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Steroidal composition and cytotoxic activity from fruiting body of Cortinarius xiphidipus.
Torres, Solange; Cajas, Daniel; Palfner, Goetz; Astuya, Allisson; Aballay, Ambbar; Pérez, Claudia; Hernández, Víctor; Becerra, José.
Afiliação
  • Torres S; a Laboratory of Natural Products Chemistry, Department of Botany , University of Concepción , Concepción , Chile.
  • Cajas D; a Laboratory of Natural Products Chemistry, Department of Botany , University of Concepción , Concepción , Chile.
  • Palfner G; b Laboratory of Mycology and Mycorrhizal, Department of Botany , University of Concepción , Concepción , Chile.
  • Astuya A; c Laboratory of Cellular Culturing and Marine Genomics, Marine Biotechnology Unit and COPAS Sur-Austral Program , University of Concepción , Concepción , Chile.
  • Aballay A; c Laboratory of Cellular Culturing and Marine Genomics, Marine Biotechnology Unit and COPAS Sur-Austral Program , University of Concepción , Concepción , Chile.
  • Pérez C; a Laboratory of Natural Products Chemistry, Department of Botany , University of Concepción , Concepción , Chile.
  • Hernández V; a Laboratory of Natural Products Chemistry, Department of Botany , University of Concepción , Concepción , Chile.
  • Becerra J; a Laboratory of Natural Products Chemistry, Department of Botany , University of Concepción , Concepción , Chile.
Nat Prod Res ; 31(4): 473-476, 2017 Feb.
Article em En | MEDLINE | ID: mdl-27198920
From the fruiting body of ectomycorrhizal fungi Cortinarius xiphidipus, sterols were identified from the crude extract and the cytotoxic effect of ergosta-4, 6, 8(14), 22-tetraen-3-one (ergone) was evaluated. Ten sterols including ergosta-3,5,7,9(11),22-pentaene, (22E)-ergosta-5,7,9(11),22-tetraen-3b-ol, (3ß,22E)-ergosta-5,7,22-trien-3-ol, (22E)-ergosta-7,22-dien-3-ol, neoergosterol, (3ß)-ergosta-5,8-dien-3-ol, (3ß)-ergosta-7-en-3-ol, stigmasterol, stigmasterol 22,23-dihydro and (22E)-ergosta-4,6,8(14),22-tetraen-3-one were identified from the crude extract. The cytotoxic activity of the sterol fraction containing ergosta-4, 6, 8(14), 22-tetraen-3-one was assessed on four tumour cell lines (Neuro-2a, Saos-2, MCF7 and LNCaP-C42). The cytotoxic activity against the four tumour cell lines tested, being Neuro-2a and Saos-2 the most sensitive, with a half-maximal inhibitory concentration (IC50) of 20.8 ± 2.2 and 27.8 ± 1.0 µg/mL, respectively. This is the first report of this Antarctic fungi collected in the Magallanes and Chilean Antarctica Region. This work represents a potential source for the development of anticancer drugs.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esteróis / Cortinarius / Antineoplásicos Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esteróis / Cortinarius / Antineoplásicos Idioma: En Ano de publicação: 2017 Tipo de documento: Article