衣壳
药效团
哌嗪
效力
体内
体外
计算生物学
化学
病毒学
组合化学
立体化学
药理学
生物
病毒
生物化学
生物技术
作者
Xin Li,Zhigao Zhang,Yang Chen,Bin Wang,Guimei Yang,Xu Xiangbin,Baihui Yechao,Ding Bai,Binqiang Feng,Yuchang Mao,Jun Feng,Chang Bai,Feng He,Weikang Tao
标识
DOI:10.1021/acsmedchemlett.2c00002
摘要
Capsid assembly modulators (CpAMs) represent a new class of antivirals targeting hepatitis B virus (HBV) core protein to disrupt the assembly process. In this work, a novel chemotype featuring a fused heterocycle amide was discovered through pharmacophore exploration. Lead optimization resulted in compound 8 with an EC50 value of 511 nM, and then methyl substitution on the piperazine was found to improve the in vitro potency remarkably. Further SAR studies established the key compound SHR5133, which showed high in vitro antiviral potency, favorable pharmacokinetic profiles across species, and robust in vivo efficacy.
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