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Bioorganic and Medicinal Chemistry

Volumn 18, Issue 18, 2010, Pages 6708-6714

Design and synthesis of biphenyl derivatives as mushroom tyrosinase inhibitors

(6) Bao, Kai a,b Dai, Yi a Zhu, Zhi Bin b Tu, Feng Juan b Zhang, Wei Ge b Yao, Xin Sheng a,b

a JINAN UNIVERSITY (China)

b SHENYANG PHARMACEUTICAL UNIVERSITY (China)

Author keywords

Biphenyls; Fortuneanoside E; Synthesis; Tyrosinase inhibitors

Indexed keywords

3,4' DIHYDROXY 3',5' DIMETHOXYBIPHENYL 4 CARBOXYLIC ACID; AGLYCONE; ARBUTIN; BIPHENYL DERIVATIVE; ENZYME INHIBITOR; FORTUNEANOSIDE E; TYROSINASE INHIBITOR; UNCLASSIFIED DRUG;

ARTICLE; DRUG ACTIVITY; DRUG DESIGN; DRUG STRUCTURE; DRUG SYNTHESIS; ENZYME INHIBITION; STRUCTURE ACTIVITY RELATION; SUZUKI REACTION;

AGARICALES; BIPHENYL COMPOUNDS; DRUG DESIGN; ENZYME INHIBITORS; KINETICS; MONOPHENOL MONOOXYGENASE; SALICYLIC ACIDS; STRUCTURE-ACTIVITY RELATIONSHIP;

BASIDIOMYCOTA;

EID: 77956343202 PISSN: 09680896 EISSN: None Source Type: Journal
DOI: 10.1016/j.bmc.2010.07.062 Document Type: Article

Times cited : (60)

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