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Updated: Sep 30, 2025

Identifying Inhibitors of the HBx-DDB1 Interaction Using a Split Luciferase Assay System
Published on: December 21, 2019
Discovery of SHR5133, a Highly Potent and Novel HBV Capsid Assembly Modulator
Xin Li1, Zhigao Zhang1, Yang Chen1
1Shanghai Hengrui Pharmaceutical Co., Ltd., R&D Center, 279 Wenjing Road, Shanghai 200245, China.
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.
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