应用天然产物 ›› 2014, Vol. 4 ›› Issue (2): 119-128.DOI: 10.1007/s13659-014-0015-5
Liang-Yan Liu1,2, Zheng-Hui Li1, Gang-Qiang Wang1, Kun Wei1, Ze-Jun Dong1, Tao Feng1, Gen-Tao Li1, Yan Li1, Ji-Kai Liu1
Liang-Yan Liu1,2, Zheng-Hui Li1, Gang-Qiang Wang1, Kun Wei1, Ze-Jun Dong1, Tao Feng1, Gen-Tao Li1, Yan Li1, Ji-Kai Liu1
摘要: Nine previously-unreported farnesylphenols, involving eight neogrifolin derivatives(1-8) and one grifolin analogue(9), together with three known compounds, were isolated from the fruiting bodies of the mushroom Albatrellus caeruleoporus. Their structures were elucidated as(S)-17-hydroxy-18, 20-ene-neogrifolin(1),(S)-18, 19-dihydroxyneogrifolin(2),(S)-9-hydroxy-10, 22-ene-neogrifolin(3),(9S, 10R)-6, 10-epoxy-9-hydroxyneo grifolin(4),(9S, 10R)-6, 9-epoxy-10-hydroxyneogrifolin(5),(-)-13, 14-dihydroxyneogrifolin(6), albatrelin G(7), albatrelin H(8), and one grifolin analogue,(S)-10-hydroxygrifolin(9), grifolin(10), neogrifolin(11), and albatrellin(12) by extensive spectroscopic analyses and chemical methods. Compounds 7 and 8 showed weak cytotoxic activity to cell lines HL-60, SMMC-7721, A-549, and MCF-7, in vitro.