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Showing metabocard for 5,6,7,8-Tetrahydrofolic acid (HMDB0243631)

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Record Information
Version5.0
StatusDetected but not Quantified
Creation Date2021-09-10 20:52:46 UTC
Update Date2021-09-26 22:50:47 UTC
HMDB IDHMDB0243631
Secondary Accession NumbersNone
Metabolite Identification
Common Name5,6,7,8-Tetrahydrofolic acid
Description5,6,7,8-Tetrahydrofolic acid, also known as tetrahydropteroylglutamate, 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. Based on a literature review a significant number of articles have been published on 5,6,7,8-Tetrahydrofolic acid. This compound has been identified in human blood as reported by (PMID: 31557052 ). 5,6,7,8-tetrahydrofolic acid is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 5,6,7,8-Tetrahydrofolic acid is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.
Structure
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MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0243631 (5,6,7,8-Tetrahydrofolic acid)


  Mrv1652305221920552D          

 32 34  0  0  0  0            999 V2000
   -2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -3.7125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5737   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  1  0  0  0  0
  4  2  2  0  0  0  0
  6  5  1  0  0  0  0
  9  1  2  0  0  0  0
  9  2  1  0  0  0  0
 10  3  2  0  0  0  0
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 11  8  1  0  0  0  0
 12  5  1  0  0  0  0
 13  6  1  0  0  0  0
 15 14  2  0  0  0  0
 16  9  1  0  0  0  0
 17 14  1  0  0  0  0
 18 12  1  0  0  0  0
 20 19  2  0  0  0  0
 21  7  1  0  0  0  0
 21 10  1  0  0  0  0
 22  8  1  0  0  0  0
 22 15  1  0  0  0  0
 23 11  1  0  0  0  0
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 25 19  1  0  0  0  0
 26 17  2  0  0  0  0
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 28 13  1  0  0  0  0
 29 16  2  0  0  0  0
 30 17  1  0  0  0  0
 31 18  2  0  0  0  0
 32 18  1  0  0  0  0
M  END
Download

3D MOL for HMDB0243631 (5,6,7,8-Tetrahydrofolic acid)

HMDB0243631
     RDKit          3D
5,6,7,8-Tetrahydrofolic acid
 55 57  0  0  0  0  0  0  0  0999 V2000
   -8.9661    2.4320    0.8218 N   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1208    1.4588    0.7589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1940    0.3564    1.5260 N   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2897   -0.6411    1.4324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3554   -1.7839    2.2199 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2370   -0.5473    0.5173 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2028    0.6015   -0.2476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1172    1.5791   -0.1324 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1175    0.6938   -1.1851 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5399   -0.5196   -1.6747 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2886   -1.5548   -0.6267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9302   -1.3440    0.0373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8729   -1.4290   -0.9350 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4948   -1.2570   -0.5793 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4802   -1.3096   -1.5500 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8146   -1.1431   -1.2434 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2252   -0.9155    0.0641 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6497   -0.7370    0.3733 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4307   -1.7290    0.4403 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1551    0.5439    0.5942 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.5778    0.7439    0.8976 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2383    1.4620   -0.2576 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6783    1.7004   -0.0336 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5267    0.5334    0.1630 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3039   -0.3330    1.0573 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6505    0.2895   -0.6327 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6259    1.5169    2.1507 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5682    1.9042    2.7553 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8321    1.8460    2.7114 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2512   -0.8635    1.0301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1012   -1.0323    0.7183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2797   -1.5768    0.4013 N   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7852    2.4171    1.4978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7834   -1.7709    3.0742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0216    2.4324   -0.7561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7704    1.6183   -1.4900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6128   -0.2903   -2.2426 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.3184   -2.5496   -1.1397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7829   -2.0665    0.8424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9344   -0.2781    0.4030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1193   -1.6188   -1.9266 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1644   -1.4838   -2.5717 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6010   -1.1831   -2.0034 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5482    1.3801    0.5510 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0275   -0.2528    0.9640 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7429    2.4482   -0.4590 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0964    0.8233   -1.1651 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0742    2.2349   -0.9608 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8437    2.4907    0.7602 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6474    0.4892   -1.6384 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3666    1.1846    3.2567 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5688   -0.6831    2.0679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8396   -0.9849    1.5050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3442   -2.3554    1.1218 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  2  0
  4  5  1  0
  4  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
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 16 17  2  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
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 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 21 27  1  0
 27 28  2  0
 27 29  1  0
 17 30  1  0
 30 31  2  0
 11 32  1  0
  8  2  1  0
 31 14  1  0
 32  6  1  0
  1 33  1  0
  5 34  1  0
  8 35  1  0
  9 36  1  0
 10 37  1  0
 10 38  1  0
 11 39  1  0
 12 40  1  0
 12 41  1  0
 13 42  1  0
 15 43  1  0
 16 44  1  0
 20 45  1  0
 21 46  1  0
 22 47  1  0
 22 48  1  0
 23 49  1  0
 23 50  1  0
 26 51  1  0
 29 52  1  0
 30 53  1  0
 31 54  1  0
 32 55  1  0
M  END
Download

3D SDF for HMDB0243631 (5,6,7,8-Tetrahydrofolic acid)


  Mrv1652305221920552D          

 32 34  0  0  0  0            999 V2000
   -2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -3.7125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5737   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  1  0  0  0  0
  4  2  2  0  0  0  0
  6  5  1  0  0  0  0
  9  1  2  0  0  0  0
  9  2  1  0  0  0  0
 10  3  2  0  0  0  0
 10  4  1  0  0  0  0
 11  7  1  0  0  0  0
 11  8  1  0  0  0  0
 12  5  1  0  0  0  0
 13  6  1  0  0  0  0
 15 14  2  0  0  0  0
 16  9  1  0  0  0  0
 17 14  1  0  0  0  0
 18 12  1  0  0  0  0
 20 19  2  0  0  0  0
 21  7  1  0  0  0  0
 21 10  1  0  0  0  0
 22  8  1  0  0  0  0
 22 15  1  0  0  0  0
 23 11  1  0  0  0  0
 23 14  1  0  0  0  0
 24 12  1  0  0  0  0
 24 16  1  0  0  0  0
 25 15  1  0  0  0  0
 25 19  1  0  0  0  0
 26 17  2  0  0  0  0
 26 19  1  0  0  0  0
 27 13  2  0  0  0  0
 28 13  1  0  0  0  0
 29 16  2  0  0  0  0
 30 17  1  0  0  0  0
 31 18  2  0  0  0  0
 32 18  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0243631

> <DATABASE_NAME>
hmdb

> <SMILES>
OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(N2)C(O)=NC(=N)N3)C=C1)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C19H23N7O6/c20-19-25-15-14(17(30)26-19)23-11(8-22-15)7-21-10-3-1-9(2-4-10)16(29)24-12(18(31)32)5-6-13(27)28/h1-4,11-12,21,23H,5-8H2,(H,24,29)(H,27,28)(H,31,32)(H4,20,22,25,26,30)

> <INCHI_KEY>
MSTNYGQPCMXVAQ-UHFFFAOYSA-N

> <FORMULA>
C19H23N7O6

> <MOLECULAR_WEIGHT>
445.4292

> <EXACT_MASS>
445.170981503

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
44.542572941364014

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(4-{[(4-hydroxy-2-imino-1,2,5,6,7,8-hexahydropteridin-6-yl)methyl]amino}phenyl)formamido]pentanedioic acid

> <ALOGPS_LOGP>
-1.43

> <JCHEM_LOGP>
-3.636316241831437

> <ALOGPS_LOGS>
-3.32

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
3.882650266532847

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.0444825037700194

> <JCHEM_PKA_STRONGEST_BASIC>
5.760080233502614

> <JCHEM_POLAR_SURFACE_AREA>
208.25999999999996

> <JCHEM_REFRACTIVITY>
132.4011

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.15e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[(4-{[(4-hydroxy-2-imino-5,6,7,8-tetrahydro-1H-pteridin-6-yl)methyl]amino}phenyl)formamido]pentanedioic acid

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0243631 (5,6,7,8-Tetrahydrofolic acid)

HMDB0243631
     RDKit          3D
5,6,7,8-Tetrahydrofolic acid
 55 57  0  0  0  0  0  0  0  0999 V2000
   -8.9661    2.4320    0.8218 N   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1208    1.4588    0.7589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1940    0.3564    1.5260 N   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2897   -0.6411    1.4324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3554   -1.7839    2.2199 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2370   -0.5473    0.5173 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2028    0.6015   -0.2476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1172    1.5791   -0.1324 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1175    0.6938   -1.1851 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5399   -0.5196   -1.6747 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2886   -1.5548   -0.6267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9302   -1.3440    0.0373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8729   -1.4290   -0.9350 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4948   -1.2570   -0.5793 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4802   -1.3096   -1.5500 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8146   -1.1431   -1.2434 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2252   -0.9155    0.0641 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6497   -0.7370    0.3733 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4307   -1.7290    0.4403 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1551    0.5439    0.5942 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.5778    0.7439    0.8976 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2383    1.4620   -0.2576 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6783    1.7004   -0.0336 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5267    0.5334    0.1630 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3039   -0.3330    1.0573 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6505    0.2895   -0.6327 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6259    1.5169    2.1507 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5682    1.9042    2.7553 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8321    1.8460    2.7114 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2512   -0.8635    1.0301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1012   -1.0323    0.7183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2797   -1.5768    0.4013 N   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7852    2.4171    1.4978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7834   -1.7709    3.0742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0216    2.4324   -0.7561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7704    1.6183   -1.4900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6128   -0.2903   -2.2426 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2695   -0.9468   -2.4135 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3184   -2.5496   -1.1397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7829   -2.0665    0.8424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9344   -0.2781    0.4030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1193   -1.6188   -1.9266 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1644   -1.4838   -2.5717 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6010   -1.1831   -2.0034 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5482    1.3801    0.5510 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0275   -0.2528    0.9640 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7429    2.4482   -0.4590 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0964    0.8233   -1.1651 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0742    2.2349   -0.9608 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8437    2.4907    0.7602 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6474    0.4892   -1.6384 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3666    1.1846    3.2567 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5688   -0.6831    2.0679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8396   -0.9849    1.5050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3442   -2.3554    1.1218 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  2  0
  4  5  1  0
  4  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 21 27  1  0
 27 28  2  0
 27 29  1  0
 17 30  1  0
 30 31  2  0
 11 32  1  0
  8  2  1  0
 31 14  1  0
 32  6  1  0
  1 33  1  0
  5 34  1  0
  8 35  1  0
  9 36  1  0
 10 37  1  0
 10 38  1  0
 11 39  1  0
 12 40  1  0
 12 41  1  0
 13 42  1  0
 15 43  1  0
 16 44  1  0
 20 45  1  0
 21 46  1  0
 22 47  1  0
 22 48  1  0
 23 49  1  0
 23 50  1  0
 26 51  1  0
 29 52  1  0
 30 53  1  0
 31 54  1  0
 32 55  1  0
M  END
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PDB for HMDB0243631 (5,6,7,8-Tetrahydrofolic acid)

HEADER    PROTEIN                                 22-MAY-19   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   22-MAY-19         0                                  
HETATM    1  C   UNK     0      -5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.668  -5.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -12.003  -6.930   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -13.337  -7.700   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -10.669  -7.700   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -14.670  -6.930   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.000   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.000   1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0     -10.669  -9.240   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       4.001   2.310   0.000  0.00  0.00           N+0
HETATM   21  N   UNK     0      -2.667  -4.620   0.000  0.00  0.00           N+0
HETATM   22  N   UNK     0       1.334  -2.310   0.000  0.00  0.00           N+0
HETATM   23  N   UNK     0      -1.334  -0.770   0.000  0.00  0.00           N+0
HETATM   24  N   UNK     0      -9.336  -6.930   0.000  0.00  0.00           N+0
HETATM   25  N   UNK     0       2.667   0.000   0.000  0.00  0.00           N+0
HETATM   26  N   UNK     0       1.334   2.310   0.000  0.00  0.00           N+0
HETATM   27  O   UNK     0     -16.004  -7.700   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0     -14.670  -5.390   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      -8.002  -9.240   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      -9.336 -10.010   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0     -12.003 -10.010   0.000  0.00  0.00           O+0
CONECT    1    3    9                                                       
CONECT    2    4    9                                                       
CONECT    3    1   10                                                       
CONECT    4    2   10                                                       
CONECT    5    6   12                                                       
CONECT    6    5   13                                                       
CONECT    7   11   21                                                       
CONECT    8   11   22                                                       
CONECT    9    1    2   16                                                  
CONECT   10    3    4   21                                                  
CONECT   11    7    8   23                                                  
CONECT   12    5   18   24                                                  
CONECT   13    6   27   28                                                  
CONECT   14   15   17   23                                                  
CONECT   15   14   22   25                                                  
CONECT   16    9   24   29                                                  
CONECT   17   14   26   30                                                  
CONECT   18   12   31   32                                                  
CONECT   19   20   25   26                                                  
CONECT   20   19                                                            
CONECT   21    7   10                                                       
CONECT   22    8   15                                                       
CONECT   23   11   14                                                       
CONECT   24   12   16                                                       
CONECT   25   15   19                                                       
CONECT   26   17   19                                                       
CONECT   27   13                                                            
CONECT   28   13                                                            
CONECT   29   16                                                            
CONECT   30   17                                                            
CONECT   31   18                                                            
CONECT   32   18                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END
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3D PDB for HMDB0243631 (5,6,7,8-Tetrahydrofolic acid)

COMPND    HMDB0243631
HETATM    1  N1  UNL     1      -8.966   2.432   0.822  1.00  0.00           N  
HETATM    2  C1  UNL     1      -8.121   1.459   0.759  1.00  0.00           C  
HETATM    3  N2  UNL     1      -8.194   0.356   1.526  1.00  0.00           N  
HETATM    4  C2  UNL     1      -7.290  -0.641   1.432  1.00  0.00           C  
HETATM    5  O1  UNL     1      -7.355  -1.784   2.220  1.00  0.00           O  
HETATM    6  C3  UNL     1      -6.237  -0.547   0.517  1.00  0.00           C  
HETATM    7  C4  UNL     1      -6.203   0.602  -0.248  1.00  0.00           C  
HETATM    8  N3  UNL     1      -7.117   1.579  -0.132  1.00  0.00           N  
HETATM    9  N4  UNL     1      -5.118   0.694  -1.185  1.00  0.00           N  
HETATM   10  C5  UNL     1      -4.540  -0.520  -1.675  1.00  0.00           C  
HETATM   11  C6  UNL     1      -4.289  -1.555  -0.627  1.00  0.00           C  
HETATM   12  C7  UNL     1      -2.930  -1.344   0.037  1.00  0.00           C  
HETATM   13  N5  UNL     1      -1.873  -1.429  -0.935  1.00  0.00           N  
HETATM   14  C8  UNL     1      -0.495  -1.257  -0.579  1.00  0.00           C  
HETATM   15  C9  UNL     1       0.480  -1.310  -1.550  1.00  0.00           C  
HETATM   16  C10 UNL     1       1.815  -1.143  -1.243  1.00  0.00           C  
HETATM   17  C11 UNL     1       2.225  -0.916   0.064  1.00  0.00           C  
HETATM   18  C12 UNL     1       3.650  -0.737   0.373  1.00  0.00           C  
HETATM   19  O2  UNL     1       4.431  -1.729   0.440  1.00  0.00           O  
HETATM   20  N6  UNL     1       4.155   0.544   0.594  1.00  0.00           N  
HETATM   21  C13 UNL     1       5.578   0.744   0.898  1.00  0.00           C  
HETATM   22  C14 UNL     1       6.238   1.462  -0.258  1.00  0.00           C  
HETATM   23  C15 UNL     1       7.678   1.700  -0.034  1.00  0.00           C  
HETATM   24  C16 UNL     1       8.527   0.533   0.163  1.00  0.00           C  
HETATM   25  O3  UNL     1       8.304  -0.333   1.057  1.00  0.00           O  
HETATM   26  O4  UNL     1       9.650   0.290  -0.633  1.00  0.00           O  
HETATM   27  C17 UNL     1       5.626   1.517   2.151  1.00  0.00           C  
HETATM   28  O5  UNL     1       4.568   1.904   2.755  1.00  0.00           O  
HETATM   29  O6  UNL     1       6.832   1.846   2.711  1.00  0.00           O  
HETATM   30  C18 UNL     1       1.251  -0.863   1.030  1.00  0.00           C  
HETATM   31  C19 UNL     1      -0.101  -1.032   0.718  1.00  0.00           C  
HETATM   32  N7  UNL     1      -5.280  -1.577   0.401  1.00  0.00           N  
HETATM   33  H1  UNL     1      -9.785   2.417   1.498  1.00  0.00           H  
HETATM   34  H2  UNL     1      -6.783  -1.771   3.074  1.00  0.00           H  
HETATM   35  H3  UNL     1      -7.022   2.432  -0.756  1.00  0.00           H  
HETATM   36  H4  UNL     1      -4.770   1.618  -1.490  1.00  0.00           H  
HETATM   37  H5  UNL     1      -3.613  -0.290  -2.243  1.00  0.00           H  
HETATM   38  H6  UNL     1      -5.269  -0.947  -2.413  1.00  0.00           H  
HETATM   39  H7  UNL     1      -4.318  -2.550  -1.140  1.00  0.00           H  
HETATM   40  H8  UNL     1      -2.783  -2.067   0.842  1.00  0.00           H  
HETATM   41  H9  UNL     1      -2.934  -0.278   0.403  1.00  0.00           H  
HETATM   42  H10 UNL     1      -2.119  -1.619  -1.927  1.00  0.00           H  
HETATM   43  H11 UNL     1       0.164  -1.484  -2.572  1.00  0.00           H  
HETATM   44  H12 UNL     1       2.601  -1.183  -2.003  1.00  0.00           H  
HETATM   45  H13 UNL     1       3.548   1.380   0.551  1.00  0.00           H  
HETATM   46  H14 UNL     1       6.028  -0.253   0.964  1.00  0.00           H  
HETATM   47  H15 UNL     1       5.743   2.448  -0.459  1.00  0.00           H  
HETATM   48  H16 UNL     1       6.096   0.823  -1.165  1.00  0.00           H  
HETATM   49  H17 UNL     1       8.074   2.235  -0.961  1.00  0.00           H  
HETATM   50  H18 UNL     1       7.844   2.491   0.760  1.00  0.00           H  
HETATM   51  H19 UNL     1       9.647   0.489  -1.638  1.00  0.00           H  
HETATM   52  H20 UNL     1       7.367   1.185   3.257  1.00  0.00           H  
HETATM   53  H21 UNL     1       1.569  -0.683   2.068  1.00  0.00           H  
HETATM   54  H22 UNL     1      -0.840  -0.985   1.505  1.00  0.00           H  
HETATM   55  H23 UNL     1      -5.344  -2.355   1.122  1.00  0.00           H  
CONECT    1    2    2   33
CONECT    2    3    8
CONECT    3    4    4
CONECT    4    5    6
CONECT    5   34
CONECT    6    7    7   32
CONECT    7    8    9
CONECT    8   35
CONECT    9   10   36
CONECT   10   11   37   38
CONECT   11   12   32   39
CONECT   12   13   40   41
CONECT   13   14   42
CONECT   14   15   15   31
CONECT   15   16   43
CONECT   16   17   17   44
CONECT   17   18   30
CONECT   18   19   19   20
CONECT   20   21   45
CONECT   21   22   27   46
CONECT   22   23   47   48
CONECT   23   24   49   50
CONECT   24   25   25   26
CONECT   26   51
CONECT   27   28   28   29
CONECT   29   52
CONECT   30   31   31   53
CONECT   31   54
CONECT   32   55
END
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SMILES for HMDB0243631 (5,6,7,8-Tetrahydrofolic acid)

OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(N2)C(O)=NC(=N)N3)C=C1)C(O)=O
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INCHI for HMDB0243631 (5,6,7,8-Tetrahydrofolic acid)

InChI=1S/C19H23N7O6/c20-19-25-15-14(17(30)26-19)23-11(8-22-15)7-21-10-3-1-9(2-4-10)16(29)24-12(18(31)32)5-6-13(27)28/h1-4,11-12,21,23H,5-8H2,(H,24,29)(H,27,28)(H,31,32)(H4,20,22,25,26,30)
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View in JSmolView NMR AssignmentsView Stereo Labels
Synonyms
ValueSource
5,6,7,8-TetrahydrofolateGenerator
TetrahydrofolateHMDB
5,6,7,8-Tetrahydrofolic acid, (D-(-))-isomerHMDB
5,6,7,8-Tetrahydrofolic acid, ion (2-)-isomerHMDB
5,6,7,8-Tetrahydrofolic acid, (L)-isomerHMDB
Tetrahydrofolic acidHMDB
TetrahydropteroylglutamateHMDB
5,6,7,8-Tetrahydrofolic acidMeSH
Chemical FormulaC19H23N7O6
Average Molecular Weight445.4292
Monoisotopic Molecular Weight445.170981503
IUPAC Name2-[(4-{[(4-hydroxy-2-imino-1,2,5,6,7,8-hexahydropteridin-6-yl)methyl]amino}phenyl)formamido]pentanedioic acid
Traditional Name2-[(4-{[(4-hydroxy-2-imino-5,6,7,8-tetrahydro-1H-pteridin-6-yl)methyl]amino}phenyl)formamido]pentanedioic acid
CAS Registry NumberNot Available
SMILES
OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(N2)C(O)=NC(=N)N3)C=C1)C(O)=O
InChI Identifier
InChI=1S/C19H23N7O6/c20-19-25-15-14(17(30)26-19)23-11(8-22-15)7-21-10-3-1-9(2-4-10)16(29)24-12(18(31)32)5-6-13(27)28/h1-4,11-12,21,23H,5-8H2,(H,24,29)(H,27,28)(H,31,32)(H4,20,22,25,26,30)
InChI KeyMSTNYGQPCMXVAQ-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.
KingdomOrganic compounds
Super ClassOrganoheterocyclic compounds
ClassPteridines and derivatives
Sub ClassPterins and derivatives
Direct ParentTetrahydrofolic 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
  • Dicarboxylic acid or derivatives
  • Monocyclic benzene moiety
  • Benzenoid
  • Pyrimidine
  • Heteroaromatic compound
  • Vinylogous amide
  • Amino acid or derivatives
  • Secondary carboxylic acid amide
  • Carboxamide group
  • Amino acid
  • Azacycle
  • Carboxylic acid derivative
  • Carboxylic acid
  • Secondary amine
  • Primary amine
  • Organic nitrogen compound
  • Carbonyl group
  • Hydrocarbon derivative
  • Organic oxide
  • Amine
  • Organopnictogen compound
  • Organic oxygen compound
  • Organonitrogen compound
  • Organooxygen compound
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Biological location
ProcessNot Available
RoleNot Available
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
logP-1.4ALOGPS
logP-3.6ChemAxon
logS-3.3ALOGPS
pKa (Strongest Acidic)2.04ChemAxon
pKa (Strongest Basic)5.76ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count12ChemAxon
Hydrogen Donor Count9ChemAxon
Polar Surface Area208.26 ŲChemAxon
Rotatable Bond Count9ChemAxon
Refractivity132.4 m³·mol⁻¹ChemAxon
Polarizability44.54 ųChemAxon
Number of Rings3ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleYesChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
AllCCS[M+H]+199.232859911
AllCCS[M+H-H2O]+197.332859911
AllCCS[M+NH4]+201.032859911
AllCCS[M+Na]+201.532859911
AllCCS[M-H]-195.432859911
AllCCS[M+Na-2H]-196.032859911
AllCCS[M+HCOO]-196.932859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
5,6,7,8-Tetrahydrofolic acidOC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(N2)C(O)=NC(=N)N3)C=C1)C(O)=O6014.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acidOC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(N2)C(O)=NC(=N)N3)C=C1)C(O)=O4357.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acidOC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(N2)C(O)=NC(=N)N3)C=C1)C(O)=O5012.7Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #1C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)C=C1)[Si](C)(C)C4410.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #1C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)C=C1)[Si](C)(C)C3773.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #1C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)C=C1)[Si](C)(C)C6832.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #10C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2)[NH]14414.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #10C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2)[NH]13941.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #10C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2)[NH]17202.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #100C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4389.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #100C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C3993.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #100C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C6059.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #101C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]14410.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #101C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]14043.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #101C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]16102.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #102C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C14395.5Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #102C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C13969.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #102C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C16192.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #103C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)N24355.5Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #103C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)N24026.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #103C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)N26517.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #104C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C14342.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #104C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C13922.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #104C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C15719.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #105C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4507.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #105C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C3857.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #105C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C6556.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #106C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C14410.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #106C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C13953.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #106C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C15970.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #107C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]14434.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #107C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]14003.8Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #107C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]16019.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #108C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4433.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #108C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C3976.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #108C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C6355.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #109C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C14444.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #109C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C14055.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #109C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C15813.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #11C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4407.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #11C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C3901.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #11C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C6314.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #110C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)N2[Si](C)(C)C4368.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #110C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)N2[Si](C)(C)C4099.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #110C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)N2[Si](C)(C)C5852.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #111C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4554.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #111C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C3996.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #111C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C6098.2Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #112C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(N1)C(O)=NC(=N)N2[Si](C)(C)C)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C14378.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #112C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(N1)C(O)=NC(=N)N2[Si](C)(C)C)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C14043.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #112C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(N1)C(O)=NC(=N)N2[Si](C)(C)C)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C16219.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #113C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)N24327.3Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #113C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)N24104.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #113C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)N26531.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #114C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(O)=NC(=N)[NH]2)N1[Si](C)(C)C)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C14319.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #114C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(O)=NC(=N)[NH]2)N1[Si](C)(C)C)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C13986.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #114C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(O)=NC(=N)[NH]2)N1[Si](C)(C)C)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C15765.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #115C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4461.3Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #115C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C3919.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #115C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C6577.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #116C[Si](C)(C)N(CC1CNC2=C(C(O)=NC(=N)N2[Si](C)(C)C)N1[Si](C)(C)C)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C14393.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #116C[Si](C)(C)N(CC1CNC2=C(C(O)=NC(=N)N2[Si](C)(C)C)N1[Si](C)(C)C)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C14032.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #116C[Si](C)(C)N(CC1CNC2=C(C(O)=NC(=N)N2[Si](C)(C)C)N1[Si](C)(C)C)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C16020.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #117C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]14406.3Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #117C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]14083.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #117C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]16063.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #118C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N2[Si](C)(C)C4339.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #118C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N2[Si](C)(C)C4174.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #118C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N2[Si](C)(C)C5904.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #119C[Si](C)(C)N1CC(CNC2=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)C(=N)N=C2O4430.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #119C[Si](C)(C)N1CC(CNC2=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)C(=N)N=C2O4127.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #119C[Si](C)(C)N1CC(CNC2=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)C(=N)N=C2O5868.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #12C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)C(=O)O4342.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #12C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)C(=O)O3885.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #12C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)C(=O)O6656.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #120C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4397.3Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #120C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4051.8Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #120C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C6380.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #121C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4503.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #121C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4083.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #121C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C6151.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #122C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4484.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #122C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4080.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #122C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C6335.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #123C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(O)=NC(=N)N2[Si](C)(C)C)N1[Si](C)(C)C)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C14466.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #123C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(O)=NC(=N)N2[Si](C)(C)C)N1[Si](C)(C)C)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C14131.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #123C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(O)=NC(=N)N2[Si](C)(C)C)N1[Si](C)(C)C)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C15805.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #124C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)N2[Si](C)(C)C4372.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #124C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)N2[Si](C)(C)C4165.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #124C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)N2[Si](C)(C)C5846.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #125C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C4556.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #125C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C4077.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #125C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C6089.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #126C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4524.5Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #126C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4146.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #126C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C5891.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #13C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O4419.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #13C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O3852.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #13C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O6703.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #14C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2)[NH]14495.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #14C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2)[NH]13915.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #14C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2)[NH]17174.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #15C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O4452.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #15C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O3888.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #15C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O6246.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #16C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)C(=O)O4382.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #16C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)C(=O)O3996.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #16C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)C(=O)O6563.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #17C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)N24385.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #17C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)N24025.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #17C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)N26923.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #18C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O4390.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #18C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O3956.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #18C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O6131.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #19C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2)N1[Si](C)(C)C4537.5Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #19C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2)N1[Si](C)(C)C3895.8Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #19C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2)N1[Si](C)(C)C6981.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #2C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4432.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #2C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3727.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #2C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C6778.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #20C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O4476.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #20C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O3982.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #20C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O6377.2Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #21C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C)[NH]14493.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #21C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C)[NH]14034.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #21C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C)[NH]16363.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #22C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C4359.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #22C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C3725.8Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #22C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C6494.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #23C[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(N2)C(O)=NC(=N)[NH]3)C=C1)[Si](C)(C)C4255.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #23C[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(N2)C(O)=NC(=N)[NH]3)C=C1)[Si](C)(C)C3855.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #23C[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(N2)C(O)=NC(=N)[NH]3)C=C1)[Si](C)(C)C6407.2Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #24C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4357.3Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #24C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C3835.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #24C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C6476.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #25C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=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=C3)N2)[NH]14356.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #25C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=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=C3)N2)[NH]13894.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #25C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=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=C3)N2)[NH]16892.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #26C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4346.1Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #26C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C3875.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #26C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C5958.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #27C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4293.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #27C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3827.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #27C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C6353.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #28C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4379.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #28C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3789.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #28C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C6412.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #29C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)[NH]14406.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #29C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)[NH]13845.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #29C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)[NH]16841.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #3C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)C=C1)C(=O)O[Si](C)(C)C4283.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #3C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)C=C1)C(=O)O[Si](C)(C)C3845.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #3C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)C=C1)C(=O)O[Si](C)(C)C6652.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #30C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4370.5Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #30C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3831.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #30C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C5878.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #31C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4315.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #31C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3922.8Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #31C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C6282.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #32C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)N24318.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #32C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)N23978.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #32C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)N26599.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #33C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4309.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #33C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3909.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #33C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C5779.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #34C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4472.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #34C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C3830.8Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #34C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C6648.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #35C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4405.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #35C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3929.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #35C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C6038.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #36C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]14437.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #36C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]13975.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #36C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]16077.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #37C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C4279.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #37C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C3893.8Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #37C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C6373.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #38C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4363.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #38C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3872.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #38C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C6448.2Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #39C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)[NH]14367.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #39C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)[NH]13911.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #39C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)[NH]16845.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #4C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4392.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #4C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3806.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #4C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C6718.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #40C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4354.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #40C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3900.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #40C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C5943.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #41C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4309.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #41C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4012.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #41C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C6314.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #42C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)N24286.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #42C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)N24057.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #42C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)N26623.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #43C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4296.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #43C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C3974.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #43C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C5846.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #44C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4412.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #44C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C3914.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #44C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C6676.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #45C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4368.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #45C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4019.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #45C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C6111.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #46C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]14399.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #46C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]14063.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #46C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]16152.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #47C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O4366.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #47C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O4011.8Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #47C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O6268.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #48C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)N24353.5Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #48C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)N24071.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #48C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)N26592.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #49C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O4330.5Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #49C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O3964.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #49C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O5792.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #5C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2)[NH]14455.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #5C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2)[NH]13870.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #5C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2)[NH]17195.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #50C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4493.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #50C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C3891.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #50C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C6636.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #51C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O4398.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #51C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O3996.8Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #51C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O6049.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #52C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]14436.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #52C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]14048.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #52C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]16097.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #53C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2)N1[Si](C)(C)C4430.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #53C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2)N1[Si](C)(C)C4020.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #53C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2)N1[Si](C)(C)C6432.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #54C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O4427.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #54C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O4107.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #54C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O5890.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #55C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)N2[Si](C)(C)C4368.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #55C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)N2[Si](C)(C)C4139.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #55C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)N2[Si](C)(C)C5926.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #56C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4557.5Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #56C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4035.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #56C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C6177.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #57C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C4396.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #57C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C3747.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #57C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C6747.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #58C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)C=C1)[Si](C)(C)C4280.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #58C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)C=C1)[Si](C)(C)C3876.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #58C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)C=C1)[Si](C)(C)C6647.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #59C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4389.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #59C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C3872.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #59C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C6697.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #6C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4449.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #6C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3840.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #6C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C6250.2Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #60C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)[NH]14413.3Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #60C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)[NH]13919.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #60C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)[NH]17153.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #61C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4408.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #61C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C3874.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #61C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C6266.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #62C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C14351.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #62C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C13840.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #62C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C16585.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #63C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C14425.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #63C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C13816.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #63C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C16623.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #64C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)[NH]14472.1Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #64C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)[NH]13871.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #64C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)[NH]17099.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #65C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C14450.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #65C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C13845.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #65C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C16171.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #66C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C14393.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #66C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C13952.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #66C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C16488.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #67C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)N24353.5Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #67C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)N23977.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #67C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)N26851.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #68C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C14391.5Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #68C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C13914.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #68C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C16059.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #69C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4513.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #69C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C3858.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #69C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C6904.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #7C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C4385.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #7C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C3772.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #7C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C6797.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #70C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C14471.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #70C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C13940.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #70C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C16298.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #71C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]14478.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #71C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]13992.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #71C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]16286.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #72C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)N2)N1[Si](C)(C)C4493.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #72C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)N2)N1[Si](C)(C)C4014.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #72C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)N2)N1[Si](C)(C)C6650.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #73C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4568.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #73C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C3906.8Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #73C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C6875.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #74C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4466.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #74C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C3935.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #74C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C6914.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #75C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4614.1Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #75C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4045.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #75C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C6328.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #76C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)N24433.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #76C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)N24065.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #76C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)N26823.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #77C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N24341.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #77C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N24048.8Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #77C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N26858.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #78C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)N2[Si](C)(C)C4469.3Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #78C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)N2[Si](C)(C)C4135.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #78C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)N2[Si](C)(C)C6076.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #79C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)[NH]14430.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #79C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)[NH]13930.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #79C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)[NH]17085.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #8C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)C=C1)[Si](C)(C)C4262.1Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #8C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)C=C1)[Si](C)(C)C3904.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #8C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)C=C1)[Si](C)(C)C6693.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #80C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]14491.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #80C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]14072.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #80C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]16268.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #81C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]14440.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #81C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]14070.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #81C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]16336.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #82C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)CN24481.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #82C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)CN24020.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #82C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)CN26311.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #83C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN24438.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #83C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN24027.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #83C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN26384.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #84C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN2[Si](C)(C)C4531.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #84C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN2[Si](C)(C)C4109.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #84C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN2[Si](C)(C)C6118.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #85C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1NC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN24408.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #85C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1NC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN23881.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #85C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1NC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN26782.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #86C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1NC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C4465.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #86C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1NC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C4026.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #86C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1NC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C6506.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #87C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1NC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C4383.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #87C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1NC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C4032.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #87C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1NC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C6556.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #88C[Si](C)(C)OC1=NC(=N)[NH]C2=C1N([Si](C)(C)C)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)CN24417.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #88C[Si](C)(C)OC1=NC(=N)[NH]C2=C1N([Si](C)(C)C)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)CN23918.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #88C[Si](C)(C)OC1=NC(=N)[NH]C2=C1N([Si](C)(C)C)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)CN26244.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #89C[Si](C)(C)OC1=NC(=N)[NH]C2=C1N([Si](C)(C)C)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C4421.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #89C[Si](C)(C)OC1=NC(=N)[NH]C2=C1N([Si](C)(C)C)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C3976.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #89C[Si](C)(C)OC1=NC(=N)[NH]C2=C1N([Si](C)(C)C)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C6038.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #9C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4373.1Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #9C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C3895.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #9C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C6751.2Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #90C[Si](C)(C)OC1=NC(=N)[NH]C2=C1N([Si](C)(C)C)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C4374.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #90C[Si](C)(C)OC1=NC(=N)[NH]C2=C1N([Si](C)(C)C)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C3975.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #90C[Si](C)(C)OC1=NC(=N)[NH]C2=C1N([Si](C)(C)C)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C6100.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #91C[Si](C)(C)OC1=NC(=N)[NH]C2=C1NC(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)C4341.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #91C[Si](C)(C)OC1=NC(=N)[NH]C2=C1NC(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)C3915.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #91C[Si](C)(C)OC1=NC(=N)[NH]C2=C1NC(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)C6640.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #92C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C4307.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #92C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C3867.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #92C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C6324.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #93C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4391.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #93C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3852.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #93C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C6393.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #94C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)[NH]14377.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #94C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)[NH]13890.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #94C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)[NH]16792.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #95C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4360.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #95C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3876.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #95C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C5893.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #96C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4345.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #96C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C3984.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #96C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C6262.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #97C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N24300.5Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #97C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N24033.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #97C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N26574.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #98C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4314.1Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #98C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C3944.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #98C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C5800.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #99C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4433.3Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #99C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C3896.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,4TMS,isomer #99C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C6621.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #1C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C4307.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #1C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C3721.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #1C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C6434.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #10C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4280.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #10C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3905.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #10C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C6164.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #100C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]14319.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #100C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]14014.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #100C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]15919.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #101C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)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)CN24358.5Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #101C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)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)CN23969.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #101C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)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)CN25975.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #102C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C4439.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #102C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C4038.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #102C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C5726.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #103C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C4386.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #103C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C4076.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #103C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C5798.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #104C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1NC(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)C4326.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #104C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1NC(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)C3978.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #104C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1NC(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)C6169.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #105C[Si](C)(C)OC1=NC(=N)[NH]C2=C1N([Si](C)(C)C)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)C4289.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #105C[Si](C)(C)OC1=NC(=N)[NH]C2=C1N([Si](C)(C)C)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)C3926.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #105C[Si](C)(C)OC1=NC(=N)[NH]C2=C1N([Si](C)(C)C)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)C5730.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #106C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4286.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #106C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3956.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #106C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C5864.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #107C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N24204.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #107C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N24009.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #107C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N26203.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #108C[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)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4236.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #108C[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)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3903.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #108C[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)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C5445.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #109C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4337.3Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #109C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C3831.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #109C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C6217.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #11C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)N24275.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #11C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)N23922.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #11C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)N26564.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #110C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4308.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #110C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3947.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #110C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C5663.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #111C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]14280.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #111C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]13986.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #111C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]15692.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #112C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4286.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #112C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C3984.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #112C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C6019.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #113C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4330.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #113C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4060.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #113C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C5528.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #114C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N2[Si](C)(C)C4222.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #114C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N2[Si](C)(C)C4086.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #114C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N2[Si](C)(C)C5562.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #115C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4364.3Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #115C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C3989.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #115C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C5781.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #116C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4360.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #116C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C3962.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #116C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C5955.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #117C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C14362.3Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #117C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C14006.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #117C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C15447.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #118C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)N2[Si](C)(C)C4272.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #118C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)N2[Si](C)(C)C4037.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #118C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)N2[Si](C)(C)C5485.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #119C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C4420.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #119C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C3935.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #119C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C5702.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #12C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4279.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #12C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3885.8Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #12C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C5748.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #120C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4386.1Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #120C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4037.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #120C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C5514.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #121C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4321.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #121C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4027.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #121C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C5976.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #122C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(O)=NC(=N)N2[Si](C)(C)C)N1[Si](C)(C)C)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C14340.1Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #122C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(O)=NC(=N)N2[Si](C)(C)C)N1[Si](C)(C)C)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C14071.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #122C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(O)=NC(=N)N2[Si](C)(C)C)N1[Si](C)(C)C)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C15500.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #123C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)N2[Si](C)(C)C4229.3Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #123C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)N2[Si](C)(C)C4110.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #123C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)N2[Si](C)(C)C5534.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #124C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C4373.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #124C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C4010.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #124C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C5751.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #125C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4338.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #125C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4113.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #125C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C5569.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #126C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C4411.1Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #126C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C4085.8Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #126C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C5508.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #13C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4404.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #13C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C3800.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #13C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C6603.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #14C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4374.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #14C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3877.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #14C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C5965.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #15C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]14373.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #15C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]13918.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #15C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]15943.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #16C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C4212.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #16C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C3844.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #16C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C6322.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #17C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4309.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #17C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3816.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #17C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C6337.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #18C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)[NH]14312.3Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #18C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)[NH]13879.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #18C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)[NH]16827.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #19C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4308.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #19C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3851.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #19C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C5903.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #2C[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(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)C=C1)[Si](C)(C)C4183.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #2C[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(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)C=C1)[Si](C)(C)C3860.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #2C[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(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)C=C1)[Si](C)(C)C6341.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #20C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4257.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #20C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C3984.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #20C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C6216.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #21C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)N24226.1Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #21C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)N23996.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #21C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)N26603.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #22C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4252.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #22C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C3940.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #22C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C5819.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #23C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4333.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #23C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C3873.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #23C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C6629.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #24C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4329.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #24C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C3960.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #24C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C6033.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #25C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]14310.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #25C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]13996.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #25C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]16010.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #26C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O4343.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #26C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O3939.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #26C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O6166.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #27C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)N24325.5Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #27C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)N23980.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #27C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)N26571.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #28C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O4305.1Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #28C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O3906.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #28C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O5756.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #29C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4427.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #29C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C3827.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #29C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C6595.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #3C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4319.1Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #3C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C3818.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #3C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C6367.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #30C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O4379.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #30C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O3908.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #30C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O5960.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #31C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]14374.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #31C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]13969.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #31C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]15945.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #32C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2)N1[Si](C)(C)C4387.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #32C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2)N1[Si](C)(C)C3968.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #32C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2)N1[Si](C)(C)C6359.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #33C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O4395.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #33C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O4035.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #33C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O5818.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #34C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)N2[Si](C)(C)C4347.1Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #34C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)N2[Si](C)(C)C4057.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #34C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)N2[Si](C)(C)C5773.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #35C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4475.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #35C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C3960.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #35C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C6006.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #36C[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(N2)C(O)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C4174.5Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #36C[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(N2)C(O)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C3817.8Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #36C[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(N2)C(O)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C6022.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #37C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4286.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #37C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3784.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #37C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C6050.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #38C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=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=C3)[Si](C)(C)C)N2)[NH]14260.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #38C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=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=C3)[Si](C)(C)C)N2)[NH]13832.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #38C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=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=C3)[Si](C)(C)C)N2)[NH]16474.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #39C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4264.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #39C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3829.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #39C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C5557.2Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #4C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=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=C3)N2)[NH]14333.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #4C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=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=C3)N2)[NH]13884.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #4C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=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=C3)N2)[NH]16865.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #40C[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(N2)C(O)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4239.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #40C[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(N2)C(O)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C3936.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #40C[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(N2)C(O)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C5934.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #41C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N24171.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #41C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N23975.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #41C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N26271.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #42C[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)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4197.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #42C[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)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C3916.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #42C[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)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C5493.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #43C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=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=C3)N2)N1[Si](C)(C)C4310.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #43C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=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=C3)N2)N1[Si](C)(C)C3834.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #43C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=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=C3)N2)N1[Si](C)(C)C6288.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #44C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4298.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #44C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C3932.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #44C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C5716.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #45C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=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=C3)N2[Si](C)(C)C)[NH]14281.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #45C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=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=C3)N2[Si](C)(C)C)[NH]13972.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #45C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=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=C3)N2[Si](C)(C)C)[NH]15739.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #46C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4278.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #46C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3890.8Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #46C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C5871.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #47C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N24242.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #47C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N23943.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #47C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N26221.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #48C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4231.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #48C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3860.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #48C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C5418.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #49C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4366.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #49C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C3780.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #49C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C6232.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #5C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4314.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #5C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C3856.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #5C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C5926.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #50C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4319.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #50C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3867.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #50C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C5636.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #51C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]14313.5Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #51C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]13909.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #51C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]15665.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #52C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4321.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #52C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C3925.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #52C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C6023.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #53C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4315.1Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #53C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3996.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #53C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C5497.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #54C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)N2[Si](C)(C)C4256.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #54C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)N2[Si](C)(C)C4020.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #54C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)N2[Si](C)(C)C5528.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #55C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4395.5Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #55C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C3916.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #55C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C5749.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #56C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4256.1Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #56C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3965.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #56C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C5908.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #57C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N24190.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #57C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N24018.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #57C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N26246.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #58C[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)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4216.1Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #58C[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)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3916.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #58C[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)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C5484.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #59C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4320.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #59C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C3840.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #59C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C6262.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #6C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4247.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #6C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3799.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #6C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C6292.2Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #60C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4292.3Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #60C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3955.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #60C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C5705.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #61C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]14274.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #61C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]13994.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #61C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]15734.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #62C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4270.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #62C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4000.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #62C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C6062.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #63C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4303.1Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #63C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4075.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #63C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C5568.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #64C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)N2[Si](C)(C)C4202.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #64C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)N2[Si](C)(C)C4099.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #64C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)N2[Si](C)(C)C5601.2Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #65C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4345.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #65C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4002.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #65C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C5823.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #66C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4351.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #66C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C3986.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #66C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C6021.2Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #67C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O4347.1Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #67C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O4032.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #67C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O5509.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #68C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)N2[Si](C)(C)C4261.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #68C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)N2[Si](C)(C)C4060.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #68C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)N2[Si](C)(C)C5546.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #69C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C4414.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #69C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C3956.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #69C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C5767.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #7C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4321.5Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #7C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3753.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #7C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C6304.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #70C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4379.5Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #70C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4068.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #70C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C5576.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #71C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C4231.1Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #71C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C3826.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #71C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C6282.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #72C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4325.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #72C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3802.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #72C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C6292.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #73C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)[NH]14321.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #73C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)[NH]13862.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #73C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)[NH]16783.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #74C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4315.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #74C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3834.8Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #74C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C5861.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #75C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4281.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #75C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C3969.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #75C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C6173.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #76C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N24230.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #76C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N23981.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #76C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N26562.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #77C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4271.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #77C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C3918.8Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #77C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C5780.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #78C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4346.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #78C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C3856.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #78C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C6586.2Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #79C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4347.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #79C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C3945.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #79C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C5990.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #8C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)[NH]14375.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #8C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)[NH]13821.8Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #8C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)[NH]16826.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #80C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]14320.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #80C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]13980.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #80C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]15968.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #81C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C14350.1Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #81C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C13912.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #81C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C16101.2Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #82C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)N24314.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #82C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)N23950.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #82C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)N26508.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #83C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C14312.3Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #83C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C13876.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #83C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C15695.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #84C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4426.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #84C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C3800.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #84C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C6528.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #85C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C14379.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #85C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C13890.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #85C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C15893.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #86C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]14366.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #86C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]13940.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #86C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]15880.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #87C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4369.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #87C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C3935.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #87C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C6294.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #88C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C14403.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #88C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C14004.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #88C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C15756.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #89C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)N2[Si](C)(C)C4342.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #89C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)N2[Si](C)(C)C4029.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #89C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)N2[Si](C)(C)C5712.2Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #9C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4348.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #9C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3795.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #9C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C5845.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #90C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4471.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #90C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C3931.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #90C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C5940.2Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #91C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4424.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #91C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C3990.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #91C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C6260.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #92C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4313.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #92C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4002.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #92C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C6308.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #93C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4483.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #93C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4069.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #93C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C5701.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #94C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4373.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #94C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C3847.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #94C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C6529.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #95C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C4483.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #95C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C3986.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #95C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C5912.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #96C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4404.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #96C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4004.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #96C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C5986.2Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #97C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)N24273.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #97C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)N24020.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #97C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)N26506.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #98C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)N2[Si](C)(C)C4364.5Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #98C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)N2[Si](C)(C)C4066.8Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #98C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)N2[Si](C)(C)C5689.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #99C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N2[Si](C)(C)C4294.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #99C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N2[Si](C)(C)C4096.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,5TMS,isomer #99C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N2[Si](C)(C)C5756.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #1C[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(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C4150.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #1C[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(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C3798.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #1C[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(N2)C(O[Si](C)(C)C)=NC(=N)[NH]3)[Si](C)(C)C)C=C1)[Si](C)(C)C6013.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #10C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=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=C3)N2[Si](C)(C)C)[NH]14252.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #10C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=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=C3)N2[Si](C)(C)C)[NH]13926.8Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #10C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=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=C3)N2[Si](C)(C)C)[NH]15653.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #11C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4255.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #11C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3853.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #11C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C5808.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #12C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(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)N24232.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #12C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(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)N23896.8Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #12C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(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)N26235.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #13C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4242.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #13C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3836.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #13C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C5420.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #14C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4334.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #14C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C3741.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #14C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C6234.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #15C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4318.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #15C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3815.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #15C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C5582.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #16C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]14312.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #16C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]13871.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #16C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]15567.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #17C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4280.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #17C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C3898.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #17C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C5983.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #18C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4304.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #18C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3953.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #18C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C5463.2Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #19C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)N2[Si](C)(C)C4261.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #19C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)N2[Si](C)(C)C3979.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #19C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)N2[Si](C)(C)C5418.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #2C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4276.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #2C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3756.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #2C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C5981.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #20C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4352.3Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #20C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C3870.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #20C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C5626.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #21C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4247.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #21C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3912.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #21C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C5852.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #22C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(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)N24190.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #22C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(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)N23965.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #22C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(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)N26258.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #23C[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[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4209.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #23C[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[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3880.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #23C[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[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C5483.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #24C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4288.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #24C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C3791.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #24C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C6251.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #25C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4294.5Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #25C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3890.8Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #25C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C5648.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #26C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]14260.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #26C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]13950.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #26C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]15630.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #27C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4225.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #27C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C3960.8Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #27C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C6028.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #28C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4290.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #28C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4022.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #28C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C5536.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #29C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)N2[Si](C)(C)C4204.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #29C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)N2[Si](C)(C)C4052.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #29C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)N2[Si](C)(C)C5494.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #3C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=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=C3)[Si](C)(C)C)N2)[NH]14249.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #3C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=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=C3)[Si](C)(C)C)N2)[NH]13823.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #3C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=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=C3)[Si](C)(C)C)N2)[NH]16507.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #30C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4304.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #30C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C3942.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #30C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C5694.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #31C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4343.5Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #31C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C3928.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #31C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C5981.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #32C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O4349.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #32C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O3958.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #32C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O5458.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #33C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)N2[Si](C)(C)C4292.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #33C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)N2[Si](C)(C)C4002.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #33C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)N2[Si](C)(C)C5423.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #34C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C4384.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #34C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C3902.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #34C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C5618.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #35C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4369.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #35C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4016.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #35C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C5423.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #36C[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(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4192.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #36C[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(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3889.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #36C[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(N2)C(O)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C5567.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #37C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N24120.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #37C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N23947.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #37C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N25912.2Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #38C[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)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4153.3Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #38C[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)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3864.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #38C[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)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C5177.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #39C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=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=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4253.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #39C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=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=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C3771.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #39C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=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=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C5895.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #4C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4261.5Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #4C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3802.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #4C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C5568.2Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #40C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4264.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #40C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3873.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #40C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C5356.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #41C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=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=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]14228.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #41C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=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=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]13917.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #41C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=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=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]15375.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #42C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=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=C3)N2)N1[Si](C)(C)C4197.1Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #42C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=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=C3)N2)N1[Si](C)(C)C3943.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #42C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=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=C3)N2)N1[Si](C)(C)C5703.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #43C[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)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4230.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #43C[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)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4011.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #43C[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)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C5249.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #44C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N2[Si](C)(C)C4140.1Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #44C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N2[Si](C)(C)C4036.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #44C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N2[Si](C)(C)C5275.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #45C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=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=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4265.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #45C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=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=C3)N2[Si](C)(C)C)N1[Si](C)(C)C3924.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #45C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=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=C3)N2[Si](C)(C)C)N1[Si](C)(C)C5465.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #46C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4273.1Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #46C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C3893.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #46C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C5642.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #47C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4281.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #47C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3936.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #47C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C5170.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #48C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N2[Si](C)(C)C4208.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #48C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N2[Si](C)(C)C3972.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #48C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N2[Si](C)(C)C5199.2Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #49C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C4319.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #49C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C3853.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #49C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C5386.2Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #5C[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(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4203.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #5C[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(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C3928.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #5C[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(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C5872.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #50C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4277.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #50C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C3987.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #50C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C5218.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #51C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4229.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #51C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C3962.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #51C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C5689.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #52C[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)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4259.1Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #52C[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)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4005.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #52C[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)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C5244.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #53C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N2[Si](C)(C)C4162.3Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #53C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N2[Si](C)(C)C4049.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #53C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N2[Si](C)(C)C5275.2Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #54C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C4297.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #54C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C3934.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #54C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C5461.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #55C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4242.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #55C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4059.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #55C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C5298.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #56C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C4331.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #56C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C4008.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #56C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C5238.2Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #57C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4267.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #57C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3903.5Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #57C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(N2)C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C5817.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #58C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(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)N24199.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #58C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(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)N23956.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #58C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(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)N26223.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #59C[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[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4223.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #59C[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[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3868.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #59C[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[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C5450.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #6C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(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)N24151.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #6C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(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)N23942.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #6C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(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)N26279.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #60C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4306.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #60C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C3775.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #60C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C6214.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #61C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4313.0Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #61C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C3885.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #61C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C5612.2Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #62C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]14269.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #62C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]13943.6Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #62C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)[NH]15595.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #63C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4235.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #63C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C3953.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #63C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C5992.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #64C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4310.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #64C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4012.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #64C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C5502.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #65C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N2[Si](C)(C)C4218.5Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #65C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N2[Si](C)(C)C4035.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #65C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N2[Si](C)(C)C5460.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #66C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4321.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #66C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C3930.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #66C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C5659.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #67C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4342.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #67C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C3909.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #67C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C5927.8Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #68C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C14358.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #68C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C13943.3Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #68C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C15407.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #69C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)N2[Si](C)(C)C4292.3Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #69C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)N2[Si](C)(C)C3984.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #69C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)N2[Si](C)(C)C5374.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #7C[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[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4190.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #7C[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[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C3902.8Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #7C[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[Si](C)(C)C)=NC(=N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C5504.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #70C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C4389.5Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #70C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C3889.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #70C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C5565.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #71C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4369.3Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #71C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C3991.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #71C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C5372.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #72C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4290.4Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #72C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C3963.9Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #72C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C5941.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #73C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C4407.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #73C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C4011.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #73C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C5345.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #74C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4325.3Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #74C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4055.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #74C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C5424.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #75C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C4348.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #75C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C3949.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #75C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C5611.1Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #76C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)N2[Si](C)(C)C4249.5Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #76C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)N2[Si](C)(C)C4045.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #76C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)N2[Si](C)(C)C5419.9Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #77C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)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)C4335.5Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #77C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)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)C4002.8Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #77C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)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)C5454.2Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #78C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C4241.9Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #78C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C3959.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #78C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2)N1[Si](C)(C)C5654.5Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #79C[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)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4280.1Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #79C[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)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C4003.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #79C[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)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C5211.2Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #8C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=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=C3)N2)N1[Si](C)(C)C4271.8Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #8C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=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=C3)N2)N1[Si](C)(C)C3815.1Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #8C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=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=C3)N2)N1[Si](C)(C)C6282.0Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #80C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N2[Si](C)(C)C4172.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #80C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N2[Si](C)(C)C4042.0Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #80C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(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)N2[Si](C)(C)C5241.7Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #81C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C4306.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #81C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C3928.8Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #81C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C5425.6Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #82C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4252.7Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #82C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4049.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #82C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C5264.4Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #83C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C4341.2Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #83C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C3992.4Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #83C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C5189.3Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #84C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C4289.6Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #84C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C4053.2Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #84C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)C5245.2Standard polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #9C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4292.1Semi standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #9C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C3894.7Standard non polar33892256
5,6,7,8-Tetrahydrofolic acid,6TMS,isomer #9C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C5676.7Standard polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5,6,7,8-tetrahydrofolate(2-) GC-MS (Non-derivatized) - 70eV, Positivesplash10-0002-1294300000-633d8c4420228889b85d2021-09-24Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5,6,7,8-tetrahydrofolate(2-) GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5,6,7,8-tetrahydrofolate(2-) GC-MS (TMS_1_1) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5,6,7,8-tetrahydrofolate(2-) GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5,6,7,8-tetrahydrofolate(2-) GC-MS (TMS_1_3) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5,6,7,8-tetrahydrofolate(2-) GC-MS (TMS_1_4) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5,6,7,8-tetrahydrofolate(2-) GC-MS (TMS_1_5) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5,6,7,8-tetrahydrofolate(2-) GC-MS (TMS_1_6) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5,6,7,8-tetrahydrofolate(2-) GC-MS (TMS_1_7) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5,6,7,8-tetrahydrofolate(2-) GC-MS (TMS_1_8) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5,6,7,8-tetrahydrofolate(2-) GC-MS (TMS_1_9) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5,6,7,8-tetrahydrofolate(2-) GC-MS (TMS_2_1) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5,6,7,8-tetrahydrofolate(2-) GC-MS (TMS_2_2) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5,6,7,8-tetrahydrofolate(2-) GC-MS (TMS_2_3) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5,6,7,8-tetrahydrofolate(2-) GC-MS (TMS_2_4) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5,6,7,8-tetrahydrofolate(2-) GC-MS (TMS_2_5) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5,6,7,8-tetrahydrofolate(2-) GC-MS (TMS_2_6) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5,6,7,8-tetrahydrofolate(2-) GC-MS (TMS_2_7) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5,6,7,8-tetrahydrofolate(2-) GC-MS (TMS_2_8) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5,6,7,8-tetrahydrofolate(2-) GC-MS (TMS_2_9) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5,6,7,8-tetrahydrofolate(2-) GC-MS (TMS_2_10) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5,6,7,8-tetrahydrofolate(2-) GC-MS (TMS_2_11) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5,6,7,8-tetrahydrofolate(2-) GC-MS (TMS_2_12) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5,6,7,8-tetrahydrofolate(2-) GC-MS (TMS_2_13) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5,6,7,8-tetrahydrofolate(2-) GC-MS (TMS_2_14) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Experimental LC-MS/MSLC-MS/MS Spectrum - 5,6,7,8-Tetrahydrofolic acid Quattro_QQQ 10V, Positive-QTOF (Annotated)splash10-0002-7796610000-0937514a7f23431b726e2012-07-24HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - 5,6,7,8-Tetrahydrofolic acid Quattro_QQQ 25V, Positive-QTOF (Annotated)splash10-0nor-3269210000-20105ed6a7a6e24e24412012-07-24HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - 5,6,7,8-Tetrahydrofolic acid Quattro_QQQ 40V, Positive-QTOF (Annotated)splash10-00kr-1935200000-a9449c19c1ae3b0d70da2012-07-24HMDB team, MONAView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5,6,7,8-Tetrahydrofolic acid 10V, Positive-QTOFsplash10-0032-0431900000-ff1f3948e475611612932016-09-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5,6,7,8-Tetrahydrofolic acid 20V, Positive-QTOFsplash10-001i-0952300000-ed9d84bc39d490f6210e2016-09-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5,6,7,8-Tetrahydrofolic acid 40V, Positive-QTOFsplash10-001i-0920000000-0d0efcb6c323340d20b92016-09-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5,6,7,8-Tetrahydrofolic acid 10V, Negative-QTOFsplash10-0006-0001900000-abb4cec0eb79b0bd2de12016-09-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5,6,7,8-Tetrahydrofolic acid 20V, Negative-QTOFsplash10-0v4l-2356900000-2fd17d2f587bbd5e882c2016-09-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5,6,7,8-Tetrahydrofolic acid 40V, Negative-QTOFsplash10-0006-9441000000-8c630c7a3633467d6bb32016-09-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5,6,7,8-Tetrahydrofolic acid 10V, Positive-QTOFsplash10-0002-0290800000-00f48a2b40b4e602a17c2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5,6,7,8-Tetrahydrofolic acid 20V, Positive-QTOFsplash10-0002-1297200000-465db9c5756cff8e39f92021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5,6,7,8-Tetrahydrofolic acid 40V, Positive-QTOFsplash10-001i-1941000000-f6ca2e57ea63ce85dacc2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5,6,7,8-Tetrahydrofolic acid 10V, Negative-QTOFsplash10-0f7o-0006900000-fa8eb29192dbf7c6ab3c2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5,6,7,8-Tetrahydrofolic acid 20V, Negative-QTOFsplash10-0ufr-4908400000-b4e33d60be7ed7a197472021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 5,6,7,8-Tetrahydrofolic acid 40V, Negative-QTOFsplash10-0006-9721100000-5ff72a913fe80c96e7dd2021-10-12Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Experimental 2D NMR[1H, 13C]-HSQC NMR Spectrum (2D, 600 MHz, H2O, experimental)2012-12-05Wishart LabView Spectrum
Biological Properties
Cellular LocationsNot Available
Biospecimen Locations
  • Blood
Tissue LocationsNot Available
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodDetected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal details
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB022705
KNApSAcK IDNot Available
Chemspider ID1097
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkTetrahydrofolic acid
METLIN IDNot Available
PubChem Compound135402046
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]