SCOPUS 정보 검색 플랫폼

Volumn 4, Issue 4, 2009, Pages 594-614

Flavonoid dimers as bivalent modulators for P-glycoprotein-based multidrug resistance: Structure-activity relationships

(9) Chan, Kin Fai a,b Zhao, Yunzhe a,b Chow, Toby W S a Yan, Clare S W a Ma, Dik Lung a Burkett, Brendan A a Wong, Iris L K a Chow, Larry M C a Chan, Tak Hang a

a HONG KONG POLYTECHNIC UNIVERSITY (Hong Kong)

b State Key Laboratory of Chinese Medicine and Molecular Pharmacology (Incubation) (China)

Author keywords

Flavonoid Dinners; Multidrug Resistance Paclitaxel; P Glycoprotein; Structure Activity Relationships

Indexed keywords

2 (4' ALLYLOXYPHENYL) 4H CHROMEN 4 ONE; 3 (4 ALLYLOXYPHENYL) 1 (2 HYDROXY 3 NITRO 5 METHYLPHENYL)PROPENONE; 3 (4 ALLYLOXYPHENYL) 1 (2 HYDROXY 3,5 DICHLOROPHENYL)PROPENONE; 3 (4 ALLYLOXYPHENYL) 1 (2 HYDROXY 4 BENZYLOXYPHENYL)PROPENONE; 3 (4 ALLYLOXYPHENYL) 1 (2 HYDROXY 4 METHOXYPHENYL)PROPENONE; 3 (4 ALLYLOXYPHENYL) 1 (2 HYDROXY 4 METHYLPHENYL)PROPENONE; 3 (4 ALLYLOXYPHENYL) 1 (2 HYDROXY 4,5 DIMETHOXYLPHENYL)PROPENONE; 3 (4 ALLYLOXYPHENYL) 1 (2 HYDROXY 4,6 DIBENZYLOXYPHENYL)PROPENONE; 3 (4 ALLYLOXYPHENYL) 1 (2 HYDROXY 4,6 DIMETHOXYPHENYL)PROPENONE; 3 (4 ALLYLOXYPHENYL) 1 (2 HYDROXY 5 BENZYLOXYPHENYL)PROPENONE; 3 (4 ALLYLOXYPHENYL) 1 (2 HYDROXY 5 BROMOPHENYL)PROPENONE; 3 (4 ALLYLOXYPHENYL) 1 (2 HYDROXY 5 CHLOROPHENYL)PROPERNONE; 3 (4 ALLYLOXYPHENYL) 1 (2 HYDROXY 5 ETHYLPHENYL)PROPENONE; 3 (4 ALLYLOXYPHENYL) 1 (2 HYDROXY 5 FLUOROPHENYL)PROPENONE; 3 (4 ALLYLOXYPHENYL) 1 (2 HYDROXY 5 METHOXYPHENYL)PROPENONE; 3 (4 ALLYLOXYPHENYL) 1 (2 HYDROXY 5 METHYLPHENYL)PROPENONE; 3 (4 ALLYLOXYPHENYL) 1 (2 HYDROXY 6 BENZYLOXYPHENYL)PROPENONE; 3 (4 ALLYLOXYPHENYL) 1 (2 HYDROXY 6 METHOXYPHENYL)PROPENONE; 3 (4 ALLYOXYPHENYL) 1 (2 HYDROXY 4 FLUOROPHENYL)PROPENONE; 3 (4 ALLYOXYPHENYL) 1 (2 HYDROXYPHENYL)PROPENONE; 6 FLUORO 2 (4' ALLYLOXYPHENYL) 4H CHROMEN 4 ONE; 7 FLUORO 2 (4' ALLYLOXYPHENYL) 4H CHROMEN 4 ONE; DOXORUBICIN; FLAVANOID; GLYCOPROTEIN P; PACLITAXEL; TARIQUIDAR; UNCLASSIFIED DRUG; UNINDEXED DRUG; VERAPAMIL; VINBLASTINE; VINCRISTINE;

ANTINEOPLASTIC ACTIVITY; ARTICLE; BREAST CANCER; CANCER CELL; CANCER RESISTANCE; CHEMICAL MODIFICATION; CONCENTRATION RESPONSE; DRUG CYTOTOXICITY; DRUG DESIGN; DRUG POTENCY; DRUG POTENTIATION; DRUG SENSITIVITY; HUMAN; HUMAN CELL; HYDROPHILICITY; IC 50; IN VITRO STUDY; LEUKEMIA CELL; LIPOPHILICITY; MULTIDRUG RESISTANCE; PRIORITY JOURNAL; STRUCTURE ACTIVITY RELATION;

EID: 65549092069 PISSN: 18607179 EISSN: 18607187 Source Type: Journal
DOI: 10.1002/cmdc.200800413 Document Type: Article

Times cited : (50)

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