Title of article :
New lycorine-type alkaloid from Lycoris traubii and evaluation of antitrypanosomal and antimalarial activities of lycorine derivatives Original Research Article
Author/Authors :
Yosuke Toriizuka، نويسنده , , Eri Kinoshita، نويسنده , , Noriyuki Kogure، نويسنده , , Mariko Kitajima، نويسنده , , Aki Ishiyama، نويسنده , , Kazuhiko Otoguro، نويسنده , , Haruki Yamada، نويسنده , , Satoshi Omura، نويسنده , , Hiromitsu Takayama، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2008
Pages :
8
From page :
10182
To page :
10189
Abstract :
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.
Keywords :
Bioisoteric replacement , Angucyclinones , N-heterocyclic quinones , Cytotoxicity
Journal title :
Bioorganic and Medicinal Chemistry
Serial Year :
2008
Journal title :
Bioorganic and Medicinal Chemistry
Record number :
1306118
Link To Document :
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