1,3,4-Oxadiazole Scaffold in Antidiabetic Drug Discovery: An Overview
- PMID: 38644715
- DOI: 10.2174/0113895575298181240410041029
1,3,4-Oxadiazole Scaffold in Antidiabetic Drug Discovery: An Overview
Abstract
Diabetes mellitus is one of the biggest challenges for the scientific community in the 21st century. With the increasing number of cases of diabetes and drug-resistant diabetes, there is an urgent need to develop new potent molecules capable of combating this cruel disease. Medicinal chemistry concerns the discovery, development, identification, and interpretation of the mode of action of biologically active compounds at the molecular level. Oxadiazole-based derivatives have come up as a potential option for antidiabetic drug research. Oxadiazole is a five-membered heterocyclic organic compound containing two nitrogen atoms and one oxygen atom in its ring. Oxadiazole hybrids have shown the ability to improve glucose tolerance, enhance insulin sensitivity, and reduce fasting blood glucose levels. The mechanisms underlying the antidiabetic effects of oxadiazole involve the modulation of molecular _targets such as peroxisome proliferator-activated receptor gamma (PPARγ), α-glucosidase, α-amylase and GSK-3β which regulate glucose metabolism and insulin secretion. The present review article describes the chemical structure and properties of oxadiazoles and highlights the antidiabetic activity through action on different _targets. The SAR for the oxadiazole hybrids has been discussed in this article, which will pave the way for the design and development of new 1,3,4-oxadiazole derivatives as promising antidiabetic agents in the future. We expect that this article will provide comprehensive knowledge and current innovation on oxadiazole derivatives with antidiabetic potential and will fulfil the needs of the scientific community in designing and developing efficacious antidiabetic agents.
Keywords: Antidiabetic drug _targets; Diabetes; GSK-3β.; SAR; Type 2 diabetes; oxadiazole.
Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.
Similar articles
-
Anti-tuberculosis activity and its structure-activity relationship (SAR) studies of oxadiazole derivatives: A key review.Eur J Med Chem. 2021 Jan 1;209:112886. doi: 10.1016/j.ejmech.2020.112886. Epub 2020 Sep 29. Eur J Med Chem. 2021. PMID: 33032083 Review.
-
Oxadiazole: A highly versatile scaffold in drug discovery.Arch Pharm (Weinheim). 2022 Sep;355(9):e2200123. doi: 10.1002/ardp.202200123. Epub 2022 May 16. Arch Pharm (Weinheim). 2022. PMID: 35575467 Review.
-
Alpha-amylase as molecular _target for treatment of diabetes mellitus: A comprehensive review.Chem Biol Drug Des. 2021 Oct;98(4):539-560. doi: 10.1111/cbdd.13909. Epub 2021 Jul 4. Chem Biol Drug Des. 2021. PMID: 34173346 Review.
-
Substituted oxadiazoles: a patent review (2010 - 2012).Expert Opin Ther Pat. 2013 Sep;23(9):1209-32. doi: 10.1517/13543776.2013.797409. Epub 2013 May 10. Expert Opin Ther Pat. 2013. PMID: 23663160 Review.
-
Oxadiazole scaffolds in anti-tuberculosis drug discovery.Bioorg Med Chem Lett. 2019 Aug 15;29(16):1999-2007. doi: 10.1016/j.bmcl.2019.06.054. Epub 2019 Jun 28. Bioorg Med Chem Lett. 2019. PMID: 31296357 Review.
References
-
- Tattersall R.B.; Matthews D.R.; The history of diabetes mellitusTextbook of Diabetes 2010,1-23
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous