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Volumn 22, Issue 12, 2014, Pages 3220-3226
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Synthesis and biological evaluation of CHX-DAPYs as HIV-1 non-nucleoside reverse transcriptase inhibitors
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Author keywords
Antiviral activity; Diarylpyrimidine; HIV 1; NNRTIs; SAR
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Indexed keywords
4 [[4 [(3 BROMOPHENYL)CHLOROMETHYL]PYRIMIDIN 2 YL]AMINO]BENZONITRILE;
4 [[4 [(4 BROMOPHENYL)CHLOROMETHYL] 6 METHYLPYRIMIDIN 2 YL]AMINO]BENZONITRILE;
4 [[4 [(4 BROMOPHENYL)CHLOROMETHYL]PYRIMIDIN 2 YL]AMINO]BENZONITRILE;
4 [[4 [1 [4 (TERT BUTYL)PHENYL] 1 HYDROXYETHYL] 5 METHYLPYRIMIDIN 2 YL]AMINO]BENZONITRILE;
4 [[4 [BROMO(4 TOLYL)METHYL]PYRIMIDIN 2 YL]AMINO]BENZONITRILE;
4 [[4 [BROMO(PHENYL)METHYL]PYRIMIDIN 2 YL]AMINO]BENZONITRILE;
4 [[4 [CHLORO(3 CHLOROPHENYL)METHYL]PYRIMIDIN 2 YL]AMINO]BENZONITRILE;
4 [[4 [CHLORO(3 FLUOROPHENYL)METHYL]PYRIMIDIN 2 YL]AMINO]BENZONITRILE;
4 [[4 [CHLORO(4 CHLOROPHENYL)METHYL]PYRIMIDIN 2 YL]AMINO]BENZONITRILE;
4 [[4 [CHLORO(4 FLUOROPHENYL)METHYL] 5 METHYLPYRIMIDIN 2 YL]AMINO]BENZONITRILE;
4 [[4 [CHLORO(4 FLUOROPHENYL)METHYL] 6 METHYLPYRIMIDIN 2 YL]AMINO]BENZONITRILE;
4 [[4 [CHLORO(4 FLUOROPHENYL)METHYL]PYRIMIDIN 2 YL]AMINO]BENZONITRILE;
4 [[4 [CHLORO(4 METHOXYPHENYL)METHYL]PYRIMIDIN 2 YL]AMINO]BENZONITRILE;
4 [[4 [CHLORO(4 TOLYL)METHYL]PYRIMIDIN 2 YL]AMINO]BENZONITRILE;
4 [[4 [CHLORO(NAPHTHALEN 1 YL)METHYL]PYRIMIDIN 2 YL]AMINO]BENZONITRILE;
4 [[4 [CHLORO(PHENYL)METHYL]PYRIMIDIN 2 YL]AMINO]BENZONITRILE;
4 [[4 [[4 (TERT BUTYL)PHENYL]CHLOROMETHYL] 5 METHYLPYRIMIDIN 2 YL]AMINO]BENZONITRILE;
4 [[4 [[4 (TERT BUTYL)PHENYL]CHLOROMETHYL] 6 METHYLPYRIMIDIN 2 YL]AMINO]BENZONITRILE;
4 [[4 [[4 (TERT BUTYL)PHENYL]CHLOROMETHYL]PYRIMIDIN 2 YL]AMINO]BENZONITRILE;
DELAVIRDINE;
DIARYLPYRIMIDINE DERIVATIVE;
EFAVIRENZ;
ETRAVIRINE;
LAMIVUDINE;
NEVIRAPINE;
NONNUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITOR;
PYRIMIDINE DERIVATIVE;
UNCLASSIFIED DRUG;
ZIDOVUDINE;
4-((4-((3-BROMOPHENYL)CHLOROMETHYL)PYRIMIDIN-2-YL)AMINO)BENZONITRILE;
4-((4-(CHLORO(3-CHLOROPHENYL)METHYL)PYRIMIDIN-2-YL)AMINO)BENZONITRILE;
ANTI HUMAN IMMUNODEFICIENCY VIRUS AGENT;
BENZAMIDE DERIVATIVE;
NITRILE;
REVERSE TRANSCRIPTASE, HUMAN IMMUNODEFICIENCY VIRUS 1;
RNA DIRECTED DNA POLYMERASE;
RNA DIRECTED DNA POLYMERASE INHIBITOR;
ANTIVIRAL ACTIVITY;
ARTICLE;
BINDING AFFINITY;
CHEMICAL BOND;
CONCENTRATION RESPONSE;
CONTROLLED STUDY;
DRUG CONFORMATION;
DRUG CYTOTOXICITY;
DRUG DESIGN;
DRUG SCREENING;
DRUG SYNTHESIS;
HALOGEN BOND;
HUMAN IMMUNODEFICIENCY VIRUS 1;
HYDROGEN BOND;
MOLECULAR DOCKING;
MOLECULAR INTERACTION;
MOLECULAR MODEL;
NONHUMAN;
STRUCTURE ACTIVITY RELATION;
STRUCTURE ANALYSIS;
WILD TYPE;
ANTAGONISTS AND INHIBITORS;
CELL CULTURE;
CELL SURVIVAL;
CHEMICAL STRUCTURE;
CHEMISTRY;
DRUG EFFECTS;
HUMAN;
PATHOLOGY;
PRECURSOR CELL LYMPHOBLASTIC LEUKEMIA-LYMPHOMA;
SYNTHESIS;
TUMOR CELL CULTURE;
VIROLOGY;
VIRUS REPLICATION;
HUMAN IMMUNODEFICIENCY VIRUS 1;
ANTI-HIV AGENTS;
BENZAMIDES;
CELL SURVIVAL;
CELLS, CULTURED;
DRUG DESIGN;
HIV REVERSE TRANSCRIPTASE;
HIV-1;
HUMANS;
MODELS, MOLECULAR;
MOLECULAR DOCKING SIMULATION;
MOLECULAR STRUCTURE;
NITRILES;
PRECURSOR CELL LYMPHOBLASTIC LEUKEMIA-LYMPHOMA;
PYRIMIDINES;
REVERSE TRANSCRIPTASE INHIBITORS;
STRUCTURE-ACTIVITY RELATIONSHIP;
TUMOR CELLS, CULTURED;
VIRUS REPLICATION;
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EID: 84901237372
PISSN: 09680896
EISSN: 14643391
Source Type: Journal
DOI: 10.1016/j.bmc.2014.03.020 Document Type: Article |
Times cited : (19)
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References (18)
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