小分子可溶性环氧化酶抑制剂的发展:合成进步和治疗应用
Zhen-Yue Wang1, Jing-Yue Dong1, Jian-Hua Liang1
1Key Laboratory of Medicinal Molecule Science and Pharmaceutical Engineering, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing, P. R. China.
开发新的可溶性环氧化酶 (sEH) 抑制剂解决了药物开发中的局限性. 本综述强调了下一代针对性治疗的先进策略和新化学型.
科学领域:
- 药用化学 医学化学
- 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:
- 可溶性环氧化酶 (sEH) 抑制剂显示出治疗的前景.
- 临床转化受到溶解性差,AUC低,CYP抑制和hERG毒性的阻碍.
研究的目的:
- 审查最近在sEH抑制剂开发方面的进展.
- 突出克服药理动力学和毒性限制的策略.
主要方法:
- 对脚手架多样化和合理设计方法的评估.
- 分析创新的合成方法和结构-活动关系.
- 除了基于尿素的支架之外,探索新的化学类型.
主要成果:
- 在脚手架多样化和合理设计方面的突破.
- 识别新的化学类型,扩大化学空间.
- 克服诸如溶解性差和毒性等局限性.
结论:
- 先进的抑制剂为针对sEH的药物发现提供了战略路线图.
- 下一代sEH抑制剂对于治疗进步至关重要.
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