临床相关的激酶抑制剂的非激酶非位抑制活性
Nickolas R Brauer1, Allison L Kempen1, Delmis Hernandez1
1Department of Chemistry, Purdue University, 560 Oval Drive, West Lafayette, IN, 47907, USA.
European journal of medicinal chemistry
|June 9, 2024
概括
激酶抑制剂可以影响非激酶标,影响药物的疗效和毒性. 本综述检查了FDA批准的和临床试验中的激酶抑制剂,这些抑制剂与意想不到的蛋白质标结合.
科学领域:
- 生物化学 生物化学
- 药理学 药理学是指药理学的学科.
- 药物发现 药物发现 药物发现
背景情况:
- 蛋白激酶调节关键细胞功能,如细胞周期,细胞亡和增殖.
- 激酶是治疗干预的关键点,需要对抑制剂进行选择性分析.
- 标准查往往忽略了非酶目标,可能缺失的负担或疗效贡献.
研究的目的:
- 审查FDA批准的和临床试验中的酶抑制剂,与非酶标相互作用.
- 分析酶和非酶标中的结合姿势,了解多药理学.
- 探索这些非目标相互作用对药物毒性和疗效的相关性.
主要方法:
- 对已知非激酶标的激酶抑制剂的文献综述.
- 对药物标结合剂的已公布结构数据的分析.
- 检查临床试验数据和FDA对具有多种药理的化合物的批准.
主要成果:
- 几种FDA批准和临床酶抑制剂表明它们与非酶蛋白结合.
- 结构分析揭示了共享或独特的结合特征,这些特征负责酶和异相互作用.
- 目标外结合可以导致不良影响和治疗益处.
结论:
- 激酶抑制剂经常表现出超出其预期的激酶标的多药性.
- 了解非酶非向相互作用对于预测药物安全性和有效性至关重要.
- 对非标结合的进一步调查可以完善药物设计和治疗策略.
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