Renate Spitaler
University of Innsbruck
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Featured researches published by Renate Spitaler.
Zeitschrift für Naturforschung C | 2002
Christian Zidorn; Renate Spitaler; Ernst-P. Ellmerer-Müller; Nigel B. Perry; Clarissa Gerhäuser; Hermann Stuppner
A novel tyrolobibenzyl derivative, 1→6-β-ᴅ-apiosyl-β-ᴅ-glucopyranosyl 4-[2-(4-hydroxyphenyl) ethyl]benzofuran-2-carboxylate 3 (tyrolobibenzyl D) was isolated from Scorzonera humilis L. and its structure established by mass spectrometry and 1D- and 2D-NMR spectroscopy. The biological activities of the new compound and related tyrolobibenzyls A-C (1-2, 4) and the semi-synthetic peracetyl derivatives of tyrolobibenzyls B (2a) and C (4a) were assessed. The results revealed no cytotoxic activity against P388 cells and neither anti-bacterial activity against Bacillus subtilis nor antifungal activity against Candida albicans and Trichophyton mentagrophytes for any of the investigated compounds. An evaluation of potential chemopreventive activity of 2, 2a, 4, and 4a also revealed no pronounced activity in any of the employed assaying systems.
Zeitschrift für Naturforschung B | 2004
Renate Spitaler; Ernst-P. Ellmerer; Christian Zidorn; Hermann Stuppner
Abstract Besides the known compounds 2,4,6-trihydroxyacetophenone 4-O-β -D-glucopyranoside and syringaresinol 4’-O-β -D-glucopyranoside, the novel sesquiterpenoid 1,2-dehydro-3-oxocostic acid β - D-glucopyranoside ester was isolated from Leontodon tuberosus L. and its structure established by mass spectrometry and 1D- and 2D-NMR spectroscopy. Additionally, a number of fatty and phenolic acids was identified in the crude methanolic extract by HPLC-DAD and HPLC-MS. The chemosystematic impact of the new sesquiterpenoid is discussed briefly.
Scientia Pharmaceutica | 2011
Romana Krimplstätter; Benjamin Ma; Renate Spitaler; Ernst P. Ellmerer; Christian Zidorn
Rhagadiolus stellatus Gaertn., a Mediterranean member of the Cichorieae tribe of the Asteraceae family used as a food plant, was analyzed for its spectrum of phenolic compounds. Kaempferol 3-O-β-glucoside 1, kaempferol 3-O-β-rutinoside (nicotiflorin) 2, quercetin 3-O-β-glucoside 3, and luteolin 4 were isolated from the n-butanol layer of a methanolic extract of whole plants of Rh. stellatus of Spanish origin by repeated Sephadex LH-20 column chromatography. Structures were determined based on NMR and MS data as well as by comparison with literature data. Additionally, chlorogenic acid 5 and 3,5-dicaffeoylquinic acid 6 were detected by HPLC/DAD and HPLC/MS. Chemosystematic implications of the presented findings are discussed in comparison with other members of the Cichorieae tribe.
Phytochemistry | 2006
Renate Spitaler; P. Daniel Schlorhaufer; Ernst P. Ellmerer; Irmgard Merfort; Sigmar Bortenschlager; Hermann Stuppner; Christian Zidorn
Journal of Chemical Ecology | 2008
Renate Spitaler; Andrea Winkler; Isabella Lins; Sema Yanar; Hermann Stuppner; Christian Zidorn
Biochemical Systematics and Ecology | 2009
Renate Spitaler; Sara Gurschler; Ernst P. Ellmerer; Birthe Schubert; Manuela Sgarbossa; Christian Zidorn
Journal of Agricultural and Food Chemistry | 2006
Judith M. Rollinger; Renate Spitaler; Magdalena Menz; Klaus Marschall; Roland Zelger; Ernst P. Ellmerer; Peter Schneider; Hermann Stuppner
Biochemical Systematics and Ecology | 2007
Christian Zidorn; Renate Spitaler; Sandra Grass; Judith Mader; Thomas Müller; Ernst P. Ellmerer; Hermann Stuppner
Biochemical Systematics and Ecology | 2006
Christian Zidorn; Renate Spitaler; Ernst P. Ellmerer; Hermann Stuppner
Biochemical Systematics and Ecology | 2005
Christian Zidorn; Vedrana Udovičić; Renate Spitaler; Ernst P. Ellmerer; Hermann Stuppner