1,10-Epoxyhypocretenolides from the Azorean Endemic Leontodon rigens (Asteraceae)

Author(s): C. Zidorn, E.- P. Ellmerer, G. Konwalinka, K.- H. Ongania, R. Schwaha, R. Greil, K. Joehrer, N. B. Perry, H. Stuppner.

Journal Name: Letters in Organic Chemistry

Volume 2 , Issue 5 , 2005

Become EABM
Become Reviewer

Abstract:

A methanolic extract of Leontodon rigens (Dryander in Aiton) Paiva & Ormonde yielded 1,10- epoxy-14-hydroxyhypocretenolide-β-D-glucopyranoside and its 6-O-p-hydroxyphenylacetyl derivative. These compounds represent the first epoxyguaian-12,5-olide derivatives. The structures were established by means of high resolution mass spectrometry and 1-D and 2-D NMR spectroscopy. The cytotoxicity of the isolated compounds was assessed using the MTT assay and their potential to induce apoptosis by employing the annexin V-PI assay.

Keywords: asteraceae, leontodon rigens, natural products, sesquiterpene lactone epoxides, cytotoxicity

Rights & PermissionsPrintExport Cite as

Article Details

VOLUME: 2
ISSUE: 5
Year: 2005
Page: [461 - 464]
Pages: 4
DOI: 10.2174/1570178054406002
Price: $65

Article Metrics

PDF: 2