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Synthesis of quinolones and zwitterionic quinolonate derivatives with broad-spectrum antibiotic activity
Title: | Synthesis of quinolones and zwitterionic quinolonate derivatives with broad-spectrum antibiotic activity |
Authors : | Suay García, Beatriz Bueso Bordils, José Ignacio Antón Fos, Gerardo Manuel Pérez Gracia, María Teresa. Falcó Montesinos, Antonio Alemán López, Pedro |
Keywords: | Bacteria - Drug resistance - Mathematical models.; Biología molecular - Modelos matemáticos.; Molecular biology - Mathematical models.; Topología - Aplicaciones en bioquímica.; Bacterias - Resistencia a los medicamentos - Modelos matemáticos.; Quinolonas - Modelos matemáticos.; Quinolone antibacterial agents - Mathematical models.; Antibióticos - Modelos matemáticos.; Antibiotics - Mathematical models.; Topology in biochemistry. |
Publisher: | MDPI |
Citation: | Suay-García, B., Bueso-Bordils, J. I., Antón-Fos, G., Pérez-Gracia, M. T., Falcó, A. & Alemán-López, P. (2022). Synthesis of quinolones and zwitterionic quinolonate derivatives with broad-spectrum antibiotic activity. Pharmaceuticals, vol. 15, i. 7 (01 jul.), art. 818. DOI: https://doi.org/10.3390/ph15070818 |
Abstract: | Quinolones are one of the most extensively used therapeutic families of antibiotics. However, the increase in antibiotic-resistant bacteria has rendered many of the available compounds useless. After applying our prediction model of activity against E. coli to a library of 1000 quinolones, two quinolones were selected to be synthesized. Additionally, a series of zwitterionic quinolonates were also synthesized. Quinolones and zwitterionic quinolonates were obtained by coupling the corresponding amine with reagent 1 in acetonitrile. Antibacterial activity was assessed using a microdilution method. All the compounds presented antibacterial activity, especially quinolones 2 and 3, selected by the prediction model, which had broad-spectrum activity. Furthermore, a new type of zwitterionic quinolonate with antibacterial activity was found. These compounds can lead to a new line of antimicrobials, as the structures, and, therefore, their properties, are easily adjustable in the amine in position 4 of the pyridine ring. |
Description: | Este artículo se encuentra disponible en la siguiente URL: https://www.mdpi.com/1424-8247/15/7/818 Este artículo de investigación pertenece al número especial "Novel Antibacterial Agents 2022". |
URI: | http://hdl.handle.net/10637/14213 |
Rights : | http://creativecommons.org/licenses/by/4.0/deed.es |
ISSN: | 1424-8247 (Electrónico) |
Language: | es |
Issue Date: | 1-Jul-2022 |
Center : | Universidad Cardenal Herrera-CEU |
Appears in Collections: | Dpto. Farmacia |
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