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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 19:37:39 UTC

Update Date

2022-03-07 02:54:13 UTC

HMDB ID

HMDB0034725

Secondary Accession Numbers

HMDB34725

Metabolite Identification

Common Name

6-Hydroxykaempferol 7-glucoside

Description

6-Hydroxykaempferol 7-glucoside belongs to the class of organic compounds known as flavonoid-7-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position. Based on a literature review very few articles have been published on 6-Hydroxykaempferol 7-glucoside.

Structure

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

  Mrv0541 02241208442D          

 33 36  0  0  0  0            999 V2000
   -2.5012    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7862    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0712    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3576    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3574    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3574    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0712    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7861    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0710    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0710    0.8251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3574    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3576    0.8251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0712    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7862    0.8251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5012    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5012   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2148   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2148   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9298   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9298   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7861    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7861   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5011   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2147   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2147    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5011    0.8251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0712   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7862   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7862   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5012   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5012   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9298   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0712   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2 14  1  0  0  0  0
  3  4  1  0  0  0  0
  3  7  1  0  0  0  0
  4  5  1  0  0  0  0
  4 12  2  0  0  0  0
  5  6  2  0  0  0  0
  5  9  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 21  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 28  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 30  1  0  0  0  0
 19 20  1  0  0  0  0
 21 22  1  0  0  0  0
 21 26  2  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 32  1  0  0  0  0
 25 26  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 33  1  0  0  0  0
 30 31  1  0  0  0  0
M  END

HMDB0034725
     RDKit          3D
6-Hydroxykaempferol 7-glucoside
 53 56  0  0  0  0  0  0  0  0999 V2000
    3.5895   -0.5674   -3.4980 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2696   -0.3708   -2.2980 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2646   -0.1481   -1.3460 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5557   -0.1621   -1.8116 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9267    0.0664   -0.0408 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9107    0.3024    0.9902 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2433    0.3376    0.7796 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1614    0.5697    1.8181 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7236    0.7698    3.0922 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5682    1.0031    4.1577 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3569    0.7409    3.3494 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4813    0.5112    2.3117 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6297    0.0602    0.3130 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6635   -0.1446   -0.5473 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3553   -0.1407   -0.1344 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7108   -0.3573   -1.0331 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9340   -0.3483   -0.6171 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1917   -0.3558   -0.2840 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5973    0.9086    0.1674 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9234    1.0159    0.4736 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8649    0.8912   -0.7011 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6255    1.8734   -1.6583 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3409    0.1220    1.6193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6001    0.8608    2.7685 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2707   -0.9018    1.9341 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3732   -0.4027    2.8815 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6141   -1.4351    0.7095 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4337   -2.3989    0.1356 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4127   -0.5775   -2.3585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4117   -0.8022   -3.3234 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9273   -0.5792   -2.7681 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1542   -0.8021   -4.0886 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9595   -0.3680   -1.8901 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7972   -0.3228   -2.7522 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7090    0.1951   -0.1764 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2251    0.5943    1.6319 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5677    1.0284    3.9932 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9904    0.8973    4.3557 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4329    0.4914    2.5232 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1013    0.0317    0.9085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8513   -0.5517   -1.1989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0652    2.0783    0.8388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8880    1.1062   -0.2993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8200   -0.0872   -1.1977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3990    1.8944   -2.2811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2843   -0.3762    1.3164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6971    1.8300    2.6012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7920   -1.7534    2.4290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3386    0.5656    2.7821 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6791   -1.9733    1.0299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9318   -3.1432   -0.2810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3640   -0.7981   -3.0198 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8504   -0.8770   -4.7208 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
  3  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  2  0
  5 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 20 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 16 29  2  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31 33  2  0
 33  2  1  0
 12  6  1  0
 33 14  1  0
 27 18  1  0
  4 34  1  0
  7 35  1  0
  8 36  1  0
 10 37  1  0
 11 38  1  0
 12 39  1  0
 15 40  1  0
 18 41  1  0
 20 42  1  0
 21 43  1  0
 21 44  1  0
 22 45  1  0
 23 46  1  0
 24 47  1  0
 25 48  1  0
 26 49  1  0
 27 50  1  0
 28 51  1  0
 30 52  1  0
 32 53  1  0
M  END

  Mrv0541 02241208442D          

 33 36  0  0  0  0            999 V2000
   -2.5012    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7862    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0712    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3576    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3574    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3574    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0712    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7861    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0710    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0710    0.8251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3574    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3576    0.8251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0712    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7862    0.8251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5012    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5012   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2148   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2148   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9298   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9298   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7861    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7861   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5011   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2147   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2147    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5011    0.8251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0712   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7862   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7862   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5012   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5012   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9298   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0712   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2 14  1  0  0  0  0
  3  4  1  0  0  0  0
  3  7  1  0  0  0  0
  4  5  1  0  0  0  0
  4 12  2  0  0  0  0
  5  6  2  0  0  0  0
  5  9  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 21  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 28  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 30  1  0  0  0  0
 19 20  1  0  0  0  0
 21 22  1  0  0  0  0
 21 26  2  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 32  1  0  0  0  0
 25 26  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 33  1  0  0  0  0
 30 31  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0034725

> <DATABASE_NAME>
hmdb

> <SMILES>
OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(O3)C2=CC=C(O)C=C2)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C21H20O12/c22-6-11-14(25)17(28)19(30)21(33-11)32-10-5-9-12(15(26)13(10)24)16(27)18(29)20(31-9)7-1-3-8(23)4-2-7/h1-5,11,14,17,19,21-26,28-30H,6H2

