衣壳
化学
病毒学
仿形(计算机编程)
乙型肝炎病毒
病毒
计算生物学
丙型肝炎病毒
生物
计算机科学
操作系统
作者
B. Lesch,Alexander Birkmann,Susanne Bonsmann,Alastair Donald,Florian Engel,Thomas Goldner,Kamal Kumar,Tamara Pfaff,Andreas Urban,Holger Zimmermann,Alexandra E. Bosnidou,Estefanía Del Castillo,Félix Cuevas,Elena Detta,D. Font,J. Víctor García,Justine L. Raymond,Maria Ángeles Sarmentero,Arjen Cnossen,Wessel Sinnige
标识
DOI:10.1021/acs.jmedchem.4c02838
摘要
Hepatitis B Virus (HBV) infections remain a threat to the global public health. Nucleoside analogues remain the mainstay of therapy despite their discouraging cure rates achieved. Capsid assembly modulators (CAMs) have been at the center of HBV research, but despite having shown clinical efficacy on viral load in clinical studies, market entry has been elusive. Herein, we present the optimization program of our lead series. Setting our focus on potency, solubility, and hERG liability, these studies resulted in AIC263282, a new, potent capsid assembly modulator with improved physicochemical properties, which is ready for profiling as a preclinical candidate.
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