4.6 Review

Influenza Neuraminidase Inhibitors: Synthetic Approaches, Derivatives and Biological Activity

Journal

MOLECULES
Volume 21, Issue 11, Pages -

Publisher

MDPI AG
DOI: 10.3390/molecules21111513

Keywords

influenza treatment; neuraminidase inhibitors; organic synthesis; total synthesis; sialic acid analogues

Funding

  1. Natural Science Foundation of China [31471703, A0201300537, 31671854]
  2. 100 Foreign Talents Plan [JSB2014012]

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Despite being a common viral disease, influenza has very negative consequences, causing the death of around half a million people each year. A neuraminidase located on the surface of the virus plays an important role in viral reproduction by contributing to the release of viruses from infected host cells. The treatment of influenza is mainly based on the administration of neuraminidase inhibitors. The neuraminidase inhibitors zanamivir, laninamivir, oseltamivir and peramivir have been commercialized and have been demonstrated to be potent influenza viral neuraminidase inhibitors against most influenza strains. In order to create more potent neuraminidase inhibitors and fight against the surge in resistance resulting from naturally-occurring mutations, these anti-influenza drugs have been used as templates for the development of new neuraminidase inhibitors through structure-activity relationship studies. Here, we review the synthetic routes to these commercial drugs, the modifications which have been performed on these structures and the effects of these modifications on their inhibitory activity.

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