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Showing metabocard for Luteolin 7-glucoside (HMDB0035588)

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IdentificationTaxonomyOntologyPhysical propertiesSpectraBiological propertiesConcentrationsLinksReferencesXML
Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 20:35:49 UTC
Update Date2022-03-07 02:54:34 UTC
HMDB IDHMDB0035588
Secondary Accession Numbers
  • HMDB35588
Metabolite Identification
Common NameLuteolin 7-glucoside
DescriptionLuteolin 7-glucoside, also known as 7-glucoluteolin or cinaroside, 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. Thus, luteolin 7-glucoside is considered to be a flavonoid. Luteolin 7-glucoside is found, on average, in the highest concentration within a few different foods, such as mexican oreganos (Lippia graveolens), anises (Pimpinella anisum), and wild celeries (Apium graveolens) and in a lower concentration in olives (Olea europaea), celery leaves (Apium graveolens var. secalinum), and lentils (Lens culinaris). Luteolin 7-glucoside has also been detected, but not quantified in, several different foods, such as hard wheats (Triticum durum), rice (Oryza sativa), prairie turnips (Pediomelum esculentum), common sages (Salvia officinalis), and green bell peppers (Capsicum annuum). This could make luteolin 7-glucoside a potential biomarker for the consumption of these foods. Luteolin 7-glucoside is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. Based on a literature review a significant number of articles have been published on Luteolin 7-glucoside.
Structure
Data?1563862741
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0035588 (Luteolin 7-glucoside)


  Mrv1652309272007272D          

 32 35  0  0  0  0            999 V2000
10001.0655 9998.3407    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10004.635710000.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10004.635710002.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9999.6409 9998.3407    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9998.214110000.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9996.7852 9998.3510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.0707 9997.9374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9996.785210001.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9995.354210000.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9995.3542 9999.1760    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9996.784510000.8252    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9996.070010000.4127    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9996.0700 9999.5876    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9996.7845 9999.1752    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9997.4990 9999.5876    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9997.499010000.4127    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10003.207010002.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.492610001.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.492610000.8249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10003.207010000.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10003.921510000.8249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10003.921510001.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9999.641210000.8217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.926610000.4091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.9266 9999.5842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9999.6411 9999.1717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.066710000.8217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10000.352210000.4092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.3522 9999.5841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.0667 9999.1717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.7812 9999.5841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.781210000.4092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  6  7  1  0  0  0  0
 11 12  1  0  0  0  0
 11 16  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16  5  1  6  0  0  0
 14  6  1  6  0  0  0
 13 10  1  1  0  0  0
 12  9  1  6  0  0  0
 11  8  1  1  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 17  1  0  0  0  0
 21  2  1  0  0  0  0
 22  3  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 24  5  1  0  0  0  0
 26  4  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 27 28  1  0  0  0  0
 27 32  1  0  0  0  0
  1 30  2  0  0  0  0
 32 19  1  0  0  0  0
 28 23  2  0  0  0  0
 26 29  2  0  0  0  0
M  END
Download

3D MOL for HMDB0035588 (Luteolin 7-glucoside)

HMDB0035588
     RDKit          3D
Luteolin 7-glucoside
 52 55  0  0  0  0  0  0  0  0999 V2000
    1.9431   -0.4551    4.2962 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2088   -0.2638    3.0956 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5068    0.0224    2.6774 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8476    0.2413    1.3659 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1964    0.5444    0.9081 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2964    0.5955    1.7162 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5781    0.8954    1.2870 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7791    1.1675   -0.0624 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0502    1.4710   -0.5205 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6820    1.1204   -0.8920 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8787    1.3919   -2.2486 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4076    0.8201   -0.4544 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8732    0.1667    0.5015 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6103   -0.1028    0.8266 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6798   -0.1480   -0.2223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6500   -0.4185    0.0182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5509   -0.4615   -1.0098 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9173   -0.7031   -0.9600 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4015   -1.3467   -2.0641 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7609   -1.4890   -2.1124 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.3236   -0.8710   -3.3992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7110   -1.0508   -3.3926 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5301   -0.9104   -0.9739 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.6852   -1.8227    0.0854 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0035    0.4129   -0.4700 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.8295    1.4719   -0.8317 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5994    0.6858   -0.9153 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8779    1.4200    0.0218 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9989   -0.6363    1.3186 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0927   -0.5997    2.3980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5213   -0.8274    3.6607 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2336   -0.3256    2.1242 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2721    0.0711    3.4293 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1732    0.3878    2.7827 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4371    0.9308    1.9355 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8510    1.5058    0.0946 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7416    1.6179   -2.6812 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5408    0.7790   -1.0870 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9911    0.0293   -1.2325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1444   -1.2183    0.0149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0740   -2.5743   -2.1939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1358    0.2126   -3.4424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9416   -1.4118   -4.2807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1909   -0.1811   -3.3510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5780   -0.7168   -1.3441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5350   -1.6015    0.5376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0603    0.3759    0.6573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7900    1.2414   -0.7713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5279    1.1030   -1.9141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2284    1.1562    0.9150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0197   -0.8508    1.5974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0987   -0.8513    4.5174 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  1
 20 41  1  6
 21 42  1  0
 21 43  1  0
 22 44  1  0
 23 45  1  6
 24 46  1  0
 25 47  1  1
 26 48  1  0
 27 49  1  6
 28 50  1  0
 29 51  1  0
 31 52  1  0
M  END
Download

3D SDF for HMDB0035588 (Luteolin 7-glucoside)


  Mrv1652309272007272D          

 32 35  0  0  0  0            999 V2000
10001.0655 9998.3407    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10004.635710000.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10004.635710002.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9999.6409 9998.3407    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9998.214110000.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9996.7852 9998.3510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.0707 9997.9374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9996.785210001.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9995.354210000.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9995.3542 9999.1760    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9996.784510000.8252    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9996.070010000.4127    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9996.0700 9999.5876    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9996.7845 9999.1752    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9997.4990 9999.5876    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9997.499010000.4127    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10003.207010002.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.492610001.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.492610000.8249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10003.207010000.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10003.921510000.8249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10003.921510001.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9999.641210000.8217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.926610000.4091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.9266 9999.5842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9999.6411 9999.1717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.066710000.8217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10000.352210000.4092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.3522 9999.5841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.0667 9999.1717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.7812 9999.5841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.781210000.4092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  6  7  1  0  0  0  0
 11 12  1  0  0  0  0
 11 16  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16  5  1  6  0  0  0
 14  6  1  6  0  0  0
 13 10  1  1  0  0  0
 12  9  1  6  0  0  0
 11  8  1  1  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 17  1  0  0  0  0
 21  2  1  0  0  0  0
 22  3  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 24  5  1  0  0  0  0
 26  4  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 27 28  1  0  0  0  0
 27 32  1  0  0  0  0
  1 30  2  0  0  0  0
 32 19  1  0  0  0  0
 28 23  2  0  0  0  0
 26 29  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0035588

> <DATABASE_NAME>
hmdb

> <SMILES>
OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(OC3=C2)C2=CC(O)=C(O)C=C2)[C@H](O)[C@@H](O)[C@@H]1O

> <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/t16-,18-,19+,20-,21-/m1/s1

> <INCHI_KEY>
PEFNSGRTCBGNAN-QNDFHXLGSA-N

> <FORMULA>
C21H20O11

> <MOLECULAR_WEIGHT>
448.3769

> <EXACT_MASS>
448.100561482

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
42.98453166897848

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-{[(2S,3R,4S,5S,6R)-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>
8.720961662761638

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.296801688115588

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981092343758667

> <JCHEM_POLAR_SURFACE_AREA>
186.37

> <JCHEM_REFRACTIVITY>
107.0392

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.08e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
luteolin 7-O-glucoside

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0035588 (Luteolin 7-glucoside)

HMDB0035588
     RDKit          3D
Luteolin 7-glucoside
 52 55  0  0  0  0  0  0  0  0999 V2000
    1.9431   -0.4551    4.2962 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2088   -0.2638    3.0956 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5068    0.0224    2.6774 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8476    0.2413    1.3659 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1964    0.5444    0.9081 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2964    0.5955    1.7162 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5781    0.8954    1.2870 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7791    1.1675   -0.0624 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0502    1.4710   -0.5205 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6820    1.1204   -0.8920 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8787    1.3919   -2.2486 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4076    0.8201   -0.4544 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8732    0.1667    0.5015 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6103   -0.1028    0.8266 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6798   -0.1480   -0.2223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6500   -0.4185    0.0182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5509   -0.4615   -1.0098 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9173   -0.7031   -0.9600 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4015   -1.3467   -2.0641 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7609   -1.4890   -2.1124 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.3236   -0.8710   -3.3992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7110   -1.0508   -3.3926 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5301   -0.9104   -0.9739 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.6852   -1.8227    0.0854 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0035    0.4129   -0.4700 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.8295    1.4719   -0.8317 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5994    0.6858   -0.9153 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8779    1.4200    0.0218 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9989   -0.6363    1.3186 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0927   -0.5997    2.3980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5213   -0.8274    3.6607 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2336   -0.3256    2.1242 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2721    0.0711    3.4293 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1732    0.3878    2.7827 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4371    0.9308    1.9355 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8510    1.5058    0.0946 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7416    1.6179   -2.6812 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5408    0.7790   -1.0870 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9911    0.0293   -1.2325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1444   -1.2183    0.0149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0740   -2.5743   -2.1939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1358    0.2126   -3.4424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9416   -1.4118   -4.2807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1909   -0.1811   -3.3510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5780   -0.7168   -1.3441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5350   -1.6015    0.5376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0603    0.3759    0.6573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7900    1.2414   -0.7713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5279    1.1030   -1.9141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2284    1.1562    0.9150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0197   -0.8508    1.5974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0987   -0.8513    4.5174 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  1
 20 41  1  6
 21 42  1  0
 21 43  1  0
 22 44  1  0
 23 45  1  6
 24 46  1  0
 25 47  1  1
 26 48  1  0
 27 49  1  6
 28 50  1  0
 29 51  1  0
 31 52  1  0
M  END
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PDB for HMDB0035588 (Luteolin 7-glucoside)

HEADER    PROTEIN                                 27-SEP-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-SEP-20         0                                  
HETATM    1  O   UNK     0    8668.6568663.569   0.000  0.00  0.00           O+0
HETATM    2  O   UNK     0    8675.3208667.437   0.000  0.00  0.00           O+0
HETATM    3  O   UNK     0    8675.3208670.517   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0    8665.9968663.569   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0    8663.3338668.207   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0    8660.6668663.589   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0    8659.3328662.816   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0    8660.6668669.747   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0    8657.9958668.207   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0    8657.9958665.129   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0    8660.6648668.207   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0    8659.3318667.437   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0    8659.3318665.897   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0    8660.6648665.127   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0    8661.9988665.897   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0    8661.9988667.437   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0    8672.6538670.517   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0    8671.3208669.747   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0    8671.3208668.206   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0    8672.6538667.436   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0    8673.9878668.206   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0    8673.9878669.747   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0    8665.9978668.201   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0    8664.6638667.430   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0    8664.6638665.891   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0    8665.9978665.121   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0    8668.6588668.201   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0    8667.3248667.431   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0    8667.3248665.890   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0    8668.6588665.121   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0    8669.9928665.890   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0    8669.9928667.431   0.000  0.00  0.00           C+0
CONECT    1   30                                                            
CONECT    2   21                                                            
CONECT    3   22                                                            
CONECT    4   26                                                            
CONECT    5   16   24                                                       
CONECT    6    7   14                                                       
CONECT    7    6                                                            
CONECT    8   11                                                            
CONECT    9   12                                                            
CONECT   10   13                                                            
CONECT   11   12   16    8                                                  
CONECT   12   11   13    9                                                  
CONECT   13   12   14   10                                                  
CONECT   14   13   15    6                                                  
CONECT   15   14   16                                                       
CONECT   16   11   15    5                                                  
CONECT   17   18   22                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   32                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22    2                                                  
CONECT   22   21   17    3                                                  
CONECT   23   24   28                                                       
CONECT   24   23   25    5                                                  
CONECT   25   24   26                                                       
CONECT   26   25    4   29                                                  
CONECT   27   28   32                                                       
CONECT   28   29   27   23                                                  
CONECT   29   28   30   26                                                  
CONECT   30   29   31    1                                                  
CONECT   31   30   32                                                       
CONECT   32   31   27   19                                                  
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END
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3D PDB for HMDB0035588 (Luteolin 7-glucoside)

COMPND    HMDB0035588
HETATM    1  O1  UNL     1       1.943  -0.455   4.296  1.00  0.00           O  
HETATM    2  C1  UNL     1       2.209  -0.264   3.096  1.00  0.00           C  
HETATM    3  C2  UNL     1       3.507   0.022   2.677  1.00  0.00           C  
HETATM    4  C3  UNL     1       3.848   0.241   1.366  1.00  0.00           C  
HETATM    5  C4  UNL     1       5.196   0.544   0.908  1.00  0.00           C  
HETATM    6  C5  UNL     1       6.296   0.596   1.716  1.00  0.00           C  
HETATM    7  C6  UNL     1       7.578   0.895   1.287  1.00  0.00           C  
HETATM    8  C7  UNL     1       7.779   1.168  -0.062  1.00  0.00           C  
HETATM    9  O2  UNL     1       9.050   1.471  -0.520  1.00  0.00           O  
HETATM   10  C8  UNL     1       6.682   1.120  -0.892  1.00  0.00           C  
HETATM   11  O3  UNL     1       6.879   1.392  -2.249  1.00  0.00           O  
HETATM   12  C9  UNL     1       5.408   0.820  -0.454  1.00  0.00           C  
HETATM   13  O4  UNL     1       2.873   0.167   0.501  1.00  0.00           O  
HETATM   14  C10 UNL     1       1.610  -0.103   0.827  1.00  0.00           C  
HETATM   15  C11 UNL     1       0.680  -0.148  -0.222  1.00  0.00           C  
HETATM   16  C12 UNL     1      -0.650  -0.418   0.018  1.00  0.00           C  
HETATM   17  O5  UNL     1      -1.551  -0.461  -1.010  1.00  0.00           O  
HETATM   18  C13 UNL     1      -2.917  -0.703  -0.960  1.00  0.00           C  
HETATM   19  O6  UNL     1      -3.402  -1.347  -2.064  1.00  0.00           O  
HETATM   20  C14 UNL     1      -4.761  -1.489  -2.112  1.00  0.00           C  
HETATM   21  C15 UNL     1      -5.324  -0.871  -3.399  1.00  0.00           C  
HETATM   22  O7  UNL     1      -6.711  -1.051  -3.393  1.00  0.00           O  
HETATM   23  C16 UNL     1      -5.530  -0.910  -0.974  1.00  0.00           C  
HETATM   24  O8  UNL     1      -5.685  -1.823   0.085  1.00  0.00           O  
HETATM   25  C17 UNL     1      -5.004   0.413  -0.470  1.00  0.00           C  
HETATM   26  O9  UNL     1      -5.829   1.472  -0.832  1.00  0.00           O  
HETATM   27  C18 UNL     1      -3.599   0.686  -0.915  1.00  0.00           C  
HETATM   28  O10 UNL     1      -2.878   1.420   0.022  1.00  0.00           O  
HETATM   29  C19 UNL     1      -0.999  -0.636   1.319  1.00  0.00           C  
HETATM   30  C20 UNL     1      -0.093  -0.600   2.398  1.00  0.00           C  
HETATM   31  O11 UNL     1      -0.521  -0.827   3.661  1.00  0.00           O  
HETATM   32  C21 UNL     1       1.234  -0.326   2.124  1.00  0.00           C  
HETATM   33  H1  UNL     1       4.272   0.071   3.429  1.00  0.00           H  
HETATM   34  H2  UNL     1       6.173   0.388   2.783  1.00  0.00           H  
HETATM   35  H3  UNL     1       8.437   0.931   1.935  1.00  0.00           H  
HETATM   36  H4  UNL     1       9.851   1.506   0.095  1.00  0.00           H  
HETATM   37  H5  UNL     1       7.742   1.618  -2.681  1.00  0.00           H  
HETATM   38  H6  UNL     1       4.541   0.779  -1.087  1.00  0.00           H  
HETATM   39  H7  UNL     1       0.991   0.029  -1.232  1.00  0.00           H  
HETATM   40  H8  UNL     1      -3.144  -1.218   0.015  1.00  0.00           H  
HETATM   41  H9  UNL     1      -5.074  -2.574  -2.194  1.00  0.00           H  
HETATM   42  H10 UNL     1      -5.136   0.213  -3.442  1.00  0.00           H  
HETATM   43  H11 UNL     1      -4.942  -1.412  -4.281  1.00  0.00           H  
HETATM   44  H12 UNL     1      -7.191  -0.181  -3.351  1.00  0.00           H  
HETATM   45  H13 UNL     1      -6.578  -0.717  -1.344  1.00  0.00           H  
HETATM   46  H14 UNL     1      -6.535  -1.602   0.538  1.00  0.00           H  
HETATM   47  H15 UNL     1      -5.060   0.376   0.657  1.00  0.00           H  
HETATM   48  H16 UNL     1      -6.790   1.241  -0.771  1.00  0.00           H  
HETATM   49  H17 UNL     1      -3.528   1.103  -1.914  1.00  0.00           H  
HETATM   50  H18 UNL     1      -3.228   1.156   0.915  1.00  0.00           H  
HETATM   51  H19 UNL     1      -2.020  -0.851   1.597  1.00  0.00           H  
HETATM   52  H20 UNL     1      -0.099  -0.851   4.517  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
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SMILES for HMDB0035588 (Luteolin 7-glucoside)

OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(OC3=C2)C2=CC(O)=C(O)C=C2)[C@H](O)[C@@H](O)[C@@H]1O
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INCHI for HMDB0035588 (Luteolin 7-glucoside)

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/t16-,18-,19+,20-,21-/m1/s1
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View in JSmolView Stereo Labels
Synonyms
ValueSource
2-(3,4-Dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-yl beta-D-glucopyranosideChEBI
2-(3,4-Dihydroxyphenyl)-7-(beta-D-glucopyranosyloxy)-5-hydroxy-4H-1-benzopyran-4-oneChEBI
7-GlucoluteolinChEBI
7-GlucosylluteolinChEBI
7-O-beta-D-Glucosyl-5,7,3',4'-tetrahydroxyflavoneChEBI
CinarosideChEBI
CynarosideChEBI
Luteolin 7-monoglucosideChEBI
Luteolin 7-O-glucopyranosideChEBI
Luteolin 7-O-glucosideChEBI
Luteolin-7-glucosideChEBI
LuteolosideChEBI
2-(3,4-Dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-yl b-D-glucopyranosideGenerator
2-(3,4-Dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-yl β-D-glucopyranosideGenerator
2-(3,4-Dihydroxyphenyl)-7-(b-D-glucopyranosyloxy)-5-hydroxy-4H-1-benzopyran-4-oneGenerator
2-(3,4-Dihydroxyphenyl)-7-(β-D-glucopyranosyloxy)-5-hydroxy-4H-1-benzopyran-4-oneGenerator
7-O-b-D-Glucosyl-5,7,3',4'-tetrahydroxyflavoneGenerator
7-O-Β-D-glucosyl-5,7,3',4'-tetrahydroxyflavoneGenerator
Luteolin 7-glucosideChEBI
DaphneflavonolosideHMDB
FlavopurposideHMDB
GlucoluteolinHMDB
Luteolin 7-O-beta-D-glucosideHMDB
Luteolin 7-O-b-D-glucosideGenerator
Luteolin 7-O-β-D-glucosideGenerator
NephrocizinMeSH
Luteolin-7-O-monoglucosideMeSH
Luteolin-7-O-beta-D-glucopyranosideMeSH
Luteolin-7-beta-D-glucosideMeSH
3',4',5,7-Tetrahydroxyflavone 7-beta-D-glucopyranosidePhytoBank
3',4',5,7-Tetrahydroxyflavone 7-β-D-glucopyranosidePhytoBank
3’,4’,5,7-Tetrahydroxyflavone 7-β-D-glucopyranosidePhytoBank
3',4',5-Trihydroxyflavone 7-O-beta-D-glucopyranosidePhytoBank
3',4',5-Trihydroxyflavone 7-O-β-D-glucopyranosidePhytoBank
3’,4’,5-Trihydroxyflavone 7-O-β-D-glucopyranosidePhytoBank
7-(beta-D-Glucosyloxy)-3',4',5-trihydroxyflavonePhytoBank
7-(β-D-Glucosyloxy)-3',4',5-trihydroxyflavonePhytoBank
7-(β-D-Glucosyloxy)-3’,4’,5-trihydroxyflavonePhytoBank
7-O-beta-D-GlucosylluteolinPhytoBank
7-O-β-D-GlucosylluteolinPhytoBank
Luteolin 7-O-beta-D-glucopyranosidePhytoBank
Luteolin 7-O-β-D-glucopyranosidePhytoBank
Luteolin 7-O-beta-glucopyranosidePhytoBank
Luteolin 7-O-β-glucopyranosidePhytoBank
Luteolin 7-O-beta-glucosidePhytoBank
Luteolin 7-O-β-glucosidePhytoBank
Luteolin 7-beta-D-glucosidePhytoBank
Luteolin 7-β-D-glucosidePhytoBank
Chemical FormulaC21H20O11
Average Molecular Weight448.3769
Monoisotopic Molecular Weight448.100561482
IUPAC Name2-(3,4-dihydroxyphenyl)-5-hydroxy-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H-chromen-4-one
Traditional Nameluteolin 7-O-glucoside
CAS Registry Number5373-11-5
SMILES
OC[C@H]1O[C@@H](OC2=CC3=C(C(O)=C2)C(=O)C=C(O3)C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O)[C@@H]1O
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/t16-,18-,19+,20-,21-/m1/s1
InChI KeyPEFNSGRTCBGNAN-QNDFHXLGSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as flavonoid-7-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position.
KingdomOrganic compounds
Super ClassPhenylpropanoids and polyketides
ClassFlavonoids
Sub ClassFlavonoid glycosides
Direct ParentFlavonoid-7-O-glycosides
Alternative Parents
Substituents
  • Flavonoid-7-o-glycoside
  • 3'-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 FrameworkAromatic heteropolycyclic compounds
External Descriptors
Ontology
Not AvailableNot Available
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point256 - 258 °CNot Available
Boiling Point838.10 °C. @ 760.00 mm Hg (est)The Good Scents Company Information System
Water Solubility2888 mg/L @ 25 °C (est)The Good Scents Company Information System
LogP-0.090 (est)The Good Scents Company Information System
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility1.08 g/LALOGPS
logP0.58ALOGPS
logP0.14ChemAxon
logS-2.6ALOGPS
pKa (Strongest Acidic)7.3ChemAxon
pKa (Strongest Basic)-3ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count11ChemAxon
Hydrogen Donor Count7ChemAxon
Polar Surface Area186.37 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity107.04 m³·mol⁻¹ChemAxon
Polarizability42.98 ųChemAxon
Number of Rings4ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+201.63831661259
DarkChem[M-H]-199.00331661259
DeepCCS[M+H]+193.34830932474
DeepCCS[M-H]-190.95230932474
DeepCCS[M-2H]-224.28730932474
DeepCCS[M+Na]+199.23630932474
AllCCS[M+H]+202.832859911
AllCCS[M+H-H2O]+200.432859911
AllCCS[M+NH4]+205.032859911
AllCCS[M+Na]+205.632859911
AllCCS[M-H]-199.232859911
AllCCS[M+Na-2H]-199.632859911
AllCCS[M+HCOO]-200.232859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Luteolin 7-glucosideOC[C@H]1O[C@@H](OC2=CC3=C(C(O)=C2)C(=O)C=C(O3)C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O)[C@@H]1O5468.0Standard polar33892256
Luteolin 7-glucosideOC[C@H]1O[C@@H](OC2=CC3=C(C(O)=C2)C(=O)C=C(O3)C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O)[C@@H]1O4223.4Standard non polar33892256
Luteolin 7-glucosideOC[C@H]1O[C@@H](OC2=CC3=C(C(O)=C2)C(=O)C=C(O3)C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O)[C@@H]1O4403.6Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Luteolin 7-glucoside,1TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O4353.8Semi standard non polar33892256
Luteolin 7-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)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O24381.0Semi standard non polar33892256
Luteolin 7-glucoside,1TMS,isomer #3C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C=C3O2)C=C1O4449.3Semi standard non polar33892256
Luteolin 7-glucoside,1TMS,isomer #4C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C=C3O2)=CC=C1O4417.6Semi standard non polar33892256
Luteolin 7-glucoside,1TMS,isomer #5C[Si](C)(C)O[C@H]1[C@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)O[C@H](CO)[C@@H](O)[C@@H]1O4397.1Semi standard non polar33892256
Luteolin 7-glucoside,1TMS,isomer #6C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)O[C@H](CO)[C@H]1O4376.7Semi standard non polar33892256
Luteolin 7-glucoside,1TMS,isomer #7C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@H]1O4361.4Semi standard non polar33892256
Luteolin 7-glucoside,2TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O4196.5Semi standard non polar33892256
Luteolin 7-glucoside,2TMS,isomer #10C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C=C3O2)C=C1O4301.8Semi standard non polar33892256
Luteolin 7-glucoside,2TMS,isomer #11C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C=C3O2)=CC=C1O4280.1Semi standard non polar33892256
Luteolin 7-glucoside,2TMS,isomer #12C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3O2)C=C1O4231.4Semi standard non polar33892256
Luteolin 7-glucoside,2TMS,isomer #13C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3O2)C=C1O4239.4Semi standard non polar33892256
Luteolin 7-glucoside,2TMS,isomer #14C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3O2)C=C1O4259.5Semi standard non polar33892256
Luteolin 7-glucoside,2TMS,isomer #15C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C=C3O2)C=C1O[Si](C)(C)C4233.1Semi standard non polar33892256
Luteolin 7-glucoside,2TMS,isomer #16C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3O2)=CC=C1O4205.5Semi standard non polar33892256
Luteolin 7-glucoside,2TMS,isomer #17C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3O2)=CC=C1O4204.3Semi standard non polar33892256
Luteolin 7-glucoside,2TMS,isomer #18C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3O2)=CC=C1O4229.6Semi standard non polar33892256
Luteolin 7-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)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)O[C@@H]1CO4220.8Semi standard non polar33892256
Luteolin 7-glucoside,2TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O4232.1Semi standard non polar33892256
Luteolin 7-glucoside,2TMS,isomer #20C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)O[C@H](CO)[C@H]1O4242.4Semi standard non polar33892256
Luteolin 7-glucoside,2TMS,isomer #21C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@H]1O[Si](C)(C)C4209.4Semi standard non polar33892256
Luteolin 7-glucoside,2TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O4208.7Semi standard non polar33892256
Luteolin 7-glucoside,2TMS,isomer #4C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O4230.1Semi standard non polar33892256
Luteolin 7-glucoside,2TMS,isomer #5C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O4207.1Semi standard non polar33892256
Luteolin 7-glucoside,2TMS,isomer #6C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C4219.7Semi standard non polar33892256
Luteolin 7-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)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O24202.1Semi standard non polar33892256
Luteolin 7-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)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O24211.0Semi standard non polar33892256
Luteolin 7-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)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O24227.1Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O)[C@@H](O)[C@@H]1O4122.5Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #10C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O4061.4Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #11C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O4037.7Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #12C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C4073.0Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #13C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O4105.5Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #14C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C4146.7Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #15C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4111.6Semi standard non polar33892256
Luteolin 7-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)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O24078.3Semi standard non polar33892256
Luteolin 7-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)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O24085.1Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #18C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3O2)C=C1O4144.6Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #19C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3O2)=CC=C1O4136.6Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O)[C@@H](O)[C@@H]1O4102.8Semi standard non polar33892256
Luteolin 7-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)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O24109.2Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #21C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3O2)C=C1O4152.3Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #22C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3O2)=CC=C1O4138.1Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #23C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3O2)C=C1O4142.9Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #24C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3O2)=CC=C1O4136.8Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #25C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C=C3O2)C=C1O[Si](C)(C)C4183.3Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #26C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3O2)C=C1O4055.1Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #27C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3O2)C=C1O4063.5Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #28C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3O2)C=C1O[Si](C)(C)C4094.4Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #29C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C=C3O2)C=C1O4094.5Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O4092.5Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #30C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3O2)C=C1O[Si](C)(C)C4085.0Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #31C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C4103.3Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #32C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3O2)=CC=C1O4047.9Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #33C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3O2)=CC=C1O4054.2Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #34C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C=C3O2)=CC=C1O4083.6Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #35C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)O[C@H](CO)[C@H]1O[Si](C)(C)C4099.5Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #4C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O4064.4Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #5C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C4098.4Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #6C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O)[C@@H](O)[C@@H]1O4068.1Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #7C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O4077.1Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #8C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O4058.9Semi standard non polar33892256
Luteolin 7-glucoside,3TMS,isomer #9C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C4091.1Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O)[C@@H](O)[C@@H]1O4061.0Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #10C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4034.4Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #11C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O4013.7Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #12C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O3985.5Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #13C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C4024.1Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #14C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O4003.3Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #15C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C4025.3Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #16C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4011.8Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #17C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O3992.0Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #18C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C4006.0Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #19C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4001.2Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O4048.8Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #20C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4123.9Semi standard non polar33892256
Luteolin 7-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)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O24039.5Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #22C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3O2)C=C1O4070.5Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #23C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3O2)=CC=C1O4065.4Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #24C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3O2)C=C1O4073.9Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #25C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3O2)=CC=C1O4062.9Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #26C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)C=C3O2)C=C1O[Si](C)(C)C4097.7Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #27C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C=C3O2)C=C1O4081.0Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #28C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C=C3O2)=CC=C1O4076.6Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #29C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3O2)C=C1O[Si](C)(C)C4098.5Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O4037.8Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #30C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C4090.6Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #31C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(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)C=C3O2)C=C1O4014.3Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #32C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3O2)C=C1O[Si](C)(C)C4013.4Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #33C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C4009.7Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #34C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C4031.0Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #35C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(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)C=C3O2)=CC=C1O4009.1Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #4C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C4059.5Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #5C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O4033.3Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #6C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O4020.0Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #7C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C4043.3Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #8C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O4029.6Semi standard non polar33892256
Luteolin 7-glucoside,4TMS,isomer #9C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C4048.5Semi standard non polar33892256
Luteolin 7-glucoside,5TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O4031.6Semi standard non polar33892256
Luteolin 7-glucoside,5TMS,isomer #10C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O[Si](C)(C)C)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4042.4Semi standard non polar33892256
Luteolin 7-glucoside,5TMS,isomer #11C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O4004.3Semi standard non polar33892256
Luteolin 7-glucoside,5TMS,isomer #12C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C4012.9Semi standard non polar33892256
Luteolin 7-glucoside,5TMS,isomer #13C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4013.3Semi standard non polar33892256
Luteolin 7-glucoside,5TMS,isomer #14C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4033.1Semi standard non polar33892256
Luteolin 7-glucoside,5TMS,isomer #15C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4024.4Semi standard non polar33892256
Luteolin 7-glucoside,5TMS,isomer #16C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(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)C=C3O2)C=C1O4059.4Semi standard non polar33892256
Luteolin 7-glucoside,5TMS,isomer #17C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(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)C=C3O2)=CC=C1O4058.0Semi standard non polar33892256
Luteolin 7-glucoside,5TMS,isomer #18C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)C=C3O2)C=C1O[Si](C)(C)C4060.5Semi standard non polar33892256
Luteolin 7-glucoside,5TMS,isomer #19C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C4050.2Semi standard non polar33892256
Luteolin 7-glucoside,5TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O4013.9Semi standard non polar33892256
Luteolin 7-glucoside,5TMS,isomer #20C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C4067.0Semi standard non polar33892256
Luteolin 7-glucoside,5TMS,isomer #21C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(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)C=C3O2)C=C1O[Si](C)(C)C4031.2Semi standard non polar33892256
Luteolin 7-glucoside,5TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C4041.9Semi standard non polar33892256
Luteolin 7-glucoside,5TMS,isomer #4C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O4028.5Semi standard non polar33892256
Luteolin 7-glucoside,5TMS,isomer #5C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C4038.1Semi standard non polar33892256
Luteolin 7-glucoside,5TMS,isomer #6C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4045.0Semi standard non polar33892256
Luteolin 7-glucoside,5TMS,isomer #7C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O4019.8Semi standard non polar33892256
Luteolin 7-glucoside,5TMS,isomer #8C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C4027.3Semi standard non polar33892256
Luteolin 7-glucoside,5TMS,isomer #9C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4034.9Semi standard non polar33892256
Luteolin 7-glucoside,6TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O4022.9Semi standard non polar33892256
Luteolin 7-glucoside,6TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C4023.1Semi standard non polar33892256
Luteolin 7-glucoside,6TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4036.3Semi standard non polar33892256
Luteolin 7-glucoside,6TMS,isomer #4C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4049.5Semi standard non polar33892256
Luteolin 7-glucoside,6TMS,isomer #5C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4046.4Semi standard non polar33892256
Luteolin 7-glucoside,6TMS,isomer #6C[Si](C)(C)OC[C@H]1O[C@@H](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@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4050.5Semi standard non polar33892256
Luteolin 7-glucoside,6TMS,isomer #7C[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(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)C=C3O2)C=C1O[Si](C)(C)C4054.9Semi standard non polar33892256
Luteolin 7-glucoside,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O4649.8Semi standard non polar33892256
Luteolin 7-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)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O24651.6Semi standard non polar33892256
Luteolin 7-glucoside,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C=C3O2)C=C1O4703.4Semi standard non polar33892256
Luteolin 7-glucoside,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C=C3O2)=CC=C1O4656.9Semi standard non polar33892256
Luteolin 7-glucoside,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)O[C@H]1[C@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)O[C@H](CO)[C@@H](O)[C@@H]1O4662.1Semi standard non polar33892256
Luteolin 7-glucoside,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)O[C@H](CO)[C@H]1O4645.8Semi standard non polar33892256
Luteolin 7-glucoside,1TBDMS,isomer #7CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@H]1O4637.0Semi standard non polar33892256
Luteolin 7-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)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O4704.5Semi standard non polar33892256
Luteolin 7-glucoside,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C=C3O2)C=C1O4808.1Semi standard non polar33892256
Luteolin 7-glucoside,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C=C3O2)=CC=C1O4763.8Semi standard non polar33892256
Luteolin 7-glucoside,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)C=C3O2)C=C1O4742.1Semi standard non polar33892256
Luteolin 7-glucoside,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)C=C3O2)C=C1O4747.0Semi standard non polar33892256
Luteolin 7-glucoside,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1O4747.5Semi standard non polar33892256
Luteolin 7-glucoside,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C4733.0Semi standard non polar33892256
Luteolin 7-glucoside,2TBDMS,isomer #16CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)C=C3O2)=CC=C1O4704.8Semi standard non polar33892256
Luteolin 7-glucoside,2TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)C=C3O2)=CC=C1O4705.5Semi standard non polar33892256
Luteolin 7-glucoside,2TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)C=C3O2)=CC=C1O4710.0Semi standard non polar33892256
Luteolin 7-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)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)O[C@@H]1CO4717.0Semi standard non polar33892256
Luteolin 7-glucoside,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O4756.4Semi standard non polar33892256
Luteolin 7-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)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)O[C@H](CO)[C@H]1O4739.7Semi standard non polar33892256
Luteolin 7-glucoside,2TBDMS,isomer #21CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4704.1Semi standard non polar33892256
Luteolin 7-glucoside,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O4713.9Semi standard non polar33892256
Luteolin 7-glucoside,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O4734.9Semi standard non polar33892256
Luteolin 7-glucoside,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4699.6Semi standard non polar33892256
Luteolin 7-glucoside,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4723.1Semi standard non polar33892256
Luteolin 7-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)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O24700.4Semi standard non polar33892256
Luteolin 7-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)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O24692.3Semi standard non polar33892256
Luteolin 7-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)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O24705.8Semi standard non polar33892256
Luteolin 7-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)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O4908.8Semi standard non polar33892256
Luteolin 7-glucoside,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)OC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O4786.3Semi standard non polar33892256
Luteolin 7-glucoside,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4774.2Semi standard non polar33892256
Luteolin 7-glucoside,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4797.4Semi standard non polar33892256
Luteolin 7-glucoside,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4801.0Semi standard non polar33892256
Luteolin 7-glucoside,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4830.3Semi standard non polar33892256
Luteolin 7-glucoside,3TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C4796.7Semi standard non polar33892256
Luteolin 7-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)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O24780.9Semi standard non polar33892256
Luteolin 7-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)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O24790.9Semi standard non polar33892256
Luteolin 7-glucoside,3TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)C=C3O2)C=C1O4919.8Semi standard non polar33892256
Luteolin 7-glucoside,3TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)C=C3O2)=CC=C1O4870.8Semi standard non polar33892256
Luteolin 7-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)=C3C(=O)C=C(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O4854.1Semi standard non polar33892256
Luteolin 7-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)=CC2=C1C(=O)C=C(C1=CC=C(O)C(O)=C1)O24811.6Semi standard non polar33892256
Luteolin 7-glucoside,3TBDMS,isomer #21CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)C=C3O2)C=C1O4934.6Semi standard non polar33892256
Luteolin 7-glucoside,3TBDMS,isomer #22CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)C=C3O2)=CC=C1O4882.2Semi standard non polar33892256
Luteolin 7-glucoside,3TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1O4912.5Semi standard non polar33892256
Luteolin 7-glucoside,3TBDMS,isomer #24CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)C=C3O2)=CC=C1O4864.0Semi standard non polar33892256
Luteolin 7-glucoside,3TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C4915.2Semi standard non polar33892256
Luteolin 7-glucoside,3TBDMS,isomer #26CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(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)C=C3O2)C=C1O4819.8Semi standard non polar33892256
Luteolin 7-glucoside,3TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(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)C=C3O2)C=C1O4835.3Semi standard non polar33892256
Luteolin 7-glucoside,3TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C4837.7Semi standard non polar33892256
Luteolin 7-glucoside,3TBDMS,isomer #29CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(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)C=C3O2)C=C1O4848.9Semi standard non polar33892256
Luteolin 7-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)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O4787.0Semi standard non polar33892256
Luteolin 7-glucoside,3TBDMS,isomer #30CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C4833.8Semi standard non polar33892256
Luteolin 7-glucoside,3TBDMS,isomer #31CC(C)(C)[Si](C)(C)OC1=CC=C(C2=CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C4829.8Semi standard non polar33892256
Luteolin 7-glucoside,3TBDMS,isomer #32CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(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)C=C3O2)=CC=C1O4785.6Semi standard non polar33892256
Luteolin 7-glucoside,3TBDMS,isomer #33CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(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)C=C3O2)=CC=C1O4797.2Semi standard non polar33892256
Luteolin 7-glucoside,3TBDMS,isomer #34CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(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)C=C3O2)=CC=C1O4811.5Semi standard non polar33892256
Luteolin 7-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)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)O[C@H](CO)[C@H]1O[Si](C)(C)C(C)(C)C4812.8Semi standard non polar33892256
Luteolin 7-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)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4759.1Semi standard non polar33892256
Luteolin 7-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)=C3C(=O)C=C(C4=CC=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4787.5Semi standard non polar33892256
Luteolin 7-glucoside,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](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@H](O)[C@@H](O)[C@@H]1O4823.8Semi standard non polar33892256
Luteolin 7-glucoside,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O4832.1Semi standard non polar33892256
Luteolin 7-glucoside,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4819.2Semi standard non polar33892256
Luteolin 7-glucoside,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4843.6Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 7-glucoside GC-MS (Non-derivatized) - 70eV, Positivesplash10-001r-8934600000-7e7c6044b90fb9c114632017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 7-glucoside GC-MS (3 TMS) - 70eV, Positivesplash10-0f72-4730119000-f82ba729f371b8abdbda2017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 7-glucoside GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 7-glucoside ESI-TOF 10V, Negative-QTOFsplash10-0002-0010900030-c10d893db863fa97d0a82017-08-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 7-glucoside ESI-TOF 10V, Negative-QTOFsplash10-0002-0010900030-c10d893db863fa97d0a82017-09-12HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 7-glucoside DI-ESI-qTof , Positive-QTOFsplash10-000i-0090000000-f076599705f9f223d3602017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 7-glucoside DI-ESI-qTof , Negative-QTOFsplash10-000i-0090100000-fe6850abbcec4fe56dd92017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 7-glucoside LC-ESI-QTOF , negative-QTOFsplash10-0012-0190500000-bcf45c556204b1713d582017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 7-glucoside LC-ESI-QTOF , negative-QTOFsplash10-0002-0030900020-65868b413ea8969c46722017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 7-glucoside LC-ESI-QTOF , negative-QTOFsplash10-0019-0090000000-0908e4e690a4acb6edfc2017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 7-glucoside LC-ESI-QTOF , negative-QTOFsplash10-0002-0000900000-f15806fb1fd62f75af542017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 7-glucoside LC-ESI-QTOF , negative-QTOFsplash10-001a-0190400000-862638c136c541fb742b2017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 7-glucoside Linear Ion Trap , negative-QTOFsplash10-000i-0091000000-f63c0d3cebcf6fc2e5072017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 7-glucoside , negative-QTOFsplash10-0002-0040900000-e3f9043e8fac7872cb662017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 7-glucoside LC-ESI-QTOF , positive-QTOFsplash10-000i-0090000000-1ff8e42522b8a1f6961a2017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 7-glucoside LC-ESI-QTOF , positive-QTOFsplash10-000i-0090100000-cb0df3f467ea51e6ab182017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 7-glucoside LC-ESI-QTOF , positive-QTOFsplash10-000j-0090600000-8f1dad507334d836e2a82017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 7-glucoside LC-ESI-QTOF , positive-QTOFsplash10-000i-0190000000-e3aa1461dda1c7043d2d2017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 7-glucoside LC-ESI-ITTOF , positive-QTOFsplash10-000i-0090000000-31bb8bd03bfd2eff538b2017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 7-glucoside Linear Ion Trap , positive-QTOFsplash10-000i-0091100000-ea4c2b653cea6f4747662017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 7-glucoside , positive-QTOFsplash10-000i-0090000000-8392154e4309f46037d52017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 7-glucoside 40V, Negative-QTOFsplash10-0019-0090000000-a15f658ade963370f0c32021-09-20HMDB team, MONAView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolin 7-glucoside 10V, Positive-QTOFsplash10-000j-0190600000-49dfd37238ba14bc6c112016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolin 7-glucoside 20V, Positive-QTOFsplash10-00kr-0190000000-8733c538660a8dd11d052016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolin 7-glucoside 40V, Positive-QTOFsplash10-014i-1390000000-ceeece13914238abed462016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolin 7-glucoside 10V, Negative-QTOFsplash10-000b-1261900000-e1ec4112e692ec8fbbd62016-08-04Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolin 7-glucoside 20V, Negative-QTOFsplash10-000i-1190100000-bcbf2a30e128889e80472016-08-04Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolin 7-glucoside 40V, Negative-QTOFsplash10-00ku-2190000000-954ea2eef82d3bedfb362016-08-04Wishart 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 ID245
FooDB IDFDB014280
KNApSAcK IDC00004266
Chemspider ID4444241
KEGG Compound IDC03951
BioCyc IDLUTEOLIN-7-O-BETA-D-GLUCOSIDE
BiGG IDNot Available
Wikipedia LinkCynaroside
METLIN IDNot Available
PubChem Compound5280637
PDB IDNot Available
ChEBI ID27994
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1699821
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .