Jump To Section:

Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References XML

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 17:32:32 UTC

Update Date

2022-03-07 02:52:17 UTC

HMDB ID

HMDB0029770

Secondary Accession Numbers

HMDB29770

Metabolite Identification

Common Name

7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside]

Description

7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol. Based on a literature review a small amount of articles have been published on 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside].

Structure

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

  Mrv0541 02241208462D          

 37 39  0  0  0  0            999 V2000
   -4.6421   -1.2395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6421   -2.0646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3571   -2.4771    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9285   -2.4771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2149   -2.0646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4998   -2.4771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4579   -0.1945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9285   -0.8271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3963   -0.1945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2149   -1.2395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4998   -0.8271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7875   -1.2395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0739   -0.8271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3603   -1.2395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0739   -0.0034    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4998   -1.6521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3603    0.4091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3547   -0.0034    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0725    0.4091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0725    1.2355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3547    1.6521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3603    1.2355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0739    1.6521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3547    2.4771    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7875    1.6521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7875   -0.0034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5011    0.4091    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2162   -0.0034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2162   -0.8284    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9298   -1.2409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6421   -0.8284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6421   -0.0034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9298    0.4077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9298    1.2327    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3571    0.4091    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3571   -1.2409    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9298   -2.0659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  8  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  5 10  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 16  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 22  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 26  1  0  0  0  0
 20 21  1  0  0  0  0
 20 25  1  0  0  0  0
 21 22  1  0  0  0  0
 21 24  1  0  0  0  0
 22 23  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 33  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 37  1  0  0  0  0
 31 32  1  0  0  0  0
 31 36  1  0  0  0  0
 32 33  1  0  0  0  0
 32 35  1  0  0  0  0
 33 34  1  0  0  0  0
M  END

HMDB0029770
     RDKit          3D
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside]
 79 81  0  0  0  0  0  0  0  0999 V2000
   -5.5126    0.6872    1.9750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7191    0.0817    0.6618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9050   -0.3717    0.3181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1274   -0.9864   -1.0075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1071   -1.7625   -1.1626 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2251   -0.6986   -2.1215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1679    0.2719   -1.7182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0345    0.3529   -2.6861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7983    1.6620   -1.6290 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5939   -0.0307   -0.3132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6086    0.9157   -0.1074 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0433   -1.4066   -0.3911 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4989   -1.9779    0.8828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3601   -1.2785    1.4890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0194   -2.0683    2.7977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2157   -1.1081    0.7642 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6300    0.0954    0.6791 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5844    0.0689    1.3996 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5702   -0.6850    0.8644 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8643    0.1454    0.9266 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9241   -0.5869    0.4002 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1180    0.1289    0.4258 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0380   -0.4393    1.3057 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1117    0.4131    1.4213 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7218    1.8100    1.8272 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9111    0.4791    0.1684 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0169   -0.3904    0.3148 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1409    0.1223   -1.0710 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6068    0.9339   -2.1067 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6619    0.3191   -0.9479 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2656    1.5369   -1.4964 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4182   -1.1020   -0.5727 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6404   -2.2634   -0.6324 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8443    0.0247   -1.3721 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7979    0.9903   -1.6974 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3027    0.6401   -0.6653 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0055    2.0121   -0.4589 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3558    1.3465    2.2942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4916   -0.1357    2.7398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5519    1.2251    2.0794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7659   -0.3206    0.9715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8182   -1.6503   -2.5227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7798   -0.2309   -2.9778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5962   -0.6234   -2.9366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3086    1.0955   -2.2863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4571    0.8009   -3.6279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4799    1.7790   -0.7892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3449    1.9118   -2.5529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0107    2.4431   -1.5181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9254    1.8055    0.1043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7514   -2.1500   -0.8127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1793   -1.3674   -1.1101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3666   -1.9156    1.6142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3676   -3.0837    0.7854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6706   -0.2996    1.8792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0471   -1.7512    3.1917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7832   -1.8261    3.5650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1122   -3.1531    2.5910 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1950    0.9053    1.2427 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8199   -1.5945    1.4734 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7615    1.1075    0.3967 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0674    0.3711    1.9991 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8812    1.1256    0.8568 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7540    0.0186    2.2532 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5991    2.2720    2.3252 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8871    1.8428    2.5478 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5268    2.4448    0.9210 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3657    1.4907    0.0943 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2837   -0.4465    1.2732 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3972   -0.9255   -1.3633 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6058    1.0065   -2.1120 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1909   -0.4680   -1.6117 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7383    1.6772   -2.3608 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4346   -1.2974   -1.0124 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2729   -3.0379   -0.5742 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4666   -0.4703   -2.3308 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5592    0.4965   -2.1296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1729    0.6728   -1.3546 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5477    2.3737   -1.2024 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  7 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 19 32  1  0
 32 33  1  0
 32 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  1  0
 10  2  1  0
 36 17  1  0
 30 22  1  0
  1 38  1  0
  1 39  1  0
  1 40  1  0
  3 41  1  0
  6 42  1  0
  6 43  1  0
  8 44  1  0
  8 45  1  0
  8 46  1  0
  9 47  1  0
  9 48  1  0
  9 49  1  0
 11 50  1  0
 12 51  1  0
 12 52  1  0
 13 53  1  0
 13 54  1  0
 14 55  1  0
 15 56  1  0
 15 57  1  0
 15 58  1  0
 17 59  1  0
 19 60  1  0
 20 61  1  0
 20 62  1  0
 22 63  1  0
 24 64  1  0
 25 65  1  0
 25 66  1  0
 25 67  1  0
 26 68  1  0
 27 69  1  0
 28 70  1  0
 29 71  1  0
 30 72  1  0
 31 73  1  0
 32 74  1  0
 33 75  1  0
 34 76  1  0
 35 77  1  0
 36 78  1  0
 37 79  1  0
M  END

  Mrv0541 02241208462D          

 37 39  0  0  0  0            999 V2000
   -4.6421   -1.2395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6421   -2.0646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3571   -2.4771    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9285   -2.4771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2149   -2.0646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4998   -2.4771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4579   -0.1945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9285   -0.8271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3963   -0.1945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2149   -1.2395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4998   -0.8271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7875   -1.2395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0739   -0.8271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3603   -1.2395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0739   -0.0034    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4998   -1.6521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3603    0.4091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3547   -0.0034    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0725    0.4091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0725    1.2355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3547    1.6521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3603    1.2355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0739    1.6521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3547    2.4771    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7875    1.6521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7875   -0.0034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5011    0.4091    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2162   -0.0034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2162   -0.8284    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9298   -1.2409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6421   -0.8284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6421   -0.0034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9298    0.4077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9298    1.2327    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3571    0.4091    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3571   -1.2409    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9298   -2.0659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  8  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  5 10  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 16  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 22  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 26  1  0  0  0  0
 20 21  1  0  0  0  0
 20 25  1  0  0  0  0
 21 22  1  0  0  0  0
 21 24  1  0  0  0  0
 22 23  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 33  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 37  1  0  0  0  0
 31 32  1  0  0  0  0
 31 36  1  0  0  0  0
 32 33  1  0  0  0  0
 32 35  1  0  0  0  0
 33 34  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0029770

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(CCC1(O)C(C)=CC(=O)CC1(C)C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C25H42O12/c1-11-8-14(26)9-24(4,5)25(11,33)7-6-12(2)35-23-21(32)19(30)17(28)15(37-23)10-34-22-20(31)18(29)16(27)13(3)36-22/h8,12-13,15-23,27-33H,6-7,9-10H2,1-5H3

> <INCHI_KEY>
JDTFCGGOAXAFRS-UHFFFAOYSA-N

> <FORMULA>
C25H42O12

> <MOLECULAR_WEIGHT>
534.5938

> <EXACT_MASS>
534.267626808

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_AVERAGE_POLARIZABILITY>
55.90662308845132

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-hydroxy-3,5,5-trimethyl-4-{3-[(3,4,5-trihydroxy-6-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}oxan-2-yl)oxy]butyl}cyclohex-2-en-1-one

> <ALOGPS_LOGP>
-0.75

> <JCHEM_LOGP>
-1.0256555530000007

> <ALOGPS_LOGS>
-2.11

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.431112652714624

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.911714993346855

> <JCHEM_PKA_STRONGEST_BASIC>
-3.325702908087968

> <JCHEM_POLAR_SURFACE_AREA>
195.6

> <JCHEM_REFRACTIVITY>
127.40149999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.16e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-hydroxy-3,5,5-trimethyl-4-{3-[(3,4,5-trihydroxy-6-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}oxan-2-yl)oxy]butyl}cyclohex-2-en-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0029770
     RDKit          3D
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside]
 79 81  0  0  0  0  0  0  0  0999 V2000
   -5.5126    0.6872    1.9750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7191    0.0817    0.6618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9050   -0.3717    0.3181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1274   -0.9864   -1.0075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1071   -1.7625   -1.1626 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2251   -0.6986   -2.1215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1679    0.2719   -1.7182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0345    0.3529   -2.6861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7983    1.6620   -1.6290 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5939   -0.0307   -0.3132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6086    0.9157   -0.1074 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0433   -1.4066   -0.3911 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4989   -1.9779    0.8828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3601   -1.2785    1.4890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0194   -2.0683    2.7977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2157   -1.1081    0.7642 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6300    0.0954    0.6791 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5844    0.0689    1.3996 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5702   -0.6850    0.8644 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8643    0.1454    0.9266 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9241   -0.5869    0.4002 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1180    0.1289    0.4258 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0380   -0.4393    1.3057 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1117    0.4131    1.4213 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7218    1.8100    1.8272 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9111    0.4791    0.1684 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0169   -0.3904    0.3148 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1409    0.1223   -1.0710 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6068    0.9339   -2.1067 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6619    0.3191   -0.9479 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2656    1.5369   -1.4964 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4182   -1.1020   -0.5727 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6404   -2.2634   -0.6324 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8443    0.0247   -1.3721 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7979    0.9903   -1.6974 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3027    0.6401   -0.6653 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0055    2.0121   -0.4589 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3558    1.3465    2.2942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4916   -0.1357    2.7398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5519    1.2251    2.0794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7659   -0.3206    0.9715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8182   -1.6503   -2.5227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7798   -0.2309   -2.9778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5962   -0.6234   -2.9366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3086    1.0955   -2.2863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4571    0.8009   -3.6279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4799    1.7790   -0.7892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3449    1.9118   -2.5529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0107    2.4431   -1.5181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9254    1.8055    0.1043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7514   -2.1500   -0.8127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1793   -1.3674   -1.1101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3666   -1.9156    1.6142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3676   -3.0837    0.7854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6706   -0.2996    1.8792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0471   -1.7512    3.1917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7832   -1.8261    3.5650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1122   -3.1531    2.5910 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1950    0.9053    1.2427 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8199   -1.5945    1.4734 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7615    1.1075    0.3967 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0674    0.3711    1.9991 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8812    1.1256    0.8568 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7540    0.0186    2.2532 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5991    2.2720    2.3252 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8871    1.8428    2.5478 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5268    2.4448    0.9210 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3657    1.4907    0.0943 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2837   -0.4465    1.2732 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3972   -0.9255   -1.3633 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6058    1.0065   -2.1120 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1909   -0.4680   -1.6117 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7383    1.6772   -2.3608 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4346   -1.2974   -1.0124 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2729   -3.0379   -0.5742 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4666   -0.4703   -2.3308 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5592    0.4965   -2.1296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1729    0.6728   -1.3546 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5477    2.3737   -1.2024 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  7 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 19 32  1  0
 32 33  1  0
 32 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  1  0
 10  2  1  0
 36 17  1  0
 30 22  1  0
  1 38  1  0
  1 39  1  0
  1 40  1  0
  3 41  1  0
  6 42  1  0
  6 43  1  0
  8 44  1  0
  8 45  1  0
  8 46  1  0
  9 47  1  0
  9 48  1  0
  9 49  1  0
 11 50  1  0
 12 51  1  0
 12 52  1  0
 13 53  1  0
 13 54  1  0
 14 55  1  0
 15 56  1  0
 15 57  1  0
 15 58  1  0
 17 59  1  0
 19 60  1  0
 20 61  1  0
 20 62  1  0
 22 63  1  0
 24 64  1  0
 25 65  1  0
 25 66  1  0
 25 67  1  0
 26 68  1  0
 27 69  1  0
 28 70  1  0
 29 71  1  0
 30 72  1  0
 31 73  1  0
 32 74  1  0
 33 75  1  0
 34 76  1  0
 35 77  1  0
 36 78  1  0
 37 79  1  0
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -8.665  -2.314   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -8.665  -3.854   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0     -10.000  -4.624   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -7.333  -4.624   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.001  -3.854   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.666  -4.624   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -8.321  -0.363   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -7.333  -1.544   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -6.340  -0.363   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -6.001  -2.314   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.666  -1.544   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.337  -2.314   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.005  -1.544   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.673  -2.314   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -2.005  -0.006   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      -4.666  -3.084   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -0.673   0.764   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       0.662  -0.006   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.002   0.764   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.002   2.306   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.662   3.084   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.673   2.306   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -2.005   3.084   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       0.662   4.624   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       3.337   3.084   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       3.337  -0.006   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       4.669   0.764   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       6.004  -0.006   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       6.004  -1.546   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       7.336  -2.316   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       8.665  -1.546   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.665  -0.006   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       7.336   0.761   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       7.336   2.301   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      10.000   0.764   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      10.000  -2.316   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       7.336  -3.856   0.000  0.00  0.00           C+0
CONECT    1    2    8                                                       
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5                                                            
CONECT    7    8                                                            
CONECT    8    1    7    9   10                                             
CONECT    9    8                                                            
CONECT   10    5    8   11   16                                             
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   17                                                       
CONECT   16   10                                                            
CONECT   17   15   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   26                                                  
CONECT   20   19   21   25                                                  
CONECT   21   20   22   24                                                  
CONECT   22   17   21   23                                                  
CONECT   23   22                                                            
CONECT   24   21                                                            
CONECT   25   20                                                            
CONECT   26   19   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   33                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   37                                                  
CONECT   31   30   32   36                                                  
CONECT   32   31   33   35                                                  
CONECT   33   28   32   34                                                  
CONECT   34   33                                                            
CONECT   35   32                                                            
CONECT   36   31                                                            
CONECT   37   30                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   78    0
END

