中文关键词:氨基恶唑啉呫吨BACE1抑制剂特征结构 分子对接作用机制 英文关键词:Aminooxazolinexanthene BACE1 inhibitors, Structuralfeatures, Moleculardocking, Interactionmechanism 基金项目:

作者	单位	E-mail
吴倩	潍坊学院化学化工与环境工程学院	wuqianwq2006@163.com
高庆平	潍坊职业学院化学工程学院
刘莉	潍坊学院化学化工与环境工程学院
李丹	潍坊学院化学化工与环境工程学院
李燕	大连理工大学化工与环境生命学部材料科学与化工系
杨凌	中国科学院大连化学物理研究所药物资源开发研究组

摘要点击次数:1612 全文下载次数:0 中文摘要: β-分泌酶(BACE1)是治疗阿尔兹海默症(AD)的潜在靶点,BACE1抑制剂的开发已成为治疗AD的重要方向。本文运用比较分子相似性指数(CoMSIA)和分子对接法对66个氨基恶唑啉呫吨类BACE1抑制剂进行模拟分析,建立了可靠的构效关系预测模型(Q₂=0.86, R_ncv2=0.97, R_pre2=0.88),揭示了影响分子抑制活性的重要特征结构信息,发现抑制剂通过与BACE1之间形成的氢键作用和π-π堆积作用占据了分泌酶的S3、S1和S2"三个活性位点。实验所得模型和信息为后续新型高效BACE1抑制剂的结构优化和改造提供了重要的理论指导。 英文摘要: β-secretase (BACE1) is a potent target for Alzheimer"s disease (AD). Inhibition of BACE1 has gained considerable attention as a potential disease-modifying treatment of AD. In this study, 66 aminooxazoline xanthene-based BACE1 inhibitors were simulated by comparative molecular similarity index (CoMSIA) and molecular docking methods. A reliable prediction model of structure-activity relationship (Q₂= 0.86, R_ncv2=0.97, R_pre2= 0.88) was constructed, revealing the important structural features information that influences the inhibitory activity of the molecules. Moreover, it was found that the inhibitor occupies S3, S1 and S2" active sites of target through hydrogen bonding and π-π stacking interactions formed with BACE1. The model and information deduced from this in silico analysis provide important theoretical guidance for the structural optimization and modification of new and efficient BACE1 inhibitors. 查看全文查看/发表评论下载PDF阅读器 相关附件：附件1附件2附件3版权转让声明书附件1附件2 -->