化学
磷酸二酯酶
药效团
亚科
第二信使系统
药理学
生物化学
酶
生物
基因
作者
Jiaxi Huang,Bolin Zhu,Jiang Xu,Zhong‐Zhen Zhou
标识
DOI:10.1016/j.ejmech.2023.115194
摘要
Phosphodiesterase 7 (PDE7) specifically hydrolyzes cyclic adenosine monophosphate (cAMP), a second messenger that plays essential roles in cell signaling and physiological processes. Many PDE7 inhibitors used to investigate the role of PDE7 have displayed efficacy in the treatment of a wide range of diseases, such as asthma and central nervous system (CNS) disorders. Although PDE7 inhibitors are developed more slowly than PDE4 inhibitors, there is increasing recognition of PDE7 inhibitors as potential therapeutics for no nausea and vomiting secondary. Herein, we summarized the advances in PDE7 inhibitors over the past decade, focusing on their crystal structures, key pharmacophores, subfamily selectivity, and therapeutic potential. Hopefully, this summary will lead to a better understanding of PDE7 inhibitors and provide strategies for developing novel therapies targeting PDE7.
科研通智能强力驱动
Strongly Powered by AbleSci AI