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Lentinoids A–D, New Natural Products Isolated from Lentinus strigellus

Four novel lentinoids (1–4), along with the known compounds striguellone A (5), isopanepoxydone (6) and panepoxydone (7), were isolated as part of our studies on Lentinus strigellus. The structures of 1–4 have been established by 1D- and 2D-NMR and MS analysis. Compounds (1–3) and (5–7) were tested...

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Autores principales: Vásquez, Roger, Rios, Nivia, Solano, Godofredo, Cubilla-Rios, Luis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017980/
https://www.ncbi.nlm.nih.gov/pubmed/29597242
http://dx.doi.org/10.3390/molecules23040773
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author Vásquez, Roger
Rios, Nivia
Solano, Godofredo
Cubilla-Rios, Luis
author_facet Vásquez, Roger
Rios, Nivia
Solano, Godofredo
Cubilla-Rios, Luis
author_sort Vásquez, Roger
collection PubMed
description Four novel lentinoids (1–4), along with the known compounds striguellone A (5), isopanepoxydone (6) and panepoxydone (7), were isolated as part of our studies on Lentinus strigellus. The structures of 1–4 have been established by 1D- and 2D-NMR and MS analysis. Compounds (1–3) and (5–7) were tested against Listeria monocytogenes, Enterococcus faecalis, Pseudomonas aeruginosa and Klebsiella pneumoniae. These compounds showed inhibition diameters ranging from 7.5–9.5 mm, however, when the minimum inhibitory concentration (MIC) was determined, only compound 1 showed a significant activity of 200 μg/mL. Intermediates for the biosynthesis of the oxygenated cyclohexenyl derivatives isolated from lentinoid fungi (genera Lentinus and Panus) are proposed.
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spelling pubmed-60179802018-11-13 Lentinoids A–D, New Natural Products Isolated from Lentinus strigellus Vásquez, Roger Rios, Nivia Solano, Godofredo Cubilla-Rios, Luis Molecules Article Four novel lentinoids (1–4), along with the known compounds striguellone A (5), isopanepoxydone (6) and panepoxydone (7), were isolated as part of our studies on Lentinus strigellus. The structures of 1–4 have been established by 1D- and 2D-NMR and MS analysis. Compounds (1–3) and (5–7) were tested against Listeria monocytogenes, Enterococcus faecalis, Pseudomonas aeruginosa and Klebsiella pneumoniae. These compounds showed inhibition diameters ranging from 7.5–9.5 mm, however, when the minimum inhibitory concentration (MIC) was determined, only compound 1 showed a significant activity of 200 μg/mL. Intermediates for the biosynthesis of the oxygenated cyclohexenyl derivatives isolated from lentinoid fungi (genera Lentinus and Panus) are proposed. MDPI 2018-03-28 /pmc/articles/PMC6017980/ /pubmed/29597242 http://dx.doi.org/10.3390/molecules23040773 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Vásquez, Roger
Rios, Nivia
Solano, Godofredo
Cubilla-Rios, Luis
Lentinoids A–D, New Natural Products Isolated from Lentinus strigellus
title Lentinoids A–D, New Natural Products Isolated from Lentinus strigellus
title_full Lentinoids A–D, New Natural Products Isolated from Lentinus strigellus
title_fullStr Lentinoids A–D, New Natural Products Isolated from Lentinus strigellus
title_full_unstemmed Lentinoids A–D, New Natural Products Isolated from Lentinus strigellus
title_short Lentinoids A–D, New Natural Products Isolated from Lentinus strigellus
title_sort lentinoids a–d, new natural products isolated from lentinus strigellus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017980/
https://www.ncbi.nlm.nih.gov/pubmed/29597242
http://dx.doi.org/10.3390/molecules23040773
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