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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 22:38:37 UTC

Update Date

2022-03-07 02:55:18 UTC

HMDB ID

HMDB0037399

Secondary Accession Numbers

HMDB37399

Metabolite Identification

Common Name

(-)-Epicatechin 6-C-glucoside

Description

(-)-Epicatechin 6-C-glucoside belongs to the class of organic compounds known as biflavonoids and polyflavonoids. These are organic compounds containing at least two flavan/flavone units. These units are usually linked through CC or C-O-C bonds. Some examples include C2-O-C3, C2-O-C4, C3'-C3''', and C6-C8'' (-)-Epicatechin 6-C-glucoside has been detected, but not quantified in, chinese cinnamons (Cinnamomum aromaticum) and herbs and spices. This could make (-)-epicatechin 6-C-glucoside a potential biomarker for the consumption of these foods. Based on a literature review a significant number of articles have been published on (-)-Epicatechin 6-C-glucoside.

Structure

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


  Mrv0541 02241209352D          

 32 35  0  0  0  0            999 V2000
   -1.2964   -2.5928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0109   -3.0053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0109   -3.8304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2964   -4.2429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5820   -3.8304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5820   -3.0053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1325   -2.5928    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1325   -4.2429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8470   -3.8304    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8470   -3.0053    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5614   -2.5929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2759   -1.3553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5614   -1.7678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2759   -3.0054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9904   -2.5929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9904   -1.7678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7048   -1.3553    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7048   -3.0053    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5614   -4.2429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7254   -4.2429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7254   -2.5929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2964   -5.0679    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4398   -3.8304    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1543   -4.2429    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1543   -5.0679    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4398   -5.4804    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7254   -5.0679    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8688   -3.8304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5832   -4.2429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8688   -5.4804    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4398   -6.3054    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0109   -5.4804    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  1  6  2  0  0  0  0
  7  6  1  0  0  0  0
  6  5  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  6  0  0  0
 13 11  1  0  0  0  0
 11 14  2  0  0  0  0
 12 13  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 12 16  1  0  0  0  0
 16 17  1  0  0  0  0
 15 18  1  0  0  0  0
  9 19  1  6  0  0  0
  2 21  1  0  0  0  0
  4 22  1  0  0  0  0
 27 20  1  0  0  0  0
 23 20  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 24 28  1  1  0  0  0
 28 29  1  0  0  0  0
 25 30  1  6  0  0  0
 26 31  1  1  0  0  0
 27 32  1  6  0  0  0
 20  3  1  0  0  0  0
M  END

HMDB0037399
     RDKit          3D
(-)-Epicatechin 6-C-glucoside
 56 59  0  0  0  0  0  0  0  0999 V2000
   -7.0855   -1.7395   -0.6265 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7439   -1.6043   -1.0118 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9107   -0.8492   -0.0103 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6237   -0.7321   -0.5047 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9071    0.2555    0.0768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4585    0.0854   -0.0669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0377   -0.3738   -1.3294 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9884   -0.5458   -2.3479 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2912   -0.6338   -1.5053 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1943   -0.4411   -0.4500 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7922   -0.0007    0.7803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5905    0.2738    0.9801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9290    0.7077    2.2417 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6801    0.1292    1.9826 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9855   -0.6071    1.6406 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6529   -1.9411    1.4515 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4101   -0.0468    0.2814 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8394   -0.1796   -0.0062 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4345   -1.3355   -0.4325 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7873   -1.3633   -0.6609 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5805   -0.2622   -0.4773 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9440   -0.2312   -0.6907 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9905    0.9112   -0.0483 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7398    2.0486    0.1539 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6334    0.9592    0.1860 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5626   -0.6993   -0.6572 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4252    1.6623   -0.0283 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6798    2.5471    0.6983 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8491    1.6634    0.4523 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.6011    2.6176   -0.3051 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5438    0.3664    0.5243 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.0025    0.1927    1.8639 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6373   -1.3488   -1.3814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7338   -1.1798   -2.0317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3642   -2.6560   -1.1465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7902   -1.5723    0.8625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0684    0.0344    1.2265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7371   -0.8713   -3.2795 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7019   -0.9860   -2.4415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8562    0.8947    2.5073 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8526    1.2001    2.1437 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2145   -0.3752    2.8812 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7500   -0.4424    2.4239 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6422   -2.2181    0.5235 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1154    1.0460    0.2956 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8465   -2.2423   -0.5885 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2847   -2.2651   -1.0011 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4933   -1.0155   -1.0097 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7305    2.0898    0.0101 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2047    1.8875    0.5227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4443    1.9804   -1.1325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0964    3.0631    0.0354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8311    2.1533    1.4710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2776    2.0656   -0.7867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5125    0.4893   -0.0487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6292   -0.5655    1.9096 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 11 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  2  0
 17 26  1  0
  5 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31  3  1  0
 12  6  1  0
 25 18  1  0
 26 10  1  0
  1 33  1  0
  2 34  1  0
  2 35  1  0
  3 36  1  1
  5 37  1  0
  8 38  1  0
  9 39  1  0
 13 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  1
 16 44  1  0
 17 45  1  1
 19 46  1  0
 20 47  1  0
 22 48  1  0
 24 49  1  0
 25 50  1  0
 27 51  1  6
 28 52  1  0
 29 53  1  1
 30 54  1  0
 31 55  1  6
 32 56  1  0
M  END


  Mrv0541 02241209352D          

 32 35  0  0  0  0            999 V2000
   -1.2964   -2.5928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0109   -3.0053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0109   -3.8304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2964   -4.2429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5820   -3.8304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5820   -3.0053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1325   -2.5928    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1325   -4.2429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8470   -3.8304    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8470   -3.0053    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5614   -2.5929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2759   -1.3553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5614   -1.7678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2759   -3.0054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9904   -2.5929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9904   -1.7678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7048   -1.3553    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7048   -3.0053    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5614   -4.2429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7254   -4.2429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7254   -2.5929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2964   -5.0679    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4398   -3.8304    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1543   -4.2429    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1543   -5.0679    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4398   -5.4804    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7254   -5.0679    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8688   -3.8304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5832   -4.2429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8688   -5.4804    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4398   -6.3054    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0109   -5.4804    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  1  6  2  0  0  0  0
  7  6  1  0  0  0  0
  6  5  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  6  0  0  0
 13 11  1  0  0  0  0
 11 14  2  0  0  0  0
 12 13  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 12 16  1  0  0  0  0
 16 17  1  0  0  0  0
 15 18  1  0  0  0  0
  9 19  1  6  0  0  0
  2 21  1  0  0  0  0
  4 22  1  0  0  0  0
 27 20  1  0  0  0  0
 23 20  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 24 28  1  1  0  0  0
 28 29  1  0  0  0  0
 25 30  1  6  0  0  0
 26 31  1  1  0  0  0
 27 32  1  6  0  0  0
 20  3  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0037399

