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Mutagenicity in a Molecule: Identification of Core Structural Features of Mutagenicity Using a Scaffold Analysis

机译:分子的致突变性:使用支架分析法鉴定致突变性的核心结构特征

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摘要

With advances in the development and application of Ames mutagenicity in silico prediction tools, the International Conference on Harmonisation (ICH) has amended its M7 guideline to reflect the use of such prediction models for the detection of mutagenic activity in early drug safety evaluation processes. Since current Ames mutagenicity prediction tools only focus on functional group alerts or side chain modifications of an analog series, these tools are unable to identify mutagenicity derived from core structures or specific scaffolds of a compound. In this study, a large collection of 6512 compounds are used to perform scaffold tree analysis. By relating different scaffolds on constructed scaffold trees with Ames mutagenicity, four major and one minor novel mutagenic groups of scaffold are identified. The recognized mutagenic groups of scaffold can serve as a guide for medicinal chemists to prevent the development of potentially mutagenic therapeutic agents in early drug design or development phases, by modifying the core structures of mutagenic compounds to form non-mutagenic compounds. In addition, five series of substructures are provided as recommendations, for direct modification of potentially mutagenic scaffolds to decrease associated mutagenic activities.
机译:随着Ames致突变性在计算机预测工具中的开发和应用的进步,国际协调会议(ICH)修改了其M7指南,以反映出在预测早期药物安全性评估过程中使用此类预测模型检测致突变活性。由于当前的Ames致突变性预测工具仅侧重于类似系列的功能组警报或侧链修饰,因此这些工具无法识别源自化合物核心结构或特定支架的致突变性。在这项研究中,大量的6512种化合物用于进行支架树分析。通过使构筑的支架树上的不同支架具有Ames致突变性,确定了四个主要和一个次要的新颖诱变组。公认的诱变支架基团可以通过修饰诱变化合物的核心结构以形成非诱变化合物,作为药物化学家在早期药物设计或开发阶段中防止潜在诱变治疗剂发展的指南。另外,作为推荐提供了五个系列的亚结构,用于直接修饰潜在的诱变支​​架以减少相关的诱变活性。

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