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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 00:13:45 UTC

Update Date

2021-09-26 22:56:46 UTC

HMDB ID

HMDB0247218

Secondary Accession Numbers

None

Metabolite Identification

Common Name

(6R)-Folinic acid

Description

N5-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

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

  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

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

  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

$$$$

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

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

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

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

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
Leucovorin	Kegg
Rescuvolin	Kegg
5-Formyltetrahydrofolate	Kegg
L(-)-5-Formyl-5,6,7,8-tetrahydrofolic acid	Kegg
5-Formyltetrahydrofolic acid	Generator
L(-)-5-Formyl-5,6,7,8-tetrahydrofolate	Generator
(6R,S)-5-Formyltetrahydrofolate	HMDB
10-Formyl-7,8-dihydrofolate	HMDB
10-Formyl-7,8-dihydrofolic acid	HMDB
5-Formyl-5,6,7,8-tetrahydrofolate	HMDB
5-Formyl-5,6,7,8-tetrahydrofolic acid	HMDB
5-Formyltetrahydropteroylglutamate	HMDB
5-Formyltetrahydropteroylglutamic acid	HMDB
Folinate	HMDB, Generator
Folinic acid	HMDB, MeSH
Folinic acid-SF	HMDB
L-Leucovorin	HMDB
L-N-[P-[[(2-amino-5-Formyl-5,6,7,8-tetrahydro-4-hydroxy-6-pteridinyl)methyl]amino]benzoyl]-glutamic acid	HMDB
Leucal	HMDB
Levoleucovorin	HMDB
N5-Formyl-5,6,7,8-tetrahydrofolate	HMDB
N5-Formyl-5,6,7,8-tetrahydrofolic acid	HMDB
N5-Formyltetrahydrofolate	HMDB
N5-Formyltetrahydrofolic acid	HMDB
Welcovorin	HMDB
Acid, folinic	MeSH, HMDB
Folinate, calcium	MeSH, HMDB
Leucovorin, (D)-isomer	MeSH, HMDB
Leucovorin, (DL)-isomer	MeSH, HMDB
Leucovorin, calcium (1:1) salt	MeSH, HMDB
5 Formyltetrahydrofolate	MeSH, HMDB
Citrovorum factor	MeSH, HMDB
Factor, citrovorum	MeSH, HMDB
Folinic acid SF	MeSH, HMDB
Leucovorin, calcium (1:1) salt, pentahydrate	MeSH, HMDB
Leukovorin	MeSH, HMDB
N(5)-Formyltetrahydrofolate	MeSH, HMDB
Leucovorin, (R)-isomer	MeSH, HMDB
Leucovorin, calcium (1:1) salt, (DL)-isomer	MeSH, HMDB
Leukovorum	MeSH, HMDB
Monosodium salt leucovorin	MeSH, HMDB
Wellcovorin	MeSH, HMDB
5 Formyltetrahydropteroylglutamate	MeSH, HMDB
Calcium folinate	MeSH, HMDB
Calcium leucovorin	MeSH, HMDB
Leucovorin, calcium	MeSH, HMDB
Leucovorin, monosodium salt	MeSH, HMDB
5-Formlyl-5,6,7,8-tetrahydrofolate,calcium salt	Generator

Chemical Formula

C₂₀H₂₃N₇O₇

Average Molecular Weight

473.4393

Monoisotopic Molecular Weight

473.165896125

IUPAC Name

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

Traditional Name

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

CAS Registry Number

Not 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 Key

VVIAGPKUTFNRDU-UHFFFAOYSA-N

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pteridines and derivatives

Sub Class

Pterins and derivatives

Direct Parent

Tetrahydrofolic acids

Alternative Parents

Substituents

Tetrahydrofolic acid
Glutamic acid or derivatives
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 Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Cytoplasm (HMDB: HMDB01562)

Organelle

Mitochondrion (HMDB: HMDB01562)

Source

Exogenous

Exogenous (HMDB: HMDB01562)

Food

Vegetable

Leaf vegetable

Lettuce (FooDB: FOOD00095)

Process

Naturally occurring process

Biological process

Biochemical pathway

Metabolic pathway

Folate Metabolism (HMDB: HMDB01562)

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	-1.6	ALOGPS
logP	-2.3	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	3.47	ChemAxon
pKa (Strongest Basic)	2.81	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	215.55 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	126.66 m³·mol⁻¹	ChemAxon
Polarizability	46.54 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	202.972	30932474
DeepCCS	[M-H]-	200.604	30932474
DeepCCS	[M-2H]-	233.77	30932474
DeepCCS	[M+Na]+	209.055	30932474
AllCCS	[M+H]+	203.2	32859911
AllCCS	[M+H-H2O]+	201.5	32859911
AllCCS	[M+NH4]+	204.8	32859911
AllCCS	[M+Na]+	205.3	32859911
AllCCS	[M-H]-	199.7	32859911
AllCCS	[M+Na-2H]-	200.5	32859911
AllCCS	[M+HCOO]-	201.4	32859911

Predicted Kovats Retention Indices

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
(6R)-Folinic acid,1TMS,isomer #4	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)O	4852.4	Semi standard non polar	33892256
(6R)-Folinic acid,1TMS,isomer #4	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)O	4085.8	Standard non polar	33892256
(6R)-Folinic acid,1TMS,isomer #4	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)O	7712.0	Standard polar	33892256
(6R)-Folinic acid,1TMS,isomer #8	C[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)CN2	4871.2	Semi standard non polar	33892256
(6R)-Folinic acid,1TMS,isomer #8	C[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)CN2	4219.4	Standard non polar	33892256
(6R)-Folinic acid,1TMS,isomer #8	C[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)CN2	7804.8	Standard polar	33892256
(6R)-Folinic acid,2TMS,isomer #1	C[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	4765.5	Semi standard non polar	33892256
(6R)-Folinic acid,2TMS,isomer #1	C[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	4040.1	Standard non polar	33892256
(6R)-Folinic acid,2TMS,isomer #1	C[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	7456.4	Standard polar	33892256
(6R)-Folinic acid,2TMS,isomer #18	C[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]1	4774.7	Semi standard non polar	33892256
(6R)-Folinic acid,2TMS,isomer #18	C[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]1	4179.8	Standard non polar	33892256
(6R)-Folinic acid,2TMS,isomer #18	C[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]1	7213.8	Standard polar	33892256
(6R)-Folinic acid,2TMS,isomer #23	C[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=C1	4587.9	Semi standard non polar	33892256
(6R)-Folinic acid,2TMS,isomer #23	C[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=C1	4136.7	Standard non polar	33892256
(6R)-Folinic acid,2TMS,isomer #23	C[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=C1	6739.6	Standard polar	33892256
(6R)-Folinic acid,2TMS,isomer #3	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	4665.1	Semi standard non polar	33892256
(6R)-Folinic acid,2TMS,isomer #3	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	4049.2	Standard non polar	33892256
(6R)-Folinic acid,2TMS,isomer #3	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	7178.5	Standard polar	33892256
(6R)-Folinic acid,2TMS,isomer #4	C[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	4654.9	Semi standard non polar	33892256
(6R)-Folinic acid,2TMS,isomer #4	C[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	4052.3	Standard non polar	33892256
(6R)-Folinic acid,2TMS,isomer #4	C[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	7098.2	Standard polar	33892256
(6R)-Folinic acid,2TMS,isomer #5	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O	4563.6	Semi standard non polar	33892256
(6R)-Folinic acid,2TMS,isomer #5	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O	4086.8	Standard non polar	33892256
(6R)-Folinic acid,2TMS,isomer #5	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O	6872.3	Standard polar	33892256
(6R)-Folinic acid,2TMS,isomer #6	C[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	4700.1	Semi standard non polar	33892256
(6R)-Folinic acid,2TMS,isomer #6	C[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	4177.6	Standard non polar	33892256
(6R)-Folinic acid,2TMS,isomer #6	C[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	7272.4	Standard polar	33892256
(6R)-Folinic acid,3TMS,isomer #1	C[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)C	4611.6	Semi standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #1	C[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)C	3919.4	Standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #1	C[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)C	6876.1	Standard polar	33892256
(6R)-Folinic acid,3TMS,isomer #10	C[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)C	4531.0	Semi standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #10	C[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)C	4041.8	Standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #10	C[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)C	6663.4	Standard polar	33892256
(6R)-Folinic acid,3TMS,isomer #11	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(=O)O[Si](C)(C)C)C=C3)N2C=O)[NH]1	4582.0	Semi standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #11	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(=O)O[Si](C)(C)C)C=C3)N2C=O)[NH]1	4081.4	Standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #11	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(=O)O[Si](C)(C)C)C=C3)N2C=O)[NH]1	6722.5	Standard polar	33892256
(6R)-Folinic acid,3TMS,isomer #14	C[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)C	4494.4	Semi standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #14	C[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)C	4124.4	Standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #14	C[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)C	6735.2	Standard polar	33892256
(6R)-Folinic acid,3TMS,isomer #17	C[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	4500.3	Semi standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #17	C[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	4118.8	Standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #17	C[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	6656.8	Standard polar	33892256
(6R)-Folinic acid,3TMS,isomer #2	C[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)C	4556.0	Semi standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #2	C[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)C	3993.9	Standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #2	C[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)C	6929.4	Standard polar	33892256
(6R)-Folinic acid,3TMS,isomer #20	C[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=O	4498.4	Semi standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #20	C[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=O	4232.7	Standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #20	C[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=O	6503.9	Standard polar	33892256
(6R)-Folinic acid,3TMS,isomer #24	C[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=C1	4521.4	Semi standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #24	C[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=C1	3988.3	Standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #24	C[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=C1	6603.0	Standard polar	33892256
(6R)-Folinic acid,3TMS,isomer #3	C[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	4584.2	Semi standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #3	C[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	3993.5	Standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #3	C[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	6850.5	Standard polar	33892256
(6R)-Folinic acid,3TMS,isomer #32	C[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	4569.6	Semi standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #32	C[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	4137.6	Standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #32	C[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	6993.9	Standard polar	33892256
(6R)-Folinic acid,3TMS,isomer #36	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=C1)CN2[Si](C)(C)C	4479.8	Semi standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #36	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=C1)CN2[Si](C)(C)C	4061.3	Standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #36	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=C1)CN2[Si](C)(C)C	6638.2	Standard polar	33892256
(6R)-Folinic acid,3TMS,isomer #4	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O	4506.3	Semi standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #4	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O	4042.1	Standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #4	C[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O	6690.9	Standard polar	33892256
(6R)-Folinic acid,3TMS,isomer #42	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)N2C=O)[Si](C)(C)C)C=C1	4509.8	Semi standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #42	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)N2C=O)[Si](C)(C)C)C=C1	4060.8	Standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #42	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)N2C=O)[Si](C)(C)C)C=C1	6557.3	Standard polar	33892256
(6R)-Folinic acid,3TMS,isomer #44	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1	4520.1	Semi standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #44	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1	4134.1	Standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #44	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1	6376.9	Standard polar	33892256
(6R)-Folinic acid,3TMS,isomer #48	C[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=C1	4488.6	Semi standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #48	C[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=C1	4138.2	Standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #48	C[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=C1	6622.7	Standard polar	33892256
(6R)-Folinic acid,3TMS,isomer #49	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=C3)[Si](C)(C)C)N2C=O)[NH]1	4534.5	Semi standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #49	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=C3)[Si](C)(C)C)N2C=O)[NH]1	4195.1	Standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #49	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=C3)[Si](C)(C)C)N2C=O)[NH]1	6680.8	Standard polar	33892256
(6R)-Folinic acid,3TMS,isomer #50	C[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=O	4463.5	Semi standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #50	C[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=O	4264.5	Standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #50	C[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=O	6468.1	Standard polar	33892256
(6R)-Folinic acid,3TMS,isomer #53	C[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=C1	4522.9	Semi standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #53	C[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=C1	4236.1	Standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #53	C[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=C1	6360.2	Standard polar	33892256
(6R)-Folinic acid,3TMS,isomer #6	C[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]1	4692.3	Semi standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #6	C[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]1	4198.6	Standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #6	C[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]1	6999.6	Standard polar	33892256
(6R)-Folinic acid,3TMS,isomer #8	C[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)C	4495.0	Semi standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #8	C[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)C	3920.3	Standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #8	C[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)C	6485.1	Standard polar	33892256
(6R)-Folinic acid,3TMS,isomer #9	C[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)C	4409.2	Semi standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #9	C[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)C	3974.2	Standard non polar	33892256
(6R)-Folinic acid,3TMS,isomer #9	C[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)C	6335.4	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #1	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C	4468.4	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #1	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C	3931.3	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #1	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C	6467.5	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #10	C[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	4387.1	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #10	C[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	4003.0	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #10	C[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	6242.0	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #11	C[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	4476.0	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #11	C[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	4030.9	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #11	C[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	6482.0	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #12	C[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]1	4535.0	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #12	C[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]1	4109.7	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #12	C[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]1	6488.2	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #13	C[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	4475.8	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #13	C[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	4143.9	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #13	C[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	6330.2	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #14	C[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=O	4471.1	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #14	C[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=O	4158.6	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #14	C[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=O	6287.7	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #15	C[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)C	4638.1	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #15	C[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)C	4114.4	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #15	C[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)C	6553.2	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #16	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4363.2	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #16	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	3898.3	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #16	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	6070.3	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #17	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C	4271.7	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #17	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C	3971.6	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #17	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C	5974.2	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #18	C[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)C	4394.0	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #18	C[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)C	4029.6	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #18	C[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)C	6245.2	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #19	C[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]1	4412.7	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #19	C[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]1	4074.4	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #19	C[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]1	6290.3	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #2	C[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)C	4463.7	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #2	C[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)C	3881.4	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #2	C[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)C	6374.2	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #20	C[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)C	4290.0	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #20	C[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)C	3935.7	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #20	C[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)C	5889.1	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #21	C[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)C	4398.9	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #21	C[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)C	3964.5	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #21	C[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)C	6150.0	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #22	C[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]1	4406.5	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #22	C[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]1	4006.5	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #22	C[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]1	6203.4	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #23	C[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)C	4366.4	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #23	C[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)C	4077.1	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #23	C[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)C	5988.9	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #24	C[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=O	4379.1	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #24	C[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=O	4105.7	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #24	C[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=O	6028.8	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #25	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(=O)O[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C	4531.9	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #25	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(=O)O[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C	4038.7	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #25	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(=O)O[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)C	6281.3	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #26	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4286.6	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #26	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	3999.8	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #26	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	5948.2	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #27	C[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)C	4368.7	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #27	C[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)C	4047.3	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #27	C[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)C	6215.0	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #28	C[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]1	4373.5	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #28	C[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]1	4092.8	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #28	C[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]1	6268.2	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #29	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C	4341.0	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #29	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C	4155.9	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #29	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C	6055.7	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #3	C[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)C	4393.2	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #3	C[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)C	3954.8	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #3	C[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)C	6247.0	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #30	C[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=O	4307.7	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #30	C[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=O	4194.9	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #30	C[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=O	6099.8	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #31	C[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)C	4453.8	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #31	C[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)C	4133.6	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #31	C[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)C	6353.3	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #32	C[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	4376.5	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #32	C[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	4153.8	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #32	C[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	5988.0	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #33	C[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=O	4347.7	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #33	C[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=O	4173.3	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #33	C[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=O	6036.6	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #34	C[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)C	4514.3	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #34	C[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)C	4080.2	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #34	C[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)C	6285.0	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #35	C[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)C	4455.4	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #35	C[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)C	4189.9	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #35	C[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)C	6080.4	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #36	C[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)C	4433.6	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #36	C[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)C	3924.4	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #36	C[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)C	6372.2	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #37	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C	4379.5	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #37	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C	3991.7	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #37	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C	6265.7	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #38	C[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)C	4468.0	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #38	C[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)C	4049.6	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #38	C[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)C	6515.8	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #39	C[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]1	4491.2	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #39	C[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]1	4120.3	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #39	C[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]1	6510.8	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #4	C[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)C	4490.4	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #4	C[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)C	3981.7	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #4	C[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)C	6512.3	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #40	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1	4394.4	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #40	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1	3968.9	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #40	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1	6168.7	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #41	C[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=C1	4479.6	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #41	C[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=C1	4000.6	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #41	C[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=C1	6402.6	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #42	C[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]1	4513.1	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #42	C[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]1	4067.5	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #42	C[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]1	6410.0	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #43	C[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=C1	4488.8	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #43	C[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=C1	4100.6	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #43	C[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=C1	6254.3	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #44	C[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=O	4461.0	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #44	C[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=O	4124.9	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #44	C[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=O	6214.5	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #45	C[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)C	4636.2	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #45	C[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)C	4076.6	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #45	C[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)C	6473.6	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #46	C[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)C	4566.8	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #46	C[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)C	4199.4	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #46	C[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)C	6212.1	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #47	C[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)C	4609.9	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #47	C[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)C	4124.5	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #47	C[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)C	6430.4	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #48	C[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)C	4548.9	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #48	C[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)C	4156.3	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #48	C[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)C	6517.3	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #49	C[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=O	4439.8	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #49	C[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=O	4185.8	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #49	C[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=O	6179.2	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #5	C[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]1	4543.2	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #5	C[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]1	4047.3	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #5	C[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]1	6499.8	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #50	C[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=O	4392.1	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #50	C[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=O	4203.6	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #50	C[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=O	6256.4	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #51	C[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]1	4458.6	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #51	C[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]1	4140.9	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #51	C[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]1	6443.6	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #52	C[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	4452.5	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #52	C[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	4080.0	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #52	C[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	6485.6	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #53	C[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)C	4498.0	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #53	C[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)C	4161.9	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #53	C[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)C	6208.5	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #54	C[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)C	4447.1	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #54	C[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)C	4169.9	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #54	C[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)C	6294.1	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #55	C[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)C	4373.3	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #55	C[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)C	4032.2	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #55	C[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)C	6197.9	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #56	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4312.0	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #56	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	3978.5	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #56	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	5901.3	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #57	C[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)C	4390.5	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #57	C[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)C	4031.3	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #57	C[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)C	6162.3	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #58	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)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]1	4385.3	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #58	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)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]1	4081.6	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #58	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)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]1	6217.0	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #59	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C	4369.7	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #59	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C	4131.5	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #59	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C	6006.2	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #6	C[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)C	4424.3	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #6	C[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)C	3944.2	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #6	C[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)C	6422.7	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #60	C[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=O	4326.0	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #60	C[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=O	4176.3	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #60	C[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=O	6051.9	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #61	C[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)C	4475.8	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #61	C[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)C	4116.8	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #61	C[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)C	6300.6	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #62	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1	4400.5	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #62	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1	4109.2	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #62	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1	5910.8	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #63	C[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=O	4356.6	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #63	C[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=O	4140.2	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #63	C[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=O	5962.7	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #64	C[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)C	4520.2	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #64	C[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)C	4050.1	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #64	C[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)C	6205.7	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #65	C[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)C	4454.6	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #65	C[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)C	4148.8	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #65	C[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)C	6002.9	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #66	C[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=C1	4375.1	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #66	C[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=C1	4174.0	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #66	C[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=C1	5963.4	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #67	C[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=O	4316.4	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #67	C[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=O	4215.7	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #67	C[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=O	6008.8	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #68	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=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C	4468.5	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #68	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=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C	4119.3	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #68	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=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C	6256.9	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #69	C[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)C	4399.0	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #69	C[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)C	4219.4	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #69	C[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)C	6057.9	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #7	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C	4353.7	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #7	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C	4017.4	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #7	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C	6313.9	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #70	C[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)C	4461.6	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #70	C[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)C	4212.6	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #70	C[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)C	5988.3	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #8	C[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)C	4446.3	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #8	C[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)C	4073.4	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #8	C[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)C	6568.6	Standard polar	33892256
(6R)-Folinic acid,4TMS,isomer #9	C[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]1	4484.7	Semi standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #9	C[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]1	4137.4	Standard non polar	33892256
(6R)-Folinic acid,4TMS,isomer #9	C[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]1	6562.2	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #1	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4353.5	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #1	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	3883.4	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #1	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	6014.4	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #10	C[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)C	4495.5	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #10	C[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)C	3998.5	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #10	C[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)C	6104.9	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #11	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4268.2	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #11	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	3969.9	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #11	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	5897.0	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #12	C[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)C	4365.9	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #12	C[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)C	3998.7	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #12	C[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)C	6107.5	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #13	C[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]1	4354.2	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #13	C[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]1	4063.8	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #13	C[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]1	6099.5	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #14	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C	4340.7	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #14	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C	4117.1	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #14	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C	5972.8	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #15	C[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=O	4290.8	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #15	C[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=O	4144.5	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #15	C[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=O	5932.0	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #16	C[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)C	4419.4	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #16	C[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)C	4076.6	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #16	C[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)C	6171.9	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #17	C[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)O	4400.7	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #17	C[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)O	4072.6	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #17	C[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)O	5886.5	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #18	C[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=O	4357.1	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #18	C[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=O	4104.3	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #18	C[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=O	5854.6	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #19	C[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)C	4488.9	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #19	C[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)C	4022.7	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #19	C[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)C	6086.3	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #2	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C	4272.7	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #2	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C	3968.8	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #2	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C	5923.2	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #20	C[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)C	4450.8	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #20	C[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)C	