Synthesis of 1,2,3-benzotriazin-4(3H)-one derivatives as α-glucosidase inhibitor and their in-silico study
Author:
Publisher
Springer Science and Business Media LLC
Subject
Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics
Link
https://link.springer.com/content/pdf/10.1007/s00044-022-02883-1.pdf
Reference25 articles.
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2. Alomari M, Taha M, Rahim F, Selvaraj M, Iqbal N, Chigurupati S, et al. Synthesis of indole-based-thiadiazole derivatives as a potent inhibitor of α-glucosidase enzyme along with in silico study. Bioorg Chem. 2021;108:104638 https://doi.org/10.1016/j.bioorg.2021.104638
3. Seo WD, Kim JH, Kang JE, Ryu HW, Curtis-Long MJ, Lee HS, et al. Sulfonamide chalcone as a new class of α-glucosidase inhibitors. Bioorg Med Chem Lett. 2005;15:5514–6. https://doi.org/10.1016/j.bmcl.2005.08.087
4. Kausar N, Ullah S, Khan MA, Zafar H, Choudhary MI, Yousuf S. Celebrex derivatives: synthesis, α-glucosidase inhibition, crystal structures and molecular docking studies. Bioorg Chem. 2021;106:104499 https://doi.org/10.1016/j.bioorg.2020.104499
5. Akocak S, Taslimi P, Lolak N, Işık M, Durgun M, Budak Y, et al. Synthesis, Characterization, and Inhibition Study of Novel Substituted Phenylureido Sulfaguanidine Derivatives as α‐Glycosidase and Cholinesterase Inhibitors. Chem Biodivers. 2021;18:e2000958 https://doi.org/10.1002/cbdv.202000958
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