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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 22:40:26 UTC

Update Date

2022-03-07 02:55:19 UTC

HMDB ID

HMDB0037426

Secondary Accession Numbers

HMDB37426

Metabolite Identification

Common Name

Astragalin 7-rhamnoside

Description

Astragalin 7-rhamnoside belongs to the class of organic compounds known as flavonoid-7-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position. Thus, astragalin 7-rhamnoside is considered to be a flavonoid. Astragalin 7-rhamnoside is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. Based on a literature review very few articles have been published on Astragalin 7-rhamnoside.

Structure

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

            
  Mrv1652310191718582D          

 42 46  0  0  0  0            999 V2000
 2501.7980 2502.5513    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2503.2269 2501.7263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2504.6559 2501.7263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2506.0848 2504.2013    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2504.6559 2505.0263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2504.6559 2506.6763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2507.5138 2506.6763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2506.0848 2507.5013    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2499.6546 2505.4388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2503.2269 2500.0763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2503.2269 2499.2513    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2500.3691 2501.7263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2500.3691 2500.0763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2501.7980 2499.2513    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2505.3704 2505.4388    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 2505.3704 2506.2638    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 2506.0848 2506.6763    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 2506.7993 2506.2638    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 2506.7993 2505.4388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2506.0848 2505.0263    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 2501.7980 2501.7263    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 2501.0835 2501.3138    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 2501.0835 2500.4888    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 2501.7980 2500.0763    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 2502.5125 2500.4888    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 2502.5125 2501.3138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2503.2269 2504.2013    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2503.2269 2502.5513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2502.5125 2502.9638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2502.5125 2503.7888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2501.7980 2505.0263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2501.7980 2504.2013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2501.0835 2503.7888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2500.3691 2504.2013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2500.3691 2505.0263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2501.0835 2505.4388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2505.3704 2503.7888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2505.3704 2502.9638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2504.6559 2502.5513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2503.9414 2502.9638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2503.9414 2503.7888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2504.6559 2504.2013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 10 11  1  0  0  0  0
 15 16  1  0  0  0  0
 15 20  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 21 26  1  0  0  0  0
 25 26  1  0  0  0  0
 18  7  1  6  0  0  0
 17  8  1  1  0  0  0
 16  6  1  6  0  0  0
 15  5  1  6  0  0  0
 20  4  1  1  0  0  0
 22 12  1  1  0  0  0
 23 13  1  6  0  0  0
 24 14  1  6  0  0  0
 25 10  1  6  0  0  0
 21  1  1  6  0  0  0
 27 30  1  0  0  0  0
 28  2  2  0  0  0  0
  1 29  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 31  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 37  1  0  0  0  0
 37  4  1  0  0  0  0
 39  3  1  0  0  0  0
 27 41  1  0  0  0  0
 40 28  1  0  0  0  0
 35  9  1  0  0  0  0
 30 32  1  0  0  0  0
M  END

HMDB0037426
     RDKit          3D
Astragalin 7-rhamnoside
 72 76  0  0  0  0  0  0  0  0999 V2000
    6.9676    2.1228    2.1665 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3979    1.7042    0.7736 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3002    1.8673   -0.0672 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5005    0.7292   -0.1038 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2678    0.9264   -0.6883 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0084    0.8055   -0.2029 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7639    0.4298    1.0723 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4672    0.2946    1.6079 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3404   -0.0900    2.9057 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4192    0.5738    0.7381 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8610    0.4604    1.1866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1091    0.1138    2.3605 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9155    0.7400    0.3074 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1864    0.6089    0.7843 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8766   -0.6260    0.8472 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8440   -0.7028   -0.1448 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4071   -1.9607   -0.2280 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.9122   -1.9212   -0.3164 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2844   -1.2111   -1.4486 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9787   -2.9238    0.8262 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.9635   -3.9380    0.8796 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8629   -2.3644    2.2051 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.9611   -2.6318    3.0134 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5945   -0.8625    2.1447 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9734   -0.3978    3.2681 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6189    1.1188   -0.9601 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5936    1.4510   -1.9828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1885    1.4870   -3.3162 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0078    1.8488   -4.3429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3112    2.2042   -4.0885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1922    2.5806   -5.0894 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7329    2.1771   -2.7834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8892    1.8064   -1.7375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3422    1.2117   -1.3497 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6723    0.9644   -0.5871 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9641    1.0754   -1.0413 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1643   -0.4381   -0.7998 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5669   -1.5962   -0.3044 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6116   -0.4663   -0.4516 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.0003   -1.7958   -0.2668 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8114    0.2485    0.8665 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.1707    0.2201    1.1737 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8785    2.1698    2.8327 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3867    1.2445    2.5728 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3966    3.0500    2.1919 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2128    2.3689    0.4611 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3747    0.4166    0.9502 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5761    0.2004    1.7891 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5831   -0.2394    3.4561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1642   -1.4662    0.6010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0576   -2.3873   -1.2145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3262   -1.4643    0.6138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2811   -2.9560   -0.4167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5827   -0.4964   -1.5647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0463   -3.4680    0.5022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3177   -4.0715    1.7727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9542   -2.8067    2.6809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5536   -1.8192    2.9853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6192   -0.3991    2.0957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8903    0.5730    3.2511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1610    1.2117   -3.5693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6665    1.8667   -5.3619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9678    2.6263   -6.0543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7501    2.4458   -2.5107 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2682    1.8271   -0.7273 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1211    1.3768   -2.0619 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9629   -0.4066   -1.8892 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2313   -2.1843   -1.0190 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2313   -0.0332   -1.2506 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9404   -1.9455   -0.4985 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2769   -0.2592    1.6862 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6461    1.0422    0.8697 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 17 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 13 26  2  0
 26 27  1  0
 27 28  2  0
 28 29  1  0
 29 30  2  0
 30 31  1  0
 30 32  1  0
 32 33  2  0
 26 34  1  0
 34 35  1  0
 35 36  2  0
  4 37  1  0
 37 38  1  0
 37 39  1  0
 39 40  1  0
 39 41  1  0
 41 42  1  0
 41  2  1  0
 36  6  1  0
 35 10  1  0
 24 15  1  0
 33 27  1  0
  1 43  1  0
  1 44  1  0
  1 45  1  0
  2 46  1  6
  4 47  1  1
  7 48  1  0
  9 49  1  0
 15 50  1  6
 17 51  1  6
 18 52  1  0
 18 53  1  0
 19 54  1  0
 20 55  1  6
 21 56  1  0
 22 57  1  1
 23 58  1  0
 24 59  1  6
 25 60  1  0
 28 61  1  0
 29 62  1  0
 31 63  1  0
 32 64  1  0
 33 65  1  0
 36 66  1  0
 37 67  1  6
 38 68  1  0
 39 69  1  6
 40 70  1  0
 41 71  1  1
 42 72  1  0
M  END