> <INCHI_KEY>
IYEWEDZIDUAUTD-UHFFFAOYSA-N

> <FORMULA>
C21H20O12

> <MOLECULAR_WEIGHT>
464.3763

> <EXACT_MASS>
464.095476104

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_AVERAGE_POLARIZABILITY>
43.96383118954054

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

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

> <ALOGPS_LOGP>
0.50

> <JCHEM_LOGP>
-0.11176862933333384

> <ALOGPS_LOGS>
-2.33

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.856978595000946

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.06238331759832

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810923549784256

> <JCHEM_POLAR_SURFACE_AREA>
206.6

> <JCHEM_REFRACTIVITY>
109.0066

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.16e+00 g/l

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

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0034725
     RDKit          3D
6-Hydroxykaempferol 7-glucoside
 53 56  0  0  0  0  0  0  0  0999 V2000
    3.5895   -0.5674   -3.4980 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2696   -0.3708   -2.2980 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2646   -0.1481   -1.3460 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5557   -0.1621   -1.8116 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9267    0.0664   -0.0408 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9107    0.3024    0.9902 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2433    0.3376    0.7796 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1614    0.5697    1.8181 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7236    0.7698    3.0922 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5682    1.0031    4.1577 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3569    0.7409    3.3494 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4813    0.5112    2.3117 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6297    0.0602    0.3130 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6635   -0.1446   -0.5473 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3553   -0.1407   -0.1344 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7108   -0.3573   -1.0331 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9340   -0.3483   -0.6171 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1917   -0.3558   -0.2840 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5973    0.9086    0.1674 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9234    1.0159    0.4736 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8649    0.8912   -0.7011 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6255    1.8734   -1.6583 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3409    0.1220    1.6193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6001    0.8608    2.7685 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2707   -0.9018    1.9341 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3732   -0.4027    2.8815 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6141   -1.4351    0.7095 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4337   -2.3989    0.1356 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4127   -0.5775   -2.3585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4117   -0.8022   -3.3234 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9273   -0.5792   -2.7681 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1542   -0.8021   -4.0886 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9595   -0.3680   -1.8901 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7972   -0.3228   -2.7522 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7090    0.1951   -0.1764 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2251    0.5943    1.6319 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5677    1.0284    3.9932 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9904    0.8973    4.3557 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4329    0.4914    2.5232 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1013    0.0317    0.9085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8513   -0.5517   -1.1989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0652    2.0783    0.8388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8880    1.1062   -0.2993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8200   -0.0872   -1.1977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3990    1.8944   -2.2811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2843   -0.3762    1.3164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6971    1.8300    2.6012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7920   -1.7534    2.4290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3386    0.5656    2.7821 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6791   -1.9733    1.0299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9318   -3.1432   -0.2810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3640   -0.7981   -3.0198 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8504   -0.8770   -4.7208 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
  3  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  2  0
  5 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 20 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 16 29  2  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31 33  2  0
 33  2  1  0
 12  6  1  0
 33 14  1  0
 27 18  1  0
  4 34  1  0
  7 35  1  0
  8 36  1  0
 10 37  1  0
 11 38  1  0
 12 39  1  0
 15 40  1  0
 18 41  1  0
 20 42  1  0
 21 43  1  0
 21 44  1  0
 22 45  1  0
 23 46  1  0
 24 47  1  0
 25 48  1  0
 26 49  1  0
 27 50  1  0
 28 51  1  0
 30 52  1  0
 32 53  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  O   UNK     0      -4.669   3.850   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -3.334   3.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.000   3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.668   3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.667   3.850   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       0.667   5.390   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      -2.000   5.390   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0       3.334   3.850   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       1.999   3.080   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.999   1.540   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.667   0.770   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -0.668   1.540   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.000   0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.334   1.540   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -4.669   0.770   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -4.669  -0.770   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -6.001  -1.540   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -6.001  -3.080   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -7.336  -3.850   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -7.336  -5.390   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       3.334   0.770   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.334  -0.770   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.669  -1.540   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.001  -0.770   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.001   0.770   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.669   1.540   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -2.000  -0.770   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -3.334  -1.540   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -3.334  -3.080   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -4.669  -3.850   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -4.669  -5.390   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       7.336  -1.540   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0      -2.000  -3.850   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   14                                                  
CONECT    3    2    4    7                                                  
CONECT    4    3    5   12                                                  
CONECT    5    4    6    9                                                  
CONECT    6    5                                                            
CONECT    7    3                                                            
CONECT    8    9                                                            
CONECT    9    5    8   10                                                  
CONECT   10    9   11   21                                                  
CONECT   11   10   12                                                       
CONECT   12    4   11   13                                                  
CONECT   13   12   14                                                       
CONECT   14    2   13   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   28                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   30                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   10   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   32                                                  
CONECT   25   24   26                                                       
CONECT   26   21   25                                                       
CONECT   27   28                                                            
CONECT   28   16   27   29                                                  
CONECT   29   28   30   33                                                  
CONECT   30   18   29   31                                                  
CONECT   31   30                                                            
CONECT   32   24                                                            
CONECT   33   29                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   72    0
END

