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Volumn 20, Issue 3, 2010, Pages 1263-1268
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Synthesis and antituberculosis activity of novel mefloquine-isoxazole carboxylic esters as prodrugs
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Author keywords
Antituberculosis; Ester; Isoxazole; Quinoline; SAR
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Indexed keywords
5 (2,8 BIS(TRIFLUOROMETHYL)QUINOLIN 4 YLOXYMETHYL)ISOXAZOLE 3 CARBOXYLIC ACID ETHYL ESTER;
ESTER;
MEFLOQUINE;
PRODRUG;
RIFAMPICIN;
TUBERCULOSTATIC AGENT;
UNCLASSIFIED DRUG;
CARBOXYLIC ACID;
ISOXAZOLE DERIVATIVE;
ACIDITY;
ARTICLE;
BACILLUS ANTHRACIS;
BACTERIAL COUNT;
BACTERICIDAL ACTIVITY;
CANDIDA ALBICANS;
DRUG ACTIVITY;
DRUG POTENCY;
DRUG SYNTHESIS;
ESCHERICHIA COLI;
HUMAN;
IN VITRO STUDY;
IN VIVO STUDY;
INFLAMMATION;
MACROPHAGE;
MINIMUM INHIBITORY CONCENTRATION;
MYCOBACTERIUM BOVIS;
MYCOBACTERIUM SMEGMATIS;
MYCOBACTERIUM TUBERCULOSIS;
PH;
STAPHYLOCOCCUS AUREUS;
STRUCTURE ACTIVITY RELATION;
TUBERCULOSIS;
COMPARATIVE STUDY;
DRUG EFFECTS;
GROWTH, DEVELOPMENT AND AGING;
MICROBIAL SENSITIVITY TEST;
SYNTHESIS;
BACTERIA (MICROORGANISMS);
MYCOBACTERIUM TUBERCULOSIS;
ANTITUBERCULAR AGENTS;
CARBOXYLIC ACIDS;
ESTERS;
HUMANS;
ISOXAZOLES;
MEFLOQUINE;
MICROBIAL SENSITIVITY TESTS;
MYCOBACTERIUM TUBERCULOSIS;
PRODRUGS;
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EID: 74049097181
PISSN: 0960894X
EISSN: None
Source Type: Journal
DOI: 10.1016/j.bmcl.2009.11.105 Document Type: Article |
Times cited : (67)
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References (13)
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