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5-Arylaminouracil Derivatives as Potential Dual-Action Agents
Several 5-aminouracil derivatives that have previously been shown to inhibit Mycobacterium tuberculosis growth at concentrations of 5–40 μg/mL are demonstrated to act also as noncompetitive non-nucleoside inhibitors of HIV-1 reverse transcriptase without causing toxicity in vitro (MT-4 cells) and ex...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
A.I. Gordeyev
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4610172/ https://www.ncbi.nlm.nih.gov/pubmed/26483967 |
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author | Matyugina, E. S. Novikov, M. S. Babkov, D. A. Valuev-Elliston, V. T. Vanpouille, C. Zicari, S. Corona, A. Tramontano, E. Margolis, L. B. Khandazhinskaya, A. L. Kochetkov, S. N. |
author_facet | Matyugina, E. S. Novikov, M. S. Babkov, D. A. Valuev-Elliston, V. T. Vanpouille, C. Zicari, S. Corona, A. Tramontano, E. Margolis, L. B. Khandazhinskaya, A. L. Kochetkov, S. N. |
author_sort | Matyugina, E. S. |
collection | PubMed |
description | Several 5-aminouracil derivatives that have previously been shown to inhibit Mycobacterium tuberculosis growth at concentrations of 5–40 μg/mL are demonstrated to act also as noncompetitive non-nucleoside inhibitors of HIV-1 reverse transcriptase without causing toxicity in vitro (MT-4 cells) and ex vivo (human tonsillar tissue). |
format | Online Article Text |
id | pubmed-4610172 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | A.I. Gordeyev |
record_format | MEDLINE/PubMed |
spelling | pubmed-46101722015-10-19 5-Arylaminouracil Derivatives as Potential Dual-Action Agents Matyugina, E. S. Novikov, M. S. Babkov, D. A. Valuev-Elliston, V. T. Vanpouille, C. Zicari, S. Corona, A. Tramontano, E. Margolis, L. B. Khandazhinskaya, A. L. Kochetkov, S. N. Acta Naturae Research Article Several 5-aminouracil derivatives that have previously been shown to inhibit Mycobacterium tuberculosis growth at concentrations of 5–40 μg/mL are demonstrated to act also as noncompetitive non-nucleoside inhibitors of HIV-1 reverse transcriptase without causing toxicity in vitro (MT-4 cells) and ex vivo (human tonsillar tissue). A.I. Gordeyev 2015 /pmc/articles/PMC4610172/ /pubmed/26483967 Text en Copyright ® 2015 Park-media Ltd. http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of 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 Matyugina, E. S. Novikov, M. S. Babkov, D. A. Valuev-Elliston, V. T. Vanpouille, C. Zicari, S. Corona, A. Tramontano, E. Margolis, L. B. Khandazhinskaya, A. L. Kochetkov, S. N. 5-Arylaminouracil Derivatives as Potential Dual-Action Agents |
title | 5-Arylaminouracil Derivatives as Potential Dual-Action Agents |
title_full | 5-Arylaminouracil Derivatives as Potential Dual-Action Agents |
title_fullStr | 5-Arylaminouracil Derivatives as Potential Dual-Action Agents |
title_full_unstemmed | 5-Arylaminouracil Derivatives as Potential Dual-Action Agents |
title_short | 5-Arylaminouracil Derivatives as Potential Dual-Action Agents |
title_sort | 5-arylaminouracil derivatives as potential dual-action agents |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4610172/ https://www.ncbi.nlm.nih.gov/pubmed/26483967 |
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