Hmdb loader

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

Jump To Section:
IdentificationTaxonomyOntologyPhysical propertiesSpectraBiological propertiesConcentrationsLinksReferencesXML
Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 19:37:39 UTC
Update Date2022-03-07 02:54:13 UTC
HMDB IDHMDB0034725
Secondary Accession Numbers
  • HMDB34725
Metabolite Identification
Common Name6-Hydroxykaempferol 7-glucoside
Description6-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
Data?1563862610
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0034725 (6-Hydroxykaempferol 7-glucoside)


  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
Download

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

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
Download

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


  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

$$$$
Download

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

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
Download

PDB for HMDB0034725 (6-Hydroxykaempferol 7-glucoside)

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
Download

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

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
Download

SMILES for HMDB0034725 (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
Download

INCHI for HMDB0034725 (6-Hydroxykaempferol 7-glucoside)

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
Download
View in JSmolView NMR AssignmentsView Stereo Labels
Synonyms
ValueSource
6-Hydroxykaempferol 7-allosideHMDB
7-(beta-D-Allopyranosyloxy)-3,5,6-trihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-oneHMDB
Chemical FormulaC21H20O12
Average Molecular Weight464.3763
Monoisotopic Molecular Weight464.095476104
IUPAC Name3,5,6-trihydroxy-2-(4-hydroxyphenyl)-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H-chromen-4-one
Traditional Name3,5,6-trihydroxy-2-(4-hydroxyphenyl)-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one
CAS Registry Number205496-87-3
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 KeyIYEWEDZIDUAUTD-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.
KingdomOrganic compounds
Super ClassPhenylpropanoids and polyketides
ClassFlavonoids
Sub ClassFlavonoid glycosides
Direct ParentFlavonoid-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 FrameworkAromatic heteropolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Biological location
ProcessNot Available
RoleNot Available
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility2.16 g/LALOGPS
logP0.5ALOGPS
logP-0.11ChemAxon
logS-2.3ALOGPS
pKa (Strongest Acidic)8.06ChemAxon
pKa (Strongest Basic)-3ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count12ChemAxon
Hydrogen Donor Count8ChemAxon
Polar Surface Area206.6 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity109.01 m³·mol⁻¹ChemAxon
Polarizability43.96 ųChemAxon
Number of Rings4ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+198.86630932474
DeepCCS[M-H]-196.4730932474
DeepCCS[M-2H]-229.37330932474
DeepCCS[M+Na]+204.77830932474
AllCCS[M+H]+205.132859911
AllCCS[M+H-H2O]+202.832859911
AllCCS[M+NH4]+207.232859911
AllCCS[M+Na]+207.832859911
AllCCS[M-H]-201.532859911
AllCCS[M+Na-2H]-202.032859911
AllCCS[M+HCOO]-202.732859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
6-Hydroxykaempferol 7-glucosideOCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(O3)C2=CC=C(O)C=C2)C(O)C(O)C1O5478.6Standard polar33892256
6-Hydroxykaempferol 7-glucosideOCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(O3)C2=CC=C(O)C=C2)C(O)C(O)C1O4440.3Standard non polar33892256
6-Hydroxykaempferol 7-glucosideOCC1OC(OC2=CC3=C(C(O)=C2O)C(=O)C(O)=C(O3)C2=CC=C(O)C=C2)C(O)C(O)C1O4526.9Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
6-Hydroxykaempferol 7-glucoside,1TMS,isomer #1C[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)C1O4544.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,1TMS,isomer #2C[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)O24479.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,1TMS,isomer #3C[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=C1O4469.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,1TMS,isomer #4C[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=O4464.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,1TMS,isomer #5C[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=C14562.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,1TMS,isomer #6C[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)C1O4545.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,1TMS,isomer #7C[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)C1O4539.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,1TMS,isomer #8C[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)C1O4541.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #1C[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)C1O4416.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #10C[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)O24339.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #11C[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)O24361.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #12C[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=C14374.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #13C[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=O4322.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #14C[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=C1O4332.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #15C[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=C1O4319.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #16C[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=C1O4347.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #17C[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=C14358.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #18C[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=C1O4311.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #19C[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=C14353.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #2C[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)C1O4356.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #20C[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=O4332.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #21C[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=O4315.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #22C[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=O4343.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #23C[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=C14381.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #24C[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=C14357.6Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #25C[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=C14390.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #26C[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)C1O4385.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #27C[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)C4410.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #28C[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)C4385.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #3C[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)C1O4372.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #4C[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)C1O4358.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #5C[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)C1O4421.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #6C[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)C1O4403.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #7C[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)C4410.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #8C[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)C4332.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TMS,isomer #9C[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)O24348.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #1C[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)C1O4220.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #10C[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)C1O4193.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #11C[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)C4221.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #12C[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)C1O4196.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #13C[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)C1O4236.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #14C[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)C1O4196.6Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #15C[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)C4224.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #16C[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)C1O4233.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #17C[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)C1O4193.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #18C[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)C4223.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #19C[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)C1O4301.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #2C[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)C1O4209.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #20C[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)C4309.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #21C[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)C4276.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #22C[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)C4191.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #23C[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)C4162.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #24C[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)C4204.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #25C[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=C14220.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #26C[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)C4187.6Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #27C[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)O24184.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #28C[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)O24195.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #29C[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=C14197.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #3C[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)C1O4212.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #30C[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=O4157.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #31C[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)O24215.6Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #32C[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=C14178.6Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #33C[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=O4123.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #34C[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=C14202.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #35C[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=O4170.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #36C[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=C14183.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #37C[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=C1O4192.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #38C[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=C1O4199.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #39C[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=C14198.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #4C[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)C1O4284.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #40C[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=C1O4161.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #41C[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=C1O4225.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #42C[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=C14175.6Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #43C[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=C1O4115.6Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #44C[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=C14211.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #45C[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=C1O4175.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #46C[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=C14176.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #47C[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=C14199.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #48C[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=C14155.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #49C[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=C14212.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #5C[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)C1O4227.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #50C[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=O4195.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #51C[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=O4203.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #52C[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=O4218.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #53C[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=C14241.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #54C[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=C14248.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #55C[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=C14279.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #56C[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)C4315.6Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #6C[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)C4272.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #7C[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)C1O4175.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #8C[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)C1O4165.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TMS,isomer #9C[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)C1O4229.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #1C[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)C1O4070.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #10C[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)C1O4139.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #11C[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)C1O4093.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #12C[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)C4130.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #13C[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)C1O4180.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #14C[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)C4203.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #15C[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)C4166.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #16C[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)C1O4061.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #17C[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)C1O4096.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #18C[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)C1O4046.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #19C[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)C4079.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #2C[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)C1O4072.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #20C[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)C1O4098.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #21C[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)C1O4023.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #22C[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)C4083.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #23C[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)C1O4159.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #24C[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)C4202.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #25C[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)C4141.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #26C[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)C1O4131.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #27C[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)C1O4063.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #28C[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)C4116.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #29C[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)C1O4139.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #3C[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)C1O4149.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #30C[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)C4171.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #31C[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)C4123.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #32C[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)C1O4146.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #33C[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)C4157.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #34C[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)C4133.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #35C[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)C4254.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #36C[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)C4080.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #37C[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)C4104.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #38C[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=C14112.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #39C[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)C4073.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #4C[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)C1O4074.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #40C[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)C4098.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #41C[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=C14081.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #42C[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)C4023.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #43C[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=C14123.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #44C[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)C4091.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #45C[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=C14096.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #46C[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)O24122.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #47C[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=C14081.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #48C[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=O4048.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #49C[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=C14099.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #5C[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)C4130.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #50C[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=O4068.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #51C[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=C14077.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #52C[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=C14105.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #53C[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=O4064.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #54C[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=C14057.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #55C[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=C14080.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #56C[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=C1O4137.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #57C[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=C14090.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #58C[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=C1O4049.6Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #59C[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=C14116.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #6C[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)C1O4097.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #60C[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=C1O4072.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #61C[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=C14086.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #62C[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=C14114.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #63C[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=C1O4064.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #64C[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=C14056.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #65C[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=C14099.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #66C[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=C14095.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #67C[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=C14119.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #68C[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=C14120.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #69C[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=O4140.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #7C[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)C1O4130.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #70C[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=C14182.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #8C[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)C1O4099.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,4TMS,isomer #9C[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)C4123.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #1C[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)C1O4020.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #10C[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)C4066.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #11C[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)C1O4078.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #12C[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)C1O4025.6Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #13C[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)C4062.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #14C[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)C1O4075.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #15C[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)C4097.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #16C[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)C4064.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #17C[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)C1O4077.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #18C[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)C4085.6Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #19C[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)C4060.6Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #2C[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)C1O4046.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #20C[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)C4161.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #21C[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)C1O4022.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #22C[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)C1O3969.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #23C[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)C4006.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #24C[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)C1O4027.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #25C[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)C4055.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #26C[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)C4015.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #27C[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)C1O4027.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #28C[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)C4053.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #29C[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)C4015.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #3C[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)C1O4023.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #30C[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)C4148.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #31C[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)C1O4056.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #32C[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)C4086.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #33C[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)C4045.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #34C[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)C4117.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #35C[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)C4102.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #36C[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)C4068.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #37C[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=C14042.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #38C[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)C4003.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #39C[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=C14074.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #4C[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)C4035.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #40C[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)C4022.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #41C[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=C14037.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #42C[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=C14058.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #43C[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)C4009.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #44C[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=C14004.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #45C[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=C14045.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #46C[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=C14068.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #47C[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=O4023.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #48C[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=C14010.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #49C[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=C14037.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #5C[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)C1O4050.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #50C[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=C14021.6Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #51C[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=C14072.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #52C[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=C1O4032.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #53C[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=C14015.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #54C[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=C14042.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #55C[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=C14024.6Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #56C[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=C14077.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #6C[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)C1O4002.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #7C[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)C4032.6Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #8C[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)C1O4080.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,5TMS,isomer #9C[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)C4109.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #1C[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)C1O4008.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #10C[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)C4065.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #11C[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)C1O4029.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #12C[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)C4054.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #13C[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)C4016.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #14C[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)C4051.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #15C[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)C4024.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #16C[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)C1O3991.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #17C[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)C4011.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #18C[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)C3977.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #19C[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)C4028.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #2C[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)C1O3979.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #20C[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)C4022.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #21C[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)C4064.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #22C[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=C14036.6Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #23C[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)C4003.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #24C[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=C13994.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #25C[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=C14013.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #26C[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=C13996.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #27C[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=C14000.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #28C[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=C13996.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #3C[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)C3996.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #4C[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)C1O4011.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #5C[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)C4031.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #6C[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)C4001.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #7C[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)C1O4000.6Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #8C[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)C4021.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,6TMS,isomer #9C[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)C3989.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,1TBDMS,isomer #1CC(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)C1O4780.6Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,1TBDMS,isomer #2CC(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)O24736.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,1TBDMS,isomer #3CC(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=C1O4721.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,1TBDMS,isomer #4CC(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=O4749.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,1TBDMS,isomer #5CC(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=C14781.6Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,1TBDMS,isomer #6CC(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)C1O4819.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,1TBDMS,isomer #7CC(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)C1O4812.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,1TBDMS,isomer #8CC(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)C1O4819.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #1CC(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)C1O4894.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #10CC(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)O24834.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #11CC(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)O24832.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #12CC(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=C14872.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #13CC(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=O4810.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #14CC(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=C1O4824.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #15CC(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=C1O4824.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #16CC(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=C1O4825.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #17CC(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=C14865.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #18CC(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=C1O4799.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #19CC(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=C14858.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #2CC(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)C1O4840.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #20CC(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=O4813.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #21CC(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=O4808.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #22CC(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=O4812.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #23CC(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=C14887.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #24CC(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=C14886.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #25CC(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=C14885.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #26CC(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)C1O4876.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #27CC(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)C4884.6Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #28CC(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)C4863.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #3CC(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)C1O4857.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #4CC(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)C1O4841.6Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #5CC(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)C1O4891.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #6CC(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)C1O4888.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #7CC(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)C4878.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #8CC(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)C4833.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,2TBDMS,isomer #9CC(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)O24831.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #1CC(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)C1O4927.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #10CC(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)C1O4880.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #11CC(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)C4874.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #12CC(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)C1O4907.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #13CC(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)C1O4927.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #14CC(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)C1O4927.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #15CC(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)C4917.6Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #16CC(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)C1O4924.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #17CC(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)C1O4924.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #18CC(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)C4915.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #19CC(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)C1O4955.6Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #2CC(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)C1O4976.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #20CC(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)C4966.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #21CC(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)C4944.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #22CC(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)C4907.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #23CC(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)C4902.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #24CC(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)C4900.6Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #25CC(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=C14978.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #26CC(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)C4872.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #27CC(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)O24899.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #28CC(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)O24907.6Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #29CC(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=C14980.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #3CC(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)C1O4966.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #30CC(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=O4860.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #31CC(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)O24916.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #32CC(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=C14986.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #33CC(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=O4861.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #34CC(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=C14963.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #35CC(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=O4850.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #36CC(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=C14951.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #37CC(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=C1O4910.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #38CC(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=C1O4920.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #39CC(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=C14978.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #4CC(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)C1O4973.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #40CC(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=C1O4871.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #41CC(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=C1O4932.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #42CC(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=C14977.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #43CC(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=C1O4864.5Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #44CC(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=C14967.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #45CC(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=C1O4864.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #46CC(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=C14947.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #47CC(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=C14914.8Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #48CC(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=C14905.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #49CC(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=C14914.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #5CC(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)C1O4977.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #50CC(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=O4850.2Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #51CC(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=O4869.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #52CC(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=O4874.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #53CC(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=C14956.4Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #54CC(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=C14968.0Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #55CC(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=C14974.6Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #56CC(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)C4936.7Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #6CC(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)C4960.3Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #7CC(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)C1O4871.1Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #8CC(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)C1O4876.9Semi standard non polar33892256
6-Hydroxykaempferol 7-glucoside,3TBDMS,isomer #9CC(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)C1O4887.7Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - 6-Hydroxykaempferol 7-glucoside GC-MS (Non-derivatized) - 70eV, Positivesplash10-0w31-7804900000-17fd51cdcb09d54954f12017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6-Hydroxykaempferol 7-glucoside GC-MS (3 TMS) - 70eV, Positivesplash10-014r-3620009000-b176a82f44c98681b28f2017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6-Hydroxykaempferol 7-glucoside GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6-Hydroxykaempferol 7-glucoside GC-MS (TBDMS_3_41) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6-Hydroxykaempferol 7-glucoside GC-MS ("6-Hydroxykaempferol 7-glucoside,3TBDMS,#41" TMS) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-Hydroxykaempferol 7-glucoside 10V, Positive-QTOFsplash10-0uxr-0148900000-8955561f40f2fd68693e2016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-Hydroxykaempferol 7-glucoside 20V, Positive-QTOFsplash10-0udi-0169100000-2cb64ed98fcc461a44602016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-Hydroxykaempferol 7-glucoside 40V, Positive-QTOFsplash10-0zmu-2952000000-6d601ba9fb35bcee8df42016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-Hydroxykaempferol 7-glucoside 10V, Negative-QTOFsplash10-0ik9-2305900000-72d39793c5f9d96de4142016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-Hydroxykaempferol 7-glucoside 20V, Negative-QTOFsplash10-0udi-2349200000-d26ce68ba81ef239e8622016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-Hydroxykaempferol 7-glucoside 40V, Negative-QTOFsplash10-0zfu-8694000000-520410b219aadf84d3782016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-Hydroxykaempferol 7-glucoside 10V, Positive-QTOFsplash10-0uxr-0009400000-82ee0af7a45dc332bf032021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-Hydroxykaempferol 7-glucoside 20V, Positive-QTOFsplash10-0udi-0009100000-7cb9d26c1cc75ab3087e2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-Hydroxykaempferol 7-glucoside 40V, Positive-QTOFsplash10-0udi-0009000000-83a0d85bdd6b793b4e432021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-Hydroxykaempferol 7-glucoside 10V, Negative-QTOFsplash10-03di-0000900000-0c99867ed0f73f18e8ae2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-Hydroxykaempferol 7-glucoside 20V, Negative-QTOFsplash10-0ik9-0005900000-e1e3f4f430433969300b2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-Hydroxykaempferol 7-glucoside 40V, Negative-QTOFsplash10-0udi-0009100000-e11df97ed7c4b30b148e2021-09-23Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Cytoplasm
  • Extracellular
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB013262
KNApSAcK IDC00013823
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound14825511
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .