Synthesis, α-glucosidase and α-amylase inhibitory activities, acute toxicity and molecular docking studies of thiazolidine-2,4-diones derivatives


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Output type: Journal article

UM6P affiliated Publication?: Yes

Author list: Fettach S., Thari F.Z., Hafidi Z., Tachallait H., Karrouchi K., El achouri M., Cherrah Y., Sefrioui H., Bougrin K., Faouzi M.E.A.

Publisher: Taylor & Francis: STM, Behavioural Science and Public Health Titles

Publication year: 2021

Journal: Journal of Biomolecular Structure and Dynamics (0739-1102)

ISSN: 0739-1102

eISSN: 1538-0254

URL: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85104427316&doi=10.1080%2f07391102.2021.1911854&partnerID=40&md5=118c16bfcdbf3ebd47dfab34687a7134

Languages: English (EN-GB)


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Abstract

In the present study, a series of thiazolidine-2,4-diones derivatives (3a–3e) and (4a–4e) were synthesized and characterized by 1H NMR, 13C NMR and ESI-MS spectrometry. All compounds were screened for their α-glucosidase and α-amylase inhibitory activities. In vitro biological investigations revealed that most of compounds were active against α-glucosidase with IC50 values in the range of 43.85 ± 1.06 to 380.10 ± 1.02 µM, and α-amylase with IC50 in the range of 18.19 ± 0.11 to 208.10 ± 1.80 µM. Some of the tested compounds were found to be more potent inhibitors than the clinical drug Acarbose (IC50glucosidase = 97.12 ± 0.35 µM and IC50amylase = 2.97 ± 0.004 μM). The lead compounds were evaluated for their acute toxicity on Swiss mice and found to be completely non-toxic with LD > 2000 mg/kg BW. Furthermore, the Structure–activity relationship (SAR) and the binding interactions of all compounds with the active site of α-glucosidase and α-amylase were confirmed through molecular docking and stabilizing energy calculations. This study has identified the inhibitory potential a new class of synthesized thiazolidine-2,4-diones in controlling both hyperglycemia and type 2 diabetes mellitus. Furthermore, the theoretical binding mode of the target molecules was evaluated by molecular docking studies against the 3D Crystal Structure of human pancreatic α-amylase (PDB ID: 1B2Y) and α-glucosidase (PDB ID: 3W37) Communicated by Ramaswamy H. Sarma. © 2021 Informa UK Limited, trading as Taylor & Francis Group.


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Last updated on 2021-30-11 at 23:20