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Volumn 4, Issue 2, 2012, Pages 517-531

Biological activities of thiadiazole derivatives: A Review

Author keywords

Biological activity; Synthesis; Thiadiazole

Indexed keywords

1,2,3 THIADIAZOLE DERIVATIVE; 1,2,4 THIADIAZOLE DERIVATIVE; 1,2,5 THIADIZOLE DERIVATIVE; 1,3,4 THIADIAZOLE DERIVATIVE; 2 AMINO 5 SULFANYL 1,3,4 THIADIAZOLE; 3 CHLORO 1 [5 (5 CHLORO 2 PHENYL BENZOIMIDAZOL 1 YLMETHYL) 1,3,4]THIADIAZOL 2 YL]AZETIDIN 2 ONE; 3 PHENYL 1,2,4 THIADIAZOLE; 5 [2 (PHENYLTHIO)PHENYL] 1,3,4 THIADIAZOLE DERIVATIVE; 5 ACETYLAMINO[1,3,4]THIADIAZOLE 2 SULFONYL CHLORIDE; 5 ADAMANTYLCARBOXAMIDO 1,3,4 THIADIAZOLE 2 SULFONAMIDE; 5 AMINO 1,3,4 THIADIAZOLE DERIVATIVE; 5 BENZOYLAMIDO 1,3,4 THIADIAZOLE 2 SULFONAMIDE; 5 CYCLOHEXYLAMINO 1,3,4 THIADIAZOLE; 5 PIVALOYLAMIDO 1,3,4 THIADIAZOLE 2 SULFONAMIDE; 5 TOLUENESULFONYLAMIDO 1,3,4 THIADIAZOLE 2 SULFONAMIDE; 7 [4 (5 AMINO[1,3,4]THIADIAZOLE 2 SULFONYL)PIPERAZIN 1 YL]FLUOROQUINOLONES; ANALGESIC AGENT; ANTICONVULSIVE AGENT; ANTIDEPRESSANT AGENT; ANTIDIABETIC AGENT; ANTIINFECTIVE AGENT; ANTIINFLAMMATORY AGENT; ANTINEOPLASTIC AGENT; ANTIOXIDANT; CHEMICAL COMPOUND; DIURETIC AGENT; RADIOPROTECTIVE AGENT; THIADIAZOLE DERIVATIVE; TUBERCULOSTATIC AGENT; UNCLASSIFIED DRUG; UNINDEXED DRUG; 2 (NITROARYL) 5 (NITROBENZYLSULFINYL AND SULFONYL) 1, 3, 4 THIADIAZOLE DERIVATIVE; 3 [5 SUBSTITUTED PHENYL 1, 3, 4 THIADIAZOLE 2 YL] 2 STYRYL QUINAZOLINE 4(3H) ONES; 3 CHLORO 1 [5 (5 CHLORO 2 PHENYL BENZOIMIDAZOL 1 YLMETHYL) 1, 3, 4] THIADIAZOL 2 YL] AZETIDIN 2 ONE; 4 AMINO 2 {5 [(4 SUBSTITUTED PHENYL) AMINO] 1, 3, 4 THIADIAZOLE 2 YL} PHENOL; 5 [2 (PHENYLTHIO) PHENYL]1, 3, 4 THIADIAZOLE DERIVATIVE; 5 AMINO L,3,4 THIADIAZOLE DERIVATIVE; 7[4 (5 AMINO [1,3,4]THIADIAZOLE 2 SULFONYL) PIPERAZIN 1 YL] FLUOROQUINOLONE DERIVATIVE; ACETAZOLAMIDE; ANTIFUNGAL AGENT; ANTIHISTAMINIC AGENT; ANTIMALARIAL AGENT; ANTITHROMBOCYTIC AGENT; DIARYL SUBSTITUTED 2 AMINO 5 SULFANYL 1, 3, 4 THIADIAZOLE DERIVATIVE; DITHIZONE; GLIBENCLAMIDE; MUSCLE RELAXANT AGENT; NONSTEROID ANTIINFLAMMATORY AGENT; PESTICIDE;

EID: 84860608555     PISSN: None     EISSN: 09744290     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (68)

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