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通过从头进化、合成、生物评价和分子动力学模拟鉴定蛋白酪氨酸磷酸酶 1B(PTP1B)抑制剂。

Identification of protein tyrosine phosphatase 1B (PTP1B) inhibitors through De Novo Evoluton, synthesis, biological evaluation and molecular dynamics simulation.

机构信息

Tianjin Key Laboratory on Technologies Enabling Development of Clinical Therapeutics and Diagnostics (Theranostics), School of Pharmacy, Tianjin Medical University, Tianjin, 300070, China.

Tianjin Key Laboratory on Technologies Enabling Development of Clinical Therapeutics and Diagnostics (Theranostics), School of Pharmacy, Tianjin Medical University, Tianjin, 300070, China.

出版信息

Biochem Biophys Res Commun. 2020 May 21;526(1):273-280. doi: 10.1016/j.bbrc.2020.03.075. Epub 2020 Mar 21.

Abstract

Protein tyrosine phosphatase 1B (PTP1B) is a widely expressed 50 kDa enzyme and the first intracellular PTP to be purified from human placental tissue. It has been proved that protein tyrosine phosphatase 1B played a significant role in the negative regulation of insulin signaling pathway and overexpression of PTP1B could lead to the decrease of insulin resistance. Therefore PTP1B has emerged as a novel promising therapeutic target for the treatment of type-2 diabetes mellitus. Computer aided drug design (CADD), chemical synthesis and biological activity assay resulted in the identification of a novel potent PTP1B inhibitor, compound 1a, which shared an IC value of 4.46 μM. Finally, the analysis of molecular dynamics simulation provided the theoretical basis for favorable activity of compound 1a.

摘要

蛋白酪氨酸磷酸酶 1B(PTP1B)是一种广泛表达的 50kDa 酶,也是第一个从人胎盘组织中纯化出来的细胞内 PTP。已经证明,蛋白酪氨酸磷酸酶 1B 在胰岛素信号通路的负调控中发挥着重要作用,而过表达 PTP1B 会导致胰岛素抵抗的降低。因此,PTP1B 已成为治疗 2 型糖尿病的一个有前途的新型治疗靶点。计算机辅助药物设计(CADD)、化学合成和生物活性测定,确定了一种新型有效的 PTP1B 抑制剂,化合物 1a,其 IC 值为 4.46μM。最后,分子动力学模拟分析为化合物 1a 的良好活性提供了理论依据。

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