冠状动脉疾病
体内
药理学
药代动力学
磷脂酶
临床试验
疾病
磷脂酶A2
医学
化学
计算生物学
生物信息学
生物化学
内科学
酶
生物
生物技术
作者
Fabrizio Giordanetto,Daniel Pettersen,Ingemar Starke,Peter Nordberg,Mikael Dahlström,Laurent Knerr,Nidhal Selmi,Birgitta Rosengren,Lars-Olof Larsson,Jenny Sandmark,Marie Castaldo,Niek Dekker,Ulla Karlsson,Eva Hurt‐Camejo
标识
DOI:10.1021/acsmedchemlett.6b00188
摘要
Expedited structure-based optimization of the initial fragment hit 1 led to the design of (R)-7 (AZD2716) a novel, potent secreted phospholipase A2 (sPLA2) inhibitor with excellent preclinical pharmacokinetic properties across species, clear in vivo efficacy, and minimized safety risk. Based on accumulated profiling data, (R)-7 was selected as a clinical candidate for the treatment of coronary artery disease.
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