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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2021-09-23 06:29:04 UTC

Update Date

2021-09-23 06:29:04 UTC

HMDB ID

HMDB0302090

Secondary Accession Numbers

None

Metabolite Identification

Common Name

(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside

Description

(2R)-8-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2R,3R,4R,5R,6R)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}oxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one belongs to the class of organic compounds known as flavonoid 8-c-glycosides. Flavonoid 8-C-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to 8-position of a 2-phenylchromen-4-one flavonoid backbone. Based on a literature review very few articles have been published on (2R)-8-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2R,3R,4R,5R,6R)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}oxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one.

Structure

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

  Mrv0541 02241212132D          

 42 46  0  0  0  0            999 V2000
   -4.0661    1.6795    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7805    1.2670    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7805    0.4420    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0661    0.0294    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3516    0.4420    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3516    1.2670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0661    2.5045    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4950    1.6795    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4950    0.0295    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0661   -0.7956    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9227    0.4420    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2082    1.6795    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9227    1.2670    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2082    0.0295    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4937    0.4420    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4937    1.2670    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6518    0.8839    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6371    1.6795    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2082    2.5045    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2207    1.6795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9352    1.2670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2082   -0.7955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9227   -1.2081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9227   -2.0331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2082   -2.4456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4937   -2.0331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4937   -1.2081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2207   -0.7955    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2207   -2.4456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9352   -2.0331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9352   -1.2081    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6371   -0.7956    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2082   -3.2706    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2207   -3.2706    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6497   -0.7956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3641    0.4420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6497    0.0295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3641   -1.2081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0786   -0.7956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0786    0.0295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7931    0.4420    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6371    0.0295    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  7  1  6  0  0  0
  2  8  1  1  0  0  0
  3  9  1  6  0  0  0
  4 10  1  6  0  0  0
 13 11  1  0  0  0  0
 11 14  1  0  0  0  0
 12 13  1  0  0  0  0
 12 16  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  5 17  1  6  0  0  0
 13 18  1  1  0  0  0
 12 19  1  6  0  0  0
 16 20  1  1  0  0  0
 20 21  1  0  0  0  0
 14 22  1  1  0  0  0
 22 23  2  0  0  0  0
 22 27  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 28 27  1  0  0  0  0
 26 27  2  0  0  0  0
 26 29  1  0  0  0  0
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 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 23 32  1  0  0  0  0
 25 33  1  0  0  0  0
 29 34  2  0  0  0  0
 31 35  1  1  0  0  0
 37 35  2  0  0  0  0
 35 38  1  0  0  0  0
 36 37  1  0  0  0  0
 36 40  2  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
  5 42  1  0  0  0  0
 11 42  1  6  0  0  0
M  END

HMDB0302090
     RDKit          3D
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside
 71 75  0  0  0  0  0  0  0  0999 V2000
   -3.9807   -0.1664   -4.2894 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3874    0.0584   -3.2323 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0640    0.7003   -2.0508 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7872   -0.2670   -0.8769 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4621    0.2959    0.2992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6735   -0.1953    0.7226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3287    0.3569    1.8334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7674    1.4112    2.5272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4394    1.9486    3.6281 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5525    1.8999    2.0974 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9187    1.3457    1.0020 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4514   -0.5826   -0.7296 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5531   -0.5959   -1.7570 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9819   -0.2808   -3.0300 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1530   -0.2671   -4.1298 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5354    0.0500   -5.4200 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1757   -0.6024   -3.8837 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6144   -0.9235   -2.6109 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9559   -1.2701   -2.5594 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2103   -0.9301   -1.4988 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2754   -1.3218   -0.1613 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6345   -1.9193    0.6884 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1685   -2.6250    1.6183 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4603   -3.8243    2.2174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6111   -3.6136    2.9319 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7641   -1.6642    2.6047 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0622   -2.0921    2.9450 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8929   -0.2840    1.9960 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1965    0.5137    2.2215 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2373   -0.3807    0.4796 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5801   -0.5394    0.4485 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2546    0.5179   -0.1972 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2375   -0.0155   -0.9668 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0866    0.7974   -1.6336 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9347    0.7359   -3.0401 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1274    2.2124   -1.1490 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3956    2.7786   -1.4506 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0491    2.1963    0.3600 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8037    3.5307    0.7391 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9352    1.3543    0.9070 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9595    2.1978    1.4884 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6435    1.6869   -1.7989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1599    0.7277   -2.1677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3308   -1.2080   -1.1979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1480   -1.0160    0.2091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2835   -0.0407    2.1547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1042    2.7115    3.4888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1199    2.7213    2.6432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9717    1.7512    0.6935 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.9623   -2.2485   -0.4311 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.8522   -4.5069    3.3344 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2165   -1.5690    3.5464 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5663   -2.3231    2.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.7516    0.0745    2.9147 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9740    0.6500    0.0510 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5164    1.1679   -0.7116 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1305    0.3727   -1.4746 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.0830    2.0581   -1.2881 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.4337    2.9485    1.9004 H   0  0  0  0  0  0  0  0  0  0  0  0
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  2  3  1  0
  3  4  1  0
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 14  2  1  0
 30 21  1  0
 40 32  1  0
 11  5  1  0
 20 13  1  0
  3 42  1  0
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  9 47  1  0
 10 48  1  0
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 16 50  1  0
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 30 62  1  6
 32 63  1  6
 34 64  1  6
 35 65  1  0
 36 66  1  6
 37 67  1  0
 38 68  1  1
 39 69  1  0
 40 70  1  1
 41 71  1  0
M  END

  Mrv0541 02241212132D          

 42 46  0  0  0  0            999 V2000
   -4.0661    1.6795    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7805    1.2670    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7805    0.4420    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -3.3516    0.4420    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -4.0661   -0.7956    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9227    0.4420    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    0.9352   -1.2081    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6371   -0.7956    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2082   -3.2706    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2207   -3.2706    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6497   -0.7956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3641    0.4420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6497    0.0295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3641   -1.2081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0786   -0.7956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0786    0.0295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7931    0.4420    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6371    0.0295    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  7  1  6  0  0  0
  2  8  1  1  0  0  0
  3  9  1  6  0  0  0
  4 10  1  6  0  0  0
 13 11  1  0  0  0  0
 11 14  1  0  0  0  0
 12 13  1  0  0  0  0
 12 16  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  5 17  1  6  0  0  0
 13 18  1  1  0  0  0
 12 19  1  6  0  0  0
 16 20  1  1  0  0  0
 20 21  1  0  0  0  0
 14 22  1  1  0  0  0
 22 23  2  0  0  0  0
 22 27  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 28 27  1  0  0  0  0
 26 27  2  0  0  0  0
 26 29  1  0  0  0  0
 28 31  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 23 32  1  0  0  0  0
 25 33  1  0  0  0  0
 29 34  2  0  0  0  0
 31 35  1  1  0  0  0
 37 35  2  0  0  0  0
 35 38  1  0  0  0  0
 36 37  1  0  0  0  0
 36 40  2  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
  5 42  1  0  0  0  0
 11 42  1  6  0  0  0
M  END
> <DATABASE_ID>
HMDB0302090

> <DATABASE_NAME>
hmdb

> <SMILES>
[H][C@@]1(O[C@@H]2[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]2C2=C(O)C=C(O)C3=C2O[C@H](CC3=O)C2=CC=C(O)C=C2)O[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C26H30O15/c27-7-14-17(32)19(34)24(40-26-21(36)18(33)20(35)25(37)41-26)23(39-14)16-11(30)5-10(29)15-12(31)6-13(38-22(15)16)8-1-3-9(28)4-2-8/h1-5,13-14,17-21,23-30,32-37H,6-7H2/t13-,14-,17-,18-,19+,20-,21-,23+,24-,25-,26-/m1/s1

> <INCHI_KEY>
RSOASCRBGDBQFY-VCLDZDMQSA-N

> <FORMULA>
C26H30O15

> <MOLECULAR_WEIGHT>
582.5074

> <EXACT_MASS>
582.15847029

> <JCHEM_ACCEPTOR_COUNT>
15

> <JCHEM_AVERAGE_POLARIZABILITY>
55.38920360638205

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
10

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R)-8-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2R,3R,4R,5R,6R)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}oxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one

> <ALOGPS_LOGP>
-0.91

> <JCHEM_LOGP>
-1.4269375000000002

> <ALOGPS_LOGS>
-1.63

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.437402765199268

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.480769421766415

> <JCHEM_PKA_STRONGEST_BASIC>
-3.655996436320149

> <JCHEM_POLAR_SURFACE_AREA>
256.28999999999996

> <JCHEM_REFRACTIVITY>
131.8888

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.36e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-8-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2R,3R,4R,5R,6R)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}oxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzopyran-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0302090
     RDKit          3D
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside
 71 75  0  0  0  0  0  0  0  0999 V2000
   -3.9807   -0.1664   -4.2894 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3874    0.0584   -3.2323 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0640    0.7003   -2.0508 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7872   -0.2670   -0.8769 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4621    0.2959    0.2992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6735   -0.1953    0.7226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3287    0.3569    1.8334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7674    1.4112    2.5272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4394    1.9486    3.6281 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5525    1.8999    2.0974 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9187    1.3457    1.0020 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4514   -0.5826   -0.7296 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5531   -0.5959   -1.7570 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9819   -0.2808   -3.0300 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1530   -0.2671   -4.1298 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5354    0.0500   -5.4200 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1757   -0.6024   -3.8837 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6144   -0.9235   -2.6109 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9559   -1.2701   -2.5594 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2103   -0.9301   -1.4988 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2754   -1.3218   -0.1613 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6345   -1.9193    0.6884 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1685   -2.6250    1.6183 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4603   -3.8243    2.2174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6111   -3.6136    2.9319 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7641   -1.6642    2.6047 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0622   -2.0921    2.9450 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8929   -0.2840    1.9960 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1965    0.5137    2.2215 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2373   -0.3807    0.4796 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5801   -0.5394    0.4485 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2546    0.5179   -0.1972 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2375   -0.0155   -0.9668 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0866    0.7974   -1.6336 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9347    0.7359   -3.0401 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1274    2.2124   -1.1490 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3956    2.7786   -1.4506 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0491    2.1963    0.3600 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8037    3.5307    0.7391 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9352    1.3543    0.9070 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9595    2.1978    1.4884 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6435    1.6869   -1.7989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1599    0.7277   -2.1677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3308   -1.2080   -1.1979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1480   -1.0160    0.2091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2835   -0.0407    2.1547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1042    2.7115    3.4888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1199    2.7213    2.6432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9717    1.7512    0.6935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4472    0.3127   -5.6585 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8345   -0.5964   -4.7421 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4286   -1.6687   -1.7996 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9623   -2.2485   -0.4311 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0450   -3.0130    1.0070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5419   -4.6174    1.4433 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2954   -4.2340    2.9638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8522   -4.5069    3.3344 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2165   -1.5690    3.5464 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5663   -2.3231    2.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7618    0.1735    2.4923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7516    0.0745    2.9147 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9740    0.6500    0.0510 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5164    1.1679   -0.7116 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1305    0.3727   -1.4746 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8667   -0.2335   -3.2514 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3015    2.8297   -1.5491 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0830    2.0581   -1.2881 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0231    1.8665    0.7789 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2285    3.9695    0.0327 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3254    0.7125    1.7087 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4337    2.9485    1.9004 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 11  2  0
  4 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
 17 18  1  0
 18 19  1  0
 18 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 23 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  1  0
 36 38  1  0
 38 39  1  0
 38 40  1  0
 40 41  1  0
 14  2  1  0
 30 21  1  0
 40 32  1  0
 11  5  1  0
 20 13  1  0
  3 42  1  0
  3 43  1  0
  4 44  1  6
  6 45  1  0
  7 46  1  0
  9 47  1  0
 10 48  1  0
 11 49  1  0
 16 50  1  0
 17 51  1  0
 19 52  1  0
 21 53  1  6
 23 54  1  6
 24 55  1  0
 24 56  1  0
 25 57  1  0
 26 58  1  1
 27 59  1  0
 28 60  1  1
 29 61  1  0
 30 62  1  6
 32 63  1  6
 34 64  1  6
 35 65  1  0
 36 66  1  6
 37 67  1  0
 38 68  1  1
 39 69  1  0
 40 70  1  1
 41 71  1  0
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -7.590   3.135   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -8.924   2.365   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -8.924   0.825   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -7.590   0.055   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.256   0.825   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -6.256   2.365   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      -7.590   4.675   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0     -10.257   3.135   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0     -10.257   0.055   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      -7.590  -1.485   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -3.589   0.825   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.255   3.135   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.589   2.365   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.255   0.055   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -0.922   0.825   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -0.922   2.365   0.000  0.00  0.00           C+0
HETATM   17  H   UNK     0      -4.950   1.650   0.000  0.00  0.00           H+0
HETATM   18  O   UNK     0      -4.923   3.135   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -2.255   4.675   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.412   3.135   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       1.746   2.365   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -2.255  -1.485   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -3.589  -2.255   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -3.589  -3.795   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.255  -4.565   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.922  -3.795   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.922  -2.255   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       0.412  -1.485   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       0.412  -4.565   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.746  -3.795   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.746  -2.255   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -4.923  -1.485   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0      -2.255  -6.105   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0       0.412  -6.105   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       3.079  -1.485   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       4.413   0.825   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       3.079   0.055   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       4.413  -2.255   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       5.747  -1.485   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       5.747   0.055   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       7.080   0.825   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0      -4.923   0.055   0.000  0.00  0.00           O+0
CONECT    1    2    6    7                                                  
CONECT    2    1    3    8                                                  
CONECT    3    2    4    9                                                  
CONECT    4    3    5   10                                                  
CONECT    5    4    6   17   42                                             
CONECT    6    1    5                                                       
CONECT    7    1                                                            
CONECT    8    2                                                            
CONECT    9    3                                                            
CONECT   10    4                                                            
CONECT   11   13   14   42                                                  
CONECT   12   13   16   19                                                  
CONECT   13   11   12   18                                                  
CONECT   14   11   15   22                                                  
CONECT   15   14   16                                                       
CONECT   16   12   15   20                                                  
CONECT   17    5                                                            
CONECT   18   13                                                            
CONECT   19   12                                                            
CONECT   20   16   21                                                       
CONECT   21   20                                                            
CONECT   22   14   23   27                                                  
CONECT   23   22   24   32                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   33                                                  
CONECT   26   25   27   29                                                  
CONECT   27   22   28   26                                                  
CONECT   28   27   31                                                       
CONECT   29   26   30   34                                                  
CONECT   30   29   31                                                       
CONECT   31   28   30   35                                                  
CONECT   32   23                                                            
CONECT   33   25                                                            
CONECT   34   29                                                            
CONECT   35   31   37   38                                                  
CONECT   36   37   40                                                       
CONECT   37   35   36                                                       
CONECT   38   35   39                                                       
CONECT   39   38   40                                                       
CONECT   40   36   39   41                                                  
CONECT   41   40                                                            
CONECT   42    5   11                                                       
MASTER        0    0    0    0    0    0    0    0   42    0   92    0
END

