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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 polar