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Bioorganic and Medicinal Chemistry Letters

Volumn 24, Issue 17, 2014, Pages 4162-4165

Structure-activity studies of (-)-epigallocatechin gallate derivatives as HCV entry inhibitors

(7) Bhat, Rohit a Adam, Amna T a Lee, Jungeun Jasmine a Deloison, Gaspard b Rouillé, Yves c Séron, Karin c Rotella, David P a

a MONTCLAIR STATE UNIVERSITY (United States)

b INSTITUT PASTEUR DE LILLE (France)

c UNIV LILLE (France)

Author keywords

Antiviral; HCV entry; Natural product

Indexed keywords

ANTIVIRUS AGENT; EPIGALLOCATECHIN GALLATE; EPIGALLOCATECHIN GALLATE DERIVATIVE; UNCLASSIFIED DRUG; CATECHIN;

ANTIVIRAL ACTIVITY; ARTICLE; CELL VIABILITY; DRUG EFFICACY; DRUG POTENCY; HEPATITIS C VIRUS; IC 50; NONHUMAN; STEREOCHEMISTRY; STRUCTURE ACTIVITY RELATION; VIRUS ENTRY; VIRUS INHIBITION; ANALOGS AND DERIVATIVES; CELL SURVIVAL; CHEMICAL STRUCTURE; CHEMISTRY; DOSE RESPONSE; DRUG EFFECTS; HEPACIVIRUS; HUMAN; MICROBIAL SENSITIVITY TEST; PHYSIOLOGY; STEREOISOMERISM; SYNTHESIS; TUMOR CELL CULTURE;

HEPATITIS C VIRUS;

ANTIVIRAL AGENTS; CATECHIN; CELL SURVIVAL; DOSE-RESPONSE RELATIONSHIP, DRUG; HEPACIVIRUS; HUMANS; MICROBIAL SENSITIVITY TESTS; MOLECULAR STRUCTURE; STEREOISOMERISM; STRUCTURE-ACTIVITY RELATIONSHIP; TUMOR CELLS, CULTURED; VIRUS INTERNALIZATION;

EID: 84906934972 PISSN: 0960894X EISSN: 14643405 Source Type: Journal
DOI: 10.1016/j.bmcl.2014.07.051 Document Type: Article

Times cited : (15)

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