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Volumn 11, Issue 18, 2001, Pages 2465-2468
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Design and synthesis of new inhibitors of HIV-1 protease dimerization with conformationally constrained templates
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Author keywords
[No Author keywords available]
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Indexed keywords
2 [3 [[2 [(9 FLUORENYLMETHOXY)CARBONYL]HYDRAZINO]CARBONYL] 4 METHOXYANILIN] 2 OXOACETIC ACID;
4 (2 AMINOETHYL) 6 DIBENZOFURANPROPIONIC ACID;
ASPARTIC PROTEINASE;
ASPARTIC PROTEINASE INHIBITOR;
MACROPHAGE INFLAMMATORY PROTEIN 1ALPHA;
PROPIONIC ACID;
TRYPTOPHYLLEUCYLTHREONYLISOLEUCYL 4 (2 AMINOETHYL) 6 DIBENZOFURANPROPIONIC ACID THREONYLTYROSYLASPARAGINYLPHENYLALANYLHYDROXIDE;
UNCLASSIFIED DRUG;
VIRUS ENZYME;
ARTICLE;
BETA SHEET;
CONTROLLED STUDY;
DIMERIZATION;
DISSOCIATION;
DRUG CONFORMATION;
DRUG DESIGN;
DRUG MECHANISM;
DRUG POTENCY;
DRUG SCREENING;
DRUG SYNTHESIS;
ENZYME ACTIVE SITE;
ENZYME ACTIVITY;
ENZYME INHIBITION;
HUMAN IMMUNODEFICIENCY VIRUS 1;
KINETICS;
NONHUMAN;
VIRUS INHIBITION;
DIMERIZATION;
DRUG DESIGN;
DRUG EVALUATION, PRECLINICAL;
HIV PROTEASE;
HIV PROTEASE INHIBITORS;
HYDRAZINES;
KINETICS;
MOLECULAR CONFORMATION;
MOLECULAR MIMICRY;
STRUCTURE-ACTIVITY RELATIONSHIP;
HUMAN IMMUNODEFICIENCY VIRUS 1;
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EID: 0035903892
PISSN: 0960894X
EISSN: None
Source Type: Journal
DOI: 10.1016/S0960-894X(01)00468-1 Document Type: Article |
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Times cited : (34)
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References (28)
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