Discovery of novel thiazole derivatives containing pyrazole scaffold as PPAR-γ Agonists, α-Glucosidase, α-Amylase and COX-2 inhibitors; Design, synthesis and in silico study-Reference-Cited by-同舟云学术

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Discovery of novel thiazole derivatives containing pyrazole scaffold as PPAR-γ Agonists, α-Glucosidase, α-Amylase and COX-2 inhibitors; Design, synthesis and in silico study

Published:2024-11 Issue: Volume:152 Page:107760
ISSN:0045-2068
Container-title:Bioorganic Chemistry
language:en
Short-container-title:Bioorganic Chemistry

Author:

Fadaly Wael A.A.,Elshewy Ahmed,Nemr Mohamed T.M.,Abdou Kareem,Sayed Ahmed M.,Kahk Nesma M.

Publisher

Elsevier BV

Reference54 articles.

1. Potential of Potentilla Inclinata and its polyphenolic compounds in α-glucosidase inhibition: Kinetics and interaction mechanism merged with docking simulations;Sohretoglu;J. Biol. Macromol.,2018

2. Screening of α-glucosidase inhibitors from houttuynia cordata and evaluation of the binding mechanisms;Zhang;ChemistrySelect,2020

3. Alpha-amylase inhibition can treat diabetes mellitus;Agarwal;J. Health Sci. Res.,2016

4. Therapeutic potential of α-glucosidase inhibitors in type 2 diabetes mellitus: an evidence-based review;Joshi;Expert Opin Pharmacother.,2015

5. Design and synthesis of novel thiazolidine-2,4-diones as hypoglycemic agents;Datar;J. Saudi Chem. Soc.,2016

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