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Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References enzymes (1) Show 1 protein XML

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2005-11-16 15:48:42 UTC

Update Date

2021-09-14 15:48:26 UTC

HMDB ID

HMDB0001534

Secondary Accession Numbers

HMDB01534

Metabolite Identification

Common Name

5-Formiminotetrahydrofolic acid

Description

5-Formiminotetrahydrofolic acid belongs to the class of organic compounds known as tetrahydrofolic acids. These are heterocyclic compounds based on the 5,6,7,8-tetrahydropteroic acid skeleton conjugated with at least one L-glutamic acid unit. In humans, 5-formiminotetrahydrofolic acid is involved in the metabolic disorder called the methylenetetrahydrofolate reductase deficiency (mthfrd) pathway. 5-Formiminotetrahydrofolic acid has been detected, but not quantified in, a few different foods, such as anatidaes (Anatidae), chickens (Gallus gallus), and domestic pigs (Sus scrofa domestica). This could make 5-formiminotetrahydrofolic acid a potential biomarker for the consumption of these foods. 5-Formiminotetrahydrofolic acid is a primary metabolite. Primary metabolites are metabolically or physiologically essential metabolites. They are directly involved in an organism’s growth, development or reproduction. Based on a literature review a significant number of articles have been published on 5-Formiminotetrahydrofolic acid.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI


  Mrv0541 02231219122D          

 34 36  0  0  0  0            999 V2000
   11.7507  -12.9322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4659  -12.5196    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.7507  -13.7572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0358  -12.5196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1807  -12.9322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4659  -11.6947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4659  -14.1700    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.0358  -14.1700    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.3207  -12.9322    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.0358  -11.6947    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.1807  -13.7572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8959  -12.5197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1807  -11.2883    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.3207  -13.7572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6107  -12.9322    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.6055  -14.1700    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   15.3145  -12.5197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3145  -11.6947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0293  -12.9322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0293  -11.2883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7445  -12.5197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7445  -11.6947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.4594  -11.2883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.1744  -11.6947    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   17.4594  -10.4633    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.8893  -11.2883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.8876  -10.4630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.6029  -11.7013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.5977  -10.0476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.6011  -12.5270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.3349  -11.3199    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.6047   -9.2252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.3216   -8.8169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.8968   -8.8017    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  3  2  0  0  0  0
  1  4  1  0  0  0  0
  2  5  1  0  0  0  0
  2  6  1  0  0  0  0
  3  7  1  0  0  0  0
  3  8  1  0  0  0  0
  4  9  1  0  0  0  0
  4 10  2  0  0  0  0
  5 11  1  0  0  0  0
  5 12  1  0  0  0  0
  6 13  2  0  0  0  0
  8 14  2  0  0  0  0
 12 15  1  0  0  0  0
 14 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 18 20  1  0  0  0  0
 19 21  2  0  0  0  0
 20 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 27 29  1  0  0  0  0
 28 30  1  0  0  0  0
 28 31  2  0  0  0  0
 29 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
  7 11  1  0  0  0  0
  9 14  1  0  0  0  0
 21 22  1  0  0  0  0
M  END

HMDB0001534
     RDKit          3D
5-Formiminotetrahydrofolic acid
 58 60  0  0  0  0  0  0  0  0999 V2000
    5.6394   -3.4968    1.2533 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8463   -2.8614    0.4135 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6806   -1.4882    0.7096 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2865   -0.5758   -0.2476 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9037    0.7756   -0.2137 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4480    1.6376   -1.0955 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.3458    1.2306   -1.9957 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9582    2.1364   -2.9033 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.7157   -0.0581   -2.0402 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1946   -0.9648   -1.1706 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5547   -2.2042   -1.2114 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0010    1.1527    0.7607 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0789    0.4670    2.0684 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9619   -1.0579    1.8622 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4902   -1.3988    1.8993 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7543   -0.8573    0.8175 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3412   -0.7816    0.9061 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4809   -0.1327    0.0125 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8766   -0.0571    0.1835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4797   -0.6333    1.2593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9033   -0.6326    1.5696 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2922   -0.9923    2.7311 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8203   -0.2642    0.6509 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7704    0.1171   -0.2997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4550    1.4285    0.0719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4709    1.8804   -0.8764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1946    2.3336   -2.1845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4363    2.4756   -2.8721 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2121    2.6709   -2.9692 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2928    0.0992   -1.6907 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2551    0.5954   -2.1356 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1157   -0.5816   -2.6361 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6531   -1.3236    2.2188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3283   -1.3482    1.9736 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1082   -3.0585    2.0550 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4094   -3.3757   -0.3998 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7029    1.8490   -3.5667 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6696    3.1578   -2.9336 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4140   -0.3633   -2.7460 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3020    1.8876    0.6256 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2732    0.8029    2.7263 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1003    0.6331    2.4498 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4079   -1.4706    2.8218 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0874   -0.9336    2.8406 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3450   -2.4832    1.9914 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1661   -0.4657   -0.0628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0677    0.3237   -0.8562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4327    0.4734   -0.5316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8057   -0.2040    1.6321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6829   -0.6155   -0.2456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9397    1.2185    1.0633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7319    2.2415    0.2879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0837    2.7095   -0.3383 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2954    1.0455   -0.8952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2908    3.4342   -3.6649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9622   -1.5771   -2.8203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1591   -1.7761    3.0601 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3019   -1.8956    2.6875 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  2  0
  5 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  2  0
 27 29  1  0
 24 30  1  0
 30 31  2  0
 30 32  1  0
 20 33  1  0
 33 34  2  0
 14  3  1  0
 34 17  1  0
 10  4  1  0
  1 35  1  0
  2 36  1  0
  8 37  1  0
  8 38  1  0
  9 39  1  0
 12 40  1  0
 13 41  1  0
 13 42  1  0
 14 43  1  0
 15 44  1  0
 15 45  1  0
 16 46  1  0
 18 47  1  0
 19 48  1  0
 23 49  1  0
 24 50  1  0
 25 51  1  0
 25 52  1  0
 26 53  1  0
 26 54  1  0
 29 55  1  0
 32 56  1  0
 33 57  1  0
 34 58  1  0
M  END


  Mrv0541 02231219122D          

 34 36  0  0  0  0            999 V2000
   11.7507  -12.9322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4659  -12.5196    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.7507  -13.7572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0358  -12.5196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1807  -12.9322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4659  -11.6947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4659  -14.1700    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.0358  -14.1700    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.3207  -12.9322    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.0358  -11.6947    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.1807  -13.7572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8959  -12.5197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1807  -11.2883    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.3207  -13.7572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6107  -12.9322    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.6055  -14.1700    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   15.3145  -12.5197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3145  -11.6947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0293  -12.9322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0293  -11.2883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7445  -12.5197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7445  -11.6947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.4594  -11.2883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.1744  -11.6947    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   17.4594  -10.4633    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.8893  -11.2883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.8876  -10.4630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.6029  -11.7013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.5977  -10.0476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.6011  -12.5270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.3349  -11.3199    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.6047   -9.2252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.3216   -8.8169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.8968   -8.8017    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  3  2  0  0  0  0
  1  4  1  0  0  0  0
  2  5  1  0  0  0  0
  2  6  1  0  0  0  0
  3  7  1  0  0  0  0
  3  8  1  0  0  0  0
  4  9  1  0  0  0  0
  4 10  2  0  0  0  0
  5 11  1  0  0  0  0
  5 12  1  0  0  0  0
  6 13  2  0  0  0  0
  8 14  2  0  0  0  0
 12 15  1  0  0  0  0
 14 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 18 20  1  0  0  0  0
 19 21  2  0  0  0  0
 20 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 27 29  1  0  0  0  0
 28 30  1  0  0  0  0
 28 31  2  0  0  0  0
 29 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
  7 11  1  0  0  0  0
  9 14  1  0  0  0  0
 21 22  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0001534

> <DATABASE_NAME>
hmdb

> <SMILES>
NC1=NC2=C(N(C=N)C(CNC3=CC=C(C=C3)C(=O)NC(CCC(O)=O)C(O)=O)CN2)C(=O)N1

> <INCHI_IDENTIFIER>
InChI=1S/C20H24N8O6/c21-9-28-12(8-24-16-15(28)18(32)27-20(22)26-16)7-23-11-3-1-10(2-4-11)17(31)25-13(19(33)34)5-6-14(29)30/h1-4,9,12-13,21,23H,5-8H2,(H,25,31)(H,29,30)(H,33,34)(H4,22,24,26,27,32)

> <INCHI_KEY>
YCWUVLPMLLBDCU-UHFFFAOYSA-N

> <FORMULA>
C20H24N8O6

> <MOLECULAR_WEIGHT>
472.4546

> <EXACT_MASS>
472.18188054

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_AVERAGE_POLARIZABILITY>
47.05771689075006

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(4-{[(2-amino-5-carboximidoyl-4-oxo-3,4,5,6,7,8-hexahydropteridin-6-yl)methyl]amino}phenyl)formamido]pentanedioic acid

> <ALOGPS_LOGP>
-1.83

> <JCHEM_LOGP>
-3.7565652768720494

> <ALOGPS_LOGS>
-3.46

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
3.944706211888484

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.856143553781271

> <JCHEM_PKA_STRONGEST_BASIC>
6.042592508856188

> <JCHEM_POLAR_SURFACE_AREA>
222.32999999999996

> <JCHEM_REFRACTIVITY>
139.53200000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.63e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[(4-{[(2-amino-5-carboximidoyl-4-oxo-3,6,7,8-tetrahydropteridin-6-yl)methyl]amino}phenyl)formamido]pentanedioic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0001534
     RDKit          3D
5-Formiminotetrahydrofolic acid
 58 60  0  0  0  0  0  0  0  0999 V2000
    5.6394   -3.4968    1.2533 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8463   -2.8614    0.4135 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6806   -1.4882    0.7096 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2865   -0.5758   -0.2476 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9037    0.7756   -0.2137 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4480    1.6376   -1.0955 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.3458    1.2306   -1.9957 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9582    2.1364   -2.9033 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.7157   -0.0581   -2.0402 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1946   -0.9648   -1.1706 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5547   -2.2042   -1.2114 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0010    1.1527    0.7607 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0789    0.4670    2.0684 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9619   -1.0579    1.8622 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4902   -1.3988    1.8993 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7543   -0.8573    0.8175 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3412   -0.7816    0.9061 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4809   -0.1327    0.0125 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8766   -0.0571    0.1835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4797   -0.6333    1.2593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9033   -0.6326    1.5696 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2922   -0.9923    2.7311 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8203   -0.2642    0.6509 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7704    0.1171   -0.2997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4550    1.4285    0.0719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4709    1.8804   -0.8764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1946    2.3336   -2.1845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4363    2.4756   -2.8721 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2121    2.6709   -2.9692 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2928    0.0992   -1.6907 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2551    0.5954   -2.1356 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1157   -0.5816   -2.6361 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6531   -1.3236    2.2188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3283   -1.3482    1.9736 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1082   -3.0585    2.0550 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4094   -3.3757   -0.3998 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7029    1.8490   -3.5667 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6696    3.1578   -2.9336 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4140   -0.3633   -2.7460 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3020    1.8876    0.6256 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2732    0.8029    2.7263 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1003    0.6331    2.4498 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4079   -1.4706    2.8218 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0874   -0.9336    2.8406 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3450   -2.4832    1.9914 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1661   -0.4657   -0.0628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0677    0.3237   -0.8562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4327    0.4734   -0.5316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8057   -0.2040    1.6321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6829   -0.6155   -0.2456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9397    1.2185    1.0633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7319    2.2415    0.2879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0837    2.7095   -0.3383 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2954    1.0455   -0.8952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2908    3.4342   -3.6649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9622   -1.5771   -2.8203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1591   -1.7761    3.0601 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3019   -1.8956    2.6875 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  2  0
  5 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  2  0
 27 29  1  0
 24 30  1  0
 30 31  2  0
 30 32  1  0
 20 33  1  0
 33 34  2  0
 14  3  1  0
 34 17  1  0
 10  4  1  0
  1 35  1  0
  2 36  1  0
  8 37  1  0
  8 38  1  0
  9 39  1  0
 12 40  1  0
 13 41  1  0
 13 42  1  0
 14 43  1  0
 15 44  1  0
 15 45  1  0
 16 46  1  0
 18 47  1  0
 19 48  1  0
 23 49  1  0
 24 50  1  0
 25 51  1  0
 25 52  1  0
 26 53  1  0
 26 54  1  0
 29 55  1  0
 32 56  1  0
 33 57  1  0
 34 58  1  0
M  END

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  C   UNK     0      21.935 -24.140   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0      23.270 -23.370   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0      21.935 -25.680   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      20.600 -23.370   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      24.604 -24.140   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      23.270 -21.830   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0      23.270 -26.451   0.000  0.00  0.00           N+0
HETATM    8  N   UNK     0      20.600 -26.451   0.000  0.00  0.00           N+0
HETATM    9  N   UNK     0      19.265 -24.140   0.000  0.00  0.00           N+0
HETATM   10  O   UNK     0      20.600 -21.830   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      24.604 -25.680   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      25.939 -23.370   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      24.604 -21.071   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0      19.265 -25.680   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0      27.273 -24.140   0.000  0.00  0.00           N+0
HETATM   16  N   UNK     0      17.930 -26.451   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0      28.587 -23.370   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      28.587 -21.830   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      29.921 -24.140   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      29.921 -21.071   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      31.256 -23.370   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      31.256 -21.830   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      32.591 -21.071   0.000  0.00  0.00           C+0
HETATM   24  N   UNK     0      33.926 -21.830   0.000  0.00  0.00           N+0
HETATM   25  O   UNK     0      32.591 -19.531   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      35.260 -21.071   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      35.257 -19.531   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      36.592 -21.842   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      36.582 -18.756   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      36.589 -23.384   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      37.958 -21.130   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      36.595 -17.220   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      37.934 -16.458   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      35.274 -16.430   0.000  0.00  0.00           O+0
CONECT    1    2    3    4                                                  
CONECT    2    1    5    6                                                  
CONECT    3    1    7    8                                                  
CONECT    4    1    9   10                                                  
CONECT    5    2   11   12                                                  
CONECT    6    2   13                                                       
CONECT    7    3   11                                                       
CONECT    8    3   14                                                       
CONECT    9    4   14                                                       
CONECT   10    4                                                            
CONECT   11    5    7                                                       
CONECT   12    5   15                                                       
CONECT   13    6                                                            
CONECT   14    8   16    9                                                  
CONECT   15   12   17                                                       
CONECT   16   14                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17   20                                                       
CONECT   19   17   21                                                       
CONECT   20   18   22                                                       
CONECT   21   19   22                                                       
CONECT   22   20   23   21                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23   26                                                       
CONECT   25   23                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26   29                                                       
CONECT   28   26   30   31                                                  
CONECT   29   27   32                                                       
CONECT   30   28                                                            
CONECT   31   28                                                            
CONECT   32   29   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   72    0
END

COMPND    HMDB0001534
HETATM    1  N1  UNL     1       5.639  -3.497   1.253  1.00  0.00           N  
HETATM    2  C1  UNL     1       4.846  -2.861   0.413  1.00  0.00           C  
HETATM    3  N2  UNL     1       4.681  -1.488   0.710  1.00  0.00           N  
HETATM    4  C2  UNL     1       5.287  -0.576  -0.248  1.00  0.00           C  
HETATM    5  C3  UNL     1       4.904   0.776  -0.214  1.00  0.00           C  
HETATM    6  N3  UNL     1       5.448   1.638  -1.096  1.00  0.00           N  
HETATM    7  C4  UNL     1       6.346   1.231  -1.996  1.00  0.00           C  
HETATM    8  N4  UNL     1       6.958   2.136  -2.903  1.00  0.00           N  
HETATM    9  N5  UNL     1       6.716  -0.058  -2.040  1.00  0.00           N  
HETATM   10  C5  UNL     1       6.195  -0.965  -1.171  1.00  0.00           C  
HETATM   11  O1  UNL     1       6.555  -2.204  -1.211  1.00  0.00           O  
HETATM   12  N6  UNL     1       4.001   1.153   0.761  1.00  0.00           N  
HETATM   13  C6  UNL     1       4.079   0.467   2.068  1.00  0.00           C  
HETATM   14  C7  UNL     1       3.962  -1.058   1.862  1.00  0.00           C  
HETATM   15  C8  UNL     1       2.490  -1.399   1.899  1.00  0.00           C  
HETATM   16  N7  UNL     1       1.754  -0.857   0.818  1.00  0.00           N  
HETATM   17  C9  UNL     1       0.341  -0.782   0.906  1.00  0.00           C  
HETATM   18  C10 UNL     1      -0.481  -0.133   0.013  1.00  0.00           C  
HETATM   19  C11 UNL     1      -1.877  -0.057   0.183  1.00  0.00           C  
HETATM   20  C12 UNL     1      -2.480  -0.633   1.259  1.00  0.00           C  
HETATM   21  C13 UNL     1      -3.903  -0.633   1.570  1.00  0.00           C  
HETATM   22  O2  UNL     1      -4.292  -0.992   2.731  1.00  0.00           O  
HETATM   23  N8  UNL     1      -4.820  -0.264   0.651  1.00  0.00           N  
HETATM   24  C14 UNL     1      -5.770   0.117  -0.300  1.00  0.00           C  
HETATM   25  C15 UNL     1      -6.455   1.429   0.072  1.00  0.00           C  
HETATM   26  C16 UNL     1      -7.471   1.880  -0.876  1.00  0.00           C  
HETATM   27  C17 UNL     1      -7.195   2.334  -2.185  1.00  0.00           C  
HETATM   28  O3  UNL     1      -8.436   2.476  -2.872  1.00  0.00           O  
HETATM   29  O4  UNL     1      -6.212   2.671  -2.969  1.00  0.00           O  
HETATM   30  C18 UNL     1      -5.293   0.099  -1.691  1.00  0.00           C  
HETATM   31  O5  UNL     1      -4.255   0.595  -2.136  1.00  0.00           O  
HETATM   32  O6  UNL     1      -6.116  -0.582  -2.636  1.00  0.00           O  
HETATM   33  C19 UNL     1      -1.653  -1.324   2.219  1.00  0.00           C  
HETATM   34  C20 UNL     1      -0.328  -1.348   1.974  1.00  0.00           C  
HETATM   35  H1  UNL     1       6.108  -3.058   2.055  1.00  0.00           H  
HETATM   36  H2  UNL     1       4.409  -3.376  -0.400  1.00  0.00           H  
HETATM   37  H3  UNL     1       7.703   1.849  -3.567  1.00  0.00           H  
HETATM   38  H4  UNL     1       6.670   3.158  -2.934  1.00  0.00           H  
HETATM   39  H5  UNL     1       7.414  -0.363  -2.746  1.00  0.00           H  
HETATM   40  H6  UNL     1       3.302   1.888   0.626  1.00  0.00           H  
HETATM   41  H7  UNL     1       3.273   0.803   2.726  1.00  0.00           H  
HETATM   42  H8  UNL     1       5.100   0.633   2.450  1.00  0.00           H  
HETATM   43  H9  UNL     1       4.408  -1.471   2.822  1.00  0.00           H  
HETATM   44  H10 UNL     1       2.087  -0.934   2.841  1.00  0.00           H  
HETATM   45  H11 UNL     1       2.345  -2.483   1.991  1.00  0.00           H  
HETATM   46  H12 UNL     1       2.166  -0.466  -0.063  1.00  0.00           H  
HETATM   47  H13 UNL     1      -0.068   0.324  -0.856  1.00  0.00           H  
HETATM   48  H14 UNL     1      -2.433   0.473  -0.532  1.00  0.00           H  
HETATM   49  H15 UNL     1      -5.806  -0.204   1.632  1.00  0.00           H  
HETATM   50  H16 UNL     1      -6.683  -0.616  -0.246  1.00  0.00           H  
HETATM   51  H17 UNL     1      -6.940   1.218   1.063  1.00  0.00           H  
HETATM   52  H18 UNL     1      -5.732   2.242   0.288  1.00  0.00           H  
HETATM   53  H19 UNL     1      -8.084   2.710  -0.338  1.00  0.00           H  
HETATM   54  H20 UNL     1      -8.295   1.045  -0.895  1.00  0.00           H  
HETATM   55  H21 UNL     1      -6.291   3.434  -3.665  1.00  0.00           H  
HETATM   56  H22 UNL     1      -5.962  -1.577  -2.820  1.00  0.00           H  
HETATM   57  H23 UNL     1      -2.159  -1.776   3.060  1.00  0.00           H  
HETATM   58  H24 UNL     1       0.302  -1.896   2.687  1.00  0.00           H  
CONECT    1    2    2   35
CONECT    2    3   36
CONECT    3    4   14
CONECT    4    5    5   10
CONECT    5    6   12
CONECT    6    7    7
CONECT    7    8    9
CONECT    8   37   38
CONECT    9   10   39
CONECT   10   11   11
CONECT   12   13   40
CONECT   13   14   41   42
CONECT   14   15   43
CONECT   15   16   44   45
CONECT   16   17   46
CONECT   17   18   18   34
CONECT   18   19   47
CONECT   19   20   20   48
CONECT   20   21   33
CONECT   21   22   22   23
CONECT   23   24   49
CONECT   24   25   30   50
CONECT   25   26   51   52
CONECT   26   27   53   54
CONECT   27   28   28   29
CONECT   29   55
CONECT   30   31   31   32
CONECT   32   56
CONECT   33   34   34   57
CONECT   34   58
END

HMDB0001534
     RDKit          3D
5-Formiminotetrahydrofolic acid
 58 60  0  0  0  0  0  0  0  0999 V2000
    5.6394   -3.4968    1.2533 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8463   -2.8614    0.4135 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6806   -1.4882    0.7096 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2865   -0.5758   -0.2476 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9037    0.7756   -0.2137 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4480    1.6376   -1.0955 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.3458    1.2306   -1.9957 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9582    2.1364   -2.9033 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.7157   -0.0581   -2.0402 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1946   -0.9648   -1.1706 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5547   -2.2042   -1.2114 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0010    1.1527    0.7607 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0789    0.4670    2.0684 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9619   -1.0579    1.8622 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4902   -1.3988    1.8993 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7543   -0.8573    0.8175 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3412   -0.7816    0.9061 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4809   -0.1327    0.0125 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8766   -0.0571    0.1835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4797   -0.6333    1.2593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9033   -0.6326    1.5696 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2922   -0.9923    2.7311 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8203   -0.2642    0.6509 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7704    0.1171   -0.2997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4550    1.4285    0.0719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4709    1.8804   -0.8764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1946    2.3336   -2.1845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4363    2.4756   -2.8721 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2121    2.6709   -2.9692 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2928    0.0992   -1.6907 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2551    0.5954   -2.1356 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1157   -0.5816   -2.6361 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6531   -1.3236    2.2188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3283   -1.3482    1.9736 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1082   -3.0585    2.0550 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4094   -3.3757   -0.3998 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7029    1.8490   -3.5667 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6696    3.1578   -2.9336 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4140   -0.3633   -2.7460 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3020    1.8876    0.6256 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2732    0.8029    2.7263 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1003    0.6331    2.4498 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4079   -1.4706    2.8218 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0874   -0.9336    2.8406 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3450   -2.4832    1.9914 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1661   -0.4657   -0.0628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0677    0.3237   -0.8562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4327    0.4734   -0.5316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8057   -0.2040    1.6321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6829   -0.6155   -0.2456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9397    1.2185    1.0633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7319    2.2415    0.2879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0837    2.7095   -0.3383 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2954    1.0455   -0.8952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2908    3.4342   -3.6649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9622   -1.5771   -2.8203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1591   -1.7761    3.0601 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3019   -1.8956    2.6875 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  2  0
  5 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  2  0
 27 29  1  0
 24 30  1  0
 30 31  2  0
 30 32  1  0
 20 33  1  0
 33 34  2  0
 14  3  1  0
 34 17  1  0
 10  4  1  0
  1 35  1  0
  2 36  1  0
  8 37  1  0
  8 38  1  0
  9 39  1  0
 12 40  1  0
 13 41  1  0
 13 42  1  0
 14 43  1  0
 15 44  1  0
 15 45  1  0
 16 46  1  0
 18 47  1  0
 19 48  1  0
 23 49  1  0
 24 50  1  0
 25 51  1  0
 25 52  1  0
 26 53  1  0
 26 54  1  0
 29 55  1  0
 32 56  1  0
 33 57  1  0
 34 58  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
5-Formimidoyltetrahydrofolate	Kegg
5-Formimidoyltetrahydrofolic acid	Generator
5-Formiminotetrahydrofolate	Generator

Chemical Formula

C₂₀H₂₄N₈O₆

Average Molecular Weight

472.4546

Monoisotopic Molecular Weight

472.18188054

IUPAC Name

2-[(4-{[(2-amino-5-carboximidoyl-4-oxo-3,4,5,6,7,8-hexahydropteridin-6-yl)methyl]amino}phenyl)formamido]pentanedioic acid

Traditional Name

2-[(4-{[(2-amino-5-carboximidoyl-4-oxo-3,6,7,8-tetrahydropteridin-6-yl)methyl]amino}phenyl)formamido]pentanedioic acid

CAS Registry Number

2311-81-1

SMILES

NC1=NC2=C(N(C=N)C(CNC3=CC=C(C=C3)C(=O)NC(CCC(O)=O)C(O)=O)CN2)C(=O)N1

InChI Identifier

InChI=1S/C20H24N8O6/c21-9-28-12(8-24-16-15(28)18(32)27-20(22)26-16)7-23-11-3-1-10(2-4-11)17(31)25-13(19(33)34)5-6-14(29)30/h1-4,9,12-13,21,23H,5-8H2,(H,25,31)(H,29,30)(H,33,34)(H4,22,24,26,27,32)

InChI Key

YCWUVLPMLLBDCU-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetrahydrofolic acids. These are heterocyclic compounds based on the 5,6,7,8-tetrahydropteroic acid skeleton conjugated with at least one L-glutamic acid unit.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pteridines and derivatives

Sub Class

Pterins and derivatives

Direct Parent

Tetrahydrofolic acids

Alternative Parents

Substituents

Tetrahydrofolic acid
Glutamic acid or derivatives
Hippuric acid or derivatives
Hippuric acid
N-acyl-alpha-amino acid
N-acyl-alpha amino acid or derivatives
Alpha-amino acid or derivatives
Aminobenzamide
Aminobenzoic acid or derivatives
Benzamide
Benzoic acid or derivatives
Benzoyl
Phenylalkylamine
Aniline or substituted anilines
Aminopyrimidine
Pyrimidone
Secondary aliphatic/aromatic amine
Monocyclic benzene moiety
Dicarboxylic acid or derivatives
Benzenoid
Pyrimidine
Heteroaromatic compound
Vinylogous amide
Carboxamide group
Amino acid or derivatives
Amino acid
Secondary carboxylic acid amide
Azacycle
Formamidine
Amidine
Carboxylic acid amidine
Carboxylic acid
Carboxylic acid derivative
Secondary amine
Amine
Organic nitrogen compound
Organic oxide
Carbonyl group
Organopnictogen compound
Hydrocarbon derivative
Organic oxygen compound
Imine
Organonitrogen compound
Organooxygen compound
Primary amine
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Cytoplasm (HMDB: HMDB0001534)

Source

Endogenous

Endogenous (HMDB: HMDB0001534)

Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)
Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Equine

Horse (FooDB: FOOD00378)

Process

Naturally occurring process

Biological process

Biochemical pathway

Disease pathway

Folate Malabsorption, Hereditary (HMDB: HMDB0001534)
Histidinemia (PathBank: SMP0120493)
Methylenetetrahydrofolate Reductase Deficiency (MTHFRD) (PathBank: SMP0120522)
Folate Malabsorption, Hereditary (PathBank: SMP0120656)

Drug action pathway

Methotrexate Action Pathway (HMDB: HMDB0001534)
Methotrexate Action Pathway (PathBank: SMP0000432)

Metabolic pathway

Folate Metabolism (PathBank: SMP0000801)
Histidine Metabolism (PathBank: SMP0063632)
Folate Metabolism (HMDB: HMDB0001534)

Role

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.16 g/L	ALOGPS
logP	-1.8	ALOGPS
logP	-3.8	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	2.86	ChemAxon
pKa (Strongest Basic)	6.04	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	222.33 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	139.53 m³·mol⁻¹	ChemAxon
Polarizability	47.06 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	208.554	31661259
DarkChem	[M-H]-	202.45	31661259
AllCCS	[M+H]+	204.067	32859911
AllCCS	[M-H]-	200.207	32859911
DeepCCS	[M+H]+	203.591	30932474
DeepCCS	[M-H]-	201.233	30932474
DeepCCS	[M-2H]-	234.154	30932474
DeepCCS	[M+Na]+	209.684	30932474
AllCCS	[M+H]+	204.1	32859911
AllCCS	[M+H-H2O]+	202.3	32859911
AllCCS	[M+NH4]+	205.7	32859911
AllCCS	[M+Na]+	206.1	32859911
AllCCS	[M-H]-	200.2	32859911
AllCCS	[M+Na-2H]-	201.0	32859911
AllCCS	[M+HCOO]-	202.0	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.	1.57 minutes	32390414
Predicted by Siyang on May 30, 2022	10.7215 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	8.61 minutes	32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid	430.0 seconds	40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	397.3 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	203.5 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	82.4 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	171.1 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	58.3 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	263.1 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	329.0 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	1025.9 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	592.8 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	88.6 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	742.2 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	203.7 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	269.0 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	666.9 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	569.3 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	511.6 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
5-Formiminotetrahydrofolic acid	NC1=NC2=C(N(C=N)C(CNC3=CC=C(C=C3)C(=O)NC(CCC(O)=O)C(O)=O)CN2)C(=O)N1	5906.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid	NC1=NC2=C(N(C=N)C(CNC3=CC=C(C=C3)C(=O)NC(CCC(O)=O)C(O)=O)CN2)C(=O)N1	4117.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid	NC1=NC2=C(N(C=N)C(CNC3=CC=C(C=C3)C(=O)NC(CCC(O)=O)C(O)=O)CN2)C(=O)N1	5180.3	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
5-Formiminotetrahydrofolic acid,1TMS,isomer #1	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)C(=O)O	5060.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,1TMS,isomer #2	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1	5068.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,1TMS,isomer #3	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN2	5252.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,1TMS,isomer #4	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	5081.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,1TMS,isomer #5	C[Si](C)(C)N(CC1CNC2=C(C(=O)[NH]C(N)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	5042.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,1TMS,isomer #6	C[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)C(CCC(=O)O)C(=O)O	5044.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,1TMS,isomer #7	C[Si](C)(C)N1CC(CNC2=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C2)N(C=N)C2=C1N=C(N)[NH]C2=O	4952.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,1TMS,isomer #8	C[Si](C)(C)N1C(N)=NC2=C(C1=O)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN2	5127.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #1	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)C(=O)O[Si](C)(C)C	4844.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #10	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1	4812.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #11	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1	4750.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #12	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1	4973.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #13	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	4839.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #14	C[Si](C)(C)N(C1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN2)[Si](C)(C)C	5055.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #15	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN2	5153.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #16	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	5031.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #17	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)CN2	5036.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #18	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN2	5026.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #19	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN2[Si](C)(C)C	4961.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #2	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)CN2	5026.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #20	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4967.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #21	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4748.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #22	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	4837.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #23	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4824.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #24	C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4719.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #25	C[Si](C)(C)N(CC1CNC2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4949.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #26	C[Si](C)(C)N(CC1CNC2=C(C(=O)[NH]C(N)=N2)N1C=N)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4794.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #27	C[Si](C)(C)N1CC(CNC2=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)N(C=N)C2=C1N=C(N)[NH]C2=O	4717.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #28	C[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)C(CCC(=O)O)C(=O)O	4935.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #29	C[Si](C)(C)N1CC(CNC2=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C2)N(C=N)C2=C1N=C(N)N([Si](C)(C)C)C2=O	4919.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #3	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	4816.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #4	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O	4799.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #5	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)C(=O)O	4724.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #6	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)C(=O)O	4953.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #7	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	4827.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #8	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)CN2	5035.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TMS,isomer #9	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	4850.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #1	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)CN2	4822.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #1	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)CN2	4111.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #1	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)CN2	7081.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #10	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)CN2	4808.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #10	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)CN2	4177.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #10	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)CN2	7047.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #11	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)CN2	4789.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #11	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)CN2	4183.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #11	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)CN2	7130.5	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #12	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)CN2[Si](C)(C)C	4752.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #12	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)CN2[Si](C)(C)C	4282.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #12	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)CN2[Si](C)(C)C	6832.6	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #13	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	4584.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #13	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	4075.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #13	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	6832.5	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #14	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	4496.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #14	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	4162.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #14	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	6808.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #15	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	4722.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #15	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	4189.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #15	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	7114.3	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #16	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1	4601.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #16	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1	4147.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #16	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1	7063.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #17	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O	4513.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #17	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O	4176.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #17	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O	6751.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #18	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O	4744.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #18	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O	4195.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #18	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O	7045.6	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #19	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C	4602.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #19	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C	4130.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #19	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C	7003.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #2	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	4655.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #2	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	4063.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #2	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	6924.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #20	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)C(=O)O	4739.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #20	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)C(=O)O	4270.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #20	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)C(=O)O	7021.5	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #21	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	4510.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #21	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	4198.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #21	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	6921.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #22	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	4761.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #22	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	4226.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #22	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	7256.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #23	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1	4864.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #23	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1	4251.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #23	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1	6901.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #24	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)CN2	4967.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #24	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)CN2	4208.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #24	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)CN2	6988.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #25	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	4809.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #25	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	4218.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #25	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	7201.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #26	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	4818.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #26	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	4106.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #26	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	6944.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #27	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)CN2	4817.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #27	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)CN2	4140.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #27	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)CN2	7060.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #28	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	4768.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #28	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	4204.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #28	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	6739.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #29	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	4598.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #29	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	4041.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #29	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	6761.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #3	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C	4621.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #3	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C	4019.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #3	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C	6828.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #30	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	4525.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #30	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	4121.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #30	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	6743.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #31	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	4753.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #31	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	4148.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #31	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	7044.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #32	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	4632.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #32	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	4111.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #32	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	6993.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #33	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1	4522.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #33	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1	4110.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #33	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1	6656.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #34	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1	4757.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #34	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1	4130.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #34	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1	6941.3	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #35	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	4614.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #35	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	4079.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #35	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	6900.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #36	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1	4755.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #36	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1	4201.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #36	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1	6923.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #37	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	4519.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #37	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	4145.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #37	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	6826.5	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #38	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	4771.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #38	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	4166.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #38	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	7154.5	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #39	C[Si](C)(C)N(C1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN2)[Si](C)(C)C	5047.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #39	C[Si](C)(C)N(C1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN2)[Si](C)(C)C	4429.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #39	C[Si](C)(C)N(C1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN2)[Si](C)(C)C	7036.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #4	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)C(=O)O[Si](C)(C)C	4517.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #4	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)C(=O)O[Si](C)(C)C	4109.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #4	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)C(=O)O[Si](C)(C)C	6802.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #40	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4842.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #40	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4429.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #40	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	7159.6	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #41	C[Si](C)(C)N(CC1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4876.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #41	C[Si](C)(C)N(CC1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4337.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #41	C[Si](C)(C)N(CC1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	6857.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #42	C[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(CCC(=O)O)C(=O)O	4825.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #42	C[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(CCC(=O)O)C(=O)O	4315.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #42	C[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(CCC(=O)O)C(=O)O	6954.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #43	C[Si](C)(C)N1CC(CNC2=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C2)N(C=N)C2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O	4794.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #43	C[Si](C)(C)N1CC(CNC2=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C2)N(C=N)C2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O	4399.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #43	C[Si](C)(C)N1CC(CNC2=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C2)N(C=N)C2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O	6706.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #44	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4961.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #44	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4390.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #44	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	7197.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #45	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)CN2	4968.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #45	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)CN2	4290.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #45	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)CN2	6942.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #46	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN2	4947.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #46	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN2	4278.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #46	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN2	7034.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #47	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN2[Si](C)(C)C	4949.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #47	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN2[Si](C)(C)C	4375.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #47	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN2[Si](C)(C)C	6762.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #48	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4766.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #48	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4340.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #48	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	6946.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #49	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	4834.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #49	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	4278.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #49	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	7159.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #5	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)C(=O)O[Si](C)(C)C	4771.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #5	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)C(=O)O[Si](C)(C)C	4130.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #5	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)C(=O)O[Si](C)(C)C	7098.3	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #50	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4803.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #50	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4298.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #50	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	7246.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #51	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	4803.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #51	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	4171.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #51	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	6977.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #52	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	4765.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #52	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	4288.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #52	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	6699.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #53	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	4745.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #53	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	4272.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #53	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	6777.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #54	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4764.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #54	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4293.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #54	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	7045.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #55	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	4793.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #55	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	4237.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #55	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	7116.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #56	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4762.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #56	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4233.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #56	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	7182.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #57	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	4539.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #57	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	4231.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #57	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	6787.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #58	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4514.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #58	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4200.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #58	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	6843.5	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #59	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4593.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #59	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4136.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #59	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	6913.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #6	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1	4643.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #6	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1	4076.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #6	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1	7047.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #60	C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4746.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #60	C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4296.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #60	C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	6883.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #61	C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1C=N)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4480.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #61	C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1C=N)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4165.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #61	C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1C=N)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	6664.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #62	C[Si](C)(C)N(CC1CNC2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1C=N)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4717.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #62	C[Si](C)(C)N(CC1CNC2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1C=N)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4189.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #62	C[Si](C)(C)N(CC1CNC2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1C=N)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	6963.6	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #63	C[Si](C)(C)N1CC(CNC2=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)N(C=N)C2=C1N=C(N)N([Si](C)(C)C)C2=O	4710.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #63	C[Si](C)(C)N1CC(CNC2=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)N(C=N)C2=C1N=C(N)N([Si](C)(C)C)C2=O	4253.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #63	C[Si](C)(C)N1CC(CNC2=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)N(C=N)C2=C1N=C(N)N([Si](C)(C)C)C2=O	6949.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #7	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(=O)O	4846.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #7	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(=O)O	4323.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #7	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(=O)O	7007.3	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #8	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)CN2	4957.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #8	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)CN2	4281.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #8	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)CN2	7092.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #9	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	4811.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #9	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	4288.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TMS,isomer #9	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	7303.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #1	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(=O)O[Si](C)(C)C	4682.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #1	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(=O)O[Si](C)(C)C	4196.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #1	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(=O)O[Si](C)(C)C	6463.3	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #10	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	4464.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #10	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	4041.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #10	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	6651.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #11	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C	4346.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #11	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C	4015.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #11	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C	6368.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #12	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C	4577.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #12	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C	4043.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #12	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C	6620.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #13	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	4455.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #13	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	3973.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #13	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	6568.3	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #14	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)C(=O)O[Si](C)(C)C	4558.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #14	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)C(=O)O[Si](C)(C)C	4145.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #14	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)C(=O)O[Si](C)(C)C	6640.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #15	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1	4334.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #15	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1	4062.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #15	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1	6537.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #16	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1	4582.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #16	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1	4077.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #16	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1	6833.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #17	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)[Si](C)(C)C	4613.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #17	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)[Si](C)(C)C	4258.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #17	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)[Si](C)(C)C	6522.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #18	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O	4674.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #18	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O	4230.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #18	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O	6438.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #19	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(=O)O	4623.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #19	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(=O)O	4325.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #19	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(=O)O	6320.3	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #2	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)CN2	4770.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #2	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)CN2	4139.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #2	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)CN2	6567.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #20	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(=O)O	4871.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #20	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(=O)O	4364.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #20	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(=O)O	6542.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #21	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	4663.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #21	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	4313.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #21	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	6726.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #22	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	4793.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #22	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	4259.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #22	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	6778.5	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #23	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)CN2	4773.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #23	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)CN2	4172.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #23	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)CN2	6544.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #24	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)CN2	4727.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #24	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)CN2	4203.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #24	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)CN2	6622.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #25	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)CN2[Si](C)(C)C	4768.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #25	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)CN2[Si](C)(C)C	4285.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #25	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)CN2[Si](C)(C)C	6392.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #26	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	4590.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #26	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	4230.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #26	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	6576.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #27	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C	4650.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #27	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C	4136.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #27	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C	6752.3	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #28	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1	4615.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #28	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1	4192.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #28	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1	6825.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #29	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	4596.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #29	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	4063.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #29	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	6577.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #3	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1	4648.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #3	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1	4113.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #3	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1	6769.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #30	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	4577.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #30	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	4163.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #30	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	6337.5	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #31	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	4545.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #31	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	4193.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #31	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	6413.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #32	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	4330.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #32	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	4062.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #32	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	6365.6	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #33	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	4530.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #33	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	4093.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #33	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	6623.6	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #34	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4417.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #34	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4033.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #34	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	6566.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #35	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	4512.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #35	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	4197.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #35	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	6647.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #36	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1	4310.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #36	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1	4121.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #36	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1	6542.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #37	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1	4556.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #37	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1	4142.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #37	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1	6841.5	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #38	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O	4560.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #38	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O	4188.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #38	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O	6583.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #39	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C	4358.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #39	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C	4109.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #39	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C	6485.6	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #4	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	4631.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #4	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	4004.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #4	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	6532.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #40	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C	4597.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #40	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C	4108.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #40	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C	6781.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #41	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	4584.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #41	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	4198.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #41	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	6747.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #42	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)[Si](C)(C)C	4634.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #42	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)[Si](C)(C)C	4231.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #42	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)[Si](C)(C)C	6466.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #43	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1	4682.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #43	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1	4182.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #43	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1	6354.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #44	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1	4633.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #44	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1	4275.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #44	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1	6240.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #45	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1	4861.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #45	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1	4311.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #45	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1	6458.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #46	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	4658.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #46	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	4273.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #46	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	6642.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #47	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	4787.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #47	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	4210.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #47	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	6696.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #48	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	4780.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #48	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	4120.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #48	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	6462.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #49	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)CN2	4755.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #49	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)CN2	4177.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #49	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)CN2	6568.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #5	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)CN2	4645.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #5	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)CN2	4082.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #5	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)CN2	6628.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #50	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	4777.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #50	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	4230.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #50	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	6314.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #51	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	4598.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #51	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	4186.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #51	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	6499.3	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #52	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	4646.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #52	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	4096.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #52	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	6670.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #53	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	4632.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #53	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	4173.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #53	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	6770.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #54	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	4612.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #54	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	4044.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #54	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	6523.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #55	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	4593.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #55	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	4115.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #55	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	6260.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #56	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	4570.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #56	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	4164.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #56	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	6362.6	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #57	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	4347.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #57	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	4044.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #57	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	6310.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #58	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	4550.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #58	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	4076.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #58	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	6565.5	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #59	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C	4429.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #59	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C	4019.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #59	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C	6509.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #6	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	4580.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #6	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	4130.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #6	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	6349.6	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #60	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	4543.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #60	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	4170.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #60	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	6590.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #61	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	4339.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #61	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	4100.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #61	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	6487.3	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #62	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	4582.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #62	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	4123.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #62	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	6783.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #63	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1	4575.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #63	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1	4145.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #63	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1	6501.5	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #64	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	4369.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #64	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	4079.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #64	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	6405.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #65	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	4604.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #65	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	4079.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #65	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	6695.6	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #66	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	4599.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #66	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	4164.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #66	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	6665.3	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #67	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4883.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #67	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4441.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #67	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	6710.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #68	C[Si](C)(C)N(CC1CNC2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4876.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #68	C[Si](C)(C)N(CC1CNC2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4361.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #68	C[Si](C)(C)N(CC1CNC2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	6414.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #69	C[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(CCC(=O)O)C(=O)O	4808.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #69	C[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(CCC(=O)O)C(=O)O	4368.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #69	C[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(CCC(=O)O)C(=O)O	6504.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #7	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	4454.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #7	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	3965.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #7	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	6426.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #70	C[Si](C)(C)N1CC(CNC2=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C2)N(C=N)C2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O	4865.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #70	C[Si](C)(C)N1CC(CNC2=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C2)N(C=N)C2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O	4444.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #70	C[Si](C)(C)N1CC(CNC2=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C2)N(C=N)C2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O	6321.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #71	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4628.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #71	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4387.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #71	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	6443.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #72	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	4688.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #72	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	4311.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #72	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	6612.3	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #73	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4613.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #73	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4344.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #73	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	6689.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #74	C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4649.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #74	C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4337.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #74	C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	6198.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #75	C[Si](C)(C)N(CC1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1C=N)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4637.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #75	C[Si](C)(C)N(CC1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1C=N)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4243.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #75	C[Si](C)(C)N(CC1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1C=N)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	6393.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #76	C[Si](C)(C)N1CC(CNC2=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)N(C=N)C2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O	4577.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #76	C[Si](C)(C)N1CC(CNC2=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)N(C=N)C2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O	4332.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #76	C[Si](C)(C)N1CC(CNC2=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)N(C=N)C2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O	6283.6	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #77	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4799.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #77	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4338.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #77	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	6506.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #78	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	4823.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #78	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	4255.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #78	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	6656.5	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #79	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4770.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #79	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4287.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #79	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	6737.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #8	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	4349.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #8	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	4066.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #8	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	6452.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #80	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	4760.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #80	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	4183.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #80	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	6494.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #81	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	4776.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #81	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	4287.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #81	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	6272.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #82	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	4732.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #82	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	4297.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #82	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	6352.5	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #83	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	4618.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #83	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	4253.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #83	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	6463.6	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #84	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4559.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #84	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4258.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #84	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	6538.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #85	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4619.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #85	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4162.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #85	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	6700.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #86	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	4557.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #86	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	4177.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #86	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	6288.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #87	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	4608.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #87	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	4234.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #87	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	6617.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #88	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4558.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #88	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4219.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #88	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	6678.6	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #89	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4578.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #89	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4136.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #89	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	6703.3	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #9	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	4564.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #9	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	4100.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #9	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	6711.3	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #90	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4337.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #90	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4132.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #90	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	6408.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #91	C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1C=N)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4531.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #91	C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1C=N)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4198.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,4TMS,isomer #91	C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1C=N)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	6511.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #1	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)[Si](C)(C)C	4533.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #1	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)[Si](C)(C)C	4179.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #1	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)[Si](C)(C)C	6073.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #10	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1	4468.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #10	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1	4102.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #10	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1	6128.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #11	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	4522.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #11	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	4000.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #11	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	6291.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #12	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	4522.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #12	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	4084.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #12	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	6379.5	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #13	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	4493.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #13	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	3976.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #13	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	6141.5	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #14	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	4452.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #14	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	4035.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #14	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	5897.6	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #15	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	4423.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #15	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	4108.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #15	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	5993.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #16	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	4242.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #16	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	3981.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #16	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	6062.6	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #17	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	4448.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #17	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	4020.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #17	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	6300.6	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #18	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C	4333.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #18	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C	3957.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #18	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C	6236.5	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #19	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	4412.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #19	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	4133.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #19	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)C=C1)[Si](C)(C)C	6351.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #2	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C	4566.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #2	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C	4104.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #2	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C	5966.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #20	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	4208.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #20	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	4033.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #20	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	6240.5	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #21	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	4444.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #21	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	4046.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #21	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	6515.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #22	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C	4453.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #22	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C	4077.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #22	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C	6264.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #23	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	4244.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #23	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	3993.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #23	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	6161.3	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #24	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	4475.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #24	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	3994.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #24	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	6431.6	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #25	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1	4437.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #25	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1	4098.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #25	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1	6422.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #26	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	4518.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #26	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	4158.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #26	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	6028.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #27	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)[Si](C)(C)C	4453.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #27	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)[Si](C)(C)C	4274.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #27	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)[Si](C)(C)C	5944.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #28	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)[Si](C)(C)C	4643.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #28	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)[Si](C)(C)C	4303.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #28	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)[Si](C)(C)C	6127.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #29	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1	4482.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #29	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1	4248.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #29	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1	6313.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #3	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(=O)O[Si](C)(C)C	4509.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #3	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(=O)O[Si](C)(C)C	4221.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #3	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(=O)O[Si](C)(C)C	5870.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #30	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O	4531.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #30	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O	4237.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #30	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O	5857.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #31	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O	4723.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #31	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O	4254.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #31	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1)C(=O)O	6037.3	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #32	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C	4571.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #32	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C	4181.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #32	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C	6234.3	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #33	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(=O)O	4704.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #33	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(=O)O	4374.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #33	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(=O)O	5973.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #34	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	4505.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #34	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	4289.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #34	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	6093.5	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #35	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	4720.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #35	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	4322.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #35	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	6323.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #36	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	4652.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #36	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	4230.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #36	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1	6170.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #37	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C	4652.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #37	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C	4122.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #37	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C	6300.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #38	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1	4590.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #38	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1	4180.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #38	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1	6377.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #39	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	4584.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #39	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	4095.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #39	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	6149.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #4	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(=O)O[Si](C)(C)C	4698.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #4	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(=O)O[Si](C)(C)C	4249.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #4	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)C(=O)O[Si](C)(C)C	6055.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #40	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	4620.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #40	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	4178.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #40	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	5946.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #41	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	4566.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #41	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	4228.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #41	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	6030.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #42	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C	4482.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #42	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C	4129.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #42	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C	6125.3	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #43	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1	4419.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #43	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1	4166.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #43	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1	6199.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #44	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4482.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #44	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4070.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #44	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	6340.5	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #45	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	4428.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #45	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	4091.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #45	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	5962.6	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #46	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	4419.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #46	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	4125.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #46	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	6266.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #47	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4217.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #47	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4048.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #47	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	6159.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #48	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4438.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #48	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4053.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #48	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	6431.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #49	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1	4409.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #49	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1	4145.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #49	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1	6429.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #5	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1	4549.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #5	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1	4178.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #5	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1	6253.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #50	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C	4465.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #50	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C	4129.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #50	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C	6367.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #51	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	4532.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #51	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	4148.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #51	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	5983.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #52	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)[Si](C)(C)C	4479.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #52	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)[Si](C)(C)C	4257.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #52	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)[Si](C)(C)C	5901.5	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #53	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)[Si](C)(C)C	4656.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #53	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)[Si](C)(C)C	4289.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #53	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1)[Si](C)(C)C	6082.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #54	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	4499.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #54	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	4239.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #54	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	6267.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #55	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1	4538.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #55	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1	4210.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #55	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1	5793.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #56	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1	4724.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #56	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1	4225.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #56	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)[Si](C)(C)C)C=C1	5970.5	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #57	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	4562.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #57	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	4164.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #57	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	6166.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #58	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1	4707.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #58	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1	4339.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #58	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N3)N2C=N)C=C1	5907.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #59	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	4512.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #59	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	4266.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #59	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	6028.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #6	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1	4626.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #6	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1	4114.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #6	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1	6315.6	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #60	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	4717.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #60	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	4291.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #60	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	6254.6	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #61	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	4664.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #61	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	4207.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #61	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1	6107.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #62	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	4666.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #62	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	4102.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #62	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	6233.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #63	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	4613.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #63	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	4173.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #63	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	6332.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #64	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	4608.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #64	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	4085.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #64	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	6104.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #65	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	4637.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #65	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	4153.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #65	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	5882.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #66	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	4593.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #66	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	4209.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #66	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	5988.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #67	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	4496.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #67	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	4112.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #67	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	6060.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #68	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	4445.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #68	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	4157.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #68	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	6155.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #69	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C	4502.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #69	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C	4063.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #69	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C	6295.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #7	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	4607.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #7	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	4041.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #7	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2	6091.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #70	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	4447.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #70	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	4080.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #70	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	5919.3	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #71	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	4441.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #71	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	4117.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #71	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(=O)N([Si](C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C)C=C1)[Si](C)(C)C	6217.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #72	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C	4237.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #72	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C	4041.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #72	C[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C	6109.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #73	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C	4463.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #73	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C	4045.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #73	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C	6381.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #74	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	4441.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #74	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	4136.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #74	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1	6381.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #75	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	4487.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #75	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	4113.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #75	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C	6297.3	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #76	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4745.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #76	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4419.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #76	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	6097.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #77	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	4757.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #77	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	4308.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #77	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	6220.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #78	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4667.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #78	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4363.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #78	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	6303.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #79	C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4730.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #79	C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4370.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #79	C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	5870.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #8	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)CN2	4588.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #8	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)CN2	4120.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #8	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)CN2	6189.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #80	C[Si](C)(C)N(CC1CNC2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1C=N)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4685.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #80	C[Si](C)(C)N(CC1CNC2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1C=N)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4279.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #80	C[Si](C)(C)N(CC1CNC2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1C=N)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	6017.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #81	C[Si](C)(C)N1CC(CNC2=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)N(C=N)C2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O	4657.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #81	C[Si](C)(C)N1CC(CNC2=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)N(C=N)C2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O	4393.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #81	C[Si](C)(C)N1CC(CNC2=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)N(C=N)C2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O	5959.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #82	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	4546.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #82	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	4310.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #82	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	5994.3	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #83	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4450.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #83	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4330.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #83	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	6074.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #84	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4519.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #84	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4231.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #84	C[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	6205.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #85	C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1C=N)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4494.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #85	C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1C=N)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4265.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #85	C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1C=N)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	5839.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #86	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	4674.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #86	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	4244.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #86	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C	6067.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #87	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4612.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #87	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	4268.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #87	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1	6147.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #88	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4639.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #88	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4167.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #88	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)N([Si](C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	6268.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #89	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	4603.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #89	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	4206.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #89	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C	5922.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #9	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	4604.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #9	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	4174.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #9	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)CN2[Si](C)(C)C	5958.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #90	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4444.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #90	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4177.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #90	C[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C)[NH]C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	6093.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #91	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4441.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #91	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4163.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,5TMS,isomer #91	C[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C)C2=O)N([Si](C)(C)C)CC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C	6302.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)C(=O)O	5319.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1	5312.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN2	5432.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	5308.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N(CC1CNC2=C(C(=O)[NH]C(N)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	5261.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)C(CCC(=O)O)C(=O)O	5302.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N1CC(CNC2=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C2)N(C=N)C2=C1N=C(N)[NH]C2=O	5208.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,1TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N1C(N)=NC2=C(C1=O)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN2	5319.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)C(=O)O[Si](C)(C)C(C)(C)C	5345.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C(C)(C)C)C=C1	5300.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1	5234.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N3)N2C=N)C=C1	5431.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C1	5320.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)N(C1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN2)[Si](C)(C)C(C)(C)C	5445.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN2	5531.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C(C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	5423.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C(C)(C)C)CN2	5421.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)CN2	5441.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN2[Si](C)(C)C(C)(C)C	5362.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C1)CN2	5453.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #20	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C(C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	5392.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C(C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	5216.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #22	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C(C)(C)C	5282.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #23	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1	5292.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #24	CC(C)(C)[Si](C)(C)N(CC1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	5200.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #25	CC(C)(C)[Si](C)(C)N(CC1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	5378.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #26	CC(C)(C)[Si](C)(C)N(CC1CNC2=C(C(=O)[NH]C(N)=N2)N1C=N)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1	5262.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #27	CC(C)(C)[Si](C)(C)N1CC(CNC2=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C2)N(C=N)C2=C1N=C(N)[NH]C2=O	5212.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #28	CC(C)(C)[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N3)N2C=N)C=C1)C(CCC(=O)O)C(=O)O	5387.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #29	CC(C)(C)[Si](C)(C)N1CC(CNC2=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C2)N(C=N)C2=C1N=C(N)N([Si](C)(C)C(C)(C)C)C2=O	5375.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)[Si](C)(C)C(C)(C)C	5329.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C(C)(C)C)C=C1)C(=O)O	5298.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)C(=O)O	5219.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N3)N2C=N)C=C1)C(=O)O	5413.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C1	5312.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C1)CN2	5469.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)[Si](C)(C)C(C)(C)C	5344.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C=C1)CN2	5422.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C=C1)CN2	4729.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C=C1)CN2	6736.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C1)[Si](C)(C)C(C)(C)C)CN2	5386.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C1)[Si](C)(C)C(C)(C)C)CN2	4711.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C1)[Si](C)(C)C(C)(C)C)CN2	6730.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)CN2	5374.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)CN2	4742.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)CN2	6784.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C1)CN2[Si](C)(C)C(C)(C)C	5311.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C1)CN2[Si](C)(C)C(C)(C)C	4836.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C1)CN2[Si](C)(C)C(C)(C)C	6584.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C	5236.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C	4591.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C	6581.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)[Si](C)(C)C(C)(C)C	5154.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)[Si](C)(C)C(C)(C)C	4676.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)[Si](C)(C)C(C)(C)C	6610.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N3)N2C=N)C=C1)[Si](C)(C)C(C)(C)C	5355.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N3)N2C=N)C=C1)[Si](C)(C)C(C)(C)C	4753.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N3)N2C=N)C=C1)[Si](C)(C)C(C)(C)C	6766.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1	5242.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1	4595.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1	6776.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C(C)(C)C)C=C1)C(=O)O	5185.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C(C)(C)C)C=C1)C(=O)O	4675.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C(C)(C)C)C=C1)C(=O)O	6559.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C(C)(C)C)C=C1)C(=O)O	5397.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C(C)(C)C)C=C1)C(=O)O	4742.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C(C)(C)C)C=C1)C(=O)O	6713.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C1)[Si](C)(C)C(C)(C)C	5246.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C1)[Si](C)(C)C(C)(C)C	4556.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C1)[Si](C)(C)C(C)(C)C	6728.6	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)[Si](C)(C)C(C)(C)C	5315.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)[Si](C)(C)C(C)(C)C	4631.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)[Si](C)(C)C(C)(C)C	6644.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N3)N2C=N)C=C1)C(=O)O	5386.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N3)N2C=N)C=C1)C(=O)O	4842.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N3)N2C=N)C=C1)C(=O)O	6743.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #21	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C(C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C1	5169.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #21	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C(C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C1	4648.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #21	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C(C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C1	6707.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #22	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C(C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C1	5388.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #22	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C(C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C1	4715.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #22	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C(C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C1	6894.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N3)N2C=N)C=C1	5458.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N3)N2C=N)C=C1	4844.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N3)N2C=N)C=C1	6568.5	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #24	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C1)CN2	5538.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #24	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C1)CN2	4842.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #24	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C1)CN2	6641.3	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #25	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C(C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C1	5401.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #25	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C(C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C1	4747.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #25	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C(C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C1	6863.6	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #26	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)CN2	5407.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #26	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)CN2	4684.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #26	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)CN2	6667.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #27	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1)CN2	5406.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #27	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1)CN2	4740.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #27	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1)CN2	6747.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #28	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C1)CN2[Si](C)(C)C(C)(C)C	5343.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #28	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C1)CN2[Si](C)(C)C(C)(C)C	4804.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #28	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C1)CN2[Si](C)(C)C(C)(C)C	6523.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C	5246.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C	4592.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C	6539.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C(C)(C)C)C=C1)C(=O)O[Si](C)(C)C(C)(C)C	5272.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C(C)(C)C)C=C1)C(=O)O[Si](C)(C)C(C)(C)C	4586.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C(C)(C)C)C=C1)C(=O)O[Si](C)(C)C(C)(C)C	6567.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)[Si](C)(C)C(C)(C)C	5173.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)[Si](C)(C)C(C)(C)C	4669.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)[Si](C)(C)C(C)(C)C	6570.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N3)N2C=N)C=C1)[Si](C)(C)C(C)(C)C	5380.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N3)N2C=N)C=C1)[Si](C)(C)C(C)(C)C	4754.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N3)N2C=N)C=C1)[Si](C)(C)C(C)(C)C	6725.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #32	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1	5263.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #32	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1	4592.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #32	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1	6735.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C(C)(C)C)C=C1	5189.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C(C)(C)C)C=C1	4639.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)[Si](C)(C)C(C)(C)C)C=C1	6494.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C(C)(C)C)C=C1	5404.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C(C)(C)C)C=C1	4710.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N3)N2C=N)[Si](C)(C)C(C)(C)C)C=C1	6646.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #35	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C	5260.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #35	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C	4538.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #35	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C	6663.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #36	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N3)N2C=N)C=C1	5403.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #36	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N3)N2C=N)C=C1	4807.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #36	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N3)N2C=N)C=C1	6679.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #37	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C(C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C1	5181.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #37	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C(C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C1	4624.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #37	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C(C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C1	6644.5	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #38	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C(C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C1	5406.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #38	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C(C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C1	4691.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #38	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C(C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C1	6829.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #39	CC(C)(C)[Si](C)(C)N(C1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN2)[Si](C)(C)C(C)(C)C	5585.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #39	CC(C)(C)[Si](C)(C)N(C1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN2)[Si](C)(C)C(C)(C)C	4974.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #39	CC(C)(C)[Si](C)(C)N(C1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN2)[Si](C)(C)C(C)(C)C	6644.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)C(=O)O[Si](C)(C)C(C)(C)C	5177.9	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)C(=O)O[Si](C)(C)C(C)(C)C	4678.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)[NH]C(N)=N3)N2C=N)C=C1)C(=O)O[Si](C)(C)C(C)(C)C	6592.7	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #40	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	5444.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #40	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4897.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #40	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	6791.3	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #41	CC(C)(C)[Si](C)(C)N(CC1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	5433.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #41	CC(C)(C)[Si](C)(C)N(CC1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4833.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #41	CC(C)(C)[Si](C)(C)N(CC1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	6552.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #42	CC(C)(C)[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N3)N2C=N)C=C1)C(CCC(=O)O)C(=O)O	5394.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #42	CC(C)(C)[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N3)N2C=N)C=C1)C(CCC(=O)O)C(=O)O	4849.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #42	CC(C)(C)[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N3)N2C=N)C=C1)C(CCC(=O)O)C(=O)O	6616.5	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #43	CC(C)(C)[Si](C)(C)N1CC(CNC2=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C2)N(C=N)C2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C2=O	5363.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #43	CC(C)(C)[Si](C)(C)N1CC(CNC2=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C2)N(C=N)C2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C2=O	4920.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #43	CC(C)(C)[Si](C)(C)N1CC(CNC2=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C2)N(C=N)C2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C2=O	6468.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #44	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	5531.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #44	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4865.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #44	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	6818.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #45	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C(C)(C)C)CN2	5534.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #45	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C(C)(C)C)CN2	4832.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #45	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C(C)(C)C)CN2	6630.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #46	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)CN2	5506.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #46	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)CN2	4851.4	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #46	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)CN2	6691.0	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #47	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN2[Si](C)(C)C(C)(C)C	5527.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #47	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN2[Si](C)(C)C(C)(C)C	4933.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #47	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN2[Si](C)(C)C(C)(C)C	6511.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #48	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C(C)(C)C)[NH]C2=O)N([Si](C)(C)C(C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	5339.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #48	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C(C)(C)C)[NH]C2=O)N([Si](C)(C)C(C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4812.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #48	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C(C)(C)C)[NH]C2=O)N([Si](C)(C)C(C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	6711.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #49	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C(C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C(C)(C)C	5414.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #49	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C(C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C(C)(C)C	4726.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #49	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C(C)(C)C)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C(C)(C)C	6854.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N3)N2C=N)C=C1)C(=O)O[Si](C)(C)C(C)(C)C	5404.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N3)N2C=N)C=C1)C(=O)O[Si](C)(C)C(C)(C)C	4754.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N3)N2C=N)C=C1)C(=O)O[Si](C)(C)C(C)(C)C	6745.3	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #50	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C(C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1	5391.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #50	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C(C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1	4773.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #50	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C(C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1	6910.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #51	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)CN2	5380.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #51	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)CN2	4701.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #51	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)CN2	6709.6	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #52	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C(C)(C)C)CN2[Si](C)(C)C(C)(C)C	5341.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #52	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C(C)(C)C)CN2[Si](C)(C)C(C)(C)C	4798.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #52	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C(C)(C)C)CN2[Si](C)(C)C(C)(C)C	6517.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #53	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)CN2[Si](C)(C)C(C)(C)C	5305.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #53	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)CN2[Si](C)(C)C(C)(C)C	4814.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #53	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N(C=N)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)CN2[Si](C)(C)C(C)(C)C	6576.3	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #54	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C(C)(C)C)C2=O)N([Si](C)(C)C(C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	5395.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #54	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C(C)(C)C)C2=O)N([Si](C)(C)C(C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4775.8	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #54	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C(C)(C)C)C2=O)N([Si](C)(C)C(C)(C)C)CC1CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	6790.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #55	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C(C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C(C)(C)C	5411.1	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #55	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C(C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C(C)(C)C	4678.9	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #55	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C(C)(C)C)C2=O)NCC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C(C)(C)C	6803.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #56	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C(C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1	5373.7	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #56	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C(C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1	4709.0	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #56	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)N([Si](C)(C)C(C)(C)C)C2=O)NCC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1	6852.4	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #57	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C(C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C(C)(C)C	5199.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #57	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C(C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C(C)(C)C	4638.1	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #57	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C(C)(C)C)CC1CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C(C)(C)C	6618.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #58	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C(C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1	5160.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #58	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C(C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1	4636.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #58	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)N([Si](C)(C)C(C)(C)C)CC1CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1	6665.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #59	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C	5239.6	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #59	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C	4556.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #59	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C	6678.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C=C1	5276.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C=C1	4585.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C=C1	6759.3	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #60	CC(C)(C)[Si](C)(C)N(CC1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	5405.4	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #60	CC(C)(C)[Si](C)(C)N(CC1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	4812.6	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #60	CC(C)(C)[Si](C)(C)N(CC1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1C=N)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1	6653.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #61	CC(C)(C)[Si](C)(C)N(CC1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1C=N)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1	5150.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #61	CC(C)(C)[Si](C)(C)N(CC1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1C=N)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1	4656.2	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #61	CC(C)(C)[Si](C)(C)N(CC1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1C=N)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1	6512.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #62	CC(C)(C)[Si](C)(C)N(CC1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1C=N)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1	5354.0	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #62	CC(C)(C)[Si](C)(C)N(CC1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1C=N)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1	4725.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #62	CC(C)(C)[Si](C)(C)N(CC1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1C=N)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1	6670.1	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #63	CC(C)(C)[Si](C)(C)N1CC(CNC2=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C2)N(C=N)C2=C1N=C(N)N([Si](C)(C)C(C)(C)C)C2=O	5356.8	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #63	CC(C)(C)[Si](C)(C)N1CC(CNC2=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C2)N(C=N)C2=C1N=C(N)N([Si](C)(C)C(C)(C)C)C2=O	4816.7	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #63	CC(C)(C)[Si](C)(C)N1CC(CNC2=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C2)N(C=N)C2=C1N=C(N)N([Si](C)(C)C(C)(C)C)C2=O	6705.2	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N3)N2C=N)C=C1)C(=O)O	5443.2	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N3)N2C=N)C=C1)C(=O)O	4877.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N3)N2C=N)C=C1)C(=O)O	6631.8	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C1)CN2	5526.3	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C1)CN2	4869.3	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N(C=N)C(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C1)CN2	6702.9	Standard polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C(C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C1	5369.5	Semi standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C(C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C1	4770.5	Standard non polar	33892256
5-Formiminotetrahydrofolic acid,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=CN1C2=C(N=C(N[Si](C)(C)C(C)(C)C)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C1	6925.5	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Formiminotetrahydrofolic acid GC-MS (Non-derivatized) - 70eV, Positive	splash10-004i-1444900000-227217d565370340172f	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Formiminotetrahydrofolic acid GC-MS (2 TMS) - 70eV, Positive	splash10-0uk9-3331397000-01cb800442c1e1c96e39	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Formiminotetrahydrofolic acid GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-Formiminotetrahydrofolic acid GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-Formiminotetrahydrofolic acid 10V, Positive-QTOF	splash10-0a4i-0031900000-bf344326ac22f287aa35	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-Formiminotetrahydrofolic acid 20V, Positive-QTOF	splash10-0a6r-0393500000-8fc7ac6d67efd44cfedc	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-Formiminotetrahydrofolic acid 40V, Positive-QTOF	splash10-0zfr-1791000000-b39eab982a3930dc5ed6	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-Formiminotetrahydrofolic acid 10V, Negative-QTOF	splash10-00di-0000900000-d1729aece34f4a1b8ce0	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-Formiminotetrahydrofolic acid 20V, Negative-QTOF	splash10-0ufu-0012900000-ff4f88b4c580913c8482	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-Formiminotetrahydrofolic acid 40V, Negative-QTOF	splash10-0006-9463200000-b3fbdf5da75999d625c5	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-Formiminotetrahydrofolic acid 10V, Negative-QTOF	splash10-0zmi-0000900000-f515f485aa42a19ee541	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-Formiminotetrahydrofolic acid 20V, Negative-QTOF	splash10-004i-0100900000-9ce99e7432941cb7fab8	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-Formiminotetrahydrofolic acid 40V, Negative-QTOF	splash10-0fbc-3921300000-4463ee0ccf9cabfe0511	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-Formiminotetrahydrofolic acid 10V, Positive-QTOF	splash10-00fr-0006900000-7715c5fc87f9023ea537	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-Formiminotetrahydrofolic acid 20V, Positive-QTOF	splash10-004i-1229100000-ab66a6f2441632392430	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-Formiminotetrahydrofolic acid 40V, Positive-QTOF	splash10-001i-0931000000-f3b5c77212f13c77a8dd	2021-09-22	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm (predicted from logP)

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Name	SMPDB/PathBank	KEGG
Histidine metabolism
One carbon pool by folate	Not Available
Methylenetetrahydrofolate Reductase Deficiency (MTHFRD)		Not Available
Methotrexate Action Pathway		Not Available
Folate malabsorption, hereditary		Not Available

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB022676

KNApSAcK ID

Not Available

Chemspider ID

11267158

KEGG Compound ID

C00664

BioCyc ID

Not Available

BiGG ID

35643

Wikipedia Link

5-Formiminotetrahydrofolate

METLIN ID

6305

PubChem Compound

530

PDB ID

Not Available

ChEBI ID

15639

Food Biomarker Ontology

Not Available

VMH ID

5FORTHF

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Not Available

Enzymes

Enzyme Details

1. Formimidoyltransferase-cyclodeaminase

General function:: Involved in catalytic activity
Specific function:: Folate-dependent enzyme, that displays both transferase and deaminase activity. Serves to channel one-carbon units from formiminoglutamate to the folate pool. Binds and promotes bundling of vimentin filaments originating from the Golgi (By similarity).
Gene Name:: FTCD
Uniprot ID:: O95954
Molecular weight:: 58925.93

Reactions

5-Formiminotetrahydrofolic acid + Glutamic acid → Tetrahydrofolic acid + Formiminoglutamic acid	details
5-Formiminotetrahydrofolic acid → 5,10-Methenyltetrahydrofolic acid + Ammonia	details
5-Formiminotetrahydrofolic acid + Glutamic acid → Tetrahydrofolic acid + Formiminoglutamic acid	details
5-Formiminotetrahydrofolic acid + Hydrogen Ion → 5,10-Methenyltetrahydrofolic acid + Ammonia	details

Showing metabocard for 5-Formiminotetrahydrofolic acid (HMDB0001534)

MOL for HMDB0001534 (5-Formiminotetrahydrofolic acid)

3D MOL for HMDB0001534 (5-Formiminotetrahydrofolic acid)

3D SDF for HMDB0001534 (5-Formiminotetrahydrofolic acid)

3D-SDF for HMDB0001534 (5-Formiminotetrahydrofolic acid)

PDB for HMDB0001534 (5-Formiminotetrahydrofolic acid)

3D PDB for HMDB0001534 (5-Formiminotetrahydrofolic acid)

SMILES for HMDB0001534 (5-Formiminotetrahydrofolic acid)

INCHI for HMDB0001534 (5-Formiminotetrahydrofolic acid)

Structure for HMDB0001534 (5-Formiminotetrahydrofolic acid)

3D Structure for HMDB0001534 (5-Formiminotetrahydrofolic acid)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

Enzymes

Reactions