Synthesis of novel indazole derivatives as inhibitors of diabetics II along with molecular docking and simulation study

In the light of the pharmacological significance of the indazole and 1, 3, 4-thiadiazole scaffold, hybrid analogs of indazole and 1, 3, 4-thiadiazole (1–14) were synthesized, identified using HREI-MS, 1H, and 13CNMR, and their capability for inhibition of α-amylase and α-glucosidase enzymes was eval...

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发表在:Journal of Molecular Structure
主要作者: 2-s2.0-85207018388
格式: 文件
语言:English
出版: Elsevier B.V. 2025
在线阅读:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85207018388&doi=10.1016%2fj.molstruc.2024.140394&partnerID=40&md5=e5be6169fdf74e8e5fb1445f9c0aed02