| Literature DB >> 28094179 |
Sebastien Boucle1, Xiao Lu1, Leda Bassit1, Tugba Ozturk1, Olivia Ollinger Russell1, Franck Amblard1, Steven J Coats2, Raymond F Schinazi3.
Abstract
New modifications to the scaffold of previously reported HBV capsid assembly effectors such as BAY 41-4109, HAP-12 and GLS4 were explored. The anti-HBV activity in the HepAD38 system, and cytotoxicity profiles of each of the new compounds has been assessed. Among them, five new iodo- and bromo-heteroarylpyrimidines analogs displayed anti-HBV activity in the low micromolar range.Entities:
Keywords: Capsid assembly effectors; HAP; HBV; Heteroarylpyrimidine
Mesh:
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Year: 2017 PMID: 28094179 PMCID: PMC5314961 DOI: 10.1016/j.bmcl.2017.01.010
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823