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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 00:06:22 UTC

Update Date

2022-03-07 02:55:54 UTC

HMDB ID

HMDB0038763

Secondary Accession Numbers

HMDB38763

Metabolite Identification

Common Name

Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside)

Description

Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside) belongs to the class of organic compounds known as flavonoid-7-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position. Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside) has been detected, but not quantified in, several different foods, such as green onion, garden onions (Allium cepa), garden onion (var.), red onion, and onion-family vegetables. This could make kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside) a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside).

Structure

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


  Mrv0541 05061310382D          

 67 73  0  0  0  0            999 V2000
   -2.8579   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    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
   -2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    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
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    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
   -2.8579   -4.9500    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
   -2.1434   -5.3625    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
    5.7158    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -0.4125    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
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    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
    1.4289   -1.6500    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
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    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
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    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
   -2.1434   -1.2375    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
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -1.6500    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
    3.5724    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -6.1875    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
   -1.4289    0.0000    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
    5.7158    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.0000    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
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  4  1  0  0  0  0
  7  5  2  0  0  0  0
  8  2  2  0  0  0  0
  9  3  2  0  0  0  0
 16  2  1  0  0  0  0
 16  3  1  0  0  0  0
 16 10  2  0  0  0  0
 17  4  2  0  0  0  0
 17  5  1  0  0  0  0
 18  6  2  0  0  0  0
 18  7  1  0  0  0  0
 19 11  2  0  0  0  0
 19 12  1  0  0  0  0
 20  8  1  0  0  0  0
 21 11  1  0  0  0  0
 22 10  1  0  0  0  0
 22 20  2  0  0  0  0
 23 12  2  0  0  0  0
 24 13  1  0  0  0  0
 25 14  1  0  0  0  0
 26 15  1  0  0  0  0
 27  9  1  0  0  0  0
 28 21  2  0  0  0  0
 28 23  1  0  0  0  0
 29 24  1  0  0  0  0
 30 25  1  0  0  0  0
 31 26  1  0  0  0  0
 32 28  1  0  0  0  0
 33 29  1  0  0  0  0
 34 30  1  0  0  0  0
 35 31  1  0  0  0  0
 36 33  1  0  0  0  0
 37 34  1  0  0  0  0
 38 17  1  0  0  0  0
 39 32  1  0  0  0  0
 39 38  2  0  0  0  0
 40 35  1  0  0  0  0
 41 36  1  0  0  0  0
 42 37  1  0  0  0  0
 43 40  1  0  0  0  0
 44 13  1  0  0  0  0
 45 14  1  0  0  0  0
 46 15  1  0  0  0  0
 47 20  1  0  0  0  0
 48 21  1  0  0  0  0
 49 27  2  0  0  0  0
 50 29  1  0  0  0  0
 51 30  1  0  0  0  0
 52 31  1  0  0  0  0
 53 32  2  0  0  0  0
 54 33  1  0  0  0  0
 55 34  1  0  0  0  0
 56 35  1  0  0  0  0
 57 36  1  0  0  0  0
 58 37  1  0  0  0  0
 59  1  1  0  0  0  0
 59 22  1  0  0  0  0
 60 18  1  0  0  0  0
 60 41  1  0  0  0  0
 61 19  1  0  0  0  0
 61 43  1  0  0  0  0
 62 23  1  0  0  0  0
 62 38  1  0  0  0  0
 63 24  1  0  0  0  0
 63 41  1  0  0  0  0
 64 25  1  0  0  0  0
 64 42  1  0  0  0  0
 65 26  1  0  0  0  0
 65 43  1  0  0  0  0
 66 27  1  0  0  0  0
 66 40  1  0  0  0  0
 67 39  1  0  0  0  0
 67 42  1  0  0  0  0
M  END

HMDB0038763
     RDKit          3D
Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside)
115121  0  0  0  0  0  0  0  0999 V2000
   10.6053   -0.8257   -0.9999 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4234   -2.1773   -1.0125 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7799   -3.0570   -0.2257 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1007   -2.6950    0.9085 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4719   -3.5935    1.6992 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6946   -3.3272    2.8833 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9311   -2.3381    3.0742 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5273   -1.2139    2.3265 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7704   -0.4051    3.0114 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7143   -0.7503    1.0588 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1348    0.4554    0.6719 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1488    0.4837   -0.4170 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8596    0.3929   -0.0164 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7261    1.1098   -0.1189 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5933    2.4070   -0.5255 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3734    3.0469   -0.5942 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2784    4.3579   -1.0069 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2315    2.3773   -0.2492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0151    2.9572   -0.2975 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0843    4.1463   -0.6669 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1855    2.2617    0.0520 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3381    2.9514   -0.0418 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0297    3.2615   -1.2390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1834    4.6585   -1.3060 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4606    5.0606   -2.6042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6949    6.5554   -2.5212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9695    7.1254   -3.7344 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6273    4.3085   -3.1877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5455    5.2293   -3.6826 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3242    3.4445   -2.1797 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1631    2.5196   -2.7769 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3892    2.6742   -1.2608 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3455    1.3260   -1.6735 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0444    0.9689    0.4507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1626    0.1208    0.8434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3524    0.6476    1.2246 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4623   -0.1695    1.5191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3706   -1.5396    1.4292 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4041   -2.4052    1.6946 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7059   -2.0972    2.1011 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0266   -2.8167    3.2613 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6269   -4.1173    3.0834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9240   -4.8883    4.3691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2426   -4.3498    5.4429 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3888   -4.8281    1.9879 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6688   -5.9780    1.6477 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5402   -3.9921    0.7481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6767   -4.4555    0.0895 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7283   -2.5343    1.0620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9918   -2.2497    1.5327 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1350   -2.0765    1.0375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0663   -1.2438    0.7548 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8105    0.4418    0.4847 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2899    1.0540    0.1690 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5307    0.4595    0.2237 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2457    1.7991   -1.0753 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2997    1.7122   -1.9902 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4852    3.0595   -2.6184 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5170    3.0663   -3.5623 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4913    1.2400   -1.1811 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5840   -0.1551   -1.4251 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2346    1.4687    0.3008 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3698    1.3344    1.0345 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5091   -4.9576    1.3481 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1767   -5.3269    0.2233 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8113   -4.4257   -0.5728 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4969   -4.7756   -1.7239 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1587   -0.3124   -0.1281 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2722   -0.3539   -1.9514 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.7097   -0.6237   -0.9377 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0981   -1.6416    1.1971 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8267   -4.1112    3.7125 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4559   -2.3776    4.1311 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6218    0.9612    1.5569 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3238   -0.1416   -1.3272 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4634    2.9648   -0.7979 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0244    4.9499   -1.2860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4549    2.9551   -2.1373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5493    4.9077   -3.1996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8158    7.0631   -2.0786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5479    6.7174   -1.8218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9345    8.0944   -3.7108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2846    3.6966   -4.0376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0234    4.7921   -4.4358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9601    4.0735   -1.5173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6181    1.9512   -3.3973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8147    2.6740   -0.2426 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv0541 05061310382D          

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M  END
> <DATABASE_ID>
HMDB0038763

> <DATABASE_NAME>
hmdb

> <SMILES>
COC1=C(O)C=CC(\C=C/C(=O)OC2C(OC3=CC(O)=C4C(OC(C5=CC=C(OC6OC(CO)C(O)C(O)C6O)C=C5)=C(OC5OC(CO)C(O)C(O)C5O)C4=O)=C3)OC(CO)C(O)C2O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C43H48O24/c1-59-22-10-16(2-8-20(22)47)3-9-27(49)66-40-35(56)31(52)26(15-46)65-43(40)61-19-11-21(48)28-23(12-19)62-38(39(32(28)53)67-42-37(58)34(55)30(51)25(14-45)64-42)17-4-6-18(7-5-17)60-41-36(57)33(54)29(50)24(13-44)63-41/h2-12,24-26,29-31,33-37,40-48,50-52,54-58H,13-15H2,1H3/b9-3-

> <INCHI_KEY>
SJOFKYITWVGVEV-OQFOIZHKSA-N

> <FORMULA>
C43H48O24

> <MOLECULAR_WEIGHT>
948.8268

> <EXACT_MASS>
948.253552464

> <JCHEM_ACCEPTOR_COUNT>
23

> <JCHEM_AVERAGE_POLARIZABILITY>
93.15744402863768

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
13

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4,5-dihydroxy-2-[(5-hydroxy-4-oxo-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2-(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-4H-chromen-7-yl)oxy]-6-(hydroxymethyl)oxan-3-yl (2Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

> <ALOGPS_LOGP>
0.40

> <JCHEM_LOGP>
-1.8047520303333338

> <ALOGPS_LOGS>
-2.92

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.87519150111278

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.287061398532243

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6491251505882287

> <JCHEM_POLAR_SURFACE_AREA>
380.20000000000016

> <JCHEM_REFRACTIVITY>
219.5952000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.14e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,5-dihydroxy-2-[(5-hydroxy-4-oxo-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2-(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)chromen-7-yl)oxy]-6-(hydroxymethyl)oxan-3-yl (2Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0038763
     RDKit          3D
Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside)
115121  0  0  0  0  0  0  0  0999 V2000
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   -7.6900   -4.1153    0.0355 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2960   -3.7291   -0.1513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4894   -1.9513    0.1363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9808   -1.2907    1.8378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0620   -3.1526    0.9715 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.5779   -0.5839    0.5564 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9852    0.9521   -2.7555 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5385    3.4295   -3.0521 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7861    3.8348   -1.8620 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5111    2.1404   -3.9661 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4014    1.7208   -1.5137 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9097   -0.3515   -2.3202 H   0  0  0  0  0  0  0  0  0  0  0  0
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    8.0034   -5.6798    1.9819 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2011   -6.3813   -0.0461 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.5232   -5.7497   -1.9810 H   0  0  0  0  0  0  0  0  0  0  0  0
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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      -5.335 -12.320   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.667  -9.240   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       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.003   6.930   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -8.002   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -5.335  -9.240   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      -4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.669   6.160   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.336   6.930   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.002   6.160   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       9.336   3.850   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      12.003   8.470   0.000  0.00  0.00           O+0
HETATM   45  O   UNK     0       1.334  -6.930   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0      -8.002   1.540   0.000  0.00  0.00           O+0
HETATM   47  O   UNK     0      -6.668 -10.010   0.000  0.00  0.00           O+0
HETATM   48  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   49  O   UNK     0      -4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0       9.336   8.470   0.000  0.00  0.00           O+0
HETATM   51  O   UNK     0       5.335  -9.240   0.000  0.00  0.00           O+0
HETATM   52  O   UNK     0      -8.002  -3.080   0.000  0.00  0.00           O+0
HETATM   53  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   54  O   UNK     0       6.668   6.930   0.000  0.00  0.00           O+0
HETATM   55  O   UNK     0       8.002  -7.700   0.000  0.00  0.00           O+0
HETATM   56  O   UNK     0      -5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   57  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM   58  O   UNK     0       8.002  -4.620   0.000  0.00  0.00           O+0
HETATM   59  O   UNK     0      -4.001 -11.550   0.000  0.00  0.00           O+0
HETATM   60  O   UNK     0       9.336   2.310   0.000  0.00  0.00           O+0
HETATM   61  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
HETATM   62  O   UNK     0       2.667   0.000   0.000  0.00  0.00           O+0
HETATM   63  O   UNK     0      10.669   4.620   0.000  0.00  0.00           O+0
HETATM   64  O   UNK     0       4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   65  O   UNK     0      -5.335   0.000   0.000  0.00  0.00           O+0
HETATM   66  O   UNK     0      -2.667  -3.080   0.000  0.00  0.00           O+0
HETATM   67  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
CONECT    1   59                                                            
CONECT    2    8   16                                                       
CONECT    3    9   16                                                       
CONECT    4    6   17                                                       
CONECT    5    7   17                                                       
CONECT    6    4   18                                                       
CONECT    7    5   18                                                       
CONECT    8    2   20                                                       
CONECT    9    3   27                                                       
CONECT   10   16   22                                                       
CONECT   11   19   21                                                       
CONECT   12   19   23                                                       
CONECT   13   24   44                                                       
CONECT   14   25   45                                                       
CONECT   15   26   46                                                       
CONECT   16    2    3   10                                                  
CONECT   17    4    5   38                                                  
CONECT   18    6    7   60                                                  
CONECT   19   11   12   61                                                  
CONECT   20    8   22   47                                                  
CONECT   21   11   28   48                                                  
CONECT   22   10   20   59                                                  
CONECT   23   12   28   62                                                  
CONECT   24   13   29   63                                                  
CONECT   25   14   30   64                                                  
CONECT   26   15   31   65                                                  
CONECT   27    9   49   66                                                  
CONECT   28   21   23   32                                                  
CONECT   29   24   33   50                                                  
CONECT   30   25   34   51                                                  
CONECT   31   26   35   52                                                  
CONECT   32   28   39   53                                                  
CONECT   33   29   36   54                                                  
CONECT   34   30   37   55                                                  
CONECT   35   31   40   56                                                  
CONECT   36   33   41   57                                                  
CONECT   37   34   42   58                                                  
CONECT   38   17   39   62                                                  
CONECT   39   32   38   67                                                  
CONECT   40   35   43   66                                                  
CONECT   41   36   60   63                                                  
CONECT   42   37   64   67                                                  
CONECT   43   40   61   65                                                  
CONECT   44   13                                                            
CONECT   45   14                                                            
CONECT   46   15                                                            
CONECT   47   20                                                            
CONECT   48   21                                                            
CONECT   49   27                                                            
CONECT   50   29                                                            
CONECT   51   30                                                            
CONECT   52   31                                                            
CONECT   53   32                                                            
CONECT   54   33                                                            
CONECT   55   34                                                            
CONECT   56   35                                                            
CONECT   57   36                                                            
CONECT   58   37                                                            
CONECT   59    1   22                                                       
CONECT   60   18   41                                                       
CONECT   61   19   43                                                       
CONECT   62   23   38                                                       
CONECT   63   24   41                                                       
CONECT   64   25   42                                                       
CONECT   65   26   43                                                       
CONECT   66   27   40                                                       
CONECT   67   39   42                                                       
MASTER        0    0    0    0    0    0    0    0   67    0  146    0
END

COMPND    HMDB0038763
HETATM    1  C1  UNL     1      10.605  -0.826  -1.000  1.00  0.00           C  
HETATM    2  O1  UNL     1      10.423  -2.177  -1.013  1.00  0.00           O  
HETATM    3  C2  UNL     1       9.780  -3.057  -0.226  1.00  0.00           C  
HETATM    4  C3  UNL     1       9.101  -2.695   0.908  1.00  0.00           C  
HETATM    5  C4  UNL     1       8.472  -3.593   1.699  1.00  0.00           C  
HETATM    6  C5  UNL     1       7.695  -3.327   2.883  1.00  0.00           C  
HETATM    7  C6  UNL     1       6.931  -2.338   3.074  1.00  0.00           C  
HETATM    8  C7  UNL     1       6.527  -1.214   2.326  1.00  0.00           C  
HETATM    9  O2  UNL     1       5.770  -0.405   3.011  1.00  0.00           O  
HETATM   10  O3  UNL     1       6.714  -0.750   1.059  1.00  0.00           O  
HETATM   11  C8  UNL     1       6.135   0.455   0.672  1.00  0.00           C  
HETATM   12  C9  UNL     1       5.149   0.484  -0.417  1.00  0.00           C  
HETATM   13  O4  UNL     1       3.860   0.393  -0.016  1.00  0.00           O  
HETATM   14  C10 UNL     1       2.726   1.110  -0.119  1.00  0.00           C  
HETATM   15  C11 UNL     1       2.593   2.407  -0.526  1.00  0.00           C  
HETATM   16  C12 UNL     1       1.373   3.047  -0.594  1.00  0.00           C  
HETATM   17  O5  UNL     1       1.278   4.358  -1.007  1.00  0.00           O  
HETATM   18  C13 UNL     1       0.231   2.377  -0.249  1.00  0.00           C  
HETATM   19  C14 UNL     1      -1.015   2.957  -0.298  1.00  0.00           C  
HETATM   20  O6  UNL     1      -1.084   4.146  -0.667  1.00  0.00           O  
HETATM   21  C15 UNL     1      -2.186   2.262   0.052  1.00  0.00           C  
HETATM   22  O7  UNL     1      -3.338   2.951  -0.042  1.00  0.00           O  
HETATM   23  C16 UNL     1      -4.030   3.261  -1.239  1.00  0.00           C  
HETATM   24  O8  UNL     1      -4.183   4.658  -1.306  1.00  0.00           O  
HETATM   25  C17 UNL     1      -4.461   5.061  -2.604  1.00  0.00           C  
HETATM   26  C18 UNL     1      -4.695   6.555  -2.521  1.00  0.00           C  
HETATM   27  O9  UNL     1      -4.969   7.125  -3.734  1.00  0.00           O  
HETATM   28  C19 UNL     1      -5.627   4.309  -3.188  1.00  0.00           C  
HETATM   29  O10 UNL     1      -6.546   5.229  -3.683  1.00  0.00           O  
HETATM   30  C20 UNL     1      -6.324   3.444  -2.180  1.00  0.00           C  
HETATM   31  O11 UNL     1      -7.163   2.520  -2.777  1.00  0.00           O  
HETATM   32  C21 UNL     1      -5.389   2.674  -1.261  1.00  0.00           C  
HETATM   33  O12 UNL     1      -5.345   1.326  -1.674  1.00  0.00           O  
HETATM   34  C22 UNL     1      -2.044   0.969   0.451  1.00  0.00           C  
HETATM   35  C23 UNL     1      -3.163   0.121   0.843  1.00  0.00           C  
HETATM   36  C24 UNL     1      -4.352   0.648   1.225  1.00  0.00           C  
HETATM   37  C25 UNL     1      -5.462  -0.170   1.519  1.00  0.00           C  
HETATM   38  C26 UNL     1      -5.371  -1.540   1.429  1.00  0.00           C  
HETATM   39  O13 UNL     1      -6.404  -2.405   1.695  1.00  0.00           O  
HETATM   40  C27 UNL     1      -7.706  -2.097   2.101  1.00  0.00           C  
HETATM   41  O14 UNL     1      -8.027  -2.817   3.261  1.00  0.00           O  
HETATM   42  C28 UNL     1      -7.627  -4.117   3.083  1.00  0.00           C  
HETATM   43  C29 UNL     1      -7.924  -4.888   4.369  1.00  0.00           C  
HETATM   44  O15 UNL     1      -7.243  -4.350   5.443  1.00  0.00           O  
HETATM   45  C30 UNL     1      -8.389  -4.828   1.988  1.00  0.00           C  
HETATM   46  O16 UNL     1      -7.669  -5.978   1.648  1.00  0.00           O  
HETATM   47  C31 UNL     1      -8.540  -3.992   0.748  1.00  0.00           C  
HETATM   48  O17 UNL     1      -9.677  -4.455   0.089  1.00  0.00           O  
HETATM   49  C32 UNL     1      -8.728  -2.534   1.062  1.00  0.00           C  
HETATM   50  O18 UNL     1      -9.992  -2.250   1.533  1.00  0.00           O  
HETATM   51  C33 UNL     1      -4.135  -2.077   1.038  1.00  0.00           C  
HETATM   52  C34 UNL     1      -3.066  -1.244   0.755  1.00  0.00           C  
HETATM   53  O19 UNL     1      -0.810   0.442   0.485  1.00  0.00           O  
HETATM   54  C35 UNL     1       0.290   1.054   0.169  1.00  0.00           C  
HETATM   55  C36 UNL     1       1.531   0.460   0.224  1.00  0.00           C  
HETATM   56  O20 UNL     1       5.246   1.799  -1.075  1.00  0.00           O  
HETATM   57  C37 UNL     1       6.300   1.712  -1.990  1.00  0.00           C  
HETATM   58  C38 UNL     1       6.485   3.059  -2.618  1.00  0.00           C  
HETATM   59  O21 UNL     1       7.517   3.066  -3.562  1.00  0.00           O  
HETATM   60  C39 UNL     1       7.491   1.240  -1.181  1.00  0.00           C  
HETATM   61  O22 UNL     1       7.584  -0.155  -1.425  1.00  0.00           O  
HETATM   62  C40 UNL     1       7.235   1.469   0.301  1.00  0.00           C  
HETATM   63  O23 UNL     1       8.370   1.334   1.035  1.00  0.00           O  
HETATM   64  C41 UNL     1       8.509  -4.958   1.348  1.00  0.00           C  
HETATM   65  C42 UNL     1       9.177  -5.327   0.223  1.00  0.00           C  
HETATM   66  C43 UNL     1       9.811  -4.426  -0.573  1.00  0.00           C  
HETATM   67  O24 UNL     1      10.497  -4.776  -1.724  1.00  0.00           O  
HETATM   68  H1  UNL     1      10.159  -0.312  -0.128  1.00  0.00           H  
HETATM   69  H2  UNL     1      10.272  -0.354  -1.951  1.00  0.00           H  
HETATM   70  H3  UNL     1      11.710  -0.624  -0.938  1.00  0.00           H  
HETATM   71  H4  UNL     1       9.098  -1.642   1.197  1.00  0.00           H  
HETATM   72  H5  UNL     1       7.827  -4.111   3.712  1.00  0.00           H  
HETATM   73  H6  UNL     1       6.456  -2.378   4.131  1.00  0.00           H  
HETATM   74  H7  UNL     1       5.622   0.961   1.557  1.00  0.00           H  
HETATM   75  H8  UNL     1       5.324  -0.142  -1.327  1.00  0.00           H  
HETATM   76  H9  UNL     1       3.463   2.965  -0.798  1.00  0.00           H  
HETATM   77  H10 UNL     1       2.024   4.950  -1.286  1.00  0.00           H  
HETATM   78  H11 UNL     1      -3.455   2.955  -2.137  1.00  0.00           H  
HETATM   79  H12 UNL     1      -3.549   4.908  -3.200  1.00  0.00           H  
HETATM   80  H13 UNL     1      -3.816   7.063  -2.079  1.00  0.00           H  
HETATM   81  H14 UNL     1      -5.548   6.717  -1.822  1.00  0.00           H  
HETATM   82  H15 UNL     1      -4.934   8.094  -3.711  1.00  0.00           H  
HETATM   83  H16 UNL     1      -5.285   3.697  -4.038  1.00  0.00           H  
HETATM   84  H17 UNL     1      -7.023   4.792  -4.436  1.00  0.00           H  
HETATM   85  H18 UNL     1      -6.960   4.073  -1.517  1.00  0.00           H  
HETATM   86  H19 UNL     1      -6.618   1.951  -3.397  1.00  0.00           H  
HETATM   87  H20 UNL     1      -5.815   2.674  -0.243  1.00  0.00           H  
HETATM   88  H21 UNL     1      -4.418   1.120  -1.911  1.00  0.00           H  
HETATM   89  H22 UNL     1      -4.537   1.701   1.364  1.00  0.00           H  
HETATM   90  H23 UNL     1      -6.397   0.290   1.822  1.00  0.00           H  
HETATM   91  H24 UNL     1      -7.790  -1.013   2.263  1.00  0.00           H  
HETATM   92  H25 UNL     1      -6.534  -4.140   2.950  1.00  0.00           H  
HETATM   93  H26 UNL     1      -9.004  -4.925   4.553  1.00  0.00           H  
HETATM   94  H27 UNL     1      -7.525  -5.916   4.219  1.00  0.00           H  
HETATM   95  H28 UNL     1      -7.879  -3.960   6.085  1.00  0.00           H  
HETATM   96  H29 UNL     1      -9.377  -5.147   2.397  1.00  0.00           H  
HETATM   97  H30 UNL     1      -7.883  -6.263   0.712  1.00  0.00           H  
HETATM   98  H31 UNL     1      -7.690  -4.115   0.035  1.00  0.00           H  
HETATM   99  H32 UNL     1     -10.296  -3.729  -0.151  1.00  0.00           H  
HETATM  100  H33 UNL     1      -8.489  -1.951   0.136  1.00  0.00           H  
HETATM  101  H34 UNL     1      -9.981  -1.291   1.838  1.00  0.00           H  
HETATM  102  H35 UNL     1      -4.062  -3.153   0.971  1.00  0.00           H  
HETATM  103  H36 UNL     1      -2.143  -1.752   0.460  1.00  0.00           H  
HETATM  104  H37 UNL     1       1.578  -0.584   0.556  1.00  0.00           H  
HETATM  105  H38 UNL     1       5.985   0.952  -2.756  1.00  0.00           H  
HETATM  106  H39 UNL     1       5.539   3.429  -3.052  1.00  0.00           H  
HETATM  107  H40 UNL     1       6.786   3.835  -1.862  1.00  0.00           H  
HETATM  108  H41 UNL     1       7.511   2.140  -3.966  1.00  0.00           H  
HETATM  109  H42 UNL     1       8.401   1.721  -1.514  1.00  0.00           H  
HETATM  110  H43 UNL     1       7.910  -0.352  -2.320  1.00  0.00           H  
HETATM  111  H44 UNL     1       6.756   2.480   0.361  1.00  0.00           H  
HETATM  112  H45 UNL     1       8.137   1.476   2.001  1.00  0.00           H  
HETATM  113  H46 UNL     1       8.003  -5.680   1.982  1.00  0.00           H  
HETATM  114  H47 UNL     1       9.201  -6.381  -0.046  1.00  0.00           H  
HETATM  115  H48 UNL     1      10.523  -5.750  -1.981  1.00  0.00           H  
CONECT    1    2   68   69   70
CONECT    2    3
CONECT    3    4    4   66
CONECT    4    5   71
CONECT    5    6   64   64
CONECT    6    7    7   72
CONECT    7    8   73
CONECT    8    9    9   10
CONECT   10   11
CONECT   11   12   62   74
CONECT   12   13   56   75
CONECT   13   14
CONECT   14   15   15   55
CONECT   15   16   76
CONECT   16   17   18   18
CONECT   17   77
CONECT   18   19   54
CONECT   19   20   20   21
CONECT   21   22   34   34
CONECT   22   23
CONECT   23   24   32   78
CONECT   24   25
CONECT   25   26   28   79
CONECT   26   27   80   81
CONECT   27   82
CONECT   28   29   30   83
CONECT   29   84
CONECT   30   31   32   85
CONECT   31   86
CONECT   32   33   87
CONECT   33   88
CONECT   34   35   53
CONECT   35   36   36   52
CONECT   36   37   89
CONECT   37   38   38   90
CONECT   38   39   51
CONECT   39   40
CONECT   40   41   49   91
CONECT   41   42
CONECT   42   43   45   92
CONECT   43   44   93   94
CONECT   44   95
CONECT   45   46   47   96
CONECT   46   97
CONECT   47   48   49   98
CONECT   48   99
CONECT   49   50  100
CONECT   50  101
CONECT   51   52   52  102
CONECT   52  103
CONECT   53   54
CONECT   54   55   55
CONECT   55  104
CONECT   56   57
CONECT   57   58   60  105
CONECT   58   59  106  107
CONECT   59  108
CONECT   60   61   62  109
CONECT   61  110
CONECT   62   63  111
CONECT   63  112
CONECT   64   65  113
CONECT   65   66   66  114
CONECT   66   67
CONECT   67  115
END

HMDB0038763
     RDKit          3D
Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside)
115121  0  0  0  0  0  0  0  0999 V2000
   10.6053   -0.8257   -0.9999 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4234   -2.1773   -1.0125 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7799   -3.0570   -0.2257 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1007   -2.6950    0.9085 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4719   -3.5935    1.6992 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6946   -3.3272    2.8833 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9311   -2.3381    3.0742 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5273   -1.2139    2.3265 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7704   -0.4051    3.0114 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7143   -0.7503    1.0588 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1348    0.4554    0.6719 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1488    0.4837   -0.4170 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8596    0.3929   -0.0164 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7261    1.1098   -0.1189 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5933    2.4070   -0.5255 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3734    3.0469   -0.5942 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2784    4.3579   -1.0069 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2315    2.3773   -0.2492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0151    2.9572   -0.2975 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0843    4.1463   -0.6669 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1855    2.2617    0.0520 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3381    2.9514   -0.0418 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0297    3.2615   -1.2390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1834    4.6585   -1.3060 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4606    5.0606   -2.6042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6949    6.5554   -2.5212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9695    7.1254   -3.7344 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6273    4.3085   -3.1877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5455    5.2293   -3.6826 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3242    3.4445   -2.1797 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1631    2.5196   -2.7769 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3892    2.6742   -1.2608 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3455    1.3260   -1.6735 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0444    0.9689    0.4507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1626    0.1208    0.8434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3524    0.6476    1.2246 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4623   -0.1695    1.5191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3706   -1.5396    1.4292 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4041   -2.4052    1.6946 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7059   -2.0972    2.1011 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0266   -2.8167    3.2613 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6269   -4.1173    3.0834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9240   -4.8883    4.3691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2426   -4.3498    5.4429 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3888   -4.8281    1.9879 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6688   -5.9780    1.6477 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5402   -3.9921    0.7481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6767   -4.4555    0.0895 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7283   -2.5343    1.0620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9918   -2.2497    1.5327 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1350   -2.0765    1.0375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0663   -1.2438    0.7548 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8105    0.4418    0.4847 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2899    1.0540    0.1690 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5307    0.4595    0.2237 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2457    1.7991   -1.0753 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2997    1.7122   -1.9902 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4852    3.0595   -2.6184 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5170    3.0663   -3.5623 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4913    1.2400   -1.1811 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5840   -0.1551   -1.4251 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2346    1.4687    0.3008 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3698    1.3344    1.0345 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5091   -4.9576    1.3481 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1767   -5.3269    0.2233 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8113   -4.4257   -0.5728 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4969   -4.7756   -1.7239 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1587   -0.3124   -0.1281 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2722   -0.3539   -1.9514 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.7097   -0.6237   -0.9377 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0981   -1.6416    1.1971 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8267   -4.1112    3.7125 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4559   -2.3776    4.1311 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6218    0.9612    1.5569 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3238   -0.1416   -1.3272 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4634    2.9648   -0.7979 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0244    4.9499   -1.2860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4549    2.9551   -2.1373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5493    4.9077   -3.1996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8158    7.0631   -2.0786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5479    6.7174   -1.8218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9345    8.0944   -3.7108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2846    3.6966   -4.0376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0234    4.7921   -4.4358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9601    4.0735   -1.5173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6181    1.9512   -3.3973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8147    2.6740   -0.2426 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4180    1.1204   -1.9107 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5374    1.7011    1.3636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3969    0.2896    1.8217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7905   -1.0134    2.2632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5340   -4.1405    2.9501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0037   -4.9249    4.5530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5248   -5.9161    4.2191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8788   -3.9602    6.0850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3767   -5.1472    2.3971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8829   -6.2627    0.7118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6900   -4.1153    0.0355 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2960   -3.7291   -0.1513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4894   -1.9513    0.1363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9808   -1.2907    1.8378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0620   -3.1526    0.9715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1429   -1.7519    0.4597 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5779   -0.5839    0.5564 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9852    0.9521   -2.7555 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5385    3.4295   -3.0521 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7861    3.8348   -1.8620 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5111    2.1404   -3.9661 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4014    1.7208   -1.5137 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9097   -0.3515   -2.3202 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7562    2.4804    0.3612 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1372    1.4760    2.0015 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0034   -5.6798    1.9819 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2011   -6.3813   -0.0461 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.5232   -5.7497   -1.9810 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
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M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
Kaempferol 3,4'-diglucoside-7-(2''-ferulylglucoside)	HMDB
4,5-Dihydroxy-2-[(5-hydroxy-4-oxo-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2-(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-4H-chromen-7-yl)oxy]-6-(hydroxymethyl)oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoic acid	Generator

Chemical Formula

C₄₃H₄₈O₂₄

Average Molecular Weight

948.8268

Monoisotopic Molecular Weight

948.253552464

IUPAC Name

4,5-dihydroxy-2-[(5-hydroxy-4-oxo-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2-(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-4H-chromen-7-yl)oxy]-6-(hydroxymethyl)oxan-3-yl (2Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

Traditional Name

4,5-dihydroxy-2-[(5-hydroxy-4-oxo-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2-(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)chromen-7-yl)oxy]-6-(hydroxymethyl)oxan-3-yl (2Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

CAS Registry Number

108887-46-3

SMILES

COC1=C(O)C=CC(\C=C/C(=O)OC2C(OC3=CC(O)=C4C(OC(C5=CC=C(OC6OC(CO)C(O)C(O)C6O)C=C5)=C(OC5OC(CO)C(O)C(O)C5O)C4=O)=C3)OC(CO)C(O)C2O)=C1

InChI Identifier

InChI=1S/C43H48O24/c1-59-22-10-16(2-8-20(22)47)3-9-27(49)66-40-35(56)31(52)26(15-46)65-43(40)61-19-11-21(48)28-23(12-19)62-38(39(32(28)53)67-42-37(58)34(55)30(51)25(14-45)64-42)17-4-6-18(7-5-17)60-41-36(57)33(54)29(50)24(13-44)63-41/h2-12,24-26,29-31,33-37,40-48,50-52,54-58H,13-15H2,1H3/b9-3-

InChI Key

SJOFKYITWVGVEV-OQFOIZHKSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavonoid-7-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Flavonoid-7-O-glycosides

Alternative Parents

Substituents

Flavonoid-3-o-glycoside
Flavonoid-7-o-glycoside
5-hydroxyflavonoid
Hydroxyflavonoid
Flavone
Phenolic glycoside
Cinnamic acid ester
Cinnamic acid or derivatives
Coumaric acid or derivatives
Hydroxycinnamic acid or derivatives
O-glycosyl compound
Chromone
Glycosyl compound
Methoxyphenol
Benzopyran
1-benzopyran
Styrene
Phenol ether
Anisole
Methoxybenzene
Phenoxy compound
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Fatty acid ester
Phenol
Pyranone
Pyran
Oxane
Monocyclic benzene moiety
Fatty acyl
Monosaccharide
Benzenoid
Enoate ester
Heteroaromatic compound
Alpha,beta-unsaturated carboxylic ester
Vinylogous acid
Secondary alcohol
Carboxylic acid ester
Oxacycle
Acetal
Ether
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Carboxylic acid derivative
Polyol
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
Alcohol
Carbonyl group
Organic oxide
Primary alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	214 - 217 °C	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	1.14 g/L	ALOGPS
logP	0.4	ALOGPS
logP	-1.8	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	8.29	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	23	ChemAxon
Hydrogen Donor Count	13	ChemAxon
Polar Surface Area	380.2 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	219.6 m³·mol⁻¹	ChemAxon
Polarizability	93.16 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	296.473	30932474
DeepCCS	[M-H]-	294.16	30932474
DeepCCS	[M-2H]-	327.958	30932474
DeepCCS	[M+Na]+	302.532	30932474
AllCCS	[M+H]+	278.2	32859911
AllCCS	[M+H-H2O]+	278.7	32859911
AllCCS	[M+NH4]+	277.7	32859911
AllCCS	[M+Na]+	277.5	32859911
AllCCS	[M-H]-	271.2	32859911
AllCCS	[M+Na-2H]-	276.4	32859911
AllCCS	[M+HCOO]-	282.2	32859911

Predicted Kovats Retention Indices

Not Available

Spectra

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside) 10V, Positive-QTOF	splash10-00m4-0300443904-95afcc3c8ed5f70c67a0	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside) 20V, Positive-QTOF	splash10-0002-0300935400-d13c2776f521bce48205	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside) 40V, Positive-QTOF	splash10-0002-0300914200-3c5f4d712bba54728f16	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside) 10V, Negative-QTOF	splash10-002p-0700127928-e4f874e4a99a29ac49a7	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside) 20V, Negative-QTOF	splash10-002f-0900243513-7ec10e473e586f8d9b36	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside) 40V, Negative-QTOF	splash10-002g-0900403000-17a32564012802f99a7f	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside) 10V, Negative-QTOF	splash10-0002-0000000009-803f69f065bfc3b879b1	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside) 20V, Negative-QTOF	splash10-0002-0000000509-4c5f552c7b8ea823768e	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside) 40V, Negative-QTOF	splash10-001i-0000000901-ad023746ad8c47d1e40f	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside) 10V, Positive-QTOF	splash10-000i-0000000902-6bdd95752f4fbf5ac556	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside) 20V, Positive-QTOF	splash10-000k-0000000909-9e731af607f5470d2733	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside) 40V, Positive-QTOF	splash10-000i-0000000900-18589d4f34dcca3daef3	2021-09-25	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
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, 100 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, 1000 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, 200 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, 300 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, 400 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, 500 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, 600 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, 700 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, 800 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
Predicted 1D NMR	¹³C 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

FDB018180

KNApSAcK ID

C00005925

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

131752457

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

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MarkerDB ID

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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 Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside) (HMDB0038763)

MOL for HMDB0038763 (Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside))

3D MOL for HMDB0038763 (Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside))

3D SDF for HMDB0038763 (Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside))

3D-SDF for HMDB0038763 (Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside))

PDB for HMDB0038763 (Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside))

3D PDB for HMDB0038763 (Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside))

SMILES for HMDB0038763 (Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside))

INCHI for HMDB0038763 (Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside))

Structure for HMDB0038763 (Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside))

3D Structure for HMDB0038763 (Kaempferol 3,4'-diglucoside 7-(2-feruloylglucoside))

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

MS/MS Spectra

NMR Spectra