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通过基于结构的虚拟筛选发现新型糖原合成酶激酶-3β抑制剂

Discovery of new GSK-3β inhibitors through structure-based virtual screening.

作者信息

Dou Xiaodong, Jiang Lan, Wang Yanxing, Jin Hongwei, Liu Zhenming, Zhang Liangren

机构信息

State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing 100191, China.

State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing 100191, China.

出版信息

Bioorg Med Chem Lett. 2018 Jan 15;28(2):160-166. doi: 10.1016/j.bmcl.2017.11.036. Epub 2017 Nov 24.

Abstract

Glycogen synthase kinase-3β (GSK-3β) is an attractive therapeutic target for human diseases, such as diabetes, cancer, neurodegenerative diseases, and inflammation. Thus, structure-based virtual screening was performed to identify novel scaffolds of GSK-3β inhibitors, and we observed that conserved water molecules of GSK-3β were suitable for virtual screening. We found 14 hits and D1 (IC of 0.71 μM) were identified. Furthermore, the neuroprotection activity of D1-D3 was validated on a cellular level. 2D similarity searches were used to find derivatives of high inhibitory compounds and an enriched structure-activity relationship suggested that these skeletons were worthy of study as potent GSK-3β inhibitors.

摘要

糖原合酶激酶-3β(GSK-3β)是治疗糖尿病、癌症、神经退行性疾病和炎症等人类疾病的一个有吸引力的治疗靶点。因此,进行了基于结构的虚拟筛选以识别GSK-3β抑制剂的新型骨架,并且我们观察到GSK-3β的保守水分子适用于虚拟筛选。我们发现了14个命中化合物,并鉴定出D1(IC为0.71μM)。此外,在细胞水平上验证了D1-D3的神经保护活性。使用二维相似性搜索来寻找高抑制性化合物的衍生物,并且丰富的构效关系表明这些骨架作为有效的GSK-3β抑制剂值得研究。

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