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Antiviral Metal Complexes

The initial events (virus adsorption and fusion with the cells) in the replicative cycle of human immunodeficiency virus (HIV) can serve as targets for the antiviral action of metal-binding compounds such as polyanionic compounds (polysulfates, polysulfonates, polycarboxylates, polyoxometalates, and...

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Detalles Bibliográficos
Autor principal: De Clercq, Erik
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2365060/
https://www.ncbi.nlm.nih.gov/pubmed/18475787
http://dx.doi.org/10.1155/MBD.1997.173
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author De Clercq, Erik
author_facet De Clercq, Erik
author_sort De Clercq, Erik
collection PubMed
description The initial events (virus adsorption and fusion with the cells) in the replicative cycle of human immunodeficiency virus (HIV) can serve as targets for the antiviral action of metal-binding compounds such as polyanionic compounds (polysulfates, polysulfonates, polycarboxylates, polyoxometalates, and sulfonated or carboxylated metalloporphyrins), bicyclams and G-octet-forming oligonucleotides. The adsorption and fusion of HIV with its target cells depends on the interaction of the viral envelope glycoproteins (gp 120) with the receptors (CD4, CXCR4) at the outer cell membrane. We are currently investigating how the aforementioned compounds interfere with these viral glycoproteins and/or cell receptor.
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spelling pubmed-23650602008-05-12 Antiviral Metal Complexes De Clercq, Erik Met Based Drugs Research Article The initial events (virus adsorption and fusion with the cells) in the replicative cycle of human immunodeficiency virus (HIV) can serve as targets for the antiviral action of metal-binding compounds such as polyanionic compounds (polysulfates, polysulfonates, polycarboxylates, polyoxometalates, and sulfonated or carboxylated metalloporphyrins), bicyclams and G-octet-forming oligonucleotides. The adsorption and fusion of HIV with its target cells depends on the interaction of the viral envelope glycoproteins (gp 120) with the receptors (CD4, CXCR4) at the outer cell membrane. We are currently investigating how the aforementioned compounds interfere with these viral glycoproteins and/or cell receptor. Hindawi Publishing Corporation 1997 /pmc/articles/PMC2365060/ /pubmed/18475787 http://dx.doi.org/10.1155/MBD.1997.173 Text en Copyright © 1997 Hindawi Publishing Corporation. http://creativecommons.org/licenses/by/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
De Clercq, Erik
Antiviral Metal Complexes
title Antiviral Metal Complexes
title_full Antiviral Metal Complexes
title_fullStr Antiviral Metal Complexes
title_full_unstemmed Antiviral Metal Complexes
title_short Antiviral Metal Complexes
title_sort antiviral metal complexes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2365060/
https://www.ncbi.nlm.nih.gov/pubmed/18475787
http://dx.doi.org/10.1155/MBD.1997.173
work_keys_str_mv AT declercqerik antiviralmetalcomplexes