Cargando…
Antifungal Activity of Extracts and Prenylated Coumarins Isolated from Baccharis darwinii Hook & Arn. (Asteraceae)
The petroleum ether extract of Baccharis darwinii showed activity against Cryptococcus neoformans and dermatophytes. Bioactivity-guided fractionation of Baccharis darwinii has resulted in the isolation of three coumarins: 5’-hydroxy aurapten (anisocoumarin H, 1), aurapten (7-geranyloxycoumarin, 2) a...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257657/ https://www.ncbi.nlm.nih.gov/pubmed/20657398 http://dx.doi.org/10.3390/molecules15074898 |
_version_ | 1783374364455993344 |
---|---|
author | Kurdelas, Rita R. Lima, Beatriz Tapia, Alejandro Egly Feresin, Gabriela Gonzalez Sierra, Manuel Rodríguez, María Victoria Zacchino, Susana Enriz, Ricardo D. Freile, Monica L. |
author_facet | Kurdelas, Rita R. Lima, Beatriz Tapia, Alejandro Egly Feresin, Gabriela Gonzalez Sierra, Manuel Rodríguez, María Victoria Zacchino, Susana Enriz, Ricardo D. Freile, Monica L. |
author_sort | Kurdelas, Rita R. |
collection | PubMed |
description | The petroleum ether extract of Baccharis darwinii showed activity against Cryptococcus neoformans and dermatophytes. Bioactivity-guided fractionation of Baccharis darwinii has resulted in the isolation of three coumarins: 5’-hydroxy aurapten (anisocoumarin H, 1), aurapten (7-geranyloxycoumarin, 2) and 5’-oxoaurapten (diversinin, 3). The structures of these compounds were characterized by spectroscopic methods. These compounds were evaluated for their antimicrobial activity against a panel of each, bacteria and fungi. Compound 3 showed the best activities against Microsporum gypseum, Trichophyton rubrum and Trichophyton mentagrophytes with MICs = 15.6 µg/mL, followed by compound 1 whose MICs against the same fungi were 62.5 µg/mL. In addition they showed fungicidal rather than fungistatic activity. Both compounds showed moderate activity (MICs = 125 µg/mL) against Cryptococcus neoformans. This is the first report of the presence of compound 1 in B. darwinii. |
format | Online Article Text |
id | pubmed-6257657 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62576572018-12-06 Antifungal Activity of Extracts and Prenylated Coumarins Isolated from Baccharis darwinii Hook & Arn. (Asteraceae) Kurdelas, Rita R. Lima, Beatriz Tapia, Alejandro Egly Feresin, Gabriela Gonzalez Sierra, Manuel Rodríguez, María Victoria Zacchino, Susana Enriz, Ricardo D. Freile, Monica L. Molecules Article The petroleum ether extract of Baccharis darwinii showed activity against Cryptococcus neoformans and dermatophytes. Bioactivity-guided fractionation of Baccharis darwinii has resulted in the isolation of three coumarins: 5’-hydroxy aurapten (anisocoumarin H, 1), aurapten (7-geranyloxycoumarin, 2) and 5’-oxoaurapten (diversinin, 3). The structures of these compounds were characterized by spectroscopic methods. These compounds were evaluated for their antimicrobial activity against a panel of each, bacteria and fungi. Compound 3 showed the best activities against Microsporum gypseum, Trichophyton rubrum and Trichophyton mentagrophytes with MICs = 15.6 µg/mL, followed by compound 1 whose MICs against the same fungi were 62.5 µg/mL. In addition they showed fungicidal rather than fungistatic activity. Both compounds showed moderate activity (MICs = 125 µg/mL) against Cryptococcus neoformans. This is the first report of the presence of compound 1 in B. darwinii. MDPI 2010-07-13 /pmc/articles/PMC6257657/ /pubmed/20657398 http://dx.doi.org/10.3390/molecules15074898 Text en © 2010 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 license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Kurdelas, Rita R. Lima, Beatriz Tapia, Alejandro Egly Feresin, Gabriela Gonzalez Sierra, Manuel Rodríguez, María Victoria Zacchino, Susana Enriz, Ricardo D. Freile, Monica L. Antifungal Activity of Extracts and Prenylated Coumarins Isolated from Baccharis darwinii Hook & Arn. (Asteraceae) |
title | Antifungal Activity of Extracts and Prenylated Coumarins Isolated from Baccharis darwinii Hook & Arn. (Asteraceae) |
title_full | Antifungal Activity of Extracts and Prenylated Coumarins Isolated from Baccharis darwinii Hook & Arn. (Asteraceae) |
title_fullStr | Antifungal Activity of Extracts and Prenylated Coumarins Isolated from Baccharis darwinii Hook & Arn. (Asteraceae) |
title_full_unstemmed | Antifungal Activity of Extracts and Prenylated Coumarins Isolated from Baccharis darwinii Hook & Arn. (Asteraceae) |
title_short | Antifungal Activity of Extracts and Prenylated Coumarins Isolated from Baccharis darwinii Hook & Arn. (Asteraceae) |
title_sort | antifungal activity of extracts and prenylated coumarins isolated from baccharis darwinii hook & arn. (asteraceae) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257657/ https://www.ncbi.nlm.nih.gov/pubmed/20657398 http://dx.doi.org/10.3390/molecules15074898 |
work_keys_str_mv | AT kurdelasritar antifungalactivityofextractsandprenylatedcoumarinsisolatedfrombaccharisdarwiniihookarnasteraceae AT limabeatriz antifungalactivityofextractsandprenylatedcoumarinsisolatedfrombaccharisdarwiniihookarnasteraceae AT tapiaalejandro antifungalactivityofextractsandprenylatedcoumarinsisolatedfrombaccharisdarwiniihookarnasteraceae AT eglyferesingabriela antifungalactivityofextractsandprenylatedcoumarinsisolatedfrombaccharisdarwiniihookarnasteraceae AT gonzalezsierramanuel antifungalactivityofextractsandprenylatedcoumarinsisolatedfrombaccharisdarwiniihookarnasteraceae AT rodriguezmariavictoria antifungalactivityofextractsandprenylatedcoumarinsisolatedfrombaccharisdarwiniihookarnasteraceae AT zacchinosusana antifungalactivityofextractsandprenylatedcoumarinsisolatedfrombaccharisdarwiniihookarnasteraceae AT enrizricardod antifungalactivityofextractsandprenylatedcoumarinsisolatedfrombaccharisdarwiniihookarnasteraceae AT freilemonical antifungalactivityofextractsandprenylatedcoumarinsisolatedfrombaccharisdarwiniihookarnasteraceae |