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Volumn 12, Issue 4, 2002, Pages 641-643
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Solution and solid-phase synthesis of potent inhibitors of Hepatitis C Virus NS3 proteinase
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Author keywords
[No Author keywords available]
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Indexed keywords
AMINO ACID;
ENZYME INHIBITOR;
FLUORENE DERIVATIVE;
N(ALPHA) FLUORENYLMETHYLOXYCARBONYLAMINO ACIDS;
N(ALPHA)-FLUORENYLMETHYLOXYCARBONYLAMINO ACIDS;
NS3 PROTEIN, HEPATITIS C VIRUS;
OLIGOPEPTIDE;
VIRUS PROTEIN;
AMIDE;
PROTEINASE;
PROTEINASE INHIBITOR;
ARTICLE;
COMBINATORIAL CHEMISTRY;
DRUG ANTAGONISM;
ENZYMOLOGY;
HEPATITIS C VIRUS;
HUMAN;
IC 50;
STRUCTURE ACTIVITY RELATION;
SYNTHESIS;
AMINO ACID SEQUENCE;
DRUG POTENCY;
DRUG SYNTHESIS;
ENZYME INHIBITION;
SOLID;
AMINO ACIDS;
COMBINATORIAL CHEMISTRY TECHNIQUES;
ENZYME INHIBITORS;
FLUORENES;
HEPACIVIRUS;
HUMANS;
INHIBITORY CONCENTRATION 50;
OLIGOPEPTIDES;
STRUCTURE-ACTIVITY RELATIONSHIP;
VIRAL NONSTRUCTURAL PROTEINS;
HEPATITIS C VIRUS;
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EID: 0037169975
PISSN: 0960894X
EISSN: None
Source Type: Journal
DOI: 10.1016/S0960-894X(01)00816-2 Document Type: Article |
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Times cited : (29)
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References (12)
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