COMPND    HMDB0034725
HETATM    1  O1  UNL     1       3.589  -0.567  -3.498  1.00  0.00           O  
HETATM    2  C1  UNL     1       3.270  -0.371  -2.298  1.00  0.00           C  
HETATM    3  C2  UNL     1       4.265  -0.148  -1.346  1.00  0.00           C  
HETATM    4  O2  UNL     1       5.556  -0.162  -1.812  1.00  0.00           O  
HETATM    5  C3  UNL     1       3.927   0.066  -0.041  1.00  0.00           C  
HETATM    6  C4  UNL     1       4.911   0.302   0.990  1.00  0.00           C  
HETATM    7  C5  UNL     1       6.243   0.338   0.780  1.00  0.00           C  
HETATM    8  C6  UNL     1       7.161   0.570   1.818  1.00  0.00           C  
HETATM    9  C7  UNL     1       6.724   0.770   3.092  1.00  0.00           C  
HETATM   10  O3  UNL     1       7.568   1.003   4.158  1.00  0.00           O  
HETATM   11  C8  UNL     1       5.357   0.741   3.349  1.00  0.00           C  
HETATM   12  C9  UNL     1       4.481   0.511   2.312  1.00  0.00           C  
HETATM   13  O4  UNL     1       2.630   0.060   0.313  1.00  0.00           O  
HETATM   14  C10 UNL     1       1.664  -0.145  -0.547  1.00  0.00           C  
HETATM   15  C11 UNL     1       0.355  -0.141  -0.134  1.00  0.00           C  
HETATM   16  C12 UNL     1      -0.711  -0.357  -1.033  1.00  0.00           C  
HETATM   17  O5  UNL     1      -1.934  -0.348  -0.617  1.00  0.00           O  
HETATM   18  C13 UNL     1      -3.192  -0.356  -0.284  1.00  0.00           C  
HETATM   19  O6  UNL     1      -3.597   0.909   0.167  1.00  0.00           O  
HETATM   20  C14 UNL     1      -4.923   1.016   0.474  1.00  0.00           C  
HETATM   21  C15 UNL     1      -5.865   0.891  -0.701  1.00  0.00           C  
HETATM   22  O7  UNL     1      -5.626   1.873  -1.658  1.00  0.00           O  
HETATM   23  C16 UNL     1      -5.341   0.122   1.619  1.00  0.00           C  
HETATM   24  O8  UNL     1      -5.600   0.861   2.768  1.00  0.00           O  
HETATM   25  C17 UNL     1      -4.271  -0.902   1.934  1.00  0.00           C  
HETATM   26  O9  UNL     1      -3.373  -0.403   2.881  1.00  0.00           O  
HETATM   27  C18 UNL     1      -3.614  -1.435   0.710  1.00  0.00           C  
HETATM   28  O10 UNL     1      -4.434  -2.399   0.136  1.00  0.00           O  
HETATM   29  C19 UNL     1      -0.413  -0.577  -2.358  1.00  0.00           C  
HETATM   30  O11 UNL     1      -1.412  -0.802  -3.323  1.00  0.00           O  
HETATM   31  C20 UNL     1       0.927  -0.579  -2.768  1.00  0.00           C  
HETATM   32  O12 UNL     1       1.154  -0.802  -4.089  1.00  0.00           O  
HETATM   33  C21 UNL     1       1.959  -0.368  -1.890  1.00  0.00           C  
HETATM   34  H1  UNL     1       5.797  -0.323  -2.752  1.00  0.00           H  
HETATM   35  H2  UNL     1       6.709   0.195  -0.176  1.00  0.00           H  
HETATM   36  H3  UNL     1       8.225   0.594   1.632  1.00  0.00           H  
HETATM   37  H4  UNL     1       8.568   1.028   3.993  1.00  0.00           H  
HETATM   38  H5  UNL     1       4.990   0.897   4.356  1.00  0.00           H  
HETATM   39  H6  UNL     1       3.433   0.491   2.523  1.00  0.00           H  
HETATM   40  H7  UNL     1       0.101   0.032   0.908  1.00  0.00           H  
HETATM   41  H8  UNL     1      -3.851  -0.552  -1.199  1.00  0.00           H  
HETATM   42  H9  UNL     1      -5.065   2.078   0.839  1.00  0.00           H  
HETATM   43  H10 UNL     1      -6.888   1.106  -0.299  1.00  0.00           H  
HETATM   44  H11 UNL     1      -5.820  -0.087  -1.198  1.00  0.00           H  
HETATM   45  H12 UNL     1      -6.399   1.894  -2.281  1.00  0.00           H  
HETATM   46  H13 UNL     1      -6.284  -0.376   1.316  1.00  0.00           H  
HETATM   47  H14 UNL     1      -5.697   1.830   2.601  1.00  0.00           H  
HETATM   48  H15 UNL     1      -4.792  -1.753   2.429  1.00  0.00           H  
HETATM   49  H16 UNL     1      -3.339   0.566   2.782  1.00  0.00           H  
HETATM   50  H17 UNL     1      -2.679  -1.973   1.030  1.00  0.00           H  
HETATM   51  H18 UNL     1      -3.932  -3.143  -0.281  1.00  0.00           H  
HETATM   52  H19 UNL     1      -2.364  -0.798  -3.020  1.00  0.00           H  
HETATM   53  H20 UNL     1       1.850  -0.877  -4.721  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   33
CONECT    3    4    5    5
CONECT    4   34
CONECT    5    6   13
CONECT    6    7    7   12
CONECT    7    8   35
CONECT    8    9    9   36
CONECT    9   10   11
CONECT   10   37
CONECT   11   12   12   38
CONECT   12   39
CONECT   13   14
CONECT   14   15   15   33
CONECT   15   16   40
CONECT   16   17   29   29
CONECT   17   18
CONECT   18   19   27   41
CONECT   19   20
CONECT   20   21   23   42
CONECT   21   22   43   44
CONECT   22   45
CONECT   23   24   25   46
CONECT   24   47
CONECT   25   26   27   48
CONECT   26   49
CONECT   27   28   50
CONECT   28   51
CONECT   29   30   31
CONECT   30   52
CONECT   31   32   33   33
CONECT   32   53
END

HMDB0034725
     RDKit          3D
6-Hydroxykaempferol 7-glucoside
 53 56  0  0  0  0  0  0  0  0999 V2000
    3.5895   -0.5674   -3.4980 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2696   -0.3708   -2.2980 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2646   -0.1481   -1.3460 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5557   -0.1621   -1.8116 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9267    0.0664   -0.0408 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9107    0.3024    0.9902 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2433    0.3376    0.7796 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1614    0.5697    1.8181 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7236    0.7698    3.0922 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5682    1.0031    4.1577 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3569    0.7409    3.3494 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4813    0.5112    2.3117 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6297    0.0602    0.3130 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6635   -0.1446   -0.5473 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3553   -0.1407   -0.1344 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7108   -0.3573   -1.0331 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9340   -0.3483   -0.6171 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1917   -0.3558   -0.2840 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5973    0.9086    0.1674 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9234    1.0159    0.4736 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8649    0.8912   -0.7011 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6255    1.8734   -1.6583 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3409    0.1220    1.6193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6001    0.8608    2.7685 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2707   -0.9018    1.9341 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3732   -0.4027    2.8815 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6141   -1.4351    0.7095 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4337   -2.3989    0.1356 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4127   -0.5775   -2.3585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4117   -0.8022   -3.3234 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9273   -0.5792   -2.7681 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1542   -0.8021   -4.0886 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9595   -0.3680   -1.8901 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7972   -0.3228   -2.7522 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7090    0.1951   -0.1764 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2251    0.5943    1.6319 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5677    1.0284    3.9932 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9904    0.8973    4.3557 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4329    0.4914    2.5232 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1013    0.0317    0.9085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8513   -0.5517   -1.1989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0652    2.0783    0.8388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8880    1.1062   -0.2993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8200   -0.0872   -1.1977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3990    1.8944   -2.2811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2843   -0.3762    1.3164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6971    1.8300    2.6012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7920   -1.7534    2.4290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3386    0.5656    2.7821 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6791   -1.9733    1.0299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9318   -3.1432   -0.2810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3640   -0.7981   -3.0198 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8504   -0.8770   -4.7208 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
  3  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  2  0
  5 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 20 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 16 29  2  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31 33  2  0
 33  2  1  0
 12  6  1  0
 33 14  1  0
 27 18  1  0
  4 34  1  0
  7 35  1  0
  8 36  1  0
 10 37  1  0
 11 38  1  0
 12 39  1  0
 15 40  1  0
 18 41  1  0
 20 42  1  0
 21 43  1  0
 21 44  1  0
 22 45  1  0
 23 46  1  0
 24 47  1  0
 25 48  1  0
 26 49  1  0
 27 50  1  0
 28 51  1  0
 30 52  1  0
 32 53  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
6-Hydroxykaempferol 7-alloside	HMDB
7-(beta-D-Allopyranosyloxy)-3,5,6-trihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one	HMDB

Chemical Formula

C₂₁H₂₀O₁₂

Average Molecular Weight

464.3763

Monoisotopic Molecular Weight

464.095476104

IUPAC Name

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

Traditional Name

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

CAS Registry Number

205496-87-3

SMILES

OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(O3)C2=CC=C(O)C=C2)C(O)C(O)C1O

InChI Identifier

InChI=1S/C21H20O12/c22-6-11-14(25)17(28)19(30)21(33-11)32-10-5-9-12(15(26)13(10)24)16(27)18(29)20(31-9)7-1-3-8(23)4-2-7/h1-5,11,14,17,19,21-26,28-30H,6H2

InChI Key

IYEWEDZIDUAUTD-UHFFFAOYSA-N

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Flavonoid-7-O-glycosides

Alternative Parents

Substituents

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

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Extracellular (HMDB: HMDB0034725)
Cytoplasm (HMDB: HMDB0034725)

