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Showing metabocard for Luteolinidin 3-O-glucoside (HMDB0029248)

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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 17:29:10 UTC
Update Date2022-03-07 02:52:05 UTC
HMDB IDHMDB0029248
Secondary Accession Numbers
  • HMDB29248
Metabolite Identification
Common NameLuteolinidin 3-O-glucoside
DescriptionLuteolinidin 3-O-glucoside belongs to the class of organic compounds known as anthocyanidin-5-o-glycosides. These are phenolic compounds containing one anthocyanidin moiety which is O-glycosidically linked to a carbohydrate moiety at the C5-position. Luteolinidin 3-O-glucoside is an extremely weak basic (essentially neutral) compound (based on its pKa). A polyphenol compound found in foods of plant origin (PhenolExplorer).
Structure
Data?1582753392
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0029248 (Luteolinidin 3-O-glucoside)


  Mrv0541 02241220442D          

 31 34  0  0  0  0            999 V2000
   -2.3868   -0.8656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3868   -0.0406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6723   -1.2781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1013   -1.2781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6723    0.3719    0.0000 O   0  3  0  0  0  0  0  0  0  0  0  0
   -3.1013    0.3719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9579   -0.8656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8158   -0.8656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9579   -0.0406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8158   -0.0406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2434    0.3719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5302    0.3719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4711   -0.0406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2434    1.1969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1855    0.3719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4711    1.6094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1855    1.1969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9000   -0.0406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9000    1.6094    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1013   -2.1031    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5302   -2.1031    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2447   -2.5156    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2447   -3.3406    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5302   -3.7531    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8158   -3.3406    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8158   -2.5156    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1013   -3.7531    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5302   -4.5781    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9592   -3.7531    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9592   -2.1031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6736   -2.5156    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  3  2  0  0  0  0
  1  4  1  0  0  0  0
  2  5  2  0  0  0  0
  2  6  1  0  0  0  0
  3  7  1  0  0  0  0
  4  8  2  0  0  0  0
  5  9  1  0  0  0  0
  6 10  2  0  0  0  0
  9 11  1  0  0  0  0
 10 12  1  0  0  0  0
 11 13  2  0  0  0  0
 11 14  1  0  0  0  0
 13 15  1  0  0  0  0
 14 16  2  0  0  0  0
 15 17  2  0  0  0  0
 15 18  1  0  0  0  0
 17 19  1  0  0  0  0
  7  9  2  0  0  0  0
  8 10  1  0  0  0  0
 16 17  1  0  0  0  0
  4 20  1  0  0  0  0
 26 20  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 21 26  1  0  0  0  0
 25 27  1  6  0  0  0
 24 28  1  1  0  0  0
 23 29  1  6  0  0  0
 22 30  1  1  0  0  0
 30 31  1  0  0  0  0
M  CHG  1   5   1
M  END
Download

3D MOL for HMDB0029248 (Luteolinidin 3-O-glucoside)

HMDB0029248
     RDKit          3D
Luteolinidin 3-O-glucoside
 52 55  0  0  0  0  0  0  0  0999 V2000
   -6.8209    1.8687    1.3680 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4236    1.9043    1.5364 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8273    0.9028    0.5854 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4396    0.8648    0.6791 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8745    0.1815   -0.3882 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5067    0.0743   -0.1578 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4654    0.5382   -0.8974 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284    1.2350   -2.0726 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4672    1.6960   -2.8052 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2674    2.4027   -3.9984 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7488    1.4607   -2.3627 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9306    0.7629   -1.1850 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1428    0.5264   -0.7428 O   0  0  0  0  0  3  0  0  0  0  0  0
    3.4153   -0.1284    0.3661 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8026   -0.3306    0.7571 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1372   -1.0068    1.9023 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4865   -1.1805    2.2444 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4999   -0.6943    1.4682 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8073   -0.9067    1.8735 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1686   -0.0167    0.3208 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1819    0.4850   -0.4813 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8452    0.1502   -0.0089 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3560   -0.5945    1.1087 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0533   -0.3703    0.6838 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8276    0.3155   -0.4755 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4198   -1.2203   -0.5309 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1370   -1.6921   -1.8285 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8847   -1.3365   -0.3212 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1652   -2.6906   -0.0357 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3188   -0.5020    0.8516 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.6758   -0.5741    1.0561 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0443    1.7788    0.4049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1182    2.9286    1.2437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2274    1.6602    2.5904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0890    1.1617   -0.4528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1476    0.7278   -1.3111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6150    1.4324   -2.4406 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2255    1.8058   -4.8380 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6172    1.8191   -2.9315 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3910   -1.4201    2.5664 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7464   -1.7168    3.1521 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6278   -0.5967    1.3853 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1559    0.4077   -0.3153 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5682    0.6842   -0.9139 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4859   -1.1403    2.0298 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1975   -0.7220    1.2421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8977   -1.8631    0.2083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0870   -2.6762   -1.8105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4555   -1.0353   -1.2369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2677   -3.2090   -0.8553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7683   -0.8633    1.7479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8484   -0.3809    2.0257 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  2  0
 14 23  2  0
 23 24  1  0
 24 25  2  0
  5 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 30  3  1  0
 25  7  1  0
 25 12  1  0
 22 15  1  0
  1 32  1  0
  2 33  1  0
  2 34  1  0
  3 35  1  6
  5 36  1  6
  8 37  1  0
 10 38  1  0
 11 39  1  0
 16 40  1  0
 17 41  1  0
 19 42  1  0
 21 43  1  0
 22 44  1  0
 23 45  1  0
 24 46  1  0
 26 47  1  1
 27 48  1  0
 28 49  1  6
 29 50  1  0
 30 51  1  1
 31 52  1  0
M  CHG  1  13   1
M  END
Download

3D SDF for HMDB0029248 (Luteolinidin 3-O-glucoside)


  Mrv0541 02241220442D          

 31 34  0  0  0  0            999 V2000
   -2.3868   -0.8656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3868   -0.0406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6723   -1.2781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1013   -1.2781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6723    0.3719    0.0000 O   0  3  0  0  0  0  0  0  0  0  0  0
   -3.1013    0.3719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9579   -0.8656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8158   -0.8656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9579   -0.0406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8158   -0.0406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2434    0.3719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5302    0.3719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4711   -0.0406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2434    1.1969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1855    0.3719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4711    1.6094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1855    1.1969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9000   -0.0406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9000    1.6094    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1013   -2.1031    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5302   -2.1031    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2447   -2.5156    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2447   -3.3406    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5302   -3.7531    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8158   -3.3406    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8158   -2.5156    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1013   -3.7531    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5302   -4.5781    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9592   -3.7531    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9592   -2.1031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6736   -2.5156    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  3  2  0  0  0  0
  1  4  1  0  0  0  0
  2  5  2  0  0  0  0
  2  6  1  0  0  0  0
  3  7  1  0  0  0  0
  4  8  2  0  0  0  0
  5  9  1  0  0  0  0
  6 10  2  0  0  0  0
  9 11  1  0  0  0  0
 10 12  1  0  0  0  0
 11 13  2  0  0  0  0
 11 14  1  0  0  0  0
 13 15  1  0  0  0  0
 14 16  2  0  0  0  0
 15 17  2  0  0  0  0
 15 18  1  0  0  0  0
 17 19  1  0  0  0  0
  7  9  2  0  0  0  0
  8 10  1  0  0  0  0
 16 17  1  0  0  0  0
  4 20  1  0  0  0  0
 26 20  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 21 26  1  0  0  0  0
 25 27  1  6  0  0  0
 24 28  1  1  0  0  0
 23 29  1  6  0  0  0
 22 30  1  1  0  0  0
 30 31  1  0  0  0  0
M  CHG  1   5   1
M  END
> <DATABASE_ID>
HMDB0029248

> <DATABASE_NAME>
hmdb

> <SMILES>
OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(=CC=C23)C2=CC(O)=C(O)C=C2)[C@H](O)[C@@H](O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C21H20O10/c22-8-17-18(26)19(27)20(28)21(31-17)30-16-7-10(23)6-15-11(16)2-4-14(29-15)9-1-3-12(24)13(25)5-9/h1-7,17-22,26-28H,8H2,(H2-,23,24,25)/p+1/t17-,18-,19+,20-,21-/m1/s1

> <INCHI_KEY>
RXQNESSHTIRLBK-YMQHIKHWSA-O

> <FORMULA>
C21H21O10

> <MOLECULAR_WEIGHT>
433.3854

> <EXACT_MASS>
433.113471892

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_AVERAGE_POLARIZABILITY>
42.79730206962095

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
1

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(3,4-dihydroxyphenyl)-7-hydroxy-5-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1λ⁴-chromen-1-ylium

> <ALOGPS_LOGP>
1.29

> <JCHEM_LOGP>
0.6713999999999993

> <ALOGPS_LOGS>
-3.02

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.141740835091433

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.830158159903804

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810923463387162

> <JCHEM_POLAR_SURFACE_AREA>
173.21

> <JCHEM_REFRACTIVITY>
114.27659999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.43e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(3,4-dihydroxyphenyl)-7-hydroxy-5-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1λ⁴-chromen-1-ylium

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0029248 (Luteolinidin 3-O-glucoside)

HMDB0029248
     RDKit          3D
Luteolinidin 3-O-glucoside
 52 55  0  0  0  0  0  0  0  0999 V2000
   -6.8209    1.8687    1.3680 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4236    1.9043    1.5364 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8273    0.9028    0.5854 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4396    0.8648    0.6791 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8745    0.1815   -0.3882 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5067    0.0743   -0.1578 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4654    0.5382   -0.8974 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284    1.2350   -2.0726 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4672    1.6960   -2.8052 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2674    2.4027   -3.9984 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7488    1.4607   -2.3627 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9306    0.7629   -1.1850 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1428    0.5264   -0.7428 O   0  0  0  0  0  3  0  0  0  0  0  0
    3.4153   -0.1284    0.3661 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8026   -0.3306    0.7571 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1372   -1.0068    1.9023 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4865   -1.1805    2.2444 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4999   -0.6943    1.4682 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8073   -0.9067    1.8735 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1686   -0.0167    0.3208 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1819    0.4850   -0.4813 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8452    0.1502   -0.0089 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3560   -0.5945    1.1087 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0533   -0.3703    0.6838 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8276    0.3155   -0.4755 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4198   -1.2203   -0.5309 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1370   -1.6921   -1.8285 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8847   -1.3365   -0.3212 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1652   -2.6906   -0.0357 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3188   -0.5020    0.8516 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.6758   -0.5741    1.0561 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0443    1.7788    0.4049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1182    2.9286    1.2437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2274    1.6602    2.5904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0890    1.1617   -0.4528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1476    0.7278   -1.3111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6150    1.4324   -2.4406 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2255    1.8058   -4.8380 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6172    1.8191   -2.9315 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3910   -1.4201    2.5664 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7464   -1.7168    3.1521 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6278   -0.5967    1.3853 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1559    0.4077   -0.3153 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5682    0.6842   -0.9139 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4859   -1.1403    2.0298 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1975   -0.7220    1.2421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8977   -1.8631    0.2083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0870   -2.6762   -1.8105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4555   -1.0353   -1.2369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2677   -3.2090   -0.8553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7683   -0.8633    1.7479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8484   -0.3809    2.0257 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  2  0
 14 23  2  0
 23 24  1  0
 24 25  2  0
  5 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 30  3  1  0
 25  7  1  0
 25 12  1  0
 22 15  1  0
  1 32  1  0
  2 33  1  0
  2 34  1  0
  3 35  1  6
  5 36  1  6
  8 37  1  0
 10 38  1  0
 11 39  1  0
 16 40  1  0
 17 41  1  0
 19 42  1  0
 21 43  1  0
 22 44  1  0
 23 45  1  0
 24 46  1  0
 26 47  1  1
 27 48  1  0
 28 49  1  6
 29 50  1  0
 30 51  1  1
 31 52  1  0
M  CHG  1  13   1
M  END
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PDB for HMDB0029248 (Luteolinidin 3-O-glucoside)

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -4.455  -1.616   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.455  -0.076   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.122  -2.386   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.789  -2.386   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -3.122   0.694   0.000  0.00  0.00           O+1
HETATM    6  C   UNK     0      -5.789   0.694   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.788  -1.616   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -7.123  -1.616   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.788  -0.076   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -7.123  -0.076   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.454   0.694   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -8.456   0.694   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.879  -0.076   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.454   2.234   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.213   0.694   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.879   3.004   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.213   2.234   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       3.547  -0.076   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       3.547   3.004   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -5.789  -3.926   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -8.456  -3.926   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -9.790  -4.696   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -9.790  -6.236   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -8.456  -7.006   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -7.123  -6.236   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -7.123  -4.696   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -5.789  -7.006   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      -8.456  -8.546   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0     -11.124  -7.006   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0     -11.124  -3.926   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0     -12.457  -4.696   0.000  0.00  0.00           O+0
CONECT    1    2    3    4                                                  
CONECT    2    1    5    6                                                  
CONECT    3    1    7                                                       
CONECT    4    1    8   20                                                  
CONECT    5    2    9                                                       
CONECT    6    2   10                                                       
CONECT    7    3    9                                                       
CONECT    8    4   10                                                       
CONECT    9    5   11    7                                                  
CONECT   10    6   12    8                                                  
CONECT   11    9   13   14                                                  
CONECT   12   10                                                            
CONECT   13   11   15                                                       
CONECT   14   11   16                                                       
CONECT   15   13   17   18                                                  
CONECT   16   14   17                                                       
CONECT   17   15   19   16                                                  
CONECT   18   15                                                            
CONECT   19   17                                                            
CONECT   20    4   26                                                       
CONECT   21   22   26                                                       
CONECT   22   21   23   30                                                  
CONECT   23   22   24   29                                                  
CONECT   24   23   25   28                                                  
CONECT   25   24   26   27                                                  
CONECT   26   20   25   21                                                  
CONECT   27   25                                                            
CONECT   28   24                                                            
CONECT   29   23                                                            
CONECT   30   22   31                                                       
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END
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3D PDB for HMDB0029248 (Luteolinidin 3-O-glucoside)