COMPND    HMDB0029770
HETATM    1  C1  UNL     1      -5.513   0.687   1.975  1.00  0.00           C  
HETATM    2  C2  UNL     1      -5.719   0.082   0.662  1.00  0.00           C  
HETATM    3  C3  UNL     1      -6.905  -0.372   0.318  1.00  0.00           C  
HETATM    4  C4  UNL     1      -7.127  -0.986  -1.007  1.00  0.00           C  
HETATM    5  O1  UNL     1      -8.107  -1.763  -1.163  1.00  0.00           O  
HETATM    6  C5  UNL     1      -6.225  -0.699  -2.121  1.00  0.00           C  
HETATM    7  C6  UNL     1      -5.168   0.272  -1.718  1.00  0.00           C  
HETATM    8  C7  UNL     1      -4.035   0.353  -2.686  1.00  0.00           C  
HETATM    9  C8  UNL     1      -5.798   1.662  -1.629  1.00  0.00           C  
HETATM   10  C9  UNL     1      -4.594  -0.031  -0.313  1.00  0.00           C  
HETATM   11  O2  UNL     1      -3.609   0.916  -0.107  1.00  0.00           O  
HETATM   12  C10 UNL     1      -4.043  -1.407  -0.391  1.00  0.00           C  
HETATM   13  C11 UNL     1      -3.499  -1.978   0.883  1.00  0.00           C  
HETATM   14  C12 UNL     1      -2.360  -1.278   1.489  1.00  0.00           C  
HETATM   15  C13 UNL     1      -2.019  -2.068   2.798  1.00  0.00           C  
HETATM   16  O3  UNL     1      -1.216  -1.108   0.764  1.00  0.00           O  
HETATM   17  C14 UNL     1      -0.630   0.095   0.679  1.00  0.00           C  
HETATM   18  O4  UNL     1       0.584   0.069   1.400  1.00  0.00           O  
HETATM   19  C15 UNL     1       1.570  -0.685   0.864  1.00  0.00           C  
HETATM   20  C16 UNL     1       2.864   0.145   0.927  1.00  0.00           C  
HETATM   21  O5  UNL     1       3.924  -0.587   0.400  1.00  0.00           O  
HETATM   22  C17 UNL     1       5.118   0.129   0.426  1.00  0.00           C  
HETATM   23  O6  UNL     1       6.038  -0.439   1.306  1.00  0.00           O  
HETATM   24  C18 UNL     1       7.112   0.413   1.421  1.00  0.00           C  
HETATM   25  C19 UNL     1       6.722   1.810   1.827  1.00  0.00           C  
HETATM   26  C20 UNL     1       7.911   0.479   0.168  1.00  0.00           C  
HETATM   27  O7  UNL     1       9.017  -0.390   0.315  1.00  0.00           O  
HETATM   28  C21 UNL     1       7.141   0.122  -1.071  1.00  0.00           C  
HETATM   29  O8  UNL     1       7.607   0.934  -2.107  1.00  0.00           O  
HETATM   30  C22 UNL     1       5.662   0.319  -0.948  1.00  0.00           C  
HETATM   31  O9  UNL     1       5.266   1.537  -1.496  1.00  0.00           O  
HETATM   32  C23 UNL     1       1.418  -1.102  -0.573  1.00  0.00           C  
HETATM   33  O10 UNL     1       0.640  -2.263  -0.632  1.00  0.00           O  
HETATM   34  C24 UNL     1       0.844   0.025  -1.372  1.00  0.00           C  
HETATM   35  O11 UNL     1       1.798   0.990  -1.697  1.00  0.00           O  
HETATM   36  C25 UNL     1      -0.303   0.640  -0.665  1.00  0.00           C  
HETATM   37  O12 UNL     1       0.006   2.012  -0.459  1.00  0.00           O  
HETATM   38  H1  UNL     1      -6.356   1.346   2.294  1.00  0.00           H  
HETATM   39  H2  UNL     1      -5.492  -0.136   2.740  1.00  0.00           H  
HETATM   40  H3  UNL     1      -4.552   1.225   2.079  1.00  0.00           H  
HETATM   41  H4  UNL     1      -7.766  -0.321   0.972  1.00  0.00           H  
HETATM   42  H5  UNL     1      -5.818  -1.650  -2.523  1.00  0.00           H  
HETATM   43  H6  UNL     1      -6.780  -0.231  -2.978  1.00  0.00           H  
HETATM   44  H7  UNL     1      -3.596  -0.623  -2.937  1.00  0.00           H  
HETATM   45  H8  UNL     1      -3.309   1.096  -2.286  1.00  0.00           H  
HETATM   46  H9  UNL     1      -4.457   0.801  -3.628  1.00  0.00           H  
HETATM   47  H10 UNL     1      -6.480   1.779  -0.789  1.00  0.00           H  
HETATM   48  H11 UNL     1      -6.345   1.912  -2.553  1.00  0.00           H  
HETATM   49  H12 UNL     1      -5.011   2.443  -1.518  1.00  0.00           H  
HETATM   50  H13 UNL     1      -3.925   1.806   0.104  1.00  0.00           H  
HETATM   51  H14 UNL     1      -4.751  -2.150  -0.813  1.00  0.00           H  
HETATM   52  H15 UNL     1      -3.179  -1.367  -1.110  1.00  0.00           H  
HETATM   53  H16 UNL     1      -4.367  -1.916   1.614  1.00  0.00           H  
HETATM   54  H17 UNL     1      -3.368  -3.084   0.785  1.00  0.00           H  
HETATM   55  H18 UNL     1      -2.671  -0.300   1.879  1.00  0.00           H  
HETATM   56  H19 UNL     1      -1.047  -1.751   3.192  1.00  0.00           H  
HETATM   57  H20 UNL     1      -2.783  -1.826   3.565  1.00  0.00           H  
HETATM   58  H21 UNL     1      -2.112  -3.153   2.591  1.00  0.00           H  
HETATM   59  H22 UNL     1      -1.195   0.905   1.243  1.00  0.00           H  
HETATM   60  H23 UNL     1       1.820  -1.594   1.473  1.00  0.00           H  
HETATM   61  H24 UNL     1       2.762   1.107   0.397  1.00  0.00           H  
HETATM   62  H25 UNL     1       3.067   0.371   1.999  1.00  0.00           H  
HETATM   63  H26 UNL     1       4.881   1.126   0.857  1.00  0.00           H  
HETATM   64  H27 UNL     1       7.754   0.019   2.253  1.00  0.00           H  
HETATM   65  H28 UNL     1       7.599   2.272   2.325  1.00  0.00           H  
HETATM   66  H29 UNL     1       5.887   1.843   2.548  1.00  0.00           H  
HETATM   67  H30 UNL     1       6.527   2.445   0.921  1.00  0.00           H  
HETATM   68  H31 UNL     1       8.366   1.491   0.094  1.00  0.00           H  
HETATM   69  H32 UNL     1       9.284  -0.447   1.273  1.00  0.00           H  
HETATM   70  H33 UNL     1       7.397  -0.925  -1.363  1.00  0.00           H  
HETATM   71  H34 UNL     1       8.606   1.006  -2.112  1.00  0.00           H  
HETATM   72  H35 UNL     1       5.191  -0.468  -1.612  1.00  0.00           H  
HETATM   73  H36 UNL     1       5.738   1.677  -2.361  1.00  0.00           H  
HETATM   74  H37 UNL     1       2.435  -1.297  -1.012  1.00  0.00           H  
HETATM   75  H38 UNL     1       1.273  -3.038  -0.574  1.00  0.00           H  
HETATM   76  H39 UNL     1       0.467  -0.470  -2.331  1.00  0.00           H  
HETATM   77  H40 UNL     1       2.559   0.496  -2.130  1.00  0.00           H  
HETATM   78  H41 UNL     1      -1.173   0.673  -1.355  1.00  0.00           H  
HETATM   79  H42 UNL     1       0.548   2.374  -1.202  1.00  0.00           H  
CONECT    1    2   38   39   40
CONECT    2    3    3   10
CONECT    3    4   41
CONECT    4    5    5    6
CONECT    6    7   42   43
CONECT    7    8    9   10
CONECT    8   44   45   46
CONECT    9   47   48   49
CONECT   10   11   12
CONECT   11   50
CONECT   12   13   51   52
CONECT   13   14   53   54
CONECT   14   15   16   55
CONECT   15   56   57   58
CONECT   16   17
CONECT   17   18   36   59
CONECT   18   19
CONECT   19   20   32   60
CONECT   20   21   61   62
CONECT   21   22
CONECT   22   23   30   63
CONECT   23   24
CONECT   24   25   26   64
CONECT   25   65   66   67
CONECT   26   27   28   68
CONECT   27   69
CONECT   28   29   30   70
CONECT   29   71
CONECT   30   31   72
CONECT   31   73
CONECT   32   33   34   74
CONECT   33   75
CONECT   34   35   36   76
CONECT   35   77
CONECT   36   37   78
CONECT   37   79
END

