使用典型相关分析的化合物-转运体相互作用研究

IF 0.4 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
M. Kitajima, Yohsuke Minowa, H. Matsuda, Y. Okuno
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引用次数: 0

摘要

在药物开发的早期阶段,有效筛选先导化合物或候选药物的有效性和安全性至关重要。化合物通常仅根据其药理作用从不同的“化学空间”中筛选,但这种筛选不足以保证药物安全性。为了解决这个问题,我们设计了一个化学空间,考虑到与蛋白质(如药物转运体)的相互作用信息。我们还创建并评估了预测化合物-转运体相互作用的数学模型。这是通过首先生成基于药物转运体及其相应抑制剂化合物的相互作用相关矩阵来实现的。为了实施考虑到药物转运体相互作用的筛选方案,我们使用典型相关分析(CCA)创建了一个模型,该模型利用了药物转运体与其相应抑制剂之间相互作用的已知信息。模型的交叉验证得到了满意的检验结果,并在此基础上构建了生理相关的化学空间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Compound-Transporter Interaction Studies using Canonical Correlation Analysis
The efficient screening of lead compounds or drug candidates for efficacy and safety is critically important during the early stage of drug development. Compounds are usually screened from a diverse ‘chemical space’ based only on its pharmacological effects, but this screening is not enough to guarantee drug safety. To solve this problem, we devised a chemical space that takes into account interaction information with proteins such as drug transporters. We also created and evaluated a mathematical model for predicting compound-transporter interactions. This was achieved by first generating an interaction correlation matrix based on drug transporters and their corresponding inhibitor compounds. To implement a screening scheme that takes into account interaction with drug transporters, we created a model using Canonical Correlation Analysis (CCA) that makes use of the known information on interaction between drug transporters and their corresponding inhibitors. Cross-validation of the model gave satisfactory test results and a physiologically relevant chemical space was constructed based on the model.
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来源期刊
Chem-Bio Informatics Journal
Chem-Bio Informatics Journal BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
0.60
自引率
0.00%
发文量
8
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