COMPND    HMDB0029248
HETATM    1  O1  UNL     1      -6.821   1.869   1.368  1.00  0.00           O  
HETATM    2  C1  UNL     1      -5.424   1.904   1.536  1.00  0.00           C  
HETATM    3  C2  UNL     1      -4.827   0.903   0.585  1.00  0.00           C  
HETATM    4  O2  UNL     1      -3.440   0.865   0.679  1.00  0.00           O  
HETATM    5  C3  UNL     1      -2.874   0.182  -0.388  1.00  0.00           C  
HETATM    6  O3  UNL     1      -1.507   0.074  -0.158  1.00  0.00           O  
HETATM    7  C4  UNL     1      -0.465   0.538  -0.897  1.00  0.00           C  
HETATM    8  C5  UNL     1      -0.628   1.235  -2.073  1.00  0.00           C  
HETATM    9  C6  UNL     1       0.467   1.696  -2.805  1.00  0.00           C  
HETATM   10  O4  UNL     1       0.267   2.403  -3.998  1.00  0.00           O  
HETATM   11  C7  UNL     1       1.749   1.461  -2.363  1.00  0.00           C  
HETATM   12  C8  UNL     1       1.931   0.763  -1.185  1.00  0.00           C  
HETATM   13  O5  UNL     1       3.143   0.526  -0.743  1.00  0.00           O1+
HETATM   14  C9  UNL     1       3.415  -0.128   0.366  1.00  0.00           C  
HETATM   15  C10 UNL     1       4.803  -0.331   0.757  1.00  0.00           C  
HETATM   16  C11 UNL     1       5.137  -1.007   1.902  1.00  0.00           C  
HETATM   17  C12 UNL     1       6.487  -1.181   2.244  1.00  0.00           C  
HETATM   18  C13 UNL     1       7.500  -0.694   1.468  1.00  0.00           C  
HETATM   19  O6  UNL     1       8.807  -0.907   1.873  1.00  0.00           O  
HETATM   20  C14 UNL     1       7.169  -0.017   0.321  1.00  0.00           C  
HETATM   21  O7  UNL     1       8.182   0.485  -0.481  1.00  0.00           O  
HETATM   22  C15 UNL     1       5.845   0.150  -0.009  1.00  0.00           C  
HETATM   23  C16 UNL     1       2.356  -0.594   1.109  1.00  0.00           C  
HETATM   24  C17 UNL     1       1.053  -0.370   0.684  1.00  0.00           C  
HETATM   25  C18 UNL     1       0.828   0.316  -0.475  1.00  0.00           C  
HETATM   26  C19 UNL     1      -3.420  -1.220  -0.531  1.00  0.00           C  
HETATM   27  O8  UNL     1      -3.137  -1.692  -1.828  1.00  0.00           O  
HETATM   28  C20 UNL     1      -4.885  -1.336  -0.321  1.00  0.00           C  
HETATM   29  O9  UNL     1      -5.165  -2.691  -0.036  1.00  0.00           O  
HETATM   30  C21 UNL     1      -5.319  -0.502   0.852  1.00  0.00           C  
HETATM   31  O10 UNL     1      -6.676  -0.574   1.056  1.00  0.00           O  
HETATM   32  H1  UNL     1      -7.044   1.779   0.405  1.00  0.00           H  
HETATM   33  H2  UNL     1      -5.118   2.929   1.244  1.00  0.00           H  
HETATM   34  H3  UNL     1      -5.227   1.660   2.590  1.00  0.00           H  
HETATM   35  H4  UNL     1      -5.089   1.162  -0.453  1.00  0.00           H  
HETATM   36  H5  UNL     1      -3.148   0.728  -1.311  1.00  0.00           H  
HETATM   37  H6  UNL     1      -1.615   1.432  -2.441  1.00  0.00           H  
HETATM   38  H7  UNL     1       0.226   1.806  -4.838  1.00  0.00           H  
HETATM   39  H8  UNL     1       2.617   1.819  -2.931  1.00  0.00           H  
HETATM   40  H9  UNL     1       4.391  -1.420   2.566  1.00  0.00           H  
HETATM   41  H10 UNL     1       6.746  -1.717   3.152  1.00  0.00           H  
HETATM   42  H11 UNL     1       9.628  -0.597   1.385  1.00  0.00           H  
HETATM   43  H12 UNL     1       9.156   0.408  -0.315  1.00  0.00           H  
HETATM   44  H13 UNL     1       5.568   0.684  -0.914  1.00  0.00           H  
HETATM   45  H14 UNL     1       2.486  -1.140   2.030  1.00  0.00           H  
HETATM   46  H15 UNL     1       0.197  -0.722   1.242  1.00  0.00           H  
HETATM   47  H16 UNL     1      -2.898  -1.863   0.208  1.00  0.00           H  
HETATM   48  H17 UNL     1      -3.087  -2.676  -1.810  1.00  0.00           H  
HETATM   49  H18 UNL     1      -5.455  -1.035  -1.237  1.00  0.00           H  
HETATM   50  H19 UNL     1      -5.268  -3.209  -0.855  1.00  0.00           H  
HETATM   51  H20 UNL     1      -4.768  -0.863   1.748  1.00  0.00           H  
HETATM   52  H21 UNL     1      -6.848  -0.381   2.026  1.00  0.00           H  
CONECT    1    2   32
CONECT    2    3   33   34
CONECT    3    4   30   35
CONECT    4    5
CONECT    5    6   26   36
CONECT    6    7
CONECT    7    8    8   25
CONECT    8    9   37
CONECT    9   10   11   11
CONECT   10   38
CONECT   11   12   39
CONECT   12   13   13   25
CONECT   13   14
CONECT   14   15   23   23
CONECT   15   16   16   22
CONECT   16   17   40
CONECT   17   18   18   41
CONECT   18   19   20
CONECT   19   42
CONECT   20   21   22   22
CONECT   21   43
CONECT   22   44
CONECT   23   24   45
CONECT   24   25   25   46
CONECT   26   27   28   47
CONECT   27   48
CONECT   28   29   30   49
CONECT   29   50
CONECT   30   31   51
CONECT   31   52
END
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SMILES for HMDB0029248 (Luteolinidin 3-O-glucoside)

OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(=CC=C23)C2=CC(O)=C(O)C=C2)[C@H](O)[C@@H](O)[C@@H]1O
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INCHI for HMDB0029248 (Luteolinidin 3-O-glucoside)

InChI=1S/C21H20O10/c22-8-17-18(26)19(27)20(28)21(31-17)30-16-7-10(23)6-15-11(16)2-4-14(29-15)9-1-3-12(24)13(25)5-9/h1-7,17-22,26-28H,8H2,(H2-,23,24,25)/p+1/t17-,18-,19+,20-,21-/m1/s1
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View in JSmolView Stereo Labels
SynonymsNot Available
Chemical FormulaC21H21O10
Average Molecular Weight433.3854
Monoisotopic Molecular Weight433.113471892
IUPAC Name2-(3,4-dihydroxyphenyl)-7-hydroxy-5-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1λ⁴-chromen-1-ylium
Traditional Name2-(3,4-dihydroxyphenyl)-7-hydroxy-5-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1λ⁴-chromen-1-ylium
CAS Registry NumberNot Available
SMILES
OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(=CC=C23)C2=CC(O)=C(O)C=C2)[C@H](O)[C@@H](O)[C@@H]1O
InChI Identifier
InChI=1S/C21H20O10/c22-8-17-18(26)19(27)20(28)21(31-17)30-16-7-10(23)6-15-11(16)2-4-14(29-15)9-1-3-12(24)13(25)5-9/h1-7,17-22,26-28H,8H2,(H2-,23,24,25)/p+1/t17-,18-,19+,20-,21-/m1/s1
InChI KeyRXQNESSHTIRLBK-YMQHIKHWSA-O
Chemical Taxonomy
Description Belongs to the class of organic compounds known as anthocyanidin-5-o-glycosides. These are phenolic compounds containing one anthocyanidin moiety which is O-glycosidically linked to a carbohydrate moiety at the C5-position.
KingdomOrganic compounds
Super ClassPhenylpropanoids and polyketides
ClassFlavonoids
Sub ClassFlavonoid glycosides
Direct ParentAnthocyanidin-5-O-glycosides
Alternative Parents
Substituents
  • Anthocyanidin-5-o-glycoside
  • 3'-hydroxyflavonoid
  • 4'-hydroxyflavonoid
  • 7-hydroxyflavonoid
  • Hydroxyflavonoid
  • Anthocyanidin
  • Phenolic glycoside
  • Hexose monosaccharide
  • Glycosyl compound
  • O-glycosyl compound
  • Benzopyran
  • 1-benzopyran
  • Catechol
  • 1-hydroxy-4-unsubstituted benzenoid
  • 1-hydroxy-2-unsubstituted benzenoid
  • Phenol
  • Monocyclic benzene moiety
  • Benzenoid
  • Monosaccharide
  • Oxane
  • Heteroaromatic compound
  • Secondary alcohol
  • Organoheterocyclic compound
  • Oxacycle
  • Polyol
  • Acetal
  • Primary alcohol
  • Hydrocarbon derivative
  • Organic oxygen compound
  • Alcohol
  • Organooxygen compound
  • Organic cation
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Biological locationSource
ProcessNot Available
RoleNot Available
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.44 g/LALOGPS
logP1.29ALOGPS
logP0.67ChemAxon
logS-3ALOGPS
pKa (Strongest Acidic)6.83ChemAxon
pKa (Strongest Basic)-3ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count9ChemAxon
Hydrogen Donor Count7ChemAxon
Polar Surface Area173.21 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity114.28 m³·mol⁻¹ChemAxon
Polarizability42.8 ųChemAxon
Number of Rings4ChemAxon
BioavailabilityYesChemAxon
Rule of FiveNoChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+197.51231661259
DarkChem[M-H]-193.48131661259
DeepCCS[M-2H]-221.75430932474
DeepCCS[M+Na]+196.67530932474
AllCCS[M+H]+200.832859911
AllCCS[M+H-H2O]+198.332859911
AllCCS[M+NH4]+203.132859911
AllCCS[M+Na]+203.732859911
AllCCS[M-H]-198.232859911
AllCCS[M+Na-2H]-198.532859911
AllCCS[M+HCOO]-199.032859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Luteolinidin 3-O-glucosideOC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(=CC=C23)C2=CC(O)=C(O)C=C2)[C@H](O)[C@@H](O)[C@@H]1O5829.6Standard polar33892256
Luteolinidin 3-O-glucosideOC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(=CC=C23)C2=CC(O)=C(O)C=C2)[C@H](O)[C@@H](O)[C@@H]1O4294.7Standard non polar33892256
Luteolinidin 3-O-glucosideOC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(=CC=C23)C2=CC(O)=C(O)C=C2)[C@H](O)[C@@H](O)[C@@H]1O4347.8Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Luteolinidin 3-O-glucoside,1TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O4147.3Semi standard non polar33892256
Luteolinidin 3-O-glucoside,1TMS,isomer #2C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)=C2C=CC(C3=CC=C(O)C(O)=C3)=[O+]C2=C14229.3Semi standard non polar33892256
Luteolinidin 3-O-glucoside,1TMS,isomer #3C[Si](C)(C)OC1=CC(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)=CC(O)=CC3=[O+]2)=CC=C1O4150.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,1TMS,isomer #4C[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)=CC(O)=CC3=[O+]2)C=C1O4179.0Semi standard non polar33892256
Luteolinidin 3-O-glucoside,1TMS,isomer #5C[Si](C)(C)O[C@H]1[C@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)O[C@H](CO)[C@@H](O)[C@@H]1O4189.6Semi standard non polar33892256
Luteolinidin 3-O-glucoside,1TMS,isomer #6C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)O[C@H](CO)[C@H]1O4171.9Semi standard non polar33892256
Luteolinidin 3-O-glucoside,1TMS,isomer #7C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O)[C@H]1O4153.0Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O4015.6Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TMS,isomer #10C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)=C2C=CC(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C14077.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TMS,isomer #11C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)=C2C=CC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C14064.3Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TMS,isomer #12C[Si](C)(C)OC1=CC(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=CC(O)=CC3=[O+]2)=CC=C1O3994.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TMS,isomer #13C[Si](C)(C)OC1=CC(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O)=CC3=[O+]2)=CC=C1O3990.3Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TMS,isomer #14C[Si](C)(C)OC1=CC(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O)=CC3=[O+]2)=CC=C1O4015.5Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TMS,isomer #15C[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)=CC(O)=CC3=[O+]2)C=C1O[Si](C)(C)C4043.3Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TMS,isomer #16C[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=CC(O)=CC3=[O+]2)C=C1O3999.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TMS,isomer #17C[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O)=CC3=[O+]2)C=C1O4000.7Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TMS,isomer #18C[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O)=CC3=[O+]2)C=C1O4029.9Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TMS,isomer #19C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)O[C@@H]1CO4017.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O4020.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TMS,isomer #20C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)O[C@H](CO)[C@H]1O4041.6Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TMS,isomer #21C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O)[C@H]1O[Si](C)(C)C4007.9Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O3999.3Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TMS,isomer #4C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O4042.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TMS,isomer #5C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O4022.8Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TMS,isomer #6C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C4029.7Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TMS,isomer #7C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)=C2C=CC(C3=CC=C(O)C(O)=C3)=[O+]C2=C14013.6Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TMS,isomer #8C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)=C2C=CC(C3=CC=C(O)C(O)=C3)=[O+]C2=C14017.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TMS,isomer #9C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)=C2C=CC(C3=CC=C(O)C(O)=C3)=[O+]C2=C14038.7Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O3926.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #10C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O3870.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #11C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O3839.5Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #12C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C3873.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #13C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O3947.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #14C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C3975.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #15C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3944.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #16C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)=C2C=CC(C3=CC=C(O)C(O)=C3)=[O+]C2=C13912.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #17C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)=C2C=CC(C3=CC=C(O)C(O)=C3)=[O+]C2=C13918.0Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #18C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)=C2C=CC(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C13933.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #19C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)=C2C=CC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C13930.0Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O3908.9Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #20C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=C2C=CC(C3=CC=C(O)C(O)=C3)=[O+]C2=C13934.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #21C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)=C2C=CC(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C13934.6Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #22C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)=C2C=CC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C13930.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #23C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)=C2C=CC(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C13941.7Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #24C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)=C2C=CC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C13936.5Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #25C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)=C2C=CC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=[O+]C2=C13968.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #26C[Si](C)(C)OC1=CC(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O)=CC3=[O+]2)=CC=C1O3852.5Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #27C[Si](C)(C)OC1=CC(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O)=CC3=[O+]2)=CC=C1O3860.7Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #28C[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=CC(O)=CC3=[O+]2)C=C1O[Si](C)(C)C3901.9Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #29C[Si](C)(C)OC1=CC(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC(O)=CC3=[O+]2)=CC=C1O3878.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O3929.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #30C[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O)=CC3=[O+]2)C=C1O[Si](C)(C)C3887.9Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #31C[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O)=CC3=[O+]2)C=C1O[Si](C)(C)C3915.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #32C[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O)=CC3=[O+]2)C=C1O3862.3Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #33C[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O)=CC3=[O+]2)C=C1O3875.7Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #34C[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC(O)=CC3=[O+]2)C=C1O3890.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #35C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)O[C@H](CO)[C@H]1O[Si](C)(C)C3957.8Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #4C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O3899.0Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #5C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C3928.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #6C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O3893.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #7C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O3888.9Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #8C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O3862.8Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TMS,isomer #9C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C3892.3Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O3886.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #10C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3865.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #11C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O3833.6Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #12C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O3804.5Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #13C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C3841.8Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #14C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O3796.6Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #15C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C3825.0Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #16C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3807.0Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #17C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O3780.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #18C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C3805.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #19C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3790.3Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O3865.7Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #20C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3947.6Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #21C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=C2C=CC(C3=CC=C(O)C(O)=C3)=[O+]C2=C13877.3Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #22C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)=C2C=CC(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C13874.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #23C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)=C2C=CC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C13864.6Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #24C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)=C2C=CC(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C13879.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #25C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)=C2C=CC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C13864.6Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #26C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)=C2C=CC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=[O+]C2=C13908.8Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #27C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=C2C=CC(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C13879.6Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #28C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=C2C=CC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C13869.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #29C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)=C2C=CC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=[O+]C2=C13907.0Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O3857.5Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #30C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)=C2C=CC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=[O+]C2=C13909.9Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #31C[Si](C)(C)OC1=CC(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC(O)=CC3=[O+]2)=CC=C1O3817.0Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #32C[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O)=CC3=[O+]2)C=C1O[Si](C)(C)C3831.3Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #33C[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O)=CC3=[O+]2)C=C1O[Si](C)(C)C3832.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #34C[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC(O)=CC3=[O+]2)C=C1O[Si](C)(C)C3840.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #35C[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC(O)=CC3=[O+]2)C=C1O3829.3Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #4C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C3870.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #5C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O3847.7Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #6C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O3838.8Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #7C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C3851.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #8C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O3860.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TMS,isomer #9C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C3880.8Semi standard non polar33892256
Luteolinidin 3-O-glucoside,5TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O3867.7Semi standard non polar33892256
Luteolinidin 3-O-glucoside,5TMS,isomer #10C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3870.3Semi standard non polar33892256
Luteolinidin 3-O-glucoside,5TMS,isomer #11C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O3820.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,5TMS,isomer #12C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C3831.8Semi standard non polar33892256
Luteolinidin 3-O-glucoside,5TMS,isomer #13C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3829.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,5TMS,isomer #14C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3833.8Semi standard non polar33892256
Luteolinidin 3-O-glucoside,5TMS,isomer #15C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3819.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,5TMS,isomer #16C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=C2C=CC(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C13869.8Semi standard non polar33892256
Luteolinidin 3-O-glucoside,5TMS,isomer #17C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=C2C=CC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C13862.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,5TMS,isomer #18C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)=C2C=CC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=[O+]C2=C13885.5Semi standard non polar33892256
Luteolinidin 3-O-glucoside,5TMS,isomer #19C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)=C2C=CC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=[O+]C2=C13879.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,5TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O3856.0Semi standard non polar33892256
Luteolinidin 3-O-glucoside,5TMS,isomer #20C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=C2C=CC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=[O+]C2=C13885.8Semi standard non polar33892256
Luteolinidin 3-O-glucoside,5TMS,isomer #21C[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC(O)=CC3=[O+]2)C=C1O[Si](C)(C)C3851.0Semi standard non polar33892256
Luteolinidin 3-O-glucoside,5TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C3877.5Semi standard non polar33892256
Luteolinidin 3-O-glucoside,5TMS,isomer #4C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O3843.0Semi standard non polar33892256
Luteolinidin 3-O-glucoside,5TMS,isomer #5C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C3858.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,5TMS,isomer #6C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3860.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,5TMS,isomer #7C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O3832.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,5TMS,isomer #8C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C3846.5Semi standard non polar33892256
Luteolinidin 3-O-glucoside,5TMS,isomer #9C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3848.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,6TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O3858.9Semi standard non polar33892256
Luteolinidin 3-O-glucoside,6TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C3869.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,6TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3876.7Semi standard non polar33892256
Luteolinidin 3-O-glucoside,6TMS,isomer #4C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3872.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,6TMS,isomer #5C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3865.6Semi standard non polar33892256
Luteolinidin 3-O-glucoside,6TMS,isomer #6C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)=CC=C23)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3875.5Semi standard non polar33892256
Luteolinidin 3-O-glucoside,6TMS,isomer #7C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=C2C=CC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=[O+]C2=C13891.9Semi standard non polar33892256
Luteolinidin 3-O-glucoside,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O4435.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)=C2C=CC(C3=CC=C(O)C(O)=C3)=[O+]C2=C14481.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1=CC(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)=CC(O)=CC3=[O+]2)=CC=C1O4414.5Semi standard non polar33892256
Luteolinidin 3-O-glucoside,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)=CC(O)=CC3=[O+]2)C=C1O4456.3Semi standard non polar33892256
Luteolinidin 3-O-glucoside,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)O[C@H]1[C@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)O[C@H](CO)[C@@H](O)[C@@H]1O4456.7Semi standard non polar33892256
Luteolinidin 3-O-glucoside,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)O[C@H](CO)[C@H]1O4439.9Semi standard non polar33892256
Luteolinidin 3-O-glucoside,1TBDMS,isomer #7CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O)[C@H]1O4421.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C(C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O4544.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)=C2C=CC(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)=[O+]C2=C14625.8Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)=C2C=CC(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)=[O+]C2=C14589.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC1=CC(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)=CC(O)=CC3=[O+]2)=CC=C1O4503.7Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC1=CC(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)=CC(O)=CC3=[O+]2)=CC=C1O4507.9Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC1=CC(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=CC(O)=CC3=[O+]2)=CC=C1O4514.6Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)=CC(O)=CC3=[O+]2)C=C1O[Si](C)(C)C(C)(C)C4533.9Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TBDMS,isomer #16CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)=CC(O)=CC3=[O+]2)C=C1O4536.5Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)=CC(O)=CC3=[O+]2)C=C1O4541.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=CC(O)=CC3=[O+]2)C=C1O4548.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TBDMS,isomer #19CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)O[C@@H]1CO4545.9Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O4532.0Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TBDMS,isomer #20CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)O[C@H](CO)[C@H]1O4548.6Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TBDMS,isomer #21CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4525.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O4492.9Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O4532.5Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4515.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4520.8Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)=C2C=CC(C3=CC=C(O)C(O)=C3)=[O+]C2=C14547.7Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)=C2C=CC(C3=CC=C(O)C(O)=C3)=[O+]C2=C14553.6Semi standard non polar33892256
Luteolinidin 3-O-glucoside,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)=C2C=CC(C3=CC=C(O)C(O)=C3)=[O+]C2=C14558.3Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C(C)(C)C)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O4755.7Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC=C23)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O4590.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4575.8Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4590.9Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4595.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4639.6Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C4596.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #16CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)=C2C=CC(C3=CC=C(O)C(O)=C3)=[O+]C2=C14642.5Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)=C2C=CC(C3=CC=C(O)C(O)=C3)=[O+]C2=C14654.3Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)=C2C=CC(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)=[O+]C2=C14773.7Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)=C2C=CC(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)=[O+]C2=C14730.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C(C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O4713.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #20CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)=C2C=CC(C3=CC=C(O)C(O)=C3)=[O+]C2=C14664.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #21CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)=C2C=CC(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)=[O+]C2=C14790.9Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #22CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)=C2C=CC(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)=[O+]C2=C14746.0Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)=C2C=CC(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)=[O+]C2=C14778.3Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #24CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)=C2C=CC(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)=[O+]C2=C14736.7Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)=C2C=CC(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C3)=[O+]C2=C14759.9Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #26CC(C)(C)[Si](C)(C)OC1=CC(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)=CC(O)=CC3=[O+]2)=CC=C1O4589.3Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC1=CC(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=CC(O)=CC3=[O+]2)=CC=C1O4603.0Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)=CC(O)=CC3=[O+]2)C=C1O[Si](C)(C)C(C)(C)C4650.6Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #29CC(C)(C)[Si](C)(C)OC1=CC(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O[Si](C)(C)C(C)(C)C)=CC(O)=CC3=[O+]2)=CC=C1O4615.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C(C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O4643.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #30CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)=CC(O)=CC3=[O+]2)C=C1O[Si](C)(C)C(C)(C)C4651.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #31CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=CC(O)=CC3=[O+]2)C=C1O[Si](C)(C)C(C)(C)C4648.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #32CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)=CC(O)=CC3=[O+]2)C=C1O4627.6Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #33CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=CC(O)=CC3=[O+]2)C=C1O4642.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #34CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O[Si](C)(C)C(C)(C)C)=CC(O)=CC3=[O+]2)C=C1O4652.0Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #35CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)O[C@H](CO)[C@H]1O[Si](C)(C)C(C)(C)C4616.7Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C(C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4633.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C(C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4642.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O4627.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O4636.7Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4622.3Semi standard non polar33892256
Luteolinidin 3-O-glucoside,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4637.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C(C)(C)C)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O4847.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C(C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C4719.5Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C4)=CC=C23)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O4726.3Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4707.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4717.7Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4728.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4763.5Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #16CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C4738.6Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC=C23)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4683.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC=C23)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4713.6Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C4692.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C(C)(C)C)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O4875.9Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #20CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C4728.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #21CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)=C2C=CC(C3=CC=C(O)C(O)=C3)=[O+]C2=C14721.9Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #22CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)=C2C=CC(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)=[O+]C2=C14860.5Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)=C2C=CC(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)=[O+]C2=C14820.7Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #24CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)=C2C=CC(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)=[O+]C2=C14867.6Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)=C2C=CC(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)=[O+]C2=C14827.5Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #26CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)=C2C=CC(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C3)=[O+]C2=C14866.6Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)=C2C=CC(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)=[O+]C2=C14880.0Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)=C2C=CC(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)=[O+]C2=C14837.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #29CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)=C2C=CC(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C3)=[O+]C2=C14866.4Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C(C)(C)C)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4857.9Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #30CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)=C2C=CC(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C3)=[O+]C2=C14872.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #31CC(C)(C)[Si](C)(C)OC1=CC(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O[Si](C)(C)C(C)(C)C)=CC(O)=CC3=[O+]2)=CC=C1O4699.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #32CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)=CC(O)=CC3=[O+]2)C=C1O[Si](C)(C)C(C)(C)C4708.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #33CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=CC(O)=CC3=[O+]2)C=C1O[Si](C)(C)C(C)(C)C4719.3Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #34CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O[Si](C)(C)C(C)(C)C)=CC(O)=CC3=[O+]2)C=C1O[Si](C)(C)C(C)(C)C4730.7Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #35CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC=C3C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O[Si](C)(C)C(C)(C)C)=CC(O)=CC3=[O+]2)C=C1O4737.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C(C)(C)C)=CC3=[O+]C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4870.5Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C(C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC=C23)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O4831.3Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C(C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4813.2Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C(C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)=CC=C23)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4825.3Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C(C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4715.1Semi standard non polar33892256
Luteolinidin 3-O-glucoside,4TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C(C)(C)C)=CC3=[O+]C(C4=CC=C(O)C(O)=C4)=CC=C23)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4742.3Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Luteolinidin 3-O-glucoside GC-MS (Non-derivatized) - 70eV, Positivesplash10-0fk9-9623500000-e160984c9e0121a052312017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolinidin 3-O-glucoside GC-MS (3 TMS) - 70eV, Positivesplash10-001i-3520029000-c6e3526e9399e950a8652017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolinidin 3-O-glucoside GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolinidin 3-O-glucoside 10V, Positive-QTOFsplash10-001i-0100900000-1a37c1bfb429f2afad1e2016-06-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolinidin 3-O-glucoside 20V, Positive-QTOFsplash10-01q9-1400900000-d9a48ed162f202a92eed2016-06-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolinidin 3-O-glucoside 40V, Positive-QTOFsplash10-0002-9720000000-d4508f3cbae0bd32bc6d2016-06-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolinidin 3-O-glucoside 10V, Negative-QTOFsplash10-001i-1200900000-3e317cfbb3d4496cfa182016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolinidin 3-O-glucoside 20V, Negative-QTOFsplash10-001i-6700900000-c178b2beba394e10f6d32016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolinidin 3-O-glucoside 40V, Negative-QTOFsplash10-0596-9100000000-54575f143aff4b5aaed12016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolinidin 3-O-glucoside 10V, Positive-QTOFsplash10-00yi-0182900000-80800f3eef19d52356d52021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolinidin 3-O-glucoside 20V, Positive-QTOFsplash10-00di-0091000000-7f035318031ee963dc462021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolinidin 3-O-glucoside 40V, Positive-QTOFsplash10-05fs-6391000000-47956e79990f475a72842021-09-24Wishart 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 ID94
FooDB IDFDB000074
KNApSAcK IDNot Available
Chemspider ID10236767
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound21604000
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. Neveu V, Perez-Jimenez J, Vos F, Crespy V, du Chaffaut L, Mennen L, Knox C, Eisner R, Cruz J, Wishart D, Scalbert A: Phenol-Explorer: an online comprehensive database on polyphenol contents in foods. Database (Oxford). 2010;2010:bap024. doi: 10.1093/database/bap024. Epub 2010 Jan 8. [PubMed:20428313 ]