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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 22:50:55 UTC

Update Date

2022-03-07 02:55:25 UTC

HMDB ID

HMDB0037595

Secondary Accession Numbers

HMDB37595

Metabolite Identification

Common Name

6-Hydroxyluteolin 6-xyloside

Description

6-Hydroxyluteolin 6-xyloside belongs to the class of organic compounds known as flavonoid o-glycosides. Flavonoid O-glycosides are compounds containing a carbohydrate moiety which is O-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone. 6-Hydroxyluteolin 6-xyloside has been detected, but not quantified in, fruits. This could make 6-hydroxyluteolin 6-xyloside a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on 6-Hydroxyluteolin 6-xyloside.

Structure

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

  Mrv0541 05061309532D          

 31 34  0  0  0  0            999 V2000
   -2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  7  1  1  0  0  0  0
  7  3  2  0  0  0  0
  8  2  1  0  0  0  0
  9  3  1  0  0  0  0
  9  8  2  0  0  0  0
 10  4  1  0  0  0  0
 11  5  2  0  0  0  0
 12  6  1  0  0  0  0
 13  4  2  0  0  0  0
 13  7  1  0  0  0  0
 14  5  1  0  0  0  0
 15 10  1  0  0  0  0
 15 14  2  0  0  0  0
 16 12  1  0  0  0  0
 17 15  1  0  0  0  0
 18 16  1  0  0  0  0
 19 11  1  0  0  0  0
 19 17  2  0  0  0  0
 20 18  1  0  0  0  0
 21  8  1  0  0  0  0
 22  9  1  0  0  0  0
 23 10  2  0  0  0  0
 24 11  1  0  0  0  0
 25 12  1  0  0  0  0
 26 16  1  0  0  0  0
 27 17  1  0  0  0  0
 28 18  1  0  0  0  0
 29  6  1  0  0  0  0
 29 20  1  0  0  0  0
 30 13  1  0  0  0  0
 30 14  1  0  0  0  0
 31 19  1  0  0  0  0
 31 20  1  0  0  0  0
M  END

HMDB0037595
     RDKit          3D
6-Hydroxyluteolin 6-xyloside
 49 52  0  0  0  0  0  0  0  0999 V2000
   -0.7756   -2.8815    1.6165 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4049   -1.9075    1.1343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7750   -2.0174    0.8884 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4419   -0.9569    0.3671 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8690   -0.9548    0.0690 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6204   -2.0706    0.3147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9932   -2.1116    0.0434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5840   -0.9764   -0.4890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9335   -0.9882   -0.7659 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8556    0.1604   -0.7470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5180    1.2542   -1.2793 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5061    0.1618   -0.4663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7975    0.1574    0.0997 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5178    0.2970    0.3161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8970    1.5078    0.0090 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4449    1.6747    0.2278 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0400    2.8801   -0.0828 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2221    0.6333    0.7644 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5497    0.9000    0.9438 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4687    0.7705   -0.1603 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0047    2.0344   -0.3208 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1379    2.1074   -1.0876 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2473    1.2306   -0.5345 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3050    1.2916   -1.4523 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8069   -0.1876   -0.3826 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6926   -0.8223    0.5035 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4282   -0.3155    0.1698 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8806   -1.5107   -0.3419 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5944   -0.5573    1.0641 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3410   -1.6051    1.6030 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7678   -0.7232    0.8401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2806   -2.9253    1.1103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2267   -2.9865    0.7269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5876   -2.9944    0.2378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3646   -0.1666   -1.1519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9556    2.0832   -1.4610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9148    1.0391   -0.6593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5109    2.2951   -0.4022 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4744    3.6213   -0.4673 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8558    0.4619   -1.0397 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9949    1.8670   -2.1471 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5113    3.1496   -1.0321 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6075    1.5907    0.4570 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0991    1.7120   -1.0348 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8808   -0.7116   -1.3843 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3448   -0.1800    0.8875 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5048   -0.4269    1.2801 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3604   -2.3009    0.0291 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2999   -1.6026    1.8243 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  2  0
  4 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 18 29  1  0
 29 30  1  0
 29 31  2  0
 31  2  1  0
 12  5  1  0
 31 14  1  0
 27 20  1  0
  3 32  1  0
  6 33  1  0
  7 34  1  0
  9 35  1  0
 11 36  1  0
 12 37  1  0
 15 38  1  0
 17 39  1  0
 20 40  1  0
 22 41  1  0
 22 42  1  0
 23 43  1  0
 24 44  1  0
 25 45  1  0
 26 46  1  0
 27 47  1  0
 28 48  1  0
 30 49  1  0
M  END

  Mrv0541 05061309532D          

 31 34  0  0  0  0            999 V2000
   -2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  7  1  1  0  0  0  0
  7  3  2  0  0  0  0
  8  2  1  0  0  0  0
  9  3  1  0  0  0  0
  9  8  2  0  0  0  0
 10  4  1  0  0  0  0
 11  5  2  0  0  0  0
 12  6  1  0  0  0  0
 13  4  2  0  0  0  0
 13  7  1  0  0  0  0
 14  5  1  0  0  0  0
 15 10  1  0  0  0  0
 15 14  2  0  0  0  0
 16 12  1  0  0  0  0
 17 15  1  0  0  0  0
 18 16  1  0  0  0  0
 19 11  1  0  0  0  0
 19 17  2  0  0  0  0
 20 18  1  0  0  0  0
 21  8  1  0  0  0  0
 22  9  1  0  0  0  0
 23 10  2  0  0  0  0
 24 11  1  0  0  0  0
 25 12  1  0  0  0  0
 26 16  1  0  0  0  0
 27 17  1  0  0  0  0
 28 18  1  0  0  0  0
 29  6  1  0  0  0  0
 29 20  1  0  0  0  0
 30 13  1  0  0  0  0
 30 14  1  0  0  0  0
 31 19  1  0  0  0  0
 31 20  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0037595

> <DATABASE_NAME>
hmdb

> <SMILES>
OC1COC(OC2=C(O)C3=C(OC(=CC3=O)C3=CC(O)=C(O)C=C3)C=C2O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C20H18O11/c21-8-2-1-7(3-9(8)22)13-4-10(23)15-14(30-13)5-11(24)19(17(15)27)31-20-18(28)16(26)12(25)6-29-20/h1-5,12,16,18,20-22,24-28H,6H2

> <INCHI_KEY>
ROVSWYFYBQYCAJ-UHFFFAOYSA-N

> <FORMULA>
C20H18O11

> <MOLECULAR_WEIGHT>
434.3503

> <EXACT_MASS>
434.084911418

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_AVERAGE_POLARIZABILITY>
41.679215860944716

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]-4H-chromen-4-one

> <ALOGPS_LOGP>
0.71

> <JCHEM_LOGP>
0.4618253389999998

> <ALOGPS_LOGS>
-2.59

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.669214011426543

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.007288593039783

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5265985443108088

> <JCHEM_POLAR_SURFACE_AREA>
186.36999999999998

> <JCHEM_REFRACTIVITY>
103.0576

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.12e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]chromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0037595
     RDKit          3D
6-Hydroxyluteolin 6-xyloside
 49 52  0  0  0  0  0  0  0  0999 V2000
   -0.7756   -2.8815    1.6165 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4049   -1.9075    1.1343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7750   -2.0174    0.8884 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4419   -0.9569    0.3671 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8690   -0.9548    0.0690 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6204   -2.0706    0.3147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9932   -2.1116    0.0434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5840   -0.9764   -0.4890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9335   -0.9882   -0.7659 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8556    0.1604   -0.7470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5180    1.2542   -1.2793 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5061    0.1618   -0.4663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7975    0.1574    0.0997 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5178    0.2970    0.3161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8970    1.5078    0.0090 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4449    1.6747    0.2278 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0400    2.8801   -0.0828 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2221    0.6333    0.7644 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5497    0.9000    0.9438 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4687    0.7705   -0.1603 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0047    2.0344   -0.3208 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1379    2.1074   -1.0876 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2473    1.2306   -0.5345 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3050    1.2916   -1.4523 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8069   -0.1876   -0.3826 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6926   -0.8223    0.5035 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4282   -0.3155    0.1698 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8806   -1.5107   -0.3419 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5944   -0.5573    1.0641 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3410   -1.6051    1.6030 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7678   -0.7232    0.8401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2806   -2.9253    1.1103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2267   -2.9865    0.7269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5876   -2.9944    0.2378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3646   -0.1666   -1.1519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9556    2.0832   -1.4610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9148    1.0391   -0.6593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5109    2.2951   -0.4022 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4744    3.6213   -0.4673 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8558    0.4619   -1.0397 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9949    1.8670   -2.1471 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5113    3.1496   -1.0321 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6075    1.5907    0.4570 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0991    1.7120   -1.0348 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8808   -0.7116   -1.3843 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3448   -0.1800    0.8875 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5048   -0.4269    1.2801 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3604   -2.3009    0.0291 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2999   -1.6026    1.8243 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  2  0
  4 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 18 29  1  0
 29 30  1  0
 29 31  2  0
 31  2  1  0
 12  5  1  0
 31 14  1  0
 27 20  1  0
  3 32  1  0
  6 33  1  0
  7 34  1  0
  9 35  1  0
 11 36  1  0
 12 37  1  0
 15 38  1  0
 17 39  1  0
 20 40  1  0
 22 41  1  0
 22 42  1  0
 23 43  1  0
 24 44  1  0
 25 45  1  0
 26 46  1  0
 27 47  1  0
 28 48  1  0
 30 49  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.335   1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.667   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.335   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.336   3.850   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -6.668  -0.770   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       0.000   6.160   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       5.335   1.540   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      10.669   1.540   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      10.669   4.620   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       2.667   6.160   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       8.002   6.160   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       6.668   2.310   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       0.000   1.540   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       5.335   4.620   0.000  0.00  0.00           O+0
CONECT    1    2    7                                                       
CONECT    2    1    8                                                       
CONECT    3    7    9                                                       
CONECT    4   10   13                                                       
CONECT    5   11   14                                                       
CONECT    6   12   29                                                       
CONECT    7    1    3   13                                                  
CONECT    8    2    9   21                                                  
CONECT    9    3    8   22                                                  
CONECT   10    4   15   23                                                  
CONECT   11    5   19   24                                                  
CONECT   12    6   16   25                                                  
CONECT   13    4    7   30                                                  
CONECT   14    5   15   30                                                  
CONECT   15   10   14   17                                                  
CONECT   16   12   18   26                                                  
CONECT   17   15   19   27                                                  
CONECT   18   16   20   28                                                  
CONECT   19   11   17   31                                                  
CONECT   20   18   29   31                                                  
CONECT   21    8                                                            
CONECT   22    9                                                            
CONECT   23   10                                                            
CONECT   24   11                                                            
CONECT   25   12                                                            
CONECT   26   16                                                            
CONECT   27   17                                                            
CONECT   28   18                                                            
CONECT   29    6   20                                                       
CONECT   30   13   14                                                       
CONECT   31   19   20                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

COMPND    HMDB0037595
HETATM    1  O1  UNL     1      -0.776  -2.881   1.616  1.00  0.00           O  
HETATM    2  C1  UNL     1      -1.405  -1.908   1.134  1.00  0.00           C  
HETATM    3  C2  UNL     1      -2.775  -2.017   0.888  1.00  0.00           C  
HETATM    4  C3  UNL     1      -3.442  -0.957   0.367  1.00  0.00           C  
HETATM    5  C4  UNL     1      -4.869  -0.955   0.069  1.00  0.00           C  
HETATM    6  C5  UNL     1      -5.620  -2.071   0.315  1.00  0.00           C  
HETATM    7  C6  UNL     1      -6.993  -2.112   0.043  1.00  0.00           C  
HETATM    8  C7  UNL     1      -7.584  -0.976  -0.489  1.00  0.00           C  
HETATM    9  O2  UNL     1      -8.933  -0.988  -0.766  1.00  0.00           O  
HETATM   10  C8  UNL     1      -6.856   0.160  -0.747  1.00  0.00           C  
HETATM   11  O3  UNL     1      -7.518   1.254  -1.279  1.00  0.00           O  
HETATM   12  C9  UNL     1      -5.506   0.162  -0.466  1.00  0.00           C  
HETATM   13  O4  UNL     1      -2.798   0.157   0.100  1.00  0.00           O  
HETATM   14  C10 UNL     1      -1.518   0.297   0.316  1.00  0.00           C  
HETATM   15  C11 UNL     1      -0.897   1.508   0.009  1.00  0.00           C  
HETATM   16  C12 UNL     1       0.445   1.675   0.228  1.00  0.00           C  
HETATM   17  O5  UNL     1       1.040   2.880  -0.083  1.00  0.00           O  
HETATM   18  C13 UNL     1       1.222   0.633   0.764  1.00  0.00           C  
HETATM   19  O6  UNL     1       2.550   0.900   0.944  1.00  0.00           O  
HETATM   20  C14 UNL     1       3.469   0.770  -0.160  1.00  0.00           C  
HETATM   21  O7  UNL     1       4.005   2.034  -0.321  1.00  0.00           O  
HETATM   22  C15 UNL     1       5.138   2.107  -1.088  1.00  0.00           C  
HETATM   23  C16 UNL     1       6.247   1.231  -0.534  1.00  0.00           C  
HETATM   24  O8  UNL     1       7.305   1.292  -1.452  1.00  0.00           O  
HETATM   25  C17 UNL     1       5.807  -0.188  -0.383  1.00  0.00           C  
HETATM   26  O9  UNL     1       6.693  -0.822   0.503  1.00  0.00           O  
HETATM   27  C18 UNL     1       4.428  -0.315   0.170  1.00  0.00           C  
HETATM   28  O10 UNL     1       3.881  -1.511  -0.342  1.00  0.00           O  
HETATM   29  C19 UNL     1       0.594  -0.557   1.064  1.00  0.00           C  
HETATM   30  O11 UNL     1       1.341  -1.605   1.603  1.00  0.00           O  
HETATM   31  C20 UNL     1      -0.768  -0.723   0.840  1.00  0.00           C  
HETATM   32  H1  UNL     1      -3.281  -2.925   1.110  1.00  0.00           H  
HETATM   33  H2  UNL     1      -5.227  -2.986   0.727  1.00  0.00           H  
HETATM   34  H3  UNL     1      -7.588  -2.994   0.238  1.00  0.00           H  
HETATM   35  H4  UNL     1      -9.365  -0.167  -1.152  1.00  0.00           H  
HETATM   36  H5  UNL     1      -6.956   2.083  -1.461  1.00  0.00           H  
HETATM   37  H6  UNL     1      -4.915   1.039  -0.659  1.00  0.00           H  
HETATM   38  H7  UNL     1      -1.511   2.295  -0.402  1.00  0.00           H  
HETATM   39  H8  UNL     1       0.474   3.621  -0.467  1.00  0.00           H  
HETATM   40  H9  UNL     1       2.856   0.462  -1.040  1.00  0.00           H  
HETATM   41  H10 UNL     1       4.995   1.867  -2.147  1.00  0.00           H  
HETATM   42  H11 UNL     1       5.511   3.150  -1.032  1.00  0.00           H  
HETATM   43  H12 UNL     1       6.608   1.591   0.457  1.00  0.00           H  
HETATM   44  H13 UNL     1       8.099   1.712  -1.035  1.00  0.00           H  
HETATM   45  H14 UNL     1       5.881  -0.712  -1.384  1.00  0.00           H  
HETATM   46  H15 UNL     1       7.345  -0.180   0.887  1.00  0.00           H  
HETATM   47  H16 UNL     1       4.505  -0.427   1.280  1.00  0.00           H  
HETATM   48  H17 UNL     1       4.360  -2.301   0.029  1.00  0.00           H  
HETATM   49  H18 UNL     1       2.300  -1.603   1.824  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   31
CONECT    3    4    4   32
CONECT    4    5   13
CONECT    5    6    6   12
CONECT    6    7   33
CONECT    7    8    8   34
CONECT    8    9   10
CONECT    9   35
CONECT   10   11   12   12
CONECT   11   36
CONECT   12   37
CONECT   13   14
CONECT   14   15   15   31
CONECT   15   16   38
CONECT   16   17   18   18
CONECT   17   39
CONECT   18   19   29
CONECT   19   20
CONECT   20   21   27   40
CONECT   21   22
CONECT   22   23   41   42
CONECT   23   24   25   43
CONECT   24   44
CONECT   25   26   27   45
CONECT   26   46
CONECT   27   28   47
CONECT   28   48
CONECT   29   30   31   31
CONECT   30   49
END

HMDB0037595
     RDKit          3D
6-Hydroxyluteolin 6-xyloside
 49 52  0  0  0  0  0  0  0  0999 V2000
   -0.7756   -2.8815    1.6165 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4049   -1.9075    1.1343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7750   -2.0174    0.8884 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4419   -0.9569    0.3671 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8690   -0.9548    0.0690 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6204   -2.0706    0.3147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9932   -2.1116    0.0434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5840   -0.9764   -0.4890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9335   -0.9882   -0.7659 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8556    0.1604   -0.7470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5180    1.2542   -1.2793 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5061    0.1618   -0.4663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7975    0.1574    0.0997 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5178    0.2970    0.3161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8970    1.5078    0.0090 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4449    1.6747    0.2278 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0400    2.8801   -0.0828 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2221    0.6333    0.7644 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5497    0.9000    0.9438 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4687    0.7705   -0.1603 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0047    2.0344   -0.3208 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1379    2.1074   -1.0876 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2473    1.2306   -0.5345 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3050    1.2916   -1.4523 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8069   -0.1876   -0.3826 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6926   -0.8223    0.5035 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4282   -0.3155    0.1698 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8806   -1.5107   -0.3419 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5944   -0.5573    1.0641 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3410   -1.6051    1.6030 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7678   -0.7232    0.8401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2806   -2.9253    1.1103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2267   -2.9865    0.7269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5876   -2.9944    0.2378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3646   -0.1666   -1.1519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9556    2.0832   -1.4610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9148    1.0391   -0.6593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5109    2.2951   -0.4022 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4744    3.6213   -0.4673 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8558    0.4619   -1.0397 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9949    1.8670   -2.1471 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5113    3.1496   -1.0321 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6075    1.5907    0.4570 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0991    1.7120   -1.0348 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8808   -0.7116   -1.3843 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3448   -0.1800    0.8875 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5048   -0.4269    1.2801 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3604   -2.3009    0.0291 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2999   -1.6026    1.8243 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  2  0
  4 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 18 29  1  0
 29 30  1  0
 29 31  2  0
 31  2  1  0
 12  5  1  0
 31 14  1  0
 27 20  1  0
  3 32  1  0
  6 33  1  0
  7 34  1  0
  9 35  1  0
 11 36  1  0
 12 37  1  0
 15 38  1  0
 17 39  1  0
 20 40  1  0
 22 41  1  0
 22 42  1  0
 23 43  1  0
 24 44  1  0
 25 45  1  0
 26 46  1  0
 27 47  1  0
 28 48  1  0
 30 49  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₀H₁₈O₁₁

Average Molecular Weight

434.3503

Monoisotopic Molecular Weight

434.084911418

IUPAC Name

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]-4H-chromen-4-one

Traditional Name

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]chromen-4-one

CAS Registry Number

65876-67-7

SMILES

OC1COC(OC2=C(O)C3=C(OC(=CC3=O)C3=CC(O)=C(O)C=C3)C=C2O)C(O)C1O

InChI Identifier

InChI=1S/C20H18O11/c21-8-2-1-7(3-9(8)22)13-4-10(23)15-14(30-13)5-11(24)19(17(15)27)31-20-18(28)16(26)12(25)6-29-20/h1-5,12,16,18,20-22,24-28H,6H2

InChI Key

ROVSWYFYBQYCAJ-UHFFFAOYSA-N

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Flavonoid O-glycosides

Alternative Parents

Substituents

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

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Extracellular (HMDB: HMDB0037595)
Cytoplasm (HMDB: HMDB0037595)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0037595)

Source

Exogenous

Exogenous (HMDB: HMDB0037595)

Food

Food (HMDB: HMDB0037595)

Fruit

Fruits (FooDB: FOOD00871)

Endogenous

Plant

Plant (HMDB: HMDB0037595)

Process

Not Available

Role

Biological role

Nutrient (HMDB: HMDB0037595)

Physical Properties

State

Not Available

Experimental Molecular Properties

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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	1.12 g/L	ALOGPS
logP	0.71	ALOGPS
logP	0.46	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	7.01	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	186.37 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	103.06 m³·mol⁻¹	ChemAxon
Polarizability	41.68 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	197.524	30932474
DeepCCS	[M-H]-	195.128	30932474
DeepCCS	[M-2H]-	228.492	30932474
DeepCCS	[M+Na]+	203.562	30932474
AllCCS	[M+H]+	199.4	32859911
AllCCS	[M+H-H2O]+	196.9	32859911
AllCCS	[M+NH4]+	201.8	32859911
AllCCS	[M+Na]+	202.4	32859911
AllCCS	[M-H]-	196.0	32859911
AllCCS	[M+Na-2H]-	196.2	32859911
AllCCS	[M+HCOO]-	196.6	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
6-Hydroxyluteolin 6-xyloside	OC1COC(OC2=C(O)C3=C(OC(=CC3=O)C3=CC(O)=C(O)C=C3)C=C2O)C(O)C1O	5230.4	Standard polar	33892256
6-Hydroxyluteolin 6-xyloside	OC1COC(OC2=C(O)C3=C(OC(=CC3=O)C3=CC(O)=C(O)C=C3)C=C2O)C(O)C1O	4186.8	Standard non polar	33892256
6-Hydroxyluteolin 6-xyloside	OC1COC(OC2=C(O)C3=C(OC(=CC3=O)C3=CC(O)=C(O)C=C3)C=C2O)C(O)C1O	4332.2	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
6-Hydroxyluteolin 6-xyloside,1TMS,isomer #1	C[Si](C)(C)OC1COC(OC2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O)C1O	4424.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,1TMS,isomer #2	C[Si](C)(C)OC1=C(OC2OCC(O)C(O)C2O)C(O)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4344.0	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,1TMS,isomer #3	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O)=C(O)C=C3O2)=CC=C1O	4437.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,1TMS,isomer #4	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O)=C(O)C=C3O2)C=C1O	4440.2	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,1TMS,isomer #5	C[Si](C)(C)OC1=CC2=C(C(O)=C1OC1OCC(O)C(O)C1O)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4392.2	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,1TMS,isomer #6	C[Si](C)(C)OC1C(OC2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)OCC(O)C1O	4391.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,1TMS,isomer #7	C[Si](C)(C)OC1C(O)COC(OC2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C1O	4389.6	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #1	C[Si](C)(C)OC1=CC2=C(C(O)=C1OC1OCC(O[Si](C)(C)C)C(O)C1O)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4284.5	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #10	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O)C(O)C4O)=C(O)C=C3O2)C=C1O	4295.6	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #11	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O)C(O)C4O)=C(O)C=C3O2)=CC=C1O	4277.8	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #12	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(O)C=C3O2)=CC=C1O	4288.7	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #13	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(O)C=C3O2)=CC=C1O	4242.7	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #14	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O)=C(O[Si](C)(C)C)C=C3O2)=CC=C1O	4278.2	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #15	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O)=C(O)C=C3O2)C=C1O[Si](C)(C)C	4241.1	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #16	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(O)C=C3O2)C=C1O	4313.2	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #17	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(O)C=C3O2)C=C1O	4263.6	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #18	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O)=C(O[Si](C)(C)C)C=C3O2)C=C1O	4293.4	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #19	C[Si](C)(C)OC1=CC2=C(C(O)=C1OC1OCC(O)C(O[Si](C)(C)C)C1O)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4261.4	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #2	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(O)C=C3O2)C=C1O	4294.8	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #20	C[Si](C)(C)OC1=CC2=C(C(O)=C1OC1OCC(O)C(O)C1O[Si](C)(C)C)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4269.4	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #21	C[Si](C)(C)OC1C(O)COC(OC2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C1O[Si](C)(C)C	4232.8	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #3	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(O)C=C3O2)=CC=C1O	4273.8	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #4	C[Si](C)(C)OC1=C(OC2OCC(O[Si](C)(C)C)C(O)C2O)C(O)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4240.8	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #5	C[Si](C)(C)OC1COC(OC2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C1O	4211.7	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #6	C[Si](C)(C)OC1COC(OC2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O)C1O[Si](C)(C)C	4239.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #7	C[Si](C)(C)OC1=C(OC2OCC(O)C(O[Si](C)(C)C)C2O)C(O)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4208.6	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #8	C[Si](C)(C)OC1=C(OC2OCC(O)C(O)C2O[Si](C)(C)C)C(O)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4213.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #9	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1OC1OCC(O)C(O)C1O)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4281.0	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #1	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(O[Si](C)(C)C)C=C3O2)C=C1O	4162.7	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #10	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(O)C=C3O2)=CC=C1O	4106.4	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #11	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C(O)C=C3O2)=CC=C1O	4128.5	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #12	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=C(O)C=C3O2)=CC=C1O	4111.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #13	C[Si](C)(C)OC1=C(OC2OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4086.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #14	C[Si](C)(C)OC1=C(OC2OCC(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4116.6	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #15	C[Si](C)(C)OC1COC(OC2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4146.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #16	C[Si](C)(C)OC1=C(OC2OCC(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4075.2	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #17	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1OC1OCC(O)C(O[Si](C)(C)C)C1O)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4121.7	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #18	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(O)C=C3O2)C=C1O	4132.0	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #19	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(O)C=C3O2)=CC=C1O	4112.4	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #2	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(O[Si](C)(C)C)C=C3O2)=CC=C1O	4149.6	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #20	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1OC1OCC(O)C(O)C1O[Si](C)(C)C)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4144.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #21	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(O)C=C3O2)C=C1O	4080.8	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #22	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(O)C=C3O2)=CC=C1O	4064.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #23	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O)C(O)C4O)=C(O[Si](C)(C)C)C=C3O2)C=C1O	4162.0	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #24	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O)C(O)C4O)=C(O[Si](C)(C)C)C=C3O2)=CC=C1O	4148.2	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #25	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O)C(O)C4O)=C(O)C=C3O2)C=C1O[Si](C)(C)C	4096.4	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #26	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(O)C=C3O2)=CC=C1O	4121.1	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #27	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(O[Si](C)(C)C)C=C3O2)=CC=C1O	4165.6	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #28	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(O)C=C3O2)C=C1O[Si](C)(C)C	4138.0	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #29	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C3O2)=CC=C1O	4119.0	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #3	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1OC1OCC(O[Si](C)(C)C)C(O)C1O)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4159.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #30	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(O)C=C3O2)C=C1O[Si](C)(C)C	4108.8	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #31	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O)=C(O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	4151.7	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #32	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(O)C=C3O2)C=C1O	4141.6	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #33	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(O[Si](C)(C)C)C=C3O2)C=C1O	4182.8	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #34	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C3O2)C=C1O	4132.6	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #35	C[Si](C)(C)OC1=CC2=C(C(O)=C1OC1OCC(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4143.8	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #4	C[Si](C)(C)OC1=CC2=C(C(O)=C1OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4152.7	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #5	C[Si](C)(C)OC1=CC2=C(C(O)=C1OC1OCC(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4137.5	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #6	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(O)C=C3O2)C=C1O	4120.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #7	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C(O)C=C3O2)C=C1O	4153.8	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #8	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=C(O)C=C3O2)C=C1O	4137.1	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #9	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(O)C=C3O2)C=C1O[Si](C)(C)C	4135.0	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #1	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(O[Si](C)(C)C)C=C3O2)C=C1O	4061.0	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #10	C[Si](C)(C)OC1=CC2=C(C(O)=C1OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4069.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #11	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C(O)C=C3O2)C=C1O	4005.8	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #12	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=C(O)C=C3O2)C=C1O	4021.1	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #13	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(O)C=C3O2)C=C1O[Si](C)(C)C	4018.1	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #14	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(O)C=C3O2)C=C1O	4016.7	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #15	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C(O)C=C3O2)C=C1O[Si](C)(C)C	3997.0	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #16	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=C(O)C=C3O2)C=C1O[Si](C)(C)C	3997.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #17	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C(O)C=C3O2)=CC=C1O	3981.1	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #18	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=C(O)C=C3O2)=CC=C1O	3997.6	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #19	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(O)C=C3O2)=CC=C1O	3982.7	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #2	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C(O[Si](C)(C)C)C=C3O2)C=C1O	4031.0	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #20	C[Si](C)(C)OC1=C(OC2OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4033.4	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #21	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1OC1OCC(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4040.6	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #22	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(O)C=C3O2)C=C1O	3994.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #23	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(O)C=C3O2)=CC=C1O	3966.7	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #24	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(O[Si](C)(C)C)C=C3O2)C=C1O	4055.6	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #25	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(O[Si](C)(C)C)C=C3O2)=CC=C1O	4035.2	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #26	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(O)C=C3O2)C=C1O[Si](C)(C)C	4005.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #27	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C3O2)C=C1O	4027.5	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #28	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C3O2)=CC=C1O	4007.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #29	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(O)C=C3O2)C=C1O[Si](C)(C)C	3981.0	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #3	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C3O2)C=C1O	4037.7	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #30	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O)C(O)C4O)=C(O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	4059.2	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #31	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C3O2)=CC=C1O	4005.0	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #32	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(O)C=C3O2)C=C1O[Si](C)(C)C	3998.8	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #33	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	4039.0	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #34	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	4019.0	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #35	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C3O2)C=C1O	4030.0	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #4	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	4050.0	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #5	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(O[Si](C)(C)C)C=C3O2)=CC=C1O	4048.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #6	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C(O[Si](C)(C)C)C=C3O2)=CC=C1O	4006.5	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #7	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C3O2)=CC=C1O	4010.6	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #8	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4051.8	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #9	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1OC1OCC(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4082.0	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #1	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C(O[Si](C)(C)C)C=C3O2)C=C1O	3982.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #10	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4002.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #11	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(O)C=C3O2)C=C1O	3949.0	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #12	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C(O)C=C3O2)C=C1O[Si](C)(C)C	3952.6	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #13	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=C(O)C=C3O2)C=C1O[Si](C)(C)C	3970.1	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #14	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(O)C=C3O2)C=C1O[Si](C)(C)C	3946.6	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #15	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(O)C=C3O2)=CC=C1O	3923.7	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #16	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C3O2)C=C1O	3976.6	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #17	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C3O2)=CC=C1O	3954.6	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #18	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(O)C=C3O2)C=C1O[Si](C)(C)C	3947.4	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #19	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	3997.5	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #2	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C3O2)C=C1O	3994.4	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #20	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	3980.8	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #21	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	3973.5	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #3	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	4009.0	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #4	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C3O2)C=C1O	3978.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #5	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C(O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	3968.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #6	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	3984.5	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #7	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C(O[Si](C)(C)C)C=C3O2)=CC=C1O	3964.5	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #8	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C3O2)=CC=C1O	3976.0	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #9	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C3O2)=CC=C1O	3950.7	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,6TMS,isomer #1	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C3O2)C=C1O	3928.0	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,6TMS,isomer #2	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C(O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	3941.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,6TMS,isomer #3	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	3955.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,6TMS,isomer #4	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	3928.5	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,6TMS,isomer #5	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C3O2)=CC=C1O	3916.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,6TMS,isomer #6	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(O)C=C3O2)C=C1O[Si](C)(C)C	3904.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,6TMS,isomer #7	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C(OC4OCC(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	3934.4	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1COC(OC2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O)C1O	4719.4	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=C(OC2OCC(O)C(O)C2O)C(O)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4625.4	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O)=C(O)C=C3O2)=CC=C1O	4647.4	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O)=C(O)C=C3O2)C=C1O	4658.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O)=C1OC1OCC(O)C(O)C1O)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4633.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1C(OC2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)OCC(O)C1O	4694.2	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1C(O)COC(OC2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C1O	4699.1	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O)=C1OC1OCC(O[Si](C)(C)C(C)(C)C)C(O)C1O)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4783.7	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O)C(O)C4O)=C(O)C=C3O2)C=C1O	4779.8	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O)C(O)C4O)=C(O)C=C3O2)=CC=C1O	4746.7	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O[Si](C)(C)C(C)(C)C)C4O)=C(O)C=C3O2)=CC=C1O	4792.5	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C(C)(C)C)=C(O)C=C3O2)=CC=C1O	4738.4	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)=CC=C1O	4742.4	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O)=C(O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C	4709.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O[Si](C)(C)C(C)(C)C)C4O)=C(O)C=C3O2)C=C1O	4827.7	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C(C)(C)C)=C(O)C=C3O2)C=C1O	4771.5	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1O	4773.8	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O)=C1OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4769.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O)C4O)=C(O)C=C3O2)C=C1O	4797.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O)=C1OC1OCC(O)C(O)C1O[Si](C)(C)C(C)(C)C)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4760.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC1C(O)COC(OC2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C1O[Si](C)(C)C(C)(C)C	4783.5	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O)C4O)=C(O)C=C3O2)=CC=C1O	4765.1	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1=C(OC2OCC(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4776.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1COC(OC2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C1O	4778.2	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1COC(OC2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O)C1O[Si](C)(C)C(C)(C)C	4804.2	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1=C(OC2OCC(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4756.1	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1=C(OC2OCC(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4751.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1OC1OCC(O)C(O)C1O)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4783.5	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O)C4O)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1O	4902.7	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O)C4O)=C(O)C=C3O2)=CC=C1O	4832.5	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C4O)=C(O)C=C3O2)=CC=C1O	4881.5	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O)C4O[Si](C)(C)C(C)(C)C)=C(O)C=C3O2)=CC=C1O	4862.7	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1=C(OC2OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4816.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC1=C(OC2OCC(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4829.7	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1COC(OC2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4850.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1=C(OC2OCC(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4794.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4829.6	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O)C(O[Si](C)(C)C(C)(C)C)C4O)=C(O)C=C3O2)C=C1O	4893.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O)C(O[Si](C)(C)C(C)(C)C)C4O)=C(O)C=C3O2)=CC=C1O	4836.7	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O)C4O)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)=CC=C1O	4857.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1OC1OCC(O)C(O)C1O[Si](C)(C)C(C)(C)C)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4823.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O)C(O)C4O[Si](C)(C)C(C)(C)C)=C(O)C=C3O2)C=C1O	4841.7	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O)C(O)C4O[Si](C)(C)C(C)(C)C)=C(O)C=C3O2)=CC=C1O	4794.1	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O)C(O)C4O)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1O	4914.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O)C(O)C4O)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)=CC=C1O	4869.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O)C(O)C4O)=C(O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C	4805.1	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O[Si](C)(C)C(C)(C)C)C4O[Si](C)(C)C(C)(C)C)=C(O)C=C3O2)=CC=C1O	4859.6	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O[Si](C)(C)C(C)(C)C)C4O)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)=CC=C1O	4876.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O[Si](C)(C)C(C)(C)C)C4O)=C(O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C	4851.5	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)=CC=C1O	4823.6	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1OC1OCC(O[Si](C)(C)C(C)(C)C)C(O)C1O)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4847.0	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C(C)(C)C)=C(O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C	4802.7	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C	4855.1	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O[Si](C)(C)C(C)(C)C)C4O[Si](C)(C)C(C)(C)C)=C(O)C=C3O2)C=C1O	4903.4	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O[Si](C)(C)C(C)(C)C)C4O)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1O	4927.0	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1O	4869.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O)=C1OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4820.0	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O)=C1OC1OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4837.4	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O)=C1OC1OCC(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4836.2	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O)C4O)=C(O)C=C3O2)C=C1O	4881.5	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C4O)=C(O)C=C3O2)C=C1O	4923.2	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O)C4O[Si](C)(C)C(C)(C)C)=C(O)C=C3O2)C=C1O	4908.2	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O)C4O)=C(O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C	4835.7	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O)C4O)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1O	5003.8	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O)=C1OC1OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4917.6	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C4O)=C(O)C=C3O2)C=C1O	4985.7	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O)C4O[Si](C)(C)C(C)(C)C)=C(O)C=C3O2)C=C1O	4990.5	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O)C4O)=C(O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C	4907.1	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C4O[Si](C)(C)C(C)(C)C)=C(O)C=C3O2)C=C1O	5008.1	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C4O)=C(O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C	4964.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O)C4O[Si](C)(C)C(C)(C)C)=C(O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C	4959.2	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C4O)=C(O)C=C3O2)=CC=C1O	4931.7	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O)C4O[Si](C)(C)C(C)(C)C)=C(O)C=C3O2)=CC=C1O	4933.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C4O[Si](C)(C)C(C)(C)C)=C(O)C=C3O2)=CC=C1O	4966.5	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C4O)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1O	5016.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC1=C(OC2OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4908.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4897.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O)C(O[Si](C)(C)C(C)(C)C)C4O[Si](C)(C)C(C)(C)C)=C(O)C=C3O2)C=C1O	4958.4	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O)C(O[Si](C)(C)C(C)(C)C)C4O[Si](C)(C)C(C)(C)C)=C(O)C=C3O2)=CC=C1O	4902.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O)C(O[Si](C)(C)C(C)(C)C)C4O)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1O	5004.5	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O)C(O[Si](C)(C)C(C)(C)C)C4O)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)=CC=C1O	4950.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O)C(O[Si](C)(C)C(C)(C)C)C4O)=C(O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C	4911.4	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O)C(O)C4O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1O	4958.5	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O)C(O)C4O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)=CC=C1O	4905.6	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O)C(O)C4O[Si](C)(C)C(C)(C)C)=C(O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C	4853.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O)C4O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1O	5014.2	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O)C(O)C4O)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C	4953.6	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O[Si](C)(C)C(C)(C)C)C4O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)=CC=C1O	4944.0	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O[Si](C)(C)C(C)(C)C)C4O[Si](C)(C)C(C)(C)C)=C(O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C	4940.6	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O[Si](C)(C)C(C)(C)C)C4O)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C	4975.6	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C	4913.4	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O[Si](C)(C)C(C)(C)C)C4O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1O	4993.2	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O)C4O)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C	4961.9	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O)C4O)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)=CC=C1O	4950.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C4O)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)=CC=C1O	4969.6	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O)C4O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C=C3O2)=CC=C1O	4961.3	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1OC1OCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4908.4	Semi standard non polar	33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1OC1OCC(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4935.8	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Hydroxyluteolin 6-xyloside GC-MS (Non-derivatized) - 70eV, Positive	splash10-106r-9107600000-e457a7bacbfa26ab4b30	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Hydroxyluteolin 6-xyloside GC-MS (3 TMS) - 70eV, Positive	splash10-000i-4600129000-81f17367ce245261de97	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Hydroxyluteolin 6-xyloside GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Hydroxyluteolin 6-xyloside GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Hydroxyluteolin 6-xyloside GC-MS (TBDMS_4_22) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Hydroxyluteolin 6-xyloside GC-MS (TBDMS_4_23) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Hydroxyluteolin 6-xyloside GC-MS ("6-Hydroxyluteolin 6-xyloside,4TBDMS,#22" TMS) - 70eV, Positive	Not Available	2021-10-14	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxyluteolin 6-xyloside 10V, Positive-QTOF	splash10-0udr-0139800000-f3b9339c16337a60a763	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxyluteolin 6-xyloside 20V, Positive-QTOF	splash10-0udi-0279100000-fb7da1f576c6bee0ca3f	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxyluteolin 6-xyloside 40V, Positive-QTOF	splash10-000l-2591000000-d627c1bed36cb6a469c0	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxyluteolin 6-xyloside 10V, Negative-QTOF	splash10-0f89-1215900000-c5e59f54e01819099fec	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxyluteolin 6-xyloside 20V, Negative-QTOF	splash10-0ue9-1459200000-0c4f2d08d4109031e55c	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxyluteolin 6-xyloside 40V, Negative-QTOF	splash10-0006-7592000000-e63ddf70b6f71b58e6a2	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxyluteolin 6-xyloside 10V, Positive-QTOF	splash10-000i-0000900000-1453f61e7eeaeb92b36b	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxyluteolin 6-xyloside 20V, Positive-QTOF	splash10-000i-0000900000-1453f61e7eeaeb92b36b	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxyluteolin 6-xyloside 40V, Positive-QTOF	splash10-0f79-0309400000-330bfdd0973588f54e96	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxyluteolin 6-xyloside 10V, Negative-QTOF	splash10-001i-0000900000-42f5f679c004d65ed93d	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxyluteolin 6-xyloside 20V, Negative-QTOF	splash10-001i-0000900000-85bbf452212130c5a29d	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxyluteolin 6-xyloside 40V, Negative-QTOF	splash10-004j-0791200000-7fa77202c15abf3668b8	2021-09-23	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm
Extracellular

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB016699

KNApSAcK ID

C00004378

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

74977865

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

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

Showing metabocard for 6-Hydroxyluteolin 6-xyloside (HMDB0037595)

MOL for HMDB0037595 (6-Hydroxyluteolin 6-xyloside)

3D MOL for HMDB0037595 (6-Hydroxyluteolin 6-xyloside)

3D SDF for HMDB0037595 (6-Hydroxyluteolin 6-xyloside)

3D-SDF for HMDB0037595 (6-Hydroxyluteolin 6-xyloside)

PDB for HMDB0037595 (6-Hydroxyluteolin 6-xyloside)

3D PDB for HMDB0037595 (6-Hydroxyluteolin 6-xyloside)

SMILES for HMDB0037595 (6-Hydroxyluteolin 6-xyloside)

INCHI for HMDB0037595 (6-Hydroxyluteolin 6-xyloside)

Structure for HMDB0037595 (6-Hydroxyluteolin 6-xyloside)

3D Structure for HMDB0037595 (6-Hydroxyluteolin 6-xyloside)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra