Your browser doesn't support javascript.
loading
Development of Simple and Accurate in Silico Ligand-Based Models for Predicting ABCG2 Inhibition.
Huang, Shuheng; Gao, Yingjie; Zhang, Xuelian; Lu, Ji; Wei, Jun; Mei, Hu; Xing, Juan; Pan, Xianchao.
Afiliação
  • Huang S; Department of Medicinal Chemistry, School of Pharmacy, Southwest Medical University, Luzhou, China.
  • Gao Y; Key Laboratory of Biorheological Science and Technology (Ministry of Education), College of Bioengineering, Chongqing University, Chongqing, China.
  • Zhang X; Department of Medicinal Chemistry, School of Pharmacy, Southwest Medical University, Luzhou, China.
  • Lu J; Department of Pathophysiology, School of Basic Medical Science, Southwest Medical University, Luzhou, China.
  • Wei J; Department of Medicinal Chemistry, School of Pharmacy, Southwest Medical University, Luzhou, China.
  • Mei H; Department of Medicinal Chemistry, School of Pharmacy, Southwest Medical University, Luzhou, China.
  • Xing J; Key Laboratory of Biorheological Science and Technology (Ministry of Education), College of Bioengineering, Chongqing University, Chongqing, China.
  • Pan X; Department of Pathophysiology, School of Basic Medical Science, Southwest Medical University, Luzhou, China.
Front Chem ; 10: 863146, 2022.
Article em En | MEDLINE | ID: mdl-35665065
ABSTRACT
The ATP binding cassette transporter ABCG2 is a physiologically important drug transporter that has a central role in determining the ADMET (absorption, distribution, metabolism, elimination, and toxicity) profile of therapeutics, and contributes to multidrug resistance. Thus, development of predictive in silico models for the identification of ABCG2 inhibitors is of great interest in the early stage of drug discovery. In this work, by exploiting a large public dataset, a number of ligand-based classification models were developed using partial least squares-discriminant analysis (PLS-DA) with molecular interaction field- and fingerprint-based structural description methods, regarding physicochemical and fragmental properties related to ABCG2 inhibition. An in-house dataset compiled from recently experimental studies was used to rigorously validated the model performance. The key molecular properties and fragments favored to inhibitor binding were discussed in detail, which was further explored by docking simulations. A highly informative chemical property was identified as the principal determinant of ABCG2 inhibition, which was utilized to derive a simple rule that had a strong capability for differentiating inhibitors from non-inhibitors. Furthermore, the incorporation of the rule into the best PLS-DA model significantly improved the classification performance, particularly achieving a high prediction accuracy on the independent in-house set. The integrative model is simple and accurate, which could be applied to the evaluation of drug-transporter interactions in drug development. Also, the dominant molecular features derived from the models may help medicinal chemists in the molecular design of novel inhibitors to circumvent ABCG2-mediated drug resistance.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article