摘要
背景:在领导确定和优化过程中,推进标准可以根据科学原理,先前的经验和/或通过审查经批准的药物铺平道路来推动。然而,获取批准的激酶抑制剂的物理化学和ADME性质的发现数据是一项巨大的任务,因为它们分散在文献中或尚未发表。 目标:我们的目标是:1)编制2016年前批准的所有激酶抑制剂的相关数据,以便生物制药界轻松获取; 2)提供回顾性分析,突出可能对“可发展性”有促进作用的趋势和属性的这些药物,3)点燃关于什么构成“可行”,“不错”和不必要的数据的重点辩论,这样的辩论会使不同类型信息的舞台适合性更加清晰,防止由于丰富而引起的混乱的不必要的数据,导致更有效和更便宜的药物发现计划。 方法:对已发表的手稿和可用的管理文件等不同的数据体进行仔细,全面的分析。 结果:我们能够从2001年起批准美国FDA批准的前三十种激酶抑制剂的大量数据。 结论:总结来说,我们已经编制了第30批批准的激酶抑制剂的物理化学和ADME数据,并提供了我们的回顾性分析,我们希望有助于在发现程序中构建进步标准。对这些数据的检查提供了一个机会来发现数据优先级和分析的阶段适当性的意见。
关键词: 激酶,抑制剂,药物,ADME,物理化学,发现,批准,FDA,药物性。
Current Medicinal Chemistry
Title:A Systematic Analysis of Physicochemical and ADME Properties of All Small Molecule Kinase Inhibitors Approved by US FDA from January 2001 to October 2015
Volume: 24 Issue: 29
关键词: 激酶,抑制剂,药物,ADME,物理化学,发现,批准,FDA,药物性。
摘要: Background: During lead identification and optimization, the advancement criteria may be driven based on scientific principles, prior experiences, and/or by examining the path paved by approved drugs. However, accessing the discovery data on physicochemical and ADME properties of the approved kinase inhibitors is a monumental task as these are either scattered in the literature or have not been published.
Objective: Our goals were: 1) To compile the relevant data on all kinase inhibitors approved prior to 2016 for easy access by the biopharmaceutical community, 2) To provide a retrospective analysis to highlight trends and attributes which may have contributed to the "developability” of these drugs, and 3) To ignite focused debates on what constitutes “actionable”, “nice-to-have”, and unnecessary data. Such debates bring about more clarity on stage appropriateness of different types of information and prevent confusion due to abundance of unnecessary data, leading to more efficient and less costly drug discovery programs.
Methods: A careful and thorough analysis of different bodies of data such as published manuscripts, and available regulatory documents were employed.
Results: We were able to assemble a large body of data on the first thirty kinase inhibitors approved by US FDA since 2001.
Conclusion: In conclusion, we have compiled physicochemical and ADME data on the first 30 approved kinase inhibitors and provided our retrospective analysis, which we hope is helpful in constructing advancement criteria in discovery programs. The examination of this data provides an opportunity to develop an opinion on data prioritization and stage appropriateness of assays.
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Cite this article as:
A Systematic Analysis of Physicochemical and ADME Properties of All Small Molecule Kinase Inhibitors Approved by US FDA from January 2001 to October 2015, Current Medicinal Chemistry 2017; 24 (29) . https://dx.doi.org/10.2174/0929867324666170523124441
DOI https://dx.doi.org/10.2174/0929867324666170523124441 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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