COMPND    HMDB0302090
HETATM    1  O1  UNL     1      -3.981  -0.166  -4.289  1.00  0.00           O  
HETATM    2  C1  UNL     1      -3.387   0.058  -3.232  1.00  0.00           C  
HETATM    3  C2  UNL     1      -4.064   0.700  -2.051  1.00  0.00           C  
HETATM    4  C3  UNL     1      -3.787  -0.267  -0.877  1.00  0.00           C  
HETATM    5  C4  UNL     1      -4.462   0.296   0.299  1.00  0.00           C  
HETATM    6  C5  UNL     1      -5.673  -0.195   0.723  1.00  0.00           C  
HETATM    7  C6  UNL     1      -6.329   0.357   1.833  1.00  0.00           C  
HETATM    8  C7  UNL     1      -5.767   1.411   2.527  1.00  0.00           C  
HETATM    9  O2  UNL     1      -6.439   1.949   3.628  1.00  0.00           O  
HETATM   10  C8  UNL     1      -4.552   1.900   2.097  1.00  0.00           C  
HETATM   11  C9  UNL     1      -3.919   1.346   1.002  1.00  0.00           C  
HETATM   12  O3  UNL     1      -2.451  -0.583  -0.730  1.00  0.00           O  
HETATM   13  C10 UNL     1      -1.553  -0.596  -1.757  1.00  0.00           C  
HETATM   14  C11 UNL     1      -1.982  -0.281  -3.030  1.00  0.00           C  
HETATM   15  C12 UNL     1      -1.153  -0.267  -4.130  1.00  0.00           C  
HETATM   16  O4  UNL     1      -1.535   0.050  -5.420  1.00  0.00           O  
HETATM   17  C13 UNL     1       0.176  -0.602  -3.884  1.00  0.00           C  
HETATM   18  C14 UNL     1       0.614  -0.924  -2.611  1.00  0.00           C  
HETATM   19  O5  UNL     1       1.956  -1.270  -2.559  1.00  0.00           O  
HETATM   20  C15 UNL     1      -0.210  -0.930  -1.499  1.00  0.00           C  
HETATM   21  C16 UNL     1       0.275  -1.322  -0.161  1.00  0.00           C  
HETATM   22  O6  UNL     1      -0.635  -1.919   0.688  1.00  0.00           O  
HETATM   23  C17 UNL     1       0.169  -2.625   1.618  1.00  0.00           C  
HETATM   24  C18 UNL     1      -0.460  -3.824   2.217  1.00  0.00           C  
HETATM   25  O7  UNL     1      -1.611  -3.614   2.932  1.00  0.00           O  
HETATM   26  C19 UNL     1       0.764  -1.664   2.605  1.00  0.00           C  
HETATM   27  O8  UNL     1       2.062  -2.092   2.945  1.00  0.00           O  
HETATM   28  C20 UNL     1       0.893  -0.284   1.996  1.00  0.00           C  
HETATM   29  O9  UNL     1      -0.197   0.514   2.222  1.00  0.00           O  
HETATM   30  C21 UNL     1       1.237  -0.381   0.480  1.00  0.00           C  
HETATM   31  O10 UNL     1       2.580  -0.539   0.448  1.00  0.00           O  
HETATM   32  C22 UNL     1       3.255   0.518  -0.197  1.00  0.00           C  
HETATM   33  O11 UNL     1       4.237  -0.015  -0.967  1.00  0.00           O  
HETATM   34  C23 UNL     1       5.087   0.797  -1.634  1.00  0.00           C  
HETATM   35  O12 UNL     1       4.935   0.736  -3.040  1.00  0.00           O  
HETATM   36  C24 UNL     1       5.127   2.212  -1.149  1.00  0.00           C  
HETATM   37  O13 UNL     1       6.396   2.779  -1.451  1.00  0.00           O  
HETATM   38  C25 UNL     1       5.049   2.196   0.360  1.00  0.00           C  
HETATM   39  O14 UNL     1       4.804   3.531   0.739  1.00  0.00           O  
HETATM   40  C26 UNL     1       3.935   1.354   0.907  1.00  0.00           C  
HETATM   41  O15 UNL     1       2.959   2.198   1.488  1.00  0.00           O  
HETATM   42  H1  UNL     1      -3.643   1.687  -1.799  1.00  0.00           H  
HETATM   43  H2  UNL     1      -5.160   0.728  -2.168  1.00  0.00           H  
HETATM   44  H3  UNL     1      -4.331  -1.208  -1.198  1.00  0.00           H  
HETATM   45  H4  UNL     1      -6.148  -1.016   0.209  1.00  0.00           H  
HETATM   46  H5  UNL     1      -7.283  -0.041   2.155  1.00  0.00           H  
HETATM   47  H6  UNL     1      -7.104   2.711   3.489  1.00  0.00           H  
HETATM   48  H7  UNL     1      -4.120   2.721   2.643  1.00  0.00           H  
HETATM   49  H8  UNL     1      -2.972   1.751   0.694  1.00  0.00           H  
HETATM   50  H9  UNL     1      -2.447   0.313  -5.659  1.00  0.00           H  
HETATM   51  H10 UNL     1       0.835  -0.596  -4.742  1.00  0.00           H  
HETATM   52  H11 UNL     1       2.429  -1.669  -1.800  1.00  0.00           H  
HETATM   53  H12 UNL     1       0.962  -2.249  -0.431  1.00  0.00           H  
HETATM   54  H13 UNL     1       1.045  -3.013   1.007  1.00  0.00           H  
HETATM   55  H14 UNL     1      -0.542  -4.617   1.443  1.00  0.00           H  
HETATM   56  H15 UNL     1       0.295  -4.234   2.964  1.00  0.00           H  
HETATM   57  H16 UNL     1      -1.852  -4.507   3.334  1.00  0.00           H  
HETATM   58  H17 UNL     1       0.216  -1.569   3.546  1.00  0.00           H  
HETATM   59  H18 UNL     1       2.566  -2.323   2.137  1.00  0.00           H  
HETATM   60  H19 UNL     1       1.762   0.173   2.492  1.00  0.00           H  
HETATM   61  H20 UNL     1      -0.752   0.075   2.915  1.00  0.00           H  
HETATM   62  H21 UNL     1       0.974   0.650   0.051  1.00  0.00           H  
HETATM   63  H22 UNL     1       2.516   1.168  -0.712  1.00  0.00           H  
HETATM   64  H23 UNL     1       6.130   0.373  -1.475  1.00  0.00           H  
HETATM   65  H24 UNL     1       4.867  -0.234  -3.251  1.00  0.00           H  
HETATM   66  H25 UNL     1       4.301   2.830  -1.549  1.00  0.00           H  
HETATM   67  H26 UNL     1       7.083   2.058  -1.288  1.00  0.00           H  
HETATM   68  H27 UNL     1       6.023   1.866   0.779  1.00  0.00           H  
HETATM   69  H28 UNL     1       4.229   3.970   0.033  1.00  0.00           H  
HETATM   70  H29 UNL     1       4.325   0.712   1.709  1.00  0.00           H  
HETATM   71  H30 UNL     1       3.434   2.948   1.900  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   14
CONECT    3    4   42   43
CONECT    4    5   12   44
CONECT    5    6    6   11
CONECT    6    7   45
CONECT    7    8    8   46
CONECT    8    9   10
CONECT    9   47
CONECT   10   11   11   48
CONECT   11   49
CONECT   12   13
CONECT   13   14   14   20
CONECT   14   15
CONECT   15   16   17   17
CONECT   16   50
CONECT   17   18   51
CONECT   18   19   20   20
CONECT   19   52
CONECT   20   21
CONECT   21   22   30   53
CONECT   22   23
CONECT   23   24   26   54
CONECT   24   25   55   56
CONECT   25   57
CONECT   26   27   28   58
CONECT   27   59
CONECT   28   29   30   60
CONECT   29   61
CONECT   30   31   62
CONECT   31   32
CONECT   32   33   40   63
CONECT   33   34
CONECT   34   35   36   64
CONECT   35   65
CONECT   36   37   38   66
CONECT   37   67
CONECT   38   39   40   68
CONECT   39   69
CONECT   40   41   70
CONECT   41   71
END