> <DATABASE_NAME>
hmdb

> <SMILES>
OC[C@H]1OC([C@H](O)[C@@H](O)[C@@H]1O)C1=C(O)C=C2O[C@@H]([C@H](O)CC2=C1O)C1=CC(O)=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C21H24O11/c22-6-14-17(28)18(29)19(30)21(32-14)15-11(25)5-13-8(16(15)27)4-12(26)20(31-13)7-1-2-9(23)10(24)3-7/h1-3,5,12,14,17-30H,4,6H2/t12-,14-,17-,18+,19-,20-,21?/m1/s1

> <INCHI_KEY>
PWMSPKVTJLJDDS-NOCOPWLTSA-N

> <FORMULA>
C21H24O11

> <MOLECULAR_WEIGHT>
452.4087

> <EXACT_MASS>
452.13186161

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_AVERAGE_POLARIZABILITY>
44.847449352552374

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3R)-2-(3,4-dihydroxyphenyl)-6-[(3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,4-dihydro-2H-1-benzopyran-3,5,7-triol

> <ALOGPS_LOGP>
-0.64

> <JCHEM_LOGP>
-0.9622138896666665

> <ALOGPS_LOGS>
-2.08

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.38099296581375

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.781192058058062

> <JCHEM_PKA_STRONGEST_BASIC>
-3.292320040483612

> <JCHEM_POLAR_SURFACE_AREA>
200.52999999999997

> <JCHEM_REFRACTIVITY>
107.11799999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.77e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-C-glucopyranosylepicatechin

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0037399
     RDKit          3D
(-)-Epicatechin 6-C-glucoside
 56 59  0  0  0  0  0  0  0  0999 V2000
   -7.0855   -1.7395   -0.6265 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7439   -1.6043   -1.0118 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9107   -0.8492   -0.0103 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6237   -0.7321   -0.5047 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9071    0.2555    0.0768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4585    0.0854   -0.0669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0377   -0.3738   -1.3294 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9884   -0.5458   -2.3479 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2912   -0.6338   -1.5053 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1943   -0.4411   -0.4500 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7922   -0.0007    0.7803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5905    0.2738    0.9801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9290    0.7077    2.2417 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6801    0.1292    1.9826 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9855   -0.6071    1.6406 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6529   -1.9411    1.4515 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4101   -0.0468    0.2814 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8394   -0.1796   -0.0062 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4345   -1.3355   -0.4325 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7873   -1.3633   -0.6609 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5805   -0.2622   -0.4773 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9440   -0.2312   -0.6907 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9905    0.9112   -0.0483 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7398    2.0486    0.1539 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6334    0.9592    0.1860 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5626   -0.6993   -0.6572 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4252    1.6623   -0.0283 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6798    2.5471    0.6983 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8491    1.6634    0.4523 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.6011    2.6176   -0.3051 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5438    0.3664    0.5243 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.0025    0.1927    1.8639 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6373   -1.3488   -1.3814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7338   -1.1798   -2.0317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3642   -2.6560   -1.1465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7902   -1.5723    0.8625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0684    0.0344    1.2265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7371   -0.8713   -3.2795 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7019   -0.9860   -2.4415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8562    0.8947    2.5073 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8526    1.2001    2.1437 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2145   -0.3752    2.8812 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7500   -0.4424    2.4239 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6422   -2.2181    0.5235 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1154    1.0460    0.2956 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8465   -2.2423   -0.5885 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2847   -2.2651   -1.0011 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4933   -1.0155   -1.0097 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7305    2.0898    0.0101 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2047    1.8875    0.5227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4443    1.9804   -1.1325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0964    3.0631    0.0354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8311    2.1533    1.4710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2776    2.0656   -0.7867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5125    0.4893   -0.0487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6292   -0.5655    1.9096 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 11 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  2  0
 17 26  1  0
  5 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31  3  1  0
 12  6  1  0
 25 18  1  0
 26 10  1  0
  1 33  1  0
  2 34  1  0
  2 35  1  0
  3 36  1  1
  5 37  1  0
  8 38  1  0
  9 39  1  0
 13 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  1
 16 44  1  0
 17 45  1  1
 19 46  1  0
 20 47  1  0
 22 48  1  0
 24 49  1  0
 25 50  1  0
 27 51  1  6
 28 52  1  0
 29 53  1  1
 30 54  1  0
 31 55  1  6
 32 56  1  0
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -2.420  -4.840   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.754  -5.610   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.754  -7.150   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.420  -7.920   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.086  -7.150   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.086  -5.610   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       0.247  -4.840   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.247  -7.920   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.581  -7.150   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.581  -5.610   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.915  -4.840   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.248  -2.530   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.915  -3.300   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.248  -5.610   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.582  -4.840   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.582  -3.300   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.916  -2.530   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       6.916  -5.610   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       2.915  -7.920   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -5.087  -7.920   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -5.087  -4.840   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -2.420  -9.460   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      -6.421  -7.150   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -7.755  -7.920   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -7.755  -9.460   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -6.421 -10.230   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -5.087  -9.460   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -9.088  -7.150   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0     -10.422  -7.920   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -9.088 -10.230   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      -6.421 -11.770   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      -3.754 -10.230   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   21                                                  
CONECT    3    2    4   20                                                  
CONECT    4    3    5   22                                                  
CONECT    5    4    6    8                                                  
CONECT    6    1    7    5                                                  
CONECT    7    6   10                                                       
CONECT    8    5    9                                                       
CONECT    9    8   10   19                                                  
CONECT   10    9    7   11                                                  
CONECT   11   10   13   14                                                  
CONECT   12   13   16                                                       
CONECT   13   11   12                                                       
CONECT   14   11   15                                                       
CONECT   15   14   16   18                                                  
CONECT   16   15   12   17                                                  
CONECT   17   16                                                            
CONECT   18   15                                                            
CONECT   19    9                                                            
CONECT   20   27   23    3                                                  
CONECT   21    2                                                            
CONECT   22    4                                                            
CONECT   23   20   24                                                       
CONECT   24   23   25   28                                                  
CONECT   25   24   26   30                                                  
CONECT   26   25   27   31                                                  
CONECT   27   20   26   32                                                  
CONECT   28   24   29                                                       
CONECT   29   28                                                            
CONECT   30   25                                                            
CONECT   31   26                                                            
CONECT   32   27                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

COMPND    HMDB0037399
HETATM    1  O1  UNL     1      -7.085  -1.739  -0.626  1.00  0.00           O  
HETATM    2  C1  UNL     1      -5.744  -1.604  -1.012  1.00  0.00           C  
HETATM    3  C2  UNL     1      -4.911  -0.849  -0.010  1.00  0.00           C  
HETATM    4  O2  UNL     1      -3.624  -0.732  -0.505  1.00  0.00           O  
HETATM    5  C3  UNL     1      -2.907   0.256   0.077  1.00  0.00           C  
HETATM    6  C4  UNL     1      -1.458   0.085  -0.067  1.00  0.00           C  
HETATM    7  C5  UNL     1      -1.038  -0.374  -1.329  1.00  0.00           C  
HETATM    8  O3  UNL     1      -1.988  -0.546  -2.348  1.00  0.00           O  
HETATM    9  C6  UNL     1       0.291  -0.634  -1.505  1.00  0.00           C  
HETATM   10  C7  UNL     1       1.194  -0.441  -0.450  1.00  0.00           C  
HETATM   11  C8  UNL     1       0.792  -0.001   0.780  1.00  0.00           C  
HETATM   12  C9  UNL     1      -0.591   0.274   0.980  1.00  0.00           C  
HETATM   13  O4  UNL     1      -0.929   0.708   2.242  1.00  0.00           O  
HETATM   14  C10 UNL     1       1.680   0.129   1.983  1.00  0.00           C  
HETATM   15  C11 UNL     1       2.986  -0.607   1.641  1.00  0.00           C  
HETATM   16  O5  UNL     1       2.653  -1.941   1.451  1.00  0.00           O  
HETATM   17  C12 UNL     1       3.410  -0.047   0.281  1.00  0.00           C  
HETATM   18  C13 UNL     1       4.839  -0.180  -0.006  1.00  0.00           C  
HETATM   19  C14 UNL     1       5.435  -1.335  -0.433  1.00  0.00           C  
HETATM   20  C15 UNL     1       6.787  -1.363  -0.661  1.00  0.00           C  
HETATM   21  C16 UNL     1       7.580  -0.262  -0.477  1.00  0.00           C  
HETATM   22  O6  UNL     1       8.944  -0.231  -0.691  1.00  0.00           O  
HETATM   23  C17 UNL     1       6.991   0.911  -0.048  1.00  0.00           C  
HETATM   24  O7  UNL     1       7.740   2.049   0.154  1.00  0.00           O  
HETATM   25  C18 UNL     1       5.633   0.959   0.186  1.00  0.00           C  
HETATM   26  O8  UNL     1       2.563  -0.699  -0.657  1.00  0.00           O  
HETATM   27  C19 UNL     1      -3.425   1.662  -0.028  1.00  0.00           C  
HETATM   28  O9  UNL     1      -2.680   2.547   0.698  1.00  0.00           O  
HETATM   29  C20 UNL     1      -4.849   1.663   0.452  1.00  0.00           C  
HETATM   30  O10 UNL     1      -5.601   2.618  -0.305  1.00  0.00           O  
HETATM   31  C21 UNL     1      -5.544   0.366   0.524  1.00  0.00           C  
HETATM   32  O11 UNL     1      -6.003   0.193   1.864  1.00  0.00           O  
HETATM   33  H1  UNL     1      -7.637  -1.349  -1.381  1.00  0.00           H  
HETATM   34  H2  UNL     1      -5.734  -1.180  -2.032  1.00  0.00           H  
HETATM   35  H3  UNL     1      -5.364  -2.656  -1.146  1.00  0.00           H  
HETATM   36  H4  UNL     1      -4.790  -1.572   0.863  1.00  0.00           H  
HETATM   37  H5  UNL     1      -3.068   0.034   1.226  1.00  0.00           H  
HETATM   38  H6  UNL     1      -1.737  -0.871  -3.279  1.00  0.00           H  
HETATM   39  H7  UNL     1       0.702  -0.986  -2.442  1.00  0.00           H  
HETATM   40  H8  UNL     1      -1.856   0.895   2.507  1.00  0.00           H  
HETATM   41  H9  UNL     1       1.853   1.200   2.144  1.00  0.00           H  
HETATM   42  H10 UNL     1       1.215  -0.375   2.881  1.00  0.00           H  
HETATM   43  H11 UNL     1       3.750  -0.442   2.424  1.00  0.00           H  
HETATM   44  H12 UNL     1       2.642  -2.218   0.524  1.00  0.00           H  
HETATM   45  H13 UNL     1       3.115   1.046   0.296  1.00  0.00           H  
HETATM   46  H14 UNL     1       4.846  -2.242  -0.588  1.00  0.00           H  
HETATM   47  H15 UNL     1       7.285  -2.265  -1.001  1.00  0.00           H  
HETATM   48  H16 UNL     1       9.493  -1.015  -1.010  1.00  0.00           H  
HETATM   49  H17 UNL     1       8.731   2.090   0.010  1.00  0.00           H  
HETATM   50  H18 UNL     1       5.205   1.888   0.523  1.00  0.00           H  
HETATM   51  H19 UNL     1      -3.444   1.980  -1.132  1.00  0.00           H  
HETATM   52  H20 UNL     1      -2.096   3.063   0.035  1.00  0.00           H  
HETATM   53  H21 UNL     1      -4.831   2.153   1.471  1.00  0.00           H  
HETATM   54  H22 UNL     1      -6.278   2.066  -0.787  1.00  0.00           H  
HETATM   55  H23 UNL     1      -6.513   0.489  -0.049  1.00  0.00           H  
HETATM   56  H24 UNL     1      -6.629  -0.565   1.910  1.00  0.00           H  
CONECT    1    2   33
CONECT    2    3   34   35
CONECT    3    4   31   36
CONECT    4    5
CONECT    5    6   27   37
CONECT    6    7    7   12
CONECT    7    8    9
CONECT    8   38
CONECT    9   10   10   39
CONECT   10   11   26
CONECT   11   12   12   14
CONECT   12   13
CONECT   13   40
CONECT   14   15   41   42
CONECT   15   16   17   43
CONECT   16   44
CONECT   17   18   26   45
CONECT   18   19   19   25
CONECT   19   20   46
CONECT   20   21   21   47
CONECT   21   22   23
CONECT   22   48
CONECT   23   24   25   25
CONECT   24   49
CONECT   25   50
CONECT   27   28   29   51
CONECT   28   52
CONECT   29   30   31   53
CONECT   30   54
CONECT   31   32   55
CONECT   32   56
END

