新型激酶抑制剂的“复古设计”概念。

Idrugs Pub Date : 2010-07-01
Gerhard Müller, Peter C Sennhenn, Timothy Woodcock, Lars Neumann
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引用次数: 0

摘要

蛋白激酶是多种疾病中最具吸引力的治疗靶点之一。本专题综述强调并分类了用于产生活性和选择性激酶抑制剂的主要设计原则。特别是,重点集中在基于片段的导联生成方法,这构成了开发具有不同结合动力学属性的II型激酶抑制剂的新设计方法。这种“复古设计”策略依赖于定制的片段库,与II型抑制剂设计中使用的传统方法形成对比。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The 'retro-design' concept for novel kinase inhibitors.

Protein kinases are among the most attractive therapeutic targets for a broad range of diseases. This feature review highlights and classifies the main design principles employed to generate active and selective kinase inhibitors. In particular, emphasis is focused on a fragment-based lead-generation approach, which constitutes a novel design method for developing type II kinase inhibitors with distinct binding kinetic attributes. This 'retro-design' strategy relies on a customized fragment library, and contrasts the traditional approach used in the design of type II inhibitors.

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Idrugs
Idrugs 医学-药学
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