School of Pharmacy, Henan University , Kaifeng, Henan, China.
Expert Opin Ther Pat. 2021 Feb;31(2):169-187. doi: 10.1080/13543776.2021.1854225. Epub 2020 Dec 30.
: Transient receptor potential vanilloid 1 (TRPV1) is a nonselective cation channel with high permeability to calcium, which is widely expressed in the central nervous system (CNS) and peripheral nervous system. Since the TRPV1 was molecularly cloned more than 20 years ago, a series of research activities have been carried out on the possibility of new drugs. : This review summarizes the patents on TRPV1 regulators (including agonists and antagonists) that were published during 2014-present and predicts the development direction in the future. The patent description is organized according to the applicant company and focuses on the representative compounds and their and data. : At present, TRPV1 is considered to be a molecular integrator of a broad range of chemical and physical stimuli. The desensitization of nociceptive neurons caused by TRPV1 agonists and the pharmacological blockade of TRPV1 by powerful small molecular antagonists are different treatments, both of which have analgesic effects. Unfortunately, TRPV1 modulators have suffered from adverse effects related to the role of TRPV1 channel in body temperature regulation and noxious heat sensation. What we need to know is whether these adverse effects are on-target (unavoidable), and whether chemical modification can be used to avoid or reduce these adverse reactions in the process of designing drug molecules, so as to develop a TRPV1 regulator with potent analgesic effect and no obvious adverse effects. Despite the difficulties and roadblocks, TRPV1 modulators remain powerful tools in pain research and represent promising therapeutic agents.
辣椒素受体 TRPV1 是一种非选择性阳离子通道,对钙离子具有高通透性,广泛表达于中枢神经系统(CNS)和外周神经系统。自 TRPV1 于 20 多年前被分子克隆以来,人们围绕其开展了一系列新药研发相关的研究。本综述总结了 2014 年至今发表的 TRPV1 调节剂(包括激动剂和拮抗剂)的专利,并对未来的发展方向进行了预测。专利描述按照申请人公司进行组织,重点介绍了有代表性的化合物及其作用机制和相关的临床前数据。目前认为 TRPV1 是多种化学和物理刺激的分子整合器。TRPV1 激动剂引起伤害感受神经元脱敏,以及强力小分子拮抗剂对 TRPV1 的药理学阻断,是两种不同的治疗方法,均具有镇痛作用。不幸的是,TRPV1 调节剂由于 TRPV1 通道在体温调节和有害热感觉中的作用而遭受与不良反应相关的困扰。我们需要知道的是,这些不良反应是否是针对靶点(不可避免的),以及在设计药物分子的过程中,是否可以通过化学修饰来避免或减少这些不良反应,从而开发出具有强大镇痛作用且无明显不良反应的 TRPV1 调节剂。尽管存在困难和障碍,但 TRPV1 调节剂仍然是疼痛研究中的有力工具,并代表着有前途的治疗药物。