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Antiviral Activity of 4′-thioIDU and Thymidine Analogs against Orthopoxviruses

The search for effective therapies for orthopoxvirus infections has identified diverse classes of molecules with antiviral activity. Pyrimidine analogs, such as 5-iodo-2′-deoxyuridine (idoxuridine, IDU) were among the first compounds identified with antiviral activity against a number of orthopoxvir...

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Detalles Bibliográficos
Autores principales: Prichard, Mark N., Kern, Earl R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185742/
https://www.ncbi.nlm.nih.gov/pubmed/21994716
http://dx.doi.org/10.3390/v2091968
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author Prichard, Mark N.
Kern, Earl R.
author_facet Prichard, Mark N.
Kern, Earl R.
author_sort Prichard, Mark N.
collection PubMed
description The search for effective therapies for orthopoxvirus infections has identified diverse classes of molecules with antiviral activity. Pyrimidine analogs, such as 5-iodo-2′-deoxyuridine (idoxuridine, IDU) were among the first compounds identified with antiviral activity against a number of orthopoxviruses and have been reported to be active both in vitro and in animal models of infection. More recently, additional analogs have been reported to have improved antiviral activity against orthopoxviruses including several derivatives of deoxyuridine with large substituents in the 5 position, as well as analogs with modifications in the deoxyribose moiety including (north)-methanocarbathymidine, and 5-iodo-4′-thio-2′-deoxyuridine (4′-thioIDU). The latter molecule has proven to have good antiviral activity against the orthopoxviruses both in vitro and in vivo and has the potential to be an effective therapy in humans.
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spelling pubmed-31857422011-10-12 Antiviral Activity of 4′-thioIDU and Thymidine Analogs against Orthopoxviruses Prichard, Mark N. Kern, Earl R. Viruses Review The search for effective therapies for orthopoxvirus infections has identified diverse classes of molecules with antiviral activity. Pyrimidine analogs, such as 5-iodo-2′-deoxyuridine (idoxuridine, IDU) were among the first compounds identified with antiviral activity against a number of orthopoxviruses and have been reported to be active both in vitro and in animal models of infection. More recently, additional analogs have been reported to have improved antiviral activity against orthopoxviruses including several derivatives of deoxyuridine with large substituents in the 5 position, as well as analogs with modifications in the deoxyribose moiety including (north)-methanocarbathymidine, and 5-iodo-4′-thio-2′-deoxyuridine (4′-thioIDU). The latter molecule has proven to have good antiviral activity against the orthopoxviruses both in vitro and in vivo and has the potential to be an effective therapy in humans. Molecular Diversity Preservation International (MDPI) 2010-09-16 /pmc/articles/PMC3185742/ /pubmed/21994716 http://dx.doi.org/10.3390/v2091968 Text en © 2010 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Prichard, Mark N.
Kern, Earl R.
Antiviral Activity of 4′-thioIDU and Thymidine Analogs against Orthopoxviruses
title Antiviral Activity of 4′-thioIDU and Thymidine Analogs against Orthopoxviruses
title_full Antiviral Activity of 4′-thioIDU and Thymidine Analogs against Orthopoxviruses
title_fullStr Antiviral Activity of 4′-thioIDU and Thymidine Analogs against Orthopoxviruses
title_full_unstemmed Antiviral Activity of 4′-thioIDU and Thymidine Analogs against Orthopoxviruses
title_short Antiviral Activity of 4′-thioIDU and Thymidine Analogs against Orthopoxviruses
title_sort antiviral activity of 4′-thioidu and thymidine analogs against orthopoxviruses
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185742/
https://www.ncbi.nlm.nih.gov/pubmed/21994716
http://dx.doi.org/10.3390/v2091968
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