Article ID Journal Published Year Pages File Type
1400025 European Journal of Medicinal Chemistry 2006 11 Pages PDF
Abstract

Several 3,6-disubstituted-1,2,4-triazolo[3,4-b]-1,3,4-thiadizoles were prepared by the condensation of 4-amino-3-aryl/aralkyl substituted-5-mercapto-1,2,4-triazoles 3(a–c) with various substituted aromatic/hetero aromatic acids through a single step reaction. Elemental analysis, IR, 1H NMR and mass spectral data confirmed the structure of the newly synthesized compounds. Synthesized triazolo thiadiazoles investigated for their antibacterial, antifungal, anti-inflammatory and analgesic activities. Some of the tested compounds showed moderate antimicrobial activity against various tested bacterial and fungal strains. None of the synthesized compounds have significant anti-inflammatory and analgesic activities.

Graphical abstractA series of 3,6-disubstituted 1,2,4-triazolo[3,4-b]-thiadiazoles was synthesized and evaluated for their antibacterial, antifungal, anti-inflammatory and analgesic activities. Some of synthesized compounds showed moderate antimicrobial activities against tested bacterial and fungal strains.Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
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