锡克
医学
计算生物学
计算机科学
癌症研究
免疫学
内科学
生物
受体
酪氨酸激酶
作者
Hong Jia,Wei Deng,Baoyu Hao,Min Cai,Dong Guo,Yu Cai,Xiaoming Dai,Zhipeng Wu,Weigang He,Jian Wang,Guanglin Wang,Sumei Xia,Na Li,Weiguo Su,Guangxiu Dai
标识
DOI:10.1021/acsmedchemlett.3c00553
摘要
Herein we describe the medicinal chemistry efforts that led to the discovery of the clinical-staged Syk inhibitor sovleplenib (41) via a structure–activity relationship investigation and pharmacokinetics (PK) optimization of a pyrido[3,4-b]pyrazine scaffold. Sovleplenib is a potent and selective Syk inhibitor with favorable preclinical PK profiles and robust anti-inflammation efficacy in a preclinical collagen-induced arthritis model. Sovleplenib is now being developed for treating autoimmune diseases such as immune thrombocytopenic purpura and warm antibody hemolytic anemia as well as hematological malignancies.
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