            
  Mrv1652310191718582D          

 42 46  0  0  0  0            999 V2000
 2501.7980 2502.5513    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2503.2269 2501.7263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2504.6559 2501.7263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2506.0848 2504.2013    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2504.6559 2505.0263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2504.6559 2506.6763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2507.5138 2506.6763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2506.0848 2507.5013    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2499.6546 2505.4388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2503.2269 2500.0763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2503.2269 2499.2513    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2500.3691 2501.7263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2500.3691 2500.0763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2501.7980 2499.2513    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2505.3704 2505.4388    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 2505.3704 2506.2638    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 2506.0848 2506.6763    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 2506.7993 2506.2638    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 2506.7993 2505.4388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2506.0848 2505.0263    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 2501.7980 2501.7263    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 2501.0835 2501.3138    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 2501.0835 2500.4888    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 2501.7980 2500.0763    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 2502.5125 2500.4888    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 2502.5125 2501.3138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2503.2269 2504.2013    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2503.2269 2502.5513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2502.5125 2502.9638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2502.5125 2503.7888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2501.7980 2505.0263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2501.7980 2504.2013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2501.0835 2503.7888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2500.3691 2504.2013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2500.3691 2505.0263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2501.0835 2505.4388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2505.3704 2503.7888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2505.3704 2502.9638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2504.6559 2502.5513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2503.9414 2502.9638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2503.9414 2503.7888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2504.6559 2504.2013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 10 11  1  0  0  0  0
 15 16  1  0  0  0  0
 15 20  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 21 26  1  0  0  0  0
 25 26  1  0  0  0  0
 18  7  1  6  0  0  0
 17  8  1  1  0  0  0
 16  6  1  6  0  0  0
 15  5  1  6  0  0  0
 20  4  1  1  0  0  0
 22 12  1  1  0  0  0
 23 13  1  6  0  0  0
 24 14  1  6  0  0  0
 25 10  1  6  0  0  0
 21  1  1  6  0  0  0
 27 30  1  0  0  0  0
 28  2  2  0  0  0  0
  1 29  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 31  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 37  1  0  0  0  0
 37  4  1  0  0  0  0
 39  3  1  0  0  0  0
 27 41  1  0  0  0  0
 40 28  1  0  0  0  0
 35  9  1  0  0  0  0
 30 32  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0037426

> <DATABASE_NAME>
hmdb

> <SMILES>
C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(OC3=C2)C2=CC=C(O)C=C2)[C@H](O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C27H30O15/c1-9-17(31)20(34)22(36)26(38-9)39-12-6-13(30)16-14(7-12)40-24(10-2-4-11(29)5-3-10)25(19(16)33)42-27-23(37)21(35)18(32)15(8-28)41-27/h2-7,9,15,17-18,20-23,26-32,34-37H,8H2,1H3/t9-,15+,17-,18-,20+,21-,22+,23+,26-,27-/m0/s1

> <INCHI_KEY>
JYXSWDCPHRTYGU-VYARGGPUSA-N

> <FORMULA>
C27H30O15

> <MOLECULAR_WEIGHT>
594.522

> <EXACT_MASS>
594.158470266

> <JCHEM_ACCEPTOR_COUNT>
15

> <JCHEM_ATOM_COUNT>
72

> <JCHEM_AVERAGE_POLARIZABILITY>
57.260292289051975

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <ALOGPS_LOGP>
-0.18

> <JCHEM_LOGP>
-1.0624281009999996

> <ALOGPS_LOGS>
-2.36

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.556776212864888

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.083349784459057

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6122003587144

> <JCHEM_POLAR_SURFACE_AREA>
245.28999999999994

> <JCHEM_REFRACTIVITY>
137.89529999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.61e+00 g/l

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

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0037426
     RDKit          3D
Astragalin 7-rhamnoside
 72 76  0  0  0  0  0  0  0  0999 V2000
    6.9676    2.1228    2.1665 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3979    1.7042    0.7736 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3002    1.8673   -0.0672 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5005    0.7292   -0.1038 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2678    0.9264   -0.6883 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0084    0.8055   -0.2029 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7639    0.4298    1.0723 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4672    0.2946    1.6079 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3404   -0.0900    2.9057 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4192    0.5738    0.7381 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8610    0.4604    1.1866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1091    0.1138    2.3605 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9155    0.7400    0.3074 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1864    0.6089    0.7843 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8766   -0.6260    0.8472 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8440   -0.7028   -0.1448 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4071   -1.9607   -0.2280 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.9122   -1.9212   -0.3164 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2844   -1.2111   -1.4486 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9787   -2.9238    0.8262 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.9635   -3.9380    0.8796 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8629   -2.3644    2.2051 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.9611   -2.6318    3.0134 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5945   -0.8625    2.1447 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9734   -0.3978    3.2681 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6189    1.1188   -0.9601 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5936    1.4510   -1.9828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1885    1.4870   -3.3162 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0078    1.8488   -4.3429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3112    2.2042   -4.0885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1922    2.5806   -5.0894 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7329    2.1771   -2.7834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8892    1.8064   -1.7375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3422    1.2117   -1.3497 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6723    0.9644   -0.5871 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9641    1.0754   -1.0413 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1643   -0.4381   -0.7998 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5669   -1.5962   -0.3044 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6116   -0.4663   -0.4516 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.0003   -1.7958   -0.2668 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8114    0.2485    0.8665 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.1707    0.2201    1.1737 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8785    2.1698    2.8327 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3867    1.2445    2.5728 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3966    3.0500    2.1919 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2128    2.3689    0.4611 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3747    0.4166    0.9502 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5761    0.2004    1.7891 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5831   -0.2394    3.4561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1642   -1.4662    0.6010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0576   -2.3873   -1.2145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3262   -1.4643    0.6138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2811   -2.9560   -0.4167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5827   -0.4964   -1.5647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0463   -3.4680    0.5022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3177   -4.0715    1.7727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9542   -2.8067    2.6809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5536   -1.8192    2.9853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6192   -0.3991    2.0957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8903    0.5730    3.2511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1610    1.2117   -3.5693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6665    1.8667   -5.3619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9678    2.6263   -6.0543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7501    2.4458   -2.5107 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2682    1.8271   -0.7273 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1211    1.3768   -2.0619 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9629   -0.4066   -1.8892 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2313   -2.1843   -1.0190 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2313   -0.0332   -1.2506 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9404   -1.9455   -0.4985 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2769   -0.2592    1.6862 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6461    1.0422    0.8697 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 17 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 13 26  2  0
 26 27  1  0
 27 28  2  0
 28 29  1  0
 29 30  2  0
 30 31  1  0
 30 32  1  0
 32 33  2  0
 26 34  1  0
 34 35  1  0
 35 36  2  0
  4 37  1  0
 37 38  1  0
 37 39  1  0
 39 40  1  0
 39 41  1  0
 41 42  1  0
 41  2  1  0
 36  6  1  0
 35 10  1  0
 24 15  1  0
 33 27  1  0
  1 43  1  0
  1 44  1  0
  1 45  1  0
  2 46  1  6
  4 47  1  1
  7 48  1  0
  9 49  1  0
 15 50  1  6
 17 51  1  6
 18 52  1  0
 18 53  1  0
 19 54  1  0
 20 55  1  6
 21 56  1  0
 22 57  1  1
 23 58  1  0
 24 59  1  6
 25 60  1  0
 28 61  1  0
 29 62  1  0
 31 63  1  0
 32 64  1  0
 33 65  1  0
 36 66  1  0
 37 67  1  6
 38 68  1  0
 39 69  1  6
 40 70  1  0
 41 71  1  1
 42 72  1  0
M  END

HEADER    PROTEIN                                 19-OCT-17   NONE
TITLE     NULL                                                        
COMPND    MOLECULE:                                                   
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-OCT-17         0                                  
HETATM    1  O   UNK     0    4670.0234671.429   0.000  0.00  0.00           O+0
HETATM    2  O   UNK     0    4672.6904669.889   0.000  0.00  0.00           O+0
HETATM    3  O   UNK     0    4675.3584669.889   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0    4678.0254674.509   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0    4675.3584676.049   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0    4675.3584679.129   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0    4680.6924679.129   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0    4678.0254680.669   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0    4666.0224676.819   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0    4672.6904666.809   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0    4672.6904665.269   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0    4667.3564669.889   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0    4667.3564666.809   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0    4670.0234665.269   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0    4676.6914676.819   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0    4676.6914678.359   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0    4678.0254679.129   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0    4679.3594678.359   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0    4679.3594676.819   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0    4678.0254676.049   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0    4670.0234669.889   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0    4668.6894669.119   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0    4668.6894667.579   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0    4670.0234666.809   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0    4671.3574667.579   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0    4671.3574669.119   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0    4672.6904674.509   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0    4672.6904671.429   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0    4671.3574672.199   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0    4671.3574673.739   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0    4670.0234676.049   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0    4670.0234674.509   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0    4668.6894673.739   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0    4667.3564674.509   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0    4667.3564676.049   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0    4668.6894676.819   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0    4676.6914673.739   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0    4676.6914672.199   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0    4675.3584671.429   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0    4674.0244672.199   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0    4674.0244673.739   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0    4675.3584674.509   0.000  0.00  0.00           C+0
CONECT    1   21   29                                                       
CONECT    2   28                                                            
CONECT    3   39                                                            
CONECT    4   20   37                                                       
CONECT    5   15                                                            
CONECT    6   16                                                            
CONECT    7   18                                                            
CONECT    8   17                                                            
CONECT    9   35                                                            
CONECT   10   11   25                                                       
CONECT   11   10                                                            
CONECT   12   22                                                            
CONECT   13   23                                                            
CONECT   14   24                                                            
CONECT   15   16   20    5                                                  
CONECT   16   15   17    6                                                  
CONECT   17   16   18    8                                                  
CONECT   18   17   19    7                                                  
CONECT   19   18   20                                                       
CONECT   20   15   19    4                                                  
CONECT   21   22   26    1                                                  
CONECT   22   21   23   12                                                  
CONECT   23   22   24   13                                                  
CONECT   24   23   25   14                                                  
CONECT   25   24   26   10                                                  
CONECT   26   21   25                                                       
CONECT   27   30   41                                                       
CONECT   28   29    2   40                                                  
CONECT   29   28   30    1                                                  
CONECT   30   29   27   32                                                  
CONECT   31   32   36                                                       
CONECT   32   31   33   30                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36    9                                                  
CONECT   36   35   31                                                       
CONECT   37   38   42    4                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40    3                                                  
CONECT   40   39   41   28                                                  
CONECT   41   40   42   27                                                  
CONECT   42   41   37                                                       
MASTER        0    0    0    0    0    0    0    0   42    0   92    0
END

COMPND    HMDB0037426
HETATM    1  C1  UNL     1       6.968   2.123   2.167  1.00  0.00           C  
HETATM    2  C2  UNL     1       7.398   1.704   0.774  1.00  0.00           C  
HETATM    3  O1  UNL     1       6.300   1.867  -0.067  1.00  0.00           O  
HETATM    4  C3  UNL     1       5.500   0.729  -0.104  1.00  0.00           C  
HETATM    5  O2  UNL     1       4.268   0.926  -0.688  1.00  0.00           O  
HETATM    6  C4  UNL     1       3.008   0.805  -0.203  1.00  0.00           C  
HETATM    7  C5  UNL     1       2.764   0.430   1.072  1.00  0.00           C  
HETATM    8  C6  UNL     1       1.467   0.295   1.608  1.00  0.00           C  
HETATM    9  O3  UNL     1       1.340  -0.090   2.906  1.00  0.00           O  
HETATM   10  C7  UNL     1       0.419   0.574   0.738  1.00  0.00           C  
HETATM   11  C8  UNL     1      -0.861   0.460   1.187  1.00  0.00           C  
HETATM   12  O4  UNL     1      -1.109   0.114   2.360  1.00  0.00           O  
HETATM   13  C9  UNL     1      -1.915   0.740   0.307  1.00  0.00           C  
HETATM   14  O5  UNL     1      -3.186   0.609   0.784  1.00  0.00           O  
HETATM   15  C10 UNL     1      -3.877  -0.626   0.847  1.00  0.00           C  
HETATM   16  O6  UNL     1      -4.844  -0.703  -0.145  1.00  0.00           O  
HETATM   17  C11 UNL     1      -5.407  -1.961  -0.228  1.00  0.00           C  
HETATM   18  C12 UNL     1      -6.912  -1.921  -0.316  1.00  0.00           C  
HETATM   19  O7  UNL     1      -7.284  -1.211  -1.449  1.00  0.00           O  
HETATM   20  C13 UNL     1      -4.979  -2.924   0.826  1.00  0.00           C  
HETATM   21  O8  UNL     1      -5.964  -3.938   0.880  1.00  0.00           O  
HETATM   22  C14 UNL     1      -4.863  -2.364   2.205  1.00  0.00           C  
HETATM   23  O9  UNL     1      -5.961  -2.632   3.013  1.00  0.00           O  
HETATM   24  C15 UNL     1      -4.594  -0.863   2.145  1.00  0.00           C  
HETATM   25  O10 UNL     1      -3.973  -0.398   3.268  1.00  0.00           O  
HETATM   26  C16 UNL     1      -1.619   1.119  -0.960  1.00  0.00           C  
HETATM   27  C17 UNL     1      -2.594   1.451  -1.983  1.00  0.00           C  
HETATM   28  C18 UNL     1      -2.189   1.487  -3.316  1.00  0.00           C  
HETATM   29  C19 UNL     1      -3.008   1.849  -4.343  1.00  0.00           C  
HETATM   30  C20 UNL     1      -4.311   2.204  -4.089  1.00  0.00           C  
HETATM   31  O11 UNL     1      -5.192   2.581  -5.089  1.00  0.00           O  
HETATM   32  C21 UNL     1      -4.733   2.177  -2.783  1.00  0.00           C  
HETATM   33  C22 UNL     1      -3.889   1.806  -1.737  1.00  0.00           C  
HETATM   34  O12 UNL     1      -0.342   1.212  -1.350  1.00  0.00           O  
HETATM   35  C23 UNL     1       0.672   0.964  -0.587  1.00  0.00           C  
HETATM   36  C24 UNL     1       1.964   1.075  -1.041  1.00  0.00           C  
HETATM   37  C25 UNL     1       6.164  -0.438  -0.800  1.00  0.00           C  
HETATM   38  O13 UNL     1       5.567  -1.596  -0.304  1.00  0.00           O  
HETATM   39  C26 UNL     1       7.612  -0.466  -0.452  1.00  0.00           C  
HETATM   40  O14 UNL     1       8.000  -1.796  -0.267  1.00  0.00           O  
HETATM   41  C27 UNL     1       7.811   0.249   0.867  1.00  0.00           C  
HETATM   42  O15 UNL     1       9.171   0.220   1.174  1.00  0.00           O  
HETATM   43  H1  UNL     1       7.878   2.170   2.833  1.00  0.00           H  
HETATM   44  H2  UNL     1       6.387   1.245   2.573  1.00  0.00           H  
HETATM   45  H3  UNL     1       6.397   3.050   2.192  1.00  0.00           H  
HETATM   46  H4  UNL     1       8.213   2.369   0.461  1.00  0.00           H  
HETATM   47  H5  UNL     1       5.375   0.417   0.950  1.00  0.00           H  
HETATM   48  H6  UNL     1       3.576   0.200   1.789  1.00  0.00           H  
HETATM   49  H7  UNL     1       0.583  -0.239   3.456  1.00  0.00           H  
HETATM   50  H8  UNL     1      -3.164  -1.466   0.601  1.00  0.00           H  
HETATM   51  H9  UNL     1      -5.058  -2.387  -1.214  1.00  0.00           H  
HETATM   52  H10 UNL     1      -7.326  -1.464   0.614  1.00  0.00           H  
HETATM   53  H11 UNL     1      -7.281  -2.956  -0.417  1.00  0.00           H  
HETATM   54  H12 UNL     1      -6.583  -0.496  -1.565  1.00  0.00           H  
HETATM   55  H13 UNL     1      -4.046  -3.468   0.502  1.00  0.00           H  
HETATM   56  H14 UNL     1      -6.318  -4.072   1.773  1.00  0.00           H  
HETATM   57  H15 UNL     1      -3.954  -2.807   2.681  1.00  0.00           H  
HETATM   58  H16 UNL     1      -6.554  -1.819   2.985  1.00  0.00           H  
HETATM   59  H17 UNL     1      -5.619  -0.399   2.096  1.00  0.00           H  
HETATM   60  H18 UNL     1      -3.890   0.573   3.251  1.00  0.00           H  
HETATM   61  H19 UNL     1      -1.161   1.212  -3.569  1.00  0.00           H  
HETATM   62  H20 UNL     1      -2.666   1.867  -5.362  1.00  0.00           H  
HETATM   63  H21 UNL     1      -4.968   2.626  -6.054  1.00  0.00           H  
HETATM   64  H22 UNL     1      -5.750   2.446  -2.511  1.00  0.00           H  
HETATM   65  H23 UNL     1      -4.268   1.827  -0.727  1.00  0.00           H  
HETATM   66  H24 UNL     1       2.121   1.377  -2.062  1.00  0.00           H  
HETATM   67  H25 UNL     1       5.963  -0.407  -1.889  1.00  0.00           H  
HETATM   68  H26 UNL     1       5.231  -2.184  -1.019  1.00  0.00           H  
HETATM   69  H27 UNL     1       8.231  -0.033  -1.251  1.00  0.00           H  
HETATM   70  H28 UNL     1       8.940  -1.945  -0.498  1.00  0.00           H  
HETATM   71  H29 UNL     1       7.277  -0.259   1.686  1.00  0.00           H  
HETATM   72  H30 UNL     1       9.646   1.042   0.870  1.00  0.00           H  
CONECT    1    2   43   44   45
CONECT    2    3   41   46
CONECT    3    4
CONECT    4    5   37   47
CONECT    5    6
CONECT    6    7    7   36
CONECT    7    8   48
CONECT    8    9   10   10
CONECT    9   49
CONECT   10   11   35
CONECT   11   12   12   13
CONECT   13   14   26   26
CONECT   14   15
CONECT   15   16   24   50
CONECT   16   17
CONECT   17   18   20   51
CONECT   18   19   52   53
CONECT   19   54
CONECT   20   21   22   55
CONECT   21   56
CONECT   22   23   24   57
CONECT   23   58
CONECT   24   25   59
CONECT   25   60
CONECT   26   27   34
CONECT   27   28   28   33
CONECT   28   29   61
CONECT   29   30   30   62
CONECT   30   31   32
CONECT   31   63
CONECT   32   33   33   64
CONECT   33   65
CONECT   34   35
CONECT   35   36   36
CONECT   36   66
CONECT   37   38   39   67
CONECT   38   68
CONECT   39   40   41   69
CONECT   40   70
CONECT   41   42   71
CONECT   42   72
END

HMDB0037426
     RDKit          3D
Astragalin 7-rhamnoside
 72 76  0  0  0  0  0  0  0  0999 V2000
    6.9676    2.1228    2.1665 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3979    1.7042    0.7736 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3002    1.8673   -0.0672 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5005    0.7292   -0.1038 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2678    0.9264   -0.6883 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0084    0.8055   -0.2029 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7639    0.4298    1.0723 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4672    0.2946    1.6079 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3404   -0.0900    2.9057 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4192    0.5738    0.7381 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8610    0.4604    1.1866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1091    0.1138    2.3605 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9155    0.7400    0.3074 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1864    0.6089    0.7843 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8766   -0.6260    0.8472 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8440   -0.7028   -0.1448 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4071   -1.9607   -0.2280 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.9122   -1.9212   -0.3164 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2844   -1.2111   -1.4486 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9787   -2.9238    0.8262 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.9635   -3.9380    0.8796 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8629   -2.3644    2.2051 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.9611   -2.6318    3.0134 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5945   -0.8625    2.1447 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9734   -0.3978    3.2681 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6189    1.1188   -0.9601 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5936    1.4510   -1.9828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1885    1.4870   -3.3162 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0078    1.8488   -4.3429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3112    2.2042   -4.0885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1922    2.5806   -5.0894 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7329    2.1771   -2.7834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8892    1.8064   -1.7375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3422    1.2117   -1.3497 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6723    0.9644   -0.5871 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9641    1.0754   -1.0413 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1643   -0.4381   -0.7998 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5669   -1.5962   -0.3044 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6116   -0.4663   -0.4516 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.0003   -1.7958   -0.2668 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8114    0.2485    0.8665 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.1707    0.2201    1.1737 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8785    2.1698    2.8327 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3867    1.2445    2.5728 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3966    3.0500    2.1919 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2128    2.3689    0.4611 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3747    0.4166    0.9502 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5761    0.2004    1.7891 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5831   -0.2394    3.4561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1642   -1.4662    0.6010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0576   -2.3873   -1.2145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3262   -1.4643    0.6138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2811   -2.9560   -0.4167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5827   -0.4964   -1.5647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0463   -3.4680    0.5022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3177   -4.0715    1.7727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9542   -2.8067    2.6809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5536   -1.8192    2.9853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6192   -0.3991    2.0957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8903    0.5730    3.2511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1610    1.2117   -3.5693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6665    1.8667   -5.3619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9678    2.6263   -6.0543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7501    2.4458   -2.5107 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2682    1.8271   -0.7273 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1211    1.3768   -2.0619 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9629   -0.4066   -1.8892 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2313   -2.1843   -1.0190 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2313   -0.0332   -1.2506 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9404   -1.9455   -0.4985 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2769   -0.2592    1.6862 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6461    1.0422    0.8697 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 17 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 13 26  2  0
 26 27  1  0
 27 28  2  0
 28 29  1  0
 29 30  2  0
 30 31  1  0
 30 32  1  0
 32 33  2  0
 26 34  1  0
 34 35  1  0
 35 36  2  0
  4 37  1  0
 37 38  1  0
 37 39  1  0
 39 40  1  0
 39 41  1  0
 41 42  1  0
 41  2  1  0
 36  6  1  0
 35 10  1  0
 24 15  1  0
 33 27  1  0
  1 43  1  0
  1 44  1  0
  1 45  1  0
  2 46  1  6
  4 47  1  1
  7 48  1  0
  9 49  1  0
 15 50  1  6
 17 51  1  6
 18 52  1  0
 18 53  1  0
 19 54  1  0
 20 55  1  6
 21 56  1  0
 22 57  1  1
 23 58  1  0
 24 59  1  6
 25 60  1  0
 28 61  1  0
 29 62  1  0
 31 63  1  0
 32 64  1  0
 33 65  1  0
 36 66  1  0
 37 67  1  6
 38 68  1  0
 39 69  1  6
 40 70  1  0
 41 71  1  1
 42 72  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
Kaempferol 3-O-b-D-galactopyranosyl-7-O-a-L-rhamnopyranoside	HMDB
Kaempferol 3-O-β-D-galactopyranosyl-7-O-α-L-rhamnopyranoside	HMDB

Chemical Formula

C₂₇H₃₀O₁₅

Average Molecular Weight

594.522

Monoisotopic Molecular Weight

594.158470266

IUPAC Name

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

Traditional Name

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

CAS Registry Number

38784-79-1

SMILES

C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(OC3=C2)C2=CC=C(O)C=C2)[C@H](O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C27H30O15/c1-9-17(31)20(34)22(36)26(38-9)39-12-6-13(30)16-14(7-12)40-24(10-2-4-11(29)5-3-10)25(19(16)33)42-27-23(37)21(35)18(32)15(8-28)41-27/h2-7,9,15,17-18,20-23,26-32,34-37H,8H2,1H3/t9-,15+,17-,18-,20+,21-,22+,23+,26-,27-/m0/s1

InChI Key

JYXSWDCPHRTYGU-VYARGGPUSA-N

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Flavonoid-7-O-glycosides

Alternative Parents

Substituents

Flavonoid-7-o-glycoside
Flavonoid-3-o-glycoside
4'-hydroxyflavonoid
5-hydroxyflavonoid
Flavone
Hydroxyflavonoid
Phenolic glycoside
Chromone
Glycosyl compound
O-glycosyl compound
Benzopyran
1-benzopyran
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Pyranone
Pyran
Monosaccharide
Benzenoid
Monocyclic benzene moiety
Oxane
Heteroaromatic compound
Vinylogous acid
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Acetal
Polyol
Primary alcohol
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
Alcohol
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

beta-D-galactoside (CHEBI:68881 )
dihydroxyflavone (CHEBI:68881 )
glycosyloxyflavone (CHEBI:68881 )
alpha-L-rhamnoside (CHEBI:68881 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Extracellular (HMDB: HMDB0037426)
Cytoplasm (HMDB: HMDB0037426)

Source

Exogenous

Exogenous (HMDB: HMDB0037426)

Food

Pulse

Bean

Broad bean (FooDB: FOOD00197)

Pea

Grass pea (FooDB: FOOD00096)

Herb and spice

Herb

Linden (FooDB: FOOD00184)
Silver linden (FooDB: FOOD00003)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	2.61 g/L	ALOGPS
logP	-0.18	ALOGPS
logP	-1.1	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Acidic)	7.08	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	15	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	245.29 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	137.9 m³·mol⁻¹	ChemAxon
Polarizability	57.26 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	224.066	30932474
DeepCCS	[M-H]-	222.236	30932474
DeepCCS	[M-2H]-	256.128	30932474
DeepCCS	[M+Na]+	229.909	30932474
AllCCS	[M+H]+	230.3	32859911
AllCCS	[M+H-H2O]+	229.0	32859911
AllCCS	[M+NH4]+	231.5	32859911
AllCCS	[M+Na]+	231.8	32859911
AllCCS	[M-H]-	225.0	32859911
AllCCS	[M+Na-2H]-	227.0	32859911
AllCCS	[M+HCOO]-	229.4	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.	4.29 minutes	32390414
Predicted by Siyang on May 30, 2022	11.0417 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	5.85 minutes	32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid	221.4 seconds	40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	1907.2 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	198.0 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	108.3 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	179.8 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	78.8 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	337.5 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	374.5 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	538.4 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	666.2 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	408.8 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	1220.5 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	243.1 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	264.2 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	427.8 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	410.2 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	197.4 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Astragalin 7-rhamnoside	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(OC3=C2)C2=CC=C(O)C=C2)[C@H](O)[C@H](O)[C@H]1O	5804.8	Standard polar	33892256
Astragalin 7-rhamnoside	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(OC3=C2)C2=CC=C(O)C=C2)[C@H](O)[C@H](O)[C@H]1O	4923.8	Standard non polar	33892256
Astragalin 7-rhamnoside	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(OC3=C2)C2=CC=C(O)C=C2)[C@H](O)[C@H](O)[C@H]1O	5477.9	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Astragalin 7-rhamnoside,1TMS,isomer #1	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5095.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,1TMS,isomer #2	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5057.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,1TMS,isomer #3	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5054.6	Semi standard non polar	33892256
Astragalin 7-rhamnoside,1TMS,isomer #4	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5066.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,1TMS,isomer #5	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5082.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,1TMS,isomer #6	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5114.8	Semi standard non polar	33892256
Astragalin 7-rhamnoside,1TMS,isomer #7	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5088.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,1TMS,isomer #8	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5061.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,1TMS,isomer #9	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5083.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #1	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4919.3	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #10	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4905.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #11	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4924.4	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #12	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4947.6	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #13	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4918.4	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #14	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4897.8	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #15	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4916.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #16	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4913.3	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #17	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4915.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #18	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4938.6	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #19	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4911.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #2	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4916.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #20	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4889.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #21	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4912.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #22	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4935.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #23	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4941.4	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #24	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4915.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #25	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4892.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #26	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4919.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #27	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4957.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #28	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4930.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #29	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4906.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #3	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4918.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #30	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4930.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #31	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4958.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #32	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4936.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #33	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4957.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #34	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4926.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #35	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4930.4	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #36	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4926.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #4	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4930.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #5	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4983.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #6	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4931.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #7	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4906.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #8	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4936.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TMS,isomer #9	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4930.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #1	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4797.8	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #10	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4829.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #11	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4781.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #12	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4748.4	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #13	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4787.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #14	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4794.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #15	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4814.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #16	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4770.4	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #17	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4734.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #18	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4777.3	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #19	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4827.3	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #2	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4767.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #20	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4787.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #21	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4753.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #22	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4790.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #23	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4830.3	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #24	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4799.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #25	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4840.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #26	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4793.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #27	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4794.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #28	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4785.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #29	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4824.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #3	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4788.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #30	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4831.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #31	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4836.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #32	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4827.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #33	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4799.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #34	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4830.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #35	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4816.6	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #36	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4809.4	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #37	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4799.6	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #38	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4770.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #39	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4803.8	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #4	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4823.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #40	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4829.3	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #41	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4825.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #42	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4796.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #43	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4827.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #44	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4823.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #45	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4798.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #46	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4825.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #47	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4815.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #48	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4822.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #49	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4815.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #5	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4787.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #50	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4827.4	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #51	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4810.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #52	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4806.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #53	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4776.8	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #54	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4809.6	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #55	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4813.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #56	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4806.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #57	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4778.3	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #58	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4810.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #59	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4810.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #6	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4756.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #60	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4787.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #61	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4816.6	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #62	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4804.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #63	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4809.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #64	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4804.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #65	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4827.8	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #66	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4820.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #67	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4793.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #68	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4824.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #69	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4805.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #7	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4791.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #70	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4778.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #71	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4811.8	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #72	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4801.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #73	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4805.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #74	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4798.3	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #75	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4822.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #76	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4795.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #77	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4825.8	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #78	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4815.8	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #79	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4822.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #8	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4779.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #80	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4814.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #81	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4826.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #82	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4828.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #83	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4823.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #84	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4839.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,3TMS,isomer #9	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4776.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #1	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4716.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #10	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4648.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #100	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4739.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #101	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4732.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #102	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4729.8	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #103	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4705.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #104	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4743.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #105	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4736.6	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #106	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4742.8	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #107	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4735.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #108	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4734.8	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #109	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4740.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #11	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4685.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #110	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4733.3	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #111	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4764.8	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #112	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4741.6	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #113	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4716.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #114	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4750.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #115	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4750.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #116	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4759.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #117	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4748.6	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #118	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4723.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #119	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4727.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #12	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4727.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #120	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4719.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #121	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4756.4	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #122	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4742.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #123	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4749.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #124	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4740.6	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #125	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4780.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #126	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4772.3	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #13	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4712.3	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #14	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4678.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #15	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4717.4	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #16	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4723.6	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #17	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4703.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #18	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4735.4	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #19	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4710.3	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #2	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4718.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #20	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4717.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #21	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4709.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #22	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4724.6	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #23	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4721.3	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #24	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4692.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #25	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4658.8	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #26	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4697.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #27	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4721.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #28	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4691.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #29	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4659.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #3	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4737.4	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #30	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4698.3	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #31	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4722.6	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #32	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4698.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #33	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4733.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #34	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4696.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #35	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4700.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #36	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4694.3	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #37	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4731.8	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #38	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4704.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #39	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4670.4	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #4	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4715.4	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #40	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4709.3	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #41	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4707.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #42	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4684.8	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #43	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4717.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #44	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4678.8	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #45	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4683.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #46	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4674.8	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #47	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4723.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #48	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4703.6	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #49	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4735.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #5	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4682.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #50	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4702.4	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #51	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4705.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #52	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4699.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #53	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4735.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #54	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4739.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #55	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4738.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #56	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4738.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #57	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4795.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #58	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4757.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #59	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4765.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #6	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4719.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #60	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4733.8	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #61	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4769.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #62	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4762.6	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #63	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4767.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #64	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4735.6	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #65	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4769.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #66	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4755.8	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #67	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4728.8	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #68	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4764.3	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #69	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4764.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #7	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4709.6	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #70	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4769.8	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #71	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4762.4	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #72	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4749.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #73	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4761.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #74	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4728.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #75	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4764.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #76	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4725.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #77	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4694.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #78	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4732.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #79	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4729.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #8	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4708.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #80	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4736.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #81	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4726.3	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #82	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4746.8	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #83	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4723.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #84	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4757.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #85	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4764.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #86	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4770.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #87	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4764.4	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #88	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4749.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #89	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4756.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #9	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4681.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #90	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4746.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #91	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4784.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #92	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	4760.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #93	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4764.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #94	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4734.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #95	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4770.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #96	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4726.6	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #97	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4699.6	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #98	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4737.3	Semi standard non polar	33892256
Astragalin 7-rhamnoside,4TMS,isomer #99	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4735.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,1TBDMS,isomer #1	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5308.3	Semi standard non polar	33892256
Astragalin 7-rhamnoside,1TBDMS,isomer #2	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5279.4	Semi standard non polar	33892256
Astragalin 7-rhamnoside,1TBDMS,isomer #3	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5259.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,1TBDMS,isomer #4	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5262.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,1TBDMS,isomer #5	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5273.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,1TBDMS,isomer #6	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5314.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,1TBDMS,isomer #7	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5280.6	Semi standard non polar	33892256
Astragalin 7-rhamnoside,1TBDMS,isomer #8	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5260.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,1TBDMS,isomer #9	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5292.4	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #1	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5338.3	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #10	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5304.6	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #11	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5321.6	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #12	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5361.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #13	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5310.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #14	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5293.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #15	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5324.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #16	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5302.3	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #17	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5304.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #18	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5351.0	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #19	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5304.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #2	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5331.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #20	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5287.6	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #21	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5317.6	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #22	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O[Si](C)(C)C(C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5322.8	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #23	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5353.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #24	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5306.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #25	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5289.8	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #26	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5320.8	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #27	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5357.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #28	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5313.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #29	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5298.3	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #3	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5337.3	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #30	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5329.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #31	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)OC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5356.3	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #32	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5344.2	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #33	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5372.6	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #34	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5315.1	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #35	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5321.4	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #36	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	5315.5	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #4	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5336.9	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #5	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5407.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #6	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5335.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #7	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5326.3	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #8	C[C@@H]1O[C@@H](OC2=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C(O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5355.7	Semi standard non polar	33892256
Astragalin 7-rhamnoside,2TBDMS,isomer #9	C[C@@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O[C@@H]4O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)=C(C4=CC=C(O)C=C4)OC3=C2)[C@H](O)[C@H](O)[C@H]1O	5319.0	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 - Astragalin 7-rhamnoside GC-MS (Non-derivatized) - 70eV, Positive	splash10-020r-6600190000-d2505426d23a9dcab764	2017-11-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Astragalin 7-rhamnoside GC-MS ("Astragalin 7-rhamnoside,1TMS,#1" TMS) - 70eV, Positive	Not Available	2021-10-14	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Astragalin 7-rhamnoside GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Astragalin 7-rhamnoside GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Astragalin 7-rhamnoside GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Astragalin 7-rhamnoside GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Astragalin 7-rhamnoside GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Astragalin 7-rhamnoside GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Astragalin 7-rhamnoside GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Astragalin 7-rhamnoside GC-MS (TMS_1_8) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Astragalin 7-rhamnoside GC-MS (TMS_1_9) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Astragalin 7-rhamnoside GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Astragalin 7-rhamnoside GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Astragalin 7-rhamnoside GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Astragalin 7-rhamnoside GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Astragalin 7-rhamnoside GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Astragalin 7-rhamnoside GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Astragalin 7-rhamnoside GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Astragalin 7-rhamnoside GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Astragalin 7-rhamnoside GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Astragalin 7-rhamnoside GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Astragalin 7-rhamnoside GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Astragalin 7-rhamnoside GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Astragalin 7-rhamnoside GC-MS (TMS_2_13) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Astragalin 7-rhamnoside GC-MS (TMS_2_14) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Experimental LC-MS/MS	LC-MS/MS Spectrum - Astragalin 7-rhamnoside 10V, Positive-QTOF	splash10-000i-0090320000-52692353619835c7cb68	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Astragalin 7-rhamnoside 6V, Positive-QTOF	splash10-000i-0090000000-79d3a7095e8de0aaba76	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Astragalin 7-rhamnoside 10V, Positive-QTOF	splash10-000t-0000790000-7f86833e870b4eff35e4	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Astragalin 7-rhamnoside 50V, Positive-QTOF	splash10-000i-0090000000-9a034e6feb774278967d	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Astragalin 7-rhamnoside 30V, Positive-QTOF	splash10-000i-0090000000-82edccc0ce044362d721	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Astragalin 7-rhamnoside 30V, Positive-QTOF	splash10-000i-0090000000-58d2100ae6027ee604f8	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Astragalin 7-rhamnoside 6V, Positive-QTOF	splash10-000i-0090320000-71fc30bcb79d456d4b1b	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Astragalin 7-rhamnoside 50V, Positive-QTOF	splash10-000i-0090000000-52b5fb2d57c2252e862f	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Astragalin 7-rhamnoside 10V, Positive-QTOF	splash10-001j-0000980000-15dbcbf80ea3fe422460	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Astragalin 7-rhamnoside 6V, Positive-QTOF	splash10-000i-0090000000-52b5d388679d0ce69849	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Astragalin 7-rhamnoside 10V, Positive-QTOF	splash10-0019-0090510000-79ff4e287f266a453f84	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Astragalin 7-rhamnoside 10V, Positive-QTOF	splash10-001j-0000970000-59a2e9b9895ae6172045	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Astragalin 7-rhamnoside 50V, Positive-QTOF	splash10-000i-0090000000-1cb1d337dea13ffeba5d	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Astragalin 7-rhamnoside 30V, Positive-QTOF	splash10-000i-0090000000-5766f8ee9f790af1a18e	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Astragalin 7-rhamnoside 10V, Positive-QTOF	splash10-000i-0090420000-dfc8b9fc4a6e52d167e7	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Astragalin 7-rhamnoside 30V, Negative-QTOF	splash10-001i-0090800000-253481210b8f01981c8d	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Astragalin 7-rhamnoside 6V, Positive-QTOF	splash10-000i-0090000000-ffd93d99903c56ef1617	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Astragalin 7-rhamnoside 6V, Positive-QTOF	splash10-000t-0000790000-faf4e4d9f31389b72327	2021-09-20	HMDB team, MONA	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Astragalin 7-rhamnoside 10V, Positive-QTOF	splash10-00ls-0020940000-152be68c0c9c9915445f	2018-11-27	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Astragalin 7-rhamnoside 20V, Positive-QTOF	splash10-000i-0190600000-36705d8ceb82dbae9f85	2018-11-27	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Astragalin 7-rhamnoside 40V, Positive-QTOF	splash10-000i-1390200000-3b0e1393af3dad7896ed	2018-11-27	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Astragalin 7-rhamnoside 10V, Positive-QTOF	splash10-001i-0000920000-b79bbf42cd3de726bb3c	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Astragalin 7-rhamnoside 20V, Positive-QTOF	splash10-001k-0000990000-8899639ff6650a87219c	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Astragalin 7-rhamnoside 40V, Positive-QTOF	splash10-001i-0000900000-fa0a1381502338409394	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Astragalin 7-rhamnoside 10V, Negative-QTOF	splash10-0006-0000090000-d429407c55c06e0fc931	2021-09-23	Wishart Lab	View Spectrum

NMR Spectra

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

Biological Properties

Cellular Locations

Cytoplasm
Extracellular

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

C00005178

Chemspider ID

28481780

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

57390614

PDB ID

Not Available

ChEBI ID

68881

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

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

Showing metabocard for Astragalin 7-rhamnoside (HMDB0037426)

MOL for HMDB0037426 (Astragalin 7-rhamnoside)

3D MOL for HMDB0037426 (Astragalin 7-rhamnoside)

3D SDF for HMDB0037426 (Astragalin 7-rhamnoside)

3D-SDF for HMDB0037426 (Astragalin 7-rhamnoside)

PDB for HMDB0037426 (Astragalin 7-rhamnoside)

3D PDB for HMDB0037426 (Astragalin 7-rhamnoside)

SMILES for HMDB0037426 (Astragalin 7-rhamnoside)

INCHI for HMDB0037426 (Astragalin 7-rhamnoside)

Structure for HMDB0037426 (Astragalin 7-rhamnoside)

3D Structure for HMDB0037426 (Astragalin 7-rhamnoside)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra