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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Main Authors: Roger Vásquez, Nivia Rios, Godofredo Solano, Luis Cubilla-Rios
Format: Article
Language:English
Published: MDPI AG 2018-03-01
Series:Molecules
Subjects:
Online Access:http://www.mdpi.com/1420-3049/23/4/773
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spelling doaj-d04ccfea0273441d90e986b399b3d1512020-11-24T20:59:55ZengMDPI AGMolecules1420-30492018-03-0123477310.3390/molecules23040773molecules23040773Lentinoids A–D, New Natural Products Isolated from Lentinus strigellusRoger Vásquez0Nivia Rios1Godofredo Solano2Luis Cubilla-Rios3Laboratory of Tropical Bioorganic Chemistry, Faculty of Natural, Exact Sciences and Technology, University of Panama, Panama 0824, PanamaDepartment of Microbiology, Faculty of Natural, Exact Sciences and Technology, University of Panama, Panama 0824, PanamaCentro de Investigaciones en Productos Naturales (CIPRONA), Universidad de Costa Rica, San José 2060, Costa RicaLaboratory of Tropical Bioorganic Chemistry, Faculty of Natural, Exact Sciences and Technology, University of Panama, Panama 0824, PanamaFour 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.http://www.mdpi.com/1420-3049/23/4/773Lentinus strigelluslentinoidsantibacterialpanepoxydoneisopanepoxydone
collection DOAJ
language English
format Article
sources DOAJ
author Roger Vásquez
Nivia Rios
Godofredo Solano
Luis Cubilla-Rios
spellingShingle Roger Vásquez
Nivia Rios
Godofredo Solano
Luis Cubilla-Rios
Lentinoids A–D, New Natural Products Isolated from Lentinus strigellus
Molecules
Lentinus strigellus
lentinoids
antibacterial
panepoxydone
isopanepoxydone
author_facet Roger Vásquez
Nivia Rios
Godofredo Solano
Luis Cubilla-Rios
author_sort Roger Vásquez
title Lentinoids A–D, New Natural Products Isolated from Lentinus strigellus
title_short 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_sort lentinoids a–d, new natural products isolated from lentinus strigellus
publisher MDPI AG
series Molecules
issn 1420-3049
publishDate 2018-03-01
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.
topic Lentinus strigellus
lentinoids
antibacterial
panepoxydone
isopanepoxydone
url http://www.mdpi.com/1420-3049/23/4/773
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