HMDB0302090
     RDKit          3D
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside
 71 75  0  0  0  0  0  0  0  0999 V2000
   -3.9807   -0.1664   -4.2894 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3874    0.0584   -3.2323 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0640    0.7003   -2.0508 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7872   -0.2670   -0.8769 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4621    0.2959    0.2992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6735   -0.1953    0.7226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3287    0.3569    1.8334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7674    1.4112    2.5272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4394    1.9486    3.6281 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5525    1.8999    2.0974 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9187    1.3457    1.0020 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4514   -0.5826   -0.7296 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5531   -0.5959   -1.7570 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9819   -0.2808   -3.0300 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1530   -0.2671   -4.1298 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5354    0.0500   -5.4200 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1757   -0.6024   -3.8837 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6144   -0.9235   -2.6109 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9559   -1.2701   -2.5594 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2103   -0.9301   -1.4988 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2754   -1.3218   -0.1613 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6345   -1.9193    0.6884 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1685   -2.6250    1.6183 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4603   -3.8243    2.2174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6111   -3.6136    2.9319 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7641   -1.6642    2.6047 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0622   -2.0921    2.9450 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8929   -0.2840    1.9960 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1965    0.5137    2.2215 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2373   -0.3807    0.4796 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5801   -0.5394    0.4485 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2546    0.5179   -0.1972 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2375   -0.0155   -0.9668 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0866    0.7974   -1.6336 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9347    0.7359   -3.0401 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1274    2.2124   -1.1490 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3956    2.7786   -1.4506 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0491    2.1963    0.3600 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8037    3.5307    0.7391 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9352    1.3543    0.9070 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9595    2.1978    1.4884 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6435    1.6869   -1.7989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1599    0.7277   -2.1677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3308   -1.2080   -1.1979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1480   -1.0160    0.2091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2835   -0.0407    2.1547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1042    2.7115    3.4888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1199    2.7213    2.6432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9717    1.7512    0.6935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4472    0.3127   -5.6585 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8345   -0.5964   -4.7421 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4286   -1.6687   -1.7996 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9623   -2.2485   -0.4311 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0450   -3.0130    1.0070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5419   -4.6174    1.4433 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2954   -4.2340    2.9638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8522   -4.5069    3.3344 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2165   -1.5690    3.5464 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5663   -2.3231    2.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7618    0.1735    2.4923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7516    0.0745    2.9147 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9740    0.6500    0.0510 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5164    1.1679   -0.7116 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1305    0.3727   -1.4746 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8667   -0.2335   -3.2514 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3015    2.8297   -1.5491 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0830    2.0581   -1.2881 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0231    1.8665    0.7789 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2285    3.9695    0.0327 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3254    0.7125    1.7087 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4337    2.9485    1.9004 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 11  2  0
  4 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
 17 18  1  0
 18 19  1  0
 18 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 23 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  1  0
 36 38  1  0
 38 39  1  0
 38 40  1  0
 40 41  1  0
 14  2  1  0
 30 21  1  0
 40 32  1  0
 11  5  1  0
 20 13  1  0
  3 42  1  0
  3 43  1  0
  4 44  1  6
  6 45  1  0
  7 46  1  0
  9 47  1  0
 10 48  1  0
 11 49  1  0
 16 50  1  0
 17 51  1  0
 19 52  1  0
 21 53  1  6
 23 54  1  6
 24 55  1  0
 24 56  1  0
 25 57  1  0
 26 58  1  1
 27 59  1  0
 28 60  1  1
 29 61  1  0
 30 62  1  6
 32 63  1  6
 34 64  1  6
 35 65  1  0
 36 66  1  6
 37 67  1  0
 38 68  1  1
 39 69  1  0
 40 70  1  1
 41 71  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(2R)-Naringenin 8-C-a-L-rhamnopyranosyl-(1->2)-b-D-glucopyranoside	Generator
(2R)-Naringenin 8-C-α-L-rhamnopyranosyl-(1->2)-β-D-glucopyranoside	Generator

Chemical Formula

C₂₆H₃₀O₁₅

Average Molecular Weight

582.5074

Monoisotopic Molecular Weight

582.15847029

IUPAC Name

(2R)-8-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2R,3R,4R,5R,6R)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}oxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one

Traditional Name

(2R)-8-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2R,3R,4R,5R,6R)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}oxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzopyran-4-one

CAS Registry Number

Not Available

SMILES

[H][C@@]1(O[C@@H]2[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]2C2=C(O)C=C(O)C3=C2O[C@H](CC3=O)C2=CC=C(O)C=C2)O[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O

InChI Identifier

InChI=1S/C26H30O15/c27-7-14-17(32)19(34)24(40-26-21(36)18(33)20(35)25(37)41-26)23(39-14)16-11(30)5-10(29)15-12(31)6-13(38-22(15)16)8-1-3-9(28)4-2-8/h1-5,13-14,17-21,23-30,32-37H,6-7H2/t13-,14-,17-,18-,19+,20-,21-,23+,24-,25-,26-/m1/s1

InChI Key

RSOASCRBGDBQFY-VCLDZDMQSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavonoid 8-c-glycosides. Flavonoid 8-C-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to 8-position of a 2-phenylchromen-4-one flavonoid backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Flavonoid 8-C-glycosides

Alternative Parents

Substituents

Flavonoid-8-c-glycoside
Hydroxyflavonoid
4'-hydroxyflavonoid
5-hydroxyflavonoid
7-hydroxyflavonoid
Flavanone
Flavan
Phenolic glycoside
O-glycosyl compound
Glycosyl compound
Disaccharide
Chromone
C-glycosyl compound
Chromane
1-benzopyran
Benzopyran
Aryl ketone
Aryl alkyl ketone
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Oxane
Vinylogous acid
Ketone
Hemiacetal
Secondary alcohol
Polyol
Acetal
Oxacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Organic oxygen compound
Hydrocarbon derivative
Alcohol
Organic oxide
Primary alcohol
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Exogenous (HMDB: HMDB0302090)

Food

Fruit

Tropical fruit

Loquat (FooDB: FOOD00076)

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
logP	-0.91	ALOGPS
logP	-1.4	ChemAxon
logS	-1.6	ALOGPS
pKa (Strongest Acidic)	7.48	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	15	ChemAxon
Hydrogen Donor Count	10	ChemAxon
Polar Surface Area	256.29 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	131.89 m³·mol⁻¹	ChemAxon
Polarizability	55.39 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	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
AllCCS	[M+H]+	231.985	32859911
AllCCS	[M+H-H2O]+	230.478	32859911
AllCCS	[M+Na]+	233.736	32859911
AllCCS	[M+NH4]+	233.35	32859911
AllCCS	[M-H]-	230.33	32859911
AllCCS	[M+Na-2H]-	232.523	32859911
AllCCS	[M+HCOO]-	235.08	32859911
DeepCCS	[M+H]+	222.24	30932474
DeepCCS	[M-H]-	220.312	30932474
DeepCCS	[M-2H]-	254.111	30932474
DeepCCS	[M+Na]+	228.298	30932474

Predicted Kovats Retention Indices

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,1TMS,isomer #10	C[Si](C)(C)O[C@H]1[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O)[C@@H]2O)O[C@@H](O)[C@H](O)[C@H]1O	4924.0	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,1TMS,isomer #10	C[Si](C)(C)O[C@H]1[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O)[C@@H]2O)O[C@@H](O)[C@H](O)[C@H]1O	4573.6	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,1TMS,isomer #10	C[Si](C)(C)O[C@H]1[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O)[C@@H]2O)O[C@@H](O)[C@H](O)[C@H]1O	8392.5	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,1TMS,isomer #8	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O)[C@@H]2O)O[C@H]1O	4934.7	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,1TMS,isomer #8	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O)[C@@H]2O)O[C@H]1O	4575.2	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,1TMS,isomer #8	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O)[C@@H]2O)O[C@H]1O	8286.9	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,2TMS,isomer #39	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4844.4	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,2TMS,isomer #39	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4547.4	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,2TMS,isomer #39	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	7078.4	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,2TMS,isomer #43	C[Si](C)(C)O[C@H]1[C@@H](O)[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O)[C@@H]2O)O[C@@H](O)[C@@H]1O[Si](C)(C)C	4800.8	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,2TMS,isomer #43	C[Si](C)(C)O[C@H]1[C@@H](O)[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O)[C@@H]2O)O[C@@H](O)[C@@H]1O[Si](C)(C)C	4541.5	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,2TMS,isomer #43	C[Si](C)(C)O[C@H]1[C@@H](O)[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O)[C@@H]2O)O[C@@H](O)[C@@H]1O[Si](C)(C)C	7310.5	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,2TMS,isomer #45	C[Si](C)(C)O[C@H]1[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O)[C@@H]2O)O[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4794.2	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,2TMS,isomer #45	C[Si](C)(C)O[C@H]1[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O)[C@@H]2O)O[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4536.4	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,2TMS,isomer #45	C[Si](C)(C)O[C@H]1[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O)[C@@H]2O)O[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	7435.6	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,2TMS,isomer #9	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O)[C@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)O[C@H](CO)[C@H]1O[Si](C)(C)C	4809.5	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,2TMS,isomer #9	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O)[C@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)O[C@H](CO)[C@H]1O[Si](C)(C)C	4505.8	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,2TMS,isomer #9	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O)[C@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)O[C@H](CO)[C@H]1O[Si](C)(C)C	7403.4	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #100	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O[Si](C)(C)C)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4761.8	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #100	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O[Si](C)(C)C)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4503.6	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #100	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O[Si](C)(C)C)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	6629.5	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #110	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O[Si](C)(C)C)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4754.7	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #110	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O[Si](C)(C)C)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4483.1	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #110	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O[Si](C)(C)C)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	6622.4	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #116	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4717.4	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #116	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4525.8	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #116	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	6595.4	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #15	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[C@H]1O	4671.8	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #15	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[C@H]1O	4521.5	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #15	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[C@H]1O	6702.1	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #21	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)[C@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)O[C@H](CO)[C@H]1O[Si](C)(C)C	4654.4	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #21	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)[C@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)O[C@H](CO)[C@H]1O[Si](C)(C)C	4515.5	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #21	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)[C@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)O[C@H](CO)[C@H]1O[Si](C)(C)C	6715.6	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #24	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4697.6	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #24	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4533.3	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #24	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	6577.2	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #25	C[Si](C)(C)OC[C@H]1O[C@@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)[C@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4665.5	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #25	C[Si](C)(C)OC[C@H]1O[C@@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)[C@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4556.8	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #25	C[Si](C)(C)OC[C@H]1O[C@@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)[C@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	6872.4	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #26	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)O[C@H](CO)[C@H]1O[Si](C)(C)C	4679.4	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #26	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)O[C@H](CO)[C@H]1O[Si](C)(C)C	4522.6	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #26	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)O[C@H](CO)[C@H]1O[Si](C)(C)C	6762.8	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #29	C[Si](C)(C)OC1=CC(O)=C2C(=O)C[C@H](C3=CC=C(O)C=C3)OC2=C1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O	4728.4	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #29	C[Si](C)(C)OC1=CC(O)=C2C(=O)C[C@H](C3=CC=C(O)C=C3)OC2=C1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O	4469.7	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #29	C[Si](C)(C)OC1=CC(O)=C2C(=O)C[C@H](C3=CC=C(O)C=C3)OC2=C1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O	6815.4	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #32	C[Si](C)(C)OC1=CC(O)=C([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O)C2=C1C(=O)C[C@H](C1=CC=C(O)C=C1)O2	4721.1	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #32	C[Si](C)(C)OC1=CC(O)=C([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O)C2=C1C(=O)C[C@H](C1=CC=C(O)C=C1)O2	4428.8	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #32	C[Si](C)(C)OC1=CC(O)=C([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O)C2=C1C(=O)C[C@H](C1=CC=C(O)C=C1)O2	6807.3	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #35	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O)=C3O2)C=C1	4723.6	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #35	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O)=C3O2)C=C1	4503.3	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #35	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O)=C3O2)C=C1	6580.5	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #5	C[Si](C)(C)O[C@@H]1O[C@@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4676.6	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #5	C[Si](C)(C)O[C@@H]1O[C@@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4511.4	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #5	C[Si](C)(C)O[C@@H]1O[C@@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	6781.9	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #58	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4697.3	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #58	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4538.5	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #58	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	6532.2	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #6	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)O[C@H](CO)[C@H]1O	4649.0	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #6	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)O[C@H](CO)[C@H]1O	4544.9	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,3TMS,isomer #6	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)O[C@H](CO)[C@H]1O	6782.3	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #120	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O[Si](C)(C)C)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4637.7	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #120	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O[Si](C)(C)C)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4478.5	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #120	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O[Si](C)(C)C)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	6195.4	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #130	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O[Si](C)(C)C)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4632.5	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #130	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O[Si](C)(C)C)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4470.6	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #130	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O[Si](C)(C)C)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	6191.9	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #136	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4608.1	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #136	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4508.4	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #136	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	6162.6	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #15	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]4O)=C3O2)C=C1	4626.3	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #15	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]4O)=C3O2)C=C1	4493.0	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #15	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]4O)=C3O2)C=C1	6208.3	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #185	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4642.6	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #185	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4436.4	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #185	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	6272.2	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #191	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O[Si](C)(C)C)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4634.3	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #191	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O[Si](C)(C)C)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4483.4	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #191	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O[Si](C)(C)C)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	6260.1	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #194	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O[Si](C)(C)C)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4642.4	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #194	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O[Si](C)(C)C)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4471.8	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #194	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O[Si](C)(C)C)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	6192.5	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #195	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O[Si](C)(C)C)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4646.2	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #195	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O[Si](C)(C)C)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4464.2	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #195	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O[Si](C)(C)C)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	6255.5	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #205	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O[Si](C)(C)C)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4642.4	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #205	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O[Si](C)(C)C)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4452.9	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #205	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O[Si](C)(C)C)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	6251.6	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #208	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4606.4	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #208	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4495.2	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #208	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	6205.7	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #209	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4620.5	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #209	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4498.2	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #209	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	6192.9	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #23	C[Si](C)(C)O[C@@H]1O[C@@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4564.3	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #23	C[Si](C)(C)O[C@@H]1O[C@@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4514.9	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #23	C[Si](C)(C)O[C@@H]1O[C@@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	6319.6	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #24	C[Si](C)(C)O[C@@H]1O[C@@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4555.5	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #24	C[Si](C)(C)O[C@@H]1O[C@@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4483.3	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #24	C[Si](C)(C)O[C@@H]1O[C@@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	6265.2	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #25	C[Si](C)(C)O[C@@H]1O[C@@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4591.7	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #25	C[Si](C)(C)O[C@@H]1O[C@@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4484.8	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #25	C[Si](C)(C)O[C@@H]1O[C@@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	6317.3	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #27	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)O[C@H](CO)[C@H]1O	4541.2	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #27	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)O[C@H](CO)[C@H]1O	4495.2	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #27	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)O[C@H](CO)[C@H]1O	6302.5	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #3	C[Si](C)(C)OC1=CC(O)=C2C(=O)C[C@H](C3=CC=C(O)C=C3)OC2=C1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O	4608.8	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #3	C[Si](C)(C)OC1=CC(O)=C2C(=O)C[C@H](C3=CC=C(O)C=C3)OC2=C1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O	4451.8	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #3	C[Si](C)(C)OC1=CC(O)=C2C(=O)C[C@H](C3=CC=C(O)C=C3)OC2=C1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O	6370.7	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #34	C[Si](C)(C)O[C@H]1[C@@H](O)[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[C@@H](O)[C@@H]1O[Si](C)(C)C	4575.2	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #34	C[Si](C)(C)O[C@H]1[C@@H](O)[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[C@@H](O)[C@@H]1O[Si](C)(C)C	4494.9	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #34	C[Si](C)(C)O[C@H]1[C@@H](O)[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[C@@H](O)[C@@H]1O[Si](C)(C)C	6244.3	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #39	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)O[C@H](CO)[C@H]1O[Si](C)(C)C	4577.8	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #39	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)O[C@H](CO)[C@H]1O[Si](C)(C)C	4505.0	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #39	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)O[C@H](CO)[C@H]1O[Si](C)(C)C	6238.9	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #42	C[Si](C)(C)OC1=CC(O)=C2C(=O)C[C@H](C3=CC=C(O)C=C3)OC2=C1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O	4610.8	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #42	C[Si](C)(C)OC1=CC(O)=C2C(=O)C[C@H](C3=CC=C(O)C=C3)OC2=C1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O	4463.5	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #42	C[Si](C)(C)OC1=CC(O)=C2C(=O)C[C@H](C3=CC=C(O)C=C3)OC2=C1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O	6307.8	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #45	C[Si](C)(C)OC1=CC(O)=C([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)C2=C1C(=O)C[C@H](C1=CC=C(O)C=C1)O2	4607.2	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #45	C[Si](C)(C)OC1=CC(O)=C([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)C2=C1C(=O)C[C@H](C1=CC=C(O)C=C1)O2	4443.1	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #45	C[Si](C)(C)OC1=CC(O)=C([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)C2=C1C(=O)C[C@H](C1=CC=C(O)C=C1)O2	6302.9	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #48	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]4O)=C3O2)C=C1	4620.6	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #48	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]4O)=C3O2)C=C1	4503.7	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #48	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]4O)=C3O2)C=C1	6155.7	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #52	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4605.9	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #52	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4504.9	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #52	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	6202.2	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #53	C[Si](C)(C)OC[C@H]1O[C@@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)[C@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4569.2	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #53	C[Si](C)(C)OC[C@H]1O[C@@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)[C@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4521.2	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #53	C[Si](C)(C)OC[C@H]1O[C@@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)[C@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	6398.4	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #54	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)O[C@H](CO)[C@H]1O[Si](C)(C)C	4589.1	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #54	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)O[C@H](CO)[C@H]1O[Si](C)(C)C	4495.1	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #54	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)O[C@H](CO)[C@H]1O[Si](C)(C)C	6315.2	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #57	C[Si](C)(C)OC1=CC(O)=C2C(=O)C[C@H](C3=CC=C(O)C=C3)OC2=C1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O	4595.1	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #57	C[Si](C)(C)OC1=CC(O)=C2C(=O)C[C@H](C3=CC=C(O)C=C3)OC2=C1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O	4457.8	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #57	C[Si](C)(C)OC1=CC(O)=C2C(=O)C[C@H](C3=CC=C(O)C=C3)OC2=C1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O	6319.4	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #60	C[Si](C)(C)OC1=CC(O)=C([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)C2=C1C(=O)C[C@H](C1=CC=C(O)C=C1)O2	4590.8	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #60	C[Si](C)(C)OC1=CC(O)=C([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)C2=C1C(=O)C[C@H](C1=CC=C(O)C=C1)O2	4437.0	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #60	C[Si](C)(C)OC1=CC(O)=C([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)C2=C1C(=O)C[C@H](C1=CC=C(O)C=C1)O2	6314.4	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #63	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]4O)=C3O2)C=C1	4603.3	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #63	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]4O)=C3O2)C=C1	4497.5	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #63	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]4O)=C3O2)C=C1	6167.1	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #66	C[Si](C)(C)OC[C@H]1O[C@@H](C2=C(O[Si](C)(C)C)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)[C@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4599.7	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #66	C[Si](C)(C)OC[C@H]1O[C@@H](C2=C(O[Si](C)(C)C)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)[C@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4495.1	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #66	C[Si](C)(C)OC[C@H]1O[C@@H](C2=C(O[Si](C)(C)C)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)[C@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	6440.6	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #67	C[Si](C)(C)OC1=CC(O)=C2C(=O)C[C@H](C3=CC=C(O)C=C3)OC2=C1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C	4612.6	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #67	C[Si](C)(C)OC1=CC(O)=C2C(=O)C[C@H](C3=CC=C(O)C=C3)OC2=C1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C	4466.4	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #67	C[Si](C)(C)OC1=CC(O)=C2C(=O)C[C@H](C3=CC=C(O)C=C3)OC2=C1[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C	6354.9	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #68	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O[Si](C)(C)C)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4633.6	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #68	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O[Si](C)(C)C)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4476.6	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #68	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O[Si](C)(C)C)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	6236.5	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #69	C[Si](C)(C)OC[C@H]1O[C@@H](C2=C(O)C=C(O[Si](C)(C)C)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)[C@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4596.4	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #69	C[Si](C)(C)OC[C@H]1O[C@@H](C2=C(O)C=C(O[Si](C)(C)C)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)[C@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4472.1	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #69	C[Si](C)(C)OC[C@H]1O[C@@H](C2=C(O)C=C(O[Si](C)(C)C)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)[C@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	6434.2	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #70	C[Si](C)(C)OC1=CC(O)=C([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)C2=C1C(=O)C[C@H](C1=CC=C(O)C=C1)O2	4613.3	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #70	C[Si](C)(C)OC1=CC(O)=C([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)C2=C1C(=O)C[C@H](C1=CC=C(O)C=C1)O2	4442.9	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #70	C[Si](C)(C)OC1=CC(O)=C([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)C2=C1C(=O)C[C@H](C1=CC=C(O)C=C1)O2	6349.6	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #71	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O[Si](C)(C)C)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4632.3	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #71	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O[Si](C)(C)C)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4464.8	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #71	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O[Si](C)(C)C)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	6232.2	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #72	C[Si](C)(C)OC[C@H]1O[C@@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O[Si](C)(C)C)C=C2)CC3=O)[C@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4614.3	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #72	C[Si](C)(C)OC[C@H]1O[C@@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O[Si](C)(C)C)C=C2)CC3=O)[C@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4538.0	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #72	C[Si](C)(C)OC[C@H]1O[C@@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O[Si](C)(C)C)C=C2)CC3=O)[C@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	6279.3	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #73	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4621.2	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #73	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	4506.2	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #73	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C)=C3O2)C=C1	6192.5	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #74	C[Si](C)(C)OC[C@H]1O[C@@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)[C@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4610.9	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #74	C[Si](C)(C)OC[C@H]1O[C@@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)[C@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4524.7	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #74	C[Si](C)(C)OC[C@H]1O[C@@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)[C@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	6374.1	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #76	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O)C2=C1C(=O)C[C@H](C1=CC=C(O)C=C1)O2	4621.9	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #76	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O)C2=C1C(=O)C[C@H](C1=CC=C(O)C=C1)O2	4390.5	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #76	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O)C2=C1C(=O)C[C@H](C1=CC=C(O)C=C1)O2	6376.6	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #80	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O[Si](C)(C)C)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O)=C3O2)C=C1	4659.2	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #80	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O[Si](C)(C)C)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O)=C3O2)C=C1	4447.7	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #80	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O[Si](C)(C)C)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O)=C3O2)C=C1	6236.1	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #83	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O[Si](C)(C)C)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O)=C3O2)C=C1	4655.5	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #83	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O[Si](C)(C)C)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O)=C3O2)C=C1	4427.3	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #83	C[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O[Si](C)(C)C)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O)=C3O2)C=C1	6232.8	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #9	C[Si](C)(C)OC1=CC(O)=C([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)C2=C1C(=O)C[C@H](C1=CC=C(O)C=C1)O2	4607.5	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #9	C[Si](C)(C)OC1=CC(O)=C([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)C2=C1C(=O)C[C@H](C1=CC=C(O)C=C1)O2	4427.1	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,4TMS,isomer #9	C[Si](C)(C)OC1=CC(O)=C([C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)C2=C1C(=O)C[C@H](C1=CC=C(O)C=C1)O2	6365.4	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,1TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O)[C@@H]2O)O[C@@H](O)[C@H](O)[C@H]1O	5134.0	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,1TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O)[C@@H]2O)O[C@@H](O)[C@H](O)[C@H]1O	4802.9	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,1TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O)[C@@H]2O)O[C@@H](O)[C@H](O)[C@H]1O	7961.8	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,1TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O)[C@@H]2O)O[C@H]1O	5152.9	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,1TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O)[C@@H]2O)O[C@H]1O	4805.2	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,1TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O)[C@@H]2O)O[C@H]1O	7880.6	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,2TBDMS,isomer #39	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=C3O2)C=C1	5259.7	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,2TBDMS,isomer #39	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=C3O2)C=C1	4974.9	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,2TBDMS,isomer #39	CC(C)(C)[Si](C)(C)OC1=CC=C([C@H]2CC(=O)C3=C(O)C=C(O)C([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[C@@H]4O[C@@H](O)[C@H](O)[C@@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=C3O2)C=C1	6937.8	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,2TBDMS,isomer #43	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O)[C@@H]2O)O[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	5183.7	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,2TBDMS,isomer #43	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O)[C@@H]2O)O[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4976.8	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,2TBDMS,isomer #43	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O)[C@@H]2O)O[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	7042.0	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,2TBDMS,isomer #45	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O)[C@@H]2O)O[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5172.7	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,2TBDMS,isomer #45	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O)[C@@H]2O)O[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4971.2	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,2TBDMS,isomer #45	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[C@H]2[C@H](C3=C(O)C=C(O)C4=C3O[C@@H](C3=CC=C(O)C=C3)CC4=O)O[C@H](CO)[C@@H](O)[C@@H]2O)O[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	7114.3	Standard polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O)[C@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)O[C@H](CO)[C@H]1O[Si](C)(C)C(C)(C)C	5166.5	Semi standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O)[C@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)O[C@H](CO)[C@H]1O[Si](C)(C)C(C)(C)C	4945.3	Standard non polar	33892256
(2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@H]2O)[C@H](C2=C(O)C=C(O)C3=C2O[C@@H](C2=CC=C(O)C=C2)CC3=O)O[C@H](CO)[C@H]1O[Si](C)(C)C(C)(C)C	7092.7	Standard polar	33892256

Spectra

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside 10V, Positive-QTOF	splash10-014r-0100980000-3f0fe6fd4be441a8fe62	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside 20V, Positive-QTOF	splash10-014r-0311910000-0a75f3a995d1fcf5e56e	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside 40V, Positive-QTOF	splash10-02ta-1759400000-774b6904b9cfaa7ea557	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside 10V, Negative-QTOF	splash10-001i-1100490000-c5b566ce6bed68b072f5	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside 20V, Negative-QTOF	splash10-0159-4512920000-31f74aeb773e9cbad3f7	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside 40V, Negative-QTOF	splash10-02u3-6914400000-1f9a8788f68b6b706533	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside 10V, Negative-QTOF	splash10-001i-0000090000-dea893230fea8d963272	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside 20V, Negative-QTOF	splash10-01q9-0000980000-6edda663a13988411a6e	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside 40V, Negative-QTOF	splash10-014i-0900400000-89057c5ab8f2ddeb2b3a	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside 10V, Positive-QTOF	splash10-001i-0000090000-e3cad8af02907a0a29dc	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside 20V, Positive-QTOF	splash10-03ea-0400960000-6879cd051546fe3bf5ef	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside 40V, Positive-QTOF	splash10-03di-0300900000-98e4dea931aa10bf3549	2021-10-21	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

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

FDB001846

KNApSAcK ID

Not Available

Chemspider ID

59696280

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Not Available

Showing metabocard for (2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside (HMDB0302090)

MOL for HMDB0302090 ((2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside)

3D MOL for HMDB0302090 ((2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside)

3D SDF for HMDB0302090 ((2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside)

3D-SDF for HMDB0302090 ((2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside)

PDB for HMDB0302090 ((2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside)

3D PDB for HMDB0302090 ((2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside)

SMILES for HMDB0302090 ((2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside)

INCHI for HMDB0302090 ((2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside)

Structure for HMDB0302090 ((2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside)

3D Structure for HMDB0302090 ((2R)-Naringenin 8-C-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Derivatized

MS/MS Spectra