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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 00:46:15 UTC

Update Date

2022-03-07 02:56:10 UTC

HMDB ID

HMDB0039347

Secondary Accession Numbers

HMDB39347

Metabolite Identification

Common Name

2'-Hydroxydaidzein 4',7-diglucoside

Description

2'-Hydroxydaidzein 4',7-diglucoside belongs to the class of organic compounds known as isoflavonoid o-glycosides. These are o-glycosylated derivatives of isoflavonoids, which are natural products derived from 3-phenylchromen-4-one. 2'-Hydroxydaidzein 4',7-diglucoside has been detected, but not quantified in, adzuki beans (Vigna angularis) and pulses. This could make 2'-hydroxydaidzein 4',7-diglucoside a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on 2'-Hydroxydaidzein 4',7-diglucoside.

Structure

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

  Mrv0541 05061311022D          

 42 46  0  0  0  0            999 V2000
    5.0013    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  2  0  0  0  0
  4  2  2  0  0  0  0
 10  1  1  0  0  0  0
 10  5  2  0  0  0  0
 11  2  1  0  0  0  0
 11  6  2  0  0  0  0
 12  3  1  0  0  0  0
 13  4  1  0  0  0  0
 14  9  2  0  0  0  0
 14 12  1  0  0  0  0
 15  5  1  0  0  0  0
 15 12  2  0  0  0  0
 16  6  1  0  0  0  0
 16 13  2  0  0  0  0
 17  7  1  0  0  0  0
 18  8  1  0  0  0  0
 19 13  1  0  0  0  0
 19 14  1  0  0  0  0
 20 17  1  0  0  0  0
 21 18  1  0  0  0  0
 22 20  1  0  0  0  0
 23 21  1  0  0  0  0
 24 22  1  0  0  0  0
 25 23  1  0  0  0  0
 26 24  1  0  0  0  0
 27 25  1  0  0  0  0
 28  7  1  0  0  0  0
 29  8  1  0  0  0  0
 30 15  1  0  0  0  0
 31 19  2  0  0  0  0
 32 20  1  0  0  0  0
 33 21  1  0  0  0  0
 34 22  1  0  0  0  0
 35 23  1  0  0  0  0
 36 24  1  0  0  0  0
 37 25  1  0  0  0  0
 38  9  1  0  0  0  0
 38 16  1  0  0  0  0
 39 10  1  0  0  0  0
 39 26  1  0  0  0  0
 40 11  1  0  0  0  0
 40 27  1  0  0  0  0
 41 17  1  0  0  0  0
 41 26  1  0  0  0  0
 42 18  1  0  0  0  0
 42 27  1  0  0  0  0
M  END

HMDB0039347
     RDKit          3D
2'-Hydroxydaidzein 4',7-diglucoside
 72 76  0  0  0  0  0  0  0  0999 V2000
    0.3405    0.8500   -1.2727 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5294   -0.1235   -0.4978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5652   -0.8555   -0.0615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8750   -0.4696   -0.5195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1710   -0.2802   -1.8634 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4335    0.0603   -2.2866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4958    0.2343   -1.3695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7290    0.5789   -1.8773 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8574    0.7028   -1.0481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8742    2.0483   -0.6546 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0296    2.4738   -0.0716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3770    1.8184    1.2450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5591    0.4598    1.1739 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1798    2.3274   -1.0613 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3201    2.8686   -0.5099 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3441    0.9150   -1.5169 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0749    0.9866   -2.7336 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0447    0.2665   -1.8308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2164   -1.1210   -1.5967 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1930    0.0459   -0.0509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8981   -0.3014    0.3730 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7306   -0.4531    1.7338 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2866   -1.9075    0.7821 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9435   -2.1966    1.1519 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9894   -1.5319    0.7637 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2701   -1.8267    1.1471 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3779   -1.0854    0.7093 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6251   -1.4641    1.1603 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8588   -0.8909    0.8239 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7784   -1.8663    0.5830 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9989   -1.7381    1.1982 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9904   -2.6841    0.5690 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1790   -2.4767   -0.7892 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.5018   -0.3262    0.9649 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8334   -0.2349    1.2848 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6331    0.5889    1.8034 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6965    1.8669    1.3007 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2402    0.0429    1.9611 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3508    1.1115    1.9082 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1583   -0.0348   -0.1304 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8795    0.2789   -0.5282 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8075   -0.4616   -0.0852 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3923   -0.4010   -2.6084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6623    0.2096   -3.3389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6883    0.0757   -0.1325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9230    3.5600    0.1196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5704    2.0734    1.9682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3210    2.2854    1.5913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3567    0.2086    1.6891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8814    2.9398   -1.9589 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0383    3.6355    0.0627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9906    0.2978   -0.8576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8675    1.8142   -3.2145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8140    0.3266   -2.9397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4000   -1.6209   -2.4113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9637    0.1700    0.7125 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.4302   -2.6743    1.8209 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7147   -0.2730   -0.1032 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9599   -2.0047    2.2772 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7578   -3.7396    0.8328 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9978   -2.4849    1.0439 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5503   -2.9965   -1.3597 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3140   -0.0955   -0.1114 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.3825   -0.1013    0.4612 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0869    0.6020    2.8253 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3881    1.9798    0.5830 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0931   -0.4702    2.9263 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7630    1.9960    2.0602 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9813    0.5723   -0.4974 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6799    1.1125   -1.1968 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
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 18 19  1  0
  7 20  1  0
 20 21  2  0
 21 22  1  0
  3 23  2  0
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 21  4  1  0
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 18  9  1  0
 38 29  1  0
  5 43  1  0
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 34 65  1  0
 35 66  1  0
 36 67  1  0
 37 68  1  0
 38 69  1  0
 39 70  1  0
 40 71  1  0
 41 72  1  0
M  END

