Discovery of RG7834: The First-in-Class Selective and Orally Available Small Molecule Hepatitis B Virus Expression Inhibitor with Novel Mechanism of Action.
Xingchun HanChengang ZhouMin JiangYongguang WangJianhua WangZhanling ChengMin WangYongqiang LiuChungen LiangJianping WangZhanguo WangRobert WeikertWenzhe LvJianxun XieXin YuXue ZhouSouphalone LuangsayHong C ShenAlexander V MaywegHassan JavanbakhtSong YangPublished in: Journal of medicinal chemistry (2018)
Chronic hepatitis B virus (HBV) infection is a serious public health burden, and current therapies cannot achieve satisfactory cure rate. There are high unmet medical needs of novel therapeutic agents with differentiated mechanism of action (MOA) from the current standard of care. RG7834, a compound from the dihydroquinolizinone (DHQ) chemical series, is a first-in-class highly selective and orally bioavailable HBV inhibitor which can reduce both viral antigens and viral DNA with a novel mechanism of action. Here we report the discovery of RG7834 from a phenotypic screening and the structure-activity relationship (SAR) of the DHQ chemical series. RG7834 can selectively inhibit HBV but not other DNA or RNA viruses in a virus panel screening. Both in vitro and in vivo profiles of RG7834 are described herein, and the data support further development of this compound as a chronic HBV therapy.
Keyphrases
- hepatitis b virus
- small molecule
- public health
- liver failure
- healthcare
- structure activity relationship
- sars cov
- circulating tumor
- single molecule
- cell free
- poor prognosis
- high throughput
- nucleic acid
- palliative care
- stem cells
- binding protein
- risk factors
- dendritic cells
- electronic health record
- drug induced
- immune response
- bone marrow
- genetic diversity
- global health