Comparisons of Halogenated β-Nitrostyrenes as Antimicrobial Agents

The influence of three types of halogen-substituted E-β-methyl-β-nitrostyrenes (such as Compounds B, D, H) to overcome bacterial activity that is currently a significant health threat was studied. The evaluations of their bio-potency was measured and related to their structure and activity relations...

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Main Authors: Hugh Cornell, Thu Nguyen, Gina Nicoletti, Neale Jackson, Helmut Hügel
Format: Article
Language:English
Published: MDPI AG 2014-08-01
Series:Applied Sciences
Subjects:
Online Access:http://www.mdpi.com/2076-3417/4/3/380
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spelling doaj-58ded44df8714ec29e557a1b193e90c82020-11-25T00:49:05ZengMDPI AGApplied Sciences2076-34172014-08-014338038910.3390/app4030380app4030380Comparisons of Halogenated β-Nitrostyrenes as Antimicrobial AgentsHugh Cornell0Thu Nguyen1Gina Nicoletti2Neale Jackson3Helmut Hügel4Health Innovations Research Institute & School of Applied Sciences RMIT University, Melbourne, VIC 3001, AustraliaHealth Innovations Research Institute & School of Applied Sciences RMIT University, Melbourne, VIC 3001, AustraliaHealth Innovations Research Institute & School of Applied Sciences RMIT University, Melbourne, VIC 3001, AustraliaHealth Innovations Research Institute & School of Applied Sciences RMIT University, Melbourne, VIC 3001, AustraliaHealth Innovations Research Institute & School of Applied Sciences RMIT University, Melbourne, VIC 3001, AustraliaThe influence of three types of halogen-substituted E-β-methyl-β-nitrostyrenes (such as Compounds B, D, H) to overcome bacterial activity that is currently a significant health threat was studied. The evaluations of their bio-potency was measured and related to their structure and activity relationships for the purposes of serving to inhibit and overcoming resistant microorganisms. In particular, fluorine-containing β-nitrostyrenes were found to be highly active antimicrobial agents. The addition of the β-bromo group enhanced the antibacterial activity significantly. Our work has illustrated that halogen substituents at both the 4-position in the aromatic ring and also at the β-position on the alkene side chain of nitropropenyl arenes enhanced the antimicrobial activity of these compounds.http://www.mdpi.com/2076-3417/4/3/380antimicrobial agentsmedicinal chemistryhalogenated β-methyl-β-nitrostyrenesMinimum Inhibitory Concentration
collection DOAJ
language English
format Article
sources DOAJ
author Hugh Cornell
Thu Nguyen
Gina Nicoletti
Neale Jackson
Helmut Hügel
spellingShingle Hugh Cornell
Thu Nguyen
Gina Nicoletti
Neale Jackson
Helmut Hügel
Comparisons of Halogenated β-Nitrostyrenes as Antimicrobial Agents
Applied Sciences
antimicrobial agents
medicinal chemistry
halogenated β-methyl-β-nitrostyrenes
Minimum Inhibitory Concentration
author_facet Hugh Cornell
Thu Nguyen
Gina Nicoletti
Neale Jackson
Helmut Hügel
author_sort Hugh Cornell
title Comparisons of Halogenated β-Nitrostyrenes as Antimicrobial Agents
title_short Comparisons of Halogenated β-Nitrostyrenes as Antimicrobial Agents
title_full Comparisons of Halogenated β-Nitrostyrenes as Antimicrobial Agents
title_fullStr Comparisons of Halogenated β-Nitrostyrenes as Antimicrobial Agents
title_full_unstemmed Comparisons of Halogenated β-Nitrostyrenes as Antimicrobial Agents
title_sort comparisons of halogenated β-nitrostyrenes as antimicrobial agents
publisher MDPI AG
series Applied Sciences
issn 2076-3417
publishDate 2014-08-01
description The influence of three types of halogen-substituted E-β-methyl-β-nitrostyrenes (such as Compounds B, D, H) to overcome bacterial activity that is currently a significant health threat was studied. The evaluations of their bio-potency was measured and related to their structure and activity relationships for the purposes of serving to inhibit and overcoming resistant microorganisms. In particular, fluorine-containing β-nitrostyrenes were found to be highly active antimicrobial agents. The addition of the β-bromo group enhanced the antibacterial activity significantly. Our work has illustrated that halogen substituents at both the 4-position in the aromatic ring and also at the β-position on the alkene side chain of nitropropenyl arenes enhanced the antimicrobial activity of these compounds.
topic antimicrobial agents
medicinal chemistry
halogenated β-methyl-β-nitrostyrenes
Minimum Inhibitory Concentration
url http://www.mdpi.com/2076-3417/4/3/380
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