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A Rigid Bicyclic Platform for the Generation of Conformationally Locked Neuraminidase Inhibitors
[Image: see text] Rapid mutation of the influenza virus through genetic mixing raises the prospect of new strains that are both highly transmissible and highly lethal, and which have the ability to evade both immunization strategies (through mutation of hemagglutinin) and current therapies (through...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3516865/ https://www.ncbi.nlm.nih.gov/pubmed/23181823 http://dx.doi.org/10.1021/ol3027939 |
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author | Brant, Michael G. Wulff, Jeremy E. |
author_facet | Brant, Michael G. Wulff, Jeremy E. |
author_sort | Brant, Michael G. |
collection | PubMed |
description | [Image: see text] Rapid mutation of the influenza virus through genetic mixing raises the prospect of new strains that are both highly transmissible and highly lethal, and which have the ability to evade both immunization strategies (through mutation of hemagglutinin) and current therapies (through mutation of neuraminidase). Inspired by a need for next-generation therapeutics, a synthetic strategy for a new class of rigid, bicyclic inhibitors of influenza neuraminidase is reported. |
format | Online Article Text |
id | pubmed-3516865 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-35168652012-12-07 A Rigid Bicyclic Platform for the Generation of Conformationally Locked Neuraminidase Inhibitors Brant, Michael G. Wulff, Jeremy E. Org Lett [Image: see text] Rapid mutation of the influenza virus through genetic mixing raises the prospect of new strains that are both highly transmissible and highly lethal, and which have the ability to evade both immunization strategies (through mutation of hemagglutinin) and current therapies (through mutation of neuraminidase). Inspired by a need for next-generation therapeutics, a synthetic strategy for a new class of rigid, bicyclic inhibitors of influenza neuraminidase is reported. American Chemical Society 2012-11-26 2012-12-07 /pmc/articles/PMC3516865/ /pubmed/23181823 http://dx.doi.org/10.1021/ol3027939 Text en Copyright © 2012 American Chemical Society http://pubs.acs.org This is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org. |
spellingShingle | Brant, Michael G. Wulff, Jeremy E. A Rigid Bicyclic Platform for the Generation of Conformationally Locked Neuraminidase Inhibitors |
title | A Rigid Bicyclic Platform for the Generation of Conformationally Locked Neuraminidase Inhibitors |
title_full | A Rigid Bicyclic Platform for the Generation of Conformationally Locked Neuraminidase Inhibitors |
title_fullStr | A Rigid Bicyclic Platform for the Generation of Conformationally Locked Neuraminidase Inhibitors |
title_full_unstemmed | A Rigid Bicyclic Platform for the Generation of Conformationally Locked Neuraminidase Inhibitors |
title_short | A Rigid Bicyclic Platform for the Generation of Conformationally Locked Neuraminidase Inhibitors |
title_sort | rigid bicyclic platform for the generation of conformationally locked neuraminidase inhibitors |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3516865/ https://www.ncbi.nlm.nih.gov/pubmed/23181823 http://dx.doi.org/10.1021/ol3027939 |
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