物理化学学报 >> 2003, Vol. 19 >> Issue (12): 1108-1113.doi: 10.3866/PKU.WHXB20031203

研究论文 上一篇    下一篇

二氢吡啶类化合物的三维定量构效关系

丁俊杰;丁晓琴;赵立峰;陈冀胜   

  1. 北京药物化学研究所,北京 102205
  • 收稿日期:2003-05-12 修回日期:2003-07-25 发布日期:2003-12-15
  • 通讯作者: 丁晓琴 E-mail:dingxq@cetin.net.cn

Three Dimensional Quantitative Structure-activity Relationship of Dihydropyridine Derivatives

Ding Jun-Jie;Ding Xiao-Qin;Zhao Li-Feng;Chen Ji-Sheng   

  1. Beijing Institute of Pharmaceutical Chemistry, Beijing 102205
  • Received:2003-05-12 Revised:2003-07-25 Published:2003-12-15
  • Contact: Ding Xiao-Qin E-mail:dingxq@cetin.net.cn

摘要: 通过分子力学和量子化学计算,得出两种二氢吡啶衍生物的低能构象,再应用比较分子力场分析方法(CoMFA)和比较分子相似性指数分析方法(CoMSIA)分别对两种构象的43个二氢吡啶衍生物进行3D-QSAR研究. 计算结果表明,用两种方法建立的两种构象的构效关系模型均有较好的预测能力.通过分析CoMFA和CoMSIA的系数等势图,直观地了解二氢吡啶衍生物的结构对生物活性的影响,为进一步设计高活性的二氢吡啶衍生物提供一定的理论依据.

关键词: 二氢吡啶(DHP), 钙离子通道拮抗剂, 三维定量构效关系(3D-QSAR), 比较分子力场分析(CoMFA), 比较分子相似性指数分析(CoMSIA)

Abstract: Two minimum energy conformations of DHPs were obtained by molecular mechanics and quantum chemistry calculation. In the studies of 3D-QSAR,comparative molecular fields analysis (CoMFA) and comparative similarity indices analysis (CoMSIA) were applied using a data set of 43 DHPs of two-conformations. The results indicate that the models of two-conformations, investigated by the two kinds of 3D-QSAR techniques, are significant and have good predictability. The analysis of steric and electrostatic CoMFA and CoMSIA coefficients contour maps reveals the influence of the structures on biological activity and gives insights to the further design of highly active DHPs compounds.

Key words: Dihydropyridine(DHP), Calcium antagonist, 3D-QSAR, CoMFA, CoMSIA