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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 22:54:13 UTC

Update Date

2022-03-07 02:55:26 UTC

HMDB ID

HMDB0037653

Secondary Accession Numbers

HMDB37653

Metabolite Identification

Common Name

Gallocatechin-(4alpha->8)-epicatechin

Description

Gallocatechin-(4alpha->8)-epicatechin 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''. Gallocatechin-(4alpha->8)-epicatechin is found, on average, in the highest concentration within a few different foods, such as teas (Camellia sinensis), red tea, and herbal tea and in a lower concentration in green tea and black tea. Gallocatechin-(4alpha->8)-epicatechin has also been detected, but not quantified in, broad beans (Vicia faba). This could make gallocatechin-(4alpha->8)-epicatechin a potential biomarker for the consumption of these foods. Gallocatechin-(4alpha->8)-epicatechin is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. Based on a literature review very few articles have been published on Gallocatechin-(4alpha->8)-epicatechin.

Structure

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


  Mrv0541 02241210282D          

 43 48  0  0  0  0            999 V2000
   -3.5652    1.9152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2796    1.5027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2796    0.6777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5652    0.2652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8507    0.6777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8507    1.5027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1362    1.9152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1362    0.2652    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4218    0.6777    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4218    1.5027    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7073    1.9152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0072    3.1527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7073    2.7402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.0072    3.9777    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1283   -0.7310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.9941    1.9152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  7  6  1  0  0  0  0
  6  5  2  0  0  0  0
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  7 10  1  0  0  0  0
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 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 35 40  1  0  0  0  0
 36 41  1  0  0  0  0
  8 21  1  6  0  0  0
 16 42  1  0  0  0  0
  2 43  1  0  0  0  0
M  END

HMDB0037653
     RDKit          3D
Gallocatechin-(4alpha->8)-epicatechin
 69 74  0  0  0  0  0  0  0  0999 V2000
   -1.9479    5.8137    1.2534 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6432    4.4919    1.0231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3593    4.0437    1.1953 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.0096    1.8245    0.5621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3042    2.2418    0.3807 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5924    3.5905    0.6207 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0
  2  3  2  0
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  6  7  1  0
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  8  2  1  0
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 43 29  1  0
  1 44  1  0
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 39 64  1  0
 40 65  1  0
 41 66  1  1
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 43 68  1  0
 43 69  1  0
M  END


  Mrv0541 02241210282D          

 43 48  0  0  0  0            999 V2000
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   -4.2796    1.5027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.4440   -1.1435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1585   -0.7310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1585    0.0940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5573   -0.7310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1283   -3.2060    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7295   -2.3810    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8729   -1.1435    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8729    0.5065    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4361    3.1527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9941    1.9152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  7  6  1  0  0  0  0
  6  5  2  0  0  0  0
  5  8  1  0  0  0  0
  7 10  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 13 11  2  0  0  0  0
 11 14  1  0  0  0  0
 12 13  1  0  0  0  0
 12 16  2  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
  4 17  1  0  0  0  0
  9 18  1  1  0  0  0
 15 19  1  0  0  0  0
 12 20  1  0  0  0  0
 21 22  2  0  0  0  0
 21 26  1  0  0  0  0
 22 23  1  0  0  0  0
 22 37  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 38  1  0  0  0  0
 26 25  2  0  0  0  0
 25 28  1  0  0  0  0
 27 26  1  0  0  0  0
 27 30  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 39  1  6  0  0  0
 30 31  1  6  0  0  0
 33 31  2  0  0  0  0
 31 34  1  0  0  0  0
 32 33  1  0  0  0  0
 32 36  2  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 35 40  1  0  0  0  0
 36 41  1  0  0  0  0
  8 21  1  6  0  0  0
 16 42  1  0  0  0  0
  2 43  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0037653

> <DATABASE_NAME>
hmdb

> <SMILES>
O[C@@H]1CC2=C(O[C@@H]1C1=CC=C(O)C(O)=C1)C([C@H]1[C@H](O)[C@H](OC3=C1C(O)=CC(O)=C3)C1=CC(O)=C(O)C(O)=C1)=C(O)C=C2O

> <INCHI_IDENTIFIER>
InChI=1S/C30H26O13/c31-12-6-17(35)23-22(7-12)42-29(11-4-19(37)26(40)20(38)5-11)27(41)25(23)24-18(36)9-15(33)13-8-21(39)28(43-30(13)24)10-1-2-14(32)16(34)3-10/h1-7,9,21,25,27-29,31-41H,8H2/t21-,25+,27+,28-,29-/m1/s1

> <INCHI_KEY>
ZYDDITZPGFXQSD-QKFRQTJPSA-N

> <FORMULA>
C30H26O13

> <MOLECULAR_WEIGHT>
594.5196

> <EXACT_MASS>
594.137340918

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_AVERAGE_POLARIZABILITY>
56.45469625746483

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
11

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3R)-2-(3,4-dihydroxyphenyl)-8-[(2R,3S,4S)-3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-yl]-3,4-dihydro-2H-1-benzopyran-3,5,7-triol

> <ALOGPS_LOGP>
2.22

> <JCHEM_LOGP>
2.812179691999999

> <ALOGPS_LOGS>
-3.53

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.074305970542673

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.56418332061728

> <JCHEM_PKA_STRONGEST_BASIC>
-5.176560376570383

> <JCHEM_POLAR_SURFACE_AREA>
240.98999999999995

> <JCHEM_REFRACTIVITY>
148.48890000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.76e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R)-2-(3,4-dihydroxyphenyl)-8-[(2R,3S,4S)-3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-yl]-3,4-dihydro-2H-1-benzopyran-3,5,7-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0037653
     RDKit          3D
Gallocatechin-(4alpha->8)-epicatechin
 69 74  0  0  0  0  0  0  0  0999 V2000
   -1.9479    5.8137    1.2534 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6432    4.4919    1.0231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3593    4.0437    1.1953 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0275    2.7344    0.9735 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2922    2.2709    1.1501 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0096    1.8245    0.5621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3042    2.2418    0.3807 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5924    3.5905    0.6207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3063    1.3689   -0.0266 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8933    0.2239   -0.7461 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0944   -0.6073   -0.9257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0727   -1.9574   -0.7445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2072   -2.7408   -0.9131 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1431   -4.1333   -0.7161 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4044   -2.1594   -1.2745 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4995   -2.9935   -1.4269 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4481   -0.8032   -1.4619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6676   -0.2461   -1.8256 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3134   -0.0306   -1.2918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7269   -0.4707   -0.1654 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2426   -1.3651   -1.1564 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6303    0.4032    0.3268 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1409   -0.1866    1.4461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4003   -0.3564    2.7127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6986    0.0503    2.9286 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2982   -0.9118    3.7639 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5991   -1.3246    3.5656 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2943   -1.8861    4.6425 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1789   -1.1760    2.3233 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4647   -0.6238    1.3026 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0808   -0.4912    0.0648 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4936   -0.3991    0.0508 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0355   -0.1886   -1.2958 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6046   -0.9040   -2.3837 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1637   -0.6551   -3.6410 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1459    0.2971   -3.8278 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6690    0.5042   -5.1036 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5731    1.0118   -2.7286 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5606    1.9649   -2.9334 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0094    0.7546   -1.4851 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0072   -1.6665    0.6973 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4210   -2.7411    0.0312 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5871   -1.6360    2.1499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8998    6.5362    0.5338 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4461    4.7178    1.5161 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9840    2.9465    1.4471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6147    3.8969    0.4732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6085    0.6053   -1.7716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1612   -2.4471   -0.4646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2611   -4.5491   -0.4527 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4158   -2.6802   -1.6867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8147    0.7413   -1.9898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3632    1.0344   -1.4421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0953   -1.1634    0.6488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7397   -2.0928   -0.7119 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1113    0.4718   -0.5324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1525   -0.0467    3.8336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1649   -1.0302    4.7543 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2490   -2.1818    4.4709 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7942    0.4427    0.7262 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8391   -1.6453   -2.2337 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8088   -1.2324   -4.4897 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3867    1.2043   -5.2191 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8732    2.4872   -2.1312 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3930    1.3563   -0.6555 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0972   -1.7378    0.6367 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4477   -2.7823    0.2928 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2956   -1.0756    2.7714 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5783   -2.7119    2.4896 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  4  6  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  2  0
 10 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 24 26  1  0
 26 27  2  0
 27 28  1  0
 27 29  1  0
 29 30  2  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  2  0
 34 35  1  0
 35 36  2  0
 36 37  1  0
 36 38  1  0
 38 39  1  0
 38 40  2  0
 32 41  1  0
 41 42  1  0
 41 43  1  0
  8  2  1  0
 19 11  1  0
 30 23  1  0
 40 33  1  0
 22  6  1  0
 43 29  1  0
  1 44  1  0
  3 45  1  0
  5 46  1  0
  8 47  1  0
 10 48  1  6
 12 49  1  0
 14 50  1  0
 16 51  1  0
 18 52  1  0
 19 53  1  0
 20 54  1  1
 21 55  1  0
 22 56  1  6
 25 57  1  0
 26 58  1  0
 28 59  1  0
 32 60  1  1
 34 61  1  0
 35 62  1  0
 37 63  1  0
 39 64  1  0
 40 65  1  0
 41 66  1  1
 42 67  1  0
 43 68  1  0
 43 69  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      -6.655   3.575   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -7.989   2.805   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -7.989   1.265   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.655   0.495   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.321   1.265   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.321   2.805   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -3.988   3.575   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -3.988   0.495   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.654   1.265   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.654   2.805   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.320   3.575   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.013   5.885   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.320   5.115   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.013   2.805   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.347   3.575   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.347   5.115   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -6.655  -0.525   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      -1.320   0.495   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       2.681   2.805   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       0.013   7.425   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -3.973  -1.365   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -5.307  -2.135   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -5.307  -3.675   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -3.973  -4.445   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.639  -3.675   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -2.639  -2.135   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -1.306  -1.365   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -1.306  -4.445   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.028  -3.675   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.028  -2.135   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.362  -1.365   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.695   0.945   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       1.362   0.175   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.695  -2.135   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.029  -1.365   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       4.029   0.175   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -6.640  -1.365   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      -3.973  -5.985   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0       1.362  -4.445   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       5.363  -2.135   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0       5.363   0.945   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0       2.681   5.885   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0      -9.322   3.575   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   43                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   17                                                  
CONECT    5    4    6    8                                                  
CONECT    6    1    7    5                                                  
CONECT    7    6   10                                                       
CONECT    8    5    9   21                                                  
CONECT    9    8   10   18                                                  
CONECT   10    7    9   11                                                  
CONECT   11   10   13   14                                                  
CONECT   12   13   16   20                                                  
CONECT   13   11   12                                                       
CONECT   14   11   15                                                       
CONECT   15   14   16   19                                                  
CONECT   16   12   15   42                                                  
CONECT   17    4                                                            
CONECT   18    9                                                            
CONECT   19   15                                                            
CONECT   20   12                                                            
CONECT   21   22   26    8                                                  
CONECT   22   21   23   37                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   38                                                  
CONECT   25   24   26   28                                                  
CONECT   26   21   25   27                                                  
CONECT   27   26   30                                                       
CONECT   28   25   29                                                       
CONECT   29   28   30   39                                                  
CONECT   30   27   29   31                                                  
CONECT   31   30   33   34                                                  
CONECT   32   33   36                                                       
CONECT   33   31   32                                                       
CONECT   34   31   35                                                       
CONECT   35   34   36   40                                                  
CONECT   36   32   35   41                                                  
CONECT   37   22                                                            
CONECT   38   24                                                            
CONECT   39   29                                                            
CONECT   40   35                                                            
CONECT   41   36                                                            
CONECT   42   16                                                            
CONECT   43    2                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   96    0
END

COMPND    HMDB0037653
HETATM    1  O1  UNL     1      -1.948   5.814   1.253  1.00  0.00           O  
HETATM    2  C1  UNL     1      -1.643   4.492   1.023  1.00  0.00           C  
HETATM    3  C2  UNL     1      -0.359   4.044   1.195  1.00  0.00           C  
HETATM    4  C3  UNL     1      -0.027   2.734   0.973  1.00  0.00           C  
HETATM    5  O2  UNL     1       1.292   2.271   1.150  1.00  0.00           O  
HETATM    6  C4  UNL     1      -1.010   1.825   0.562  1.00  0.00           C  
HETATM    7  C5  UNL     1      -2.304   2.242   0.381  1.00  0.00           C  
HETATM    8  C6  UNL     1      -2.592   3.591   0.621  1.00  0.00           C  
HETATM    9  O3  UNL     1      -3.306   1.369  -0.027  1.00  0.00           O  
HETATM   10  C7  UNL     1      -2.893   0.224  -0.746  1.00  0.00           C  
HETATM   11  C8  UNL     1      -4.094  -0.607  -0.926  1.00  0.00           C  
HETATM   12  C9  UNL     1      -4.073  -1.957  -0.745  1.00  0.00           C  
HETATM   13  C10 UNL     1      -5.207  -2.741  -0.913  1.00  0.00           C  
HETATM   14  O4  UNL     1      -5.143  -4.133  -0.716  1.00  0.00           O  
HETATM   15  C11 UNL     1      -6.404  -2.159  -1.275  1.00  0.00           C  
HETATM   16  O5  UNL     1      -7.500  -2.994  -1.427  1.00  0.00           O  
HETATM   17  C12 UNL     1      -6.448  -0.803  -1.462  1.00  0.00           C  
HETATM   18  O6  UNL     1      -7.668  -0.246  -1.826  1.00  0.00           O  
HETATM   19  C13 UNL     1      -5.313  -0.031  -1.292  1.00  0.00           C  
HETATM   20  C14 UNL     1      -1.727  -0.471  -0.165  1.00  0.00           C  
HETATM   21  O7  UNL     1      -1.243  -1.365  -1.156  1.00  0.00           O  
HETATM   22  C15 UNL     1      -0.630   0.403   0.327  1.00  0.00           C  
HETATM   23  C16 UNL     1       0.141  -0.187   1.446  1.00  0.00           C  
HETATM   24  C17 UNL     1      -0.400  -0.356   2.713  1.00  0.00           C  
HETATM   25  O8  UNL     1      -1.699   0.050   2.929  1.00  0.00           O  
HETATM   26  C18 UNL     1       0.298  -0.912   3.764  1.00  0.00           C  
HETATM   27  C19 UNL     1       1.599  -1.325   3.566  1.00  0.00           C  
HETATM   28  O9  UNL     1       2.294  -1.886   4.642  1.00  0.00           O  
HETATM   29  C20 UNL     1       2.179  -1.176   2.323  1.00  0.00           C  
HETATM   30  C21 UNL     1       1.465  -0.624   1.303  1.00  0.00           C  
HETATM   31  O10 UNL     1       2.081  -0.491   0.065  1.00  0.00           O  
HETATM   32  C22 UNL     1       3.494  -0.399   0.051  1.00  0.00           C  
HETATM   33  C23 UNL     1       4.036  -0.189  -1.296  1.00  0.00           C  
HETATM   34  C24 UNL     1       3.605  -0.904  -2.384  1.00  0.00           C  
HETATM   35  C25 UNL     1       4.164  -0.655  -3.641  1.00  0.00           C  
HETATM   36  C26 UNL     1       5.146   0.297  -3.828  1.00  0.00           C  
HETATM   37  O11 UNL     1       5.669   0.504  -5.104  1.00  0.00           O  
HETATM   38  C27 UNL     1       5.573   1.012  -2.729  1.00  0.00           C  
HETATM   39  O12 UNL     1       6.561   1.965  -2.933  1.00  0.00           O  
HETATM   40  C28 UNL     1       5.009   0.755  -1.485  1.00  0.00           C  
HETATM   41  C29 UNL     1       4.007  -1.666   0.697  1.00  0.00           C  
HETATM   42  O13 UNL     1       3.421  -2.741   0.031  1.00  0.00           O  
HETATM   43  C30 UNL     1       3.587  -1.636   2.150  1.00  0.00           C  
HETATM   44  H1  UNL     1      -1.900   6.536   0.534  1.00  0.00           H  
HETATM   45  H2  UNL     1       0.446   4.718   1.516  1.00  0.00           H  
HETATM   46  H3  UNL     1       1.984   2.947   1.447  1.00  0.00           H  
HETATM   47  H4  UNL     1      -3.615   3.897   0.473  1.00  0.00           H  
HETATM   48  H5  UNL     1      -2.608   0.605  -1.772  1.00  0.00           H  
HETATM   49  H6  UNL     1      -3.161  -2.447  -0.465  1.00  0.00           H  
HETATM   50  H7  UNL     1      -4.261  -4.549  -0.453  1.00  0.00           H  
HETATM   51  H8  UNL     1      -8.416  -2.680  -1.687  1.00  0.00           H  
HETATM   52  H9  UNL     1      -7.815   0.741  -1.990  1.00  0.00           H  
HETATM   53  H10 UNL     1      -5.363   1.034  -1.442  1.00  0.00           H  
HETATM   54  H11 UNL     1      -2.095  -1.163   0.649  1.00  0.00           H  
HETATM   55  H12 UNL     1      -0.740  -2.093  -0.712  1.00  0.00           H  
HETATM   56  H13 UNL     1       0.111   0.472  -0.532  1.00  0.00           H  
HETATM   57  H14 UNL     1      -2.152  -0.047   3.834  1.00  0.00           H  
HETATM   58  H15 UNL     1      -0.165  -1.030   4.754  1.00  0.00           H  
HETATM   59  H16 UNL     1       3.249  -2.182   4.471  1.00  0.00           H  
HETATM   60  H17 UNL     1       3.794   0.443   0.726  1.00  0.00           H  
HETATM   61  H18 UNL     1       2.839  -1.645  -2.234  1.00  0.00           H  
HETATM   62  H19 UNL     1       3.809  -1.232  -4.490  1.00  0.00           H  
HETATM   63  H20 UNL     1       6.387   1.204  -5.219  1.00  0.00           H  
HETATM   64  H21 UNL     1       6.873   2.487  -2.131  1.00  0.00           H  
HETATM   65  H22 UNL     1       5.393   1.356  -0.655  1.00  0.00           H  
HETATM   66  H23 UNL     1       5.097  -1.738   0.637  1.00  0.00           H  
HETATM   67  H24 UNL     1       2.448  -2.782   0.293  1.00  0.00           H  
HETATM   68  H25 UNL     1       4.296  -1.076   2.771  1.00  0.00           H  
HETATM   69  H26 UNL     1       3.578  -2.712   2.490  1.00  0.00           H  
CONECT    1    2   44
CONECT    2    3    3    8
CONECT    3    4   45
CONECT    4    5    6    6
CONECT    5   46
CONECT    6    7   22
CONECT    7    8    8    9
CONECT    8   47
CONECT    9   10
CONECT   10   11   20   48
CONECT   11   12   12   19
CONECT   12   13   49
CONECT   13   14   15   15
CONECT   14   50
CONECT   15   16   17
CONECT   16   51
CONECT   17   18   19   19
CONECT   18   52
CONECT   19   53
CONECT   20   21   22   54
CONECT   21   55
CONECT   22   23   56
CONECT   23   24   24   30
CONECT   24   25   26
CONECT   25   57
CONECT   26   27   27   58
CONECT   27   28   29
CONECT   28   59
CONECT   29   30   30   43
CONECT   30   31
CONECT   31   32
CONECT   32   33   41   60
CONECT   33   34   34   40
CONECT   34   35   61
CONECT   35   36   36   62
CONECT   36   37   38
CONECT   37   63
CONECT   38   39   40   40
CONECT   39   64
CONECT   40   65
CONECT   41   42   43   66
CONECT   42   67
CONECT   43   68   69
END

HMDB0037653
     RDKit          3D
Gallocatechin-(4alpha->8)-epicatechin
 69 74  0  0  0  0  0  0  0  0999 V2000
   -1.9479    5.8137    1.2534 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6432    4.4919    1.0231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3593    4.0437    1.1953 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0275    2.7344    0.9735 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2922    2.2709    1.1501 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0096    1.8245    0.5621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3042    2.2418    0.3807 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5924    3.5905    0.6207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3063    1.3689   -0.0266 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8933    0.2239   -0.7461 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0944   -0.6073   -0.9257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0727   -1.9574   -0.7445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2072   -2.7408   -0.9131 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1431   -4.1333   -0.7161 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4044   -2.1594   -1.2745 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4995   -2.9935   -1.4269 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4481   -0.8032   -1.4619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6676   -0.2461   -1.8256 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3134   -0.0306   -1.2918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7269   -0.4707   -0.1654 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2426   -1.3651   -1.1564 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6303    0.4032    0.3268 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1409   -0.1866    1.4461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4003   -0.3564    2.7127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6986    0.0503    2.9286 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2982   -0.9118    3.7639 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5991   -1.3246    3.5656 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2943   -1.8861    4.6425 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1789   -1.1760    2.3233 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4647   -0.6238    1.3026 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0808   -0.4912    0.0648 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4936   -0.3991    0.0508 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0355   -0.1886   -1.2958 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6046   -0.9040   -2.3837 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1637   -0.6551   -3.6410 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1459    0.2971   -3.8278 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6690    0.5042   -5.1036 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5731    1.0118   -2.7286 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5606    1.9649   -2.9334 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0094    0.7546   -1.4851 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0072   -1.6665    0.6973 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4210   -2.7411    0.0312 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5871   -1.6360    2.1499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8998    6.5362    0.5338 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4461    4.7178    1.5161 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9840    2.9465    1.4471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6147    3.8969    0.4732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6085    0.6053   -1.7716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1612   -2.4471   -0.4646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2611   -4.5491   -0.4527 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4158   -2.6802   -1.6867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8147    0.7413   -1.9898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3632    1.0344   -1.4421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0953   -1.1634    0.6488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7397   -2.0928   -0.7119 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1113    0.4718   -0.5324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1525   -0.0467    3.8336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1649   -1.0302    4.7543 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2490   -2.1818    4.4709 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7942    0.4427    0.7262 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8391   -1.6453   -2.2337 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8088   -1.2324   -4.4897 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3867    1.2043   -5.2191 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8732    2.4872   -2.1312 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3930    1.3563   -0.6555 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0972   -1.7378    0.6367 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4477   -2.7823    0.2928 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2956   -1.0756    2.7714 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5783   -2.7119    2.4896 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  4  6  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  2  0
 10 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 24 26  1  0
 26 27  2  0
 27 28  1  0
 27 29  1  0
 29 30  2  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  2  0
 34 35  1  0
 35 36  2  0
 36 37  1  0
 36 38  1  0
 38 39  1  0
 38 40  2  0
 32 41  1  0
 41 42  1  0
 41 43  1  0
  8  2  1  0
 19 11  1  0
 30 23  1  0
 40 33  1  0
 22  6  1  0
 43 29  1  0
  1 44  1  0
  3 45  1  0
  5 46  1  0
  8 47  1  0
 10 48  1  6
 12 49  1  0
 14 50  1  0
 16 51  1  0
 18 52  1  0
 19 53  1  0
 20 54  1  1
 21 55  1  0
 22 56  1  6
 25 57  1  0
 26 58  1  0
 28 59  1  0
 32 60  1  1
 34 61  1  0
 35 62  1  0
 37 63  1  0
 39 64  1  0
 40 65  1  0
 41 66  1  1
 42 67  1  0
 43 68  1  0
 43 69  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
Gallocatechin-(4a->8)-epicatechin	Generator
Gallocatechin-(4α->8)-epicatechin	Generator
Gallocatechin(4a->8)epicatechin	HMDB
(+)-Gallocatechin-(4a->8)-(-)-epicatechin	Generator
(+)-Gallocatechin-(4α->8)-(-)-epicatechin	Generator

Chemical Formula

C₃₀H₂₆O₁₃

Average Molecular Weight

594.5196

Monoisotopic Molecular Weight

594.137340918

IUPAC Name

(2R,3R)-2-(3,4-dihydroxyphenyl)-8-[(2R,3S,4S)-3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-yl]-3,4-dihydro-2H-1-benzopyran-3,5,7-triol

Traditional Name

(2R,3R)-2-(3,4-dihydroxyphenyl)-8-[(2R,3S,4S)-3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-yl]-3,4-dihydro-2H-1-benzopyran-3,5,7-triol

CAS Registry Number

79199-56-7

SMILES

O[C@@H]1CC2=C(O[C@@H]1C1=CC=C(O)C(O)=C1)C([C@H]1[C@H](O)[C@H](OC3=C1C(O)=CC(O)=C3)C1=CC(O)=C(O)C(O)=C1)=C(O)C=C2O

InChI Identifier

InChI=1S/C30H26O13/c31-12-6-17(35)23-22(7-12)42-29(11-4-19(37)26(40)20(38)5-11)27(41)25(23)24-18(36)9-15(33)13-8-21(39)28(43-30(13)24)10-1-2-14(32)16(34)3-10/h1-7,9,21,25,27-29,31-41H,8H2/t21-,25+,27+,28-,29-/m1/s1

InChI Key

ZYDDITZPGFXQSD-QKFRQTJPSA-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
Epigallocatechin
Catechin
3'-hydroxyflavonoid
Flavan-3-ol
Hydroxyflavonoid
3-hydroxyflavonoid
7-hydroxyflavonoid
5-hydroxyflavonoid
4'-hydroxyflavonoid
Flavan
Chromane
1-benzopyran
Benzopyran
Benzenetriol
Pyrogallol derivative
Catechol
Phenol
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Monocyclic benzene moiety
Secondary alcohol
Polyol
Organoheterocyclic compound
Oxacycle
Ether
Hydrocarbon derivative
Alcohol
Organic oxygen compound
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

polyphenol (CHEBI:75666 )
proanthocyanidin (CHEBI:75666 )
biflavonoid (CHEBI:75666 )
hydroxyflavan (CHEBI:75666 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Extracellular (HMDB: HMDB0037653)
Cytoplasm (HMDB: HMDB0037653)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0037653)

Source

Exogenous

Food

Food (HMDB: HMDB0037653)

Tea

Pulse

Bean

Broad bean (FooDB: FOOD00197)

Endogenous

Plant

Plant (HMDB: HMDB0037653)
Fabaceae (HMDB: HMDB0037653)

Not Available

Nutrient (HMDB: HMDB0037653)

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	0.18 g/L	ALOGPS
logP	2.22	ALOGPS
logP	2.81	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	8.56	ChemAxon
pKa (Strongest Basic)	-5.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	11	ChemAxon
Polar Surface Area	240.99 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	148.49 m³·mol⁻¹	ChemAxon
Polarizability	56.45 Å³	ChemAxon
Number of Rings	6	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
DeepCCS	[M+H]+	228.686	30932474
DeepCCS	[M-H]-	226.806	30932474
DeepCCS	[M-2H]-	260.841	30932474
DeepCCS	[M+Na]+	234.745	30932474
AllCCS	[M+H]+	238.6	32859911
AllCCS	[M+H-H2O]+	237.1	32859911
AllCCS	[M+NH4]+	240.0	32859911
AllCCS	[M+Na]+	240.4	32859911
AllCCS	[M-H]-	234.2	32859911
AllCCS	[M+Na-2H]-	236.0	32859911
AllCCS	[M+HCOO]-	238.1	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Gallocatechin-(4alpha->8)-epicatechin	O[C@@H]1CC2=C(O[C@@H]1C1=CC=C(O)C(O)=C1)C([C@H]1[C@H](O)[C@H](OC3=C1C(O)=CC(O)=C3)C1=CC(O)=C(O)C(O)=C1)=C(O)C=C2O	7787.3	Standard polar	33892256
Gallocatechin-(4alpha->8)-epicatechin	O[C@@H]1CC2=C(O[C@@H]1C1=CC=C(O)C(O)=C1)C([C@H]1[C@H](O)[C@H](OC3=C1C(O)=CC(O)=C3)C1=CC(O)=C(O)C(O)=C1)=C(O)C=C2O	5422.5	Standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin	O[C@@H]1CC2=C(O[C@@H]1C1=CC=C(O)C(O)=C1)C([C@H]1[C@H](O)[C@H](OC3=C1C(O)=CC(O)=C3)C1=CC(O)=C(O)C(O)=C1)=C(O)C=C2O	6049.0	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Gallocatechin-(4alpha->8)-epicatechin,1TMS,isomer #1	C[Si](C)(C)O[C@@H]1CC2=C(O)C=C(O)C([C@@H]3C4=C(O)C=C(O)C=C4O[C@H](C4=CC(O)=C(O)C(O)=C4)[C@H]3O)=C2O[C@@H]1C1=CC=C(O)C(O)=C1	5879.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,1TMS,isomer #10	C[Si](C)(C)OC1=CC(O)=C([C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C2=C1C[C@@H](O)[C@@H](C1=CC=C(O)C(O)=C1)O2	5827.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,1TMS,isomer #2	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O	5882.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,1TMS,isomer #3	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)=CC=C1O	5861.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,1TMS,isomer #4	C[Si](C)(C)O[C@H]1[C@H](C2=C(O)C=C(O)C3=C2O[C@H](C2=CC=C(O)C(O)=C2)[C@H](O)C3)C2=C(O)C=C(O)C=C2O[C@@H]1C1=CC(O)=C(O)C(O)=C1	5851.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,1TMS,isomer #5	C[Si](C)(C)OC1=CC(O)=CC2=C1[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5875.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,1TMS,isomer #6	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5887.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,1TMS,isomer #7	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O)=C1O	5834.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,1TMS,isomer #8	C[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)C=C1O	5826.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,1TMS,isomer #9	C[Si](C)(C)OC1=CC(O)=C2C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)OC2=C1[C@@H]1C2=C(O)C=C(O)C=C2O[C@H](C2=CC(O)=C(O)C(O)=C2)[C@H]1O	5843.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #1	C[Si](C)(C)OC1=CC(O)=C([C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC=C(O)C(O)=C1)O2	5675.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #10	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O	5653.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #11	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O	5673.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #12	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O	5697.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #13	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O)C2	5684.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #14	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O	5659.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #15	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)C=C1O	5639.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #16	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)C=C1O	5669.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #17	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O[Si](C)(C)C	5625.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #18	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)=CC=C1O	5634.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #19	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)=CC=C1O	5652.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #2	C[Si](C)(C)OC1=CC(O)=C2C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)OC2=C1[C@@H]1C2=C(O)C=C(O)C=C2O[C@H](C2=CC(O)=C(O)C(O)=C2)[C@H]1O	5696.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #20	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)=CC=C1O	5673.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #21	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O)C2	5673.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #22	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)=CC=C1O	5637.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #23	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)=CC=C1O	5613.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #24	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)=CC=C1O	5656.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #25	C[Si](C)(C)OC1=CC(O)=C2C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)OC2=C1[C@@H]1C2=C(O)C=C(O)C=C2O[C@H](C2=CC(O)=C(O)C(O)=C2)[C@H]1O[Si](C)(C)C	5667.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #26	C[Si](C)(C)OC1=CC(O)=C([C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)C2=C1C[C@@H](O)[C@@H](C1=CC=C(O)C(O)=C1)O2	5629.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #27	C[Si](C)(C)OC1=CC(O)=CC2=C1[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5703.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #28	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5695.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #29	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O[Si](C)(C)C)=CC(O)=C1O	5635.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #3	C[Si](C)(C)OC1=CC(O)=CC2=C1[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5732.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #30	C[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O[Si](C)(C)C)C=C1O	5630.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #31	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5680.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #32	C[Si](C)(C)OC1=CC(O)=CC2=C1[C@@H](C1=C(O[Si](C)(C)C)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5699.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #33	C[Si](C)(C)OC1=CC(O)=C([C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C2=C1C[C@@H](O)[C@@H](C1=CC=C(O)C(O)=C1)O2	5663.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #34	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O[Si](C)(C)C)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O)=C1O	5665.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #35	C[Si](C)(C)OC1=CC(O)=CC2=C1[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5658.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #36	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5674.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #37	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5645.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #38	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5691.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #39	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5653.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #4	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C2	5719.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #40	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O[Si](C)(C)C)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O)=C1O	5645.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #41	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O[Si](C)(C)C)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O)=C1O	5638.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #42	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O[Si](C)(C)C)=C1O	5655.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #43	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O)=C1O[Si](C)(C)C	5611.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #44	C[Si](C)(C)OC1=CC(O)=C2C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)OC2=C1[C@@H]1C2=C(O)C=C(O)C=C2O[C@H](C2=CC(O)=C(O[Si](C)(C)C)C(O)=C2)[C@H]1O	5643.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #45	C[Si](C)(C)OC1=CC(O)=C([C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)C2=C1C[C@@H](O)[C@@H](C1=CC=C(O)C(O)=C1)O2	5611.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #46	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C([C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C2=C1C[C@@H](O)[C@@H](C1=CC=C(O)C(O)=C1)O2	5616.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #5	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O[Si](C)(C)C)C4)[C@@H]2O)=CC(O)=C1O	5665.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #6	C[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O[Si](C)(C)C)C4)[C@@H]2O)C=C1O	5662.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #7	C[Si](C)(C)O[C@H]1[C@H](C2=C(O)C=C(O)C3=C2O[C@H](C2=CC=C(O)C(O)=C2)[C@H](O[Si](C)(C)C)C3)C2=C(O)C=C(O)C=C2O[C@@H]1C1=CC(O)=C(O)C(O)=C1	5700.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #8	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O	5701.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TMS,isomer #9	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)=CC=C1O	5689.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #1	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C([C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC=C(O)C(O)=C1)O2	5493.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #10	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C2	5544.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #100	C[Si](C)(C)OC1=CC(O)=CC2=C1[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5447.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #101	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5452.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #102	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5396.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #103	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O	5442.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #104	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C	5418.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #105	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O[Si](C)(C)C)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5539.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #106	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O[Si](C)(C)C)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5493.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #107	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)O2	5489.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #108	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5434.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #109	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C([C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C2=C1C[C@@H](O)[C@@H](C1=CC=C(O)C(O)=C1)O2	5519.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #11	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O[Si](C)(C)C)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O[Si](C)(C)C)C4)[C@@H]2O)=CC(O)=C1O	5487.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #110	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O[Si](C)(C)C)=C3[C@@H](C3=C(O[Si](C)(C)C)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O)=C1O	5507.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #111	C[Si](C)(C)OC1=CC(O)=CC2=C1[C@@H](C1=C(O[Si](C)(C)C)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5476.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #112	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O[Si](C)(C)C)=C3[C@@H](C3=C(O)C=C(O[Si](C)(C)C)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O)=C1O	5470.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #113	C[Si](C)(C)OC1=CC(O)=C([C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)C2=C1C[C@@H](O)[C@@H](C1=CC=C(O)C(O)=C1)O2	5432.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #114	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O[Si](C)(C)C)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O[Si](C)(C)C)=C1O	5494.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #115	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O[Si](C)(C)C)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O)=C1O[Si](C)(C)C	5461.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #116	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5455.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #117	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5426.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #118	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5488.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #119	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5432.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #12	C[Si](C)(C)OC1=CC(O)=C2C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)OC2=C1[C@@H]1C2=C(O)C=C(O)C=C2O[C@H](C2=CC(O)=C(O[Si](C)(C)C)C(O)=C2)[C@H]1O	5465.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #120	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5440.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #121	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5390.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #122	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5490.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #123	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O)=C1O	5448.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #124	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O[Si](C)(C)C)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O[Si](C)(C)C)=C1O	5479.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #125	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O[Si](C)(C)C)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O)=C1O[Si](C)(C)C	5446.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #126	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O[Si](C)(C)C)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O[Si](C)(C)C)=C1O	5427.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #127	C[Si](C)(C)OC1=CC(O)=C([C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)[C@H]2O)C2=C1C[C@@H](O)[C@@H](C1=CC=C(O)C(O)=C1)O2	5398.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #128	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	5448.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #129	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C([C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)C2=C1C[C@@H](O)[C@@H](C1=CC=C(O)C(O)=C1)O2	5404.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #13	C[Si](C)(C)OC1=CC(O)=C2C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)OC2=C1[C@@H]1C2=C(O)C=C(O)C=C2O[C@H](C2=CC(O)=C(O)C(O)=C2)[C@H]1O[Si](C)(C)C	5544.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #14	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O	5507.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #15	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)=CC=C1O	5498.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #16	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5537.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #17	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O	5523.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #18	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)=CC=C1O	5516.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #19	C[Si](C)(C)OC1=CC(O)=CC2=C1[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C3)[C@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5565.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #2	C[Si](C)(C)OC1=CC(O)=C([C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC=C(O)C(O)=C1)O2	5522.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #20	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O[Si](C)(C)C)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O[Si](C)(C)C)C4)[C@@H]2O)=CC(O)=C1O	5497.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #21	C[Si](C)(C)OC1=CC(O)=CC2=C1[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C3)[C@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5475.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #22	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C2	5481.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #23	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C2	5438.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #24	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C2	5540.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #25	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O[Si](C)(C)C)C2	5498.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #26	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O[Si](C)(C)C)C2	5495.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #27	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O	5440.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #28	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)=CC=C1O	5429.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #29	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O[Si](C)(C)C)C4)[C@@H]2O[Si](C)(C)C)=CC(O)=C1O	5476.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #3	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C2	5496.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #30	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O[Si](C)(C)C)C4)[C@@H]2O)=CC(O[Si](C)(C)C)=C1O	5463.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #31	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O[Si](C)(C)C)C4)[C@@H]2O)=CC(O)=C1O[Si](C)(C)C	5443.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #32	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)C=C1O	5394.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #33	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)=CC=C1O	5386.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #34	C[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O[Si](C)(C)C)C4)[C@@H]2O[Si](C)(C)C)C=C1O	5437.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #35	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)C=C1O	5493.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #36	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)=CC=C1O	5487.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #37	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O[Si](C)(C)C	5478.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #38	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O	5462.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #39	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O	5486.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #4	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O[Si](C)(C)C)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O[Si](C)(C)C)C4)[C@@H]2O)=CC(O)=C1O	5449.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #40	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O)C2	5437.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #41	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O	5383.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #42	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)C=C1O	5336.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #43	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)C=C1O	5425.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #44	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O[Si](C)(C)C	5446.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #45	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O	5528.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #46	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O)C2	5496.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #47	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O	5443.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #48	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)C=C1O	5406.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #49	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)C=C1O	5484.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #5	C[Si](C)(C)OC1=CC(O)=C([C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)C2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC=C(O)C(O)=C1)O2	5416.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #50	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O[Si](C)(C)C	5493.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #51	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5498.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #52	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O	5461.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #53	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)C=C1O	5422.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #54	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)C=C1O	5504.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #55	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O[Si](C)(C)C	5509.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #56	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O)C2	5411.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #57	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O)C2	5366.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #58	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O)C2	5467.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #59	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[C@H](O)C2	5487.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #6	C[Si](C)(C)OC1=CC(O)=C([C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)C2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC=C(O)C(O)=C1)O2	5497.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #60	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O	5411.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #61	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O	5395.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #62	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O[Si](C)(C)C)C=C1O	5399.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #63	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O[Si](C)(C)C	5430.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #64	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O[Si](C)(C)C)C=C1O	5349.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #65	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)C=C1O[Si](C)(C)C	5385.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #66	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	5453.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #67	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)=CC=C1O	5447.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #68	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)=CC=C1O	5473.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #69	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O)C2	5432.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #7	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O	5466.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #70	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)=CC=C1O	5376.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #71	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)=CC=C1O	5325.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #72	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)=CC=C1O	5412.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #73	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)=CC=C1O	5514.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #74	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O)C2	5484.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #75	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)=CC=C1O	5423.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #76	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)=CC=C1O	5387.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #77	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)=CC=C1O	5467.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #78	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5491.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #79	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)=CC=C1O	5447.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #8	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)=CC=C1O	5461.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #80	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)=CC=C1O	5404.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #81	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)=CC=C1O	5486.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #82	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O)C2	5404.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #83	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O)C2	5355.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #84	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O)C2	5454.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #85	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)=CC=C1O	5397.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #86	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)[C@H]2O)=CC=C1O	5378.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #87	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O[Si](C)(C)C)=CC=C1O	5381.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #88	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O[Si](C)(C)C)=CC=C1O	5333.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #89	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C([C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)C2=C1C[C@@H](O)[C@@H](C1=CC=C(O)C(O)=C1)O2	5457.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #9	C[Si](C)(C)OC1=CC(O)=CC2=C1[C@@H](C1=C(O[Si](C)(C)C)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5565.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #90	C[Si](C)(C)OC1=CC(O)=CC2=C1[C@@H](C1=C(O[Si](C)(C)C)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5541.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #91	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5515.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #92	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O[Si](C)(C)C)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O[Si](C)(C)C)=CC(O)=C1O	5464.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #93	C[Si](C)(C)OC1=CC(O)=C2C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)OC2=C1[C@@H]1C2=C(O)C=C(O)C=C2O[C@H](C2=CC(O)=C(O[Si](C)(C)C)C(O)=C2)[C@H]1O[Si](C)(C)C	5430.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #94	C[Si](C)(C)OC1=CC(O)=C([C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)C2=C1C[C@@H](O)[C@@H](C1=CC=C(O)C(O)=C1)O2	5488.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #95	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5457.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #96	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O[Si](C)(C)C)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O[Si](C)(C)C)=CC(O)=C1O	5412.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #97	C[Si](C)(C)OC1=CC(O)=C([C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O[Si](C)(C)C)C2=C1C[C@@H](O)[C@@H](C1=CC=C(O)C(O)=C1)O2	5364.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #98	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5512.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,3TMS,isomer #99	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O[Si](C)(C)C)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O[Si](C)(C)C)=CC(O)=C1O	5478.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #1	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C([C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC=C(O)C(O)=C1)O2	5428.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #10	C[Si](C)(C)OC1=CC(O)=C([C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)C2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC=C(O)C(O)=C1)O2	5326.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #100	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O	5269.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #101	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)C=C1O	5195.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #102	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)C=C1O	5333.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #103	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O[Si](C)(C)C	5374.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #104	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O)C2	5198.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #105	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O)C2	5144.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #106	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O)C2	5278.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #107	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[C@H](O)C2	5328.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #108	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O	5187.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #109	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O	5181.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #11	C[Si](C)(C)OC1=CC(O)=C([C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)C2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC=C(O)C(O)=C1)O2	5403.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #110	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O[Si](C)(C)C)C=C1O	5188.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #111	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O[Si](C)(C)C	5255.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #112	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O[Si](C)(C)C)C=C1O	5100.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #113	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)C=C1O[Si](C)(C)C	5184.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #114	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	5306.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #115	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O[Si](C)(C)C)C=C(O)C3=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5374.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #116	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O	5342.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #117	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)C=C1O	5273.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #118	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)C=C1O	5384.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #119	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O[Si](C)(C)C	5416.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #12	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O	5371.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #120	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O)C2	5268.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #121	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O)C2	5190.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #122	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O)C2	5337.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #123	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[C@H](O)C2	5378.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #124	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O	5257.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #125	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O	5248.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #126	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O[Si](C)(C)C)C=C1O	5267.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #127	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O[Si](C)(C)C	5318.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #128	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O[Si](C)(C)C)C=C1O	5182.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #129	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)C=C1O[Si](C)(C)C	5255.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #13	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)=CC=C1O	5369.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #130	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	5356.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #131	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5386.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #132	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O)C3)[C@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5344.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #133	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)O2	5277.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #134	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5199.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #135	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O	5286.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #136	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O	5276.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #137	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O[Si](C)(C)C)C=C1O	5294.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #138	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O[Si](C)(C)C	5349.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #139	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O[Si](C)(C)C)C=C1O	5218.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #14	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C2	5320.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #140	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)C=C1O[Si](C)(C)C	5286.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #141	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	5383.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #142	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O)C2	5215.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #143	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O)C2	5205.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #144	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O)C2	5215.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #145	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[C@H](O)C2	5284.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #146	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O)C2	5134.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #147	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[C@H](O)C2	5216.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #148	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[C@H](O)C2	5346.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #149	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O	5272.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #15	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C2	5261.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #150	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O[Si](C)(C)C)C=C1O	5203.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #151	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O[Si](C)(C)C	5261.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #152	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)[C@H]2O[Si](C)(C)C)C=C1O	5197.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #153	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O[Si](C)(C)C	5257.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #154	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	5270.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #155	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	5200.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #156	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)=CC=C1O	5349.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #157	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O)C2	5304.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #158	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)=CC=C1O	5233.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #159	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)=CC=C1O	5154.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #16	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C2	5370.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #160	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)=CC=C1O	5297.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #161	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O[Si](C)(C)C)C3=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5315.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #162	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)=CC=C1O	5259.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #163	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)=CC=C1O	5189.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #164	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)=CC=C1O	5324.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #165	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O)C2	5190.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #166	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O)C2	5138.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #167	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O)C2	5274.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #168	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)=CC=C1O	5173.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #169	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)[C@H]2O)=CC=C1O	5173.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #17	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O[Si](C)(C)C)C2	5322.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #170	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O[Si](C)(C)C)=CC=C1O	5181.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #171	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O[Si](C)(C)C)=CC=C1O	5091.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #172	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O[Si](C)(C)C)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5364.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #173	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)=CC=C1O	5329.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #174	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)=CC=C1O	5265.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #175	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)=CC=C1O	5377.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #176	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O)C2	5255.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #177	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O)C2	5184.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #178	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O)C2	5328.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #179	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)=CC=C1O	5240.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #18	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O[Si](C)(C)C)C2	5325.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #180	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)[C@H]2O)=CC=C1O	5240.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #181	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O[Si](C)(C)C)=CC=C1O	5255.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #182	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O[Si](C)(C)C)=CC=C1O	5170.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #183	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O)C3)[C@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5340.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #184	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)O2	5269.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #185	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5197.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #186	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)=CC=C1O	5271.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #187	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)[C@H]2O)=CC=C1O	5269.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #188	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O[Si](C)(C)C)=CC=C1O	5287.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #189	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O[Si](C)(C)C)=CC=C1O	5207.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #19	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O	5241.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #190	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O)C2	5205.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #191	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O)C2	5200.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #192	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O)C2	5209.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #193	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O)C2	5129.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #194	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)[C@H]2O)=CC=C1O	5261.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #195	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O[Si](C)(C)C)=CC=C1O	5191.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #196	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)[C@H]2O[Si](C)(C)C)=CC=C1O	5187.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #197	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C([C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)C2=C1C[C@@H](O)[C@@H](C1=CC=C(O)C(O)=C1)O2	5394.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #198	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5361.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #199	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O[Si](C)(C)C)=CC(O)=C1O	5303.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #2	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C2	5398.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #20	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)=CC=C1O	5245.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #200	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C([C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O[Si](C)(C)C)C2=C1C[C@@H](O)[C@@H](C1=CC=C(O)C(O)=C1)O2	5248.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #201	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O[Si](C)(C)C)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5422.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #202	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O[Si](C)(C)C)=C3[C@@H](C3=C(O[Si](C)(C)C)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O[Si](C)(C)C)=CC(O)=C1O	5375.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #203	C[Si](C)(C)OC1=CC(O)=CC2=C1[C@@H](C1=C(O[Si](C)(C)C)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5334.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #204	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5337.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #205	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5289.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #206	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O[Si](C)(C)C)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O	5321.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #207	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O[Si](C)(C)C)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C	5307.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #208	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O[Si](C)(C)C)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5370.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #209	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O[Si](C)(C)C)=C3[C@@H](C3=C(O)C=C(O[Si](C)(C)C)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O[Si](C)(C)C)=CC(O)=C1O	5328.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #21	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O[Si](C)(C)C)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O[Si](C)(C)C)C4)[C@@H]2O[Si](C)(C)C)=CC(O)=C1O	5310.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #210	C[Si](C)(C)OC1=CC(O)=C([C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O[Si](C)(C)C)C2=C1C[C@@H](O)[C@@H](C1=CC=C(O)C(O)=C1)O2	5285.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #211	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5281.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #212	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5213.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #213	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O[Si](C)(C)C)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O	5267.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #214	C[Si](C)(C)OC1=CC(O)=C([C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)[C@H]2O[Si](C)(C)C)C2=C1C[C@@H](O)[C@@H](C1=CC=C(O)C(O)=C1)O2	5257.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #215	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)O2	5344.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #216	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5292.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #217	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O[Si](C)(C)C)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O	5345.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #218	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O[Si](C)(C)C)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C	5329.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #219	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5299.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #22	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O[Si](C)(C)C)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O[Si](C)(C)C)C4)[C@@H]2O)=CC(O[Si](C)(C)C)=C1O	5300.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #220	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5290.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #221	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	5323.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #222	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5391.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #223	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O[Si](C)(C)C)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)O2	5374.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #224	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O[Si](C)(C)C)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5337.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #225	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O[Si](C)(C)C)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)O2	5326.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #226	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O[Si](C)(C)C)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5269.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #227	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)O2	5339.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #228	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O2	5333.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #229	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O[Si](C)(C)C)=C3[C@@H](C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O)=C1O	5354.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #23	C[Si](C)(C)OC1=CC(O)=C([C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)[C@H]2O)C2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC=C(O)C(O)=C1)O2	5298.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #230	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C([C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)C2=C1C[C@@H](O)[C@@H](C1=CC=C(O)C(O)=C1)O2	5324.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #231	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O[Si](C)(C)C)=C3[C@@H](C3=C(O[Si](C)(C)C)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O[Si](C)(C)C)=C1O	5374.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #232	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O[Si](C)(C)C)=C3[C@@H](C3=C(O[Si](C)(C)C)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O)=C1O[Si](C)(C)C	5364.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #233	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O[Si](C)(C)C)=C3[C@@H](C3=C(O)C=C(O[Si](C)(C)C)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O[Si](C)(C)C)=C1O	5325.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #234	C[Si](C)(C)OC1=CC(O)=C([C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)[C@H]2O)C2=C1C[C@@H](O)[C@@H](C1=CC=C(O)C(O)=C1)O2	5325.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #235	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O[Si](C)(C)C)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	5375.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #236	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5347.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #237	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5331.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #238	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5267.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #239	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5327.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #24	C[Si](C)(C)OC1=CC(O)=C([C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O[Si](C)(C)C)C2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC=C(O)C(O)=C1)O2	5261.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #240	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5268.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #241	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5315.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #242	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	5256.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #243	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O[Si](C)(C)C)=C1O	5295.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #244	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C([C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)[C@H]2O)C2=C1C[C@@H](O)[C@@H](C1=CC=C(O)C(O)=C1)O2	5293.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #245	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O[Si](C)(C)C)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	5355.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #246	C[Si](C)(C)OC1=CC(O)=C([C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)[C@H]2O)C2=C1C[C@@H](O)[C@@H](C1=CC=C(O)C(O)=C1)O2	5312.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #25	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)C=C1O	5159.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #26	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)=CC=C1O	5164.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #27	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)C=C1O	5321.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #28	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)=CC=C1O	5317.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #29	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O[Si](C)(C)C	5355.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #3	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O[Si](C)(C)C)C4)[C@@H]2O)=CC(O)=C1O	5339.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #30	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O[Si](C)(C)C)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5445.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #31	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O	5416.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #32	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)=CC=C1O	5415.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #33	C[Si](C)(C)OC1=CC(O)=CC2=C1[C@@H](C1=C(O[Si](C)(C)C)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C3)[C@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5439.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #34	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O[Si](C)(C)C)=C3[C@@H](C3=C(O[Si](C)(C)C)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O[Si](C)(C)C)C4)[C@@H]2O)=CC(O)=C1O	5405.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #35	C[Si](C)(C)OC1=CC(O)=CC2=C1[C@@H](C1=C(O[Si](C)(C)C)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C3)[C@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5365.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #36	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C2	5370.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #37	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C2	5325.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #38	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C2	5418.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #39	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O[Si](C)(C)C)C2	5371.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #4	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C([C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)C2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC=C(O)C(O)=C1)O2	5295.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #40	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O[Si](C)(C)C)C2	5369.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #41	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O	5306.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #42	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)=CC=C1O	5304.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #43	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O[Si](C)(C)C)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O[Si](C)(C)C)C4)[C@@H]2O[Si](C)(C)C)=CC(O)=C1O	5358.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #44	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O[Si](C)(C)C)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O[Si](C)(C)C)C4)[C@@H]2O)=CC(O[Si](C)(C)C)=C1O	5353.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #45	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O[Si](C)(C)C)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O[Si](C)(C)C)C4)[C@@H]2O)=CC(O)=C1O[Si](C)(C)C	5343.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #46	C[Si](C)(C)OC1=CC(O)=C2C[C@@H](O[Si](C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)OC2=C1[C@@H]1C2=C(O)C=C(O)C=C2O[C@H](C2=CC(O)=C(O[Si](C)(C)C)C(O)=C2)[C@H]1O[Si](C)(C)C	5313.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #47	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)C=C1O	5233.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #48	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)=CC=C1O	5232.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #49	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)C=C1O	5369.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #5	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C([C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)C2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC=C(O)C(O)=C1)O2	5386.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #50	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)=CC=C1O	5365.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #51	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O[Si](C)(C)C	5401.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #52	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O[Si](C)(C)C)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5374.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #53	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O[Si](C)(C)C)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5376.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #54	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C3)[C@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5414.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #55	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)O2	5373.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #56	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C3)[C@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5325.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #57	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O	5329.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #58	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)C=C1O	5261.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #59	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)C=C1O	5387.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #6	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O	5346.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #60	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O[Si](C)(C)C	5426.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #61	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)=CC=C1O	5328.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #62	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)=CC=C1O	5261.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #63	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)=CC=C1O	5386.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #64	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O[Si](C)(C)C)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O[Si](C)(C)C)C4)[C@@H]2O[Si](C)(C)C)=CC(O)=C1O	5375.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #65	C[Si](C)(C)OC1=CC(O)=CC2=C1[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C3)[C@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5330.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #66	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O[Si](C)(C)C)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O[Si](C)(C)C)C4)[C@@H]2O)=CC(O[Si](C)(C)C)=C1O	5370.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #67	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O[Si](C)(C)C)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O[Si](C)(C)C)C4)[C@@H]2O)=CC(O)=C1O[Si](C)(C)C	5356.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #68	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C2	5328.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #69	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C2	5324.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #7	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)=CC=C1O	5346.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #70	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C2	5333.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #71	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O[Si](C)(C)C)C2	5258.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #72	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O[Si](C)(C)C)C2	5260.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #73	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C2	5284.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #74	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O[Si](C)(C)C)C2	5180.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #75	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O[Si](C)(C)C)C2	5184.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #76	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O[Si](C)(C)C)C2	5341.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #77	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O[Si](C)(C)C)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C)=C1)[C@H](O[Si](C)(C)C)C2	5339.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #78	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[C@H](O[Si](C)(C)C)C2	5386.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #79	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O	5249.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #8	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O[Si](C)(C)C)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5400.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #80	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O	5245.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #81	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O[Si](C)(C)C)C=C1O	5262.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #82	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O[Si](C)(C)C	5312.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #83	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)=CC=C1O	5247.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #84	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)[C@H]2O)=CC=C1O	5243.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #85	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O[Si](C)(C)C)=CC=C1O	5260.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #86	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O[Si](C)(C)C)C4)[C@@H]2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O	5322.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #87	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O[Si](C)(C)C)C4)[C@@H]2O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C	5311.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #88	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O[Si](C)(C)C)C4)[C@@H]2O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	5359.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #89	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O[Si](C)(C)C)C=C1O	5185.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #9	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O[Si](C)(C)C)=C3[C@@H](C3=C(O)C=C(O[Si](C)(C)C)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O[Si](C)(C)C)C4)[C@@H]2O)=CC(O)=C1O	5357.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #90	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)C=C1O[Si](C)(C)C	5254.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #91	C[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O[Si](C)(C)C)=CC=C1O	5182.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #92	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	5371.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #93	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O[Si](C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O	5363.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #94	C[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O)C2	5311.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #95	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)[C@H]2O)C=C1O	5243.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #96	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)[C@H]2O)C=C1O	5158.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #97	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C)C=C1O	5306.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #98	C[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O[Si](C)(C)C	5349.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,4TMS,isomer #99	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)[C@@H](C1=C(O)C=C(O[Si](C)(C)C)C3=C1O[C@H](C1=CC=C(O[Si](C)(C)C)C(O)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	5321.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1CC2=C(O)C=C(O)C([C@@H]3C4=C(O)C=C(O)C=C4O[C@H](C4=CC(O)=C(O)C(O)=C4)[C@H]3O)=C2O[C@@H]1C1=CC=C(O)C(O)=C1	6063.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,1TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1=CC(O)=C([C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C2=C1C[C@@H](O)[C@@H](C1=CC=C(O)C(O)=C1)O2	6036.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O	6115.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)=CC=C1O	6096.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](C2=C(O)C=C(O)C3=C2O[C@H](C2=CC=C(O)C(O)=C2)[C@H](O)C3)C2=C(O)C=C(O)C=C2O[C@@H]1C1=CC(O)=C(O)C(O)=C1	6056.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	6082.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	6070.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O)=C1O	6071.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,1TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)C=C1O	6093.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,1TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)OC2=C1[C@@H]1C2=C(O)C=C(O)C=C2O[C@H](C2=CC(O)=C(O)C(O)=C2)[C@H]1O	6051.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC(O)=C([C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C2=C1C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C1=CC=C(O)C(O)=C1)O2	6144.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C(C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O	6122.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C(C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O	6169.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O	6206.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)[C@H](O)C2	6162.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)[C@H]2O)C=C1O	6151.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)[C@H]2O)C=C1O	6145.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C(C)(C)C)C=C1O	6158.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O[Si](C)(C)C(C)(C)C	6159.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O[Si](C)(C)C(C)(C)C)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)=CC=C1O	6096.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O[Si](C)(C)C(C)(C)C)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)=CC=C1O	6146.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C3=CC=C(O)C(O)=C3)OC2=C1[C@@H]1C2=C(O)C=C(O)C=C2O[C@H](C2=CC(O)=C(O)C(O)=C2)[C@H]1O	6171.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)=CC=C1O	6183.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)[C@H](O)C2	6140.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)[C@H]2O)=CC=C1O	6123.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)[C@H]2O)=CC=C1O	6108.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C(C)(C)C)=CC=C1O	6139.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)OC2=C1[C@@H]1C2=C(O)C=C(O)C=C2O[C@H](C2=CC(O)=C(O)C(O)=C2)[C@H]1O[Si](C)(C)C(C)(C)C	6146.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC1=CC(O)=C([C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O[Si](C)(C)C(C)(C)C)C2=C1C[C@@H](O)[C@@H](C1=CC=C(O)C(O)=C1)O2	6112.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	6188.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	6163.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O[Si](C)(C)C(C)(C)C)=CC(O)=C1O	6128.8	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C(C)(C)C)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	6205.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O[Si](C)(C)C(C)(C)C)C=C1O	6121.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1)[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	6173.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1[C@@H](C1=C(O[Si](C)(C)C(C)(C)C)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	6189.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC1=CC(O)=C([C@@H]2C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C2=C1C[C@@H](O)[C@@H](C1=CC=C(O)C(O)=C1)O2	6152.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O)=C1O	6171.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1[C@@H](C1=C(O)C=C(O)C3=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C3)[C@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)O2	6169.2	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #36	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	6136.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #37	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	6126.7	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #38	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O[Si](C)(C)C(C)(C)C)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	6161.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #39	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O[Si](C)(C)C(C)(C)C)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O)C2	6117.0	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)O[C@H](C1=CC(O)=C(O)C(O)=C1)[C@@H](O)[C@@H]2C1=C(O)C=C(O)C2=C1O[C@H](C1=CC=C(O)C(O)=C1)[C@H](O[Si](C)(C)C(C)(C)C)C2	6178.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #40	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O)=C1O	6136.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #41	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O[Si](C)(C)C(C)(C)C)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O)=C1O	6096.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #42	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O[Si](C)(C)C(C)(C)C)=C1O	6145.4	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #43	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O)C4)[C@@H]2O)=CC(O)=C1O[Si](C)(C)C(C)(C)C	6124.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #44	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C[C@@H](O)[C@@H](C3=CC=C(O)C(O)=C3)OC2=C1[C@@H]1C2=C(O)C=C(O)C=C2O[C@H](C2=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C2)[C@H]1O	6137.3	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #45	CC(C)(C)[Si](C)(C)OC1=CC(O)=C([C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)[C@H]2O)C2=C1C[C@@H](O)[C@@H](C1=CC=C(O)C(O)=C1)O2	6087.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #46	CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C([C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C2=C1C[C@@H](O)[C@@H](C1=CC=C(O)C(O)=C1)O2	6107.9	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O[Si](C)(C)C(C)(C)C)C4)[C@@H]2O)=CC(O)=C1O	6152.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O)=CC(O)=C3[C@@H](C3=C(O)C=C(O)C4=C3O[C@H](C3=CC=C(O)C(O)=C3)[C@H](O[Si](C)(C)C(C)(C)C)C4)[C@@H]2O)C=C1O	6156.6	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](C2=C(O)C=C(O)C3=C2O[C@H](C2=CC=C(O)C(O)=C2)[C@H](O[Si](C)(C)C(C)(C)C)C3)C2=C(O)C=C(O)C=C2O[C@@H]1C1=CC(O)=C(O)C(O)=C1	6160.1	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C(C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)C=C1O	6189.5	Semi standard non polar	33892256
Gallocatechin-(4alpha->8)-epicatechin,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=C(C[C@H]2O[Si](C)(C)C(C)(C)C)C(O)=CC(O)=C3[C@@H]2C3=C(O)C=C(O)C=C3O[C@H](C3=CC(O)=C(O)C(O)=C3)[C@H]2O)=CC=C1O	6172.8	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 - Gallocatechin-(4alpha->8)-epicatechin GC-MS (Non-derivatized) - 70eV, Positive	splash10-004r-0901360000-40829b1f34600bfa2d72	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin GC-MS (1 TMS) - 70eV, Positive	splash10-009i-9600124000-8e5beff5844df6ea8ea8	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin GC-MS ("Gallocatechin-(4alpha->8)-epicatechin,1TMS,#1" TMS) - 70eV, Positive	Not Available	2021-10-14	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin GC-MS (TMS_1_8) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin GC-MS (TMS_1_9) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin GC-MS (TMS_1_10) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin GC-MS (TMS_2_13) - 70eV, Positive	Not Available	2021-10-15	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 - Gallocatechin-(4alpha->8)-epicatechin 10V, Positive-QTOF	splash10-004j-0210980000-c1f8ae51d3afab5b7378	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin 20V, Positive-QTOF	splash10-0a4i-0645920000-cf118f50982fe9ad7637	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin 40V, Positive-QTOF	splash10-002o-0690110000-7d7bf8ff0cdba3de3507	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin 10V, Negative-QTOF	splash10-0006-0100290000-8266b1bc83f1c5cfcb30	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin 20V, Negative-QTOF	splash10-0udr-0921220000-9b2462cc181767bb7a8a	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin 40V, Negative-QTOF	splash10-004i-0901000000-15bcb361ba549a2d50b1	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin 10V, Positive-QTOF	splash10-0002-0000290000-4f508ef9951b3a759cd3	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin 20V, Positive-QTOF	splash10-0002-0100690000-82ac1d6b9c4fe7a8559f	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin 40V, Positive-QTOF	splash10-0109-1902660000-20d6e6cf6974a4104bc1	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin 10V, Negative-QTOF	splash10-0006-0000090000-7836921a5691dc82bc76	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin 20V, Negative-QTOF	splash10-00mo-0100590000-69250ca138f2bcfc3dc3	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gallocatechin-(4alpha->8)-epicatechin 40V, Negative-QTOF	splash10-002p-0310590000-90e2e4a266c6047ab006	2021-09-22	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

FDB016773

KNApSAcK ID

C00009112

Chemspider ID

9702000

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11527214

PDB ID

Not Available

ChEBI ID

75666

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 Gallocatechin-(4alpha->8)-epicatechin (HMDB0037653)

MOL for HMDB0037653 (Gallocatechin-(4alpha->8)-epicatechin)

3D MOL for HMDB0037653 (Gallocatechin-(4alpha->8)-epicatechin)

3D SDF for HMDB0037653 (Gallocatechin-(4alpha->8)-epicatechin)

3D-SDF for HMDB0037653 (Gallocatechin-(4alpha->8)-epicatechin)

PDB for HMDB0037653 (Gallocatechin-(4alpha->8)-epicatechin)

3D PDB for HMDB0037653 (Gallocatechin-(4alpha->8)-epicatechin)

SMILES for HMDB0037653 (Gallocatechin-(4alpha->8)-epicatechin)

INCHI for HMDB0037653 (Gallocatechin-(4alpha->8)-epicatechin)

Structure for HMDB0037653 (Gallocatechin-(4alpha->8)-epicatechin)

3D Structure for HMDB0037653 (Gallocatechin-(4alpha->8)-epicatechin)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra