Toriizuka Yosuke, Kinoshita Eri, Kogure Noriyuki, Kitajima Mariko, Ishiyama Aki, Otoguro Kazuhiko, Yamada Haruki, Omura Satoshi, Takayama Hiromitsu
Graduate School of Pharmaceutical Sciences, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba 263-8522, Japan.
Bioorg Med Chem. 2008 Dec 15;16(24):10182-9. doi: 10.1016/j.bmc.2008.10.061. Epub 2008 Oct 30.
A new lycorine derivative LT1 (4) was isolated from the aerial part and bulbs of Lycoris traubii Hayward (Amaryllidaceae). Its structure including absolute configuration was established by spectroscopic analysis and semi-synthesis to be 1-O-(3'S)-hydroxybutanoyllycorine. Some lycorine ester derivatives including LT1 were examined for their inhibitory activity against Trypanosoma brucei brucei, the parasite associated with sleeping sickness, and against Plasmodium falciparum, the causative agent of malaria. Among them, 2-O-acetyllycorine (6) showed the most potent activity against parasitic T. b. brucei, and LT1 (4), 1-O-(3'R)-hydroxybutanoyllycorine (8), 1,2-di-O-butanoyllycorine (11), and 1-O-propanoyllycorine (12) showed significant activity against P. falciparum in an in vitro experiment.
从换锦花(石蒜科)的地上部分和鳞茎中分离出一种新的石蒜碱衍生物LT1(4)。通过光谱分析和半合成确定其结构包括绝对构型为1-O-(3'S)-羟基丁酰石蒜碱。检测了包括LT1在内的一些石蒜碱酯衍生物对布氏布氏锥虫(与昏睡病相关的寄生虫)和恶性疟原虫(疟疾病原体)的抑制活性。其中,2-O-乙酰基石蒜碱(6)对寄生的布氏布氏锥虫显示出最有效的活性,而LT1(4)、1-O-(3'R)-羟基丁酰石蒜碱(8)、1,2-二-O-丁酰石蒜碱(11)和1-O-丙酰石蒜碱(12)在体外实验中对恶性疟原虫显示出显著活性。