| Literature DB >> 32071684 |
Hyo Gyeong Na1,2, Ali Imran1, Kyuneun Kim1,2, Hong Sik Han1,2, Young Jin Lee1,2, Myung-Jin Kim3, Chang-Soo Yun1, Young-Sik Jung1,2, Joo-Youn Lee4, Soo Bong Han1,2.
Abstract
Hepatitis B virus (HBV) remains a major health concern with 260 million people having been infected globally, and approximately 680,000 deaths have occurred annually from cirrhosis and liver cancer. The modulation of HBV capsid assembly has emerged as a promising therapeutic approach for curing chronic HBV infection. Small-molecule capsid assembly modulators (CAMs) can broadly be classified as heteroaryldihydropyrimidines and sulfamoylbenzamides (SBAs). SBAs are capsid activators that inhibit viral replication by achieving capsid assembly before polymerase encapsulation. Herein, we report a novel series of HBV CAMs based on NVR 3-778, a potent CAM belonging to the SBA class. The lead compound (KR-26556) exhibited improved pharmacological activity and was examined through molecular docking studies.Entities:
Year: 2020 PMID: 32071684 PMCID: PMC7025384 DOI: 10.1021/acsmedchemlett.9b00550
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345