HMDB0029770
     RDKit          3D
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside]
 79 81  0  0  0  0  0  0  0  0999 V2000
   -5.5126    0.6872    1.9750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7191    0.0817    0.6618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9050   -0.3717    0.3181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1274   -0.9864   -1.0075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1071   -1.7625   -1.1626 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2251   -0.6986   -2.1215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1679    0.2719   -1.7182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0345    0.3529   -2.6861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7983    1.6620   -1.6290 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5939   -0.0307   -0.3132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6086    0.9157   -0.1074 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0433   -1.4066   -0.3911 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4989   -1.9779    0.8828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3601   -1.2785    1.4890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0194   -2.0683    2.7977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2157   -1.1081    0.7642 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6300    0.0954    0.6791 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5844    0.0689    1.3996 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5702   -0.6850    0.8644 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8643    0.1454    0.9266 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9241   -0.5869    0.4002 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1180    0.1289    0.4258 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0380   -0.4393    1.3057 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1117    0.4131    1.4213 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7218    1.8100    1.8272 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9111    0.4791    0.1684 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0169   -0.3904    0.3148 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1409    0.1223   -1.0710 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6068    0.9339   -2.1067 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6619    0.3191   -0.9479 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2656    1.5369   -1.4964 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4182   -1.1020   -0.5727 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6404   -2.2634   -0.6324 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8443    0.0247   -1.3721 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7979    0.9903   -1.6974 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3027    0.6401   -0.6653 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0055    2.0121   -0.4589 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3558    1.3465    2.2942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4916   -0.1357    2.7398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5519    1.2251    2.0794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7659   -0.3206    0.9715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8182   -1.6503   -2.5227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7798   -0.2309   -2.9778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5962   -0.6234   -2.9366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3086    1.0955   -2.2863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4571    0.8009   -3.6279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4799    1.7790   -0.7892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3449    1.9118   -2.5529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0107    2.4431   -1.5181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9254    1.8055    0.1043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7514   -2.1500   -0.8127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1793   -1.3674   -1.1101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3666   -1.9156    1.6142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3676   -3.0837    0.7854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6706   -0.2996    1.8792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0471   -1.7512    3.1917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7832   -1.8261    3.5650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1122   -3.1531    2.5910 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1950    0.9053    1.2427 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8199   -1.5945    1.4734 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7615    1.1075    0.3967 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0674    0.3711    1.9991 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8812    1.1256    0.8568 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7540    0.0186    2.2532 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5991    2.2720    2.3252 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8871    1.8428    2.5478 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5268    2.4448    0.9210 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3657    1.4907    0.0943 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2837   -0.4465    1.2732 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3972   -0.9255   -1.3633 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6058    1.0065   -2.1120 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1909   -0.4680   -1.6117 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7383    1.6772   -2.3608 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4346   -1.2974   -1.0124 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2729   -3.0379   -0.5742 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4666   -0.4703   -2.3308 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5592    0.4965   -2.1296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1729    0.6728   -1.3546 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5477    2.3737   -1.2024 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  7 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 19 32  1  0
 32 33  1  0
 32 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  1  0
 10  2  1  0
 36 17  1  0
 30 22  1  0
  1 38  1  0
  1 39  1  0
  1 40  1  0
  3 41  1  0
  6 42  1  0
  6 43  1  0
  8 44  1  0
  8 45  1  0
  8 46  1  0
  9 47  1  0
  9 48  1  0
  9 49  1  0
 11 50  1  0
 12 51  1  0
 12 52  1  0
 13 53  1  0
 13 54  1  0
 14 55  1  0
 15 56  1  0
 15 57  1  0
 15 58  1  0
 17 59  1  0
 19 60  1  0
 20 61  1  0
 20 62  1  0
 22 63  1  0
 24 64  1  0
 25 65  1  0
 25 66  1  0
 25 67  1  0
 26 68  1  0
 27 69  1  0
 28 70  1  0
 29 71  1  0
 30 72  1  0
 31 73  1  0
 32 74  1  0
 33 75  1  0
 34 76  1  0
 35 77  1  0
 36 78  1  0
 37 79  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₅H₄₂O₁₂

Average Molecular Weight

534.5938

Monoisotopic Molecular Weight

534.267626808

IUPAC Name

4-hydroxy-3,5,5-trimethyl-4-{3-[(3,4,5-trihydroxy-6-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}oxan-2-yl)oxy]butyl}cyclohex-2-en-1-one

Traditional Name

4-hydroxy-3,5,5-trimethyl-4-{3-[(3,4,5-trihydroxy-6-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}oxan-2-yl)oxy]butyl}cyclohex-2-en-1-one

CAS Registry Number

177261-69-7

SMILES

CC(CCC1(O)C(C)=CC(=O)CC1(C)C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O)C1O

InChI Identifier

InChI=1S/C25H42O12/c1-11-8-14(26)9-24(4,5)25(11,33)7-6-12(2)35-23-21(32)19(30)17(28)15(37-23)10-34-22-20(31)18(29)16(27)13(3)36-22/h8,12-13,15-23,27-33H,6-7,9-10H2,1-5H3

InChI Key

JDTFCGGOAXAFRS-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acyl glycosides

Direct Parent

Fatty acyl glycosides of mono- and disaccharides

Alternative Parents

Substituents

Fatty acyl glycoside of mono- or disaccharide
Megastigmane sesquiterpenoid
Sesquiterpenoid
Alkyl glycoside
Disaccharide
Glycosyl compound
O-glycosyl compound
Cyclohexenone
Oxane
Tertiary alcohol
Ketone
Cyclic ketone
Secondary alcohol
Acetal
Oxacycle
Organoheterocyclic compound
Polyol
Hydrocarbon derivative
Organic oxide
Carbonyl group
Alcohol
Organic oxygen compound
Organooxygen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Excreta

Biofluid or Excreta

Urine (HMDB: HMDB0029770)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0029770)

Source

Endogenous

Endogenous (HMDB: HMDB0029770)

Plant

Plant (HMDB: HMDB0029770)

Animal

Animal (HMDB: HMDB0029770)

Exogenous

Food

Food (HMDB: HMDB0029770)

Fruit

Fruits (FooDB: FOOD00871)

Exogenous (HMDB: HMDB0029770)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0029770)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0029770)

Lipid metabolism pathway (HMDB: HMDB0029770)

Biochemical process

Lipid transport (HMDB: HMDB0029770)

Role

Biological role

Energy source (HMDB: HMDB0029770)

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	4.16 g/L	ALOGPS
logP	-0.75	ALOGPS
logP	-1	ChemAxon
logS	-2.1	ALOGPS
pKa (Strongest Acidic)	11.91	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	195.6 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	127.4 m³·mol⁻¹	ChemAxon
Polarizability	55.91 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	221.371	31661259
DarkChem	[M-H]-	214.959	31661259
DeepCCS	[M+H]+	218.285	30932474
DeepCCS	[M-H]-	215.889	30932474
DeepCCS	[M-2H]-	248.773	30932474
DeepCCS	[M+Na]+	224.291	30932474
AllCCS	[M+H]+	227.5	32859911
AllCCS	[M+H-H2O]+	226.1	32859911
AllCCS	[M+NH4]+	228.7	32859911
AllCCS	[M+Na]+	229.0	32859911
AllCCS	[M-H]-	219.8	32859911
AllCCS	[M+Na-2H]-	222.1	32859911
AllCCS	[M+HCOO]-	224.7	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside]	CC(CCC1(O)C(C)=CC(=O)CC1(C)C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O)C1O	4868.6	Standard polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside]	CC(CCC1(O)C(C)=CC(=O)CC1(C)C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O)C1O	3805.8	Standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside]	CC(CCC1(O)C(C)=CC(=O)CC1(C)C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O)C1O	4145.1	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],1TMS,isomer #1	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O)C1O)O[Si](C)(C)C	4122.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],1TMS,isomer #2	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O	4128.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],1TMS,isomer #3	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	4093.5	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],1TMS,isomer #4	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	4096.4	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],1TMS,isomer #5	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	4129.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],1TMS,isomer #6	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	4110.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],1TMS,isomer #7	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C	4115.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],1TMS,isomer #8	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O)C1O	4097.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #1	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O)O[Si](C)(C)C	4019.4	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #10	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	4046.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #11	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	4003.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #12	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C	4033.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #13	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O	3998.4	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #14	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O	4007.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #15	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O	3995.4	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #16	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O	3954.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #17	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C	3982.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #18	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	3931.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #19	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O	4021.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #2	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O)O[Si](C)(C)C	3959.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #20	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O	3977.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #21	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C	4013.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #22	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	3975.4	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #23	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4019.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #24	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4015.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #25	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	4006.5	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #26	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4021.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #27	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	3949.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #28	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C	3994.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #3	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O)O[Si](C)(C)C	3988.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #4	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O)O[Si](C)(C)C	4030.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #5	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O)O[Si](C)(C)C	3982.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #6	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C)O[Si](C)(C)C	4014.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #7	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O)C1O)O[Si](C)(C)C	3984.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #8	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	3994.4	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TMS,isomer #9	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	3986.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #1	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O)O[Si](C)(C)C	3864.5	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #10	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C)O[Si](C)(C)C	3845.4	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #11	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O)O[Si](C)(C)C	3767.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #12	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O)O[Si](C)(C)C	3896.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #13	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O)O[Si](C)(C)C	3842.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #14	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C)O[Si](C)(C)C	3883.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #15	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O)O[Si](C)(C)C	3833.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #16	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)O[Si](C)(C)C	3900.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #17	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)O[Si](C)(C)C	3907.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #18	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O)O[Si](C)(C)C	3863.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #19	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)O[Si](C)(C)C	3907.4	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #2	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O)O[Si](C)(C)C	3864.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #20	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O)O[Si](C)(C)C	3788.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #21	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C)O[Si](C)(C)C	3854.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #22	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O	3901.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #23	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O	3878.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #24	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O	3825.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #25	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C	3865.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #26	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	3802.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #27	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O	3876.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #28	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O	3823.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #29	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C	3862.5	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #3	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O)O[Si](C)(C)C	3934.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #30	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	3818.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #31	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3896.4	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #32	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3901.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #33	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	3870.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #34	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3905.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #35	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	3800.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #36	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C	3862.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #37	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O	3888.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #38	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O	3834.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #39	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C	3875.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #4	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O)O[Si](C)(C)C	3886.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #40	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O	3821.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #41	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3831.5	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #42	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3843.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #43	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O	3792.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #44	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3843.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #45	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O	3736.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #46	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C	3789.5	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #47	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3865.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #48	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3872.5	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #49	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O	3848.4	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #5	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C)O[Si](C)(C)C	3915.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #50	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3874.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #51	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O	3785.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #52	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C	3837.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #53	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3920.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #54	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3823.5	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #55	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3836.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #56	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3834.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #6	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O)O[Si](C)(C)C	3859.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #7	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O)O[Si](C)(C)C	3876.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #8	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O)O[Si](C)(C)C	3866.4	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TMS,isomer #9	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O)O[Si](C)(C)C	3822.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #1	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O)O[Si](C)(C)C	3784.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #10	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)O[Si](C)(C)C	3799.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #11	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)O[Si](C)(C)C	3804.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #12	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O)O[Si](C)(C)C	3714.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #13	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)O[Si](C)(C)C	3803.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #14	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O)O[Si](C)(C)C	3659.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #15	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C)O[Si](C)(C)C	3700.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #16	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O)O[Si](C)(C)C	3772.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #17	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O)O[Si](C)(C)C	3734.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #18	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C)O[Si](C)(C)C	3745.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #19	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O)O[Si](C)(C)C	3662.5	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #2	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O)O[Si](C)(C)C	3770.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #20	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)O[Si](C)(C)C	3738.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #21	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)O[Si](C)(C)C	3736.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #22	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O)O[Si](C)(C)C	3629.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #23	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)O[Si](C)(C)C	3738.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #24	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O)O[Si](C)(C)C	3592.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #25	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C)O[Si](C)(C)C	3608.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #26	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)O[Si](C)(C)C	3753.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #27	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)O[Si](C)(C)C	3756.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #28	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O)O[Si](C)(C)C	3677.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #29	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)O[Si](C)(C)C	3755.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #3	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O)O[Si](C)(C)C	3736.5	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #30	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O)O[Si](C)(C)C	3619.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #31	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C)O[Si](C)(C)C	3659.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #32	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)O[Si](C)(C)C	3820.4	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #33	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)O[Si](C)(C)C	3678.4	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #34	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)O[Si](C)(C)C	3690.5	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #35	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)O[Si](C)(C)C	3683.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #36	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O	3795.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #37	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O	3737.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #38	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C	3770.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #39	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O	3716.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #4	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C)O[Si](C)(C)C	3744.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #40	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3735.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #41	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3739.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #42	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O	3681.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #43	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3738.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #44	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O	3631.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #45	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C	3664.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #46	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3733.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #47	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3742.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #48	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O	3689.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #49	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3739.4	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #5	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O)O[Si](C)(C)C	3658.5	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #50	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O	3631.5	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #51	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C	3672.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #52	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3810.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #53	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3696.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #54	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3714.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #55	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3706.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #56	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3736.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #57	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3747.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #58	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O	3693.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #59	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3747.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #6	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O)O[Si](C)(C)C	3769.5	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #60	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O	3634.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #61	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C	3676.4	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #62	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3739.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #63	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3624.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #64	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3638.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #65	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3632.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #66	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3774.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #67	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3664.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #68	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3682.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #69	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3675.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #7	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O)O[Si](C)(C)C	3730.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #70	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3725.5	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #8	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C)O[Si](C)(C)C	3744.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],4TMS,isomer #9	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O)O[Si](C)(C)C	3658.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #1	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O)O[Si](C)(C)C	3705.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #10	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C)O[Si](C)(C)C	3540.5	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #11	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)O[Si](C)(C)C	3652.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #12	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)O[Si](C)(C)C	3649.4	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #13	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O)O[Si](C)(C)C	3560.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #14	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)O[Si](C)(C)C	3643.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #15	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O)O[Si](C)(C)C	3528.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #16	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C)O[Si](C)(C)C	3539.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #17	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)O[Si](C)(C)C	3721.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #18	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)O[Si](C)(C)C	3587.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #19	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)O[Si](C)(C)C	3591.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #2	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O)O[Si](C)(C)C	3664.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #20	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)O[Si](C)(C)C	3582.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #21	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)O[Si](C)(C)C	3651.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #22	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)O[Si](C)(C)C	3645.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #23	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O)O[Si](C)(C)C	3559.5	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #24	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)O[Si](C)(C)C	3639.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #25	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O)O[Si](C)(C)C	3522.5	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #26	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C)O[Si](C)(C)C	3534.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #27	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)O[Si](C)(C)C	3647.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #28	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)O[Si](C)(C)C	3524.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #29	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)O[Si](C)(C)C	3522.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #3	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C)O[Si](C)(C)C	3671.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #30	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)O[Si](C)(C)C	3514.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #31	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)O[Si](C)(C)C	3667.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #32	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)O[Si](C)(C)C	3542.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #33	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)O[Si](C)(C)C	3544.5	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #34	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)O[Si](C)(C)C	3536.4	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #35	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)O[Si](C)(C)C	3613.5	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #36	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3676.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #37	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3669.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #38	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O	3633.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #39	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3662.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #4	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O)O[Si](C)(C)C	3596.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #40	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O	3574.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #41	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C	3608.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #42	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3658.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #43	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3564.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #44	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3567.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #45	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3562.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #46	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3657.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #47	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3564.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #48	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3571.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #49	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3559.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #5	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)O[Si](C)(C)C	3651.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #50	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3634.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #51	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3655.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #52	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3565.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #53	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3564.5	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #54	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3557.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #55	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3550.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #56	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3592.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #6	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)O[Si](C)(C)C	3647.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #7	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O)O[Si](C)(C)C	3563.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #8	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)O[Si](C)(C)C	3643.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],5TMS,isomer #9	CC1=CC(O[Si](C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O)O[Si](C)(C)C	3534.4	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],1TBDMS,isomer #1	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O)C1O)O[Si](C)(C)C(C)(C)C	4323.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],1TBDMS,isomer #2	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)C(O)C1O	4354.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],1TBDMS,isomer #3	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C(O)C1O	4316.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],1TBDMS,isomer #4	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O	4325.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],1TBDMS,isomer #5	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	4349.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],1TBDMS,isomer #6	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	4328.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],1TBDMS,isomer #7	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	4337.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],1TBDMS,isomer #8	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O)C1O	4287.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #1	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)C(O)C1O)O[Si](C)(C)C(C)(C)C	4451.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #10	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	4478.5	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #11	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	4454.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #12	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	4457.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #13	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)C(O)C1O	4387.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #14	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O	4441.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #15	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	4434.5	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #16	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	4403.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #17	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	4411.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #18	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C(O)C1O	4319.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #19	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	4434.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #2	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C(O)C1O)O[Si](C)(C)C(C)(C)C	4403.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #20	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	4411.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #21	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	4411.5	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #22	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O	4351.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #23	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	4459.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #24	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	4453.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #25	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	4385.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #26	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4462.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #27	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	4345.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #28	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	4376.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #3	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O)O[Si](C)(C)C(C)(C)C	4413.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #4	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O)O[Si](C)(C)C(C)(C)C	4452.4	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #5	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O)O[Si](C)(C)C(C)(C)C	4424.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #6	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4436.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #7	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O)C1O)O[Si](C)(C)C(C)(C)C	4393.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #8	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C(O)C1O	4439.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],2TBDMS,isomer #9	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O	4429.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #1	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C(O)C1O)O[Si](C)(C)C(C)(C)C	4489.5	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #10	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4469.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #11	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C(O)C1O)O[Si](C)(C)C(C)(C)C	4337.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #12	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O)O[Si](C)(C)C(C)(C)C	4498.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #13	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O)O[Si](C)(C)C(C)(C)C	4475.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #14	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4477.4	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #15	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O)O[Si](C)(C)C(C)(C)C	4372.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #16	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O)O[Si](C)(C)C(C)(C)C	4534.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #17	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4516.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #18	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O)O[Si](C)(C)C(C)(C)C	4412.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #19	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4530.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #2	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O)O[Si](C)(C)C(C)(C)C	4484.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #20	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O)O[Si](C)(C)C(C)(C)C	4378.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #21	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4400.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #22	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O	4535.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #23	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	4528.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #24	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	4515.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #25	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	4506.5	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #26	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C(O)C1O	4385.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #27	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	4523.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #28	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	4503.4	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #29	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	4499.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #3	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O)O[Si](C)(C)C(C)(C)C	4553.4	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #30	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O	4372.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #31	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	4572.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #32	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	4556.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #33	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	4431.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #34	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4570.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #35	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	4401.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #36	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	4416.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #37	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	4534.4	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #38	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	4515.4	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #39	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	4511.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #4	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O)O[Si](C)(C)C(C)(C)C	4533.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #40	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O	4394.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #41	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	4520.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #42	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	4503.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #43	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	4368.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #44	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4516.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #45	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	4339.8	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #46	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	4353.7	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #47	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	4514.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #48	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	4497.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #49	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	4395.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #5	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4530.6	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #50	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4512.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #51	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	4359.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #52	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	4379.4	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #53	CC1=CC(=O)CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4570.1	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #54	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	4423.2	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #55	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	4407.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #56	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(O)CCC(C)OC1OC(COC2OC(C)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4415.3	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #6	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)C(O)C1O)O[Si](C)(C)C(C)(C)C	4414.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #7	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O)O[Si](C)(C)C(C)(C)C	4495.0	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #8	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O)O[Si](C)(C)C(C)(C)C	4496.9	Semi standard non polar	33892256
7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside],3TBDMS,isomer #9	CC1=CC(=O)CC(C)(C)C1(CCC(C)OC1OC(COC2OC(C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O)O[Si](C)(C)C(C)(C)C	4490.5	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 - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] GC-MS (Non-derivatized) - 70eV, Positive	splash10-066r-9544180000-8e1b5aade0d3d3f29e1f	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] GC-MS (2 TMS) - 70eV, Positive	splash10-03di-9341017000-f3613104bd39f4c53665	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] GC-MS (TMS_1_8) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] GC-MS (TMS_2_13) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] GC-MS (TMS_2_14) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] GC-MS (TMS_2_15) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] GC-MS (TMS_2_16) - 70eV, Positive	Not Available	2021-10-13	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 - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] 10V, Positive-QTOF	splash10-0ar0-1292170000-cf251353f8db3990bec9	2016-08-02	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] 20V, Positive-QTOF	splash10-0a6r-1391000000-5c1d1fa5b52b242d85d9	2016-08-02	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] 40V, Positive-QTOF	splash10-0a4i-8590000000-eae494a67038e6619d64	2016-08-02	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] 10V, Negative-QTOF	splash10-05q9-4392070000-2ff481a2b203e12a14fe	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] 20V, Negative-QTOF	splash10-056s-3492010000-1e768511737290c282bc	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] 40V, Negative-QTOF	splash10-056r-4390000000-dde622701a9b5d004471	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] 10V, Negative-QTOF	splash10-001i-0140190000-48e4c765978744365a13	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] 20V, Negative-QTOF	splash10-0zfr-4922430000-fabf01167ea44d9e8d9c	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] 40V, Negative-QTOF	splash10-0a4i-6593000000-d3a6510ed0623fd5d6fe	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] 10V, Positive-QTOF	splash10-0ap3-0593870000-743d1e1b7fee0824fa19	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] 20V, Positive-QTOF	splash10-0a4l-5691110000-6637bda010e711c30098	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] 40V, Positive-QTOF	splash10-0a4l-9141100000-cbfb5798803656fe201e	2021-09-23	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-16	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

FDB000977

KNApSAcK ID

Not Available

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

85219381

PDB ID

Not Available

ChEBI ID

168825

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

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for 7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside] (HMDB0029770)

MOL for HMDB0029770 (7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside])

3D MOL for HMDB0029770 (7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside])

3D SDF for HMDB0029770 (7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside])

3D-SDF for HMDB0029770 (7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside])

PDB for HMDB0029770 (7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside])

3D PDB for HMDB0029770 (7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside])

SMILES for HMDB0029770 (7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside])

INCHI for HMDB0029770 (7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside])

Structure for HMDB0029770 (7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside])

3D Structure for HMDB0029770 (7,8-Dihydrovomifoliol 9-[rhamnosyl-(1->6)-glucoside])

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra