Picture map of Europe with pins indicating European capital cities

Open Access research with a European policy impact...

The Strathprints institutional repository is a digital archive of University of Strathclyde's Open Access research outputs. Strathprints provides access to thousands of Open Access research papers by Strathclyde researchers, including by researchers from the European Policies Research Centre (EPRC).

EPRC is a leading institute in Europe for comparative research on public policy, with a particular focus on regional development policies. Spanning 30 European countries, EPRC research programmes have a strong emphasis on applied research and knowledge exchange, including the provision of policy advice to EU institutions and national and sub-national government authorities throughout Europe.

Explore research outputs by the European Policies Research Centre...

Anthraquinones and betaenone derivatives from the sponge-associated fungus Microsphaeropsis species : novel inhibitors of protein kinases

Brauers, Gernot and Edrada-Ebel, Ruangelie and Ebel, Rainer and Proksch, Peter and Wray, Victor and Berg, Albrecht and Gräfe, Udo and Schächtele, Christoph and Totzke, Frank and Finkenzeller, Gunter and Marme, Dieter and Kraus, Jurgen and Münchbach, Miriam and Michel, Manuela and Bringmann, Gerhard and Schaumann, Karsten (2000) Anthraquinones and betaenone derivatives from the sponge-associated fungus Microsphaeropsis species : novel inhibitors of protein kinases. Journal of Natural Products, 63 (6). pp. 739-745. ISSN 0163-3864

Full text not available in this repository. Request a copy from the Strathclyde author

Abstract

An undescribed fungus of the genus Microsphaeropsis, isolated from the Mediterranean sponge Aplysina aerophoba, produces two new betaenone derivatives (1, 2) and three new 1,3,6, 8-tetrahydroxyanthraquinone congeners (5-7). The structures of the compounds were established on the basis of NMR spectroscopic and mass spectrometric data and by CD spectroscopy. This is the first report wherein the (1)H and (13)C NMR data of the betaenone congeners are fully and unambiguously assigned on the basis of two-dimensional NMR spectroscopy. Furthermore, we describe the first elucidation of the absolute configuration of 1-(2'-anthraquinonyl)ethanols such as 5 and 6, by quantum chemical calculation of their circular dichroism (CD) and comparison with experimentally measured spectra. Moreover, it was shown that compounds 1, 5, 6, and 7 are inhibitors of PKC-epsilon, CDK4, and EGF receptor tyrosine kinases.