Abstract
A set of trimeric and tetrameric derivatives 6– 11 of the influenza virus neuraminidase inhibitor zanamivir 1 have been synthesized by coupling a common monomeric zanamivir derivative 3 onto various multimeric carboxylic acid core groups. These discrete multimeric compounds are all significantly more antiviral than zanamivir and also show outstanding long-lasting protective activity when tested in mouse influenza infectivity experiments.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have