Recent Advancement in Synthesis and Bioactivities of 1,3,4-Oxadiazole.

Oxadiazole antibacterial anticancer cyclisation heterocyclic synthetic compounds

Journal

Current organic synthesis
ISSN: 1570-1794
Titre abrégé: Curr Org Synth
Pays: United Arab Emirates
ID NLM: 101208457

Informations de publication

Date de publication:
2023
Historique:
received: 17 06 2022
revised: 31 08 2022
accepted: 21 10 2022
medline: 1 6 2023
pubmed: 2 12 2022
entrez: 1 12 2022
Statut: ppublish

Résumé

Derivatives of 1,3,4-oxadiazole are effective in the treatment and cure of a wide range of diseases in medical chemistry, while industrial development has shown that they can be utilised as corrosion inhibitors and light-emitting diodes. The researchers discovered several promising synthetic strategies that created 1,3,4-oxadiazoles in extraordinarily high yields while using environmentally friendly methods. These compounds can potentially be used in a wide range of lifechanging applications. Stable isomeric oxadiazole forms of pleconaril, raltegravir, butalamine, fasiplon, oxolamine, and several other drugs are among the numerous potent and effective pharmaceuticals that are now on the market. Fasiplon, butalamine, raltegravir, and pleconaril treat HIV/AIDS patients. This article has attempted to bring attention to the chemistry and pharmacology of oxadiazole and its derivatives. Oxadiazole derivatives have been used extensively as prospective therapeutic agents in clinical research, and this has become standard practice. The use of biological and in-silico models has enabled scientists to identify more synthetic analogues of cancer prevention, antifungal, and anti-HIV medications. This article provides recent information regarding procedures for synthesizing 1,3,4-oxadiazoles and their biological actions on the body.

Identifiants

pubmed: 36453511
pii: COS-EPUB-127909
doi: 10.2174/1570179420666221129153933
doi:

Substances chimiques

1,3,4-oxadiazole 20O2F20OUR
Raltegravir Potassium 43Y000U234
Oxadiazoles 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

663-677

Informations de copyright

Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Auteurs

Tarun Chaudhary (T)

Institute of Pharmaceutical Research, GLA University, Mathura, 281406, Uttar Pradesh, India.

Prabhat Kumar Upadhyay (PK)

Institute of Pharmaceutical Research, GLA University, Mathura, 281406, Uttar Pradesh, India.

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Classifications MeSH