Structure–Activity Relationships and Discovery of (S)-5-(tert-Butyl)-11-(difluoromethoxy)-9-methoxy-2-oxo-1,2,5,6-tetrahydropyrido[2′,1′:2,3]imidazo[4,5-h]quinoline-3-carboxylic Acid (AB-161), a Novel Orally Available and Liver-Centric HBV RNA Destabilizer
化学
立体化学
药物化学
作者
Dimitar Gotchev,Shuai Chen,Benjamin J. Dugan,Bruce D. Dorsey,Xu Wang,Muhammad Sheraz,Rose Kowalski,Fei Liu,Sunny Tang,Tim Chiu,Troy O. Harasym,Ingrid Graves,Emily P. Thi,Jeremy D. Mason,Nathan Overholt,Ravi Dugyala,Angela M. Lam,Andrew G. Cole,Michael J. Sofia
Lowering hepatitis B surface antigen (HBsAg) levels from covalently closed circular DNA (cccDNA) and the integrated genome could reduce the persistence of hepatitis B virus (HBV) infection. Since HBV replication occurs in the liver and to ameliorate the peripheral neuropathy observed with a first-generation tricyclic 4-pyridone PAPD5/7 inhibitor (