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(+)-epi-Epoformin, a Phytotoxic Fungal Cyclohexenepoxide: Structure Activity Relationships

(+)-epi-Epoformin (1), is a fungal cyclohexene epoxide isolated together with diplopimarane and sphaeropsidins A and C, a nor-ent-pimarane and two pimaranes, from the culture filtrates of Diplodia quercivora, a fungal pathogen for cork oak in Sardinia, Italy. Compound 1 possesses a plethora of biolo...

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Autores principales: Cala, Antonio, Masi, Marco, Cimmino, Alessio, Molinillo, José M. G., Macias, Francisco A., Evidente, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6100255/
https://www.ncbi.nlm.nih.gov/pubmed/29941851
http://dx.doi.org/10.3390/molecules23071529
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author Cala, Antonio
Masi, Marco
Cimmino, Alessio
Molinillo, José M. G.
Macias, Francisco A.
Evidente, Antonio
author_facet Cala, Antonio
Masi, Marco
Cimmino, Alessio
Molinillo, José M. G.
Macias, Francisco A.
Evidente, Antonio
author_sort Cala, Antonio
collection PubMed
description (+)-epi-Epoformin (1), is a fungal cyclohexene epoxide isolated together with diplopimarane and sphaeropsidins A and C, a nor-ent-pimarane and two pimaranes, from the culture filtrates of Diplodia quercivora, a fungal pathogen for cork oak in Sardinia, Italy. Compound 1 possesses a plethora of biological activities, including antifungal, zootoxic and phytotoxic activity. The last activity and the peculiar structural feature of 1 suggested to carry out a structure activity relationship study, preparing eight key hemisynthetic derivatives and the phytotoxicity was assayed. The complete spectroscopic characterization and the activity in the etiolated wheat coleoptile bioassay of all the compounds is reported. Most of the compounds inhibited growth and some of them had comparable or higher activity than the natural product and the reference herbicide Logran. As regards the structure-activity relationship, the carbonyl proved to be essential for their activity of 1, as well as the conjugated double bond, while the epoxide could be altered with no significant loss.
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spelling pubmed-61002552018-11-13 (+)-epi-Epoformin, a Phytotoxic Fungal Cyclohexenepoxide: Structure Activity Relationships Cala, Antonio Masi, Marco Cimmino, Alessio Molinillo, José M. G. Macias, Francisco A. Evidente, Antonio Molecules Article (+)-epi-Epoformin (1), is a fungal cyclohexene epoxide isolated together with diplopimarane and sphaeropsidins A and C, a nor-ent-pimarane and two pimaranes, from the culture filtrates of Diplodia quercivora, a fungal pathogen for cork oak in Sardinia, Italy. Compound 1 possesses a plethora of biological activities, including antifungal, zootoxic and phytotoxic activity. The last activity and the peculiar structural feature of 1 suggested to carry out a structure activity relationship study, preparing eight key hemisynthetic derivatives and the phytotoxicity was assayed. The complete spectroscopic characterization and the activity in the etiolated wheat coleoptile bioassay of all the compounds is reported. Most of the compounds inhibited growth and some of them had comparable or higher activity than the natural product and the reference herbicide Logran. As regards the structure-activity relationship, the carbonyl proved to be essential for their activity of 1, as well as the conjugated double bond, while the epoxide could be altered with no significant loss. MDPI 2018-06-25 /pmc/articles/PMC6100255/ /pubmed/29941851 http://dx.doi.org/10.3390/molecules23071529 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
Cala, Antonio
Masi, Marco
Cimmino, Alessio
Molinillo, José M. G.
Macias, Francisco A.
Evidente, Antonio
(+)-epi-Epoformin, a Phytotoxic Fungal Cyclohexenepoxide: Structure Activity Relationships
title (+)-epi-Epoformin, a Phytotoxic Fungal Cyclohexenepoxide: Structure Activity Relationships
title_full (+)-epi-Epoformin, a Phytotoxic Fungal Cyclohexenepoxide: Structure Activity Relationships
title_fullStr (+)-epi-Epoformin, a Phytotoxic Fungal Cyclohexenepoxide: Structure Activity Relationships
title_full_unstemmed (+)-epi-Epoformin, a Phytotoxic Fungal Cyclohexenepoxide: Structure Activity Relationships
title_short (+)-epi-Epoformin, a Phytotoxic Fungal Cyclohexenepoxide: Structure Activity Relationships
title_sort (+)-epi-epoformin, a phytotoxic fungal cyclohexenepoxide: structure activity relationships
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6100255/
https://www.ncbi.nlm.nih.gov/pubmed/29941851
http://dx.doi.org/10.3390/molecules23071529
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