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Volumn 24, Issue 13, 2014, Pages 2892-2896
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Synthesis and biological evaluation of substituted 4,6-diarylpyrimidines and 3,5-diphenyl-4,5-dihydro-1H-pyrazoles as anti-tubercular agents
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Author keywords
4,6 Diarylpyrimidine; Anti tubercular; H37Rv; Pyrazole; THP 1 cells
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Indexed keywords
1 (3,5 DIARYL 4,5 DIHYDRO 1H PYRAZOL 1 YL)ETHANONE;
3,5 DIPHENYL 4,5 DIHYDRO 1H PYRAZOLE;
4,6 DIARYL 2 (HETEROARYL)PYRIMIDINE;
4,6 DIARYLPYRIMIDIN 2 AMINE;
4,6 DIARYLPYRIMIDINE;
ISONIAZID;
PYRAZOLE DERIVATIVE;
PYRIMIDINE DERIVATIVE;
RIFAMPICIN;
STREPTOMYCIN;
TUBERCULOSTATIC AGENT;
UNCLASSIFIED DRUG;
ANTIBACTERIAL ACTIVITY;
ARTICLE;
BIOLOGICAL ACTIVITY;
CYTOTOXICITY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
HUMAN;
HUMAN CELL;
IN VITRO STUDY;
MINIMUM INHIBITORY CONCENTRATION;
MONOCYTE;
MTT ASSAY;
MYCOBACTERIUM TUBERCULOSIS;
NONHUMAN;
STRUCTURE ACTIVITY RELATION;
TUBERCULOSIS;
CELL LINE;
CELL SURVIVAL;
CHEMICAL STRUCTURE;
CHEMISTRY;
DOSE RESPONSE;
DRUG EFFECTS;
MICROBIAL SENSITIVITY TEST;
SYNTHESIS;
MYCOBACTERIUM TUBERCULOSIS;
ANTITUBERCULAR AGENTS;
CELL LINE;
CELL SURVIVAL;
DOSE-RESPONSE RELATIONSHIP, DRUG;
HUMANS;
MICROBIAL SENSITIVITY TESTS;
MOLECULAR STRUCTURE;
MYCOBACTERIUM TUBERCULOSIS;
PYRAZOLES;
PYRIMIDINES;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 84901791108
PISSN: 0960894X
EISSN: 14643405
Source Type: Journal
DOI: 10.1016/j.bmcl.2014.04.094 Document Type: Article |
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Times cited : (42)
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References (17)
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