ASK1
赫尔格
细胞凋亡
激酶
IC50型
化学
生物利用度
酰胺
效力
药代动力学
药理学
丝裂原活化蛋白激酶激酶
生物化学
体外
蛋白激酶A
内科学
医学
钾通道
作者
Lin Tang,Minxiong Li,Changlin Bai,Xuejin Feng,Hai Hu,Yufen Yao,Baiqing Li,Hongwei Li,Guohong Qin,Ning Xi,Genpin Lv,Lei Zhang
摘要
Three series of benzoheterocyclic-substituted amide derivatives were designed and synthesized as potent ASK1 inhibitors in this work. After undergoing continuous structural optimization, compound 17a was discovered to be a novel inhibitor of ASK1 with good potency (kinase, IC
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