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Volumn 57, Issue 9, 2002, Pages 765-769
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Antituberculosis agents. V. Synthesis, evaluation of in vitro antituberculosis activity and cytotoxicity of some 2-(5-nitro-2-furyl)-1,3,4-thiadiazole derivatives
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Author keywords
Antituberculosis agents; Cytotoxicity; Minimum inhibitory concentration
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Indexed keywords
2 (2 CHLORO 6 FLUOROBENZYL)SULFONYL 5 (5 NITRO 2 FURYL) 1,3,4 THIADIAZOLE;
2 (2 CHLORO 6 FLUOROBENZYL)THIO 5 (5 NITRO 2 FURYL) 1,3,4 THIADIAZOLE;
2 (2,5 DIMETHYLBENZYL)SULFONYL 5 (5 NITRO 2 FURYL) 1,3,4 THIADIAZOLE;
2 (2,5 DIMETHYLBENZYL)THIO 5 (5 NITRO 2 FURYL) 1,3,4 THIADIAZOLE;
2 (4 CHLOROBENZYL)SULFONYL 5 (5 NITRO 2 FURYL) 1,3,4 THIADIAZOLE;
2 (4 CHLOROBENZYL)THIO 5 (5 NITRO 2 FURYL) 1,3,4 THIADIAZOLE;
2 (4 METHOXYBENZYL)THIO 5 (5 NITRO 2 FURYL) 1,3,4 THIADIAZOLE;
2 (4 NITROBENZYL)SULFONYL 5 (5 NITRO 2 FURYL) 1,3,4 THIADIAZOLE;
2 (4 NITROBENZYL)THIO 5 (5 NITRO 2 FURYL) 1,3,4 THIADIAZOLE;
2 (5 NITRO 2 FURYL) 5 ETHYLSULFINYL 1,3,4 THIADIAZOLE;
2 (5 NITRO 2 FURYL) 5 ETHYLSULFONYL 1,3,4 THIADIAZOLE;
2 (5 NITRO 2 FURYL) 5 ETHYLTHIO 1,3,4 THIADIAZOLE;
2 (5 NITRO 2 FURYL) 5 METHYLSULFINYL 1,3,4 THIADIAZOLE;
2 (5 NITRO 2 FURYL) 5 METHYLSULFONYL 1,3,4 THIADIAZOLE;
2 (5 NITRO 2 FURYL) 5 METHYLTHIO 1,3,4 THIADIAZOLE;
2 BENZYLSULFONYL 5 (5 NITRO 2 FURYL) 1,3,4 THIADIAZOLE;
2 BENZYLTHIO 5 (5 NITRO 2 FURYL) 1,3,4 THIADIAZOLE;
THIADIAZOLE DERIVATIVE;
TUBERCULOSTATIC AGENT;
UNCLASSIFIED DRUG;
ANIMAL CELL;
ARTICLE;
BACTERIAL STRAIN;
CONTROLLED STUDY;
CYTOTOXICITY;
DILUTION;
DRUG ACTIVITY;
DRUG OXIDATION;
DRUG SCREENING;
DRUG SYNTHESIS;
IN VITRO STUDY;
METHODOLOGY;
MINIMUM INHIBITORY CONCENTRATION;
MYCOBACTERIUM TUBERCULOSIS;
NONHUMAN;
PROTON NUCLEAR MAGNETIC RESONANCE;
RADIOMETRY;
ANIMAL;
CELL SURVIVAL;
CERCOPITHECUS;
DRUG EFFECT;
IC 50;
MICROBIOLOGICAL EXAMINATION;
STRUCTURE ACTIVITY RELATION;
SYNTHESIS;
VERO CELL;
ANIMALS;
ANTITUBERCULAR AGENTS;
CELL SURVIVAL;
CERCOPITHECUS AETHIOPS;
INHIBITORY CONCENTRATION 50;
MICROBIAL SENSITIVITY TESTS;
MYCOBACTERIUM TUBERCULOSIS;
STRUCTURE-ACTIVITY RELATIONSHIP;
THIADIAZOLES;
VERO CELLS;
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EID: 0036754299
PISSN: 0014827X
EISSN: None
Source Type: Journal
DOI: 10.1016/S0014-827X(02)01277-6 Document Type: Article |
Times cited : (71)
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References (11)
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