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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 23:47:13 UTC

Update Date

2022-03-07 02:55:46 UTC

HMDB ID

HMDB0038467

Secondary Accession Numbers

HMDB38467

Metabolite Identification

Common Name

Luteolin 7-galactoside

Description

Luteolin 7-galactoside belongs to the class of organic compounds known as flavonoid-7-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position. Luteolin 7-galactoside has been detected, but not quantified in, fruits and herbs and spices. This could make luteolin 7-galactoside a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on Luteolin 7-galactoside.

Structure

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

  Mrv0541 05061310282D          

 32 35  0  0  0  0            999 V2000
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    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
    2.1434   -0.4125    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
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    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
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    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
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    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
   -0.7145    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    0.8250    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   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    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
   -2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   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
    0.0000    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  8  1  1  0  0  0  0
  8  3  2  0  0  0  0
  9  4  2  0  0  0  0
  9  5  1  0  0  0  0
 10  2  1  0  0  0  0
 11  3  1  0  0  0  0
 11 10  2  0  0  0  0
 12  4  1  0  0  0  0
 13  6  1  0  0  0  0
 14  6  2  0  0  0  0
 14  8  1  0  0  0  0
 15  5  2  0  0  0  0
 16  7  1  0  0  0  0
 17 12  2  0  0  0  0
 17 13  1  0  0  0  0
 17 15  1  0  0  0  0
 18 16  1  0  0  0  0
 19 18  1  0  0  0  0
 20 19  1  0  0  0  0
 21 20  1  0  0  0  0
 22  7  1  0  0  0  0
 23 10  1  0  0  0  0
 24 11  1  0  0  0  0
 25 12  1  0  0  0  0
 26 13  2  0  0  0  0
 27 18  1  0  0  0  0
 28 19  1  0  0  0  0
 29 20  1  0  0  0  0
 30  9  1  0  0  0  0
 30 21  1  0  0  0  0
 31 14  1  0  0  0  0
 31 15  1  0  0  0  0
 32 16  1  0  0  0  0
 32 21  1  0  0  0  0
M  END

HMDB0038467
     RDKit          3D
Luteolin 7-galactoside
 52 55  0  0  0  0  0  0  0  0999 V2000
    2.8142   -4.0872   -1.2092 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8464   -2.8749   -0.8391 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0297   -2.1978   -0.6240 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9907   -0.8864   -0.2242 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2187   -0.1192    0.0186 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4736   -0.6393   -0.1310 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6152    0.1173    0.1080 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4840    1.4093    0.5011 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5980    2.2023    0.7510 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2247    1.9826    0.6669 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0756    3.2937    1.0657 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1182    1.1991    0.4200 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8237   -0.2993   -0.0535 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6747   -0.8701   -0.2359 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4707   -0.1856   -0.0357 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7493   -0.8163   -0.2368 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8852   -0.0967   -0.0254 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2018   -0.4853   -0.1534 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9274    0.2392   -1.0881 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6029    1.3183   -0.5426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2917    2.0341   -1.6974 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0015    3.1371   -1.2620 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6819    0.9191    0.4268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7689    1.8339    1.4893 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3451   -0.4275    1.0296 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9148   -0.4674    2.3026 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8390   -0.4398    1.2206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5050    0.7505    1.8659 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7372   -2.1088   -0.6311 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4542   -2.8238   -0.8406 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4385   -4.1416   -1.2428 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6618   -2.1908   -0.6389 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9769   -2.7374   -0.7819 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6014   -1.6539   -0.4395 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5765   -0.3453   -0.0261 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5267    3.1560    1.0413 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1507    3.6827    1.1776 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1474    1.6699    0.5566 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5480    0.8431    0.2787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2626   -1.5390   -0.4754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9068    2.0736   -0.0956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6244    2.2341   -2.5368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0597    1.2991   -2.0779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7011    3.9905   -1.6447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6827    0.8642   -0.0275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8558    2.7410    1.1387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6884   -1.2678    0.3963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7029   -1.3518    2.6840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5021   -1.2907    1.8347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9877    0.6053    2.6855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6562   -2.6328   -0.7975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4579   -4.6198   -1.3951 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
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 20 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 16 29  2  0
 29 30  1  0
 30 31  1  0
 30 32  2  0
 32  2  1  0
 12  5  1  0
 32 14  1  0
 27 18  1  0
  3 33  1  0
  6 34  1  0
  7 35  1  0
  9 36  1  0
 11 37  1  0
 12 38  1  0
 15 39  1  0
 18 40  1  0
 20 41  1  0
 21 42  1  0
 21 43  1  0
 22 44  1  0
 23 45  1  0
 24 46  1  0
 25 47  1  0
 26 48  1  0
 27 49  1  0
 28 50  1  0
 29 51  1  0
 31 52  1  0
M  END

