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Functionalized Cyclopentenones and an Oxime Ether as Antimicrobial Agents
Several naturally occurring cyclopentenones, such as palmenones and nigrosporiones, exhibit antimicrobial activity. Herein we describe the antimicrobial activity of cyclopentenones and derivatives that can be easily accessed from biomass derivatives furfural and 5‐hydroxymethylfurfural. Upon screeni...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518054/ https://www.ncbi.nlm.nih.gov/pubmed/34115919 http://dx.doi.org/10.1002/cmdc.202100369 |
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author | Gomes, Rafael F. A. Isca, Vera M. S. Andrade, Késsia Rijo, Patrícia Afonso, Carlos A. M. |
author_facet | Gomes, Rafael F. A. Isca, Vera M. S. Andrade, Késsia Rijo, Patrícia Afonso, Carlos A. M. |
author_sort | Gomes, Rafael F. A. |
collection | PubMed |
description | Several naturally occurring cyclopentenones, such as palmenones and nigrosporiones, exhibit antimicrobial activity. Herein we describe the antimicrobial activity of cyclopentenones and derivatives that can be easily accessed from biomass derivatives furfural and 5‐hydroxymethylfurfural. Upon screening a range of functionalized trans‐diamino‐cyclopentenones (DCPs) and δ‐lactone‐fused cyclopentenones (LCPs), an oxime ether derivative of DCP was identified that exhibited remarkable antimicrobial activity against Gram‐positive bacteria, including resistant strains such as methicillin‐resistant S. aureus (MRSA) and vancomycin‐resistant E. faecalis (VRE) strains. |
format | Online Article Text |
id | pubmed-8518054 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85180542021-10-21 Functionalized Cyclopentenones and an Oxime Ether as Antimicrobial Agents Gomes, Rafael F. A. Isca, Vera M. S. Andrade, Késsia Rijo, Patrícia Afonso, Carlos A. M. ChemMedChem Communications Several naturally occurring cyclopentenones, such as palmenones and nigrosporiones, exhibit antimicrobial activity. Herein we describe the antimicrobial activity of cyclopentenones and derivatives that can be easily accessed from biomass derivatives furfural and 5‐hydroxymethylfurfural. Upon screening a range of functionalized trans‐diamino‐cyclopentenones (DCPs) and δ‐lactone‐fused cyclopentenones (LCPs), an oxime ether derivative of DCP was identified that exhibited remarkable antimicrobial activity against Gram‐positive bacteria, including resistant strains such as methicillin‐resistant S. aureus (MRSA) and vancomycin‐resistant E. faecalis (VRE) strains. John Wiley and Sons Inc. 2021-07-02 2021-09-16 /pmc/articles/PMC8518054/ /pubmed/34115919 http://dx.doi.org/10.1002/cmdc.202100369 Text en © 2021 The Authors. ChemMedChem published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Communications Gomes, Rafael F. A. Isca, Vera M. S. Andrade, Késsia Rijo, Patrícia Afonso, Carlos A. M. Functionalized Cyclopentenones and an Oxime Ether as Antimicrobial Agents |
title | Functionalized Cyclopentenones and an Oxime Ether as Antimicrobial Agents |
title_full | Functionalized Cyclopentenones and an Oxime Ether as Antimicrobial Agents |
title_fullStr | Functionalized Cyclopentenones and an Oxime Ether as Antimicrobial Agents |
title_full_unstemmed | Functionalized Cyclopentenones and an Oxime Ether as Antimicrobial Agents |
title_short | Functionalized Cyclopentenones and an Oxime Ether as Antimicrobial Agents |
title_sort | functionalized cyclopentenones and an oxime ether as antimicrobial agents |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518054/ https://www.ncbi.nlm.nih.gov/pubmed/34115919 http://dx.doi.org/10.1002/cmdc.202100369 |
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