| Literature DB >> 35300087 |
Xin Li1, Zhigao Zhang1, Yang Chen1, Bin Wang1, Guimei Yang1, Xiangbin Xu1, Baihui Yechao1, Dongdong Bai1, Binqiang Feng1, Yuchang Mao1, Jun Feng1, Chang Bai1, Feng He1, Weikang Tao1.
Abstract
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.Entities:
Year: 2022 PMID: 35300087 PMCID: PMC8919393 DOI: 10.1021/acsmedchemlett.2c00002
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345