| Literature DB >> 21306567 |
Baohe Tian1, Meizi He, Zhiwu Tan, Shixing Tang, Indira Hewlett, Shuguang Chen, Yinxue Jin, Ming Yang.
Abstract
N-acylhydrazones containing glycine residue 3a-j and 8a-h were synthesized as HIV-1 capsid protein assembly inhibitors. The structures of the novel N-acylhydrazone derivatives were characterized using different spectroscopic methods. Antiviral activity demonstrated that compound 8c bearing 4-methylphenyl moiety was the most active with low cytotoxicity.Entities:
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Year: 2011 PMID: 21306567 DOI: 10.1111/j.1747-0285.2010.01050.x
Source DB: PubMed Journal: Chem Biol Drug Des ISSN: 1747-0277 Impact factor: 2.817