| Literature DB >> 14521332 |
Grigoris Zoidis1, Nicolas Kolocouris, George B Foscolos, Antonios Kolocouris, George Fytas, P Karayannis, Elizaveta Padalko, Johan Neyts, Erik De Clercq.
Abstract
There is a lack of information in the medical chemistry literature concerning the anti-influenza A activity of the drug rimantadine's 2-isomer (2-rimantadine). We now present results showing that, although 2-adamantanamine (2-amantadine) 3 is only moderately active, some 2-rimantadine analogues are effective anti-influenza A virus agents in vitro. The 2-rimantadine analogues and their spirocyclobutane and spirocyclopentane congeners were synthesized through interesting routes. The 2-rimantadine analogues were 2-4 times more potent than rimantadine 2 against influenza virus A H2N2 strain; their spirocyclobutane congeners proved equally active to rimantadine 2. Two compounds exhibited a similar activity and one of the compounds was was fourfold more potent than rimantadine 2 against H3N2 strain.Entities:
Mesh:
Substances:
Year: 2003 PMID: 14521332 DOI: 10.1177/095632020301400305
Source DB: PubMed Journal: Antivir Chem Chemother ISSN: 0956-3202