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Synthesis and biological evaluation of formazan derivatives

The formazan derivatives (FM1–FM5) were synthesized by the reaction of benzaldehyde phenylhydrazone with substituted aromatic and hetero aromatic amines. The structures of the synthesized compounds were then elucidated using UV, IR, (1)H NMR and mass spectral data. The synthesized derivatives were s...

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Autores principales: Mariappan, Gurusamy, Korim, Rejaul, Joshi, Nand Madhwa, Alam, Faruk, Hazarika, Rajib, Kumar, Deepak, Uriah, Tiewlasubon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3255400/
https://www.ncbi.nlm.nih.gov/pubmed/22247879
http://dx.doi.org/10.4103/0110-5558.76438
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author Mariappan, Gurusamy
Korim, Rejaul
Joshi, Nand Madhwa
Alam, Faruk
Hazarika, Rajib
Kumar, Deepak
Uriah, Tiewlasubon
author_facet Mariappan, Gurusamy
Korim, Rejaul
Joshi, Nand Madhwa
Alam, Faruk
Hazarika, Rajib
Kumar, Deepak
Uriah, Tiewlasubon
author_sort Mariappan, Gurusamy
collection PubMed
description The formazan derivatives (FM1–FM5) were synthesized by the reaction of benzaldehyde phenylhydrazone with substituted aromatic and hetero aromatic amines. The structures of the synthesized compounds were then elucidated using UV, IR, (1)H NMR and mass spectral data. The synthesized derivatives were screened for anticonvulsant, antibacterial and antiviral activities. All the compounds showed remarkable antibacterial activity at 250 μg/ml, but FM4 and FM3 did not show any inhibition on Staphylococcus aureus and Vibriocholera, respectively. All the compounds showed significant anticonvulsant effect at 100 mg/kg p.o. and the experimental data were statistically significant at P<0.001 level. But none of the compounds was effective against Japanese encephalitis virus.
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spelling pubmed-32554002012-01-13 Synthesis and biological evaluation of formazan derivatives Mariappan, Gurusamy Korim, Rejaul Joshi, Nand Madhwa Alam, Faruk Hazarika, Rajib Kumar, Deepak Uriah, Tiewlasubon J Adv Pharm Technol Res Original Article The formazan derivatives (FM1–FM5) were synthesized by the reaction of benzaldehyde phenylhydrazone with substituted aromatic and hetero aromatic amines. The structures of the synthesized compounds were then elucidated using UV, IR, (1)H NMR and mass spectral data. The synthesized derivatives were screened for anticonvulsant, antibacterial and antiviral activities. All the compounds showed remarkable antibacterial activity at 250 μg/ml, but FM4 and FM3 did not show any inhibition on Staphylococcus aureus and Vibriocholera, respectively. All the compounds showed significant anticonvulsant effect at 100 mg/kg p.o. and the experimental data were statistically significant at P<0.001 level. But none of the compounds was effective against Japanese encephalitis virus. Medknow Publications & Media Pvt Ltd 2010 /pmc/articles/PMC3255400/ /pubmed/22247879 http://dx.doi.org/10.4103/0110-5558.76438 Text en Copyright: © Journal of Advanced Pharmaceutical Technology & Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Mariappan, Gurusamy
Korim, Rejaul
Joshi, Nand Madhwa
Alam, Faruk
Hazarika, Rajib
Kumar, Deepak
Uriah, Tiewlasubon
Synthesis and biological evaluation of formazan derivatives
title Synthesis and biological evaluation of formazan derivatives
title_full Synthesis and biological evaluation of formazan derivatives
title_fullStr Synthesis and biological evaluation of formazan derivatives
title_full_unstemmed Synthesis and biological evaluation of formazan derivatives
title_short Synthesis and biological evaluation of formazan derivatives
title_sort synthesis and biological evaluation of formazan derivatives
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3255400/
https://www.ncbi.nlm.nih.gov/pubmed/22247879
http://dx.doi.org/10.4103/0110-5558.76438
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