Kotsampasakou Eleni, Brenner Stefan, Jäger Walter, Ecker Gerhard F
Department of Pharmaceutical Chemistry, University of Vienna , Althanstrasse 14, 1090 Vienna, Austria.
Mol Pharm. 2015 Dec 7;12(12):4395-404. doi: 10.1021/acs.molpharmaceut.5b00583. Epub 2015 Nov 2.
Organic anion transporting polypeptides 1B1 and 1B3 are transporters selectively expressed on the basolateral membrane of the hepatocyte. Several studies reveal that they are involved in drug-drug interactions, cancer, and hyperbilirubinemia. In this study, we developed a set of classification models for OATP1B1 and 1B3 inhibition based on more than 1700 carefully curated compounds from literature, which were validated via cross-validation and by use of an external test set. After combining several sets of descriptors and classifiers, the 6 best models were selected according to their statistical performance and were used for virtual screening of DrugBank. Consensus scoring of the screened compounds resulted in the selection and purchase of nine compounds as potential dual inhibitors and of one compound as potential selective OATP1B3 inhibitor. Biological testing of the compounds confirmed the validity of the models, yielding an accuracy of 90% for OATP1B1 and 80% for OATP1B3, respectively. Moreover, at least half of the new identified inhibitors are associated with hyperbilirubinemia or hepatotoxicity, implying a relationship between OATP inhibition and these severe side effects.
有机阴离子转运多肽1B1和1B3是在肝细胞基底外侧膜上选择性表达的转运蛋白。多项研究表明,它们参与药物相互作用、癌症和高胆红素血症。在本研究中,我们基于从文献中精心挑选的1700多种化合物开发了一组OATP1B1和1B3抑制的分类模型,这些模型通过交叉验证和使用外部测试集进行了验证。在组合了几组描述符和分类器后,根据统计性能选择了6个最佳模型,并用于DrugBank的虚拟筛选。对筛选出的化合物进行共识评分,结果选择并购买了9种化合物作为潜在的双重抑制剂,以及1种化合物作为潜在的选择性OATP1B3抑制剂。对这些化合物的生物学测试证实了模型的有效性,OATP1B1的准确率分别为90%,OATP1B3的准确率为80%。此外,新鉴定的抑制剂中至少有一半与高胆红素血症或肝毒性有关,这意味着OATP抑制与这些严重副作用之间存在关联。