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Volumn 336, Issue 2, 2011, Pages 403-413

Three-dimensional quantitative structure-activity relationship studies on UGT1A9-mediated 3-O-glucuronidation of natural flavonols using a pharmacophore-based comparative molecular field analysis model

Author keywords

[No Author keywords available]

Indexed keywords

3 HYDROXY 2' METHOXYFLAVONE; 3 HYDROXY 2',3' DIMETHOXYFLAVONE; 3 HYDROXY 3' METHOXYFLAVONE; 3 HYDROXY 4' METHOXYFLAVONE; 3 HYDROXY 5 METHOXYFLAVONE; 3 HYDROXY 5,7 DIMETHOXYFLAVONE; 3 HYDROXY 6 METHOXYFLAVONE; 3 HYDROXY 6 METHYL 3',4' METHYLENEDIOXYFLAVONE; 3 HYDROXY 6 METHYLFLAVONE; 3 HYDROXY 6,4' METHOXYFLAVONE; 3 HYDROXY 7 METHOXYFLAVONE; 3 HYDROXYFLAVONE; 3,2' DIHYDROXYFLAVONE; 3,3' DIHYDROXYFLAVONE; 3,3',4' TRIHYDROXYFLAVONE; 3,4' DIHYDROXYFLAVONE; 3,5 DIHYDROXYFLAVONE; 3,6 DIHYDROXYFLAVONE; 3,6,4' TRIHYDROXYFLAVONE; 3,7 DIHYDROXYFLAVONE; FLAVONOL DERIVATIVE; GLUCURONOSYLTRANSFERASE 1A9; ISORHAMNETIN; KAEMPFEROL; MORIN; MYRICETIN; QUERCETIN; RESOKAEMPFEROL; RHAMNETIN; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 78751517809     PISSN: 00223565     EISSN: 15210103     Source Type: Journal    
DOI: 10.1124/jpet.110.175356     Document Type: Article
Times cited : (34)

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