Investigation of antibacterial activity of cinnamyl derivatives of arylpiperazine

The derivatives of cinnamic acid and N-arylpiperazine show antibacterial activity. In this work the potential synergistic effect of cinnamyl derivatives of arylpiperazine in selected bacteria was investigated. The antibacterial activities of the derivatives were evaluated against Gram-positive b...

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Main Authors: Novaković Irena, Penjišević Jelena, Šukalović V., Andrić Deana, Roglić G., Kostić-Rajačić Slađana
Format: Article
Language:English
Published: University of Belgrade, University of Novi Sad 2012-01-01
Series:Archives of Biological Sciences
Subjects:
Online Access:http://www.doiserbia.nb.rs/img/doi/0354-4664/2012/0354-46641201015N.pdf
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spelling doaj-b6f072df9a2144128874a6add0560bf52020-11-24T21:37:08ZengUniversity of Belgrade, University of Novi SadArchives of Biological Sciences0354-46641821-43392012-01-01641152010.2298/ABS1201015NInvestigation of antibacterial activity of cinnamyl derivatives of arylpiperazineNovaković IrenaPenjišević JelenaŠukalović V.Andrić DeanaRoglić G.Kostić-Rajačić SlađanaThe derivatives of cinnamic acid and N-arylpiperazine show antibacterial activity. In this work the potential synergistic effect of cinnamyl derivatives of arylpiperazine in selected bacteria was investigated. The antibacterial activities of the derivatives were evaluated against Gram-positive bacteria: Staphylococcus aureus, Streptosporangium longisporum, Sarcina lutea, Micrococcus flavus, Clostridium sporogenes and Bacillus subtilis and Gram-negative bacteria: Escherichia coli, Pseudomonas aeruginosa, Salmonella enteritidis and Proteus vulgaris by the disc diffusion method. The minimum inhibitory concentration (MIC) against the selected bacteria was determined for all compounds that showed activity in the disc diffusion method. The majority of the investigated compounds displayed in vitro antibacterial activity. The effect of the type and structure of the substituent on the aromatic ring on the antibacterial activity is discussed. It was found that two derivatives expressed activity toward S. longisporum and P. aeruginosa that was almost as strong as that of amikacin.http://www.doiserbia.nb.rs/img/doi/0354-4664/2012/0354-46641201015N.pdfarylpiperazineantibacterial activityminimum inhibitory concentrationin vitro studies
collection DOAJ
language English
format Article
sources DOAJ
author Novaković Irena
Penjišević Jelena
Šukalović V.
Andrić Deana
Roglić G.
Kostić-Rajačić Slađana
spellingShingle Novaković Irena
Penjišević Jelena
Šukalović V.
Andrić Deana
Roglić G.
Kostić-Rajačić Slađana
Investigation of antibacterial activity of cinnamyl derivatives of arylpiperazine
Archives of Biological Sciences
arylpiperazine
antibacterial activity
minimum inhibitory concentration
in vitro studies
author_facet Novaković Irena
Penjišević Jelena
Šukalović V.
Andrić Deana
Roglić G.
Kostić-Rajačić Slađana
author_sort Novaković Irena
title Investigation of antibacterial activity of cinnamyl derivatives of arylpiperazine
title_short Investigation of antibacterial activity of cinnamyl derivatives of arylpiperazine
title_full Investigation of antibacterial activity of cinnamyl derivatives of arylpiperazine
title_fullStr Investigation of antibacterial activity of cinnamyl derivatives of arylpiperazine
title_full_unstemmed Investigation of antibacterial activity of cinnamyl derivatives of arylpiperazine
title_sort investigation of antibacterial activity of cinnamyl derivatives of arylpiperazine
publisher University of Belgrade, University of Novi Sad
series Archives of Biological Sciences
issn 0354-4664
1821-4339
publishDate 2012-01-01
description The derivatives of cinnamic acid and N-arylpiperazine show antibacterial activity. In this work the potential synergistic effect of cinnamyl derivatives of arylpiperazine in selected bacteria was investigated. The antibacterial activities of the derivatives were evaluated against Gram-positive bacteria: Staphylococcus aureus, Streptosporangium longisporum, Sarcina lutea, Micrococcus flavus, Clostridium sporogenes and Bacillus subtilis and Gram-negative bacteria: Escherichia coli, Pseudomonas aeruginosa, Salmonella enteritidis and Proteus vulgaris by the disc diffusion method. The minimum inhibitory concentration (MIC) against the selected bacteria was determined for all compounds that showed activity in the disc diffusion method. The majority of the investigated compounds displayed in vitro antibacterial activity. The effect of the type and structure of the substituent on the aromatic ring on the antibacterial activity is discussed. It was found that two derivatives expressed activity toward S. longisporum and P. aeruginosa that was almost as strong as that of amikacin.
topic arylpiperazine
antibacterial activity
minimum inhibitory concentration
in vitro studies
url http://www.doiserbia.nb.rs/img/doi/0354-4664/2012/0354-46641201015N.pdf
work_keys_str_mv AT novakovicirena investigationofantibacterialactivityofcinnamylderivativesofarylpiperazine
AT penjisevicjelena investigationofantibacterialactivityofcinnamylderivativesofarylpiperazine
AT sukalovicv investigationofantibacterialactivityofcinnamylderivativesofarylpiperazine
AT andricdeana investigationofantibacterialactivityofcinnamylderivativesofarylpiperazine
AT roglicg investigationofantibacterialactivityofcinnamylderivativesofarylpiperazine
AT kosticrajacicslađana investigationofantibacterialactivityofcinnamylderivativesofarylpiperazine
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