Indexed keywords
2 [5 (PYRIDIN 4 YL) 1,3,4 THIADIAZOL 2 YLTHIO] N (2 CHLOROPHENYL)ACETAMIDE;
2 [5 (PYRIDIN 4 YL) 1,3,4 THIADIAZOL 2 YLTHIO] N (2 CHLOROPHENYL)PROPANAMIDE;
2 [5 (PYRIDIN 4 YL) 1,3,4 THIADIAZOL 2 YLTHIO] N (2,4 DICHLOROPHENYL)ACETAMIDE;
2 [5 (PYRIDIN 4 YL) 1,3,4 THIADIAZOL 2 YLTHIO] N (2,4 DICHLOROPHENYL)PROPANAMIDE;
2 [5 (PYRIDIN 4 YL) 1,3,4 THIADIAZOL 2 YLTHIO] N (2,6 DICHLOROPHENYL)ACETAMIDE;
2 [5 (PYRIDIN 4 YL) 1,3,4 THIADIAZOL 2 YLTHIO] N (2,6 DICHLOROPHENYL)PROPANAMIDE;
2 [5 (PYRIDIN 4 YL) 1,3,4 THIADIAZOL 2 YLTHIO] N (4 CHLOROPHENYL)PROPANAMIDE;
2 [5 (PYRIDIN 4 YL) 1,3,4 THIADIAZOL 2 YLTHIO] N (4CHLOROPHENYL)ACETAMIDE;
2 [5 (PYRIDIN 4 YL) 1,3,4 THIADIAZOL 2 YLTHIO] N BENZYLACETAMIDE;
2 [5 (PYRIDIN 4 YL) 1,3,4 THIADIAZOL 2 YLTHIO] N BENZYLPROPANAMIDE;
2 [5 (PYRIDIN 4 YL) 1,3,4 THIADIAZOL 2 YLTHIO] N PHENYLACETAMIDE;
2 [5 (PYRIDIN 4 YL) 1,3,4 THIADIAZOL 2 YLTHIO] N PHENYLPROPANAMIDE;
3 [5 (PYRIDIN 4 YL) 1,3,4 THIADIAZOL 2 YLTHIO] N (2 CHLOROPHENYL)PROPANAMIDE;
3 [5 (PYRIDIN 4 YL) 1,3,4 THIADIAZOL 2 YLTHIO] N (2,4 DICHLOROPHENYL)PROPANAMIDE;
3 [5 (PYRIDIN 4 YL) 1,3,4 THIADIAZOL 2 YLTHIO] N (2,6 DICHLOROPHENYL)PROPANAMIDE;
3 [5 (PYRIDIN 4 YL) 1,3,4 THIADIAZOL 2 YLTHIO] N (4 CHLOROPHENYL)PROPANAMIDE;
3 [5 (PYRIDIN 4 YL) 1,3,4 THIADIAZOL 2 YLTHIO] N BENZYLPROPANAMIDE;
3 [5 (PYRIDIN 4 YL) 1,3,4 THIADIAZOL 2 YLTHIO] N PHENYLPROPANAMIDE;
ISONIAZID;
N (2 CHLOROBENZYL) 2 [5 (PYRIDIN 4 YL) 1,3,4 THIADIAZOL 2 YLTHIO]ACETAMIDE;
N (2 CHLOROBENZYL) 2 [5 (PYRIDIN 4 YL) 1,3,4 THIADIAZOL 2 YLTHIO]PROPANAMIDE;
N (2 CHLOROBENZYL) 3 [5 (PYRIDIN 4 YL) 1,3,4 THIADIAZOL 2 YLTHIO]PROPANAMIDE;
N (4 CHLOROBENZYL) 2 [5 (PYRIDIN 4 YL) 1,3,4 THIADIAZOL 2 YLTHIO]ACETAMIDE;
N (4 CHLOROBENZYL) 2 [5 (PYRIDIN 4 YL) 1,3,4 THIADIAZOL 2 YLTHIO]PROPANAMIDE;
N (4 CHLOROBENZYL) 3 [5 (PYRIDIN 4 YL) 1,3,4 THIADIAZOL 2 YLTHIO]PROPANAMIDE;
PYRIDINE DERIVATIVE;
PYRIDINYL THIADIAZOLE DERIVATIVE;
THIADIAZOLE DERIVATIVE;
TUBERCULOSTATIC AGENT;
UNCLASSIFIED DRUG;
UNINDEXED DRUG;
ANTIBACTERIAL ACTIVITY;
ANTIBIOTIC SENSITIVITY;
ARTICLE;
BACTERIAL GROWTH;
BACTERIAL STRAIN;
BACTERIUM ISOLATE;
CELL VIABILITY;
CYTOTOXICITY;
DRUG DESIGN;
DRUG STRUCTURE;
DRUG SYNTHESIS;
EXTENSIVELY DRUG RESISTANT TUBERCULOSIS;
HEPG2 CELL LINE;
IN VITRO STUDY;
MULTIDRUG RESISTANT TUBERCULOSIS;
MYCOBACTERIUM BOVIS;
MYCOBACTERIUM TUBERCULOSIS;
NONHUMAN;
STRUCTURE ACTIVITY RELATION;
CHEMICAL STRUCTURE;
CHEMISTRY;
DOSE RESPONSE;
DRUG EFFECTS;
HUMAN;
MICROBIAL SENSITIVITY TEST;
SYNTHESIS;
TUBERCULOSIS, MULTIDRUG-RESISTANT;
ANTITUBERCULAR AGENTS;
DOSE-RESPONSE RELATIONSHIP, DRUG;
HUMANS;
MICROBIAL SENSITIVITY TESTS;
MOLECULAR STRUCTURE;
MYCOBACTERIUM TUBERCULOSIS;
PYRIDINES;
STRUCTURE-ACTIVITY RELATIONSHIP;
THIADIAZOLES;
TUBERCULOSIS, MULTIDRUG-RESISTANT;
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