Mohamad Habsah, Lajis Nordin H, Abas Faridah, Ali Abdul Manaf, Sukari Mohamad Aspollah, Kikuzaki Hiroe, Nakatani Nobuji
Laboratory of Natural Products, Institute of Bioscience, Universiti Putra Malaysia, 43400 Serdang, Selangor, Malaysia.
J Nat Prod. 2005 Feb;68(2):285-8. doi: 10.1021/np040098l.
Phytochemical studies on the rhizomes of Etlingera elatior have resulted in the isolation of 1,7-bis(4-hydroxyphenyl)-2,4,6-heptatrienone (1), demethoxycurcumin (2), 1,7-bis(4-hydroxyphenyl)-1,4,6-heptatrien-3-one (3), 16-hydroxylabda-8(17),11,13-trien-15,16-olide (4), stigmast-4-en-3-one, stigmast-4-ene-3,6-dione, stigmast-4-en-6beta-ol-3-one, and 5alpha,8alpha-epidioxyergosta-6,22-dien-3beta-ol. Compounds 1 and 4 are new, and their structures were elucidated by analysis of spectroscopic data. Diarylheptanoids 1-3 were found to inhibit lipid peroxidation in a more potent manner than alpha-tocopherol.
对火炬姜根茎进行的植物化学研究已分离出1,7-双(4-羟基苯基)-2,4,6-庚三烯酮(1)、去甲氧基姜黄素(2)、1,7-双(4-羟基苯基)-1,4,6-庚三烯-3-酮(3)、16-羟基唇形-8(17),11,13-三烯-15,16-内酯(4)、豆甾-4-烯-3-酮、豆甾-4-烯-3,6-二酮、豆甾-4-烯-6β-醇-3-酮以及5α,8α-环氧麦角甾-6,22-二烯-3β-醇。化合物1和4是新化合物,其结构通过光谱数据分析得以阐明。发现二芳基庚烷类化合物1-3比α-生育酚更有效地抑制脂质过氧化。