Key Laboratory of Marine Drugs, Ministry of Education of China, School of Medicine and Pharmacy, Ocean University of China, Qingdao, P R China.
Planta Med. 2012 Nov;78(17):1861-6. doi: 10.1055/s-0032-1315395. Epub 2012 Oct 11.
As part of our ongoing chemical investigation of biologically active metabolites from marine-derived fungi, four new polyphenols containing both phenolic bisabolane and diphenyl ether units, expansols C-F (1-4), and one new diphenyl ether derivative, 3-O-methyldiorcinol (5), as well as twelve known compounds (6-17), were isolated from Penicillium expansum 091006 endogenous with the mangrove plant Excoecaria agallocha (Euphorbiaceae). The structures of the new metabolites were determined on the basis of NMR and mass spectroscopy. Among them, expansols C (1) and E (3) exhibited weak cytotoxicity against the HL-60 cell lines with IC50 values of 18.2 and 20.8 µM, respectively. The results showed that diphenyl ether substituted phenolic bisabolanes with a Δ7 double bond in the side chain are slightly less cytotoxic to HL-60 cell lines than the 7-OH or 7-OCH3 derivatives.
作为我们对海洋来源真菌生物活性代谢产物的持续化学研究的一部分,从红树林植物海漆(Euphorbiaceae)内生的扩展青霉 091006 中分离得到了四个含有倍半萜双苯并呋喃和二苯醚单元的新多酚化合物,分别为 expansols C-F(1-4),以及一个新的二苯醚衍生物 3-O-甲基金口山姜素(5),以及 12 个已知化合物(6-17)。新代谢物的结构是基于 NMR 和质谱确定的。其中,expansols C(1)和 E(3)对 HL-60 细胞系表现出较弱的细胞毒性,IC50 值分别为 18.2 和 20.8µM。结果表明,侧链带有Δ7 双键的二苯醚取代的倍半萜双苯并呋喃对 HL-60 细胞系的细胞毒性略低于 7-OH 或 7-OCH3 衍生物。