Inhibition of HIV-1 capsid assembly: Optimization of the antiviral potency by site selective modifications at N1, C2 and C16 of a 5-(5-furan-2-yl-pyrazol-1-yl)-1H-benzimidazole scaffold

已取消 20 由小小发布于 2026/8/14 9:42:06

DOI:10.1016/j.bmcl.2012.10.034
文献类型：期刊论文
补充材料：仅需补充材料
文献链接：https://doi.org/10.1016/j.bmcl.2012.10.034
管理员驳回:官网无补充材料

Elsevier

Abstract：A uHTS campaign led to the discovery of a 5-(5-furan-2-ylpyrazol-1-yl)-1H-benzimidazole series that inhibits assembly of HIV-1 capsid. Synthetic manipulations at N1, C2 and C16 positions imp

应助信息

13小时前

何玑

202608140950240335423.pdf 已驳回

13小时前

Book学术机器人

2026/8/14 9:42:07 未找到该文献，机器人已退出，请等待人工下载

2026/8/14 9:42:06 Book学术AI机器人收到请求，开始寻找文献

2026/8/14 9:42:06 已向机器人发送请求

13小时前

小小发布求助

上一个求助:其它数据库Naturally Fractured Carbonate Reservoir Characterization: A Case Study of a Mature High-Pour Point Oil Field in Hungary 下一个求助:其它数据库[Climacteric disorders].