浙江大学学报(理学版)
浙江大學學報(理學版)
절강대학학보(이학판)
JOURNAL OF ZHEJIANG UNIVERSITY
2010年
2期
204-209
,共6页
桑鹏%邹建卫%胡桂香%蒋勇军%俞庆森
桑鵬%鄒建衛%鬍桂香%蔣勇軍%俞慶森
상붕%추건위%호계향%장용군%유경삼
互变异构现象%定量结构-活性关系%分子表面静电势%TRPV1通道拮抗剂
互變異構現象%定量結構-活性關繫%分子錶麵靜電勢%TRPV1通道拮抗劑
호변이구현상%정량결구-활성관계%분자표면정전세%TRPV1통도길항제
tautomerism%QSAR%molecular electrostatic potential%TRPVl channel antagonists
研究了吲唑脲类辣椒素受体(TRPV1)通道拮抗荆的定量构效关系(QSAR).首先,采用1H-吲唑异构形式,时27个TRPV1通道拮抗剂分子进行了HF/6·31G~*水平上的结构优化,在优化结构上进行了5类拓扑指数和分子静电势及其导出参数的计算.运用多元线性回归方法对这些化合物的生物活性与其分子结构参数进行了关联.对所有化合物采用另一异构形式重复上述过程,以探讨互变异构对QSAR建模的影响.结果表明:互变异构对QSAR结果具有一定的影响,采用1H-吲唑异构形式得到的模型,在质量上均高于采用2H-吲唑异构体,预示着1H-吲唑异构体更有可能是吲唑脲类分子的活性异构形式;分子表面静电势参数结合GETAWAY参数可以较好地用于描述TRPV1通道拮抗剂分子结构与其活性间的定量关系.
研究瞭吲唑脲類辣椒素受體(TRPV1)通道拮抗荊的定量構效關繫(QSAR).首先,採用1H-吲唑異構形式,時27箇TRPV1通道拮抗劑分子進行瞭HF/6·31G~*水平上的結構優化,在優化結構上進行瞭5類拓撲指數和分子靜電勢及其導齣參數的計算.運用多元線性迴歸方法對這些化閤物的生物活性與其分子結構參數進行瞭關聯.對所有化閤物採用另一異構形式重複上述過程,以探討互變異構對QSAR建模的影響.結果錶明:互變異構對QSAR結果具有一定的影響,採用1H-吲唑異構形式得到的模型,在質量上均高于採用2H-吲唑異構體,預示著1H-吲唑異構體更有可能是吲唑脲類分子的活性異構形式;分子錶麵靜電勢參數結閤GETAWAY參數可以較好地用于描述TRPV1通道拮抗劑分子結構與其活性間的定量關繫.
연구료신서뇨류랄초소수체(TRPV1)통도길항형적정량구효관계(QSAR).수선,채용1H-신서이구형식,시27개TRPV1통도길항제분자진행료HF/6·31G~*수평상적결구우화,재우화결구상진행료5류탁복지수화분자정전세급기도출삼수적계산.운용다원선성회귀방법대저사화합물적생물활성여기분자결구삼수진행료관련.대소유화합물채용령일이구형식중복상술과정,이탐토호변이구대QSAR건모적영향.결과표명:호변이구대QSAR결과구유일정적영향,채용1H-신서이구형식득도적모형,재질량상균고우채용2H-신서이구체,예시착1H-신서이구체경유가능시신서뇨류분자적활성이구형식;분자표면정전세삼수결합GETAWAY삼수가이교호지용우묘술TRPV1통도길항제분자결구여기활성간적정량관계.
The present paper is devoted to the study of quantitative structure-activity relationship(QSAR)for indazolyl ureas as TRPV1 antagonists.First,ab initio calculations have been performed at the HF/6-31G*level of theory for 27 indazolyl urea compounds(using 1 H-indazole tautomeric form).On the basis of optimized structures,five kinds of topological indices,electrostatic potentials as well as their statistically-drived quantities have beenobtained.Linear correlations between the biological activities and the structural descriptors have been established by using multiple linear regression method.Then,by using another tautomer(2 H-indazole form),all of the above processes were repeated to investigate the effect of tautomerism upon the QSAR modelling.It has been shown that tautomerism has a significant effect on the QSAR modelling,and the models obtained from 1 H-indazol tautomeric form always represent higher quality than those from 2H-indazol tautomer,which indicates that 1 H-indazol tautomer of the indazolyl urea is probably the active form when binding with the TRPV1 channel protein.It has also been demonstrated that the theoretical descriptors derived from electrostatic potentials on molecular surface together with the GETAWAY descriptors can be well used to express the quantitative structure-activity relationship of indazolyl urea TRPV1 channel antagonists.