• 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