敌手
化学
口服活性
药理学
口服
肾脏疾病
肾
受体
内科学
医学
生物化学
作者
Ruijia Zhang,Kaiyue Su,Letian Yang,Huaichuan Duan,T. T. Lei,Minghai Tang,Min Zhao,Neng Ye,Xiaoying Cai,Xueqin Jiang,Na Li,Jing Peng,Xinlu Zhang,Lingkai Tang,Qiang Qiu,Lijuan Chen,Wenshuang Wu,Jianping Hu,Liang Ma,Haoyu Ye
标识
DOI:10.1021/acs.jmedchem.4c01395
摘要
Chronic kidney disease (CKD) is a condition characterized by functional deterioration with sustained inflammation and progressive fibrosis of the kidneys affecting over 800 million people worldwide. The P2X7 receptor (P2X7R) plays a key role in CKD progression. Our previous P2X7R antagonists demonstrated good efficacy for treating kidney injury but were limited by low oral exposure and short half-life, restricting their application. This study reports the optimization of P2X7R antagonists for better oral pharmacokinetics. The candidate compound
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