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Synthesis and Biological Evaluation of New 3-Phenyl-1-[(4-arylpiperazin-1-yl)alkyl]-piperidine-2,6-diones
A set of 13 alkyl derivatives of 3-phenylpiperidine-2,6-dione were synthesized. Newly obtained compounds were investigated in vitro against HIV-1 and other selected viruses. The benzyl 3f and fluorophenyl 3g derivatives showed moderate protection against CVB-2 and the compound 3g also against HSV-1....
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Österreichische Apotheker-Verlagsgesellschaft
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3134852/ https://www.ncbi.nlm.nih.gov/pubmed/21773062 http://dx.doi.org/10.3797/scipharm.1012-17 |
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author | Bielenica, Anna Kossakowski, Jerzy Struga, Marta Dybała, Izabela Loddo, Roberta Ibba, Cristina La Colla, Paolo |
author_facet | Bielenica, Anna Kossakowski, Jerzy Struga, Marta Dybała, Izabela Loddo, Roberta Ibba, Cristina La Colla, Paolo |
author_sort | Bielenica, Anna |
collection | PubMed |
description | A set of 13 alkyl derivatives of 3-phenylpiperidine-2,6-dione were synthesized. Newly obtained compounds were investigated in vitro against HIV-1 and other selected viruses. The benzyl 3f and fluorophenyl 3g derivatives showed moderate protection against CVB-2 and the compound 3g also against HSV-1. Derivatives were tested also for their antibacterial and antifungal activity. The molecular structures of 3a and 3d were determined by an X-ray analysis. |
format | Online Article Text |
id | pubmed-3134852 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Österreichische Apotheker-Verlagsgesellschaft |
record_format | MEDLINE/PubMed |
spelling | pubmed-31348522011-07-19 Synthesis and Biological Evaluation of New 3-Phenyl-1-[(4-arylpiperazin-1-yl)alkyl]-piperidine-2,6-diones Bielenica, Anna Kossakowski, Jerzy Struga, Marta Dybała, Izabela Loddo, Roberta Ibba, Cristina La Colla, Paolo Sci Pharm Research Article A set of 13 alkyl derivatives of 3-phenylpiperidine-2,6-dione were synthesized. Newly obtained compounds were investigated in vitro against HIV-1 and other selected viruses. The benzyl 3f and fluorophenyl 3g derivatives showed moderate protection against CVB-2 and the compound 3g also against HSV-1. Derivatives were tested also for their antibacterial and antifungal activity. The molecular structures of 3a and 3d were determined by an X-ray analysis. Österreichische Apotheker-Verlagsgesellschaft 2011 2011-02-12 /pmc/articles/PMC3134852/ /pubmed/21773062 http://dx.doi.org/10.3797/scipharm.1012-17 Text en © Bielenica et al.; licensee Österreichische Apotheker-Verlagsgesellschaft m. b. H., Vienna, Austria. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Bielenica, Anna Kossakowski, Jerzy Struga, Marta Dybała, Izabela Loddo, Roberta Ibba, Cristina La Colla, Paolo Synthesis and Biological Evaluation of New 3-Phenyl-1-[(4-arylpiperazin-1-yl)alkyl]-piperidine-2,6-diones |
title | Synthesis and Biological Evaluation of New 3-Phenyl-1-[(4-arylpiperazin-1-yl)alkyl]-piperidine-2,6-diones |
title_full | Synthesis and Biological Evaluation of New 3-Phenyl-1-[(4-arylpiperazin-1-yl)alkyl]-piperidine-2,6-diones |
title_fullStr | Synthesis and Biological Evaluation of New 3-Phenyl-1-[(4-arylpiperazin-1-yl)alkyl]-piperidine-2,6-diones |
title_full_unstemmed | Synthesis and Biological Evaluation of New 3-Phenyl-1-[(4-arylpiperazin-1-yl)alkyl]-piperidine-2,6-diones |
title_short | Synthesis and Biological Evaluation of New 3-Phenyl-1-[(4-arylpiperazin-1-yl)alkyl]-piperidine-2,6-diones |
title_sort | synthesis and biological evaluation of new 3-phenyl-1-[(4-arylpiperazin-1-yl)alkyl]-piperidine-2,6-diones |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3134852/ https://www.ncbi.nlm.nih.gov/pubmed/21773062 http://dx.doi.org/10.3797/scipharm.1012-17 |
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