HMDB0037399
     RDKit          3D
(-)-Epicatechin 6-C-glucoside
 56 59  0  0  0  0  0  0  0  0999 V2000
   -7.0855   -1.7395   -0.6265 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7439   -1.6043   -1.0118 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9107   -0.8492   -0.0103 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6237   -0.7321   -0.5047 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9071    0.2555    0.0768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4585    0.0854   -0.0669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0377   -0.3738   -1.3294 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9884   -0.5458   -2.3479 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2912   -0.6338   -1.5053 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1943   -0.4411   -0.4500 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7922   -0.0007    0.7803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5905    0.2738    0.9801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9290    0.7077    2.2417 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6801    0.1292    1.9826 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9855   -0.6071    1.6406 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6529   -1.9411    1.4515 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4101   -0.0468    0.2814 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8394   -0.1796   -0.0062 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4345   -1.3355   -0.4325 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7873   -1.3633   -0.6609 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5805   -0.2622   -0.4773 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9440   -0.2312   -0.6907 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9905    0.9112   -0.0483 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7398    2.0486    0.1539 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6334    0.9592    0.1860 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5626   -0.6993   -0.6572 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4252    1.6623   -0.0283 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6798    2.5471    0.6983 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8491    1.6634    0.4523 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.6011    2.6176   -0.3051 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5438    0.3664    0.5243 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.0025    0.1927    1.8639 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6373   -1.3488   -1.3814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7338   -1.1798   -2.0317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3642   -2.6560   -1.1465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7902   -1.5723    0.8625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0684    0.0344    1.2265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7371   -0.8713   -3.2795 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7019   -0.9860   -2.4415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8562    0.8947    2.5073 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8526    1.2001    2.1437 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2145   -0.3752    2.8812 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7500   -0.4424    2.4239 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6422   -2.2181    0.5235 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1154    1.0460    0.2956 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8465   -2.2423   -0.5885 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2847   -2.2651   -1.0011 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4933   -1.0155   -1.0097 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7305    2.0898    0.0101 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2047    1.8875    0.5227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4443    1.9804   -1.1325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0964    3.0631    0.0354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8311    2.1533    1.4710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2776    2.0656   -0.7867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5125    0.4893   -0.0487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6292   -0.5655    1.9096 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 11 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  2  0
 17 26  1  0
  5 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31  3  1  0
 12  6  1  0
 25 18  1  0
 26 10  1  0
  1 33  1  0
  2 34  1  0
  2 35  1  0
  3 36  1  1
  5 37  1  0
  8 38  1  0
  9 39  1  0
 13 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  1
 16 44  1  0
 17 45  1  1
 19 46  1  0
 20 47  1  0
 22 48  1  0
 24 49  1  0
 25 50  1  0
 27 51  1  6
 28 52  1  0
 29 53  1  1
 30 54  1  0
 31 55  1  6
 32 56  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
6-C-Glucopyranosylepicatechin	HMDB
6-Glucopyranosyl-(-)-epicatechin	HMDB
6-Glucosyl-(-)-epicatechin	HMDB

Chemical Formula

C₂₁H₂₄O₁₁

Average Molecular Weight

452.4087

Monoisotopic Molecular Weight

452.13186161

IUPAC Name

(2R,3R)-2-(3,4-dihydroxyphenyl)-6-[(3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,4-dihydro-2H-1-benzopyran-3,5,7-triol

Traditional Name

6-C-glucopyranosylepicatechin

CAS Registry Number

103215-49-2

SMILES

OC[C@H]1OC([C@H](O)[C@@H](O)[C@@H]1O)C1=C(O)C=C2O[C@@H]([C@H](O)CC2=C1O)C1=CC(O)=C(O)C=C1

InChI Identifier

InChI=1S/C21H24O11/c22-6-14-17(28)18(29)19(30)21(32-14)15-11(25)5-13-8(16(15)27)4-12(26)20(31-13)7-1-2-9(23)10(24)3-7/h1-3,5,12,14,17-30H,4,6H2/t12-,14-,17-,18+,19-,20-,21?/m1/s1

InChI Key

PWMSPKVTJLJDDS-NOCOPWLTSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as biflavonoids and polyflavonoids. These are organic compounds containing at least two flavan/flavone units. These units are usually linked through CC or C-O-C bonds. Some examples include C2-O-C3, C2-O-C4, C3'-C3''', and C6-C8''.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Biflavonoids and polyflavonoids

Direct Parent

Biflavonoids and polyflavonoids

Alternative Parents

Substituents

B-type proanthocyanidin
Bi- and polyflavonoid skeleton
Proanthocyanidin
Flavonoid c-glycoside
Catechin
3'-hydroxyflavonoid
3-hydroxyflavonoid
4'-hydroxyflavonoid
Hydroxyflavonoid
5-hydroxyflavonoid
7-hydroxyflavonoid
Flavan-3-ol
Flavan
Phenolic glycoside
Hexose monosaccharide
Glycosyl compound
C-glycosyl compound
Chromane
Benzopyran
1-benzopyran
Catechol
Phenol
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Monosaccharide
Oxane
Monocyclic benzene moiety
Benzenoid
Secondary alcohol
Polyol
Oxacycle
Ether
Dialkyl ether
Organoheterocyclic compound
Alcohol
Primary alcohol
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

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
Water Solubility	3.77 g/L	ALOGPS
logP	-0.64	ALOGPS
logP	-0.96	ChemAxon
logS	-2.1	ALOGPS
pKa (Strongest Acidic)	8.78	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	200.53 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	107.12 m³·mol⁻¹	ChemAxon
Polarizability	44.85 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	203.359	31661259
DarkChem	[M-H]-	195.692	31661259
DeepCCS	[M+H]+	202.028	30932474
DeepCCS	[M-H]-	200.133	30932474
DeepCCS	[M-2H]-	233.373	30932474
DeepCCS	[M+Na]+	207.637	30932474
AllCCS	[M+H]+	209.0	32859911
AllCCS	[M+H-H2O]+	206.6	32859911
AllCCS	[M+NH4]+	211.2	32859911
AllCCS	[M+Na]+	211.9	32859911
AllCCS	[M-H]-	205.6	32859911
AllCCS	[M+Na-2H]-	206.5	32859911
AllCCS	[M+HCOO]-	207.8	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
(-)-Epicatechin 6-C-glucoside	OC[C@H]1OC([C@H](O)[C@@H](O)[C@@H]1O)C1=C(O)C=C2O[C@@H]([C@H](O)CC2=C1O)C1=CC(O)=C(O)C=C1	4943.0	Standard polar	33892256
(-)-Epicatechin 6-C-glucoside	OC[C@H]1OC([C@H](O)[C@@H](O)[C@@H]1O)C1=C(O)C=C2O[C@@H]([C@H](O)CC2=C1O)C1=CC(O)=C(O)C=C1	4090.8	Standard non polar	33892256
(-)-Epicatechin 6-C-glucoside	OC[C@H]1OC([C@H](O)[C@@H](O)[C@@H]1O)C1=C(O)C=C2O[C@@H]([C@H](O)CC2=C1O)C1=CC(O)=C(O)C=C1	4380.2	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
(-)-Epicatechin 6-C-glucoside,1TMS,isomer #1	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	4159.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,1TMS,isomer #2	C[Si](C)(C)O[C@H]1C(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)O[C@H](CO)[C@@H](O)[C@@H]1O	4222.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,1TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](O)C(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)O[C@H](CO)[C@H]1O	4194.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,1TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](CO)OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@H]1O	4181.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,1TMS,isomer #5	C[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	4195.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,1TMS,isomer #6	C[Si](C)(C)O[C@@H]1CC2=C(C=C(O)C(C3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)=C2O)O[C@@H]1C1=CC=C(O)C(O)=C1	4220.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,1TMS,isomer #7	C[Si](C)(C)OC1=C2C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	4153.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,1TMS,isomer #8	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O)=CC=C1O	4236.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,1TMS,isomer #9	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O	4255.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #1	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	4052.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #10	C[Si](C)(C)OC1=C2C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4054.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #11	C[Si](C)(C)O[C@H]1C(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)O[C@H](CO)[C@@H](O)[C@@H]1O	4143.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #12	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O)C=C1O	4122.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #13	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O)=CC=C1O	4100.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #14	C[Si](C)(C)O[C@@H]1[C@@H](CO)OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@H]1O	4113.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #15	C[Si](C)(C)O[C@H]1C(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C	4123.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #16	C[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4057.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #17	C[Si](C)(C)OC1=C2C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4029.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #18	C[Si](C)(C)O[C@@H]1CC2=C(C=C(O)C(C3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)=C2O)O[C@@H]1C1=CC=C(O)C(O)=C1	4117.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #19	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O	4109.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #2	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	4026.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #20	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O)=CC=C1O	4086.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #21	C[Si](C)(C)O[C@@H]1[C@@H](O)C(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)O[C@H](CO)[C@H]1O[Si](C)(C)C	4092.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #22	C[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4052.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #23	C[Si](C)(C)OC1=C2C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4027.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #24	C[Si](C)(C)O[C@@H]1[C@@H](CO)OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@H]1O	4109.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #25	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O	4105.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #26	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O)=CC=C1O	4083.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #27	C[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	4055.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #28	C[Si](C)(C)OC1=CC2=C(C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	4106.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #29	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O	4113.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #3	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	4119.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #30	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O)=CC=C1O	4092.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #31	C[Si](C)(C)OC1=C2C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	4071.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #32	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O	4163.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #33	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	4144.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #34	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O	4074.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #35	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O)=CC=C1O	4053.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #36	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O[Si](C)(C)C	4148.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #4	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	4116.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #5	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	4096.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #6	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4118.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #7	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4078.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #8	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4080.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TMS,isomer #9	C[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4079.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #1	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3929.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #10	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3898.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #11	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3963.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #12	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3929.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #13	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3948.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #14	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	3986.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #15	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	3984.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #16	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4046.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #17	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4016.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #18	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4020.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #19	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	3973.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #2	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	3986.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #20	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3973.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #21	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3945.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #22	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3965.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #23	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3968.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #24	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3937.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #25	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3959.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #26	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4021.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #27	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4023.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #28	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4001.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #29	C[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	3949.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #3	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	3933.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #30	C[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3990.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #31	C[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3994.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #32	C[Si](C)(C)OC1=CC2=C(C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4016.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #33	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O)C=C1O	3948.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #34	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O)=CC=C1O	3945.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #35	C[Si](C)(C)OC1=C2C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3969.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #36	C[Si](C)(C)OC1=C2C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3972.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #37	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O	3914.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #38	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O)=CC=C1O	3903.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #39	C[Si](C)(C)OC1=C2C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	3982.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #4	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	3925.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #40	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3995.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #41	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3996.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #42	C[Si](C)(C)O[C@@H]1[C@@H](CO)OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@H]1O	4052.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #43	C[Si](C)(C)O[C@H]1C(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C	4059.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #44	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O)C=C1O	3981.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #45	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O)C=C1O	3976.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #46	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O)C=C1O[Si](C)(C)C	4002.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #47	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O)=CC=C1O	3977.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #48	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O)=CC=C1O	3973.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #49	C[Si](C)(C)O[C@H]1C(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4049.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #5	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3979.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #50	C[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	3925.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #51	C[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3981.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #52	C[Si](C)(C)OC1=CC2=C(C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	3987.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #53	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O	3932.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #54	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O)=CC=C1O	3924.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #55	C[Si](C)(C)OC1=C2C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3963.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #56	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O	3899.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #57	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O)=CC=C1O	3888.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #58	C[Si](C)(C)OC1=C2C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	3959.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #59	C[Si](C)(C)O[C@@H]1CC2=C(C=C(O)C(C3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)=C2O)O[C@@H]1C1=CC=C(O)C(O)=C1	4038.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #6	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3943.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #60	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3966.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #61	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3966.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #62	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O	3967.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #63	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3972.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #64	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O)=CC=C1O	3963.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #65	C[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	3944.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #66	C[Si](C)(C)OC1=CC2=C(C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	3998.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #67	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O	3939.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #68	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O)=CC=C1O	3933.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #69	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O	3908.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #7	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3963.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #70	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O)=CC=C1O	3897.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #71	C[Si](C)(C)OC1=C2C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	3969.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #72	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3986.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #73	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3985.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #74	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3984.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #75	C[Si](C)(C)OC1=CC2=C(C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	3961.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #76	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O	3956.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #77	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O)=CC=C1O	3947.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #78	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3957.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #79	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3954.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #8	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3958.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #80	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3988.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #81	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3923.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #82	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3921.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #83	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	4035.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #84	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3951.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TMS,isomer #9	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3909.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #1	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3844.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #10	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3886.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #100	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3824.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #101	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3863.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #102	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O	3796.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #103	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O)=CC=C1O	3792.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #104	C[Si](C)(C)OC1=C2C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3897.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #105	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3785.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #106	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3840.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #107	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3786.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #108	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3872.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #109	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3875.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #11	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3913.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #110	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	3893.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #111	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3890.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #112	C[Si](C)(C)OC1=CC2=C(C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	3865.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #113	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O	3836.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #114	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O)=CC=C1O	3830.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #115	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3828.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #116	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3832.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #117	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3876.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #118	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3791.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #119	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3847.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #12	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	3850.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #120	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3798.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #121	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	3912.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #122	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3834.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #123	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3838.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #124	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3883.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #125	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	3899.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #126	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	3872.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #13	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3838.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #14	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3815.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #15	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3828.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #16	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3834.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #17	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3807.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #18	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3822.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #19	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3900.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #2	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3820.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #20	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3916.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #21	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3894.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #22	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3787.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #23	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3794.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #24	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3914.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #25	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3868.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #26	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3886.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #27	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3830.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #28	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3810.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #29	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3784.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #3	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3815.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #30	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3795.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #31	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3801.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #32	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3774.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #33	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3789.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #34	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3879.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #35	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3901.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #36	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3873.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #37	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	3887.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #38	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3886.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #39	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3848.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #4	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3857.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #40	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3876.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #41	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3890.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #42	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3840.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #43	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3874.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #44	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3983.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #45	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3996.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #46	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3971.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #47	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3892.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #48	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3850.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #49	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3875.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #5	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3817.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #50	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3870.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #51	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3888.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #52	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3866.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #53	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3867.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #54	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3883.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #55	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3862.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #56	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3984.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #57	C[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3862.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #58	C[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3846.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #59	C[Si](C)(C)OC1=CC2=C(C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	3877.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #6	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3843.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #60	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O	3840.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #61	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O)=CC=C1O	3835.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #62	C[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3941.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #63	C[Si](C)(C)OC1=CC2=C(C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3941.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #64	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O)C=C1O	3846.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #65	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O)=CC=C1O	3841.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #66	C[Si](C)(C)OC1=CC2=C(C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3935.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #67	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O)C=C1O	3844.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #68	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O)=CC=C1O	3838.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #69	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3834.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #7	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	3825.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #70	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3841.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #71	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3884.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #72	C[Si](C)(C)OC1=C2C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3914.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #73	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O	3813.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #74	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O)=CC=C1O	3806.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #75	C[Si](C)(C)OC1=C2C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3915.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #76	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O	3806.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #77	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O)=CC=C1O	3797.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #78	C[Si](C)(C)OC1=C2C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3907.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #79	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3807.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #8	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	3828.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #80	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3856.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #81	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3810.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #82	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3892.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #83	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3884.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #84	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	3932.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #85	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3896.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #86	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3891.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #87	C[Si](C)(C)O[C@H]1C(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4011.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #88	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O)C=C1O	3911.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #89	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3907.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #9	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3932.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #90	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3904.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #91	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O)=CC=C1O	3910.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #92	C[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3842.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #93	C[Si](C)(C)OC1=CC2=C(C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	3836.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #94	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O	3841.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #95	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O)=CC=C1O	3832.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #96	C[Si](C)(C)OC1=CC2=C(C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3926.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #97	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O	3836.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #98	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O)=CC=C1O	3833.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,4TMS,isomer #99	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3823.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #1	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3749.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #10	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3765.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #100	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	3815.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #101	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3850.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #102	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	3883.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #103	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	3875.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #104	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3856.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #105	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3886.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #106	C[Si](C)(C)OC1=CC2=C(C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3769.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #107	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O	3784.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #108	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O)=CC=C1O	3778.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #109	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3770.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #11	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3751.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #110	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3772.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #111	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3812.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #112	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3792.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #113	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3797.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #114	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3831.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #115	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	3827.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #116	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3752.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #117	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3804.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #118	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3758.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #119	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	3799.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #12	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3747.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #120	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	3862.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #121	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3759.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #122	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3766.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #123	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3815.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #124	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	3837.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #125	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	3807.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #126	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	3819.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #13	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3766.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #14	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3790.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #15	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3776.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #16	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	3814.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #17	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3790.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #18	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3776.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #19	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3783.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #2	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3757.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #20	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3796.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #21	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3774.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #22	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3782.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #23	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3861.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #24	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3884.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #25	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3861.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #26	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3830.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #27	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3800.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #28	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3815.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #29	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3796.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #3	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3785.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #30	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3811.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #31	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3803.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #32	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3792.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #33	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3805.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #34	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3795.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #35	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3884.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #36	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3790.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #37	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3765.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #38	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3744.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #39	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3743.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #4	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3744.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #40	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3773.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #41	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3746.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #42	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3748.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #43	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3837.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #44	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3859.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #45	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3838.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #46	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3814.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #47	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3779.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #48	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3789.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #49	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3768.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #5	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3772.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #50	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3781.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #51	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3770.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #52	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3760.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #53	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3770.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #54	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3759.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #55	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3862.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #56	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3871.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #57	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3825.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #58	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3852.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #59	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3818.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #6	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3803.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #60	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3839.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #61	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3826.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #62	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3817.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #63	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3836.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #64	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3822.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #65	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3969.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #66	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3845.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #67	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3864.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #68	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3844.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #69	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3860.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #7	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3774.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #70	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3852.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #71	C[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3798.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #72	C[Si](C)(C)OC1=CC2=C(C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3780.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #73	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O	3794.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #74	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O)=CC=C1O	3785.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #75	C[Si](C)(C)OC1=CC2=C(C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3765.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #76	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O	3777.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #77	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O)=CC=C1O	3770.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #78	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3757.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #79	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3765.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #8	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3759.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #80	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3811.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #81	C[Si](C)(C)OC1=CC2=C(C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3897.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #82	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O)C=C1O	3823.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #83	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O)=CC=C1O	3819.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #84	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3801.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #85	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3807.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #86	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3845.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #87	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3796.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #88	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3804.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #89	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3839.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #9	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3758.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #90	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	3843.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #91	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O	3786.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #92	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O)=CC=C1O	3779.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #93	C[Si](C)(C)OC1=C2C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3865.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #94	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3764.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #95	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3821.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #96	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3770.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #97	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3756.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #98	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3814.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,5TMS,isomer #99	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3764.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #1	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3764.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #10	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3741.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #11	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3772.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #12	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3762.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #13	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3763.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #14	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3741.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #15	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3749.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #16	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3753.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #17	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3734.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #18	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3741.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #19	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3745.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #2	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3732.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #20	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3773.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #21	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3823.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #22	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3794.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #23	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3805.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #24	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3786.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #25	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3799.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #26	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3792.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #27	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3786.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #28	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3797.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #29	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3794.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #3	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3724.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #30	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3855.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #31	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3819.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #32	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3833.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #33	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3828.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #34	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3828.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #35	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3821.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #36	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3796.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #37	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3771.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #38	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3781.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #39	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3755.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #4	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3716.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #40	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3764.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #41	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3761.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #42	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3753.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #43	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3761.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #44	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3761.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #45	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3839.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #46	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3790.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #47	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3801.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #48	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3796.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #49	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3795.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #5	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3733.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #50	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3786.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #51	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3840.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #52	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3855.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #53	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3846.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #54	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3838.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #55	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3834.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #56	C[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3872.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #57	C[Si](C)(C)OC1=CC2=C(C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3757.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #58	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O	3774.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #59	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O)=CC=C1O	3766.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #6	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3722.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #60	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3759.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #61	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3758.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #62	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3794.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #63	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3747.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #64	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3747.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #65	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3782.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #66	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	3777.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #67	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3814.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #68	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3818.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #69	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3851.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #7	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3715.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #70	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	3839.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #71	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	3836.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #72	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3776.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #73	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3817.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #74	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3778.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #75	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	3803.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #76	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	3799.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #77	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	3875.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #78	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3754.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #79	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)=CC=C1O	3756.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #8	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3726.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #80	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O)C=C1O[Si](C)(C)C	3788.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #81	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	3774.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #82	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	3831.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #83	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	3794.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #84	C[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	3772.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,6TMS,isomer #9	C[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3741.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	4395.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@H]1C(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)O[C@H](CO)[C@@H](O)[C@@H]1O	4448.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)C(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)O[C@H](CO)[C@H]1O	4434.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@H]1O	4414.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	4445.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@@H]1CC2=C(C=C(O)C(C3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)=C2O)O[C@@H]1C1=CC=C(O)C(O)=C1	4441.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1=C2C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	4428.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,1TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O)=CC=C1O	4488.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,1TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O	4512.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	4510.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1=C2C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4520.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)O[C@H]1C(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C(C)(C)C)CC3=C2O)O[C@H](CO)[C@@H](O)[C@@H]1O	4566.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)C(O)=C3C[C@H]2O)C=C1O	4595.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)C(O)=C3C[C@H]2O)=CC=C1O	4564.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4564.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)O[C@H]1C(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4563.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4537.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC1=C2C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4521.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)O[C@@H]1CC2=C(C=C(O)C(C3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)=C2O)O[C@@H]1C1=CC=C(O)C(O)=C1	4559.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O	4598.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	4496.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O)=CC=C1O	4570.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)C(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)O[C@H](CO)[C@H]1O[Si](C)(C)C(C)(C)C	4547.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	4528.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC1=C2C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	4514.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #24	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C(C)(C)C)CC3=C2O)[C@H](O)[C@H]1O	4541.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O	4578.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O)=CC=C1O	4553.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C(C)(C)C)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	4553.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC1=CC2=C(C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	4557.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C(C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O	4616.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C(C)(C)C)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	4538.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C(C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O)=CC=C1O	4586.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC1=C2C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	4533.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C(C)(C)C)C=C1O	4614.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C(C)(C)C)=CC=C1O	4597.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O[Si](C)(C)C(C)(C)C)=C3C[C@H]2O)C=C1O	4575.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O[Si](C)(C)C(C)(C)C)=C3C[C@H]2O)=CC=C1O	4550.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #36	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O[Si](C)(C)C(C)(C)C	4625.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	4571.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	4548.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	4554.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4521.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4522.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4542.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	4603.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)[C@H](O)CC3=C2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	4597.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	4598.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4573.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4577.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)[C@H](O[Si](C)(C)C(C)(C)C)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	4652.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)[C@H](O[Si](C)(C)C(C)(C)C)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	4638.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C(C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	4656.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C(C)(C)C)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4622.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C(C)(C)C)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4635.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	4669.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C(C)(C)C)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	4608.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	4669.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4653.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4655.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	4646.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4630.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4632.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4640.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4659.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	4640.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C(C)(C)C)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4619.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	4673.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4630.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	4629.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC1=CC2=C(C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4628.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C(C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)C(O)=C3C[C@H]2O)C=C1O	4687.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C(C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)C(O)=C3C[C@H]2O)=CC=C1O	4654.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OC1=C2C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4602.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #36	CC(C)(C)[Si](C)(C)OC1=C2C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	4604.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #37	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C3C[C@H]2O)C=C1O	4635.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #38	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C3C[C@H]2O)=CC=C1O	4606.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #39	CC(C)(C)[Si](C)(C)OC1=C2C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4608.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O	4643.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #40	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)C(O)=C3C[C@H]2O[Si](C)(C)C(C)(C)C)C=C1O	4667.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #41	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)C(O)=C3C[C@H]2O[Si](C)(C)C(C)(C)C)=CC=C1O	4649.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #42	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C(C)(C)C)CC3=C2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4658.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #43	CC(C)(C)[Si](C)(C)O[C@H]1C(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C(C)(C)C)CC3=C2O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4654.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #44	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)C(O)=C3C[C@H]2O)C=C1O	4679.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #45	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O[Si](C)(C)C(C)(C)C)C(O)=C3C[C@H]2O)C=C1O	4674.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #46	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)C(O)=C3C[C@H]2O)C=C1O[Si](C)(C)C(C)(C)C	4702.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #47	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)C(O)=C3C[C@H]2O)=CC=C1O	4656.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #48	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O[Si](C)(C)C(C)(C)C)C(O)=C3C[C@H]2O)=CC=C1O	4650.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #49	CC(C)(C)[Si](C)(C)O[C@H]1C(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	4666.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	4626.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #50	CC(C)(C)[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C(C)(C)C)=C1C1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4627.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #51	CC(C)(C)[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4610.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #52	CC(C)(C)[Si](C)(C)OC1=CC2=C(C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4629.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #53	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C(C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O	4703.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #54	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C(C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O)=CC=C1O	4669.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #55	CC(C)(C)[Si](C)(C)OC1=C2C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4587.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #56	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)C(O[Si](C)(C)C(C)(C)C)=C3C[C@H]2O)C=C1O	4651.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #57	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)C(O[Si](C)(C)C(C)(C)C)=C3C[C@H]2O)=CC=C1O	4617.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #58	CC(C)(C)[Si](C)(C)OC1=C2C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4602.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #59	CC(C)(C)[Si](C)(C)O[C@@H]1CC2=C(C=C(O)C(C3O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)=C2O)O[C@@H]1C1=CC=C(O)C(O)=C1	4643.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4602.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #60	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C(C)(C)C)C=C1O	4674.0	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #61	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C(C)(C)C)=CC=C1O	4656.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #62	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O	4657.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #63	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O[Si](C)(C)C(C)(C)C	4702.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #64	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)C(O)=C3C[C@H]2O)=CC=C1O	4633.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #65	CC(C)(C)[Si](C)(C)OC1=CC2=C(C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C(C)(C)C)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	4615.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #66	CC(C)(C)[Si](C)(C)OC1=CC2=C(C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	4621.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #67	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C(C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O	4682.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #68	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C(C)(C)C)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O)=CC=C1O	4651.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #69	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)C(O[Si](C)(C)C(C)(C)C)=C3C[C@H]2O)C=C1O	4633.4	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O)CC3=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4609.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #70	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)C(O[Si](C)(C)C(C)(C)C)=C3C[C@H]2O)=CC=C1O	4602.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #71	CC(C)(C)[Si](C)(C)OC1=C2C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	4596.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #72	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C(C)(C)C)C=C1O	4663.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #73	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C(C)(C)C)=CC=C1O	4646.3	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #74	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O[Si](C)(C)C(C)(C)C	4695.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #75	CC(C)(C)[Si](C)(C)OC1=CC2=C(C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C(C)(C)C)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	4637.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #76	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C(C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O[Si](C)(C)C(C)(C)C)=C3C[C@H]2O)C=C1O	4714.2	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #77	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C(C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O[Si](C)(C)C(C)(C)C)=C3C[C@H]2O)=CC=C1O	4679.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #78	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C(C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C(C)(C)C)C=C1O	4687.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #79	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[Si](C)(C)C(C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C(C)(C)C)=CC=C1O	4667.7	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O)C(O)=C4)[C@H](O[Si](C)(C)C(C)(C)C)CC3=C2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	4591.1	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #80	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O[Si](C)(C)C(C)(C)C)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O)C=C1O[Si](C)(C)C(C)(C)C	4721.5	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #81	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O[Si](C)(C)C(C)(C)C)=C3C[C@H]2O[Si](C)(C)C(C)(C)C)C=C1O	4648.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #82	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O[Si](C)(C)C(C)(C)C)=C3C[C@H]2O[Si](C)(C)C(C)(C)C)=CC=C1O	4632.6	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #83	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O)=C3C[C@H]2O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C	4718.9	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #84	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=CC(O)=C(C4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(O[Si](C)(C)C(C)(C)C)=C3C[C@H]2O)C=C1O[Si](C)(C)C(C)(C)C	4679.8	Semi standard non polar	33892256
(-)-Epicatechin 6-C-glucoside,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC[C@H]1OC(C2=C(O)C=C3O[C@H](C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)[C@H](O)CC3=C2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	4624.7	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - (-)-Epicatechin 6-C-glucoside GC-MS (Non-derivatized) - 70eV, Positive	splash10-0fkc-3109300000-be171569a03c62fe5903	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (-)-Epicatechin 6-C-glucoside GC-MS (3 TMS) - 70eV, Positive	splash10-0udi-1400549000-3d3bc28c449b945d7638	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (-)-Epicatechin 6-C-glucoside GC-MS (TMS_4_58) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (-)-Epicatechin 6-C-glucoside GC-MS (TMS_5_71) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (-)-Epicatechin 6-C-glucoside GC-MS (TMS_5_75) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (-)-Epicatechin 6-C-glucoside GC-MS (TMS_5_76) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (-)-Epicatechin 6-C-glucoside GC-MS (TMS_5_77) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (-)-Epicatechin 6-C-glucoside GC-MS (TMS_6_57) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (-)-Epicatechin 6-C-glucoside GC-MS (TMS_6_58) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (-)-Epicatechin 6-C-glucoside GC-MS (TMS_6_59) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (-)-Epicatechin 6-C-glucoside GC-MS (TMS_6_63) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (-)-Epicatechin 6-C-glucoside GC-MS (TMS_6_64) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (-)-Epicatechin 6-C-glucoside GC-MS (TMS_6_65) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (-)-Epicatechin 6-C-glucoside GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (-)-Epicatechin 6-C-glucoside GC-MS ("(-)-Epicatechin 6-C-glucoside,4TMS,#58" TMS) - 70eV, Positive	Not Available	2021-10-14	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 - (-)-Epicatechin 6-C-glucoside 10V, Positive-QTOF	splash10-0udr-0142900000-09700022461a16c885bd	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Epicatechin 6-C-glucoside 20V, Positive-QTOF	splash10-0udr-2986700000-265b0aa7720d16360b26	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Epicatechin 6-C-glucoside 40V, Positive-QTOF	splash10-0f6t-1931100000-2303eb11ad85087d3eb9	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Epicatechin 6-C-glucoside 10V, Negative-QTOF	splash10-0udi-0122900000-6457aec445fa9e2d47f5	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Epicatechin 6-C-glucoside 20V, Negative-QTOF	splash10-0udi-4934400000-19ef5ec9783391056027	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Epicatechin 6-C-glucoside 40V, Negative-QTOF	splash10-0kte-3910000000-7db00502357fe1fa532d	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Epicatechin 6-C-glucoside 10V, Positive-QTOF	splash10-0udi-0002900000-669be777badd88692440	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Epicatechin 6-C-glucoside 20V, Positive-QTOF	splash10-0udi-1319500000-b5787693fddc2333182e	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Epicatechin 6-C-glucoside 40V, Positive-QTOF	splash10-0lk9-8509000000-682ceea1b475586a7f98	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Epicatechin 6-C-glucoside 10V, Negative-QTOF	splash10-0udi-0012900000-fa0ef294f3d9ddc7529c	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Epicatechin 6-C-glucoside 20V, Negative-QTOF	splash10-0uei-1139800000-4b1322458d1486dbeeb6	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Epicatechin 6-C-glucoside 40V, Negative-QTOF	splash10-0kij-6897000000-a06211696d6ebb56482e	2021-09-24	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm
Extracellular

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

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

FDB016443

KNApSAcK ID

C00006356

Chemspider ID

35014409

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131752183

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

(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .

Showing metabocard for (-)-Epicatechin 6-C-glucoside (HMDB0037399)

MOL for HMDB0037399 ((-)-Epicatechin 6-C-glucoside)

3D MOL for HMDB0037399 ((-)-Epicatechin 6-C-glucoside)

3D SDF for HMDB0037399 ((-)-Epicatechin 6-C-glucoside)

3D-SDF for HMDB0037399 ((-)-Epicatechin 6-C-glucoside)

PDB for HMDB0037399 ((-)-Epicatechin 6-C-glucoside)

3D PDB for HMDB0037399 ((-)-Epicatechin 6-C-glucoside)

SMILES for HMDB0037399 ((-)-Epicatechin 6-C-glucoside)

INCHI for HMDB0037399 ((-)-Epicatechin 6-C-glucoside)

Structure for HMDB0037399 ((-)-Epicatechin 6-C-glucoside)

3D Structure for HMDB0037399 ((-)-Epicatechin 6-C-glucoside)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra