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

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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 22:50:55 UTC
Update Date2022-03-07 02:55:25 UTC
HMDB IDHMDB0037595
Secondary Accession Numbers
  • HMDB37595
Metabolite Identification
Common Name6-Hydroxyluteolin 6-xyloside
Description6-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
Data?1563863057
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0037595 (6-Hydroxyluteolin 6-xyloside)


  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
Download

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

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
Download

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


  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

$$$$
Download

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

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
Download

PDB for HMDB0037595 (6-Hydroxyluteolin 6-xyloside)

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
Download

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

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
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SMILES for HMDB0037595 (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
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INCHI for HMDB0037595 (6-Hydroxyluteolin 6-xyloside)

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
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View in JSmolView Stereo Labels
SynonymsNot Available
Chemical FormulaC20H18O11
Average Molecular Weight434.3503
Monoisotopic Molecular Weight434.084911418
IUPAC Name2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]-4H-chromen-4-one
Traditional Name2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]chromen-4-one
CAS Registry Number65876-67-7
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 KeyROVSWYFYBQYCAJ-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.
KingdomOrganic compounds
Super ClassPhenylpropanoids and polyketides
ClassFlavonoids
Sub ClassFlavonoid glycosides
Direct ParentFlavonoid 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 FrameworkAromatic heteropolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Biological locationRoute of exposureSource
ProcessNot Available
Role
Biological role
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 Solubility1.12 g/LALOGPS
logP0.71ALOGPS
logP0.46ChemAxon
logS-2.6ALOGPS
pKa (Strongest Acidic)7.01ChemAxon
pKa (Strongest Basic)-3.5ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count11ChemAxon
Hydrogen Donor Count7ChemAxon
Polar Surface Area186.37 ŲChemAxon
Rotatable Bond Count3ChemAxon
Refractivity103.06 m³·mol⁻¹ChemAxon
Polarizability41.68 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]+197.52430932474
DeepCCS[M-H]-195.12830932474
DeepCCS[M-2H]-228.49230932474
DeepCCS[M+Na]+203.56230932474
AllCCS[M+H]+199.432859911
AllCCS[M+H-H2O]+196.932859911
AllCCS[M+NH4]+201.832859911
AllCCS[M+Na]+202.432859911
AllCCS[M-H]-196.032859911
AllCCS[M+Na-2H]-196.232859911
AllCCS[M+HCOO]-196.632859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
6-Hydroxyluteolin 6-xylosideOC1COC(OC2=C(O)C3=C(OC(=CC3=O)C3=CC(O)=C(O)C=C3)C=C2O)C(O)C1O5230.4Standard polar33892256
6-Hydroxyluteolin 6-xylosideOC1COC(OC2=C(O)C3=C(OC(=CC3=O)C3=CC(O)=C(O)C=C3)C=C2O)C(O)C1O4186.8Standard non polar33892256
6-Hydroxyluteolin 6-xylosideOC1COC(OC2=C(O)C3=C(OC(=CC3=O)C3=CC(O)=C(O)C=C3)C=C2O)C(O)C1O4332.2Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
6-Hydroxyluteolin 6-xyloside,1TMS,isomer #1C[Si](C)(C)OC1COC(OC2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O)C1O4424.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,1TMS,isomer #2C[Si](C)(C)OC1=C(OC2OCC(O)C(O)C2O)C(O)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O24344.0Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,1TMS,isomer #3C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O)=C(O)C=C3O2)=CC=C1O4437.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,1TMS,isomer #4C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O)=C(O)C=C3O2)C=C1O4440.2Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,1TMS,isomer #5C[Si](C)(C)OC1=CC2=C(C(O)=C1OC1OCC(O)C(O)C1O)C(=O)C=C(C1=CC=C(O)C(O)=C1)O24392.2Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,1TMS,isomer #6C[Si](C)(C)OC1C(OC2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)OCC(O)C1O4391.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,1TMS,isomer #7C[Si](C)(C)OC1C(O)COC(OC2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C1O4389.6Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #1C[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)O24284.5Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #10C[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=C1O4295.6Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #11C[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=C1O4277.8Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #12C[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=C1O4288.7Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #13C[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=C1O4242.7Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #14C[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=C1O4278.2Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #15C[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)C4241.1Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #16C[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=C1O4313.2Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #17C[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=C1O4263.6Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #18C[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=C1O4293.4Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #19C[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)O24261.4Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #2C[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=C1O4294.8Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #20C[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)O24269.4Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #21C[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)C4232.8Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #3C[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=C1O4273.8Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #4C[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)O24240.8Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #5C[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)C1O4211.7Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #6C[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)C4239.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #7C[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)O24208.6Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #8C[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)O24213.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TMS,isomer #9C[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)O24281.0Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #1C[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=C1O4162.7Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #10C[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=C1O4106.4Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #11C[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=C1O4128.5Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #12C[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=C1O4111.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #13C[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)O24086.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #14C[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)O24116.6Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #15C[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)C4146.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #16C[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)O24075.2Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #17C[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)O24121.7Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #18C[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=C1O4132.0Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #19C[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=C1O4112.4Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #2C[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=C1O4149.6Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #20C[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)O24144.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #21C[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=C1O4080.8Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #22C[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=C1O4064.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #23C[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=C1O4162.0Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #24C[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=C1O4148.2Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #25C[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)C4096.4Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #26C[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=C1O4121.1Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #27C[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=C1O4165.6Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #28C[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)C4138.0Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #29C[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=C1O4119.0Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #3C[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)O24159.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #30C[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)C4108.8Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #31C[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)C4151.7Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #32C[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=C1O4141.6Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #33C[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=C1O4182.8Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #34C[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=C1O4132.6Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #35C[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)O24143.8Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #4C[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)O24152.7Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #5C[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)O24137.5Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #6C[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=C1O4120.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #7C[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=C1O4153.8Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #8C[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=C1O4137.1Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TMS,isomer #9C[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)C4135.0Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #1C[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=C1O4061.0Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #10C[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)O24069.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #11C[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=C1O4005.8Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #12C[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=C1O4021.1Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #13C[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)C4018.1Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #14C[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=C1O4016.7Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #15C[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)C3997.0Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #16C[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)C3997.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #17C[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=C1O3981.1Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #18C[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=C1O3997.6Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #19C[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=C1O3982.7Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #2C[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=C1O4031.0Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #20C[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)O24033.4Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #21C[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)O24040.6Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #22C[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=C1O3994.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #23C[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=C1O3966.7Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #24C[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=C1O4055.6Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #25C[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=C1O4035.2Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #26C[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)C4005.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #27C[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=C1O4027.5Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #28C[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=C1O4007.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #29C[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)C3981.0Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #3C[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=C1O4037.7Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #30C[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)C4059.2Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #31C[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=C1O4005.0Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #32C[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)C3998.8Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #33C[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)C4039.0Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #34C[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)C4019.0Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #35C[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=C1O4030.0Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #4C[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)C4050.0Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #5C[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=C1O4048.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #6C[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=C1O4006.5Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #7C[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=C1O4010.6Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #8C[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)O24051.8Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TMS,isomer #9C[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)O24082.0Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #1C[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=C1O3982.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #10C[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)O24002.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #11C[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=C1O3949.0Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #12C[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)C3952.6Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #13C[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)C3970.1Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #14C[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)C3946.6Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #15C[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=C1O3923.7Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #16C[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=C1O3976.6Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #17C[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=C1O3954.6Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #18C[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)C3947.4Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #19C[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)C3997.5Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #2C[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=C1O3994.4Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #20C[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)C3980.8Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #21C[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)C3973.5Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #3C[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)C4009.0Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #4C[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=C1O3978.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #5C[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)C3968.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #6C[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)C3984.5Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #7C[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=C1O3964.5Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #8C[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=C1O3976.0Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,5TMS,isomer #9C[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=C1O3950.7Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,6TMS,isomer #1C[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=C1O3928.0Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,6TMS,isomer #2C[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)C3941.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,6TMS,isomer #3C[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)C3955.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,6TMS,isomer #4C[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)C3928.5Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,6TMS,isomer #5C[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=C1O3916.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,6TMS,isomer #6C[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)C3904.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,6TMS,isomer #7C[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)C3934.4Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC1COC(OC2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C(O)C1O4719.4Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,1TBDMS,isomer #2CC(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)O24625.4Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C(OC4OCC(O)C(O)C4O)=C(O)C=C3O2)=CC=C1O4647.4Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,1TBDMS,isomer #4CC(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=C1O4658.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,1TBDMS,isomer #5CC(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)O24633.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC1C(OC2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)OCC(O)C1O4694.2Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,1TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC1C(O)COC(OC2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)=CC(=O)C3=C2O)C1O4699.1Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #1CC(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)O24783.7Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #10CC(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=C1O4779.8Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #11CC(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=C1O4746.7Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #12CC(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=C1O4792.5Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #13CC(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=C1O4738.4Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #14CC(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=C1O4742.4Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #15CC(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)C4709.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #16CC(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=C1O4827.7Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #17CC(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=C1O4771.5Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #18CC(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=C1O4773.8Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #19CC(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)O24769.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #2CC(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=C1O4797.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #20CC(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)O24760.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #21CC(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)C4783.5Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #3CC(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=C1O4765.1Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #4CC(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)O24776.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #5CC(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)C1O4778.2Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #6CC(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)C4804.2Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #7CC(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)O24756.1Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #8CC(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)O24751.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,2TBDMS,isomer #9CC(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)O24783.5Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #1CC(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=C1O4902.7Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #10CC(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=C1O4832.5Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #11CC(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=C1O4881.5Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #12CC(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=C1O4862.7Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #13CC(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)O24816.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #14CC(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)O24829.7Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #15CC(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)C4850.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #16CC(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)O24794.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #17CC(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)O24829.6Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #18CC(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=C1O4893.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #19CC(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=C1O4836.7Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #2CC(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=C1O4857.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #20CC(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)O24823.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #21CC(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=C1O4841.7Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #22CC(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=C1O4794.1Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #23CC(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=C1O4914.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #24CC(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=C1O4869.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #25CC(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)C4805.1Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #26CC(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=C1O4859.6Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #27CC(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=C1O4876.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #28CC(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)C4851.5Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #29CC(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=C1O4823.6Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #3CC(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)O24847.0Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #30CC(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)C4802.7Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #31CC(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)C4855.1Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #32CC(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=C1O4903.4Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #33CC(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=C1O4927.0Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #34CC(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=C1O4869.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #35CC(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)O24820.0Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #4CC(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)O24837.4Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #5CC(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)O24836.2Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #6CC(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=C1O4881.5Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #7CC(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=C1O4923.2Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #8CC(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=C1O4908.2Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,3TBDMS,isomer #9CC(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)C4835.7Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #1CC(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=C1O5003.8Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #10CC(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)O24917.6Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #11CC(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=C1O4985.7Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #12CC(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=C1O4990.5Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #13CC(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)C4907.1Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #14CC(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=C1O5008.1Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #15CC(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)C4964.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #16CC(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)C4959.2Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #17CC(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=C1O4931.7Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #18CC(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=C1O4933.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #19CC(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=C1O4966.5Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #2CC(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=C1O5016.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #20CC(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)O24908.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #21CC(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)O24897.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #22CC(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=C1O4958.4Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #23CC(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=C1O4902.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #24CC(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=C1O5004.5Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #25CC(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=C1O4950.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #26CC(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)C4911.4Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #27CC(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=C1O4958.5Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #28CC(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=C1O4905.6Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #29CC(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)C4853.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #3CC(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=C1O5014.2Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #30CC(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)C4953.6Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #31CC(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=C1O4944.0Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #32CC(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)C4940.6Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #33CC(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)C4975.6Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #34CC(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)C4913.4Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #35CC(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=C1O4993.2Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #4CC(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)C4961.9Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #5CC(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=C1O4950.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #6CC(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=C1O4969.6Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #7CC(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=C1O4961.3Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #8CC(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)O24908.4Semi standard non polar33892256
6-Hydroxyluteolin 6-xyloside,4TBDMS,isomer #9CC(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)O24935.8Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - 6-Hydroxyluteolin 6-xyloside GC-MS (Non-derivatized) - 70eV, Positivesplash10-106r-9107600000-e457a7bacbfa26ab4b302017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6-Hydroxyluteolin 6-xyloside GC-MS (3 TMS) - 70eV, Positivesplash10-000i-4600129000-81f17367ce245261de972017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6-Hydroxyluteolin 6-xyloside GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6-Hydroxyluteolin 6-xyloside GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6-Hydroxyluteolin 6-xyloside GC-MS (TBDMS_4_22) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6-Hydroxyluteolin 6-xyloside GC-MS (TBDMS_4_23) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6-Hydroxyluteolin 6-xyloside GC-MS ("6-Hydroxyluteolin 6-xyloside,4TBDMS,#22" TMS) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-Hydroxyluteolin 6-xyloside 10V, Positive-QTOFsplash10-0udr-0139800000-f3b9339c16337a60a7632015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-Hydroxyluteolin 6-xyloside 20V, Positive-QTOFsplash10-0udi-0279100000-fb7da1f576c6bee0ca3f2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-Hydroxyluteolin 6-xyloside 40V, Positive-QTOFsplash10-000l-2591000000-d627c1bed36cb6a469c02015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-Hydroxyluteolin 6-xyloside 10V, Negative-QTOFsplash10-0f89-1215900000-c5e59f54e01819099fec2015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-Hydroxyluteolin 6-xyloside 20V, Negative-QTOFsplash10-0ue9-1459200000-0c4f2d08d4109031e55c2015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-Hydroxyluteolin 6-xyloside 40V, Negative-QTOFsplash10-0006-7592000000-e63ddf70b6f71b58e6a22015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-Hydroxyluteolin 6-xyloside 10V, Positive-QTOFsplash10-000i-0000900000-1453f61e7eeaeb92b36b2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-Hydroxyluteolin 6-xyloside 20V, Positive-QTOFsplash10-000i-0000900000-1453f61e7eeaeb92b36b2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-Hydroxyluteolin 6-xyloside 40V, Positive-QTOFsplash10-0f79-0309400000-330bfdd0973588f54e962021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-Hydroxyluteolin 6-xyloside 10V, Negative-QTOFsplash10-001i-0000900000-42f5f679c004d65ed93d2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-Hydroxyluteolin 6-xyloside 20V, Negative-QTOFsplash10-001i-0000900000-85bbf452212130c5a29d2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6-Hydroxyluteolin 6-xyloside 40V, Negative-QTOFsplash10-004j-0791200000-7fa77202c15abf3668b82021-09-23Wishart 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 IDFDB016699
KNApSAcK IDC00004378
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound74977865
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.. .