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,...

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Detalhes bibliográficos
Autores: Kurdelas, Rita Rosa, Lima, Beatriz Viviana, Tapia, Aníbal Alejandro, Feresin, Gabriela Egly, Gonzalez Sierra, Manuel, Rodriguez, María Victoria, Zacchino, Susana Alicia Stella, Enriz, Ricardo Daniel, Freile, Monica Liliana
Tipo de documento: artigo
Estado:Versão publicada
Data de publicação:2010
País:Argentina
Recursos:Consejo Nacional de Investigaciones Científicas y Técnicas
Repositório:CONICET Digital (CONICET)
Idioma:inglês
OAI Identifier:oai:ri.conicet.gov.ar:11336/127398
Acesso em linha:http://hdl.handle.net/11336/127398
Access Level:Acceso aberto
Palavra-chave:ANTIMICROBIAL ACTIVITY
ASTERACEAE
AURAPTENE
BACCHARIS DARWINII
PRENYLATED COUMARINS
https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
Descrição
Resumo: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.