Source

Exogenous

Exogenous (HMDB: HMDB0034725)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	2.16 g/L	ALOGPS
logP	0.5	ALOGPS
logP	-0.11	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	8.06	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	206.6 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	109.01 m³·mol⁻¹	ChemAxon
Polarizability	43.96 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	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
DeepCCS	[M+H]+	198.866	30932474
DeepCCS	[M-H]-	196.47	30932474
DeepCCS	[M-2H]-	229.373	30932474
DeepCCS	[M+Na]+	204.778	30932474
AllCCS	[M+H]+	205.1	32859911
AllCCS	[M+H-H2O]+	202.8	32859911
AllCCS	[M+NH4]+	207.2	32859911
AllCCS	[M+Na]+	207.8	32859911
AllCCS	[M-H]-	201.5	32859911
AllCCS	[M+Na-2H]-	202.0	32859911
AllCCS	[M+HCOO]-	202.7	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
6-Hydroxykaempferol 7-glucoside	OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(O3)C2=CC=C(O)C=C2)C(O)C(O)C1O	5478.6	Standard polar	33892256
6-Hydroxykaempferol 7-glucoside	OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(O3)C2=CC=C(O)C=C2)C(O)C(O)C1O	4440.3	Standard non polar	33892256
6-Hydroxykaempferol 7-glucoside	OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(O3)C2=CC=C(O)C=C2)C(O)C(O)C1O	4526.9	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
6-Hydroxykaempferol 7-glucoside,1TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O	4544.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,1TMS,isomer #2	C[Si](C)(C)OC1=C(O)C(OC2OC(CO)C(O)C(O)C2O)=CC2=C1C(=O)C(O)=C(C1=CC=C(O)C=C1)O2	4479.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,1TMS,isomer #3	C[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O	4469.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,1TMS,isomer #4	C[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O)C(O)C3O)=C(O)C(O)=C2C1=O	4464.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,1TMS,isomer #5	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1	4562.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,1TMS,isomer #6	C[Si](C)(C)OC1C(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)OC(CO)C(O)C1O	4545.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,1TMS,isomer #7	C[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C1O	4539.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,1TMS,isomer #8	C[Si](C)(C)OC1C(CO)OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C1O	4541.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O)C1O	4416.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #10	C[Si](C)(C)OC1=C(O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=CC2=C1C(=O)C(O)=C(C1=CC=C(O)C=C1)O2	4339.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #11	C[Si](C)(C)OC1=C(O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=CC2=C1C(=O)C(O)=C(C1=CC=C(O)C=C1)O2	4361.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #12	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O[Si](C)(C)C)C(O)=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1	4374.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #13	C[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O)C(O)C3O)=C(O)C(O[Si](C)(C)C)=C2C1=O	4322.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #14	C[Si](C)(C)OC1=C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O	4332.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #15	C[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O	4319.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #16	C[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O	4347.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #17	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1	4358.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #18	C[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O[Si](C)(C)C)C(=O)C2=C1O	4311.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #19	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1	4353.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O	4356.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #20	C[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C(O)C(O)=C2C1=O	4332.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #21	C[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C(O)C(O)=C2C1=O	4315.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #22	C[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C(O)C(O)=C2C1=O	4343.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #23	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1	4381.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #24	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1	4357.6	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #25	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1	4390.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #26	C[Si](C)(C)OC1C(CO)OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C1O	4385.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #27	C[Si](C)(C)OC1C(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)OC(CO)C(O)C1O[Si](C)(C)C	4410.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #28	C[Si](C)(C)OC1C(CO)OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C1O[Si](C)(C)C	4385.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O	4372.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O	4358.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O	4421.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O	4403.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O[Si](C)(C)C	4410.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #8	C[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O[Si](C)(C)C	4332.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #9	C[Si](C)(C)OC1=C(O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=CC2=C1C(=O)C(O)=C(C1=CC=C(O)C=C1)O2	4348.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O)C1O	4220.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #10	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O	4193.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #11	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O[Si](C)(C)C	4221.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #12	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O	4196.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #13	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O	4236.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #14	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O	4196.6	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #15	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O[Si](C)(C)C	4224.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #16	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O	4233.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #17	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O	4193.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #18	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O[Si](C)(C)C	4223.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #19	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4301.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O)C1O	4209.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #20	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4309.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #21	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4276.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #22	C[Si](C)(C)OC1=C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O[Si](C)(C)C	4191.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #23	C[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O[Si](C)(C)C	4162.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #24	C[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O[Si](C)(C)C	4204.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #25	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1	4220.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #26	C[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O[Si](C)(C)C)C(=O)C2=C1O[Si](C)(C)C	4187.6	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #27	C[Si](C)(C)OC1=C(O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC2=C1C(=O)C(O)=C(C1=CC=C(O)C=C1)O2	4184.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #28	C[Si](C)(C)OC1=C(O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC2=C1C(=O)C(O)=C(C1=CC=C(O)C=C1)O2	4195.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #29	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O[Si](C)(C)C)C(O)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1	4197.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O)C1O	4212.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #30	C[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C(O)C(O[Si](C)(C)C)=C2C1=O	4157.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #31	C[Si](C)(C)OC1=C(O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC2=C1C(=O)C(O)=C(C1=CC=C(O)C=C1)O2	4215.6	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #32	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O[Si](C)(C)C)C(O)=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1	4178.6	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #33	C[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C(O)C(O[Si](C)(C)C)=C2C1=O	4123.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #34	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O[Si](C)(C)C)C(O)=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1	4202.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #35	C[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C2C1=O	4170.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #36	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C(O)=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1	4183.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #37	C[Si](C)(C)OC1=C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O	4192.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #38	C[Si](C)(C)OC1=C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O	4199.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #39	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1	4198.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O	4284.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #40	C[Si](C)(C)OC1=C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O[Si](C)(C)C)C(=O)C2=C1O	4161.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #41	C[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O	4225.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #42	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1	4175.6	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #43	C[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O[Si](C)(C)C)C(=O)C2=C1O	4115.6	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #44	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1	4211.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #45	C[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C=C2OC(C3=CC=C(O)C=C3)=C(O[Si](C)(C)C)C(=O)C2=C1O	4175.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #46	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1	4176.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #47	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1	4199.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #48	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1	4155.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #49	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1	4212.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O	4227.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #50	C[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C(O)C(O)=C2C1=O	4195.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #51	C[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C(O)C(O)=C2C1=O	4203.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #52	C[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C(O)C(O)=C2C1=O	4218.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #53	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1	4241.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #54	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1	4248.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #55	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1	4279.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #56	C[Si](C)(C)OC1C(CO)OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4315.6	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O)C1O[Si](C)(C)C	4272.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O	4175.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #8	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O	4165.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #9	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O	4229.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O)C1O	4070.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #10	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O	4139.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #11	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O	4093.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #12	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O)C1O[Si](C)(C)C	4130.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #13	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4180.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #14	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4203.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #15	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4166.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #16	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O	4061.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #17	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O	4096.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #18	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O	4046.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #19	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O[Si](C)(C)C	4079.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O)C1O	4072.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #20	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O	4098.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #21	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O	4023.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #22	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O[Si](C)(C)C	4083.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #23	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4159.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #24	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4202.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #25	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4141.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #26	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O	4131.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #27	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O	4063.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #28	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O[Si](C)(C)C	4116.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #29	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4139.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O	4149.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #30	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4171.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #31	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4123.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #32	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4146.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #33	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4157.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #34	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4133.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #35	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4254.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #36	C[Si](C)(C)OC1=C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O[Si](C)(C)C	4080.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #37	C[Si](C)(C)OC1=C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O[Si](C)(C)C	4104.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #38	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1	4112.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #39	C[Si](C)(C)OC1=C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O[Si](C)(C)C)C(=O)C2=C1O[Si](C)(C)C	4073.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O	4074.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #40	C[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O[Si](C)(C)C	4098.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #41	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1	4081.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #42	C[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O[Si](C)(C)C)C(=O)C2=C1O[Si](C)(C)C	4023.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #43	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1	4123.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #44	C[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C=C2OC(C3=CC=C(O)C=C3)=C(O[Si](C)(C)C)C(=O)C2=C1O[Si](C)(C)C	4091.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #45	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1	4096.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #46	C[Si](C)(C)OC1=C(O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC2=C1C(=O)C(O)=C(C1=CC=C(O)C=C1)O2	4122.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #47	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O[Si](C)(C)C)C(O)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1	4081.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #48	C[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C(O)C(O[Si](C)(C)C)=C2C1=O	4048.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #49	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O[Si](C)(C)C)C(O)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1	4099.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O)C1O[Si](C)(C)C	4130.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #50	C[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C2C1=O	4068.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #51	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C(O)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1	4077.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #52	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O[Si](C)(C)C)C(O)=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1	4105.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #53	C[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C2C1=O	4064.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #54	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C(O)=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1	4057.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #55	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C(O)=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1	4080.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #56	C[Si](C)(C)OC1=C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O	4137.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #57	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1	4090.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #58	C[Si](C)(C)OC1=C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O[Si](C)(C)C)C(=O)C2=C1O	4049.6	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #59	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1	4116.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O)C1O	4097.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #60	C[Si](C)(C)OC1=C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=C2OC(C3=CC=C(O)C=C3)=C(O[Si](C)(C)C)C(=O)C2=C1O	4072.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #61	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1	4086.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #62	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1	4114.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #63	C[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C2OC(C3=CC=C(O)C=C3)=C(O[Si](C)(C)C)C(=O)C2=C1O	4064.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #64	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1	4056.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #65	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1	4099.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #66	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1	4095.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #67	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1	4119.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #68	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1	4120.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #69	C[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C(O)C(O)=C2C1=O	4140.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O	4130.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #70	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1	4182.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #8	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O	4099.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #9	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O)C1O[Si](C)(C)C	4123.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O)C1O	4020.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #10	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4066.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #11	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O	4078.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #12	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O	4025.6	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #13	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O)C1O[Si](C)(C)C	4062.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #14	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4075.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #15	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4097.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #16	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4064.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #17	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4077.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #18	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4085.6	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #19	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4060.6	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O	4046.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #20	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4161.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #21	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O	4022.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #22	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O	3969.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #23	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O[Si](C)(C)C	4006.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #24	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4027.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #25	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4055.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #26	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4015.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #27	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4027.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #28	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4053.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #29	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4015.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O	4023.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #30	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4148.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #31	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4056.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #32	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4086.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #33	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4045.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #34	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4117.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #35	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4102.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #36	C[Si](C)(C)OC1=C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O[Si](C)(C)C	4068.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #37	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1	4042.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #38	C[Si](C)(C)OC1=C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O[Si](C)(C)C)C(=O)C2=C1O[Si](C)(C)C	4003.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #39	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1	4074.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O)C1O[Si](C)(C)C	4035.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #40	C[Si](C)(C)OC1=C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=C2OC(C3=CC=C(O)C=C3)=C(O[Si](C)(C)C)C(=O)C2=C1O[Si](C)(C)C	4022.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #41	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1	4037.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #42	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1	4058.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #43	C[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C2OC(C3=CC=C(O)C=C3)=C(O[Si](C)(C)C)C(=O)C2=C1O[Si](C)(C)C	4009.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #44	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1	4004.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #45	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1	4045.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #46	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O[Si](C)(C)C)C(O)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1	4068.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #47	C[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C2C1=O	4023.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #48	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C(O)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1	4010.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #49	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C(O)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1	4037.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O	4050.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #50	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C(O)=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1	4021.6	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #51	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1	4072.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #52	C[Si](C)(C)OC1=C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C2OC(C3=CC=C(O)C=C3)=C(O[Si](C)(C)C)C(=O)C2=C1O	4032.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #53	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1	4015.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #54	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1	4042.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #55	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1	4024.6	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #56	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1	4077.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O	4002.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O)C1O[Si](C)(C)C	4032.6	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #8	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4080.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #9	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4109.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O	4008.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #10	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4065.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #11	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4029.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #12	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4054.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #13	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4016.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #14	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4051.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #15	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4024.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #16	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3991.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #17	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4011.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #18	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3977.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #19	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4028.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O	3979.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #20	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4022.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #21	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4064.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #22	C[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1	4036.6	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #23	C[Si](C)(C)OC1=C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C2OC(C3=CC=C(O)C=C3)=C(O[Si](C)(C)C)C(=O)C2=C1O[Si](C)(C)C	4003.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #24	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1	3994.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #25	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1	4013.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #26	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1	3996.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #27	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C(O)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1	4000.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #28	C[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O)C(O[Si](C)(C)C)=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1	3996.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O[Si](C)(C)C)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O)C1O[Si](C)(C)C	3996.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4011.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4031.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C)=C2O)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4001.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4000.6	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #8	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4021.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #9	C[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C)C(=O)C(O[Si](C)(C)C)=C(C2=CC=C(O[Si](C)(C)C)C=C2)O3)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3989.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O	4780.6	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=C(O)C(OC2OC(CO)C(O)C(O)C2O)=CC2=C1C(=O)C(O)=C(C1=CC=C(O)C=C1)O2	4736.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O	4721.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O)C(O)C3O)=C(O)C(O)=C2C1=O	4749.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1	4781.6	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1C(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)OC(CO)C(O)C1O	4819.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C1O	4812.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,1TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C1O	4819.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2)O3)C(O)C(O)C1O	4894.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1=C(O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)=CC2=C1C(=O)C(O)=C(C1=CC=C(O)C=C1)O2	4834.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC1=C(O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)=CC2=C1C(=O)C(O)=C(C1=CC=C(O)C=C1)O2	4832.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(O)=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1	4872.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O)C(O)C3O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C2C1=O	4810.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC1=C(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O	4824.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O	4824.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O	4825.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O[Si](C)(C)C(C)(C)C)=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1	4865.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O[Si](C)(C)C(C)(C)C)C(=O)C2=C1O	4799.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1	4858.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O[Si](C)(C)C(C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O	4840.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C(O)C(O)=C2C1=O	4813.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C(O)C(O)=C2C1=O	4808.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C(O)C(O)=C2C1=O	4812.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C=C3O2)C=C1	4887.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C=C3O2)C=C1	4886.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1	4885.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C(C)(C)C)C1O	4876.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC1C(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	4884.6	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C1O[Si](C)(C)C(C)(C)C	4863.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C(C)(C)C)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O	4857.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C(C)(C)C)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O	4841.6	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	4891.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	4888.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	4878.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O[Si](C)(C)C(C)(C)C	4833.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1=C(O)C(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)=CC2=C1C(=O)C(O)=C(C1=CC=C(O)C=C1)O2	4831.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O[Si](C)(C)C(C)(C)C)=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2)O3)C(O)C(O)C1O	4927.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O[Si](C)(C)C(C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	4880.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O[Si](C)(C)C(C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	4874.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C(C)(C)C)=C2O[Si](C)(C)C(C)(C)C)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O	4907.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C(C)(C)C)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	4927.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C(C)(C)C)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	4927.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C(C)(C)C)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	4917.6	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C(C)(C)C)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	4924.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C(C)(C)C)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	4924.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C(C)(C)C)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	4915.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	4955.6	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C(C)(C)C)=C2O)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2)O3)C(O)C(O)C1O	4976.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	4966.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4944.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC1=C(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O[Si](C)(C)C(C)(C)C	4907.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O[Si](C)(C)C(C)(C)C	4902.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O[Si](C)(C)C(C)(C)C	4900.6	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1	4978.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O[Si](C)(C)C(C)(C)C)C(=O)C2=C1O[Si](C)(C)C(C)(C)C	4872.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC1=C(O)C(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)=CC2=C1C(=O)C(O)=C(C1=CC=C(O)C=C1)O2	4899.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC1=C(O)C(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)=CC2=C1C(=O)C(O)=C(C1=CC=C(O)C=C1)O2	4907.6	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(O)=C(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C=C3O2)C=C1	4980.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C(C)(C)C)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2)O3)C(O)C(O)C1O	4966.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C2C1=O	4860.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC1=C(O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)=CC2=C1C(=O)C(O)=C(C1=CC=C(O)C=C1)O2	4916.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(O)=C(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C=C3O2)C=C1	4986.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C2C1=O	4861.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(O)=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1	4963.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C(O)C(O[Si](C)(C)C(C)(C)C)=C2C1=O	4850.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #36	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(O)=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1	4951.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #37	CC(C)(C)[Si](C)(C)OC1=C(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O	4910.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #38	CC(C)(C)[Si](C)(C)OC1=C(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O	4920.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #39	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O[Si](C)(C)C(C)(C)C)=C(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C=C3O2)C=C1	4978.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2)O3)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	4973.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #40	CC(C)(C)[Si](C)(C)OC1=C(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O[Si](C)(C)C(C)(C)C)C(=O)C2=C1O	4871.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #41	CC(C)(C)[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=C2OC(C3=CC=C(O)C=C3)=C(O)C(=O)C2=C1O	4932.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #42	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O[Si](C)(C)C(C)(C)C)=C(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C=C3O2)C=C1	4977.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #43	CC(C)(C)[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C=C2OC(C3=CC=C(O)C=C3)=C(O[Si](C)(C)C(C)(C)C)C(=O)C2=C1O	4864.5	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #44	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O[Si](C)(C)C(C)(C)C)=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1	4967.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #45	CC(C)(C)[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C=C2OC(C3=CC=C(O)C=C3)=C(O[Si](C)(C)C(C)(C)C)C(=O)C2=C1O	4864.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #46	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O)C(O[Si](C)(C)C(C)(C)C)=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1	4947.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #47	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C=C3O2)C=C1	4914.8	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #48	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C=C3O2)C=C1	4905.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #49	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1	4914.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2)O3)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	4977.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #50	CC(C)(C)[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=C(O)C(O)=C2C1=O	4850.2	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #51	CC(C)(C)[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=C(O)C(O)=C2C1=O	4869.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #52	CC(C)(C)[Si](C)(C)OC1=C(C2=CC=C(O)C=C2)OC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C(O)C(O)=C2C1=O	4874.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #53	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C4O)C=C3O2)C=C1	4956.4	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #54	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1	4968.0	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #55	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O)=C(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1	4974.6	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #56	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4936.7	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2)O3)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	4960.3	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O[Si](C)(C)C(C)(C)C)=C2O)C(=O)C(O[Si](C)(C)C(C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O	4871.1	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O[Si](C)(C)C(C)(C)C)C(=O)C(O[Si](C)(C)C(C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1O	4876.9	Semi standard non polar	33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O[Si](C)(C)C(C)(C)C)=C(C2=CC=C(O)C=C2)O3)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	4887.7	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Hydroxykaempferol 7-glucoside GC-MS (Non-derivatized) - 70eV, Positive	splash10-0w31-7804900000-17fd51cdcb09d54954f1	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Hydroxykaempferol 7-glucoside GC-MS (3 TMS) - 70eV, Positive	splash10-014r-3620009000-b176a82f44c98681b28f	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Hydroxykaempferol 7-glucoside GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Hydroxykaempferol 7-glucoside GC-MS (TBDMS_3_41) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Hydroxykaempferol 7-glucoside GC-MS ("6-Hydroxykaempferol 7-glucoside,3TBDMS,#41" TMS) - 70eV, Positive	Not Available	2021-10-14	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxykaempferol 7-glucoside 10V, Positive-QTOF	splash10-0uxr-0148900000-8955561f40f2fd68693e	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxykaempferol 7-glucoside 20V, Positive-QTOF	splash10-0udi-0169100000-2cb64ed98fcc461a4460	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxykaempferol 7-glucoside 40V, Positive-QTOF	splash10-0zmu-2952000000-6d601ba9fb35bcee8df4	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxykaempferol 7-glucoside 10V, Negative-QTOF	splash10-0ik9-2305900000-72d39793c5f9d96de414	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxykaempferol 7-glucoside 20V, Negative-QTOF	splash10-0udi-2349200000-d26ce68ba81ef239e862	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxykaempferol 7-glucoside 40V, Negative-QTOF	splash10-0zfu-8694000000-520410b219aadf84d378	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxykaempferol 7-glucoside 10V, Positive-QTOF	splash10-0uxr-0009400000-82ee0af7a45dc332bf03	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxykaempferol 7-glucoside 20V, Positive-QTOF	splash10-0udi-0009100000-7cb9d26c1cc75ab3087e	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxykaempferol 7-glucoside 40V, Positive-QTOF	splash10-0udi-0009000000-83a0d85bdd6b793b4e43	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxykaempferol 7-glucoside 10V, Negative-QTOF	splash10-03di-0000900000-0c99867ed0f73f18e8ae	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxykaempferol 7-glucoside 20V, Negative-QTOF	splash10-0ik9-0005900000-e1e3f4f430433969300b	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxykaempferol 7-glucoside 40V, Negative-QTOF	splash10-0udi-0009100000-e11df97ed7c4b30b148e	2021-09-23	Wishart Lab	View Spectrum

NMR Spectra

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

Biological Properties

Cellular Locations

Cytoplasm
Extracellular

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB013262

KNApSAcK ID

C00013823

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14825511

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

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

Showing metabocard for 6-Hydroxykaempferol 7-glucoside (HMDB0034725)

MOL for HMDB0034725 (6-Hydroxykaempferol 7-glucoside)

3D MOL for HMDB0034725 (6-Hydroxykaempferol 7-glucoside)

3D SDF for HMDB0034725 (6-Hydroxykaempferol 7-glucoside)

3D-SDF for HMDB0034725 (6-Hydroxykaempferol 7-glucoside)

PDB for HMDB0034725 (6-Hydroxykaempferol 7-glucoside)

3D PDB for HMDB0034725 (6-Hydroxykaempferol 7-glucoside)

SMILES for HMDB0034725 (6-Hydroxykaempferol 7-glucoside)

INCHI for HMDB0034725 (6-Hydroxykaempferol 7-glucoside)

Structure for HMDB0034725 (6-Hydroxykaempferol 7-glucoside)

3D Structure for HMDB0034725 (6-Hydroxykaempferol 7-glucoside)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra