Chaetominedione, a new tyrosine kinase inhibitor isolated from the algicolous marine fungus Chaetomium sp.

被引:31
作者
Abdel-Lateff, Ahmed [1 ]
机构
[1] Menia Univ, Fac Pharm, Dept Pharmacognosy, Menia 61519, Egypt
关键词
Benzonaphthyridinedione; p56(lck) tyrosine kinase; Chaetominedione; Chaetomium sp; Fungi; Marine micro-organism;
D O I
10.1016/j.tetlet.2008.08.064
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A marine fungal isolate, identified as Chaetomium sp., was cultivated and found to produce a novel benzonaphthyridinedione derivative, chaetominedione (1). In addition to the known fungal metabolites, 2-furancarboxylic acid (2) and 5-(hydroxymethyl)-2-furancarboxylic acid (3) were obtained. The structures of all the compounds were determined based on extensive spectroscopic measurements (1D and 2D NMR, MS, UV, and IR). The total extract and compound 1 had significant inhibitory activity toward p56(lek) tyrosine kinase (18.7% and 93.6% enzyme inhibition at 200 mu g/mL, respectively). (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6398 / 6400
页数:3
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