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通过优化设置改进比较分子场分析(CoMFA)建模

Improved CoMFA modeling by optimization of settings.

作者信息

Peterson Shane D, Schaal Wesley, Karlén Anders

机构信息

Department of Medicinal Chemistry, Uppsala University, Sweden.

出版信息

J Chem Inf Model. 2006 Jan-Feb;46(1):355-64. doi: 10.1021/ci049612j.

Abstract

The possibility of improving the predictive ability of comparative molecular field analysis (CoMFA) by settings optimization has been evaluated to show that CoMFA predictive ability can be improved. Ten different CoMFA settings are evaluated, producing a total of 6120 models. This method has been applied to nine different data sets, including the widely used benchmark steroid data set, as well as eight other data sets proposed as QSAR benchmarking data sets by Sutherland et al. (J. Med. Chem. 2004, 47, 5541-5554). All data sets have been studied using training and test sets to allow for both internal (q(2)) and external (r(2)(pred)) predictive ability assessment. CoMFA settings optimization was successful in developing models with improved q(2) and r(2)(pred) as compared to default CoMFA modeling. Optimized CoMFA is compared with comparative molecular similarity indices analysis (CoMSIA) and holographic quantitative structure-activity relationship (HQSAR) models and found to consistently produce models with improved or equivalent q(2) and r(2)(pred). The ability of settings optimization to improve model predictive ability has been validated using both internal and external predictions, and the risk of chance correlation has been evaluated using response variable randomization tests.

摘要

通过设置优化来提高比较分子场分析(CoMFA)预测能力的可能性已得到评估,结果表明CoMFA的预测能力可以得到提高。对十种不同的CoMFA设置进行了评估,共生成6120个模型。该方法已应用于九个不同的数据集,包括广泛使用的类固醇基准数据集,以及由萨瑟兰等人(《药物化学杂志》,2004年,47卷,5541 - 5554页)提出作为QSAR基准数据集的其他八个数据集。所有数据集均使用训练集和测试集进行研究,以便对内部(q(2))和外部(r(2)(pred))预测能力进行评估。与默认的CoMFA建模相比,CoMFA设置优化成功开发出了具有更高q(2)和r(2)(pred)的模型。将优化后的CoMFA与比较分子相似性指数分析(CoMSIA)和全息定量构效关系(HQSAR)模型进行比较,发现其始终能生成具有更高或相当q(2)和r(2)(pred)的模型。已通过内部和外部预测验证了设置优化提高模型预测能力的能力,并使用响应变量随机化测试评估了偶然相关性的风险。

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