作为抗炎药物的黄素及其衍生物的研究进展:从分子机制到临床应用
Nan Wu1, Yue Zhang1, Chengyu Cui1
1Key Laboratory of Natural Medicines of the Changbai Mountain, Ministry of Education, Yanbian University College of Pharmacy, Yanji, 133002, PR China.
European journal of medicinal chemistry
|January 20, 2026
概括
黄素 (CUR) 在治疗炎症方面表现有前途,但面临生物可用性挑战. 结构改造和新型传递系统等策略旨在改善其作为精密医学的临床使用.
科学领域:
- 药理学 药理学是指药理学的学科.
- 自然产品 化学 化学
- 药物运输 药物运输 药物运输
背景情况:
- 黄素 (CUR) 是一种二甲,具有显著的抗炎,抗氧化,抗瘤和神经保护性质.
- 低水溶性,低生物可用性和代谢不稳定性限制了CUR的临床应用.
- 了解CUR的化学结构和结构-活性关系对于其治疗发展至关重要.
研究的目的:
- 系统地审查黄素 (CUR) 的研究进展.
- 分析CUR抗炎作用的分子机制.
- 总结克服药物动力学限制的策略,并讨论临床应用.
主要方法:
- 对CUR的化学结构特征和结构-活性关系的审查.
- 对针对抗炎作用的多个信号通路的分子机制的分析.
- 结构修改策略和新型传递系统的总结,以提高生物可用性.
- 汇编了CUR在与炎症有关的疾病当前的临床应用.
主要成果:
- CUR通过一种多目标,多途径的抗炎作用机制来起作用.
- 结构修改和先进的输送系统显示了提高CUR可溶性和生物利用性的潜力.
- 有针对性的输送系统可以减轻第一通代谢并改善治疗结果.
- 对于各种与炎症相关的疾病,正在研究CUR.
结论:
- 创新策略对于克服CUR的药理动力学限制至关重要.
- CUR有可能从食补充剂转变为精密药物.
- 进一步的研究可以释放CUR和其他天然产品的全部治疗潜力.
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