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Showing metabocard for (6R)-Folinic acid (HMDB0247218)

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Record Information
Version5.0
StatusDetected but not Quantified
Creation Date2021-09-11 00:13:45 UTC
Update Date2021-09-26 22:56:46 UTC
HMDB IDHMDB0247218
Secondary Accession NumbersNone
Metabolite Identification
Common Name(6R)-Folinic acid
DescriptionN5-Formyl-THF, also known as leucovorin or rescuvolin, 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. N5-Formyl-THF exists in all living species, ranging from bacteria to plants to humans. In humans, N5-formyl-THF is involved in the metabolic disorder called the methylenetetrahydrofolate reductase deficiency (mthfrd) pathway. N5-Formyl-THF is found, on average, in the highest concentration within lettuces (Lactuca sativa). This could make N5-formyl-THF a potential biomarker for the consumption of these foods. N5-Formyl-THF is a primary metabolite. Primary metabolites are metabolically or physiologically essential metabolites. They are directly involved in an organism’s growth, development or reproduction. Based on a literature review very few articles have been published on N5-Formyl-THF. This compound has been identified in human blood as reported by (PMID: 31557052 ). (6r)-folinic acid is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically (6R)-Folinic acid is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.
Structure
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MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0247218 ((6R)-Folinic acid)


  Mrv1652305171818262D          

 34 36  0  0  0  0            999 V2000
   -4.2868   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -7.0125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -8.2500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -9.4875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.8375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -8.2500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -9.4875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -9.4875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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  3  4  1  0  0  0  0
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 27 18  1  0  0  0  0
 33  4  1  0  0  0  0
 34 23  1  0  0  0  0
M  END
Download

3D MOL for HMDB0247218 ((6R)-Folinic acid)

HMDB0258132
     RDKit          3D
5-Formlyl-5,6,7,8-tetrahydrofolic acid,calcium salt
 57 59  0  0  0  0  0  0  0  0999 V2000
   -9.7739    0.6906   -0.5962 N   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4976    0.6619   -0.4389 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6389    1.0314   -1.4045 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2990    0.9920   -1.2204 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3906    1.3607   -2.2002 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8327    0.5592   -0.0028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6820    0.1677    1.0211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0157    0.2360    0.7562 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1656   -0.2860    2.2518 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7472   -0.3588    2.4749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0458   -0.6182    1.1582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5519   -0.6625    1.3860 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8639   -0.9095    0.1520 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4647   -1.0255    0.1247 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2406   -1.1211   -1.0718 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6048   -1.2441   -1.0764 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2783   -1.2728    0.1253 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7366   -1.3937    0.1428 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2295   -2.4679    0.5794 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5160   -0.3293   -0.3173 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.9941   -0.3810   -0.3341 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4668    0.5231    0.7573 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9423    0.6245    0.8843 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5679    1.2842   -0.2564 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7921    1.0083   -0.5278 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9384    2.2054   -1.0825 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4822   -0.1999   -1.6831 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7071    0.3052   -2.5784 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7474   -0.5389   -2.1187 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6093   -1.1806    1.3290 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2218   -1.0554    1.3184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4417    0.4978    0.2968 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5656    1.4856   -0.1740 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9515    2.5262   -0.7414 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1489    1.0147   -1.5103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5963    1.9272   -2.9999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6525   -0.0515    1.5147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8781   -0.5608    2.9770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4263    0.6118    2.9091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4904   -1.2061    3.1749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4256   -1.5503    0.7295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3020   -1.4859    2.0790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1879    0.2961    1.8148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4039   -1.0022   -0.7247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3222   -1.0927   -2.0035 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1178   -1.3156   -2.0312 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0885    0.5445   -0.6674 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2493   -1.4342    0.0098 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0064    1.5507    0.6190 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0034    0.1161    1.7146 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4185   -0.3727    1.0401 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1282    1.2704    1.8054 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3475    3.1405   -1.2180 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9555   -0.6664   -3.0986 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1604   -1.2048    2.2537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3114   -0.9809    2.2804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4767    1.3375   -0.0358 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  2  0
  4  5  1  0
  4  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
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 13 14  1  0
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 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 21 27  1  0
 27 28  2  0
 27 29  1  0
 17 30  1  0
 30 31  2  0
 11 32  1  0
 32 33  1  0
 33 34  2  0
  8  2  1  0
 31 14  1  0
 32  6  1  0
  1 35  1  0
  5 36  1  0
  8 37  1  0
  9 38  1  0
 10 39  1  0
 10 40  1  0
 11 41  1  0
 12 42  1  0
 12 43  1  0
 13 44  1  0
 15 45  1  0
 16 46  1  0
 20 47  1  0
 21 48  1  0
 22 49  1  0
 22 50  1  0
 23 51  1  0
 23 52  1  0
 26 53  1  0
 29 54  1  0
 30 55  1  0
 31 56  1  0
 33 57  1  0
M  END
Download

3D SDF for HMDB0247218 ((6R)-Folinic acid)


  Mrv1652305171818262D          

 34 36  0  0  0  0            999 V2000
   -4.2868   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -7.0125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -8.2500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -9.4875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.8375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -8.2500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -9.4875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -9.4875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 19 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 12 28  1  0  0  0  0
 28 29  2  0  0  0  0
  1 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
 29  9  1  0  0  0  0
 20 15  1  0  0  0  0
 27 18  1  0  0  0  0
 33  4  1  0  0  0  0
 34 23  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0247218

> <DATABASE_NAME>
hmdb

> <SMILES>
OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(N2C=O)C(O)=NC(=N)N3)C=C1)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H23N7O7/c21-20-25-16-15(18(32)26-20)27(9-28)12(8-23-16)7-22-11-3-1-10(2-4-11)17(31)24-13(19(33)34)5-6-14(29)30/h1-4,9,12-13,22H,5-8H2,(H,24,31)(H,29,30)(H,33,34)(H4,21,23,25,26,32)

> <INCHI_KEY>
VVIAGPKUTFNRDU-UHFFFAOYSA-N

> <FORMULA>
C20H23N7O7

> <MOLECULAR_WEIGHT>
473.4393

> <EXACT_MASS>
473.165896125

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
46.53677011400615

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <ALOGPS_LOGP>
-1.56

> <JCHEM_LOGP>
-2.3350673698750146

> <ALOGPS_LOGS>
-3.43

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
4.208497575080292

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.4738504268974917

> <JCHEM_PKA_STRONGEST_BASIC>
2.809524312386858

> <JCHEM_POLAR_SURFACE_AREA>
215.54999999999995

> <JCHEM_REFRACTIVITY>
126.66199999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.76e-01 g/l

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

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0247218 ((6R)-Folinic acid)

HMDB0258132
     RDKit          3D
5-Formlyl-5,6,7,8-tetrahydrofolic acid,calcium salt
 57 59  0  0  0  0  0  0  0  0999 V2000
   -9.7739    0.6906   -0.5962 N   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4976    0.6619   -0.4389 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6389    1.0314   -1.4045 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2990    0.9920   -1.2204 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3906    1.3607   -2.2002 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8327    0.5592   -0.0028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6820    0.1677    1.0211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0157    0.2360    0.7562 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1656   -0.2860    2.2518 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7472   -0.3588    2.4749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0458   -0.6182    1.1582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5519   -0.6625    1.3860 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8639   -0.9095    0.1520 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4647   -1.0255    0.1247 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2406   -1.1211   -1.0718 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6048   -1.2441   -1.0764 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2783   -1.2728    0.1253 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7366   -1.3937    0.1428 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2295   -2.4679    0.5794 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5160   -0.3293   -0.3173 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.9941   -0.3810   -0.3341 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4668    0.5231    0.7573 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9423    0.6245    0.8843 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5679    1.2842   -0.2564 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7921    1.0083   -0.5278 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9384    2.2054   -1.0825 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4822   -0.1999   -1.6831 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7071    0.3052   -2.5784 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7474   -0.5389   -2.1187 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6093   -1.1806    1.3290 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2218   -1.0554    1.3184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4417    0.4978    0.2968 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5656    1.4856   -0.1740 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9515    2.5262   -0.7414 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1489    1.0147   -1.5103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5963    1.9272   -2.9999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6525   -0.0515    1.5147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8781   -0.5608    2.9770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4263    0.6118    2.9091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4904   -1.2061    3.1749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4256   -1.5503    0.7295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3020   -1.4859    2.0790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1879    0.2961    1.8148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4039   -1.0022   -0.7247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3222   -1.0927   -2.0035 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1178   -1.3156   -2.0312 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0885    0.5445   -0.6674 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2493   -1.4342    0.0098 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0064    1.5507    0.6190 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0034    0.1161    1.7146 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4185   -0.3727    1.0401 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1282    1.2704    1.8054 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3475    3.1405   -1.2180 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9555   -0.6664   -3.0986 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1604   -1.2048    2.2537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3114   -0.9809    2.2804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4767    1.3375   -0.0358 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  2  0
  4  5  1  0
  4  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 21 27  1  0
 27 28  2  0
 27 29  1  0
 17 30  1  0
 30 31  2  0
 11 32  1  0
 32 33  1  0
 33 34  2  0
  8  2  1  0
 31 14  1  0
 32  6  1  0
  1 35  1  0
  5 36  1  0
  8 37  1  0
  9 38  1  0
 10 39  1  0
 10 40  1  0
 11 41  1  0
 12 42  1  0
 12 43  1  0
 13 44  1  0
 15 45  1  0
 16 46  1  0
 20 47  1  0
 21 48  1  0
 22 49  1  0
 22 50  1  0
 23 51  1  0
 23 52  1  0
 26 53  1  0
 29 54  1  0
 30 55  1  0
 31 56  1  0
 33 57  1  0
M  END
Download

PDB for HMDB0247218 ((6R)-Folinic acid)

HEADER    PROTEIN                                 17-MAY-18   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-MAY-18         0                                  
HETATM    1  C   UNK     0      -8.002 -12.320   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -9.336 -13.090   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -10.669 -12.320   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -12.003 -13.090   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0     -13.337 -12.320   0.000  0.00  0.00           O+0
HETATM    6  N   UNK     0      -6.668 -13.090   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0      -5.335 -12.320   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -5.335 -10.780   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -4.001 -13.090   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.667 -12.320   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.334 -13.090   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.334 -14.630   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0       0.000 -15.400   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0       1.334 -14.630   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.667 -15.400   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.667 -16.940   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       4.001 -17.710   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       5.335 -16.940   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.335 -15.400   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       4.001 -14.630   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       4.001 -13.090   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       2.667 -12.320   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       6.668 -14.630   0.000  0.00  0.00           C+0
HETATM   24  N   UNK     0       8.002 -15.400   0.000  0.00  0.00           N+0
HETATM   25  C   UNK     0       8.002 -16.940   0.000  0.00  0.00           C+0
HETATM   26  N   UNK     0       9.336 -17.710   0.000  0.00  0.00           N+0
HETATM   27  N   UNK     0       6.668 -17.710   0.000  0.00  0.00           N+0
HETATM   28  C   UNK     0      -2.667 -15.400   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -4.001 -14.630   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -8.002 -10.780   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -6.668 -10.010   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      -9.336 -10.010   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0     -12.003 -14.630   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0       6.668 -13.090   0.000  0.00  0.00           O+0
CONECT    1    2    6   30                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   33                                                  
CONECT    5    4                                                            
CONECT    6    1    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   29                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   28                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   27                                                  
CONECT   19   18   20   23                                                  
CONECT   20   19   21   15                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   19   24   34                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   18                                                       
CONECT   28   12   29                                                       
CONECT   29   28    9                                                       
CONECT   30    1   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33    4                                                            
CONECT   34   23                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   72    0
END
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3D PDB for HMDB0247218 ((6R)-Folinic acid)

COMPND    HMDB0258132
HETATM    1  N1  UNL     1      -9.774   0.691  -0.596  1.00  0.00           N  
HETATM    2  C1  UNL     1      -8.498   0.662  -0.439  1.00  0.00           C  
HETATM    3  N2  UNL     1      -7.639   1.031  -1.404  1.00  0.00           N  
HETATM    4  C2  UNL     1      -6.299   0.992  -1.220  1.00  0.00           C  
HETATM    5  O1  UNL     1      -5.391   1.361  -2.200  1.00  0.00           O  
HETATM    6  C3  UNL     1      -5.833   0.559  -0.003  1.00  0.00           C  
HETATM    7  C4  UNL     1      -6.682   0.168   1.021  1.00  0.00           C  
HETATM    8  N3  UNL     1      -8.016   0.236   0.756  1.00  0.00           N  
HETATM    9  N4  UNL     1      -6.166  -0.286   2.252  1.00  0.00           N  
HETATM   10  C5  UNL     1      -4.747  -0.359   2.475  1.00  0.00           C  
HETATM   11  C6  UNL     1      -4.046  -0.618   1.158  1.00  0.00           C  
HETATM   12  C7  UNL     1      -2.552  -0.662   1.386  1.00  0.00           C  
HETATM   13  N5  UNL     1      -1.864  -0.909   0.152  1.00  0.00           N  
HETATM   14  C8  UNL     1      -0.465  -1.026   0.125  1.00  0.00           C  
HETATM   15  C9  UNL     1       0.241  -1.121  -1.072  1.00  0.00           C  
HETATM   16  C10 UNL     1       1.605  -1.244  -1.076  1.00  0.00           C  
HETATM   17  C11 UNL     1       2.278  -1.273   0.125  1.00  0.00           C  
HETATM   18  C12 UNL     1       3.737  -1.394   0.143  1.00  0.00           C  
HETATM   19  O2  UNL     1       4.229  -2.468   0.579  1.00  0.00           O  
HETATM   20  N6  UNL     1       4.516  -0.329  -0.317  1.00  0.00           N  
HETATM   21  C13 UNL     1       5.994  -0.381  -0.334  1.00  0.00           C  
HETATM   22  C14 UNL     1       6.467   0.523   0.757  1.00  0.00           C  
HETATM   23  C15 UNL     1       7.942   0.624   0.884  1.00  0.00           C  
HETATM   24  C16 UNL     1       8.568   1.284  -0.256  1.00  0.00           C  
HETATM   25  O3  UNL     1       9.792   1.008  -0.528  1.00  0.00           O  
HETATM   26  O4  UNL     1       7.938   2.205  -1.082  1.00  0.00           O  
HETATM   27  C17 UNL     1       6.482  -0.200  -1.683  1.00  0.00           C  
HETATM   28  O5  UNL     1       5.707   0.305  -2.578  1.00  0.00           O  
HETATM   29  O6  UNL     1       7.747  -0.539  -2.119  1.00  0.00           O  
HETATM   30  C18 UNL     1       1.609  -1.181   1.329  1.00  0.00           C  
HETATM   31  C19 UNL     1       0.222  -1.055   1.318  1.00  0.00           C  
HETATM   32  N7  UNL     1      -4.442   0.498   0.297  1.00  0.00           N  
HETATM   33  C20 UNL     1      -3.566   1.486  -0.174  1.00  0.00           C  
HETATM   34  O7  UNL     1      -3.952   2.526  -0.741  1.00  0.00           O  
HETATM   35  H1  UNL     1     -10.149   1.015  -1.510  1.00  0.00           H  
HETATM   36  H2  UNL     1      -5.596   1.927  -3.000  1.00  0.00           H  
HETATM   37  H3  UNL     1      -8.653  -0.052   1.515  1.00  0.00           H  
HETATM   38  H4  UNL     1      -6.878  -0.561   2.977  1.00  0.00           H  
HETATM   39  H5  UNL     1      -4.426   0.612   2.909  1.00  0.00           H  
HETATM   40  H6  UNL     1      -4.490  -1.206   3.175  1.00  0.00           H  
HETATM   41  H7  UNL     1      -4.426  -1.550   0.730  1.00  0.00           H  
HETATM   42  H8  UNL     1      -2.302  -1.486   2.079  1.00  0.00           H  
HETATM   43  H9  UNL     1      -2.188   0.296   1.815  1.00  0.00           H  
HETATM   44  H10 UNL     1      -2.404  -1.002  -0.725  1.00  0.00           H  
HETATM   45  H11 UNL     1      -0.322  -1.093  -2.004  1.00  0.00           H  
HETATM   46  H12 UNL     1       2.118  -1.316  -2.031  1.00  0.00           H  
HETATM   47  H13 UNL     1       4.089   0.545  -0.667  1.00  0.00           H  
HETATM   48  H14 UNL     1       6.249  -1.434   0.010  1.00  0.00           H  
HETATM   49  H15 UNL     1       6.006   1.551   0.619  1.00  0.00           H  
HETATM   50  H16 UNL     1       6.003   0.116   1.715  1.00  0.00           H  
HETATM   51  H17 UNL     1       8.419  -0.373   1.040  1.00  0.00           H  
HETATM   52  H18 UNL     1       8.128   1.270   1.805  1.00  0.00           H  
HETATM   53  H19 UNL     1       8.348   3.140  -1.218  1.00  0.00           H  
HETATM   54  H20 UNL     1       7.955  -0.666  -3.099  1.00  0.00           H  
HETATM   55  H21 UNL     1       2.160  -1.205   2.254  1.00  0.00           H  
HETATM   56  H22 UNL     1      -0.311  -0.981   2.280  1.00  0.00           H  
HETATM   57  H23 UNL     1      -2.477   1.338  -0.036  1.00  0.00           H  
CONECT    1    2    2   35
CONECT    2    3    8
CONECT    3    4    4
CONECT    4    5    6
CONECT    5   36
CONECT    6    7    7   32
CONECT    7    8    9
CONECT    8   37
CONECT    9   10   38
CONECT   10   11   39   40
CONECT   11   12   32   41
CONECT   12   13   42   43
CONECT   13   14   44
CONECT   14   15   15   31
CONECT   15   16   45
CONECT   16   17   17   46
CONECT   17   18   30
CONECT   18   19   19   20
CONECT   20   21   47
CONECT   21   22   27   48
CONECT   22   23   49   50
CONECT   23   24   51   52
CONECT   24   25   25   26
CONECT   26   53
CONECT   27   28   28   29
CONECT   29   54
CONECT   30   31   31   55
CONECT   31   56
CONECT   32   33
CONECT   33   34   34   57
END
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SMILES for HMDB0247218 ((6R)-Folinic acid)

OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(N2C=O)C(O)=NC(=N)N3)C=C1)C(O)=O
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INCHI for HMDB0247218 ((6R)-Folinic acid)

InChI=1S/C20H23N7O7/c21-20-25-16-15(18(32)26-20)27(9-28)12(8-23-16)7-22-11-3-1-10(2-4-11)17(31)24-13(19(33)34)5-6-14(29)30/h1-4,9,12-13,22H,5-8H2,(H,24,31)(H,29,30)(H,33,34)(H4,21,23,25,26,32)
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Synonyms
ValueSource
LeucovorinKegg
RescuvolinKegg
5-FormyltetrahydrofolateKegg
L(-)-5-Formyl-5,6,7,8-tetrahydrofolic acidKegg
5-Formyltetrahydrofolic acidGenerator
L(-)-5-Formyl-5,6,7,8-tetrahydrofolateGenerator
(6R,S)-5-FormyltetrahydrofolateHMDB
10-Formyl-7,8-dihydrofolateHMDB
10-Formyl-7,8-dihydrofolic acidHMDB
5-Formyl-5,6,7,8-tetrahydrofolateHMDB
5-Formyl-5,6,7,8-tetrahydrofolic acidHMDB
5-FormyltetrahydropteroylglutamateHMDB
5-Formyltetrahydropteroylglutamic acidHMDB
FolinateHMDB, Generator
Folinic acidHMDB, MeSH
Folinic acid-SFHMDB
L-LeucovorinHMDB
L-N-[P-[[(2-amino-5-Formyl-5,6,7,8-tetrahydro-4-hydroxy-6-pteridinyl)methyl]amino]benzoyl]-glutamic acidHMDB
LeucalHMDB
LevoleucovorinHMDB
N5-Formyl-5,6,7,8-tetrahydrofolateHMDB
N5-Formyl-5,6,7,8-tetrahydrofolic acidHMDB
N5-FormyltetrahydrofolateHMDB
N5-Formyltetrahydrofolic acidHMDB
WelcovorinHMDB
Acid, folinicMeSH, HMDB
Folinate, calciumMeSH, HMDB
Leucovorin, (D)-isomerMeSH, HMDB
Leucovorin, (DL)-isomerMeSH, HMDB
Leucovorin, calcium (1:1) saltMeSH, HMDB
5 FormyltetrahydrofolateMeSH, HMDB
Citrovorum factorMeSH, HMDB
Factor, citrovorumMeSH, HMDB
Folinic acid SFMeSH, HMDB
Leucovorin, calcium (1:1) salt, pentahydrateMeSH, HMDB
LeukovorinMeSH, HMDB
N(5)-FormyltetrahydrofolateMeSH, HMDB
Leucovorin, (R)-isomerMeSH, HMDB
Leucovorin, calcium (1:1) salt, (DL)-isomerMeSH, HMDB
LeukovorumMeSH, HMDB
Monosodium salt leucovorinMeSH, HMDB
WellcovorinMeSH, HMDB
5 FormyltetrahydropteroylglutamateMeSH, HMDB
Calcium folinateMeSH, HMDB
Calcium leucovorinMeSH, HMDB
Leucovorin, calciumMeSH, HMDB
Leucovorin, monosodium saltMeSH, HMDB
5-Formlyl-5,6,7,8-tetrahydrofolate,calcium saltGenerator
Chemical FormulaC20H23N7O7
Average Molecular Weight473.4393
Monoisotopic Molecular Weight473.165896125
IUPAC Name2-[(4-{[(2-amino-5-formyl-4-oxo-3,4,5,6,7,8-hexahydropteridin-6-yl)methyl]amino}phenyl)formamido]pentanedioic acid
Traditional Name2-[(4-{[(2-amino-5-formyl-4-oxo-3,6,7,8-tetrahydropteridin-6-yl)methyl]amino}phenyl)formamido]pentanedioic acid
CAS Registry NumberNot Available
SMILES
OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(N2C=O)C(O)=NC(=N)N3)C=C1)C(O)=O
InChI Identifier
InChI=1S/C20H23N7O7/c21-20-25-16-15(18(32)26-20)27(9-28)12(8-23-16)7-22-11-3-1-10(2-4-11)17(31)24-13(19(33)34)5-6-14(29)30/h1-4,9,12-13,22H,5-8H2,(H,24,31)(H,29,30)(H,33,34)(H4,21,23,25,26,32)
InChI KeyVVIAGPKUTFNRDU-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as tetrahydrofolic acids. These are heterocyclic compounds based on the 5,6,7,8-tetrahydropteroic acid skeleton conjugated with at least one L-glutamic acid unit.
KingdomOrganic compounds
Super ClassOrganoheterocyclic compounds
ClassPteridines and derivatives
Sub ClassPterins and derivatives
Direct ParentTetrahydrofolic acids
Alternative Parents
Substituents
  • Tetrahydrofolic acid
  • Glutamic acid or derivatives
  • N-acyl-alpha amino acid or derivatives
  • N-acyl-alpha-amino acid
  • Hippuric acid
  • Hippuric acid or derivatives
  • Alpha-amino acid or derivatives
  • Aminobenzamide
  • Aminobenzoic acid or derivatives
  • Benzamide
  • Benzoic acid or derivatives
  • Benzoyl
  • Aniline or substituted anilines
  • Phenylalkylamine
  • Aminopyrimidine
  • Secondary aliphatic/aromatic amine
  • Pyrimidone
  • Dicarboxylic acid or derivatives
  • Benzenoid
  • Pyrimidine
  • Monocyclic benzene moiety
  • Heteroaromatic compound
  • Vinylogous amide
  • Tertiary carboxylic acid amide
  • Secondary carboxylic acid amide
  • Amino acid or derivatives
  • Amino acid
  • Carboxamide group
  • Secondary amine
  • Carboxylic acid
  • Carboxylic acid derivative
  • Azacycle
  • Organooxygen compound
  • Carbonyl group
  • Organic nitrogen compound
  • Hydrocarbon derivative
  • Amine
  • Organic oxide
  • Organopnictogen compound
  • Organic oxygen compound
  • Primary amine
  • 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
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
logP-1.6ALOGPS
logP-2.3ChemAxon
logS-3.4ALOGPS
pKa (Strongest Acidic)3.47ChemAxon
pKa (Strongest Basic)2.81ChemAxon
Physiological Charge-2ChemAxon
Hydrogen Acceptor Count11ChemAxon
Hydrogen Donor Count7ChemAxon
Polar Surface Area215.55 ŲChemAxon
Rotatable Bond Count9ChemAxon
Refractivity126.66 m³·mol⁻¹ChemAxon
Polarizability46.54 ųChemAxon
Number of Rings3ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleYesChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+202.97230932474
DeepCCS[M-H]-200.60430932474
DeepCCS[M-2H]-233.7730932474
DeepCCS[M+Na]+209.05530932474
AllCCS[M+H]+203.232859911
AllCCS[M+H-H2O]+201.532859911
AllCCS[M+NH4]+204.832859911
AllCCS[M+Na]+205.332859911
AllCCS[M-H]-199.732859911
AllCCS[M+Na-2H]-200.532859911
AllCCS[M+HCOO]-201.432859911

Predicted Kovats Retention Indices

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
(6R)-Folinic acid,1TMS,isomer #4C[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(CCC(=O)O)C(=O)O4852.4Semi standard non polar33892256
(6R)-Folinic acid,1TMS,isomer #4C[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(CCC(=O)O)C(=O)O4085.8Standard non polar33892256
(6R)-Folinic acid,1TMS,isomer #4C[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(CCC(=O)O)C(=O)O7712.0Standard polar33892256
(6R)-Folinic acid,1TMS,isomer #8C[Si](C)(C)N1C2=C(C(O)=NC1=N)N(C=O)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN24871.2Semi standard non polar33892256
(6R)-Folinic acid,1TMS,isomer #8C[Si](C)(C)N1C2=C(C(O)=NC1=N)N(C=O)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN24219.4Standard non polar33892256
(6R)-Folinic acid,1TMS,isomer #8C[Si](C)(C)N1C2=C(C(O)=NC1=N)N(C=O)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN27804.8Standard polar33892256
(6R)-Folinic acid,2TMS,isomer #1C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O4765.5Semi standard non polar33892256
(6R)-Folinic acid,2TMS,isomer #1C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O4040.1Standard non polar33892256
(6R)-Folinic acid,2TMS,isomer #1C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O7456.4Standard polar33892256
(6R)-Folinic acid,2TMS,isomer #18C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2C=O)[NH]14774.7Semi standard non polar33892256
(6R)-Folinic acid,2TMS,isomer #18C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2C=O)[NH]14179.8Standard non polar33892256
(6R)-Folinic acid,2TMS,isomer #18C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2C=O)[NH]17213.8Standard polar33892256
(6R)-Folinic acid,2TMS,isomer #23C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(O)=NC(=N)[NH]2)N1C=O)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C14587.9Semi standard non polar33892256
(6R)-Folinic acid,2TMS,isomer #23C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(O)=NC(=N)[NH]2)N1C=O)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C14136.7Standard non polar33892256
(6R)-Folinic acid,2TMS,isomer #23C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(O)=NC(=N)[NH]2)N1C=O)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C16739.6Standard polar33892256
(6R)-Folinic acid,2TMS,isomer #3C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C4665.1Semi standard non polar33892256
(6R)-Folinic acid,2TMS,isomer #3C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C4049.2Standard non polar33892256
(6R)-Folinic acid,2TMS,isomer #3C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C7178.5Standard polar33892256
(6R)-Folinic acid,2TMS,isomer #4C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)C(=O)O4654.9Semi standard non polar33892256
(6R)-Folinic acid,2TMS,isomer #4C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)C(=O)O4052.3Standard non polar33892256
(6R)-Folinic acid,2TMS,isomer #4C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)C(=O)O7098.2Standard polar33892256
(6R)-Folinic acid,2TMS,isomer #5C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O4563.6Semi standard non polar33892256
(6R)-Folinic acid,2TMS,isomer #5C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O4086.8Standard non polar33892256
(6R)-Folinic acid,2TMS,isomer #5C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O6872.3Standard polar33892256
(6R)-Folinic acid,2TMS,isomer #6C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)C(=O)O4700.1Semi standard non polar33892256
(6R)-Folinic acid,2TMS,isomer #6C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)C(=O)O4177.6Standard non polar33892256
(6R)-Folinic acid,2TMS,isomer #6C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)C(=O)O7272.4Standard polar33892256
(6R)-Folinic acid,3TMS,isomer #1C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O[Si](C)(C)C4611.6Semi standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #1C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O[Si](C)(C)C3919.4Standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #1C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O[Si](C)(C)C6876.1Standard polar33892256
(6R)-Folinic acid,3TMS,isomer #10C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)C(=O)O[Si](C)(C)C4531.0Semi standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #10C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)C(=O)O[Si](C)(C)C4041.8Standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #10C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)C(=O)O[Si](C)(C)C6663.4Standard polar33892256
(6R)-Folinic acid,3TMS,isomer #11C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2C=O)[NH]14582.0Semi standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #11C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2C=O)[NH]14081.4Standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #11C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2C=O)[NH]16722.5Standard polar33892256
(6R)-Folinic acid,3TMS,isomer #14C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C4494.4Semi standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #14C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C4124.4Standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #14C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C6735.2Standard polar33892256
(6R)-Folinic acid,3TMS,isomer #17C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)C(=O)O4500.3Semi standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #17C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)C(=O)O4118.8Standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #17C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)C(=O)O6656.8Standard polar33892256
(6R)-Folinic acid,3TMS,isomer #2C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C4556.0Semi standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #2C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C3993.9Standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #2C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C6929.4Standard polar33892256
(6R)-Folinic acid,3TMS,isomer #20C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)N2C=O4498.4Semi standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #20C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)N2C=O4232.7Standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #20C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)N2C=O6503.9Standard polar33892256
(6R)-Folinic acid,3TMS,isomer #24C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C14521.4Semi standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #24C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C13988.3Standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #24C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C16603.0Standard polar33892256
(6R)-Folinic acid,3TMS,isomer #3C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)C(=O)O4584.2Semi standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #3C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)C(=O)O3993.5Standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #3C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)C(=O)O6850.5Standard polar33892256
(6R)-Folinic acid,3TMS,isomer #32C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N(C=O)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN24569.6Semi standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #32C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N(C=O)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN24137.6Standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #32C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N(C=O)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN26993.9Standard polar33892256
(6R)-Folinic acid,3TMS,isomer #36C[Si](C)(C)OC1=NC(=N)[NH]C2=C1N(C=O)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C4479.8Semi standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #36C[Si](C)(C)OC1=NC(=N)[NH]C2=C1N(C=O)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C4061.3Standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #36C[Si](C)(C)OC1=NC(=N)[NH]C2=C1N(C=O)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C6638.2Standard polar33892256
(6R)-Folinic acid,3TMS,isomer #4C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O4506.3Semi standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #4C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O4042.1Standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #4C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O6690.9Standard polar33892256
(6R)-Folinic acid,3TMS,isomer #42C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C14509.8Semi standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #42C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C14060.8Standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #42C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C16557.3Standard polar33892256
(6R)-Folinic acid,3TMS,isomer #44C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C14520.1Semi standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #44C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C14134.1Standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #44C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C16376.9Standard polar33892256
(6R)-Folinic acid,3TMS,isomer #48C[Si](C)(C)N(CC1CNC2=C(C(O)=NC(=N)N2[Si](C)(C)C)N1C=O)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C14488.6Semi standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #48C[Si](C)(C)N(CC1CNC2=C(C(O)=NC(=N)N2[Si](C)(C)C)N1C=O)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C14138.2Standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #48C[Si](C)(C)N(CC1CNC2=C(C(O)=NC(=N)N2[Si](C)(C)C)N1C=O)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C16622.7Standard polar33892256
(6R)-Folinic acid,3TMS,isomer #49C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]14534.5Semi standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #49C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]14195.1Standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #49C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]16680.8Standard polar33892256
(6R)-Folinic acid,3TMS,isomer #50C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N2C=O4463.5Semi standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #50C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N2C=O4264.5Standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #50C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N2C=O6468.1Standard polar33892256
(6R)-Folinic acid,3TMS,isomer #53C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(O)=NC(=N)N2[Si](C)(C)C)N1C=O)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C14522.9Semi standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #53C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(O)=NC(=N)N2[Si](C)(C)C)N1C=O)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C14236.1Standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #53C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(O)=NC(=N)N2[Si](C)(C)C)N1C=O)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C16360.2Standard polar33892256
(6R)-Folinic acid,3TMS,isomer #6C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2C=O)[NH]14692.3Semi standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #6C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2C=O)[NH]14198.6Standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #6C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2C=O)[NH]16999.6Standard polar33892256
(6R)-Folinic acid,3TMS,isomer #8C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4495.0Semi standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #8C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3920.3Standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #8C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C6485.1Standard polar33892256
(6R)-Folinic acid,3TMS,isomer #9C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O[Si](C)(C)C4409.2Semi standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #9C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O[Si](C)(C)C3974.2Standard non polar33892256
(6R)-Folinic acid,3TMS,isomer #9C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O[Si](C)(C)C6335.4Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #1C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C4468.4Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #1C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C3931.3Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #1C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C6467.5Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #10C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)C(=O)O4387.1Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #10C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)C(=O)O4003.0Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #10C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)C(=O)O6242.0Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #11C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)C(=O)O4476.0Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #11C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)C(=O)O4030.9Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #11C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)C(=O)O6482.0Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #12C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2C=O)[NH]14535.0Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #12C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2C=O)[NH]14109.7Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #12C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2C=O)[NH]16488.2Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #13C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)C(=O)O4475.8Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #13C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)C(=O)O4143.9Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #13C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)C(=O)O6330.2Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #14C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)N2C=O4471.1Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #14C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)N2C=O4158.6Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #14C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)N2C=O6287.7Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #15C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2C=O)N1[Si](C)(C)C4638.1Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #15C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2C=O)N1[Si](C)(C)C4114.4Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #15C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2C=O)N1[Si](C)(C)C6553.2Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #16C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C4363.2Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #16C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C3898.3Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #16C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C6070.3Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #17C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C4271.7Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #17C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C3971.6Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #17C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C5974.2Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #18C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C4394.0Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #18C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C4029.6Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #18C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C6245.2Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #19C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2C=O)[NH]14412.7Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #19C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2C=O)[NH]14074.4Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #19C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2C=O)[NH]16290.3Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #2C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4463.7Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #2C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3881.4Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #2C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C6374.2Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #20C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4290.0Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #20C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3935.7Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #20C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C5889.1Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #21C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4398.9Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #21C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3964.5Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #21C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C6150.0Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #22C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]14406.5Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #22C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]14006.5Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #22C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]16203.4Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #23C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)C(=O)O[Si](C)(C)C4366.4Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #23C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)C(=O)O[Si](C)(C)C4077.1Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #23C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)C(=O)O[Si](C)(C)C5988.9Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #24C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)N2C=O4379.1Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #24C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)N2C=O4105.7Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #24C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)N2C=O6028.8Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #25C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4531.9Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #25C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4038.7Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #25C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C6281.3Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #26C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C4286.6Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #26C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C3999.8Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #26C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C5948.2Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #27C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C4368.7Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #27C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C4047.3Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #27C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C6215.0Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #28C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]14373.5Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #28C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]14092.8Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #28C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]16268.2Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #29C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C4341.0Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #29C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C4155.9Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #29C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C6055.7Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #3C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O[Si](C)(C)C4393.2Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #3C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O[Si](C)(C)C3954.8Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #3C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O[Si](C)(C)C6247.0Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #30C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)N2C=O4307.7Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #30C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)N2C=O4194.9Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #30C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)N2C=O6099.8Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #31C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4453.8Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #31C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4133.6Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #31C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C6353.3Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #32C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)C(=O)O4376.5Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #32C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)C(=O)O4153.8Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #32C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)C(=O)O5988.0Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #33C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)N2C=O4347.7Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #33C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)N2C=O4173.3Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #33C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)N2C=O6036.6Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #34C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4514.3Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #34C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4080.2Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #34C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C6285.0Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #35C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2C=O)N1[Si](C)(C)C4455.4Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #35C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2C=O)N1[Si](C)(C)C4189.9Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #35C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2C=O)N1[Si](C)(C)C6080.4Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #36C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C4433.6Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #36C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C3924.4Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #36C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C6372.2Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #37C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C4379.5Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #37C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C3991.7Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #37C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C6265.7Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #38C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C4468.0Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #38C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C4049.6Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #38C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C6515.8Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #39C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2C=O)[NH]14491.2Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #39C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2C=O)[NH]14120.3Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #39C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2C=O)[NH]16510.8Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #4C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)C(=O)O[Si](C)(C)C4490.4Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #4C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)C(=O)O[Si](C)(C)C3981.7Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #4C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)C(=O)O[Si](C)(C)C6512.3Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #40C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C14394.4Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #40C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C13968.9Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #40C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C16168.7Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #41C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C14479.6Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #41C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C14000.6Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #41C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C16402.6Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #42C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]14513.1Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #42C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]14067.5Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #42C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]16410.0Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #43C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C14488.8Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #43C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C14100.6Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #43C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C16254.3Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #44C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)N2C=O4461.0Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #44C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)N2C=O4124.9Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #44C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)N2C=O6214.5Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #45C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4636.2Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #45C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4076.6Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #45C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C6473.6Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #46C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)N2C=O)N1[Si](C)(C)C4566.8Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #46C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)N2C=O)N1[Si](C)(C)C4199.4Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #46C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)N2C=O)N1[Si](C)(C)C6212.1Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #47C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4609.9Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #47C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4124.5Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #47C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C6430.4Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #48C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4548.9Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #48C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4156.3Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #48C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C6517.3Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #49C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)N2C=O4439.8Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #49C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)N2C=O4185.8Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #49C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)N2C=O6179.2Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #5C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2C=O)[NH]14543.2Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #5C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2C=O)[NH]14047.3Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #5C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2C=O)[NH]16499.8Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #50C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N2C=O4392.1Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #50C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N2C=O4203.6Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #50C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)N2C=O6256.4Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #51C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]14458.6Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #51C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]14140.9Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #51C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]16443.6Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #52C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N(C=O)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN24452.5Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #52C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N(C=O)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN24080.0Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #52C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N(C=O)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN26485.6Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #53C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N(C=O)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C4498.0Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #53C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N(C=O)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C4161.9Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #53C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N(C=O)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C6208.5Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #54C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N(C=O)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C4447.1Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #54C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