Quinazolinone-1,2,3-triazole-acetamide conjugates as potent α-glucosidase inhibitors: synthesis, enzyme inhibition, kinetic analysis, and molecular docking study

Author:

Moghadam Farid Sara1,Iraji Aida23,Mojtabavi Somayeh4,Ghasemi Mehrnaz5,Faramarzi Mohammad Ali4ORCID,Mahdavi Mohammad1,Barazandeh Tehrani Maliheh5,Akbarzadeh Tahmineh56,Saeedi Mina67ORCID

Affiliation:

1. Endocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran

2. Stem Cells Technology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran

3. Central Research Laboratory, Shiraz University of Medical Sciences, Shiraz, Iran

4. Department of Pharmaceutical Biotechnology, Faculty of Pharmacy, Tehran University of Medical Sciences, P.O. Box 14155-6451, Tehran 1417614411, Iran

5. Department of Medicinal Chemistry, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran

6. Persian Medicine and Pharmacy Research Center, Tehran University of Medical Sciences, Tehran, Iran

7. Medicinal Plants Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran

Abstract

In this study, new hybrids of quinazolinone-1,2,3-triazole-acetamide were designed, synthesized, and screened for their α-glucosidase inhibitory activity.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,Biochemistry

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