  Mrv0541 05061311022D          

 42 46  0  0  0  0            999 V2000
    5.0013    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.0013    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  2  0  0  0  0
  4  2  2  0  0  0  0
 10  1  1  0  0  0  0
 10  5  2  0  0  0  0
 11  2  1  0  0  0  0
 11  6  2  0  0  0  0
 12  3  1  0  0  0  0
 13  4  1  0  0  0  0
 14  9  2  0  0  0  0
 14 12  1  0  0  0  0
 15  5  1  0  0  0  0
 15 12  2  0  0  0  0
 16  6  1  0  0  0  0
 16 13  2  0  0  0  0
 17  7  1  0  0  0  0
 18  8  1  0  0  0  0
 19 13  1  0  0  0  0
 19 14  1  0  0  0  0
 20 17  1  0  0  0  0
 21 18  1  0  0  0  0
 22 20  1  0  0  0  0
 23 21  1  0  0  0  0
 24 22  1  0  0  0  0
 25 23  1  0  0  0  0
 26 24  1  0  0  0  0
 27 25  1  0  0  0  0
 28  7  1  0  0  0  0
 29  8  1  0  0  0  0
 30 15  1  0  0  0  0
 31 19  2  0  0  0  0
 32 20  1  0  0  0  0
 33 21  1  0  0  0  0
 34 22  1  0  0  0  0
 35 23  1  0  0  0  0
 36 24  1  0  0  0  0
 37 25  1  0  0  0  0
 38  9  1  0  0  0  0
 38 16  1  0  0  0  0
 39 10  1  0  0  0  0
 39 26  1  0  0  0  0
 40 11  1  0  0  0  0
 40 27  1  0  0  0  0
 41 17  1  0  0  0  0
 41 26  1  0  0  0  0
 42 18  1  0  0  0  0
 42 27  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0039347

> <DATABASE_NAME>
hmdb

> <SMILES>
OCC1OC(OC2=CC(O)=C(C=C2)C2=COC3=C(C=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C2=O)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C27H30O15/c28-7-17-20(32)22(34)24(36)26(41-17)39-10-1-3-12(15(30)5-10)14-9-38-16-6-11(2-4-13(16)19(14)31)40-27-25(37)23(35)21(33)18(8-29)42-27/h1-6,9,17-18,20-30,32-37H,7-8H2

> <INCHI_KEY>
DNPGZHRLHFUCNR-UHFFFAOYSA-N

> <FORMULA>
C27H30O15

> <MOLECULAR_WEIGHT>
594.5181

> <EXACT_MASS>
594.15847029

> <JCHEM_ACCEPTOR_COUNT>
15

> <JCHEM_AVERAGE_POLARIZABILITY>
57.974155818064645

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-(2-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H-chromen-4-one

> <ALOGPS_LOGP>
-0.51

> <JCHEM_LOGP>
-2.1092637970000006

> <ALOGPS_LOGS>
-2.52

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.900140693915608

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.52981811911125

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981092343722586

> <JCHEM_POLAR_SURFACE_AREA>
245.2899999999999

> <JCHEM_REFRACTIVITY>
135.97169999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.80e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-(2-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0039347
     RDKit          3D
2'-Hydroxydaidzein 4',7-diglucoside
 72 76  0  0  0  0  0  0  0  0999 V2000
    0.3405    0.8500   -1.2727 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5294   -0.1235   -0.4978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5652   -0.8555   -0.0615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8750   -0.4696   -0.5195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1710   -0.2802   -1.8634 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4335    0.0603   -2.2866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4958    0.2343   -1.3695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7290    0.5789   -1.8773 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8574    0.7028   -1.0481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8742    2.0483   -0.6546 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0296    2.4738   -0.0716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3770    1.8184    1.2450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5591    0.4598    1.1739 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1798    2.3274   -1.0613 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3201    2.8686   -0.5099 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3441    0.9150   -1.5169 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0749    0.9866   -2.7336 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0447    0.2665   -1.8308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2164   -1.1210   -1.5967 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1930    0.0459   -0.0509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8981   -0.3014    0.3730 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7306   -0.4531    1.7338 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2866   -1.9075    0.7821 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9435   -2.1966    1.1519 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9894   -1.5319    0.7637 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2701   -1.8267    1.1471 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3779   -1.0854    0.7093 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6251   -1.4641    1.1603 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8588   -0.8909    0.8239 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7784   -1.8663    0.5830 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9989   -1.7381    1.1982 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9904   -2.6841    0.5690 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1790   -2.4767   -0.7892 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.5018   -0.3262    0.9649 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8334   -0.2349    1.2848 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6331    0.5889    1.8034 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6965    1.8669    1.3007 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2402    0.0429    1.9611 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3508    1.1115    1.9082 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1583   -0.0348   -0.1304 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8795    0.2789   -0.5282 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8075   -0.4616   -0.0852 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3923   -0.4010   -2.6084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6623    0.2096   -3.3389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6883    0.0757   -0.1325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9230    3.5600    0.1196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5704    2.0734    1.9682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3210    2.2854    1.5913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3567    0.2086    1.6891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8814    2.9398   -1.9589 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0383    3.6355    0.0627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9906    0.2978   -0.8576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8675    1.8142   -3.2145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8140    0.3266   -2.9397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4000   -1.6209   -2.4113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9637    0.1700    0.7125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8880   -0.6658    2.2205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0691   -2.5273    1.1619 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4302   -2.6743    1.8209 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7147   -0.2730   -0.1032 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9599   -2.0047    2.2772 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7578   -3.7396    0.8328 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9978   -2.4849    1.0439 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5503   -2.9965   -1.3597 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3140   -0.0955   -0.1114 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.3825   -0.1013    0.4612 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0869    0.6020    2.8253 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3881    1.9798    0.5830 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0931   -0.4702    2.9263 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7630    1.9960    2.0602 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9813    0.5723   -0.4974 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6799    1.1125   -1.1968 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 11 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
  7 20  1  0
 20 21  2  0
 21 22  1  0
  3 23  2  0
 23 24  1  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 31 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  1  0
 36 38  1  0
 38 39  1  0
 27 40  2  0
 40 41  1  0
 41 42  2  0
 42  2  1  0
 21  4  1  0
 42 25  1  0
 18  9  1  0
 38 29  1  0
  5 43  1  0
  6 44  1  0
  9 45  1  0
 11 46  1  0
 12 47  1  0
 12 48  1  0
 13 49  1  0
 14 50  1  0
 15 51  1  0
 16 52  1  0
 17 53  1  0
 18 54  1  0
 19 55  1  0
 20 56  1  0
 22 57  1  0
 23 58  1  0
 26 59  1  0
 29 60  1  0
 31 61  1  0
 32 62  1  0
 32 63  1  0
 33 64  1  0
 34 65  1  0
 35 66  1  0
 36 67  1  0
 37 68  1  0
 38 69  1  0
 39 70  1  0
 40 71  1  0
 41 72  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       9.336   6.930   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.002   6.160   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.669   4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      14.671   2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.669   6.160   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.336   3.850   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      14.671   3.850   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      16.004   4.620   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      16.004   6.160   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      14.671   6.930   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      13.337   6.160   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      16.004   1.540   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      -2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       9.336   2.310   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       5.335   6.160   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      17.338   3.850   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      17.338   6.930   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      14.671   8.470   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       2.667   0.000   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0       5.335   1.540   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      12.003   6.930   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       0.000   1.540   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0      13.337   4.620   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
CONECT    1    3   10                                                       
CONECT    2    4   11                                                       
CONECT    3    1   12                                                       
CONECT    4    2   13                                                       
CONECT    5   10   15                                                       
CONECT    6   11   16                                                       
CONECT    7   17   28                                                       
CONECT    8   18   29                                                       
CONECT    9   14   38                                                       
CONECT   10    1    5   39                                                  
CONECT   11    2    6   40                                                  
CONECT   12    3   14   15                                                  
CONECT   13    4   16   19                                                  
CONECT   14    9   12   19                                                  
CONECT   15    5   12   30                                                  
CONECT   16    6   13   38                                                  
CONECT   17    7   20   41                                                  
CONECT   18    8   21   42                                                  
CONECT   19   13   14   31                                                  
CONECT   20   17   22   32                                                  
CONECT   21   18   23   33                                                  
CONECT   22   20   24   34                                                  
CONECT   23   21   25   35                                                  
CONECT   24   22   26   36                                                  
CONECT   25   23   27   37                                                  
CONECT   26   24   39   41                                                  
CONECT   27   25   40   42                                                  
CONECT   28    7                                                            
CONECT   29    8                                                            
CONECT   30   15                                                            
CONECT   31   19                                                            
CONECT   32   20                                                            
CONECT   33   21                                                            
CONECT   34   22                                                            
CONECT   35   23                                                            
CONECT   36   24                                                            
CONECT   37   25                                                            
CONECT   38    9   16                                                       
CONECT   39   10   26                                                       
CONECT   40   11   27                                                       
CONECT   41   17   26                                                       
CONECT   42   18   27                                                       
MASTER        0    0    0    0    0    0    0    0   42    0   92    0
END

COMPND    HMDB0039347
HETATM    1  O1  UNL     1       0.340   0.850  -1.273  1.00  0.00           O  
HETATM    2  C1  UNL     1       0.529  -0.123  -0.498  1.00  0.00           C  
HETATM    3  C2  UNL     1      -0.565  -0.856  -0.061  1.00  0.00           C  
HETATM    4  C3  UNL     1      -1.875  -0.470  -0.519  1.00  0.00           C  
HETATM    5  C4  UNL     1      -2.171  -0.280  -1.863  1.00  0.00           C  
HETATM    6  C5  UNL     1      -3.433   0.060  -2.287  1.00  0.00           C  
HETATM    7  C6  UNL     1      -4.496   0.234  -1.369  1.00  0.00           C  
HETATM    8  O2  UNL     1      -5.729   0.579  -1.877  1.00  0.00           O  
HETATM    9  C7  UNL     1      -6.857   0.703  -1.048  1.00  0.00           C  
HETATM   10  O3  UNL     1      -6.874   2.048  -0.655  1.00  0.00           O  
HETATM   11  C8  UNL     1      -8.030   2.474  -0.072  1.00  0.00           C  
HETATM   12  C9  UNL     1      -8.377   1.818   1.245  1.00  0.00           C  
HETATM   13  O4  UNL     1      -8.559   0.460   1.174  1.00  0.00           O  
HETATM   14  C10 UNL     1      -9.180   2.327  -1.061  1.00  0.00           C  
HETATM   15  O5  UNL     1     -10.320   2.869  -0.510  1.00  0.00           O  
HETATM   16  C11 UNL     1      -9.344   0.915  -1.517  1.00  0.00           C  
HETATM   17  O6  UNL     1     -10.075   0.987  -2.734  1.00  0.00           O  
HETATM   18  C12 UNL     1      -8.045   0.267  -1.831  1.00  0.00           C  
HETATM   19  O7  UNL     1      -8.216  -1.121  -1.597  1.00  0.00           O  
HETATM   20  C13 UNL     1      -4.193   0.046  -0.051  1.00  0.00           C  
HETATM   21  C14 UNL     1      -2.898  -0.301   0.373  1.00  0.00           C  
HETATM   22  O8  UNL     1      -2.731  -0.453   1.734  1.00  0.00           O  
HETATM   23  C15 UNL     1      -0.287  -1.907   0.782  1.00  0.00           C  
HETATM   24  O9  UNL     1       0.943  -2.197   1.152  1.00  0.00           O  
HETATM   25  C16 UNL     1       1.989  -1.532   0.764  1.00  0.00           C  
HETATM   26  C17 UNL     1       3.270  -1.827   1.147  1.00  0.00           C  
HETATM   27  C18 UNL     1       4.378  -1.085   0.709  1.00  0.00           C  
HETATM   28  O10 UNL     1       5.625  -1.464   1.160  1.00  0.00           O  
HETATM   29  C19 UNL     1       6.859  -0.891   0.824  1.00  0.00           C  
HETATM   30  O11 UNL     1       7.778  -1.866   0.583  1.00  0.00           O  
HETATM   31  C20 UNL     1       8.999  -1.738   1.198  1.00  0.00           C  
HETATM   32  C21 UNL     1       9.990  -2.684   0.569  1.00  0.00           C  
HETATM   33  O12 UNL     1      10.179  -2.477  -0.789  1.00  0.00           O  
HETATM   34  C22 UNL     1       9.502  -0.326   0.965  1.00  0.00           C  
HETATM   35  O13 UNL     1      10.833  -0.235   1.285  1.00  0.00           O  
HETATM   36  C23 UNL     1       8.633   0.589   1.803  1.00  0.00           C  
HETATM   37  O14 UNL     1       8.696   1.867   1.301  1.00  0.00           O  
HETATM   38  C24 UNL     1       7.240   0.043   1.961  1.00  0.00           C  
HETATM   39  O15 UNL     1       6.351   1.111   1.908  1.00  0.00           O  
HETATM   40  C25 UNL     1       4.158  -0.035  -0.130  1.00  0.00           C  
HETATM   41  C26 UNL     1       2.880   0.279  -0.528  1.00  0.00           C  
HETATM   42  C27 UNL     1       1.808  -0.462  -0.085  1.00  0.00           C  
HETATM   43  H1  UNL     1      -1.392  -0.401  -2.608  1.00  0.00           H  
HETATM   44  H2  UNL     1      -3.662   0.210  -3.339  1.00  0.00           H  
HETATM   45  H3  UNL     1      -6.688   0.076  -0.133  1.00  0.00           H  
HETATM   46  H4  UNL     1      -7.923   3.560   0.120  1.00  0.00           H  
HETATM   47  H5  UNL     1      -7.570   2.073   1.968  1.00  0.00           H  
HETATM   48  H6  UNL     1      -9.321   2.285   1.591  1.00  0.00           H  
HETATM   49  H7  UNL     1      -9.357   0.209   1.689  1.00  0.00           H  
HETATM   50  H8  UNL     1      -8.881   2.940  -1.959  1.00  0.00           H  
HETATM   51  H9  UNL     1     -10.038   3.636   0.063  1.00  0.00           H  
HETATM   52  H10 UNL     1      -9.991   0.298  -0.858  1.00  0.00           H  
HETATM   53  H11 UNL     1      -9.868   1.814  -3.215  1.00  0.00           H  
HETATM   54  H12 UNL     1      -7.814   0.327  -2.940  1.00  0.00           H  
HETATM   55  H13 UNL     1      -8.400  -1.621  -2.411  1.00  0.00           H  
HETATM   56  H14 UNL     1      -4.964   0.170   0.712  1.00  0.00           H  
HETATM   57  H15 UNL     1      -1.888  -0.666   2.221  1.00  0.00           H  
HETATM   58  H16 UNL     1      -1.069  -2.527   1.162  1.00  0.00           H  
HETATM   59  H17 UNL     1       3.430  -2.674   1.821  1.00  0.00           H  
HETATM   60  H18 UNL     1       6.715  -0.273  -0.103  1.00  0.00           H  
HETATM   61  H19 UNL     1       8.960  -2.005   2.277  1.00  0.00           H  
HETATM   62  H20 UNL     1       9.758  -3.740   0.833  1.00  0.00           H  
HETATM   63  H21 UNL     1      10.998  -2.485   1.044  1.00  0.00           H  
HETATM   64  H22 UNL     1       9.550  -2.996  -1.360  1.00  0.00           H  
HETATM   65  H23 UNL     1       9.314  -0.095  -0.111  1.00  0.00           H  
HETATM   66  H24 UNL     1      11.383  -0.101   0.461  1.00  0.00           H  
HETATM   67  H25 UNL     1       9.087   0.602   2.825  1.00  0.00           H  
HETATM   68  H26 UNL     1       9.388   1.980   0.583  1.00  0.00           H  
HETATM   69  H27 UNL     1       7.093  -0.470   2.926  1.00  0.00           H  
HETATM   70  H28 UNL     1       6.763   1.996   2.060  1.00  0.00           H  
HETATM   71  H29 UNL     1       4.981   0.572  -0.497  1.00  0.00           H  
HETATM   72  H30 UNL     1       2.680   1.112  -1.197  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   42
CONECT    3    4   23   23
CONECT    4    5    5   21
CONECT    5    6   43
CONECT    6    7    7   44
CONECT    7    8   20
CONECT    8    9
CONECT    9   10   18   45
CONECT   10   11
CONECT   11   12   14   46
CONECT   12   13   47   48
CONECT   13   49
CONECT   14   15   16   50
CONECT   15   51
CONECT   16   17   18   52
CONECT   17   53
CONECT   18   19   54
CONECT   19   55
CONECT   20   21   21   56
CONECT   21   22
CONECT   22   57
CONECT   23   24   58
CONECT   24   25
CONECT   25   26   26   42
CONECT   26   27   59
CONECT   27   28   40   40
CONECT   28   29
CONECT   29   30   38   60
CONECT   30   31
CONECT   31   32   34   61
CONECT   32   33   62   63
CONECT   33   64
CONECT   34   35   36   65
CONECT   35   66
CONECT   36   37   38   67
CONECT   37   68
CONECT   38   39   69
CONECT   39   70
CONECT   40   41   71
CONECT   41   42   42   72
END

