| Literature DB >> 34173346 |
Navjot Kaur1, Vanktesh Kumar1, Surendra Kumar Nayak1, Pankaj Wadhwa1, Paranjit Kaur1, Sanjeev Kumar Sahu1.
Abstract
The alpha (α)-amylase is a calcium metalloenzyme that aids digestion by breaking down polysaccharide molecules into smaller ones such as glucose and maltose. In addition, the enzyme causes postprandial hyperglycaemia and blood glucose levels to rise. α-Amylase is a well-known therapeutic target for the treatment and maintenance of postprandial blood glucose elevations. Various enzymatic inhibitors, such as acarbose, miglitol and voglibose, have been found to be effective in targeting this enzyme, prompting researchers to express an interest in developing potent alpha-amylase inhibitor molecules. The review mainly focused on designing different derivatives of drug molecules such as benzofuran hydrazone, indole hydrazone, spiroindolone, benzotriazoles, 1,3-diaryl-3-(arylamino) propan-1-one, oxadiazole and flavonoids along with their target-receptor interactions, IC50 values and other biological activities.Entities:
Keywords: alpha-amylase; alpha-amylase inhibitors; antidiabetic drug; diabetes mellitus; molecular target
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Year: 2021 PMID: 34173346 DOI: 10.1111/cbdd.13909
Source DB: PubMed Journal: Chem Biol Drug Des ISSN: 1747-0277 Impact factor: 2.817