化学
终端(电信)
特发性肺纤维化
激酶
c-jun公司
肺纤维化
药理学
纤维化
生物化学
内科学
肺
医学
转录因子
计算机科学
基因
电信
作者
Yi Huang,Fengling Liu,Shuhua Ren,Yuanqing Ding,M.M. Chi,Weiwei Huang,Wenjing Gu,Hewen Qian,Yaxia Yuan,Shurong Hou,Xiabin Chen,Lei Ma
标识
DOI:10.1021/acs.jmedchem.4c01764
摘要
Idiopathic pulmonary fibrosis (IPF) is a progressive and lethal lung disease with an elusive etiology. Aberrant activation of c-Jun N-terminal kinase 1 (JNK1) has been implicated in its pathogenesis. Through a combination of structure-based drug design and structure-activity relationship (SAR) optimization, a series of pyrimidine-2,4-diamine scaffold derivatives have been developed as potent JNK1 inhibitors. Compound
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