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Volumn 10, Issue 18, 2000, Pages 2071-2074
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Stereochemistry of halopyridyl and thiazolyl thiourea compounds is a major determinant of their potency as nonnucleoside inhibitors of HIV-1 reverse transcriptase
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Author keywords
[No Author keywords available]
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Indexed keywords
DELAVIRDINE;
HI 509;
HI 510;
HI 511;
HI 512;
HI 513;
NEVIRAPINE;
RNA DIRECTED DNA POLYMERASE;
RNA DIRECTED DNA POLYMERASE INHIBITOR;
THIOUREA DERIVATIVE;
TROVIRDINE;
UNCLASSIFIED DRUG;
ANTIVIRAL ACTIVITY;
ARTICLE;
DRUG SYNTHESIS;
ENZYME INHIBITION;
HUMAN;
HUMAN CELL;
HUMAN IMMUNODEFICIENCY VIRUS 1;
MONONUCLEAR CELL;
STEREOCHEMISTRY;
STEREOISOMERISM;
STRUCTURE ACTIVITY RELATION;
VIRUS INHIBITION;
ANTI-HIV AGENTS;
CELL CULTURE TECHNIQUES;
DRUG RESISTANCE, MULTIPLE;
HIV-1;
HUMANS;
INHIBITORY CONCENTRATION 50;
LEUKOCYTES, MONONUCLEAR;
MODELS, MOLECULAR;
PYRIDINES;
REVERSE TRANSCRIPTASE INHIBITORS;
STEREOISOMERISM;
STRUCTURE-ACTIVITY RELATIONSHIP;
THIOUREA;
HUMAN IMMUNODEFICIENCY VIRUS;
HUMAN IMMUNODEFICIENCY VIRUS 1;
RNA VIRUSES;
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EID: 0033818253
PISSN: 0960894X
EISSN: None
Source Type: Journal
DOI: 10.1016/S0960-894X(00)00398-X Document Type: Article |
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Times cited : (46)
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References (13)
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