Wiese Jutta, Aldemir Hülya, Schmaljohann Rolf, Gulder Tobias A M, Imhoff Johannes F
GEOMAR Helmholtz Center for Ocean Research Kiel, RD3 Marine Microbiology, Düsternbrooker Weg 20, 24105 Kiel, Germany.
Department of Chemistry and Center for Integrated Protein Science Munich (CIPSM), Biosystems Chemistry, Technical University of Munich, Lichtenbergstraße 4, 85747 Garching, Germany.
Mar Drugs. 2017 Jun 21;15(6):191. doi: 10.3390/md15060191.
In the frame of studies on secondary metabolites produced by fungi from deep-sea environments we have investigated inhibitors of enzymes playing key roles in signaling cascades of biochemical pathways relevant for the treatment of diseases. Here we report on a new inhibitor of the human protein tyrosine phosphatase 1B (PTP1B), a target in the signaling pathway of insulin. A new asperentin analog is produced by an strain isolated from the sediment of the deep Mediterranean Sea. Asperentin B () contains an additional phenolic hydroxy function at C-6 and exhibits an IC value against PTP1B of 2 μM in vitro, which is six times stronger than the positive control, suramin. Interestingly, asperentin () did not show any inhibition of this enzymatic activity. Asperentin B () is discussed as possible therapeutic agents for type 2 diabetes and sleeping sickness.
在对深海环境中真菌产生的次生代谢产物的研究框架内,我们研究了在与疾病治疗相关的生化途径信号级联中起关键作用的酶的抑制剂。在此,我们报道一种新型人蛋白酪氨酸磷酸酶1B(PTP1B)抑制剂,PTP1B是胰岛素信号通路中的一个靶点。一种新的asperentin类似物由从地中海深海沉积物中分离出的一株菌株产生。Asperentin B()在C-6位含有一个额外的酚羟基官能团,在体外对PTP1B的IC值为2 μM,比阳性对照苏拉明强六倍。有趣的是,asperentin()对这种酶活性没有任何抑制作用。Asperentin B()被认为可能是治疗2型糖尿病和昏睡病的药物。