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基于药效团模型、虚拟筛选和分子对接研究发现潜在的整合素 VLA-4 拮抗剂。

Discovery of potential integrin VLA-4 antagonists using pharmacophore modeling, virtual screening and molecular docking studies.

机构信息

Department of Biochemistry and Division of Applied Life Science (BK21 Program), Environmental Biotechnology National Core Research Center, Gyeongsang National University, 900 Gazwa-dong, Jinju 660-701, Korea.

出版信息

Chem Biol Drug Des. 2011 Aug;78(2):289-300. doi: 10.1111/j.1747-0285.2011.01127.x. Epub 2011 Jun 20.

Abstract

Very late antigen-4 (VLA-4) is an integrin protein, and its antagonists are useful as anti-inflammatory drugs. The aim of this study is to discover novel virtual lead compounds to use them in designing potent VLA-4 antagonists. A best pharmacophore model was generated with correlation coefficient of 0.935, large cost difference of 114.078, comprising two hydrogen bond acceptors and three hydrophobic features. It was further validated and used in database screening for potential VLA-4 antagonists. A homology model of VLA-4 was built and employed in molecular docking of screened hit compounds. Finally, two compounds were identified as potential virtual leads to be deployed in the designing of novel potent VLA-4 antagonists.

摘要

非常晚期抗原-4(VLA-4)是一种整合素蛋白,其拮抗剂可用作抗炎药物。本研究旨在发现新的虚拟先导化合物,用于设计有效的 VLA-4 拮抗剂。生成了一个最佳药效团模型,相关系数为 0.935,成本差异大,为 114.078,包含两个氢键受体和三个疏水性特征。进一步验证并用于潜在 VLA-4 拮抗剂的数据库筛选。构建了 VLA-4 的同源模型,并将其用于筛选出的命中化合物的分子对接。最后,鉴定出两种化合物作为潜在的虚拟先导化合物,用于设计新型有效的 VLA-4 拮抗剂。

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