4137.0	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #20	C[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)C	5866.5	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #21	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4206.2	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #21	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	3933.1	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #21	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	5569.5	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #22	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4319.0	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #22	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	3952.7	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #22	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(N(CC2CNC3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	5794.3	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #23	C[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]1	4295.5	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #23	C[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]1	4007.2	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #23	C[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]1	5832.1	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #24	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C	4270.1	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #24	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C	4084.1	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #24	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C	5659.0	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #25	C[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=O	4231.7	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #25	C[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=O	4118.3	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #25	C[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=O	5696.9	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #26	C[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)C	4369.1	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #26	C[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)C	4036.1	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #26	C[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)C	5920.9	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #27	C[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)C	4303.3	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #27	C[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)C	4030.0	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #27	C[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)C	5567.9	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #28	C[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=O	4269.7	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #28	C[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=O	4057.4	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #28	C[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=O	5611.8	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #29	C[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)C	4397.5	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #29	C[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)C	3959.1	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #29	C[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)C	5831.5	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #3	C[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)C	4393.8	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #3	C[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)C	3985.3	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #3	C[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)C	6149.7	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #30	C[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)C	4352.9	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #30	C[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)C	4089.5	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #30	C[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)C	5638.0	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #31	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4284.5	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #31	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4102.9	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #31	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	5642.5	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #32	C[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=O	4224.6	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #32	C[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=O	4139.5	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #32	C[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=O	5689.0	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #33	C[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)C	4363.5	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #33	C[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)C	4038.6	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #33	C[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)C	5908.3	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #34	C[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)C	4293.2	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #34	C[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)C	4162.4	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #34	C[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)C	5720.0	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #35	C[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)C	4376.2	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #35	C[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)C	4117.5	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #35	C[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)C	5650.9	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #36	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4290.8	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #36	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	3955.5	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #36	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)[NH]3)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	5855.9	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #37	C[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)C	4389.3	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #37	C[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)C	3989.0	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #37	C[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)C	6062.3	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #38	C[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]1	4366.5	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #38	C[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]1	4060.1	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #38	C[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]1	6054.6	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #39	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C	4371.0	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #39	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C	4100.6	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #39	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(NCC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)C=C1)[Si](C)(C)C	5929.7	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #4	C[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]1	4390.4	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #4	C[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]1	4053.1	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #4	C[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]1	6134.7	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #40	C[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=O	4310.0	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #40	C[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=O	4132.2	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #40	C[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=O	5889.5	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #41	C[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)C	4438.1	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #41	C[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)C	4069.0	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #41	C[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)C	6126.8	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #42	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1	4410.0	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #42	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1	4048.7	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #42	C[Si](C)(C)OC(=O)C(CCC(=O)O)NC(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O[Si](C)(C)C)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1	5821.7	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #43	C[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=O	4354.3	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #43	C[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=O	4086.8	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #43	C[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=O	5791.3	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #44	C[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)C	4492.9	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #44	C[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)C	4001.3	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #44	C[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)C	6019.2	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #45	C[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)C	4456.3	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #45	C[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)C	4108.3	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #45	C[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)C	5802.3	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #46	C[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)C	4456.0	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #46	C[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)C	4136.2	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #46	C[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)C	5765.9	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #47	C[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)C	4380.4	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #47	C[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)C	4170.9	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #47	C[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)C	5854.7	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #48	C[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)C	4434.0	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #48	C[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)C	4072.1	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #48	C[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)C	6064.0	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #49	C[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=O	4298.8	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #49	C[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=O	4155.6	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #49	C[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=O	5835.6	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #5	C[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)C	4311.9	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #5	C[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)C	3916.3	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #5	C[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)C	5833.3	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #50	C[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)C	4381.1	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #50	C[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)C	4113.9	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #50	C[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)C	5866.8	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #51	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4314.5	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #51	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	4096.0	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #51	C[Si](C)(C)OC(=O)C(CCC(=O)O)N(C(=O)C1=CC=C(N(CC2CN([Si](C)(C)C)C3=C(C(O)=NC(=N)N3[Si](C)(C)C)N2C=O)[Si](C)(C)C)C=C1)[Si](C)(C)C	5600.8	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #52	C[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=O	4247.9	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #52	C[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=O	4129.8	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #52	C[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=O	5647.8	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #53	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)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C	4384.0	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #53	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)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C	4035.6	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #53	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)[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)C	5864.0	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #54	C[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)C	4309.6	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #54	C[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)C	4149.9	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #54	C[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)C	5679.0	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #55	C[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)C	4386.6	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #55	C[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)C	4100.1	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #55	C[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)C	5588.8	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #56	C[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)C	4330.6	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #56	C[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)C	4170.5	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #56	C[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)C	5644.7	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #6	C[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)C	4401.8	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #6	C[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)C	3915.6	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #6	C[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)C	6044.8	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #7	C[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]1	4411.8	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #7	C[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]1	3982.8	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #7	C[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]1	6042.2	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #8	C[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)C	4370.1	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #8	C[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)C	4043.7	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #8	C[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)C	5896.7	Standard polar	33892256
(6R)-Folinic acid,5TMS,isomer #9	C[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=O	4360.7	Semi standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #9	C[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=O	4068.1	Standard non polar	33892256
(6R)-Folinic acid,5TMS,isomer #9	C[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=O	5855.0	Standard polar	33892256
(6R)-Folinic acid,1TBDMS,isomer #1	CC(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	5147.9	Semi standard non polar	33892256
(6R)-Folinic acid,1TBDMS,isomer #1	CC(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	4324.4	Standard non polar	33892256
(6R)-Folinic acid,1TBDMS,isomer #1	CC(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	7518.7	Standard polar	33892256
(6R)-Folinic acid,1TBDMS,isomer #2	CC(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)CN2	5101.4	Semi standard non polar	33892256
(6R)-Folinic acid,1TBDMS,isomer #2	CC(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)CN2	4324.4	Standard non polar	33892256
(6R)-Folinic acid,1TBDMS,isomer #2	CC(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)CN2	7752.6	Standard polar	33892256
(6R)-Folinic acid,1TBDMS,isomer #3	CC(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=C1	5153.3	Semi standard non polar	33892256
(6R)-Folinic acid,1TBDMS,isomer #3	CC(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=C1	4243.6	Standard non polar	33892256
(6R)-Folinic acid,1TBDMS,isomer #3	CC(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=C1	7420.3	Standard polar	33892256
(6R)-Folinic acid,1TBDMS,isomer #4	CC(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)O	5108.5	Semi standard non polar	33892256
(6R)-Folinic acid,1TBDMS,isomer #4	CC(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)O	4289.2	Standard non polar	33892256
(6R)-Folinic acid,1TBDMS,isomer #4	CC(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)O	7464.5	Standard polar	33892256
(6R)-Folinic acid,1TBDMS,isomer #6	CC(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=C2O	5010.9	Semi standard non polar	33892256
(6R)-Folinic acid,1TBDMS,isomer #6	CC(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=C2O	4310.5	Standard non polar	33892256
(6R)-Folinic acid,1TBDMS,isomer #6	CC(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=C2O	7273.2	Standard polar	33892256
(6R)-Folinic acid,2TBDMS,isomer #12	CC(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	5172.3	Semi standard non polar	33892256
(6R)-Folinic acid,2TBDMS,isomer #12	CC(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	4447.8	Standard non polar	33892256
(6R)-Folinic acid,2TBDMS,isomer #12	CC(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	7136.6	Standard polar	33892256
(6R)-Folinic acid,2TBDMS,isomer #14	CC(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)C	5190.3	Semi standard non polar	33892256
(6R)-Folinic acid,2TBDMS,isomer #14	CC(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)C	4417.4	Standard non polar	33892256
(6R)-Folinic acid,2TBDMS,isomer #14	CC(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)C	6809.8	Standard polar	33892256
(6R)-Folinic acid,2TBDMS,isomer #15	CC(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=C1	5158.7	Semi standard non polar	33892256
(6R)-Folinic acid,2TBDMS,isomer #15	CC(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=C1	4391.6	Standard non polar	33892256
(6R)-Folinic acid,2TBDMS,isomer #15	CC(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=C1	6733.0	Standard polar	33892256
(6R)-Folinic acid,2TBDMS,isomer #19	CC(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=C1	5131.1	Semi standard non polar	33892256
(6R)-Folinic acid,2TBDMS,isomer #19	CC(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=C1	4421.8	Standard non polar	33892256
(6R)-Folinic acid,2TBDMS,isomer #19	CC(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=C1	6782.5	Standard polar	33892256
(6R)-Folinic acid,2TBDMS,isomer #2	CC(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)C	5217.7	Semi standard non polar	33892256
(6R)-Folinic acid,2TBDMS,isomer #2	CC(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)C	4412.0	Standard non polar	33892256
(6R)-Folinic acid,2TBDMS,isomer #2	CC(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)C	6792.3	Standard polar	33892256
(6R)-Folinic acid,2TBDMS,isomer #28	CC(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)C	5271.3	Semi standard non polar	33892256
(6R)-Folinic acid,2TBDMS,isomer #28	CC(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)C	4616.9	Standard non polar	33892256
(6R)-Folinic acid,2TBDMS,isomer #28	CC(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)C	6834.5	Standard polar	33892256
(6R)-Folinic acid,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C(C)(C)C	5192.0	Semi standard non polar	33892256
(6R)-Folinic acid,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C(C)(C)C	4442.2	Standard non polar	33892256
(6R)-Folinic acid,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C(C)(C)C	6856.3	Standard polar	33892256
(6R)-Folinic acid,2TBDMS,isomer #9	CC(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]1	5280.2	Semi standard non polar	33892256
(6R)-Folinic acid,2TBDMS,isomer #9	CC(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]1	4641.4	Standard non polar	33892256
(6R)-Folinic acid,2TBDMS,isomer #9	CC(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]1	7129.5	Standard polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #10	CC(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)C	5161.8	Semi standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #10	CC(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)C	4595.1	Standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #10	CC(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)C	6277.6	Standard polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #17	CC(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)O	5137.8	Semi standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #17	CC(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)O	4610.8	Standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #17	CC(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)O	6298.1	Standard polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #21	CC(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)C	5274.2	Semi standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #21	CC(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)C	4701.0	Standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #21	CC(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)C	6401.4	Standard polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #23	CC(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=C1	5210.9	Semi standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #23	CC(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=C1	4504.3	Standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #23	CC(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=C1	6564.3	Standard polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #26	CC(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]1	5288.1	Semi standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #26	CC(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]1	4694.3	Standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #26	CC(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]1	6643.7	Standard polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #29	CC(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]1	5261.7	Semi standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #29	CC(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]1	4719.6	Standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #29	CC(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]1	6631.1	Standard polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #3	CC(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)O	5202.4	Semi standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #3	CC(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)O	4536.2	Standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #3	CC(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)O	6624.5	Standard polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #30	CC(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]1	5221.1	Semi standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #30	CC(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]1	4723.9	Standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #30	CC(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]1	6689.5	Standard polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #31	CC(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)CN2	5200.7	Semi standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #31	CC(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)CN2	4616.5	Standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #31	CC(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)CN2	6564.0	Standard polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #36	CC(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)C	5123.1	Semi standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #36	CC(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)C	4600.5	Standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #36	CC(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)C	6518.0	Standard polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #39	CC(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)C	5171.7	Semi standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #39	CC(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)C	4625.3	Standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #39	CC(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)C	6316.8	Standard polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #42	CC(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=C1	5166.4	Semi standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #42	CC(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=C1	4562.6	Standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #42	CC(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=C1	6239.7	Standard polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #49	CC(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]1	5172.0	Semi standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #49	CC(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]1	4689.1	Standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #49	CC(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]1	6458.0	Standard polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #53	CC(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=C1	5143.3	Semi standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #53	CC(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=C1	4689.4	Standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #53	CC(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=C1	6176.7	Standard polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #55	CC(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)C	5279.0	Semi standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #55	CC(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)C	4673.7	Standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #55	CC(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)C	6349.4	Standard polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #56	CC(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)C	5201.4	Semi standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #56	CC(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)C	4770.8	Standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #56	CC(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)C	6242.8	Standard polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C(C)(C)C	5169.5	Semi standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C(C)(C)C	4546.3	Standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)[Si](C)(C)C(C)(C)C	6352.7	Standard polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C(C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C	5062.4	Semi standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C(C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C	4565.2	Standard non polar	33892256
(6R)-Folinic acid,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC(=O)C1=CC=C(NCC2CN([Si](C)(C)C(C)(C)C)C3=C(C(O)=NC(=N)[NH]3)N2C=O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C	6202.7	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (Non-derivatized) - 70eV, Positive	splash10-004i-2332900000-5c40a0014d3bb486cb20	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (2 TMS) - 70eV, Positive	splash10-0fk9-7225198000-aa48aa22224db36842c7	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_13) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_14) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_15) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_16) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_17) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_19) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (6S)-5-formyltetrahydrofolate(2-) GC-MS (TMS_2_20) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (6R)-Folinic acid 10V, Positive-QTOF	splash10-0a4i-0031900000-31498c227b611f3360ea	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (6R)-Folinic acid 20V, Positive-QTOF	splash10-0a6r-0393400000-f81606ae4f4b27aadbac	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (6R)-Folinic acid 40V, Positive-QTOF	splash10-0a4i-1591000000-825bc8196995ef0bc1e3	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (6R)-Folinic acid 10V, Negative-QTOF	splash10-00di-0000900000-203ae236b032df3233d7	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (6R)-Folinic acid 20V, Negative-QTOF	splash10-0umj-1131900000-5174748fd5288f6523fd	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (6R)-Folinic acid 40V, Negative-QTOF	splash10-0007-9674000000-192da85bfca095ec870e	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (6R)-Folinic acid 10V, Positive-QTOF	splash10-00b9-0018900000-5cbc8e2351f8b3ec2868	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (6R)-Folinic acid 20V, Positive-QTOF	splash10-004i-0139300000-a45a2d1a5cd350ef7860	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (6R)-Folinic acid 40V, Positive-QTOF	splash10-0012-1956000000-611d4066a036a7ff475f	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (6R)-Folinic acid 10V, Negative-QTOF	splash10-00di-0001900000-20cea700a6b8ce876f5e	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (6R)-Folinic acid 20V, Negative-QTOF	splash10-0fb9-1304900000-85021f1e80280eb64d56	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (6R)-Folinic acid 40V, Negative-QTOF	splash10-0fba-3517900000-75ddfa6e2a4565261466	2021-10-12	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB022689

KNApSAcK ID

Not Available

Chemspider ID

140

KEGG Compound ID

C03479

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

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 ]

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

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

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

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

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

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

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

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

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

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

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

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra