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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2005-11-16 15:48:42 UTC
Update Date2021-09-14 14:57:37 UTC
HMDB IDHMDB0000972
Secondary Accession Numbers
  • HMDB00972
Metabolite Identification
Common Name10-Formyltetrahydrofolate
Description10-Formyltetrahydrofolate, also known as 10-formyl-THF or 10-formyl-H4pteglu1, 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. ightleftharpoons } CH2H2F + NADH + H+In the second step 5,10-methenyltetrahydrofolate undergoes hydrolysis:CH2H2F + H2O ⇌ {\displaystyle. 10-Formyltetrahydrofolate is a strong basic compound (based on its pKa). 10-Formyltetrahydrofolate exists in all eukaryotes, ranging from yeast to humans. Within humans, 10-formyltetrahydrofolate participates in a number of enzymatic reactions. In particular, 10-formyltetrahydrofolate and glycineamideribotide can be converted into tetrahydrofolic acid and 5'-phosphoribosyl-N-formylglycinamide through the action of the enzyme trifunctional purine biosynthetic protein adenosine-3. In addition, 10-formyltetrahydrofolate and AICAR can be converted into tetrahydrofolic acid and phosphoribosyl formamidocarboxamide; which is catalyzed by the enzyme bifunctional purine biosynthesis protein purh. In these reactions 10-CHO-THF is used as a substrate in formyltransferase reactions. In humans, 10-formyltetrahydrofolate is involved in the metabolic disorder called the gout or kelley-seegmiller syndrome pathway. Outside of the human body, 10-Formyltetrahydrofolate has been detected, but not quantified in, several different foods, such as breadfruits, catjang pea, climbing beans, kai-lans, and pears. This could make 10-formyltetrahydrofolate a potential biomarker for the consumption of these foods. 10-CHO-THF is required for the formylation of methionyl-tRNA formyltransferase to give fMet-tRNA.10-CHO-THF is produced from methylenetetrahydrofolate (CH2H4F) via a two step process. Two equivalents of 10-CHO-THF are required in purine biosynthesis, where 10-CHO-THF is a substrate for phosphoribosylaminoimidazolecarboxamide formyltransferase. ightleftharpoons } 10-formyltetrahydrofolate10-CHO-THF is also produced by the reactionATP + formate + tetrahydrofolate ⇌ {\displaystyle. 10-Formyltetrahydrofolate (10-CHO-THF) is a form of tetrahydrofolate that acts as a donor of formyl groups in anabolism. It can be converted back into tetrahydrofolate (THF) by formyltetrahydrofolate dehydrogenase or THF and formate by formyltetrahydrofolate deformylase. ightleftharpoons } ADP + phosphate + 10-formyltetrahydrofolateThis reaction is catalyzed by formate-tetrahydrofolate ligase.
Structure
Data?1582752168
Synonyms
ValueSource
10-Formyl-THFKegg
10-Formyltetrahydrofolic acidGenerator
10-Formyl-(6Rs)-tetrahydrofolic acidHMDB
10-Formyl-H4pteglu1HMDB
10-Formyl-tetrahydrofolateHMDB
10-FormyltetrahydropteroylglutamateHMDB
10-Formyltetrahydropteroylglutamic acidHMDB
10-FTHFHMDB
N-[p-[N-[(2-Amino-5,6,7,8-tetrahydro-4-hydroxy-6-pteridinyl)methyl]formamido]benzoyl]-glutamateHMDB
N-[p-[N-[(2-Amino-5,6,7,8-tetrahydro-4-hydroxy-6-pteridinyl)methyl]formamido]benzoyl]-glutamic acidHMDB
N-[p-[N-[(2-Amino-5,6,7,8-tetrahydro-4-hydroxy-6-pteridinyl)methyl]formamido]benzoyl]-L-glutamateHMDB
N-[p-[N-[(2-Amino-5,6,7,8-tetrahydro-4-hydroxy-6-pteridinyl)methyl]formamido]benzoyl]-L-glutamic acidHMDB
N10-Formyl-5,6,7,8-tetrahydrofolateHMDB
N10-Formyl-5,6,7,8-tetrahydrofolic acidHMDB
N10-Formyl-H4FHMDB
N10-Formyl-THFHMDB
N10-FormyltetrahydrofolateHMDB
N10-Formyltetrahydrofolic acidHMDB
N10-FormyltetrahydropteroylglutamateHMDB
Chemical FormulaC20H23N7O7
Average Molecular Weight473.4393
Monoisotopic Molecular Weight473.165896125
IUPAC Name(2S)-2-[(4-{N-[(4-hydroxy-2-imino-1,2,5,6,7,8-hexahydropteridin-6-yl)methyl]formamido}phenyl)formamido]pentanedioic acid
Traditional Name(2S)-2-[(4-{N-[(4-hydroxy-2-imino-5,6,7,8-tetrahydro-1H-pteridin-6-yl)methyl]formamido}phenyl)formamido]pentanedioic acid
CAS Registry Number2800-34-2
SMILES
NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C=C3)C(=O)N[C@@H](CCC(O)=O)C(O)=O)N2)N1
InChI Identifier
InChI=1S/C20H23N7O7/c21-20-25-16-15(18(32)26-20)23-11(7-22-16)8-27(9-28)12-3-1-10(2-4-12)17(31)24-13(19(33)34)5-6-14(29)30/h1-4,9,11,13,23H,5-8H2,(H,24,31)(H,29,30)(H,33,34)(H4,21,22,25,26,32)/t11?,13-/m0/s1
InChI KeyAUFGTPPARQZWDO-YUZLPWPTSA-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
  • N-acyl-alpha amino acid or derivatives
  • N-acyl-alpha-amino acid
  • Hippuric acid
  • Hippuric acid or derivatives
  • Acylaminobenzoic acid or derivatives
  • Alpha-amino acid or derivatives
  • Anilide
  • Benzoic acid or derivatives
  • Benzamide
  • Benzoyl
  • Pyrimidone
  • Aminopyrimidine
  • Secondary aliphatic/aromatic amine
  • Dicarboxylic acid or derivatives
  • Benzenoid
  • Pyrimidine
  • Monocyclic benzene moiety
  • Heteroaromatic compound
  • Vinylogous amide
  • Tertiary carboxylic acid amide
  • Amino acid or derivatives
  • Amino acid
  • Carboxamide group
  • Secondary carboxylic acid amide
  • Azacycle
  • Carboxylic acid
  • Carboxylic acid derivative
  • Secondary amine
  • Organic oxygen compound
  • Organic nitrogen compound
  • Carbonyl group
  • Hydrocarbon derivative
  • Amine
  • Organic oxide
  • Organopnictogen compound
  • Primary amine
  • Organooxygen compound
  • Organonitrogen compound
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Biological locationSource
Process
Naturally occurring process
RoleNot Available
Physical Properties
StateSolid
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
Water Solubility0.34 g/LALOGPS
logP-1.5ALOGPS
logP-4ChemAxon
logS-3.2ALOGPS
pKa (Strongest Acidic)2.95ChemAxon
pKa (Strongest Basic)5.75ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count12ChemAxon
Hydrogen Donor Count8ChemAxon
Polar Surface Area216.54 ŲChemAxon
Rotatable Bond Count9ChemAxon
Refractivity135.7 m³·mol⁻¹ChemAxon
Polarizability46.38 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
DarkChem[M+H]+210.18131661259
DarkChem[M-H]-202.01131661259
AllCCS[M+H]+203.45432859911
AllCCS[M-H]-200.24332859911
DeepCCS[M+H]+203.09730932474
DeepCCS[M-H]-200.70130932474
DeepCCS[M-2H]-233.58530932474
DeepCCS[M+Na]+209.0130932474
AllCCS[M+H]+203.532859911
AllCCS[M+H-H2O]+201.732859911
AllCCS[M+NH4]+205.032859911
AllCCS[M+Na]+205.532859911
AllCCS[M-H]-200.232859911
AllCCS[M+Na-2H]-201.032859911
AllCCS[M+HCOO]-201.932859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
10-FormyltetrahydrofolateNC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C=C3)C(=O)N[C@@H](CCC(O)=O)C(O)=O)N2)N15606.4Standard polar33892256
10-FormyltetrahydrofolateNC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C=C3)C(=O)N[C@@H](CCC(O)=O)C(O)=O)N2)N14344.4Standard non polar33892256
10-FormyltetrahydrofolateNC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C=C3)C(=O)N[C@@H](CCC(O)=O)C(O)=O)N2)N15383.7Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
10-Formyltetrahydrofolate,1TMS,isomer #1C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)[NH]3)C=C1)C(=O)O4973.5Semi standard non polar33892256
10-Formyltetrahydrofolate,1TMS,isomer #2C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)[NH]3)C=C14953.5Semi standard non polar33892256
10-Formyltetrahydrofolate,1TMS,isomer #3C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2)[NH]15084.1Semi standard non polar33892256
10-Formyltetrahydrofolate,1TMS,isomer #4C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)NC2=C1[NH]C(N)=NC2=O4834.8Semi standard non polar33892256
10-Formyltetrahydrofolate,1TMS,isomer #5C[Si](C)(C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[C@@H](CCC(=O)O)C(=O)O4922.4Semi standard non polar33892256
10-Formyltetrahydrofolate,1TMS,isomer #6C[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C1)[NH]C(N)=NC2=O4883.9Semi standard non polar33892256
10-Formyltetrahydrofolate,1TMS,isomer #7C[Si](C)(C)N1C(N)=NC(=O)C2=C1NCC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C1)N24932.0Semi standard non polar33892256
10-Formyltetrahydrofolate,2TMS,isomer #1C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)[NH]3)C=C1)C(=O)O[Si](C)(C)C4803.0Semi standard non polar33892256
10-Formyltetrahydrofolate,2TMS,isomer #10C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C14793.6Semi standard non polar33892256
10-Formyltetrahydrofolate,2TMS,isomer #11C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C14690.8Semi standard non polar33892256
10-Formyltetrahydrofolate,2TMS,isomer #12C[Si](C)(C)N(C1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2)[NH]1)[Si](C)(C)C4959.8Semi standard non polar33892256
10-Formyltetrahydrofolate,2TMS,isomer #13C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2)N1[Si](C)(C)C4965.8Semi standard non polar33892256
10-Formyltetrahydrofolate,2TMS,isomer #14C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C1)N24855.5Semi standard non polar33892256
10-Formyltetrahydrofolate,2TMS,isomer #15C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2)[NH]14908.4Semi standard non polar33892256
10-Formyltetrahydrofolate,2TMS,isomer #16C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2[Si](C)(C)C)[NH]14894.1Semi standard non polar33892256
10-Formyltetrahydrofolate,2TMS,isomer #17C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)NC2=C1[NH]C(N)=NC2=O4618.4Semi standard non polar33892256
10-Formyltetrahydrofolate,2TMS,isomer #18C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)N([Si](C)(C)C)C2=C1[NH]C(N)=NC2=O4615.4Semi standard non polar33892256
10-Formyltetrahydrofolate,2TMS,isomer #19C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)NC2=C1N([Si](C)(C)C)C(N)=NC2=O4716.4Semi standard non polar33892256
10-Formyltetrahydrofolate,2TMS,isomer #2C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2)[NH]14915.2Semi standard non polar33892256
10-Formyltetrahydrofolate,2TMS,isomer #20C[Si](C)(C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)[C@@H](CCC(=O)O)C(=O)O4743.9Semi standard non polar33892256
10-Formyltetrahydrofolate,2TMS,isomer #21C[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[NH]C(N)=NC2=O4664.6Semi standard non polar33892256
10-Formyltetrahydrofolate,2TMS,isomer #22C[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C1)N([Si](C)(C)C)C(N)=NC2=O4749.9Semi standard non polar33892256
10-Formyltetrahydrofolate,2TMS,isomer #3C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[Si](C)(C)C4742.0Semi standard non polar33892256
10-Formyltetrahydrofolate,2TMS,isomer #4C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)[NH]3)C=C1)C(=O)O4665.9Semi standard non polar33892256
10-Formyltetrahydrofolate,2TMS,isomer #5C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)C(=O)O4802.7Semi standard non polar33892256
10-Formyltetrahydrofolate,2TMS,isomer #6C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O4684.6Semi standard non polar33892256
10-Formyltetrahydrofolate,2TMS,isomer #7C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2)[NH]14920.5Semi standard non polar33892256
10-Formyltetrahydrofolate,2TMS,isomer #8C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[Si](C)(C)C4769.4Semi standard non polar33892256
10-Formyltetrahydrofolate,2TMS,isomer #9C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)[NH]3)C=C14665.3Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #1C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2)[NH]14769.3Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #1C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2)[NH]14263.2Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #1C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2)[NH]18009.6Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #10C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C)[NH]14713.3Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #10C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C)[NH]14342.8Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #10C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C)[NH]16763.5Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #11C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[Si](C)(C)C4463.8Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #11C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[Si](C)(C)C4210.2Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #11C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[Si](C)(C)C6922.0Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #12C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4591.1Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #12C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4149.2Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #12C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C7188.8Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #13C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4489.7Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #13C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4189.2Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #13C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C6561.4Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #14C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)C(=O)O4611.3Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #14C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)C(=O)O4283.0Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #14C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)C(=O)O7060.5Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #15C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O4454.3Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #15C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O4268.5Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #15C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O6506.1Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #16C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O4607.6Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #16C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O4269.9Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #16C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O6819.9Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #17C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C14772.3Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #17C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C14334.1Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #17C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C17690.3Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #18C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4809.1Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #18C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4300.8Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #18C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C7709.4Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #19C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)N24689.2Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #19C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)N24336.3Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #19C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)N27583.8Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #2C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[Si](C)(C)C4624.2Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #2C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[Si](C)(C)C4088.6Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #2C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[Si](C)(C)C7077.5Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #20C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)[NH]14741.7Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #20C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)[NH]14238.5Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #20C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)[NH]17916.4Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #21C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]14718.2Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #21C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]14305.9Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #21C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]16687.4Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #22C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[Si](C)(C)C4481.8Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #22C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[Si](C)(C)C4173.3Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #22C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[Si](C)(C)C6875.2Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #23C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4599.9Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #23C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4118.1Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #23C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C7140.0Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #24C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4502.1Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #24C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4156.8Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #24C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C6516.0Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #25C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C14594.7Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #25C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C14254.4Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #25C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C16982.6Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #26C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C14444.8Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #26C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C14221.0Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #26C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C16433.4Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #27C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C14593.0Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #27C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C14236.9Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #27C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C16740.7Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #28C[Si](C)(C)N(C1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2)N1[Si](C)(C)C)[Si](C)(C)C4855.0Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #28C[Si](C)(C)N(C1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2)N1[Si](C)(C)C)[Si](C)(C)C4406.4Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #28C[Si](C)(C)N(C1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2)N1[Si](C)(C)C)[Si](C)(C)C7652.9Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #29C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)NC2=C1[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O4726.2Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #29C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)NC2=C1[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O4429.1Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #29C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)NC2=C1[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O7478.9Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #3C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)[NH]3)C=C1)C(=O)O[Si](C)(C)C4516.7Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #3C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)[NH]3)C=C1)C(=O)O[Si](C)(C)C4199.0Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #3C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)[NH]3)C=C1)C(=O)O[Si](C)(C)C6959.9Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #30C[Si](C)(C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)[C@@H](CCC(=O)O)C(=O)O4729.8Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #30C[Si](C)(C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)[C@@H](CCC(=O)O)C(=O)O4335.4Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #30C[Si](C)(C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)[C@@H](CCC(=O)O)C(=O)O7667.8Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #31C[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C1)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O4776.5Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #31C[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C1)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O4479.8Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #31C[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C1)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O6636.4Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #32C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2)N1[Si](C)(C)C4772.3Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #32C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2)N1[Si](C)(C)C4442.0Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #32C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2)N1[Si](C)(C)C7394.4Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #33C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4758.4Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #33C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4309.4Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #33C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C7681.9Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #34C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4800.0Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #34C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4457.9Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #34C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C6794.6Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #35C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N24648.5Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #35C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N24355.1Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #35C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N27547.1Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #36C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C1)N2[Si](C)(C)C4681.6Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #36C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C1)N2[Si](C)(C)C4405.0Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #36C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C1)N2[Si](C)(C)C6470.1Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #37C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]14698.8Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #37C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]14343.0Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #37C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]16720.1Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #38C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)N([Si](C)(C)C)C2=C1[NH]C(N)=NC2=O4406.4Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #38C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)N([Si](C)(C)C)C2=C1[NH]C(N)=NC2=O4250.6Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #38C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)N([Si](C)(C)C)C2=C1[NH]C(N)=NC2=O6423.8Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #39C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)NC2=C1N([Si](C)(C)C)C(N)=NC2=O4537.5Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #39C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)NC2=C1N([Si](C)(C)C)C(N)=NC2=O4260.0Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #39C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)NC2=C1N([Si](C)(C)C)C(N)=NC2=O6971.6Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #4C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4647.4Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #4C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4140.3Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #4C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C7211.5Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #40C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)C(N)=NC2=O4591.4Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #40C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)C(N)=NC2=O4366.8Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #40C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)C(N)=NC2=O6615.7Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #41C[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N([Si](C)(C)C)C(N)=NC2=O4553.5Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #41C[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N([Si](C)(C)C)C(N)=NC2=O4292.9Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #41C[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N([Si](C)(C)C)C(N)=NC2=O6784.5Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #5C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4547.5Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #5C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4153.4Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #5C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C6576.6Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #6C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)C(=O)O4758.5Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #6C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)C(=O)O4372.8Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #6C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)C(=O)O7769.8Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #7C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2)N1[Si](C)(C)C4817.6Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #7C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2)N1[Si](C)(C)C4328.3Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #7C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2)N1[Si](C)(C)C7786.0Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #8C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)N24697.2Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #8C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)N24363.4Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #8C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)N27655.2Standard polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #9C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2)[NH]14716.5Semi standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #9C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2)[NH]14270.1Standard non polar33892256
10-Formyltetrahydrofolate,3TMS,isomer #9C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2)[NH]17964.0Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #1C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)C(=O)O[Si](C)(C)C4633.8Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #1C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)C(=O)O[Si](C)(C)C4304.9Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #1C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)C(=O)O[Si](C)(C)C7344.8Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #10C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4307.1Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #10C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4149.8Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #10C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C6187.9Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #11C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4494.7Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #11C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4147.4Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #11C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C6461.4Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #12C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)[Si](C)(C)C4566.1Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #12C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)[Si](C)(C)C4317.0Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #12C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)[Si](C)(C)C7302.8Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #13C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)C(=O)O4590.3Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #13C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)C(=O)O4411.2Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #13C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)C(=O)O7168.4Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #14C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)C=C1)C(=O)O4711.5Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #14C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)C=C1)C(=O)O4366.9Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #14C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)C=C1)C(=O)O7160.4Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #15C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O4622.8Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #15C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O4352.8Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #15C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O6207.9Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #16C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2)N1[Si](C)(C)C4642.0Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #16C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2)N1[Si](C)(C)C4405.7Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #16C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2)N1[Si](C)(C)C7077.9Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #17C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4609.0Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #17C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4255.7Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #17C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C7343.7Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #18C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4676.1Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #18C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4331.2Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #18C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C6421.6Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #19C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)N24504.7Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #19C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)N24318.3Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #19C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)N27251.7Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #2C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4681.7Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #2C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4231.5Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #2C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C7385.6Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #20C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)N2[Si](C)(C)C4543.5Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #20C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)N2[Si](C)(C)C4300.7Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #20C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)N2[Si](C)(C)C6123.6Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #21C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]14546.2Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #21C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]14245.9Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #21C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]16342.3Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #22C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4417.5Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #22C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4258.5Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #22C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C6679.2Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #23C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4287.2Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #23C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4185.2Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #23C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C6161.1Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #24C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4438.8Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #24C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4192.9Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #24C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C6444.0Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #25C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O4475.9Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #25C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O4287.1Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #25C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O6347.5Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #26C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)[Si](C)(C)C4592.4Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #26C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)[Si](C)(C)C4293.0Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #26C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)[Si](C)(C)C7260.9Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #27C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C14587.1Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #27C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C14391.5Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #27C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C17107.0Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #28C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)C=C14699.2Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #28C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)C=C14346.8Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #28C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)C=C17095.2Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #29C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)N2[Si](C)(C)C)C=C14625.3Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #29C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)N2[Si](C)(C)C)C=C14329.9Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #29C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)N2[Si](C)(C)C)C=C16144.8Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #3C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)N24547.3Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #3C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)N24285.3Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #3C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)N27286.9Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #30C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4647.6Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #30C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4388.4Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #30C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C7017.7Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #31C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4624.9Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #31C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4239.4Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #31C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C7303.3Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #32C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4670.2Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #32C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4319.1Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #32C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C6360.4Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #33C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N24515.6Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #33C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N24297.8Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #33C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N27214.1Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #34C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)N2[Si](C)(C)C4541.9Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #34C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)N2[Si](C)(C)C4275.2Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #34C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)N2[Si](C)(C)C6067.6Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #35C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]14562.2Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #35C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]14231.0Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #35C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]16306.6Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #36C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4434.5Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #36C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4235.1Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #36C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C6641.5Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #37C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4291.0Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #37C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4162.3Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #37C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C6127.4Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #38C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4451.5Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #38C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4175.8Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #38C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C6406.2Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #39C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C14462.3Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #39C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C14260.8Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #39C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C16285.5Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #4C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)[NH]14598.3Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #4C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)[NH]14193.4Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #4C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)[NH]17562.6Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #40C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)NC2=C1N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O4679.8Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #40C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)NC2=C1N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O4494.9Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #40C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)NC2=C1N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O6902.6Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #41C[Si](C)(C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)C=C1)[C@@H](CCC(=O)O)C(=O)O4638.6Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #41C[Si](C)(C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)C=C1)[C@@H](CCC(=O)O)C(=O)O4361.3Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #41C[Si](C)(C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)C=C1)[C@@H](CCC(=O)O)C(=O)O7065.1Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #42C[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C1)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O4740.3Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #42C[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C1)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O4481.6Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #42C[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C1)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O6297.8Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #43C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)NC2=C1[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O4522.8Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #43C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)NC2=C1[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O4412.3Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #43C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)NC2=C1[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O7064.9Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #44C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)N([Si](C)(C)C)C2=C1[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O4567.9Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #44C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)N([Si](C)(C)C)C2=C1[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O4435.4Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #44C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)N([Si](C)(C)C)C2=C1[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O6009.4Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #45C[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O4577.1Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #45C[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O4399.8Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #45C[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O6215.3Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #46C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4584.1Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #46C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4409.3Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #46C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C6967.8Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #47C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4655.8Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #47C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4438.7Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #47C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C6075.5Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #48C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4624.5Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #48C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4357.1Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #48C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C6385.7Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #49C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N2[Si](C)(C)C4517.2Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #49C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N2[Si](C)(C)C4310.5Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #49C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N2[Si](C)(C)C6090.4Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #5C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]14581.1Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #5C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]14193.5Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #5C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)[NH]16306.8Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #50C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N([C@@H](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)=NC2=O4419.1Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #50C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N([C@@H](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)=NC2=O4281.7Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #50C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N([C@@H](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)=NC2=O6276.2Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #6C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[Si](C)(C)C4339.8Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #6C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[Si](C)(C)C4156.4Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #6C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[Si](C)(C)C6599.2Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #7C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4498.1Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #7C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4094.7Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #7C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C6825.2Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #8C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4389.7Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #8C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4104.7Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #8C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C6228.3Standard polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #9C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4465.9Semi standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #9C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4237.7Standard non polar33892256
10-Formyltetrahydrofolate,4TMS,isomer #9C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C6716.2Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #1C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)[Si](C)(C)C4494.3Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #1C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)[Si](C)(C)C4261.3Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #1C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)[Si](C)(C)C6964.3Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #10C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](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]14466.1Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #10C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](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]14147.3Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #10C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](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]15955.3Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #11C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4340.0Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #11C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4215.8Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #11C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C)C=C1)[Si](C)(C)C6414.6Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #12C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4210.9Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #12C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4110.3Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #12C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C5912.5Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #13C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4393.0Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #13C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4113.5Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #13C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C6171.9Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #14C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4376.5Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #14C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4188.7Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #14C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C6076.5Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #15C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)[Si](C)(C)C4411.1Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #15C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)[Si](C)(C)C4381.5Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #15C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)[Si](C)(C)C6794.9Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #16C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4533.4Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #16C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4310.3Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #16C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)C=C1)[Si](C)(C)C6754.6Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #17C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4469.1Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #17C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4296.0Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #17C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C5836.5Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #18C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)C=C1)C(=O)O4582.6Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #18C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)C=C1)C(=O)O4458.8Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #18C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)C=C1)C(=O)O6605.2Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #19C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O4489.2Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #19C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O4347.1Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #19C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O5696.5Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #2C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)C(=O)O[Si](C)(C)C4486.0Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #2C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)C(=O)O[Si](C)(C)C4344.1Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #2C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)C(=O)O[Si](C)(C)C6837.7Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #20C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O4621.0Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #20C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O4331.6Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #20C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)C(=O)O5920.9Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #21C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4462.8Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #21C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4362.3Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #21C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C6691.8Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #22C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4542.5Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #22C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4325.4Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #22C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C5768.2Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #23C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](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)C4511.1Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #23C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](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)C4257.0Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #23C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](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)C6062.0Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #24C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)N2[Si](C)(C)C4409.1Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #24C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)N2[Si](C)(C)C4236.5Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #24C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)N2[Si](C)(C)C5787.2Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #25C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4336.6Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #25C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4224.4Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #25C[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C6057.7Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #26C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)[Si](C)(C)C4419.7Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #26C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)[Si](C)(C)C4365.3Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #26C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)C=C1)[Si](C)(C)C6766.3Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #27C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4541.3Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #27C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)C=C1)[Si](C)(C)C4299.6Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #27C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)C=C1)[Si](C)(C)C6724.7Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #28C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4483.1Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #28C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4286.6Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #28C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)N2[Si](C)(C)C)C=C1)[Si](C)(C)C5807.9Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #29C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)C=C14581.2Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #29C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)C=C14446.6Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #29C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)C=C16556.2Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #3C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4604.6Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #3C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4278.3Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #3C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C6799.2Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #30C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)N2[Si](C)(C)C)C=C14479.0Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #30C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)N2[Si](C)(C)C)C=C14331.7Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #30C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)N2[Si](C)(C)C)C=C15652.4Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #31C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C14616.9Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #31C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C14329.4Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #31C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C15872.7Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #32C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4476.2Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #32C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4353.0Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #32C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C6662.8Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #33C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4545.4Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #33C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4314.9Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #33C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C5723.7Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #34C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](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)C4532.7Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #34C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](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)C4253.5Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #34C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](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)C6033.3Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #35C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N2[Si](C)(C)C4410.7Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #35C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N2[Si](C)(C)C4224.3Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #35C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N2[Si](C)(C)C5760.8Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #36C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4348.6Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #36C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C4212.1Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #36C[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C)C3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2[Si](C)(C)C)C=C1)[Si](C)(C)C6028.6Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #37C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)NC2=C1N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O4523.6Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #37C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)NC2=C1N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O4474.9Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #37C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)NC2=C1N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O6512.2Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #38C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O4613.5Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #38C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O4472.7Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #38C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)N([Si](C)(C)C)C2=C1N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O5671.9Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #39C[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O4557.2Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #39C[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O4411.4Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #39C[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O5947.8Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #4C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4531.7Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #4C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4235.1Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #4C[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)N2[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C5797.0Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #40C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)N([Si](C)(C)C)C2=C1[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O4433.6Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #40C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)N([Si](C)(C)C)C2=C1[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O4381.2Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #40C[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C2)N([Si](C)(C)C)C2=C1[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O5686.3Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #41C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4500.0Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #41C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C4351.8Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #41C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2[Si](C)(C)C)N1[Si](C)(C)C5751.8Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #5C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4511.3Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #5C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C4327.1Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #5C[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2)N1[Si](C)(C)C6731.1Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #6C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](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)C4510.2Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #6C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](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)C4175.9Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #6C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](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)C7012.0Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #7C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](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)C4561.0Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #7C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](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)C4196.9Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #7C[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](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)C6026.1Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #8C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N24396.9Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #8C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N24243.7Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #8C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N26937.9Standard polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #9C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)N2[Si](C)(C)C4433.3Semi standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #9C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)N2[Si](C)(C)C4184.3Standard non polar33892256
10-Formyltetrahydrofolate,5TMS,isomer #9C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)N2[Si](C)(C)C5741.6Standard polar33892256
10-Formyltetrahydrofolate,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)[NH]3)C=C1)C(=O)O5241.3Semi standard non polar33892256
10-Formyltetrahydrofolate,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)[NH]3)C=C15209.9Semi standard non polar33892256
10-Formyltetrahydrofolate,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2)[NH]15282.2Semi standard non polar33892256
10-Formyltetrahydrofolate,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)NC2=C1[NH]C(N)=NC2=O5124.0Semi standard non polar33892256
10-Formyltetrahydrofolate,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[C@@H](CCC(=O)O)C(=O)O5176.8Semi standard non polar33892256
10-Formyltetrahydrofolate,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C1)[NH]C(N)=NC2=O5187.2Semi standard non polar33892256
10-Formyltetrahydrofolate,1TBDMS,isomer #7CC(C)(C)[Si](C)(C)N1C(N)=NC(=O)C2=C1NCC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C1)N25120.8Semi standard non polar33892256
10-Formyltetrahydrofolate,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)[NH]3)C=C1)C(=O)O[Si](C)(C)C(C)(C)C5299.5Semi standard non polar33892256
10-Formyltetrahydrofolate,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C(C)(C)C)C=C15229.4Semi standard non polar33892256
10-Formyltetrahydrofolate,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C(C)(C)C)C=C15227.8Semi standard non polar33892256
10-Formyltetrahydrofolate,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)N(C1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2)[NH]1)[Si](C)(C)C(C)(C)C5364.1Semi standard non polar33892256
10-Formyltetrahydrofolate,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2)N1[Si](C)(C)C(C)(C)C5353.3Semi standard non polar33892256
10-Formyltetrahydrofolate,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C(C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C1)N25268.9Semi standard non polar33892256
10-Formyltetrahydrofolate,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C3)N2)[NH]15310.2Semi standard non polar33892256
10-Formyltetrahydrofolate,2TBDMS,isomer #16CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2[Si](C)(C)C(C)(C)C)[NH]15366.4Semi standard non polar33892256
10-Formyltetrahydrofolate,2TBDMS,isomer #17CC(C)(C)[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C2)NC2=C1[NH]C(N)=NC2=O5131.4Semi standard non polar33892256
10-Formyltetrahydrofolate,2TBDMS,isomer #18CC(C)(C)[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)N([Si](C)(C)C(C)(C)C)C2=C1[NH]C(N)=NC2=O5170.9Semi standard non polar33892256
10-Formyltetrahydrofolate,2TBDMS,isomer #19CC(C)(C)[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)NC2=C1N([Si](C)(C)C(C)(C)C)C(N)=NC2=O5145.9Semi standard non polar33892256
10-Formyltetrahydrofolate,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C3)N2)[NH]15360.8Semi standard non polar33892256
10-Formyltetrahydrofolate,2TBDMS,isomer #20CC(C)(C)[Si](C)(C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C(C)(C)C)C=C1)[C@@H](CCC(=O)O)C(=O)O5173.3Semi standard non polar33892256
10-Formyltetrahydrofolate,2TBDMS,isomer #21CC(C)(C)[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)[NH]C(N)=NC2=O5196.3Semi standard non polar33892256
10-Formyltetrahydrofolate,2TBDMS,isomer #22CC(C)(C)[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C1)N([Si](C)(C)C(C)(C)C)C(N)=NC2=O5234.2Semi standard non polar33892256
10-Formyltetrahydrofolate,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[Si](C)(C)C(C)(C)C5237.6Semi standard non polar33892256
10-Formyltetrahydrofolate,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C(C)(C)C)C3=C(N2)C(=O)N=C(N)[NH]3)C=C1)C(=O)O5196.1Semi standard non polar33892256
10-Formyltetrahydrofolate,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C(C)(C)C)C=C1)C(=O)O5254.4Semi standard non polar33892256
10-Formyltetrahydrofolate,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C(C)(C)C)C=C1)C(=O)O5240.4Semi standard non polar33892256
10-Formyltetrahydrofolate,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C3)N2)[NH]15343.7Semi standard non polar33892256
10-Formyltetrahydrofolate,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[Si](C)(C)C(C)(C)C5240.7Semi standard non polar33892256
10-Formyltetrahydrofolate,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C(C)(C)C)C3=C(N2)C(=O)N=C(N)[NH]3)C=C15175.0Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C=C3)N2)[NH]15357.2Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C=C3)N2)[NH]14797.3Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C=C3)N2)[NH]17668.9Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C(C)(C)C)[NH]15371.6Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C(C)(C)C)[NH]14880.3Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C3)N2[Si](C)(C)C(C)(C)C)[NH]16547.0Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C(C)(C)C)C3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[Si](C)(C)C(C)(C)C5160.4Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C(C)(C)C)C3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[Si](C)(C)C(C)(C)C4696.3Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C(C)(C)C)C3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[Si](C)(C)C(C)(C)C6711.9Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C5232.2Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C4636.9Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C6823.1Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C5196.0Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C4684.1Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C6385.3Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C(C)(C)C)C3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C(C)(C)C)C=C1)C(=O)O5245.6Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C(C)(C)C)C3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C(C)(C)C)C=C1)C(=O)O4801.9Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C(C)(C)C)C3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C(C)(C)C)C=C1)C(=O)O6792.4Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C(C)(C)C)C=C1)C(=O)O5198.6Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C(C)(C)C)C=C1)C(=O)O4762.0Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C(C)(C)C)C=C1)C(=O)O6388.4Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #16CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C(C)(C)C)N2[Si](C)(C)C(C)(C)C)C=C1)C(=O)O5316.7Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #16CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C(C)(C)C)N2[Si](C)(C)C(C)(C)C)C=C1)C(=O)O4769.4Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #16CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C(C)(C)C)N2[Si](C)(C)C(C)(C)C)C=C1)C(=O)O6541.2Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]3)C=C15376.3Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]3)C=C14848.4Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]3)C=C17369.0Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #18CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C3)N2)N1[Si](C)(C)C(C)(C)C5378.3Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #18CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C3)N2)N1[Si](C)(C)C(C)(C)C4794.9Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #18CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C3)N2)N1[Si](C)(C)C(C)(C)C7305.1Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #19CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C(C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C1)N25284.1Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #19CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C(C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C1)N24875.6Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #19CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C(C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C1)N27351.7Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[Si](C)(C)C(C)(C)C5270.4Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[Si](C)(C)C(C)(C)C4597.2Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[Si](C)(C)C(C)(C)C6783.7Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #20CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3)N2)[NH]15295.9Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #20CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3)N2)[NH]14765.1Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #20CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3)N2)[NH]17587.4Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #21CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C3)N2[Si](C)(C)C(C)(C)C)[NH]15365.5Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #21CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C3)N2[Si](C)(C)C(C)(C)C)[NH]14864.9Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #21CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C3)N2[Si](C)(C)C(C)(C)C)[NH]16506.4Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #22CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C(C)(C)C)C3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[Si](C)(C)C(C)(C)C5154.8Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #22CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C(C)(C)C)C3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[Si](C)(C)C(C)(C)C4681.5Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #22CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C(C)(C)C)C3=C(N2)C(=O)N=C(N)[NH]3)C=C1)[Si](C)(C)C(C)(C)C6690.4Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C5229.2Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C4621.7Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C6802.0Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #24CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C5197.9Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #24CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C4677.4Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #24CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C6363.8Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C(C)(C)C)C3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C(C)(C)C)C=C15224.9Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C(C)(C)C)C3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C(C)(C)C)C=C14777.5Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C(C)(C)C)C3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C(C)(C)C)C=C16746.1Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #26CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C(C)(C)C)C=C15180.5Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #26CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C(C)(C)C)C=C14732.8Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #26CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C(C)(C)C)C3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C(C)(C)C)C=C16343.3Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C(C)(C)C)N2[Si](C)(C)C(C)(C)C)C=C15295.4Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C(C)(C)C)N2[Si](C)(C)C(C)(C)C)C=C14751.8Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C(C)(C)C)N2[Si](C)(C)C(C)(C)C)C=C16494.6Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #28CC(C)(C)[Si](C)(C)N(C1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2)N1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C5430.5Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #28CC(C)(C)[Si](C)(C)N(C1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2)N1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4867.1Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #28CC(C)(C)[Si](C)(C)N(C1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2)N1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C7226.8Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #29CC(C)(C)[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)NC2=C1[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O5341.5Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #29CC(C)(C)[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)NC2=C1[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O4919.4Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #29CC(C)(C)[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)NC2=C1[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O7234.7Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C(C)(C)C)C3=C(N2)C(=O)N=C(N)[NH]3)C=C1)C(=O)O[Si](C)(C)C(C)(C)C5201.7Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C(C)(C)C)C3=C(N2)C(=O)N=C(N)[NH]3)C=C1)C(=O)O[Si](C)(C)C(C)(C)C4702.8Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CN([Si](C)(C)C(C)(C)C)C3=C(N2)C(=O)N=C(N)[NH]3)C=C1)C(=O)O[Si](C)(C)C(C)(C)C6747.7Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #30CC(C)(C)[Si](C)(C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]3)C=C1)[C@@H](CCC(=O)O)C(=O)O5328.4Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #30CC(C)(C)[Si](C)(C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]3)C=C1)[C@@H](CCC(=O)O)C(=O)O4832.0Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #30CC(C)(C)[Si](C)(C)N(C(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]3)C=C1)[C@@H](CCC(=O)O)C(=O)O7320.8Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #31CC(C)(C)[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C1)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O5427.7Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #31CC(C)(C)[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C1)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O4974.7Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #31CC(C)(C)[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C1)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O6403.8Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #32CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C(C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2)N1[Si](C)(C)C(C)(C)C5356.3Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #32CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C(C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2)N1[Si](C)(C)C(C)(C)C4961.7Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #32CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C(C)(C)C)CC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2)N1[Si](C)(C)C(C)(C)C7089.3Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #33CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C3)N2)N1[Si](C)(C)C(C)(C)C5334.2Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #33CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C3)N2)N1[Si](C)(C)C(C)(C)C4784.2Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #33CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C3)N2)N1[Si](C)(C)C(C)(C)C7257.0Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #34CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)C5454.6Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #34CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)C4945.3Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #34CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C3)N2[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)C6469.1Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #35CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C(C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)N25260.7Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #35CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C(C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)N24870.8Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #35CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C(C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)N27307.0Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #36CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C(C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C1)N2[Si](C)(C)C(C)(C)C5361.3Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #36CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C(C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C1)N2[Si](C)(C)C(C)(C)C4926.1Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #36CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C(C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C1)N2[Si](C)(C)C(C)(C)C6358.2Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #37CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C3)N2[Si](C)(C)C(C)(C)C)[NH]15352.6Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #37CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C3)N2[Si](C)(C)C(C)(C)C)[NH]14866.0Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #37CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C3)N2[Si](C)(C)C(C)(C)C)[NH]16512.1Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #38CC(C)(C)[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C2)N([Si](C)(C)C(C)(C)C)C2=C1[NH]C(N)=NC2=O5158.7Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #38CC(C)(C)[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C2)N([Si](C)(C)C(C)(C)C)C2=C1[NH]C(N)=NC2=O4730.7Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #38CC(C)(C)[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C2)N([Si](C)(C)C(C)(C)C)C2=C1[NH]C(N)=NC2=O6333.4Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #39CC(C)(C)[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C2)NC2=C1N([Si](C)(C)C(C)(C)C)C(N)=NC2=O5191.7Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #39CC(C)(C)[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C2)NC2=C1N([Si](C)(C)C(C)(C)C)C(N)=NC2=O4767.3Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #39CC(C)(C)[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C2)NC2=C1N([Si](C)(C)C(C)(C)C)C(N)=NC2=O6724.1Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C(C)(C)C)C=C1)C(=O)O[Si](C)(C)C(C)(C)C5271.4Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C(C)(C)C)C=C1)C(=O)O[Si](C)(C)C(C)(C)C4648.4Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N)N3[Si](C)(C)C(C)(C)C)C=C1)C(=O)O[Si](C)(C)C(C)(C)C6854.0Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #40CC(C)(C)[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)N([Si](C)(C)C(C)(C)C)C2=C1N([Si](C)(C)C(C)(C)C)C(N)=NC2=O5288.3Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #40CC(C)(C)[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)N([Si](C)(C)C(C)(C)C)C2=C1N([Si](C)(C)C(C)(C)C)C(N)=NC2=O4857.0Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #40CC(C)(C)[Si](C)(C)N1CC(CN(C=O)C2=CC=C(C(=O)N[C@@H](CCC(=O)O)C(=O)O)C=C2)N([Si](C)(C)C(C)(C)C)C2=C1N([Si](C)(C)C(C)(C)C)C(N)=NC2=O6453.1Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #41CC(C)(C)[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)C(N)=NC2=O5254.6Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #41CC(C)(C)[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)C(N)=NC2=O4770.7Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #41CC(C)(C)[Si](C)(C)N1C2=C(NCC1CN(C=O)C1=CC=C(C(=O)N([C@@H](CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)C(N)=NC2=O6517.4Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C(C)(C)C)C=C1)C(=O)O[Si](C)(C)C(C)(C)C5244.6Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C(C)(C)C)C=C1)C(=O)O[Si](C)(C)C(C)(C)C4690.3Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(C(=O)N=C(N)[NH]3)N2[Si](C)(C)C(C)(C)C)C=C1)C(=O)O[Si](C)(C)C(C)(C)C6404.1Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]3)C=C1)C(=O)O5392.1Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]3)C=C1)C(=O)O4877.1Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](NC(=O)C1=CC=C(N(C=O)CC2CNC3=C(N2)C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]3)C=C1)C(=O)O7412.5Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C3)N2)N1[Si](C)(C)C(C)(C)C5394.8Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C3)N2)N1[Si](C)(C)C(C)(C)C4817.6Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C3)N2)N1[Si](C)(C)C(C)(C)C7346.4Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C(C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C1)N25311.5Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C(C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C1)N24900.2Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C(C)(C)C)CC(CN(C=O)C1=CC=C(C(=O)N[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C1)N27392.9Standard polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C)C=C3)N2)[NH]15289.6Semi standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C)C=C3)N2)[NH]14778.7Standard non polar33892256
10-Formyltetrahydrofolate,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C=O)C3=CC=C(C(=O)N([C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C)C=C3)N2)[NH]17608.1Standard polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - 10-Formyltetrahydrofolate GC-MS (Non-derivatized) - 70eV, Positivesplash10-004j-2733900000-d416b73a1673d1220b872017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 10-Formyltetrahydrofolate GC-MS (2 TMS) - 70eV, Positivesplash10-0v4i-2913374000-7b894dbf7f83fe5cd9d72017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 10-Formyltetrahydrofolate GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 10-Formyltetrahydrofolate GC-MS (TMS_1_1) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 10-Formyltetrahydrofolate GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 10-Formyltetrahydrofolate GC-MS (TMS_1_3) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 10-Formyltetrahydrofolate GC-MS (TMS_1_4) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 10-Formyltetrahydrofolate GC-MS (TMS_1_5) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 10-Formyltetrahydrofolate GC-MS (TMS_1_6) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 10-Formyltetrahydrofolate GC-MS (TMS_1_7) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 10-Formyltetrahydrofolate GC-MS (TMS_2_2) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 10-Formyltetrahydrofolate GC-MS (TMS_2_3) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 10-Formyltetrahydrofolate GC-MS (TMS_2_4) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 10-Formyltetrahydrofolate GC-MS (TMS_2_5) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 10-Formyltetrahydrofolate GC-MS (TMS_2_6) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 10-Formyltetrahydrofolate GC-MS (TMS_2_7) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 10-Formyltetrahydrofolate GC-MS (TMS_2_8) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 10-Formyltetrahydrofolate GC-MS (TMS_2_9) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 10-Formyltetrahydrofolate GC-MS (TMS_2_10) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 10-Formyltetrahydrofolate GC-MS (TMS_2_11) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 10-Formyltetrahydrofolate GC-MS (TMS_2_12) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 10-Formyltetrahydrofolate GC-MS (TMS_2_13) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 10-Formyltetrahydrofolate GC-MS (TMS_2_14) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 10-Formyltetrahydrofolate GC-MS (TMS_2_15) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 10-Formyltetrahydrofolate GC-MS (TMS_2_16) - 70eV, PositiveNot Available2021-11-06Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10-Formyltetrahydrofolate 10V, Positive-QTOFsplash10-05cr-0401900000-21104c38dc03ca4e7a0e2016-09-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10-Formyltetrahydrofolate 20V, Positive-QTOFsplash10-003r-0935700000-2f12524764eca10dcf152016-09-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10-Formyltetrahydrofolate 40V, Positive-QTOFsplash10-001i-0910000000-03f41886e7967d0201eb2016-09-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10-Formyltetrahydrofolate 10V, Negative-QTOFsplash10-00di-0000900000-1244cea99701ed75f41c2016-09-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10-Formyltetrahydrofolate 20V, Negative-QTOFsplash10-00bc-1123900000-cdcadc51a3f47cb938862016-09-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10-Formyltetrahydrofolate 40V, Negative-QTOFsplash10-0006-9842000000-62efadef6701421ce2c52016-09-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10-Formyltetrahydrofolate 10V, Positive-QTOFsplash10-002b-0002900000-e6e9d4109ecb3ef0bbee2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10-Formyltetrahydrofolate 20V, Positive-QTOFsplash10-004i-1729400000-02f5fdbf97e3ce7a3a952021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10-Formyltetrahydrofolate 40V, Positive-QTOFsplash10-001j-0932000000-68bdb6e09b80b22288c62021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10-Formyltetrahydrofolate 10V, Negative-QTOFsplash10-004i-0000900000-19d839ffa3d1b19884502021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10-Formyltetrahydrofolate 20V, Negative-QTOFsplash10-004i-0200900000-93ad732aff1ff91aa0852021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10-Formyltetrahydrofolate 40V, Negative-QTOFsplash10-0v03-4920300000-17e6f1c09b0e093800ef2021-09-24Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-16Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Extracellular
  • Mitochondria
  • Lysosome
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB030256
KNApSAcK IDNot Available
Chemspider ID109092
KEGG Compound IDC00234
BioCyc IDNot Available
BiGG ID34337
Wikipedia Link10-Formyltetrahydrofolate
METLIN ID5912
PubChem Compound122347
PDB IDNot Available
ChEBI ID15637
Food Biomarker OntologyNot Available
VMH ID10FTHF
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceDenis V; Daignan-Fornier B Synthesis of glutamine, glycine and 10-formyl tetrahydrofolate is coregulated with purine biosynthesis in Saccharomyces cerevisiae. Molecular & general genetics : MGG (1998), 259(3), 246-55.
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Xu L, Li C, Olson AJ, Wilson IA: Crystal structure of avian aminoimidazole-4-carboxamide ribonucleotide transformylase in complex with a novel non-folate inhibitor identified by virtual ligand screening. J Biol Chem. 2004 Nov 26;279(48):50555-65. Epub 2004 Sep 7. [PubMed:15355974 ]
  2. Baggott JE, Tamura T: Bioactivity of orally administered unnatural isomers, [6R]-5-formyltetrahydrofolate and [6S]-5,10-methenyltetrahydrofolate, in humans. Biochim Biophys Acta. 1999 Oct 18;1472(1-2):323-32. [PubMed:10572954 ]
  3. Johlin FC, Swain E, Smith C, Tephly TR: Studies on the mechanism of methanol poisoning: purification and comparison of rat and human liver 10-formyltetrahydrofolate dehydrogenase. Mol Pharmacol. 1989 Jun;35(6):745-50. [PubMed:2733692 ]
  4. Kirksey TJ, Appling DR: Site-directed mutagenesis of a highly conserved aspartate in the putative 10-formyl-tetrahydrofolate binding site of yeast C1-tetrahydrofolate synthase. Arch Biochem Biophys. 1996 Sep 1;333(1):251-9. [PubMed:8806778 ]
  5. Baggott JE, Robinson CB, Johnston KE: Bioactivity of [6R]-5-formyltetrahydrofolate, an unusual isomer, in humans and Enterococcus hirae, and cytochrome c oxidation of 10-formytetrahydrofolate to 10-formyldihydrofolate. Biochem J. 2001 Feb 15;354(Pt 1):115-22. [PubMed:11171086 ]
  6. Boger DL, Labroli MA, Marsilje TH, Jin Q, Hedrick MP, Baker SJ, Shim JH, Benkovic SJ: Conformationally restricted analogues designed for selective inhibition of GAR Tfase versus thymidylate synthase or dihydrofolate reductase. Bioorg Med Chem. 2000 May;8(5):1075-86. [PubMed:10882019 ]

Enzymes

General function:
Involved in catalytic activity
Specific function:
Not Available
Gene Name:
GART
Uniprot ID:
P22102
Molecular weight:
107766.295
Reactions
10-Formyltetrahydrofolate + Glycineamideribotide → Tetrahydrofolic acid + N(2)-formyl-N(1)-(5-phospho-D-ribosyl)glycinamidedetails
10-Formyltetrahydrofolate + Glycineamideribotide → Tetrahydrofolic acid + 5'-Phosphoribosyl-N-formylglycinamidedetails
General function:
Involved in IMP cyclohydrolase activity
Specific function:
Bifunctional enzyme that catalyzes 2 steps in purine biosynthesis.
Gene Name:
ATIC
Uniprot ID:
P31939
Molecular weight:
64615.255
Reactions
10-Formyltetrahydrofolate + AICAR → Tetrahydrofolic acid + Phosphoribosyl formamidocarboxamidedetails
General function:
Involved in catalytic activity
Specific function:
Not Available
Gene Name:
MTHFD2
Uniprot ID:
P13995
Molecular weight:
37894.775
Reactions
5,10-Methenyltetrahydrofolic acid + Water → 10-Formyltetrahydrofolatedetails
5,10-Methenyltetrahydrofolic acid + Water → 10-Formyltetrahydrofolate + Hydrogen Iondetails
General function:
Involved in formate-tetrahydrofolate ligase activity
Specific function:
Not Available
Gene Name:
MTHFD1
Uniprot ID:
P11586
Molecular weight:
101530.36
Reactions
5,10-Methenyltetrahydrofolic acid + Water → 10-Formyltetrahydrofolatedetails
Adenosine triphosphate + Formic acid + Tetrahydrofolic acid → ADP + Phosphate + 10-Formyltetrahydrofolatedetails
5,10-Methenyltetrahydrofolic acid + Water → 10-Formyltetrahydrofolate + Hydrogen Iondetails
General function:
Involved in formyltetrahydrofolate dehydrogenase activity
Specific function:
Not Available
Gene Name:
ALDH1L1
Uniprot ID:
O75891
Molecular weight:
99752.535
Reactions
10-Formyltetrahydrofolate + NADP + Water → Tetrahydrofolic acid + CO(2) + NADPHdetails
10-Formyltetrahydrofolate + NADP + Water → Tetrahydrofolic acid + Carbon dioxide + NADPH + Hydrogen Iondetails
General function:
Involved in catalytic activity
Specific function:
Not Available
Gene Name:
MTHFD2L
Uniprot ID:
Q9H903
Molecular weight:
37315.11
Reactions
5,10-Methenyltetrahydrofolic acid + Water → 10-Formyltetrahydrofolatedetails
5,10-Methenyltetrahydrofolic acid + Water → 10-Formyltetrahydrofolate + Hydrogen Iondetails
General function:
Involved in formyltetrahydrofolate dehydrogenase activity
Specific function:
Not Available
Gene Name:
ALDH1L2
Uniprot ID:
Q3SY69
Molecular weight:
101744.98
Reactions
10-Formyltetrahydrofolate + NADP + Water → Tetrahydrofolic acid + CO(2) + NADPHdetails
10-Formyltetrahydrofolate + NADP + Water → Tetrahydrofolic acid + Carbon dioxide + NADPH + Hydrogen Iondetails
General function:
Involved in methionyl-tRNA formyltransferase activity
Specific function:
Formylates methionyl-tRNA in mitochondria. A single tRNA(Met) gene gives rise to both an initiator and an elongator species via an unknown mechanism (By similarity).
Gene Name:
MTFMT
Uniprot ID:
Q96DP5
Molecular weight:
43831.73
Reactions
10-Formyltetrahydrofolate + L-methionyl-tRNA(fMet) → Tetrahydrofolic acid + N-formylmethionyl-tRNA(fMet)details
L-Methionyl-tRNA + 10-Formyltetrahydrofolate → Tetrahydrofolic acid + N-Formylmethionyl-tRNAdetails
General function:
Involved in formate-tetrahydrofolate ligase activity
Specific function:
May provide the missing metabolic reaction required to link the mitochondria and the cytoplasm in the mammalian model of one-carbon folate metabolism in embryonic an transformed cells complementing thus the enzymatic activities of MTHFD2 (By similarity).
Gene Name:
MTHFD1L
Uniprot ID:
Q6UB35
Molecular weight:
105888.19
Reactions
Adenosine triphosphate + Formic acid + Tetrahydrofolic acid → ADP + Phosphate + 10-Formyltetrahydrofolatedetails
General function:
Involved in catalytic activity
Specific function:
Not Available
Gene Name:
MTHFD2
Uniprot ID:
Q7Z650
Molecular weight:
26849.1