H.E.J. Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University of Karachi, Karachi-75270, Pakistan
Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi-75270, Pakistan
Med Chem. 2020;16(6):826-840. doi: 10.2174/1573406415666190612153150.
Results of our previous studies on antiglycation activity, and the noncytotoxicity of 2-mercapto benzothiazoles, encouraged us to further widen our investigation towards the identification of leads against diabetes mellitus.
33 derivatives of 2-mercapto benzothiazoles 1-33 were evaluated for in vitro α- glucosidase inhibitory activity. Mode of inhibition was deduced by kinetic studies. To predict the interactions of 2-mercapto benzothiazole derivatives 1-33 with the binding pocket of α-glucosidase enzyme, molecular docking studies were performed on the selected inhibitors.
Compounds 2-4, 6-7, 9-26, 28 and 30 showed many folds potent α-glucosidase inhibitory activity in the range of IC50 = 31.21-208.63 μM, as compared to the standard drug acarbose (IC50 = 875.75 ± 2.08 μM). It was important to note that except derivative 28, all other derivatives were also found previously to have antiglycating potential in the range of IC50 = 187.12-707.21 μM.
A number of compounds were identified as dual nature as antiglycating agent and α- glucosidase inhibitors. These compounds may serve as potential lead candidates for the management of diabetes mellitus.
我们之前关于糖基化抑制活性和 2-巯基苯并噻唑非细胞毒性的研究结果,鼓励我们进一步扩大研究范围,以寻找抗糖尿病的潜在药物。
评估了 33 种 2-巯基苯并噻唑 1-33 的衍生物的体外α-葡萄糖苷酶抑制活性。通过动力学研究推断抑制模式。为了预测 2-巯基苯并噻唑衍生物 1-33 与α-葡萄糖苷酶酶结合口袋的相互作用,对选定的抑制剂进行了分子对接研究。
与标准药物阿卡波糖(IC50=875.75±2.08μM)相比,化合物 2-4、6-7、9-26、28 和 30 的α-葡萄糖苷酶抑制活性在 IC50=31.21-208.63μM 的范围内表现出多倍活性。值得注意的是,除了衍生物 28 之外,所有其他衍生物之前在 IC50=187.12-707.21μM 的范围内也被发现具有糖化抑制潜力。
发现一些化合物具有双重性质,既是糖化抑制剂又是α-葡萄糖苷酶抑制剂。这些化合物可能成为治疗糖尿病的潜在候选药物。