化学
缺氧诱导因子
缺氧(环境)
药理学
酶抑制剂
生物化学
缺氧诱导因子1
酶
内分泌学
基因
转录因子
氧气
医学
有机化学
作者
Takeshi Fukuda,Takeshi Kuribayashi,Rieko Takano,Koji Sasaki,Takashi Tsuji,Yasushi Niitsu,Ken J. Ishii,Masami Hashimoto,Daichi Baba,Shuichiro Ito,Naoki Tanaka
标识
DOI:10.1016/j.bmcl.2024.129799
摘要
Inhibition of the hypoxia-inducible factor prolyl hydroxylase (HIF-PHD) represents a promising strategy for discovering next-generation treatments for renal anemia. We identified a pyrimidine core with HIF-PHD inhibitory activity based on scaffold hopping of FG-2216 using crystal structures of HIF-PHD2 in complex with compound. By optimizing the substituents at the 2- and 6- positions of the pyrimidine core, we discovered DS44470011, which improves the effectiveness of erythropoietin (EPO) release in cells. Oral administration of DS44470011 to cynomolgus monkeys increased plasma EPO levels.
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