【作者】 马玉卓； 陈静波； 刘鹰翔； 阎冬； 程卯生；

【Author】 MA Yuzhuo1,CHEN Jingbo2,LIU Yingxiang1,YAN Dong3,CHEN Maosheng3 (1. Department of Medicinal Chemistry, Guangdong Pharmaceutical University, Guangzhou 510006, China; 2. College of Pharmacy, Yunnan University, Kunming 650091, China; 3. School of Pharmaceutical Engineering, Shenyang Pharmaceutical University, Shenyang 110016, China)

【机构】 广东药学院药物化学系； 云南大学教育部自然资源药物化学重点实验室； 沈阳药科大学制药工程学院；

【摘要】 目的:本文利用比较分子力场方法,建立5-脂氧合酶/环氧合酶抑制剂的三维定量构效关系,为设计新的更有效的酶抑制剂提供理论依据。方法和结果:在CoMFA分析中,交叉验证回归系数R2CV、非交叉验证回归系数r2和标准偏差SEE分别为0.639,0.744,0.148。说明系列化合物分子周围立体场和静电场的分布与抗炎活性间有良好的相关性。利用该模型对本室合成的24个化合物进行活性预测,结果与实测值相符。结论:所得模型支持了假设的抑制剂作用机理和作用模型。所得CoMFA模型具有一定的预测能力,可用来指导设计新的5-脂氧合酶/环氧合酶抑制剂。更多还原

【Abstract】 Aim Comparative molecular field analysis (CoMFA) was performed to study 3D-QSAR of (E)-4-cinnamoyloxy-3-methoxystyrene derivatives with biological activity in order to give a theoretical basis to design novel more effective enzyme dual inhibitor. Methods and Result In this analysis, the cross validated coefficient R2CV was found to be 0.639,non-cross validated coefficient r2 and the standard deviation SEE was 0.744 and 0.148 respectively, and F was 198.355. The CoMFA models for twenty four of (E)-4-cinnamoyloxy-3-methoxystyrene derivatives showed the good relationship between steric and electrostatic properties with anti-inflammatory activity, which were very helpful for designing novel compounds as 5-lipoxygenase/cyclooxygenase inhibitor.更多还原