HMDB0039347
     RDKit          3D
2'-Hydroxydaidzein 4',7-diglucoside
 72 76  0  0  0  0  0  0  0  0999 V2000
    0.3405    0.8500   -1.2727 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5294   -0.1235   -0.4978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5652   -0.8555   -0.0615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8750   -0.4696   -0.5195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1710   -0.2802   -1.8634 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4335    0.0603   -2.2866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4958    0.2343   -1.3695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7290    0.5789   -1.8773 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8574    0.7028   -1.0481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8742    2.0483   -0.6546 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0296    2.4738   -0.0716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3770    1.8184    1.2450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5591    0.4598    1.1739 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1798    2.3274   -1.0613 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3201    2.8686   -0.5099 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3441    0.9150   -1.5169 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0749    0.9866   -2.7336 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0447    0.2665   -1.8308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2164   -1.1210   -1.5967 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1930    0.0459   -0.0509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8981   -0.3014    0.3730 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7306   -0.4531    1.7338 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2866   -1.9075    0.7821 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9435   -2.1966    1.1519 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9894   -1.5319    0.7637 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2701   -1.8267    1.1471 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3779   -1.0854    0.7093 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6251   -1.4641    1.1603 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8588   -0.8909    0.8239 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7784   -1.8663    0.5830 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9989   -1.7381    1.1982 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9904   -2.6841    0.5690 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1790   -2.4767   -0.7892 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.5018   -0.3262    0.9649 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8334   -0.2349    1.2848 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6331    0.5889    1.8034 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6965    1.8669    1.3007 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2402    0.0429    1.9611 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3508    1.1115    1.9082 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1583   -0.0348   -0.1304 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8795    0.2789   -0.5282 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8075   -0.4616   -0.0852 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3923   -0.4010   -2.6084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6623    0.2096   -3.3389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6883    0.0757   -0.1325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9230    3.5600    0.1196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5704    2.0734    1.9682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3210    2.2854    1.5913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3567    0.2086    1.6891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8814    2.9398   -1.9589 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0383    3.6355    0.0627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9906    0.2978   -0.8576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8675    1.8142   -3.2145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8140    0.3266   -2.9397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4000   -1.6209   -2.4113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9637    0.1700    0.7125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8880   -0.6658    2.2205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0691   -2.5273    1.1619 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4302   -2.6743    1.8209 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7147   -0.2730   -0.1032 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9599   -2.0047    2.2772 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7578   -3.7396    0.8328 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9978   -2.4849    1.0439 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5503   -2.9965   -1.3597 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3140   -0.0955   -0.1114 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.3825   -0.1013    0.4612 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0869    0.6020    2.8253 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3881    1.9798    0.5830 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0931   -0.4702    2.9263 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7630    1.9960    2.0602 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9813    0.5723   -0.4974 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6799    1.1125   -1.1968 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 11 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
  7 20  1  0
 20 21  2  0
 21 22  1  0
  3 23  2  0
 23 24  1  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 31 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  1  0
 36 38  1  0
 38 39  1  0
 27 40  2  0
 40 41  1  0
 41 42  2  0
 42  2  1  0
 21  4  1  0
 42 25  1  0
 18  9  1  0
 38 29  1  0
  5 43  1  0
  6 44  1  0
  9 45  1  0
 11 46  1  0
 12 47  1  0
 12 48  1  0
 13 49  1  0
 14 50  1  0
 15 51  1  0
 16 52  1  0
 17 53  1  0
 18 54  1  0
 19 55  1  0
 20 56  1  0
 22 57  1  0
 23 58  1  0
 26 59  1  0
 29 60  1  0
 31 61  1  0
 32 62  1  0
 32 63  1  0
 33 64  1  0
 34 65  1  0
 35 66  1  0
 36 67  1  0
 37 68  1  0
 38 69  1  0
 39 70  1  0
 40 71  1  0
 41 72  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
2'-Hydroxydaidzein 7,4'-di-O-glucoside	HMDB

Chemical Formula

C₂₇H₃₀O₁₅

Average Molecular Weight

594.5181

Monoisotopic Molecular Weight

594.15847029

IUPAC Name

3-(2-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H-chromen-4-one

Traditional Name

3-(2-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

CAS Registry Number

88048-22-0

SMILES

OCC1OC(OC2=CC(O)=C(C=C2)C2=COC3=C(C=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C2=O)C(O)C(O)C1O

InChI Identifier

InChI=1S/C27H30O15/c28-7-17-20(32)22(34)24(36)26(41-17)39-10-1-3-12(15(30)5-10)14-9-38-16-6-11(2-4-13(16)19(14)31)40-27-25(37)23(35)21(33)18(8-29)42-27/h1-6,9,17-18,20-30,32-37H,7-8H2

InChI Key

DNPGZHRLHFUCNR-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isoflavonoid o-glycosides. These are o-glycosylated derivatives of isoflavonoids, which are natural products derived from 3-phenylchromen-4-one.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

Isoflavonoid O-glycosides

Direct Parent

Isoflavonoid O-glycosides

Alternative Parents

Substituents

Isoflavonoid-4p-o-glycoside
Isoflavonoid-7-o-glycoside
Isoflavonoid o-glycoside
Isoflavone
Hydroxyisoflavonoid
Phenolic glycoside
Chromone
O-glycosyl compound
Glycosyl compound
Benzopyran
1-benzopyran
Phenoxy compound
Phenol ether
Phenol
1-hydroxy-4-unsubstituted benzenoid
Pyranone
1-hydroxy-2-unsubstituted benzenoid
Monosaccharide
Monocyclic benzene moiety
Pyran
Benzenoid
Oxane
Heteroaromatic compound
Secondary alcohol
Acetal
Oxacycle
Organoheterocyclic compound
Polyol
Alcohol
Hydrocarbon derivative
Organic oxide
Primary alcohol
Organic oxygen compound
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Extracellular (HMDB: HMDB0039347)
Cytoplasm (HMDB: HMDB0039347)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0039347)

Source

Exogenous

Exogenous (HMDB: HMDB0039347)

Food

Food (HMDB: HMDB0039347)

Pulse

Bean

Adzuki bean (FooDB: FOOD00198)

Pulses (FooDB: FOOD00867)

Endogenous

Plant

Plant (HMDB: HMDB0039347)
Fabaceae (HMDB: HMDB0039347)

Process

Not Available

Role

Biological role

Nutrient (HMDB: HMDB0039347)

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	1.8 g/L	ALOGPS
logP	-0.51	ALOGPS
logP	-2.1	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	8.53	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	15	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	245.29 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	135.97 m³·mol⁻¹	ChemAxon
Polarizability	57.97 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	234.324	31661259
DarkChem	[M-H]-	227.177	31661259
DeepCCS	[M+H]+	230.788	30932474
DeepCCS	[M-H]-	228.392	30932474
DeepCCS	[M-2H]-	261.543	30932474
DeepCCS	[M+Na]+	236.7	30932474
AllCCS	[M+H]+	228.4	32859911
AllCCS	[M+H-H2O]+	227.2	32859911
AllCCS	[M+NH4]+	229.5	32859911
AllCCS	[M+Na]+	229.8	32859911
AllCCS	[M-H]-	222.0	32859911
AllCCS	[M+Na-2H]-	224.2	32859911
AllCCS	[M+HCOO]-	226.6	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
2'-Hydroxydaidzein 4',7-diglucoside	OCC1OC(OC2=CC(O)=C(C=C2)C2=COC3=C(C=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C2=O)C(O)C(O)C1O	5036.5	Standard polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside	OCC1OC(OC2=CC(O)=C(C=C2)C2=COC3=C(C=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C2=O)C(O)C(O)C1O	5080.6	Standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside	OCC1OC(OC2=CC(O)=C(C=C2)C2=COC3=C(C=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C2=O)C(O)C(O)C1O	5585.0	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
2'-Hydroxydaidzein 4',7-diglucoside,1TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O	5361.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,1TMS,isomer #2	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC=C2C1=O	5351.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,1TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O)=COC3=C2)C(O)C(O)C1O	5362.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,1TMS,isomer #4	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O)=COC3=C2)C(O)C1O	5350.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,1TMS,isomer #5	C[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O)=COC3=C2)C1O	5345.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,1TMS,isomer #6	C[Si](C)(C)OC1C(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O)=COC3=C2)OC(CO)C(O)C1O	5366.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,1TMS,isomer #7	C[Si](C)(C)OC1C(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)OC(CO)C(O)C1O	5367.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,1TMS,isomer #8	C[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)C1O	5343.9	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,1TMS,isomer #9	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O)C1O	5351.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO[Si](C)(C)C)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O	5215.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #10	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC=C2C1=O	5163.9	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #11	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC=C2C1=O	5213.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #12	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O[Si](C)(C)C)=COC3=C2)C(O)C(O)C1O	5192.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #13	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=CC=C2C1=O	5194.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #14	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=CC=C2C1=O	5165.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #15	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=CC=C2C1=O	5211.9	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #16	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O)C=C4O)=COC3=C2)C(O)C(O)C1O	5203.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #17	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)C=C4O)=COC3=C2)C(O)C(O)C1O	5183.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #18	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C(O)C(O)C1O	5225.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #19	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O)=COC3=C2)C(O[Si](C)(C)C)C(O)C1O	5239.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O	5201.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #20	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O)=COC3=C2)C(O)C(O[Si](C)(C)C)C1O	5197.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #21	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O)=COC3=C2)C(O)C(O)C1O[Si](C)(C)C	5218.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #22	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O)C1O	5198.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #23	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)C=C4O)=COC3=C2)C(O)C1O	5176.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #24	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C(O)C1O	5222.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #25	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O)=COC3=C2)C(O[Si](C)(C)C)C1O	5230.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #26	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O)=COC3=C2)C(O)C1O[Si](C)(C)C	5206.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #27	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)C(O)C1O	5179.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #28	C[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)C1O	5151.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #29	C[Si](C)(C)OC1C(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)OC(CO)C(O)C1O	5202.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O	5184.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #30	C[Si](C)(C)OC1C(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O)=COC3=C2)OC(CO)C(O)C1O[Si](C)(C)C	5236.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #31	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O)C1O	5224.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #32	C[Si](C)(C)OC1C(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)C=C4O)=COC3=C2)OC(CO)C(O)C1O	5201.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #33	C[Si](C)(C)OC1C(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)OC(CO)C(O)C1O	5248.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #34	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C)C1O	5229.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #35	C[Si](C)(C)OC1C(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)OC(CO)C(O)C1O[Si](C)(C)C	5236.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #36	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O)C1O[Si](C)(C)C	5205.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O	5225.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O	5192.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O	5238.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O	5195.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #8	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C	5216.6	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TMS,isomer #9	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC=C2C1=O	5194.6	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O	5058.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #10	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O)=CC=C4C3=O)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O	5016.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #11	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O	5079.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #12	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O	5040.9	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #13	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C	5058.9	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #14	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O	5071.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #15	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4990.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #16	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O	5057.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #17	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O	5020.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #18	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C	5041.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #19	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)=CC=C4C3=O)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O	5031.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O	5037.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #20	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O	5099.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #21	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O	5055.9	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #22	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C	5077.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #23	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O	5045.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #24	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O	5016.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #25	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C	5032.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #26	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5087.6	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #27	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5118.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #28	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5064.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #29	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC=C2C1=O	5025.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO[Si](C)(C)C)C(O)C(O)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O	5081.6	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #30	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC=C2C1=O	5046.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #31	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O)C=C4O[Si](C)(C)C)=COC3=C2)C(O)C(O)C1O	5016.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #32	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=CC=C2C1=O	5035.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #33	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=CC=C2C1=O	5002.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #34	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=CC=C2C1=O	5051.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #35	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC=C2C1=O	5058.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #36	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)C=C4O[Si](C)(C)C)=COC3=C2)C(O)C(O)C1O	4989.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #37	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=CC=C2C1=O	4997.9	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #38	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=CC=C2C1=O	4967.6	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #39	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=CC=C2C1=O	5018.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO[Si](C)(C)C)C(O)C(O)C5O)=CC=C4C3=O)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O	5010.6	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #40	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)C=C4O[Si](C)(C)C)=COC3=C2)C(O)C(O)C1O	5029.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #41	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=CC=C1C1=COC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=CC=C2C1=O	5051.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #42	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=CC=C2C1=O	5019.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #43	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=CC=C2C1=O	5071.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #44	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O[Si](C)(C)C)=COC3=C2)C(O[Si](C)(C)C)C(O)C1O	5048.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #45	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O[Si](C)(C)C)=COC3=C2)C(O)C(O[Si](C)(C)C)C1O	5016.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #46	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O[Si](C)(C)C)=COC3=C2)C(O)C(O)C1O[Si](C)(C)C	5030.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #47	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=CC=C2C1=O	5026.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #48	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=CC=C2C1=O	5047.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #49	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC=C2C1=O	5058.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO[Si](C)(C)C)C(O)C(O)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C(O)C(O)C1O	5080.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #50	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)C=C4O)=COC3=C2)C(O)C(O)C1O	5041.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #51	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C(O)C(O)C1O	5069.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #52	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O)C=C4O)=COC3=C2)C(O[Si](C)(C)C)C(O)C1O	5080.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #53	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O)C=C4O)=COC3=C2)C(O)C(O[Si](C)(C)C)C1O	5041.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #54	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O)C=C4O)=COC3=C2)C(O)C(O)C1O[Si](C)(C)C	5058.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #55	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C(O)C(O)C1O	5069.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #56	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)C=C4O)=COC3=C2)C(O[Si](C)(C)C)C(O)C1O	5057.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #57	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)C=C4O)=COC3=C2)C(O)C(O[Si](C)(C)C)C1O	5020.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #58	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)C=C4O)=COC3=C2)C(O)C(O)C1O[Si](C)(C)C	5038.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #59	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C(O[Si](C)(C)C)C(O)C1O	5100.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C5O)C=C4O)=COC3=C2)C(O)C(O)C1O	5035.9	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #60	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C(O)C(O[Si](C)(C)C)C1O	5057.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #61	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C(O)C(O)C1O[Si](C)(C)C	5077.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #62	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O)=COC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5088.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #63	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O)=COC3=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5121.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #64	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O)=COC3=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5066.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #65	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)C(O)C1O	5053.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #66	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O)C1O	5077.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #67	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C(O)C1O	5077.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #68	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)C=C4O)=COC3=C2)C(O)C1O	5050.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #69	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C(O)C1O	5079.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C5O)C=C4O)=COC3=C2)C(O)C(O)C1O	5058.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #70	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)C=C4O)=COC3=C2)C(O[Si](C)(C)C)C1O	5057.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #71	C[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)C1O	5034.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #72	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C(O[Si](C)(C)C)C1O	5097.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #73	C[Si](C)(C)OC1C(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)OC(CO)C(O)C1O	5071.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #74	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O)=COC3=C2)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5108.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #75	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O)C1O	5080.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #76	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C)C1O	5059.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #77	C[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)C=C4O)=COC3=C2)C1O	5034.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #78	C[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C1O	5060.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #79	C[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C1O	5061.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #8	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O	5043.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #80	C[Si](C)(C)OC1C(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)OC(CO)C(O)C1O	5096.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #81	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C)C1O	5098.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #82	C[Si](C)(C)OC1C(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)C=C4O)=COC3=C2)OC(CO)C(O)C1O	5069.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #83	C[Si](C)(C)OC1C(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)C=C4O)=COC3=C2)OC(CO)C(O)C1O	5096.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #84	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5107.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,3TMS,isomer #9	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O	5070.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O	4974.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #10	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O	4932.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #100	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O)C=C4O)=COC3=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5026.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #101	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O)C=C4O)=COC3=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4981.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #102	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C(O[Si](C)(C)C)C(O)C1O	5005.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #103	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C(O)C(O[Si](C)(C)C)C1O	4964.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #104	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C(O)C(O)C1O[Si](C)(C)C	4985.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #105	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)C=C4O)=COC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4971.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #106	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)C=C4O)=COC3=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4999.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #107	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)C=C4O)=COC3=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4950.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #108	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5014.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #109	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5045.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #11	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C5O)C=C4O)=COC3=C2)C(O)C(O[Si](C)(C)C)C1O	4962.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #110	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4999.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #111	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O)=COC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5054.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #112	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O)C1O	5004.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #113	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C)C1O	4979.9	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #114	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)C(O)C1O[Si](C)(C)C	4958.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #115	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C)C1O	4996.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #116	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)C=C4O)=COC3=C2)C(O[Si](C)(C)C)C1O	4978.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #117	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C(O)C1O	5002.9	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #118	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C(O[Si](C)(C)C)C1O	4998.9	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #119	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C(O)C1O[Si](C)(C)C	4979.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #12	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO[Si](C)(C)C)C(O)C(O)C5O[Si](C)(C)C)=CC=C4C3=O)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4947.6	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #120	C[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C1O	4980.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #121	C[Si](C)(C)OC1C(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)OC(CO)C(O)C1O	5019.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #122	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C)C1O	4999.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #123	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O)C1O[Si](C)(C)C	4978.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #124	C[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C1O	4982.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #125	C[Si](C)(C)OC1C(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)OC(CO)C(O)C1O[Si](C)(C)C	4999.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #126	C[Si](C)(C)OC1C(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O[Si](C)(C)C)C=C4O)=COC3=C2)OC(CO)C(O)C1O	5019.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #13	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO[Si](C)(C)C)C(O)C(O)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O	5028.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #14	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C5O)C=C4O)=COC3=C2)C(O[Si](C)(C)C)C(O)C1O	4978.6	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #15	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C5O)C=C4O)=COC3=C2)C(O[Si](C)(C)C)C(O)C1O	5003.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #16	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO[Si](C)(C)C)C(O)C(O)C5O[Si](C)(C)C)C=C4O[Si](C)(C)C)=COC3=C2)C(O)C(O)C1O	4946.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #17	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C5O)C=C4O[Si](C)(C)C)=COC3=C2)C(O)C(O)C1O	4905.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #18	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C5O)C=C4O[Si](C)(C)C)=COC3=C2)C(O)C(O)C1O	4924.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #19	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C(O)C(O)C1O	5013.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O	5016.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #20	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C(O)C(O)C1O	4988.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #21	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)C=C4O)=COC3=C2)C(O)C(O)C1O	4971.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #22	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O	4984.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #23	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4917.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #24	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O	4985.9	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #25	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O	4945.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #26	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C	4970.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #27	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O[Si](C)(C)C)=CC=C4C3=O)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4940.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #28	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O	5004.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #29	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O	4964.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C5O)=CC=C4C3=O)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4924.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #30	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C	4988.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #31	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O)=CC=C4C3=O)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O	4957.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #32	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O)=CC=C4C3=O)C(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O	4907.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #33	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O)=CC=C4C3=O)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C	4932.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #34	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4993.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #35	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5021.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #36	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4977.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #37	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)=CC=C4C3=O)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4938.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #38	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O	5004.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #39	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O	4964.9	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O	5000.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #40	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C	4988.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #41	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O	4926.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #42	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O	4864.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #43	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C	4899.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #44	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4971.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #45	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4999.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #46	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4951.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #47	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)=CC=C4C3=O)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O	4982.9	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #48	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)=CC=C4C3=O)C(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O	4939.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #49	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)=CC=C4C3=O)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C	4963.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O	4958.6	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #50	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5015.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #51	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5044.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #52	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4999.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #53	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4973.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #54	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4999.9	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #55	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4951.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #56	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5053.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #57	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC=C2C1=O	4988.6	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #58	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)C=C4O[Si](C)(C)C)=COC3=C2)C(O)C(O)C1O	4915.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #59	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=CC=C2C1=O	4927.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C	4979.9	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #60	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=CC=C2C1=O	4886.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #61	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=CC=C2C1=O	4956.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #62	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O[Si](C)(C)C)C=C4O[Si](C)(C)C)=COC3=C2)C(O)C(O)C1O	4936.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #63	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC=C1C1=COC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=CC=C2C1=O	4954.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #64	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=CC=C2C1=O	4918.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #65	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=CC=C2C1=O	4979.9	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #66	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O)C=C4O[Si](C)(C)C)=COC3=C2)C(O[Si](C)(C)C)C(O)C1O	4961.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #67	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O)C=C4O[Si](C)(C)C)=COC3=C2)C(O)C(O[Si](C)(C)C)C1O	4908.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #68	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O)C=C4O[Si](C)(C)C)=COC3=C2)C(O)C(O)C1O[Si](C)(C)C	4932.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #69	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=CC=C2C1=O	4929.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O	4989.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #70	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=CC=C2C1=O	4956.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #71	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC=C2C1=O	4952.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #72	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O[Si](C)(C)C)C=C4O[Si](C)(C)C)=COC3=C2)C(O)C(O)C1O	4936.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #73	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1C1=COC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=CC=C2C1=O	4951.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #74	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=CC=C2C1=O	4912.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #75	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=CC=C2C1=O	4979.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #76	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)C=C4O[Si](C)(C)C)=COC3=C2)C(O[Si](C)(C)C)C(O)C1O	4926.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #77	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)C=C4O[Si](C)(C)C)=COC3=C2)C(O)C(O[Si](C)(C)C)C1O	4863.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #78	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C)C5O)C=C4O[Si](C)(C)C)=COC3=C2)C(O)C(O)C1O[Si](C)(C)C	4896.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #79	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=CC=C2C1=O	4885.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #8	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4906.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #80	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=CC=C2C1=O	4919.6	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #81	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC=C2C1=O	4912.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #82	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)C=C4O[Si](C)(C)C)=COC3=C2)C(O[Si](C)(C)C)C(O)C1O	4981.9	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #83	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)C=C4O[Si](C)(C)C)=COC3=C2)C(O)C(O[Si](C)(C)C)C1O	4937.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #84	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C)C=C4O[Si](C)(C)C)=COC3=C2)C(O)C(O)C1O[Si](C)(C)C	4959.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #85	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=CC=C1C1=COC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=CC=C2C1=O	4955.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #86	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=CC=C1C1=COC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=CC=C2C1=O	4979.9	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #87	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC=C2C1=O	4977.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #88	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O[Si](C)(C)C)=COC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4974.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #89	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O[Si](C)(C)C)=COC3=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5002.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #9	C[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O	4978.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #90	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O[Si](C)(C)C)=COC3=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4952.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #91	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC=C2C1=O	4988.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #92	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C(O)C(O)C1O	4984.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #93	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)C=C4O)=COC3=C2)C(O[Si](C)(C)C)C(O)C1O	4986.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #94	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)C=C4O)=COC3=C2)C(O)C(O[Si](C)(C)C)C1O	4945.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #95	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C5O)C=C4O)=COC3=C2)C(O)C(O)C1O[Si](C)(C)C	4966.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #96	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C(O[Si](C)(C)C)C(O)C1O	5005.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #97	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C(O)C(O[Si](C)(C)C)C1O	4964.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #98	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O[Si](C)(C)C)C=C4O)=COC3=C2)C(O)C(O)C1O[Si](C)(C)C	4985.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,4TMS,isomer #99	C[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C)C(O)C5O)C=C4O)=COC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4996.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O	5565.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC=C2C1=O	5554.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O)=COC3=C2)C(O)C(O)C1O	5565.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O)=COC3=C2)C(O)C1O	5576.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O)=COC3=C2)C1O	5572.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1C(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O)=COC3=C2)OC(CO)C(O)C1O	5586.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1C(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)OC(CO)C(O)C1O	5587.6	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,1TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)C1O	5571.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,1TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O)C1O	5576.6	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O	5597.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC=C2C1=O	5577.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC=C2C1=O	5597.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O[Si](C)(C)C(C)(C)C)=COC3=C2)C(O)C(O)C1O	5595.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=CC=C2C1=O	5593.9	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=CC=C2C1=O	5579.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=CC=C2C1=O	5598.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C5O)C=C4O)=COC3=C2)C(O)C(O)C1O	5583.6	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C5O)C=C4O)=COC3=C2)C(O)C(O)C1O	5571.9	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C(C)(C)C)C=C4O)=COC3=C2)C(O)C(O)C1O	5592.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O)=COC3=C2)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	5612.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O	5583.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O)=COC3=C2)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	5602.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O)=COC3=C2)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	5590.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O)C1O	5577.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C5O)C=C4O)=COC3=C2)C(O)C1O	5561.8	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C(C)(C)C)C=C4O)=COC3=C2)C(O)C1O	5585.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O)=COC3=C2)C(O[Si](C)(C)C(C)(C)C)C1O	5609.2	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O)=COC3=C2)C(O)C1O[Si](C)(C)C(C)(C)C	5584.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)C(O)C1O	5564.6	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)C1O	5546.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OC1C(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)OC(CO)C(O)C1O	5564.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O	5573.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OC1C(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4O)=COC3=C2)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	5614.4	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C(C)(C)C)=CC=C4C3=O)C(O)=C2)C(O)C1O	5588.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC1C(OC2=CC=C3C(=O)C(C4=CC=C(OC5OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C5O)C=C4O)=COC3=C2)OC(CO)C(O)C1O	5565.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC1C(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C(C)(C)C)=CC=C4C3=O)C(O)=C2)OC(CO)C(O)C1O	5602.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C(C)(C)C)C1O	5608.9	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OC1C(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	5613.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #36	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O)C1O[Si](C)(C)C(C)(C)C	5584.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O[Si](C)(C)C(C)(C)C)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O	5593.0	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O[Si](C)(C)C(C)(C)C)=C2)C(O)C(O)C1O	5595.3	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	5611.1	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	5601.5	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=COC4=CC(OC5OC(CO)C(O)C(O)C5O)=CC=C4C3=O)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	5590.7	Semi standard non polar	33892256
2'-Hydroxydaidzein 4',7-diglucoside,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)=CC=C1C1=COC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC=C2C1=O	5593.8	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 - 2'-Hydroxydaidzein 4',7-diglucoside GC-MS (Non-derivatized) - 70eV, Positive	splash10-0h0r-2300390000-143d290e9eeb98911ef7	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside GC-MS ("2'-Hydroxydaidzein 4',7-diglucoside,1TMS,#1" TMS) - 70eV, Positive	Not Available	2021-10-14	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside GC-MS (TMS_1_8) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside GC-MS (TMS_1_9) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside GC-MS (TMS_2_13) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside GC-MS (TMS_2_14) - 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 - 2'-Hydroxydaidzein 4',7-diglucoside 10V, Positive-QTOF	splash10-0159-0000930000-b58a41e2692e0afa4367	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside 20V, Positive-QTOF	splash10-01b9-0150900000-ce7339959c4af70c26c2	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside 40V, Positive-QTOF	splash10-01b9-3560910000-43405ff387051f1ef5dc	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside 10V, Negative-QTOF	splash10-01po-0103890000-88096fd65483b1b6c48f	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside 20V, Negative-QTOF	splash10-03e9-0212920000-95692f8b9acc0c758c30	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside 40V, Negative-QTOF	splash10-03yi-6698600000-1f003a7114a684ab897a	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside 10V, Negative-QTOF	splash10-0006-0130490000-fb1c1e3f8a633032eb23	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside 20V, Negative-QTOF	splash10-001i-2110940000-8eb6ed7dfd138d215b60	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside 40V, Negative-QTOF	splash10-01b9-1292300000-808217c066003f6747b9	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside 10V, Positive-QTOF	splash10-00si-0120920000-80805aac4336218a849a	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside 20V, Positive-QTOF	splash10-040r-0403940000-db2727b33a0d39d4ab4b	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2'-Hydroxydaidzein 4',7-diglucoside 40V, Positive-QTOF	splash10-0592-9600780000-9e0209490831e89cb733	2021-09-25	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-24	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

FDB018902

KNApSAcK ID

C00010141

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131752613

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

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

Showing metabocard for 2'-Hydroxydaidzein 4',7-diglucoside (HMDB0039347)

MOL for HMDB0039347 (2'-Hydroxydaidzein 4',7-diglucoside)

3D MOL for HMDB0039347 (2'-Hydroxydaidzein 4',7-diglucoside)

3D SDF for HMDB0039347 (2'-Hydroxydaidzein 4',7-diglucoside)

3D-SDF for HMDB0039347 (2'-Hydroxydaidzein 4',7-diglucoside)

PDB for HMDB0039347 (2'-Hydroxydaidzein 4',7-diglucoside)

3D PDB for HMDB0039347 (2'-Hydroxydaidzein 4',7-diglucoside)

SMILES for HMDB0039347 (2'-Hydroxydaidzein 4',7-diglucoside)

INCHI for HMDB0039347 (2'-Hydroxydaidzein 4',7-diglucoside)

Structure for HMDB0039347 (2'-Hydroxydaidzein 4',7-diglucoside)

3D Structure for HMDB0039347 (2'-Hydroxydaidzein 4',7-diglucoside)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra