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Volumn 8, Issue 9, 2010, Pages 2180-2197
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Conformationally-constrained indeno[2,1-c]quinolines - A new class of anti-mycobacterial agents
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Author keywords
[No Author keywords available]
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Indexed keywords
ANTI-MYCOBACTERIAL;
ANTI-TB COMPOUNDS;
COMPLEX FORMATIONS;
CONFORMATIONAL FLEXIBILITY;
GROWTH INHIBITION;
IN-VITRO;
MINIMUM INHIBITORY CONCENTRATION;
MYCOBACTERIAL;
MYCOBACTERIUM TUBERCULOSIS;
PHENYL RINGS;
QUINOLINE MOIETY;
SINGLE-DOSE;
STRUCTURAL COMPARISON;
SYNTHETIC METHODOLOGY;
TARGET PROTEINS;
TERBIUM ALLOYS;
INDENE DERIVATIVE;
QUINOLINE DERIVATIVE;
TUBERCULOSTATIC AGENT;
ARTICLE;
CELL SURVIVAL;
CHEMISTRY;
CONFORMATION;
DRUG DESIGN;
DRUG EFFECT;
HUMAN;
MICROBIOLOGICAL EXAMINATION;
MONOCYTE;
MYCOBACTERIUM TUBERCULOSIS;
STEREOISOMERISM;
STRUCTURE ACTIVITY RELATION;
SYNTHESIS;
ANTITUBERCULAR AGENTS;
CELL SURVIVAL;
DRUG DESIGN;
HUMANS;
INDENES;
MICROBIAL SENSITIVITY TESTS;
MOLECULAR CONFORMATION;
MONOCYTES;
MYCOBACTERIUM TUBERCULOSIS;
QUINOLINES;
STEREOISOMERISM;
STRUCTURE-ACTIVITY RELATIONSHIP;
MYCOBACTERIUM TUBERCULOSIS;
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EID: 77951101719
PISSN: 14770520
EISSN: None
Source Type: Journal
DOI: 10.1039/b924102g Document Type: Article |
Times cited : (59)
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References (40)
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