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

被引:71
作者
Brauers, G
Edrada, RA
Ebel, R
Proksch, P
Wray, V
Berg, A
Gräfe, U
Schächtele, C
Totzke, F
Finkenzeller, G
Marme, D
Kraus, J
Münchbach, M
Michel, M
Bringmann, G
Schaumann, K
机构
[1] Univ Dusseldorf, Lehrstuhl Pharmazeut Biol, D-40225 Dusseldorf, Germany
[2] Gesell Biotechnol Forsch mbH, D-38124 Braunschweig, Germany
[3] Hans Knoll Inst Nat Stofforsch, D-07745 Jena, Germany
[4] Inst Mol Med & Nat Stofforsch, D-79106 Freiburg, Germany
[5] Univ Wurzburg, Inst Organ Chem, D-97074 Wurzburg, Germany
[6] Alfred Wegener Inst Polar & Marine Res, D-27570 Bremerhaven, Germany
来源
JOURNAL OF NATURAL PRODUCTS | 2000年 / 63卷 / 06期
关键词
D O I
10.1021/np9905259
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
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 H-1 and C-13 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.
引用
收藏
页码:739 / 745
页数:7
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