化学
药理学
心力衰竭
口服活性
酶抑制剂
生物化学
酶
内科学
体外
医学
作者
Ming-Jie Huang,Jiale Xu,Hui Qiao,Wen Zhao,Li‐Hua Huang
标识
DOI:10.1021/acs.jmedchem.4c01303
摘要
LSD1 has become an appealing target for the development of new pharmacologic agents to treat cardiovascular diseases, including heart failure. Herein, we reported the design, synthesis, and structure-activity relationship of a series of TCP-based derivatives targeting LSD1. Docking studies were employed to successfully elucidate the SAR. Particularly, compound
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