Discovery of novel 6-(piperidin-1-ylsulfonyl)-2H-chromenes targeting α-glucosidase, α-amylase, and PPAR-γ: Design, synthesis, virtual screening, and anti-diabetic activity for type 2 diabetes mellitus
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Published:2024-08
Issue:
Volume:111
Page:108097
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ISSN:1476-9271
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Container-title:Computational Biology and Chemistry
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language:en
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Short-container-title:Computational Biology and Chemistry
Author:
Thabet Hamdy Khamees,
Abusaif Moustafa S.,
Imran MohdORCID,
Helal Mohamed Hamdy,
Alaqel Saleh Ibrahim,
Alshehri Ahmed,
Mohd Abida Ash,
Ammar Yousry A.,
Ragab AhmedORCID
Reference68 articles.
1. Developing a new multi-featured chitosan-quinoline Schiff base with potent antibacterial, antioxidant, and antidiabetic activities: design and molecular modeling simulation;Abdel-Baky;Sci. Rep.,2023
2. A novel of quinoxaline derivatives tagged with pyrrolidinyl scaffold as a new class of antimicrobial agents: Design, synthesis, antimicrobial activity, and molecular docking simulation;Abdelgalil;J. Mol. Struct.,2023
3. Triazoloquinazolines as a new class of potent $α$-glucosidase inhibitors: in vitro evaluation and docking study;Abuelizz;PLoS One,2019
4. Multiple binding modes of inhibitors to carbonic anhydrases: how to design specific drugs targeting 15 different isoforms?;Alterio;Chem. Rev.,2012
5. Comparative metabolic study of the chloroform fraction of three Cystoseira species based on UPLC/ESI/MS analysis and biological activities;Aly;J. Enzym. Inhib. Med. Chem.,2024
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