N(C=O)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C4169.9Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #54C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N(C=O)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)CN2[Si](C)(C)C6294.1Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #55C[Si](C)(C)OC1=NC(=N)[NH]C2=C1N(C=O)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C4373.3Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #55C[Si](C)(C)OC1=NC(=N)[NH]C2=C1N(C=O)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C4032.2Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #55C[Si](C)(C)OC1=NC(=N)[NH]C2=C1N(C=O)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C6197.9Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #56C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C4312.0Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #56C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C3978.5Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #56C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C5901.3Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #57C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C4390.5Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #57C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C4031.3Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #57C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C6162.3Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #58C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]14385.3Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #58C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]14081.6Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #58C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]16217.0Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #59C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C4369.7Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #59C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C4131.5Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #59C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C6006.2Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #6C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C4424.3Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #6C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C3944.2Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #6C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C6422.7Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #60C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N2C=O4326.0Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #60C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N2C=O4176.3Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #60C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N2C=O6051.9Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #61C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4475.8Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #61C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4116.8Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #61C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C6300.6Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #62C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C14400.5Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #62C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C14109.2Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #62C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C15910.8Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #63C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)N2C=O4356.6Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #63C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)N2C=O4140.2Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #63C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)N2C=O5962.7Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #64C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4520.2Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #64C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4050.1Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #64C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C6205.7Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #65C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4454.6Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #65C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4148.8Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #65C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C6002.9Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #66C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(O)=NC(=N)N2[Si](C)(C)C)N1C=O)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C14375.1Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #66C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(O)=NC(=N)N2[Si](C)(C)C)N1C=O)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C14174.0Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #66C[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(O)=NC(=N)N2[Si](C)(C)C)N1C=O)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C15963.4Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #67C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)N2C=O4316.4Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #67C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)N2C=O4215.7Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #67C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)N2C=O6008.8Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #68C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4468.5Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #68C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4119.3Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #68C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C6256.9Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #69C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4399.0Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #69C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4219.4Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #69C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C6057.9Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #7C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C4353.7Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #7C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C4017.4Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #7C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C6313.9Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #70C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4461.6Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #70C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4212.6Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #70C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C5988.3Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #8C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C4446.3Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #8C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C4073.4Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #8C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C6568.6Standard polar33892256
(6R)-Folinic acid,4TMS,isomer #9C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2C=O)[NH]14484.7Semi standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #9C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2C=O)[NH]14137.4Standard non polar33892256
(6R)-Folinic acid,4TMS,isomer #9C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2C=O)[NH]16562.2Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #1C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C4353.5Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #1C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C3883.4Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #1C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C6014.4Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #10C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4495.5Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #10C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C3998.5Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #10C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C6104.9Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #11C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C4268.2Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #11C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C3969.9Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #11C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C5897.0Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #12C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C4365.9Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #12C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C3998.7Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #12C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C6107.5Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #13C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]14354.2Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #13C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]14063.8Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #13C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]16099.5Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #14C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C4340.7Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #14C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C4117.1Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #14C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C5972.8Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #15C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)N2C=O4290.8Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #15C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)N2C=O4144.5Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #15C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)N2C=O5932.0Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #16C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4419.4Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #16C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4076.6Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #16C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C6171.9Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #17C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)C(=O)O4400.7Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #17C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)C(=O)O4072.6Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #17C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)C(=O)O5886.5Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #18C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)N2C=O4357.1Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #18C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)N2C=O4104.3Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #18C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C1)[Si](C)(C)C)N2C=O5854.6Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #19C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4488.9Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #19C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4022.7Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #19C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C6086.3Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #2C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C4272.7Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #2C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C3968.8Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #2C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C5923.2Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #20C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2C=O)N1[Si](C)(C)C4450.8Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #20C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2C=O)N1[Si](C)(C)C4137.0Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #20C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)N2C=O)N1[Si](C)(C)C5866.5Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #21C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C4206.2Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #21C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C3933.1Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #21C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C5569.5Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #22C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C4319.0Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #22C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C3952.7Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #22C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C5794.3Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #23C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]14295.5Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #23C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]14007.2Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #23C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]15832.1Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #24C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C4270.1Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #24C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C4084.1Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #24C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C5659.0Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #25C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N2C=O4231.7Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #25C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N2C=O4118.3Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #25C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N2C=O5696.9Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #26C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4369.1Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #26C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4036.1Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #26C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C5920.9Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #27C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4303.3Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #27C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4030.0Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #27C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C5567.9Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #28C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)N2C=O4269.7Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #28C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)N2C=O4057.4Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #28C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)N2C=O5611.8Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #29C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4397.5Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #29C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C3959.1Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #29C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C5831.5Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #3C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C4393.8Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #3C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C3985.3Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #3C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C6149.7Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #30C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4352.9Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #30C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4089.5Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #30C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C5638.0Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #31C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C4284.5Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #31C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C4102.9Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #31C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C5642.5Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #32C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)N2C=O4224.6Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #32C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)N2C=O4139.5Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #32C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)N2C=O5689.0Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #33C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4363.5Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #33C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4038.6Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #33C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C5908.3Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #34C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4293.2Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #34C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4162.4Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #34C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C5720.0Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #35C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4376.2Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #35C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4117.5Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #35C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C5650.9Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #36C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C4290.8Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #36C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C3955.5Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #36C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C5855.9Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #37C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C4389.3Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #37C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C3989.0Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #37C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C6062.3Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #38C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]14366.5Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #38C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]14060.1Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #38C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]16054.6Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #39C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C4371.0Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #39C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C4100.6Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #39C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C5929.7Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #4C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2C=O)[NH]14390.4Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #4C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2C=O)[NH]14053.1Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #4C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2C=O)[NH]16134.7Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #40C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N2C=O4310.0Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #40C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N2C=O4132.2Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #40C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)N2C=O5889.5Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #41C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4438.1Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #41C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4069.0Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #41C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C6126.8Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #42C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C14410.0Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #42C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C14048.7Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #42C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C15821.7Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #43C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)N2C=O4354.3Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #43C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)N2C=O4086.8Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #43C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C1)[Si](C)(C)C)N2C=O5791.3Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #44C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4492.9Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #44C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4001.3Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #44C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C6019.2Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #45C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4456.3Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #45C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4108.3Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #45C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C5802.3Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #46C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4456.0Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #46C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4136.2Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #46C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C5765.9Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #47C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4380.4Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #47C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4170.9Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #47C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C5854.7Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #48C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4434.0Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #48C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4072.1Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #48C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C6064.0Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #49C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)N2C=O4298.8Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #49C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)N2C=O4155.6Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #49C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)N2C=O5835.6Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #5C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4311.9Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #5C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3916.3Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #5C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C5833.3Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #50C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N(C=O)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C4381.1Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #50C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N(C=O)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C4113.9Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #50C[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C)C2=C1N(C=O)C(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C1)[Si](C)(C)C)CN2[Si](C)(C)C5866.8Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #51C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C4314.5Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #51C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C4096.0Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #51C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C5600.8Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #52C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C)N2C=O4247.9Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #52C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C)N2C=O4129.8Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #52C[Si](C)(C)N=C1N=C(O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C1)[Si](C)(C)C)N2C=O5647.8Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #53C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4384.0Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #53C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4035.6Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #53C[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C5864.0Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #54C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4309.6Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #54C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C4149.9Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #54C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C5679.0Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #55C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4386.6Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #55C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4100.1Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #55C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C5588.8Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #56C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4330.6Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #56C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C4170.5Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #56C[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C)CC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C5644.7Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #6C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C4401.8Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #6C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C3915.6Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #6C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C6044.8Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #7C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]14411.8Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #7C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]13982.8Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #7C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]16042.2Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #8C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)C(=O)O[Si](C)(C)C4370.1Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #8C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)C(=O)O[Si](C)(C)C4043.7Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #8C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)C(=O)O[Si](C)(C)C5896.7Standard polar33892256
(6R)-Folinic acid,5TMS,isomer #9C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)N2C=O4360.7Semi standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #9C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)N2C=O4068.1Standard non polar33892256
(6R)-Folinic acid,5TMS,isomer #9C[Si](C)(C)N=C1N=C(O[Si](C)(C)C)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1)N2C=O5855.0Standard polar33892256
(6R)-Folinic acid,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O5147.9Semi standard non polar33892256
(6R)-Folinic acid,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O4324.4Standard non polar33892256
(6R)-Folinic acid,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O7518.7Standard polar33892256
(6R)-Folinic acid,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=NC(=N)[NH]C2=C1N(C=O)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN25101.4Semi standard non polar33892256
(6R)-Folinic acid,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=NC(=N)[NH]C2=C1N(C=O)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN24324.4Standard non polar33892256
(6R)-Folinic acid,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=NC(=N)[NH]C2=C1N(C=O)C(CNC1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)CN27752.6Standard polar33892256
(6R)-Folinic acid,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C15153.3Semi standard non polar33892256
(6R)-Folinic acid,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C14243.6Standard non polar33892256
(6R)-Folinic acid,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C17420.3Standard polar33892256
(6R)-Folinic acid,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(CCC(=O)O)C(=O)O5108.5Semi standard non polar33892256
(6R)-Folinic acid,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(CCC(=O)O)C(=O)O4289.2Standard non polar33892256
(6R)-Folinic acid,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(CCC(=O)O)C(=O)O7464.5Standard polar33892256
(6R)-Folinic acid,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)N1CC(CNC2=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C2)N(C=O)C2=C1[NH]C(=N)N=C2O5010.9Semi standard non polar33892256
(6R)-Folinic acid,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)N1CC(CNC2=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C2)N(C=O)C2=C1[NH]C(=N)N=C2O4310.5Standard non polar33892256
(6R)-Folinic acid,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)N1CC(CNC2=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C2)N(C=O)C2=C1[NH]C(=N)N=C2O7273.2Standard polar33892256
(6R)-Folinic acid,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC1=NC(=N)[NH]C2=C1N(C=O)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)CN25172.3Semi standard non polar33892256
(6R)-Folinic acid,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC1=NC(=N)[NH]C2=C1N(C=O)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)CN24447.8Standard non polar33892256
(6R)-Folinic acid,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC1=NC(=N)[NH]C2=C1N(C=O)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)CN27136.6Standard polar33892256
(6R)-Folinic acid,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C(C)(C)C5190.3Semi standard non polar33892256
(6R)-Folinic acid,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C(C)(C)C4417.4Standard non polar33892256
(6R)-Folinic acid,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C(C)(C)C6809.8Standard polar33892256
(6R)-Folinic acid,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C(C)(C)C)C=C15158.7Semi standard non polar33892256
(6R)-Folinic acid,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C(C)(C)C)C=C14391.6Standard non polar33892256
(6R)-Folinic acid,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C(C)(C)C)C=C16733.0Standard polar33892256
(6R)-Folinic acid,2TBDMS,isomer #19CC(C)(C)[Si](C)(C)N(CC1CNC2=C(C(O)=NC(=N)[NH]2)N1C=O)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C15131.1Semi standard non polar33892256
(6R)-Folinic acid,2TBDMS,isomer #19CC(C)(C)[Si](C)(C)N(CC1CNC2=C(C(O)=NC(=N)[NH]2)N1C=O)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C14421.8Standard non polar33892256
(6R)-Folinic acid,2TBDMS,isomer #19CC(C)(C)[Si](C)(C)N(CC1CNC2=C(C(O)=NC(=N)[NH]2)N1C=O)C1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C16782.5Standard polar33892256
(6R)-Folinic acid,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C5217.7Semi standard non polar33892256
(6R)-Folinic acid,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C4412.0Standard non polar33892256
(6R)-Folinic acid,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C6792.3Standard polar33892256
(6R)-Folinic acid,2TBDMS,isomer #28CC(C)(C)[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)N2C=O)N1[Si](C)(C)C(C)(C)C5271.3Semi standard non polar33892256
(6R)-Folinic acid,2TBDMS,isomer #28CC(C)(C)[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)N2C=O)N1[Si](C)(C)C(C)(C)C4616.9Standard non polar33892256
(6R)-Folinic acid,2TBDMS,isomer #28CC(C)(C)[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)N2C=O)N1[Si](C)(C)C(C)(C)C6834.5Standard polar33892256
(6R)-Folinic acid,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C(C)(C)C5192.0Semi standard non polar33892256
(6R)-Folinic acid,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C(C)(C)C4442.2Standard non polar33892256
(6R)-Folinic acid,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C(C)(C)C6856.3Standard polar33892256
(6R)-Folinic acid,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)N=C1N=C(O[Si](C)(C)C(C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)N2C=O)[NH]15280.2Semi standard non polar33892256
(6R)-Folinic acid,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)N=C1N=C(O[Si](C)(C)C(C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)N2C=O)[NH]14641.4Standard non polar33892256
(6R)-Folinic acid,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)N=C1N=C(O[Si](C)(C)C(C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)N2C=O)[NH]17129.5Standard polar33892256
(6R)-Folinic acid,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C(C)(C)C)N2C=O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C5161.8Semi standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C(C)(C)C)N2C=O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C4595.1Standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C(C)(C)C)N2C=O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C6277.6Standard polar33892256
(6R)-Folinic acid,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C(C)(C)C)N2C=O)[Si](C)(C)C(C)(C)C)C=C1)C(=O)O5137.8Semi standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C(C)(C)C)N2C=O)[Si](C)(C)C(C)(C)C)C=C1)C(=O)O4610.8Standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C(C)(C)C)N2C=O)[Si](C)(C)C(C)(C)C)C=C1)C(=O)O6298.1Standard polar33892256
(6R)-Folinic acid,3TBDMS,isomer #21CC(C)(C)[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C3)N2C=O)N1[Si](C)(C)C(C)(C)C5274.2Semi standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #21CC(C)(C)[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C3)N2C=O)N1[Si](C)(C)C(C)(C)C4701.0Standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #21CC(C)(C)[Si](C)(C)N=C1N=C(O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C=C3)N2C=O)N1[Si](C)(C)C(C)(C)C6401.4Standard polar33892256
(6R)-Folinic acid,3TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C(C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C(C)(C)C)C=C15210.9Semi standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C(C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C(C)(C)C)C=C14504.3Standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C(C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C(C)(C)C)C=C16564.3Standard polar33892256
(6R)-Folinic acid,3TBDMS,isomer #26CC(C)(C)[Si](C)(C)N=C1N=C(O[Si](C)(C)C(C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C3)N2C=O)[NH]15288.1Semi standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #26CC(C)(C)[Si](C)(C)N=C1N=C(O[Si](C)(C)C(C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C3)N2C=O)[NH]14694.3Standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #26CC(C)(C)[Si](C)(C)N=C1N=C(O[Si](C)(C)C(C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C=C3)N2C=O)[NH]16643.7Standard polar33892256
(6R)-Folinic acid,3TBDMS,isomer #29CC(C)(C)[Si](C)(C)N=C1N=C(O[Si](C)(C)C(C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C(C)(C)C)N2C=O)[NH]15261.7Semi standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #29CC(C)(C)[Si](C)(C)N=C1N=C(O[Si](C)(C)C(C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C(C)(C)C)N2C=O)[NH]14719.6Standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #29CC(C)(C)[Si](C)(C)N=C1N=C(O[Si](C)(C)C(C)(C)C)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C(C)(C)C)N2C=O)[NH]16631.1Standard polar33892256
(6R)-Folinic acid,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C(C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C(C)(C)C)C=C1)C(=O)O5202.4Semi standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C(C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C(C)(C)C)C=C1)C(=O)O4536.2Standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C(C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C(C)(C)C)C=C1)C(=O)O6624.5Standard polar33892256
(6R)-Folinic acid,3TBDMS,isomer #30CC(C)(C)[Si](C)(C)N=C1N=C(O[Si](C)(C)C(C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C3)N2C=O)[NH]15221.1Semi standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #30CC(C)(C)[Si](C)(C)N=C1N=C(O[Si](C)(C)C(C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C3)N2C=O)[NH]14723.9Standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #30CC(C)(C)[Si](C)(C)N=C1N=C(O[Si](C)(C)C(C)(C)C)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C3)N2C=O)[NH]16689.5Standard polar33892256
(6R)-Folinic acid,3TBDMS,isomer #31CC(C)(C)[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C(C)(C)C)C2=C1N(C=O)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C(C)(C)C)CN25200.7Semi standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #31CC(C)(C)[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C(C)(C)C)C2=C1N(C=O)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C(C)(C)C)CN24616.5Standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #31CC(C)(C)[Si](C)(C)OC1=NC(=N)N([Si](C)(C)C(C)(C)C)C2=C1N(C=O)C(CN(C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C1)[Si](C)(C)C(C)(C)C)CN26564.0Standard polar33892256
(6R)-Folinic acid,3TBDMS,isomer #36CC(C)(C)[Si](C)(C)OC1=NC(=N)[NH]C2=C1N(C=O)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)CN2[Si](C)(C)C(C)(C)C5123.1Semi standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #36CC(C)(C)[Si](C)(C)OC1=NC(=N)[NH]C2=C1N(C=O)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)CN2[Si](C)(C)C(C)(C)C4600.5Standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #36CC(C)(C)[Si](C)(C)OC1=NC(=N)[NH]C2=C1N(C=O)C(CNC1=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C1)CN2[Si](C)(C)C(C)(C)C6518.0Standard polar33892256
(6R)-Folinic acid,3TBDMS,isomer #39CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C(C)(C)C)N2C=O)C=C1)[Si](C)(C)C(C)(C)C5171.7Semi standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #39CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C(C)(C)C)N2C=O)C=C1)[Si](C)(C)C(C)(C)C4625.3Standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #39CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C(C)(C)C)N2C=O)C=C1)[Si](C)(C)C(C)(C)C6316.8Standard polar33892256
(6R)-Folinic acid,3TBDMS,isomer #42CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C(C)(C)C)N2C=O)[Si](C)(C)C(C)(C)C)C=C15166.4Semi standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #42CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C(C)(C)C)N2C=O)[Si](C)(C)C(C)(C)C)C=C14562.6Standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #42CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C(C)(C)C)N2C=O)[Si](C)(C)C(C)(C)C)C=C16239.7Standard polar33892256
(6R)-Folinic acid,3TBDMS,isomer #49CC(C)(C)[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C3)[Si](C)(C)C(C)(C)C)N2C=O)[NH]15172.0Semi standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #49CC(C)(C)[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C3)[Si](C)(C)C(C)(C)C)N2C=O)[NH]14689.1Standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #49CC(C)(C)[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C)C=C3)[Si](C)(C)C(C)(C)C)N2C=O)[NH]16458.0Standard polar33892256
(6R)-Folinic acid,3TBDMS,isomer #53CC(C)(C)[Si](C)(C)N(CC1CN([Si](C)(C)C(C)(C)C)C2=C(C(O)=NC(=N)N2[Si](C)(C)C(C)(C)C)N1C=O)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C15143.3Semi standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #53CC(C)(C)[Si](C)(C)N(CC1CN([Si](C)(C)C(C)(C)C)C2=C(C(O)=NC(=N)N2[Si](C)(C)C(C)(C)C)N1C=O)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C14689.4Standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #53CC(C)(C)[Si](C)(C)N(CC1CN([Si](C)(C)C(C)(C)C)C2=C(C(O)=NC(=N)N2[Si](C)(C)C(C)(C)C)N1C=O)C1=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C16176.7Standard polar33892256
(6R)-Folinic acid,3TBDMS,isomer #55CC(C)(C)[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C(C)(C)C)N2C=O)N1[Si](C)(C)C(C)(C)C5279.0Semi standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #55CC(C)(C)[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C(C)(C)C)N2C=O)N1[Si](C)(C)C(C)(C)C4673.7Standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #55CC(C)(C)[Si](C)(C)N=C1N=C(O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)[Si](C)(C)C(C)(C)C)N2C=O)N1[Si](C)(C)C(C)(C)C6349.4Standard polar33892256
(6R)-Folinic acid,3TBDMS,isomer #56CC(C)(C)[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C(C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)N2C=O)N1[Si](C)(C)C(C)(C)C5201.4Semi standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #56CC(C)(C)[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C(C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)N2C=O)N1[Si](C)(C)C(C)(C)C4770.8Standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #56CC(C)(C)[Si](C)(C)N=C1N=C(O)C2=C(N([Si](C)(C)C(C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)O)C(=O)O)C=C3)N2C=O)N1[Si](C)(C)C(C)(C)C6242.8Standard polar33892256
(6R)-Folinic acid,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C(C)(C)C5169.5Semi standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C(C)(C)C4546.3Standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C(C)(C)C6352.7Standard polar33892256
(6R)-Folinic acid,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C(C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C5062.4Semi standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C(C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C4565.2Standard non polar33892256
(6R)-Folinic acid,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C(C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C6202.7Standard polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (Non-derivatized) - 70eV, Positivesplash10-004i-2332900000-5c40a0014d3bb486cb202017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (2 TMS) - 70eV, Positivesplash10-0fk9-7225198000-aa48aa22224db36842c72017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_1_1) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_1_3) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_1_5) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_1_6) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_1_7) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_2) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_7) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_8) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_9) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_10) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_11) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_12) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_13) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_14) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_15) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_16) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_17) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_19) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_20) - 70eV, PositiveNot Available2021-11-03Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (6R)-Folinic acid 10V, Positive-QTOFsplash10-0a4i-0031900000-31498c227b611f3360ea2015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (6R)-Folinic acid 20V, Positive-QTOFsplash10-0a6r-0393400000-f81606ae4f4b27aadbac2015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (6R)-Folinic acid 40V, Positive-QTOFsplash10-0a4i-1591000000-825bc8196995ef0bc1e32015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (6R)-Folinic acid 10V, Negative-QTOFsplash10-00di-0000900000-203ae236b032df3233d72015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (6R)-Folinic acid 20V, Negative-QTOFsplash10-0umj-1131900000-5174748fd5288f6523fd2015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (6R)-Folinic acid 40V, Negative-QTOFsplash10-0007-9674000000-192da85bfca095ec870e2015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (6R)-Folinic acid 10V, Positive-QTOFsplash10-00b9-0018900000-5cbc8e2351f8b3ec28682021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (6R)-Folinic acid 20V, Positive-QTOFsplash10-004i-0139300000-a45a2d1a5cd350ef78602021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (6R)-Folinic acid 40V, Positive-QTOFsplash10-0012-1956000000-611d4066a036a7ff475f2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (6R)-Folinic acid 10V, Negative-QTOFsplash10-00di-0001900000-20cea700a6b8ce876f5e2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (6R)-Folinic acid 20V, Negative-QTOFsplash10-0fb9-1304900000-85021f1e80280eb64d562021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (6R)-Folinic acid 40V, Negative-QTOFsplash10-0fba-3517900000-75ddfa6e2a45652614662021-10-12Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Biological Properties
Cellular LocationsNot Available
Biospecimen Locations
  • Blood
Tissue LocationsNot Available
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodDetected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal details
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB022689
KNApSAcK IDNot Available
Chemspider ID140
KEGG Compound IDC03479
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem CompoundNot Available
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]