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Synthesis and antibacterial activity of a new derivative of the Meldrun acid: 2,2-dimethyl-5-(4H-1,2,4-triazol-4-ylaminomethylene)-1,3-dioxane-4,6-dione (C(9)H(10)N(4)O(4))

The discovery of new substances with proven antimicrobial activity is the current study goal of various researchers. Usage of synthetic products has grown considerably in the past few years due to processing agility, and capability of going through previous chemical modifications in order to enhance...

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Autores principales: Sampaio, Gillena M. M., Teixeira, Alexandre M. R., Coutinho, Henrique D. M., Sena Junior, Diniz M., Freire, Paulo T. C., Bento, Ricardo R. F., Silva, Luiz E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Leibniz Research Centre for Working Environment and Human Factors 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4464433/
https://www.ncbi.nlm.nih.gov/pubmed/26417318
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author Sampaio, Gillena M. M.
Teixeira, Alexandre M. R.
Coutinho, Henrique D. M.
Sena Junior, Diniz M.
Freire, Paulo T. C.
Bento, Ricardo R. F.
Silva, Luiz E.
author_facet Sampaio, Gillena M. M.
Teixeira, Alexandre M. R.
Coutinho, Henrique D. M.
Sena Junior, Diniz M.
Freire, Paulo T. C.
Bento, Ricardo R. F.
Silva, Luiz E.
author_sort Sampaio, Gillena M. M.
collection PubMed
description The discovery of new substances with proven antimicrobial activity is the current study goal of various researchers. Usage of synthetic products has grown considerably in the past few years due to processing agility, and capability of going through previous chemical modifications in order to enhance its biological activity. Widespread careless use of antimicrobials has made the number of resistant microorganisms rise significantly, thus demanding more efficient drugs to fight them. One of these synthetic candidates for this purpose is the substance 2,2-Dimethyl-5-(4H-1,2,4-triazol-4-ylaminomethylene)-1,3-dioxane-4,6-dione (C(9)H(10)N(4)O(4)), aminomethylene derivative from Meldrum's acid. This substance, alone and in association with common antibiotics, were evaluated in vitro for antimicrobial activity, and had their minimum inhibitory concentration (MIC) towards Staphylococcus aureus ATCC 25923, Escherichia coli ATCC 10536 and Pseudomonas aeruginosa ATCC 15442, as well as multiresistant strains Escherichia coli 27, Staphylococcus aureus 358 and Pseudomonas aeruginosa 03 determined. The antimicrobial modulation action tests of the aminoglycosides with C(9)H(10)N(4)O(4) were performed according to the microdilution method, and resulted in observation of a positive synergic effect.
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spelling pubmed-44644332015-09-28 Synthesis and antibacterial activity of a new derivative of the Meldrun acid: 2,2-dimethyl-5-(4H-1,2,4-triazol-4-ylaminomethylene)-1,3-dioxane-4,6-dione (C(9)H(10)N(4)O(4)) Sampaio, Gillena M. M. Teixeira, Alexandre M. R. Coutinho, Henrique D. M. Sena Junior, Diniz M. Freire, Paulo T. C. Bento, Ricardo R. F. Silva, Luiz E. EXCLI J Original Article The discovery of new substances with proven antimicrobial activity is the current study goal of various researchers. Usage of synthetic products has grown considerably in the past few years due to processing agility, and capability of going through previous chemical modifications in order to enhance its biological activity. Widespread careless use of antimicrobials has made the number of resistant microorganisms rise significantly, thus demanding more efficient drugs to fight them. One of these synthetic candidates for this purpose is the substance 2,2-Dimethyl-5-(4H-1,2,4-triazol-4-ylaminomethylene)-1,3-dioxane-4,6-dione (C(9)H(10)N(4)O(4)), aminomethylene derivative from Meldrum's acid. This substance, alone and in association with common antibiotics, were evaluated in vitro for antimicrobial activity, and had their minimum inhibitory concentration (MIC) towards Staphylococcus aureus ATCC 25923, Escherichia coli ATCC 10536 and Pseudomonas aeruginosa ATCC 15442, as well as multiresistant strains Escherichia coli 27, Staphylococcus aureus 358 and Pseudomonas aeruginosa 03 determined. The antimicrobial modulation action tests of the aminoglycosides with C(9)H(10)N(4)O(4) were performed according to the microdilution method, and resulted in observation of a positive synergic effect. Leibniz Research Centre for Working Environment and Human Factors 2014-09-01 /pmc/articles/PMC4464433/ /pubmed/26417318 Text en Copyright © 2014 Sampaio et al. http://www.excli.de/documents/assignment_of_rights.pdf This is an Open Access article distributed under the following Assignment of Rights http://www.excli.de/documents/assignment_of_rights.pdf. You are free to copy, distribute and transmit the work, provided the original author and source are credited.
spellingShingle Original Article
Sampaio, Gillena M. M.
Teixeira, Alexandre M. R.
Coutinho, Henrique D. M.
Sena Junior, Diniz M.
Freire, Paulo T. C.
Bento, Ricardo R. F.
Silva, Luiz E.
Synthesis and antibacterial activity of a new derivative of the Meldrun acid: 2,2-dimethyl-5-(4H-1,2,4-triazol-4-ylaminomethylene)-1,3-dioxane-4,6-dione (C(9)H(10)N(4)O(4))
title Synthesis and antibacterial activity of a new derivative of the Meldrun acid: 2,2-dimethyl-5-(4H-1,2,4-triazol-4-ylaminomethylene)-1,3-dioxane-4,6-dione (C(9)H(10)N(4)O(4))
title_full Synthesis and antibacterial activity of a new derivative of the Meldrun acid: 2,2-dimethyl-5-(4H-1,2,4-triazol-4-ylaminomethylene)-1,3-dioxane-4,6-dione (C(9)H(10)N(4)O(4))
title_fullStr Synthesis and antibacterial activity of a new derivative of the Meldrun acid: 2,2-dimethyl-5-(4H-1,2,4-triazol-4-ylaminomethylene)-1,3-dioxane-4,6-dione (C(9)H(10)N(4)O(4))
title_full_unstemmed Synthesis and antibacterial activity of a new derivative of the Meldrun acid: 2,2-dimethyl-5-(4H-1,2,4-triazol-4-ylaminomethylene)-1,3-dioxane-4,6-dione (C(9)H(10)N(4)O(4))
title_short Synthesis and antibacterial activity of a new derivative of the Meldrun acid: 2,2-dimethyl-5-(4H-1,2,4-triazol-4-ylaminomethylene)-1,3-dioxane-4,6-dione (C(9)H(10)N(4)O(4))
title_sort synthesis and antibacterial activity of a new derivative of the meldrun acid: 2,2-dimethyl-5-(4h-1,2,4-triazol-4-ylaminomethylene)-1,3-dioxane-4,6-dione (c(9)h(10)n(4)o(4))
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4464433/
https://www.ncbi.nlm.nih.gov/pubmed/26417318
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