Department of Medicinal Chemistry, Roche Innovation Center Shanghai, Roche Pharma Research & Early Development, Building 5, No. 371, Lishizhen Road, Shanghai 201203, China.
Lead Discovery, Roche Innovation Center Shanghai, Roche Pharma Research & Early Development, Building 5, No. 371, Lishizhen Road, Shanghai 201203, China.
J Med Chem. 2022 Aug 25;65(16):10938-10955. doi: 10.1021/acs.jmedchem.1c02215. Epub 2022 Aug 16.
Chronic hepatitis B virus (HBV) infection is a worldwide disease that causes thousands of deaths per year. Currently, there is no therapeutic that can completely cure already infected HBV patients due to the inability of humans to eliminate covalently closed circular DNA (cccDNA), which serves as the template to (re)initiate an infection even after prolonged viral suppression. Through phenotypic screening, we discovered xanthone series hits as novel HBV cccDNA reducers, and subsequent structure optimization led to the identification of a lead compound with improved antiviral activity and pharmacokinetic profiles. A representative compound demonstrated good potency and oral bioavailability with no cellular toxicity. In an HBVcircle mouse model, compound showed excellent efficacy in significantly reducing HBV antigens, DNA, and intrahepatic cccDNA levels.
慢性乙型肝炎病毒 (HBV) 感染是一种全球性疾病,每年导致数千人死亡。目前,由于人类无法消除共价闭合环状 DNA (cccDNA),而 cccDNA 是即使在病毒长期抑制后重新启动感染的模板,因此还没有能够治愈已经感染的 HBV 患者的治疗方法。通过表型筛选,我们发现了一系列新型 HBV cccDNA 降低剂的酮类化合物,随后的结构优化导致了一种具有改善的抗病毒活性和药代动力学特征的先导化合物的鉴定。代表性化合物 表现出良好的效力和口服生物利用度,且没有细胞毒性。在 HBVcircle 小鼠模型中,化合物 表现出优异的疗效,可显著降低 HBV 抗原、DNA 和肝内 cccDNA 水平。