Details
Stereochemistry | ACHIRAL |
Molecular Formula | C15H10O6 |
Molecular Weight | 286.2363 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=CC(O)=C(C=C1)C2=COC3=CC(O)=CC(O)=C3C2=O
InChI
InChIKey=GSSOWCUOWLMMRJ-UHFFFAOYSA-N
InChI=1S/C15H10O6/c16-7-1-2-9(11(18)3-7)10-6-21-13-5-8(17)4-12(19)14(13)15(10)20/h1-6,16-19H
Molecular Formula | C15H10O6 |
Molecular Weight | 286.2363 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Identification of CYP1A2 as the main isoform for the phase I hydroxylated metabolism of genistein and a prodrug converting enzyme of methylated isoflavones. | 2003 Jul |
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Profiling of flavonoid conjugates in Lupinus albus and Lupinus angustifolius responding to biotic and abiotic stimuli. | 2003 May |
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Profiling isoflavone conjugates in root extracts of lupine species with LC/ESI/MSn systems. | 2005 Aug |
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Profiling isoflavone conjugates in different organs of Lupinus exaltatus Zucc. | 2006 May-Jun |
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Comparison of plants used for skin and stomach problems in Trinidad and Tobago with Asian ethnomedicine. | 2007 Jan 5 |
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Isoflavonoids from Flemingia strobilifera (L) R. Br. roots. | 2009 May-Jun |
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2'-hydroxylation of genistein enhanced antioxidant and antiproliferative activities in mcf-7 human breast cancer cells. | 2009 Nov |
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Secondary metabolites and antimycobacterial activities from the roots of Ficus nervosa. | 2010 Jul |
|
LC-MSMS profiling of flavonoid conjugates in wild Mexican lupine, Lupinus reflexus. | 2010 Jul 23 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:17:15 GMT 2023
by
admin
on
Fri Dec 15 18:17:15 GMT 2023
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Record UNII |
1R3U5726T2
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Record Status |
Validated (UNII)
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Record Version |
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70031
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1156-78-1
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DTXSID80151145
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140306
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5282074
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1R3U5726T2
Created by
admin on Fri Dec 15 18:17:15 GMT 2023 , Edited by admin on Fri Dec 15 18:17:15 GMT 2023
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PRIMARY |