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使用MetaSite和StarDrop对CYP3A4、CYP2C9和CYP2D6底物的代谢软点预测进行比较。

Comparison of metabolic soft spot predictions of CYP3A4, CYP2C9 and CYP2D6 substrates using MetaSite and StarDrop.

作者信息

Shin Young G, Le Hoa, Khojasteh Cyrus, Hop Cornelis E C A

机构信息

Drug Metabolism and Pharmacokinetics, Genentech, Inc., 1 DNA way, MS 412a, South San Francisco, CA 94080, USA.

出版信息

Comb Chem High Throughput Screen. 2011 Nov;14(9):811-23. doi: 10.2174/138620711796957170.

Abstract

Metabolite identification study plays an important role in determining the sites of metabolic liability of new chemical entities (NCEs) in drug discovery for lead optimization. Here we compare the two predictive software, MetaSite and StarDrop, available for this purpose. They work very differently but are used to predict the site of oxidation by major human cytochrome P450 (CYP) isoforms. Neither software can predict non-CYP catalyzed metabolism nor the rates of metabolism. For the purpose of comparing the two software packages, we tested known probe substrate for these enzymes, which included 12 substrates of CYP3A4 and 18 substrates of CYP2C9 and CYP2D6 were analyzed by each software and the results were compared. It is possible that these known substrates were part of the training set but we are not aware of it. To assess the performance of each software we assigned a point system for each correct prediction. The total points assigned for each CYP isoform experimentally were compared as a percentage of the total points assigned theoretically for the first choice prediction for all substrates for each isoform. Our results show that MetaSite and StarDrop are similar in predicting the correct site of metabolism by CYP3A4 (78% vs 83%, respectively). StarDrop appears to do slightly better in predicting the correct site of metabolism by CYP2C9 and CYP2D6 metabolism (89% and 93%, respectively) compared to MetaSite (63% and 70%, respectively). The sites of metabolism (SOM) from 34 in-house NCEs incubated in human liver microsomes or human hepatocytes were also evaluated using two prediction software packages and the results showed comparable SOM predictions. What makes this comparison challenging is that the contribution of each isoform to the intrinsic clearance (Clint) is not known. Overall the software were comparable except for MetaSite performing better for CYP2D6 and that MetaSite has a liver model that is absent in StarDrop that predicted with 82% accuracy.

摘要

代谢物鉴定研究在药物发现中确定新化学实体(NCEs)的代谢易感性位点以进行先导化合物优化方面发挥着重要作用。在此,我们比较了用于此目的的两种预测软件MetaSite和StarDrop。它们的工作方式差异很大,但都用于预测主要人类细胞色素P450(CYP)同工酶的氧化位点。两种软件都无法预测非CYP催化的代谢或代谢速率。为了比较这两个软件包,我们测试了这些酶的已知探针底物,其中包括12种CYP3A4底物以及18种CYP2C9和CYP2D6底物,每种软件对其进行分析并比较结果。这些已知底物有可能是训练集的一部分,但我们并不清楚。为了评估每个软件的性能,我们为每个正确预测分配了一个评分系统。将每种CYP同工酶实验分配的总分数与理论上为每种同工酶所有底物的首选预测分配的总分数的百分比进行比较。我们的结果表明,MetaSite和StarDrop在预测CYP3A4的正确代谢位点方面相似(分别为78%和83%)。与MetaSite(分别为63%和70%)相比,StarDrop在预测CYP2C9和CYP2D6代谢的正确位点方面似乎略胜一筹(分别为89%和93%)。还使用这两种预测软件包评估了在人肝微粒体或人肝细胞中孵育的34种内部NCEs的代谢位点(SOM),结果显示SOM预测结果相当。使这种比较具有挑战性的是,每种同工酶对内在清除率(Clint)的贡献尚不清楚。总体而言,除了MetaSite在CYP2D6方面表现更好以及MetaSite具有StarDrop中不存在的肝脏模型(预测准确率为82%)外,这些软件相当。

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