Tetrazoles and Related Heterocycles as Promising Synthetic Antidiabetic Agents
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES(2023)
Abstract
Tetrazole heterocycle is a promising scaffold in drug design, and it is incorporated into active pharmaceutical ingredients of medications of various actions: hypotensives, diuretics, antihistamines, antibiotics, analgesics, and others. This heterocyclic system is metabolically stable and easily participates in various intermolecular interactions with different biological targets through hydrogen bonding, conjugation, or van der Waals forces. In the present review, a systematic analysis of the activity of tetrazole derivatives against type 2 diabetes mellitus (T2DM) has been performed. As it was shown, the tetrazolyl moiety is a key fragment of many antidiabetic agents with different activities, including the following: peroxisome proliferator-activated receptors (PPARs) agonists, protein tyrosine phosphatase 1B (PTP1B) inhibitors, aldose reductase (AR) inhibitors, dipeptidyl peptidase-4 (DPP-4) inhibitors and glucagon-like peptide 1 (GLP-1) agonists, G protein-coupled receptor (GPCRs) agonists, glycogen phosphorylases (GP) Inhibitors, alpha-glycosidase (AG) Inhibitors, sodium glucose co-transporter (SGLT) inhibitors, fructose-1,6-bisphosphatase (FBPase) inhibitors, IkB kinase epsilon (IKK epsilon) and TANK binding kinase 1 (TBK1) inhibitors, and 11 beta-hydroxysteroid dehydrogenase type 1 (11 beta-HSD1). In many cases, the tetrazole-containing leader compounds markedly exceed the activity of medications already known and used in T2DM therapy, and some of them are undergoing clinical trials. In addition, tetrazole derivatives are very often used to act on diabetes-related targets or to treat post-diabetic disorders.
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Key words
tetrazoles,antidiabetic agents,type 2 diabetes mellitus,peroxisome proliferator-activated receptors (PPARs) agonists,aldose reductase (AR) inhibitors,dipeptidyl peptidase-4 (DPP-4) inhibitors,G protein-coupled receptor (GPCRs) agonists
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