3D-quantitative structure-activity relationship and docking studies of coumarin derivatives as tissue kallikrein 7 inhibitors
3D-quantitative structure-activity relationship and docking studies of coumarin derivatives as tissue kallikrein 7 inhibitors
复制标题
香豆素衍生物作为组织激肽释放酶 7 抑制剂的 3D 定量结构-活性关系和对接研究
DOI：
10.1111/jphp.12751
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发表时间：
2017
影响因子：
3.3
通讯作者：
Liu Sen
中科院分区：
文献类型：
--
作者：
Zheng Xin;He Mengxi;Tan Xiao;Zheng Jun;Wang Fangyu;Liu Sen
ObjectivesKallikrein 7 (KLK7) is a secreted serine protease that plays important roles in skin desquamation and tumour progression, which makes it an attracting drug target. To guide the design of KLK7 inhibitors, a series of coumarin-based inhibitors were used to perform 3D-quantitative structure–activity relationship analysis.Methods3D conformations of 37 inhibitors were generated and used to construct CoMFA and CoMSIA models. Then a complex model between the inhibitors and KLK7 was built with molecular docking.Key findingsWith the training set, the CoMFA and CoMSIA models achievedq2values of 0.521 and 0.498, andr2values of 0.942 and 0.983, respectively. With the testing set, the predictedr2values were 0.663 and 0.669, respectively, for CoMFA and CoMSIA. 3D contour maps from these two models identified steric and hydrophobic interactions as the most important molecular features of these inhibitors. Furthermore, molecular docking study was performed to understand the binding modes between these compounds and KLK7, in which the critical steric and hydrophobic interactions between the inhibitors and KLK7 were confirmed.ConclusionsSteric and hydrophobic interactions are critical in the efficient binding of KLK7 inhibitors. Our analysis would provide a meaningful guideline for the rational design of novel KLK7 inhibitors.
