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Anticonvulsant Potential of Certain New (2E)-2-[1-Aryl-3-(1H-imidazol-1-yl)propylidene]-N-(aryl/H)hydrazinecarboxamides
Anticonvulsant potential and neurotoxicity of certain new imidazole-containing arylsemicarbazones 6a–p are reported. The test compounds 6a–p exhibited anticonvulsant activity mainly in the scPTZ screen. Compound 6p emerged as the most active surrogate displaying 100% protection at a dose level of 63...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3913509/ https://www.ncbi.nlm.nih.gov/pubmed/24523636 http://dx.doi.org/10.1155/2014/357403 |
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author | Attia, Mohamed I. Aboul-Enein, Mohamed N. El-Azzouny, Aida A. Maklad, Yousreya A. Ghabbour, Hazem A. |
author_facet | Attia, Mohamed I. Aboul-Enein, Mohamed N. El-Azzouny, Aida A. Maklad, Yousreya A. Ghabbour, Hazem A. |
author_sort | Attia, Mohamed I. |
collection | PubMed |
description | Anticonvulsant potential and neurotoxicity of certain new imidazole-containing arylsemicarbazones 6a–p are reported. The test compounds 6a–p exhibited anticonvulsant activity mainly in the scPTZ screen. Compound 6p emerged as the most active surrogate displaying 100% protection at a dose level of 636 μmol/kg in the scPTZ screen without any neurotoxicity. The assigned (E)-configuration of the title compounds 6a–p was confirmed via single crystal X-ray structure of compound 6g. |
format | Online Article Text |
id | pubmed-3913509 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-39135092014-02-12 Anticonvulsant Potential of Certain New (2E)-2-[1-Aryl-3-(1H-imidazol-1-yl)propylidene]-N-(aryl/H)hydrazinecarboxamides Attia, Mohamed I. Aboul-Enein, Mohamed N. El-Azzouny, Aida A. Maklad, Yousreya A. Ghabbour, Hazem A. ScientificWorldJournal Research Article Anticonvulsant potential and neurotoxicity of certain new imidazole-containing arylsemicarbazones 6a–p are reported. The test compounds 6a–p exhibited anticonvulsant activity mainly in the scPTZ screen. Compound 6p emerged as the most active surrogate displaying 100% protection at a dose level of 636 μmol/kg in the scPTZ screen without any neurotoxicity. The assigned (E)-configuration of the title compounds 6a–p was confirmed via single crystal X-ray structure of compound 6g. Hindawi Publishing Corporation 2014-01-12 /pmc/articles/PMC3913509/ /pubmed/24523636 http://dx.doi.org/10.1155/2014/357403 Text en Copyright © 2014 Mohamed I. Attia et al. https://creativecommons.org/licenses/by/3.0/ 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 Attia, Mohamed I. Aboul-Enein, Mohamed N. El-Azzouny, Aida A. Maklad, Yousreya A. Ghabbour, Hazem A. Anticonvulsant Potential of Certain New (2E)-2-[1-Aryl-3-(1H-imidazol-1-yl)propylidene]-N-(aryl/H)hydrazinecarboxamides |
title | Anticonvulsant Potential of Certain New (2E)-2-[1-Aryl-3-(1H-imidazol-1-yl)propylidene]-N-(aryl/H)hydrazinecarboxamides |
title_full | Anticonvulsant Potential of Certain New (2E)-2-[1-Aryl-3-(1H-imidazol-1-yl)propylidene]-N-(aryl/H)hydrazinecarboxamides |
title_fullStr | Anticonvulsant Potential of Certain New (2E)-2-[1-Aryl-3-(1H-imidazol-1-yl)propylidene]-N-(aryl/H)hydrazinecarboxamides |
title_full_unstemmed | Anticonvulsant Potential of Certain New (2E)-2-[1-Aryl-3-(1H-imidazol-1-yl)propylidene]-N-(aryl/H)hydrazinecarboxamides |
title_short | Anticonvulsant Potential of Certain New (2E)-2-[1-Aryl-3-(1H-imidazol-1-yl)propylidene]-N-(aryl/H)hydrazinecarboxamides |
title_sort | anticonvulsant potential of certain new (2e)-2-[1-aryl-3-(1h-imidazol-1-yl)propylidene]-n-(aryl/h)hydrazinecarboxamides |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3913509/ https://www.ncbi.nlm.nih.gov/pubmed/24523636 http://dx.doi.org/10.1155/2014/357403 |
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