A PANACROMIC REVIEW ON OXADIAZOLE SCAFFOLDS AND THEIR POTENTIAL ANTI-MYCOBACTERIAL ACTIVITY
Authors: Das P , RAMYA A, NAYAK A, GAZMER A, RAJU R AND TEJASWINI R

ABSTRACT
Heterocyclic compounds form the main family of organic compounds. These are of enormous importance for a variety of synthetic, pharmaceutical, and industrial applications and are known for their biological activities. Oxadiazole or furadiazole is a five-membered ring containing two carbons, one oxygen atom, two nitrogen atoms, and two double bonds. They are derived from furan by replacing two nitrogen atoms (N =) with two methylene groups (= CH). The particular structural feature of the 1,3,4-oxadiazole ring with pyridine nitrogen atom type is advantageous for binding effectively with various enzymes and receptors in biological systems through numerous weak interactions, thereby exhibiting various pharmacological activities. Compounds containing the 1,3,4-oxadiazole moiety have recently received attention for their antiviral, anti-inflammatory, anti-tuberculous, anti-cancer, anti- parasitic, enzyme-inhibiting, antioxidant, anti-bacterial, and anti-fungal potentials. These are the results of recent developments in the synthesis and anti-tubercular activity of 1,3,4- oxadiazole candidates over the past 15 years. It is believed that this review will be of great help for new ideas in the search for rational designs for the development of more active and less toxic 1,3,4-oxadiazole-based drugs as an anti-tubercular. Keywords: 1,3,4-Oxadiazole, Anticancer, Anti-microbial. Anti-oxidant, Furadiazole, Anti-tubercular
Publication date: 01/11/2023
    https://ijbpas.com/pdf/2023/November/MS_IJBPAS_2023_7543.pdf
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https://doi.org/10.31032/IJBPAS/2023/12.11.7543