  Mrv0541 05061310282D          

 32 35  0  0  0  0            999 V2000
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    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
    2.1434   -0.4125    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
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    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
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    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
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    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
   -0.7145    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    0.8250    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   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    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
   -2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   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
    0.0000    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  8  1  1  0  0  0  0
  8  3  2  0  0  0  0
  9  4  2  0  0  0  0
  9  5  1  0  0  0  0
 10  2  1  0  0  0  0
 11  3  1  0  0  0  0
 11 10  2  0  0  0  0
 12  4  1  0  0  0  0
 13  6  1  0  0  0  0
 14  6  2  0  0  0  0
 14  8  1  0  0  0  0
 15  5  2  0  0  0  0
 16  7  1  0  0  0  0
 17 12  2  0  0  0  0
 17 13  1  0  0  0  0
 17 15  1  0  0  0  0
 18 16  1  0  0  0  0
 19 18  1  0  0  0  0
 20 19  1  0  0  0  0
 21 20  1  0  0  0  0
 22  7  1  0  0  0  0
 23 10  1  0  0  0  0
 24 11  1  0  0  0  0
 25 12  1  0  0  0  0
 26 13  2  0  0  0  0
 27 18  1  0  0  0  0
 28 19  1  0  0  0  0
 29 20  1  0  0  0  0
 30  9  1  0  0  0  0
 30 21  1  0  0  0  0
 31 14  1  0  0  0  0
 31 15  1  0  0  0  0
 32 16  1  0  0  0  0
 32 21  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0038467

> <DATABASE_NAME>
hmdb

> <SMILES>
OCC1OC(OC2=CC(O)=C3C(=O)C=C(OC3=C2)C2=CC(O)=C(O)C=C2)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C21H20O11/c22-7-16-18(27)19(28)20(29)21(32-16)30-9-4-12(25)17-13(26)6-14(31-15(17)5-9)8-1-2-10(23)11(24)3-8/h1-6,16,18-25,27-29H,7H2

> <INCHI_KEY>
PEFNSGRTCBGNAN-UHFFFAOYSA-N

> <FORMULA>
C21H20O11

> <MOLECULAR_WEIGHT>
448.3769

> <EXACT_MASS>
448.100561482

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_AVERAGE_POLARIZABILITY>
43.216166597129416

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

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

> <ALOGPS_LOGP>
0.58

> <JCHEM_LOGP>
0.1350557186666665

> <ALOGPS_LOGS>
-2.62

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.920196947264271

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.297390217268525

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981092343758667

> <JCHEM_POLAR_SURFACE_AREA>
186.36999999999998

> <JCHEM_REFRACTIVITY>
107.03919999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.08e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
cynaroside

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0038467
     RDKit          3D
Luteolin 7-galactoside
 52 55  0  0  0  0  0  0  0  0999 V2000
    2.8142   -4.0872   -1.2092 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8464   -2.8749   -0.8391 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0297   -2.1978   -0.6240 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9907   -0.8864   -0.2242 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2187   -0.1192    0.0186 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4736   -0.6393   -0.1310 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6152    0.1173    0.1080 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4840    1.4093    0.5011 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5980    2.2023    0.7510 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2247    1.9826    0.6669 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0756    3.2937    1.0657 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1182    1.1991    0.4200 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8237   -0.2993   -0.0535 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6747   -0.8701   -0.2359 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4707   -0.1856   -0.0357 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7493   -0.8163   -0.2368 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8852   -0.0967   -0.0254 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2018   -0.4853   -0.1534 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9274    0.2392   -1.0881 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6029    1.3183   -0.5426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2917    2.0341   -1.6974 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0015    3.1371   -1.2620 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6819    0.9191    0.4268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7689    1.8339    1.4893 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3451   -0.4275    1.0296 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9148   -0.4674    2.3026 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8390   -0.4398    1.2206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5050    0.7505    1.8659 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7372   -2.1088   -0.6311 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4542   -2.8238   -0.8406 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4385   -4.1416   -1.2428 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6618   -2.1908   -0.6389 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9769   -2.7374   -0.7819 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6014   -1.6539   -0.4395 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5765   -0.3453   -0.0261 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5267    3.1560    1.0413 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1507    3.6827    1.1776 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1474    1.6699    0.5566 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5480    0.8431    0.2787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2626   -1.5390   -0.4754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9068    2.0736   -0.0956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6244    2.2341   -2.5368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0597    1.2991   -2.0779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7011    3.9905   -1.6447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6827    0.8642   -0.0275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8558    2.7410    1.1387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6884   -1.2678    0.3963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7029   -1.3518    2.6840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5021   -1.2907    1.8347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9877    0.6053    2.6855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6562   -2.6328   -0.7975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4579   -4.6198   -1.3951 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
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 20 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 16 29  2  0
 29 30  1  0
 30 31  1  0
 30 32  2  0
 32  2  1  0
 12  5  1  0
 32 14  1  0
 27 18  1  0
  3 33  1  0
  6 34  1  0
  7 35  1  0
  9 36  1  0
 11 37  1  0
 12 38  1  0
 15 39  1  0
 18 40  1  0
 20 41  1  0
 21 42  1  0
 21 43  1  0
 22 44  1  0
 23 45  1  0
 24 46  1  0
 25 47  1  0
 26 48  1  0
 27 49  1  0
 28 50  1  0
 29 51  1  0
 31 52  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       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.669   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001  -0.770   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      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.003  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.003  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.667   0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -2.667   4.620   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      13.337  -3.080   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      13.337   0.000   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      -4.001   2.310   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      -4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      -1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       6.668  -0.770   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       0.000   1.540   0.000  0.00  0.00           O+0
CONECT    1    2    8                                                       
CONECT    2    1   10                                                       
CONECT    3    8   11                                                       
CONECT    4    9   12                                                       
CONECT    5    9   15                                                       
CONECT    6   13   14                                                       
CONECT    7   16   22                                                       
CONECT    8    1    3   14                                                  
CONECT    9    4    5   30                                                  
CONECT   10    2   11   23                                                  
CONECT   11    3   10   24                                                  
CONECT   12    4   17   25                                                  
CONECT   13    6   17   26                                                  
CONECT   14    6    8   31                                                  
CONECT   15    5   17   31                                                  
CONECT   16    7   18   32                                                  
CONECT   17   12   13   15                                                  
CONECT   18   16   19   27                                                  
CONECT   19   18   20   28                                                  
CONECT   20   19   21   29                                                  
CONECT   21   20   30   32                                                  
CONECT   22    7                                                            
CONECT   23   10                                                            
CONECT   24   11                                                            
CONECT   25   12                                                            
CONECT   26   13                                                            
CONECT   27   18                                                            
CONECT   28   19                                                            
CONECT   29   20                                                            
CONECT   30    9   21                                                       
CONECT   31   14   15                                                       
CONECT   32   16   21                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

COMPND    HMDB0257807
HETATM    1  O1  UNL     1       2.609  -1.928   3.413  1.00  0.00           O  
HETATM    2  C1  UNL     1       2.708  -1.339   2.297  1.00  0.00           C  
HETATM    3  C2  UNL     1       3.935  -1.077   1.703  1.00  0.00           C  
HETATM    4  C3  UNL     1       3.934  -0.434   0.492  1.00  0.00           C  
HETATM    5  C4  UNL     1       5.213  -0.143  -0.159  1.00  0.00           C  
HETATM    6  C5  UNL     1       6.425  -0.472   0.377  1.00  0.00           C  
HETATM    7  C6  UNL     1       7.609  -0.182  -0.276  1.00  0.00           C  
HETATM    8  C7  UNL     1       7.609   0.444  -1.483  1.00  0.00           C  
HETATM    9  O2  UNL     1       8.794   0.734  -2.138  1.00  0.00           O  
HETATM   10  C8  UNL     1       6.409   0.788  -2.051  1.00  0.00           C  
HETATM   11  O3  UNL     1       6.439   1.427  -3.286  1.00  0.00           O  
HETATM   12  C9  UNL     1       5.231   0.500  -1.401  1.00  0.00           C  
HETATM   13  O4  UNL     1       2.806  -0.079  -0.084  1.00  0.00           O  
HETATM   14  C10 UNL     1       1.634  -0.303   0.435  1.00  0.00           C  
HETATM   15  C11 UNL     1       0.470   0.086  -0.204  1.00  0.00           C  
HETATM   16  C12 UNL     1      -0.790  -0.158   0.358  1.00  0.00           C  
HETATM   17  O5  UNL     1      -1.860   0.278  -0.376  1.00  0.00           O  
HETATM   18  C13 UNL     1      -3.218   0.189  -0.100  1.00  0.00           C  
HETATM   19  O6  UNL     1      -3.783  -0.641  -1.052  1.00  0.00           O  
HETATM   20  C14 UNL     1      -5.142  -0.693  -1.090  1.00  0.00           C  
HETATM   21  C15 UNL     1      -5.773  -1.530  -0.002  1.00  0.00           C  
HETATM   22  O7  UNL     1      -5.505  -1.115   1.274  1.00  0.00           O  
HETATM   23  C16 UNL     1      -5.830   0.631  -1.158  1.00  0.00           C  
HETATM   24  O8  UNL     1      -6.711   0.714  -2.240  1.00  0.00           O  
HETATM   25  C17 UNL     1      -4.864   1.793  -1.118  1.00  0.00           C  
HETATM   26  O9  UNL     1      -4.284   2.072  -2.332  1.00  0.00           O  
HETATM   27  C18 UNL     1      -3.896   1.536  -0.002  1.00  0.00           C  
HETATM   28  O10 UNL     1      -2.911   2.537   0.058  1.00  0.00           O  
HETATM   29  C19 UNL     1      -0.859  -0.795   1.563  1.00  0.00           C  
HETATM   30  C20 UNL     1       0.307  -1.175   2.183  1.00  0.00           C  
HETATM   31  O11 UNL     1       0.258  -1.818   3.397  1.00  0.00           O  
HETATM   32  C21 UNL     1       1.566  -0.945   1.647  1.00  0.00           C  
HETATM   33  H1  UNL     1       4.811  -1.399   2.238  1.00  0.00           H  
HETATM   34  H2  UNL     1       6.506  -0.965   1.325  1.00  0.00           H  
HETATM   35  H3  UNL     1       8.563  -0.444   0.153  1.00  0.00           H  
HETATM   36  H4  UNL     1       9.684   0.484  -1.728  1.00  0.00           H  
HETATM   37  H5  UNL     1       5.632   1.722  -3.789  1.00  0.00           H  
HETATM   38  H6  UNL     1       4.297   0.764  -1.834  1.00  0.00           H  
HETATM   39  H7  UNL     1       0.586   0.588  -1.156  1.00  0.00           H  
HETATM   40  H8  UNL     1      -3.354  -0.309   0.879  1.00  0.00           H  
HETATM   41  H9  UNL     1      -5.403  -1.239  -2.048  1.00  0.00           H  
HETATM   42  H10 UNL     1      -5.422  -2.601  -0.072  1.00  0.00           H  
HETATM   43  H11 UNL     1      -6.872  -1.562  -0.144  1.00  0.00           H  
HETATM   44  H12 UNL     1      -6.061  -0.311   1.529  1.00  0.00           H  
HETATM   45  H13 UNL     1      -6.486   0.758  -0.247  1.00  0.00           H  
HETATM   46  H14 UNL     1      -6.988  -0.218  -2.447  1.00  0.00           H  
HETATM   47  H15 UNL     1      -5.480   2.689  -0.839  1.00  0.00           H  
HETATM   48  H16 UNL     1      -3.314   2.256  -2.275  1.00  0.00           H  
HETATM   49  H17 UNL     1      -4.474   1.637   0.953  1.00  0.00           H  
HETATM   50  H18 UNL     1      -2.285   2.241   0.787  1.00  0.00           H  
HETATM   51  H19 UNL     1      -1.838  -0.983   1.996  1.00  0.00           H  
HETATM   52  H20 UNL     1      -0.632  -2.008   3.827  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   32
CONECT    3    4    4   33
CONECT    4    5   13
CONECT    5    6    6   12
CONECT    6    7   34
CONECT    7    8    8   35
CONECT    8    9   10
CONECT    9   36
CONECT   10   11   12   12
CONECT   11   37
CONECT   12   38
CONECT   13   14
CONECT   14   15   15   32
CONECT   15   16   39
CONECT   16   17   29   29
CONECT   17   18
CONECT   18   19   27   40
CONECT   19   20
CONECT   20   21   23   41
CONECT   21   22   42   43
CONECT   22   44
CONECT   23   24   25   45
CONECT   24   46
CONECT   25   26   27   47
CONECT   26   48
CONECT   27   28   49
CONECT   28   50
CONECT   29   30   51
CONECT   30   31   32   32
CONECT   31   52
END

HMDB0038467
     RDKit          3D
Luteolin 7-galactoside
 52 55  0  0  0  0  0  0  0  0999 V2000
    2.8142   -4.0872   -1.2092 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8464   -2.8749   -0.8391 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0297   -2.1978   -0.6240 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9907   -0.8864   -0.2242 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2187   -0.1192    0.0186 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4736   -0.6393   -0.1310 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6152    0.1173    0.1080 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4840    1.4093    0.5011 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5980    2.2023    0.7510 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2247    1.9826    0.6669 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0756    3.2937    1.0657 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1182    1.1991    0.4200 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8237   -0.2993   -0.0535 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6747   -0.8701   -0.2359 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4707   -0.1856   -0.0357 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7493   -0.8163   -0.2368 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8852   -0.0967   -0.0254 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2018   -0.4853   -0.1534 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9274    0.2392   -1.0881 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6029    1.3183   -0.5426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2917    2.0341   -1.6974 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0015    3.1371   -1.2620 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6819    0.9191    0.4268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7689    1.8339    1.4893 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3451   -0.4275    1.0296 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9148   -0.4674    2.3026 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8390   -0.4398    1.2206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5050    0.7505    1.8659 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7372   -2.1088   -0.6311 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4542   -2.8238   -0.8406 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4385   -4.1416   -1.2428 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6618   -2.1908   -0.6389 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9769   -2.7374   -0.7819 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6014   -1.6539   -0.4395 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5765   -0.3453   -0.0261 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5267    3.1560    1.0413 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1507    3.6827    1.1776 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1474    1.6699    0.5566 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5480    0.8431    0.2787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2626   -1.5390   -0.4754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9068    2.0736   -0.0956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6244    2.2341   -2.5368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0597    1.2991   -2.0779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7011    3.9905   -1.6447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6827    0.8642   -0.0275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8558    2.7410    1.1387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6884   -1.2678    0.3963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7029   -1.3518    2.6840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5021   -1.2907    1.8347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9877    0.6053    2.6855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6562   -2.6328   -0.7975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4579   -4.6198   -1.3951 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
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 20 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 16 29  2  0
 29 30  1  0
 30 31  1  0
 30 32  2  0
 32  2  1  0
 12  5  1  0
 32 14  1  0
 27 18  1  0
  3 33  1  0
  6 34  1  0
  7 35  1  0
  9 36  1  0
 11 37  1  0
 12 38  1  0
 15 39  1  0
 18 40  1  0
 20 41  1  0
 21 42  1  0
 21 43  1  0
 22 44  1  0
 23 45  1  0
 24 46  1  0
 25 47  1  0
 26 48  1  0
 27 49  1  0
 28 50  1  0
 29 51  1  0
 31 52  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₁H₂₀O₁₁

Average Molecular Weight

448.3769

Monoisotopic Molecular Weight

448.100561482

IUPAC Name

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

Traditional Name

cynaroside

CAS Registry Number

68321-11-9

SMILES

OCC1OC(OC2=CC(O)=C3C(=O)C=C(OC3=C2)C2=CC(O)=C(O)C=C2)C(O)C(O)C1O

InChI Identifier

InChI=1S/C21H20O11/c22-7-16-18(27)19(28)20(29)21(32-16)30-9-4-12(25)17-13(26)6-14(31-15(17)5-9)8-1-2-10(23)11(24)3-8/h1-6,16,18-25,27-29H,7H2

InChI Key

PEFNSGRTCBGNAN-UHFFFAOYSA-N

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Flavonoid-7-O-glycosides

Alternative Parents

Substituents

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

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

a flavanone-7-O-β-D-glucoside (LUTEOLIN-7-O-BETA-D-GLUCOSIDE )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Extracellular (HMDB: HMDB0038467)
Cytoplasm (HMDB: HMDB0038467)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0038467)

Source

Exogenous

Exogenous (HMDB: HMDB0038467)

Food

Food (HMDB: HMDB0038467)

Herb and spice

Herbs and Spices (FooDB: FOOD00866)

Fruit

Fruits (FooDB: FOOD00871)

Endogenous

Plant

Plant (HMDB: HMDB0038467)

Process

Not Available

Role

Biological role

Nutrient (HMDB: HMDB0038467)

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	1.08 g/L	ALOGPS
logP	0.58	ALOGPS
logP	0.14	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	8.3	ChemAxon
pKa (Strongest Basic)	-3	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	4	ChemAxon
Refractivity	107.04 m³·mol⁻¹	ChemAxon
Polarizability	43.22 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
DarkChem	[M+H]+	205.466	31661259
DarkChem	[M-H]-	202.398	31661259
DeepCCS	[M+H]+	201.964	30932474
DeepCCS	[M-H]-	199.569	30932474
DeepCCS	[M-2H]-	232.552	30932474
DeepCCS	[M+Na]+	207.877	30932474
AllCCS	[M+H]+	202.8	32859911
AllCCS	[M+H-H2O]+	200.4	32859911
AllCCS	[M+NH4]+	205.0	32859911
AllCCS	[M+Na]+	205.6	32859911
AllCCS	[M-H]-	199.4	32859911
AllCCS	[M+Na-2H]-	199.8	32859911
AllCCS	[M+HCOO]-	200.3	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Luteolin 7-galactoside	OCC1OC(OC2=CC(O)=C3C(=O)C=C(OC3=C2)C2=CC(O)=C(O)C=C2)C(O)C(O)C1O	5418.0	Standard polar	33892256
Luteolin 7-galactoside	OCC1OC(OC2=CC(O)=C3C(=O)C=C(OC3=C2)C2=CC(O)=C(O)C=C2)C(O)C(O)C1O	4401.2	Standard non polar	33892256
Luteolin 7-galactoside	OCC1OC(OC2=CC(O)=C3C(=O)C=C(OC3=C2)C2=CC(O)=C(O)C=C2)C(O)C(O)C1O	4522.1	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Luteolin 7-galactoside,1TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O	4508.2	Semi standard non polar	33892256
Luteolin 7-galactoside,1TMS,isomer #2	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4514.6	Semi standard non polar	33892256
Luteolin 7-galactoside,1TMS,isomer #3	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)=CC=C1O	4558.5	Semi standard non polar	33892256
Luteolin 7-galactoside,1TMS,isomer #4	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O	4565.2	Semi standard non polar	33892256
Luteolin 7-galactoside,1TMS,isomer #5	C[Si](C)(C)OC1C(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)OC(CO)C(O)C1O	4548.2	Semi standard non polar	33892256
Luteolin 7-galactoside,1TMS,isomer #6	C[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C1O	4556.1	Semi standard non polar	33892256
Luteolin 7-galactoside,1TMS,isomer #7	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C1O	4551.9	Semi standard non polar	33892256
Luteolin 7-galactoside,2TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O	4414.1	Semi standard non polar	33892256
Luteolin 7-galactoside,2TMS,isomer #10	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O	4414.0	Semi standard non polar	33892256
Luteolin 7-galactoside,2TMS,isomer #11	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)=CC=C1O	4390.6	Semi standard non polar	33892256
Luteolin 7-galactoside,2TMS,isomer #12	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)=CC=C1O	4397.6	Semi standard non polar	33892256
Luteolin 7-galactoside,2TMS,isomer #13	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	4392.7	Semi standard non polar	33892256
Luteolin 7-galactoside,2TMS,isomer #14	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	4409.1	Semi standard non polar	33892256
Luteolin 7-galactoside,2TMS,isomer #15	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	4411.5	Semi standard non polar	33892256
Luteolin 7-galactoside,2TMS,isomer #16	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O	4426.4	Semi standard non polar	33892256
Luteolin 7-galactoside,2TMS,isomer #17	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	4422.7	Semi standard non polar	33892256
Luteolin 7-galactoside,2TMS,isomer #18	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	4436.5	Semi standard non polar	33892256
Luteolin 7-galactoside,2TMS,isomer #19	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C1O	4436.6	Semi standard non polar	33892256
Luteolin 7-galactoside,2TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O)C1O	4439.3	Semi standard non polar	33892256
Luteolin 7-galactoside,2TMS,isomer #20	C[Si](C)(C)OC1C(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)OC(CO)C(O)C1O[Si](C)(C)C	4443.6	Semi standard non polar	33892256
Luteolin 7-galactoside,2TMS,isomer #21	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C1O[Si](C)(C)C	4437.0	Semi standard non polar	33892256
Luteolin 7-galactoside,2TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O	4422.2	Semi standard non polar	33892256
Luteolin 7-galactoside,2TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	4429.3	Semi standard non polar	33892256
Luteolin 7-galactoside,2TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	4432.2	Semi standard non polar	33892256
Luteolin 7-galactoside,2TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	4419.9	Semi standard non polar	33892256
Luteolin 7-galactoside,2TMS,isomer #7	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4411.9	Semi standard non polar	33892256
Luteolin 7-galactoside,2TMS,isomer #8	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4406.1	Semi standard non polar	33892256
Luteolin 7-galactoside,2TMS,isomer #9	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4420.5	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O)C1O	4229.8	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #10	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	4253.7	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #11	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	4228.5	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #12	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	4237.1	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #13	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4305.1	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #14	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4342.4	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #15	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4306.3	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #16	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4240.9	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #17	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4256.8	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #18	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O	4238.1	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #19	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)=CC=C1O	4222.5	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O	4218.9	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #20	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4257.1	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #21	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	4248.9	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #22	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	4229.5	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #23	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	4220.4	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #24	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	4201.1	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #25	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	4261.3	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #26	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	4212.9	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #27	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	4238.4	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #28	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	4252.5	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #29	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	4235.2	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	4262.8	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #30	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O[Si](C)(C)C	4228.5	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #31	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	4269.6	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #32	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	4234.9	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #33	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	4256.6	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #34	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1O	4256.3	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #35	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4317.2	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	4235.8	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	4244.1	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O	4240.3	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	4272.5	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #8	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	4245.1	Semi standard non polar	33892256
Luteolin 7-galactoside,3TMS,isomer #9	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	4254.2	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O	4118.0	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #10	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4149.1	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #11	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	4152.8	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #12	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	4114.2	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #13	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	4131.6	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #14	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4139.7	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #15	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4186.5	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #16	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4139.5	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #17	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4126.5	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #18	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4167.4	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #19	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4125.5	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	4115.3	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #20	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4277.1	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #21	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4169.2	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #22	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	4128.2	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #23	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	4102.7	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #24	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	4125.2	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #25	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	4103.0	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #26	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	4149.3	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #27	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1O	4133.9	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #28	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	4108.5	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #29	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O[Si](C)(C)C	4151.0	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	4138.8	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #30	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	4121.6	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #31	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	4133.2	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #32	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O[Si](C)(C)C	4142.0	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #33	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	4158.0	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #34	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	4156.7	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #35	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1O	4150.2	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	4119.3	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	4098.2	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	4116.2	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	4100.2	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #8	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4157.5	Semi standard non polar	33892256
Luteolin 7-galactoside,4TMS,isomer #9	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4204.5	Semi standard non polar	33892256
Luteolin 7-galactoside,5TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	4079.9	Semi standard non polar	33892256
Luteolin 7-galactoside,5TMS,isomer #10	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4138.2	Semi standard non polar	33892256
Luteolin 7-galactoside,5TMS,isomer #11	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4103.2	Semi standard non polar	33892256
Luteolin 7-galactoside,5TMS,isomer #12	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4122.2	Semi standard non polar	33892256
Luteolin 7-galactoside,5TMS,isomer #13	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4101.7	Semi standard non polar	33892256
Luteolin 7-galactoside,5TMS,isomer #14	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4133.2	Semi standard non polar	33892256
Luteolin 7-galactoside,5TMS,isomer #15	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4112.1	Semi standard non polar	33892256
Luteolin 7-galactoside,5TMS,isomer #16	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1O	4066.0	Semi standard non polar	33892256
Luteolin 7-galactoside,5TMS,isomer #17	C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	4039.3	Semi standard non polar	33892256
Luteolin 7-galactoside,5TMS,isomer #18	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O[Si](C)(C)C	4074.8	Semi standard non polar	33892256
Luteolin 7-galactoside,5TMS,isomer #19	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	4101.2	Semi standard non polar	33892256
Luteolin 7-galactoside,5TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	4087.8	Semi standard non polar	33892256
Luteolin 7-galactoside,5TMS,isomer #20	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	4089.1	Semi standard non polar	33892256
Luteolin 7-galactoside,5TMS,isomer #21	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	4111.3	Semi standard non polar	33892256
Luteolin 7-galactoside,5TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	4078.5	Semi standard non polar	33892256
Luteolin 7-galactoside,5TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4086.7	Semi standard non polar	33892256
Luteolin 7-galactoside,5TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4106.9	Semi standard non polar	33892256
Luteolin 7-galactoside,5TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4084.6	Semi standard non polar	33892256
Luteolin 7-galactoside,5TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4068.7	Semi standard non polar	33892256
Luteolin 7-galactoside,5TMS,isomer #8	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4088.4	Semi standard non polar	33892256
Luteolin 7-galactoside,5TMS,isomer #9	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4066.6	Semi standard non polar	33892256
Luteolin 7-galactoside,6TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4051.4	Semi standard non polar	33892256
Luteolin 7-galactoside,6TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4057.9	Semi standard non polar	33892256
Luteolin 7-galactoside,6TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4047.0	Semi standard non polar	33892256
Luteolin 7-galactoside,6TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4059.0	Semi standard non polar	33892256
Luteolin 7-galactoside,6TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4044.1	Semi standard non polar	33892256
Luteolin 7-galactoside,6TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4107.0	Semi standard non polar	33892256
Luteolin 7-galactoside,6TMS,isomer #7	C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	4038.6	Semi standard non polar	33892256
Luteolin 7-galactoside,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O	4772.8	Semi standard non polar	33892256
Luteolin 7-galactoside,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4760.1	Semi standard non polar	33892256
Luteolin 7-galactoside,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)=CC=C1O	4806.8	Semi standard non polar	33892256
Luteolin 7-galactoside,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O	4817.8	Semi standard non polar	33892256
Luteolin 7-galactoside,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1C(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)OC(CO)C(O)C1O	4829.2	Semi standard non polar	33892256
Luteolin 7-galactoside,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C1O	4836.4	Semi standard non polar	33892256
Luteolin 7-galactoside,1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C1O	4831.9	Semi standard non polar	33892256
Luteolin 7-galactoside,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O	4887.0	Semi standard non polar	33892256
Luteolin 7-galactoside,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=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O	4914.9	Semi standard non polar	33892256
Luteolin 7-galactoside,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=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)=CC=C1O	4884.2	Semi standard non polar	33892256
Luteolin 7-galactoside,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C=C3O2)=CC=C1O	4901.3	Semi standard non polar	33892256
Luteolin 7-galactoside,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C=C3O2)=CC=C1O	4906.7	Semi standard non polar	33892256
Luteolin 7-galactoside,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C=C3O2)=CC=C1O	4897.1	Semi standard non polar	33892256
Luteolin 7-galactoside,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C	4892.3	Semi standard non polar	33892256
Luteolin 7-galactoside,2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C=C3O2)C=C1O	4936.0	Semi standard non polar	33892256
Luteolin 7-galactoside,2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C=C3O2)C=C1O	4945.1	Semi standard non polar	33892256
Luteolin 7-galactoside,2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1O	4932.4	Semi standard non polar	33892256
Luteolin 7-galactoside,2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C(C)(C)C)C1O	4950.5	Semi standard non polar	33892256
Luteolin 7-galactoside,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)OC3=C2)C(O)C(O)C1O	4927.0	Semi standard non polar	33892256
Luteolin 7-galactoside,2TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC1C(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	4961.3	Semi standard non polar	33892256
Luteolin 7-galactoside,2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C1O[Si](C)(C)C(C)(C)C	4936.5	Semi standard non polar	33892256
Luteolin 7-galactoside,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)OC3=C2)C(O)C(O)C1O	4899.4	Semi standard non polar	33892256
Luteolin 7-galactoside,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	4943.8	Semi standard non polar	33892256
Luteolin 7-galactoside,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	4950.0	Semi standard non polar	33892256
Luteolin 7-galactoside,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	4929.2	Semi standard non polar	33892256
Luteolin 7-galactoside,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4887.5	Semi standard non polar	33892256
Luteolin 7-galactoside,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4887.3	Semi standard non polar	33892256
Luteolin 7-galactoside,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4889.5	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)OC3=C2)C(O)C(O)C1O	5008.9	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)OC3=C2)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	4926.3	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)OC3=C2)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	4952.1	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	4924.6	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	4973.2	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	5007.9	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4973.2	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4934.1	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4952.0	Semi standard non polar	33892256
Luteolin 7-galactoside,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=C(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C=C3O2)C=C1O	5023.5	Semi standard non polar	33892256
Luteolin 7-galactoside,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=C(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C=C3O2)=CC=C1O	4983.2	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)OC3=C2)C(O)C(O)C1O	4966.0	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O2	4954.8	Semi standard non polar	33892256
Luteolin 7-galactoside,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=C(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C=C3O2)C=C1O	5027.1	Semi standard non polar	33892256
Luteolin 7-galactoside,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=C(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C=C3O2)=CC=C1O	4976.7	Semi standard non polar	33892256
Luteolin 7-galactoside,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=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1O	4985.2	Semi standard non polar	33892256
Luteolin 7-galactoside,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=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C=C3O2)=CC=C1O	4943.8	Semi standard non polar	33892256
Luteolin 7-galactoside,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=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C	4994.2	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C4O)C=C3O2)=CC=C1O	4941.6	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O[Si](C)(C)C(C)(C)C)C=C3O2)=CC=C1O	4949.1	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C	4949.3	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O[Si](C)(C)C(C)(C)C)C=C3O2)=CC=C1O	4962.8	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	4944.7	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C	4946.1	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C	4945.9	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C4O)C=C3O2)C=C1O	4976.2	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1O	4986.5	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1O	5000.0	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4983.8	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	4939.8	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	4927.7	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C4)OC3=C2)C(O)C(O)C1O	4947.7	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)OC3=C2)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	4964.9	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	4991.9	Semi standard non polar	33892256
Luteolin 7-galactoside,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	4963.2	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 - Luteolin 7-galactoside GC-MS (Non-derivatized) - 70eV, Positive	splash10-001r-8934600000-bd5b067d72f1086a3dd3	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Luteolin 7-galactoside GC-MS (3 TMS) - 70eV, Positive	splash10-0f72-4730119000-f82ba729f371b8abdbda	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Luteolin 7-galactoside GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Luteolin 7-galactoside GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Luteolin 7-galactoside GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Luteolin 7-galactoside GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Luteolin 7-galactoside GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Luteolin 7-galactoside GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Luteolin 7-galactoside GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Luteolin 7-galactoside GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Luteolin 7-galactoside GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Luteolin 7-galactoside GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Luteolin 7-galactoside GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Luteolin 7-galactoside GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Luteolin 7-galactoside GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Luteolin 7-galactoside GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Luteolin 7-galactoside GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Luteolin 7-galactoside GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Luteolin 7-galactoside GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Luteolin 7-galactoside GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Luteolin 7-galactoside GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Luteolin 7-galactoside GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Luteolin 7-galactoside GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Luteolin 7-galactoside GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Luteolin 7-galactoside GC-MS (TMS_2_13) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Experimental LC-MS/MS	LC-MS/MS Spectrum - Luteolin 7-galactoside LC-ESI-QTOF , negative-QTOF	splash10-0002-0000900000-7d95b5fba9dcb9787365	2017-09-14	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Luteolin 7-galactoside LC-ESI-QTOF , negative-QTOF	splash10-000b-0090800000-c99e8cabe22d3ca5cc32	2017-09-14	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Luteolin 7-galactoside LC-ESI-QTOF , negative-QTOF	splash10-0019-0090000000-0c95adaac5b2f30f4985	2017-09-14	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Luteolin 7-galactoside LC-ESI-QTOF , positive-QTOF	splash10-000i-0090100000-f0beb197c1392edf78f3	2017-09-14	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Luteolin 7-galactoside LC-ESI-QTOF , positive-QTOF	splash10-000i-0090000000-62b9d786642d93613772	2017-09-14	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Luteolin 7-galactoside LC-ESI-QTOF , positive-QTOF	splash10-000i-0090000000-8014734e92aa9faa8e5b	2017-09-14	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Luteolin 7-galactoside 6V, Positive-QTOF	splash10-000j-0090500000-d6a733209d833eb7741b	2021-09-20	HMDB team, MONA	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Luteolin 7-galactoside 10V, Positive-QTOF	splash10-000j-0190600000-619602c845bf7730c6b4	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Luteolin 7-galactoside 20V, Positive-QTOF	splash10-00kr-0190000000-aeab6c7e88291cca5e1c	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Luteolin 7-galactoside 40V, Positive-QTOF	splash10-014r-1490000000-4baa849e1a9a4ff508ea	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Luteolin 7-galactoside 10V, Positive-QTOF	splash10-000j-0190600000-619602c845bf7730c6b4	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Luteolin 7-galactoside 20V, Positive-QTOF	splash10-00kr-0190000000-aeab6c7e88291cca5e1c	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Luteolin 7-galactoside 40V, Positive-QTOF	splash10-014r-1490000000-4baa849e1a9a4ff508ea	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Luteolin 7-galactoside 10V, Positive-QTOF	splash10-000j-0190600000-619602c845bf7730c6b4	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Luteolin 7-galactoside 20V, Positive-QTOF	splash10-00kr-0190000000-aeab6c7e88291cca5e1c	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Luteolin 7-galactoside 40V, Positive-QTOF	splash10-014r-1490000000-4baa849e1a9a4ff508ea	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Luteolin 7-galactoside 10V, Negative-QTOF	splash10-000b-1260900000-db5423c58b3e96daf2c6	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Luteolin 7-galactoside 20V, Negative-QTOF	splash10-000i-1190100000-29a6e77cf9725bc2196a	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Luteolin 7-galactoside 40V, Negative-QTOF	splash10-00ku-2190000000-d73292522d50554cdd7d	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Luteolin 7-galactoside 10V, Negative-QTOF	splash10-000b-1260900000-db5423c58b3e96daf2c6	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Luteolin 7-galactoside 20V, Negative-QTOF	splash10-000i-1190100000-29a6e77cf9725bc2196a	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Luteolin 7-galactoside 40V, Negative-QTOF	splash10-00ku-2190000000-d73292522d50554cdd7d	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Luteolin 7-galactoside 10V, Negative-QTOF	splash10-000b-1260900000-db5423c58b3e96daf2c6	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Luteolin 7-galactoside 20V, Negative-QTOF	splash10-000i-1190100000-29a6e77cf9725bc2196a	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Luteolin 7-galactoside 40V, Negative-QTOF	splash10-00ku-2190000000-d73292522d50554cdd7d	2015-04-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm
Extracellular

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB017826

KNApSAcK ID

C00004267

Chemspider ID

4453194

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5291488

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 Luteolin 7-galactoside (HMDB0038467)

MOL for HMDB0038467 (Luteolin 7-galactoside)

3D MOL for HMDB0038467 (Luteolin 7-galactoside)

3D SDF for HMDB0038467 (Luteolin 7-galactoside)

3D-SDF for HMDB0038467 (Luteolin 7-galactoside)

PDB for HMDB0038467 (Luteolin 7-galactoside)

3D PDB for HMDB0038467 (Luteolin 7-galactoside)

SMILES for HMDB0038467 (Luteolin 7-galactoside)

INCHI for HMDB0038467 (Luteolin 7-galactoside)

Structure for HMDB0038467 (Luteolin 7-galactoside)

3D Structure for HMDB0038467 (Luteolin 7-galactoside)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra