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首页> 外文期刊>SAR and QSAR in Environmental Research >Analysis of van der Waals surface area properties for human ether-a-go-go-related gene blocking activity: computational study on structurally diverse compounds
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Analysis of van der Waals surface area properties for human ether-a-go-go-related gene blocking activity: computational study on structurally diverse compounds

机译:人与人有关的基因阻断活性的范德华表面积特性分析:结构多样的化合物的计算研究

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In the present investigation, a computational analysis was performed on a data set comprised of human ether-a-go-go-related gene (hERG) blockers (triethanolamine, 1,3-thiazol-2-yl and tetrasubstituted imidazoline derivatives) in order to investigate the structural features required to reduce the hERG-induced cardiotoxicity problems in an early stage of drug discovery. The results derived from the quantitative structure-activity relationship (QSAR) analysis showed that the volume, surface area and shape descriptors (vsurf_) contributed significantly in all the models. This reveals that the hydrogen-bonding and hydrophilicity properties (vsurf_HB1, vsurf_CW4 and a_acc) on the van der Waals (vdW) surface of the molecule is negatively contributed for the hERG blocking activity and the hydrophobic property (vsurf_D6) and the total polar volume (vsurf_Wp2) on the vdW surface of the molecule are favourable for the activity. Further, the pharmacophore analysis also shows that the Aro/Hyd/Acc contour is one of the important biophore sites for the hERG blocking activity. This suggests that the presence of aromatic, hydrophobic and hydrogen-bonding groups in the molecules is favourable for interaction. In comparison with our earlier works (explaining the role of topological and hydrophobicity properties for the hERG blocking activity), these studies provided additional information on the importance of vdW surface area properties for the hERG blocking activity. These results can be used with other molecular modelling studies for the design of novel molecules that are free of cardiotoxicity.View full textDownload full textKeywordsvan der Waals surface, human ether-a-go-go-related gene, quantitative structure-activity relationship, pharmacophore, hydrophobicityRelated var addthis_config = { ui_cobrand: "Taylor & Francis Online", services_compact: "citeulike,netvibes,twitter,technorati,delicious,linkedin,facebook,stumbleupon,digg,google,more", pubid: "ra-4dff56cd6bb1830b" }; Add to shortlist Link Permalink http://dx.doi.org/10.1080/1062936X.2012.666264
机译:在本研究中,按顺序对由人类醚相关基因(hERG)阻断剂(三乙醇胺,1,3-噻唑-2-基和四取代的咪唑啉衍生物)组成的数据集进行了计算分析。研究在药物开发的早期阶段减少hERG引起的心脏毒性问题所需的结构特征。定量构效关系(QSAR)分析得出的结果表明,在所有模型中,体积,表面积和形状描述符(vsurf_)都起了重要作用。这表明分子范德华(vdW)表面的氢键键合和亲水性(vsurf_HB1,vsurf_CW4和a_acc)对hERG阻断活性和疏水性(vsurf_D6)以及总极性体积(分子的vdW表面上的Vsurf_Wp2)对于活性是有利的。此外,药效团分析还显示,Aro / Hyd / Acc等高线是hERG阻断活性的重要生物团部位之一。这表明分子中芳族,疏水和氢键基团的存在有利于相互作用。与我们以前的工作(解释拓扑和疏水性对hERG阻断活性的作用)相比,这些研究提供了有关vdW表面积特性对hERG阻断活性的重要性的其他信息。这些结果可以与其他分子建模研究一起用于设计无心脏毒性的新型分子。查看全文下载全文关键词,疏水性相关var addthis_config = {ui_cobrand:“泰勒和弗朗西斯在线”,servicescompact:“ citeulike,netvibes,twitter,technorati,delicious,linkedin,facebook,stumbleupon,digg,google,更多”,发布号:“ ra-4dff56cd6bb1830b”};添加到候选列表链接永久链接http://dx.doi.org/10.1080/1062936X.2012.666264

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