These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Search MEDLINE/PubMed
Title: Divalent oseltamivir analogues as potent influenza neuraminidase inhibitors. Author: Yan ZL, Liu AY, Wei XX, Zhang Z, Qin L, Yu Q, Yu P, Lu K, Yang Y. Journal: Carbohydr Res; 2019 May 15; 477():32-38. PubMed ID: 30954773. Abstract: A panel of divalent oseltamivir and guanidino oseltamivir analogues with esterification on the carboxyl acid group as potent inhibitors of influenza virus neuraminidase was prepared via click reaction. The primary structure activity relationship study demonstrated that appropriate distance between two oseltamivir monomers around 30 Å can crosslink two adjacent neuraminidase tetramers on the virion surface and result in highly effective NA inhibitors against three strains of influenza virus and H7N9 virus like particle. This strategy also provides a basis for the multivalent modification on oseltamivir.[Abstract] [Full Text] [Related] [New Search]