Histamine-Release Effectors from<i>Angelica</i><i>dahurica</i>var.<i>dahurica</i>Root

  • Yoshiyuki Kimura
    2nd Department of Medical Biochemistry, School of Medicine, Ehime University, Shigenobu-cho, Onsen-gun, Ehime 791-02, Japan
  • Hiromichi Okuda
    2nd Department of Medical Biochemistry, School of Medicine, Ehime University, Shigenobu-cho, Onsen-gun, Ehime 791-02, Japan
  • Kimiye Baba
    2nd Department of Pharmacognosy, Osaka University, Pharmaceutical Sciences, Nahara, Takatsuki City, Osaka 569-11 Japan

書誌事項

公開日
1997-03-01
DOI
  • 10.1021/np960407a
公開者
American Chemical Society (ACS)

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説明

Six compounds isolated from the EtOAc fraction of the dried roots of Angelica dahurica var. dahurica inhibited compound 48/80-induced histamine levels in mouse peritoneal cavity (in vivo). Bergapten, oxypeucedanin hydrate, and byakangelicin inhibited compound 48/80-induced histamine elevation at a dose of 25 mg/kg. Conversely, sec-O-acetylbyakangelicin [8-(2-acetoxy-3-hydroxy-3-methylbutoxy)-5-methoxypsoralenI enhanced compound 48/80-induced histamine elevation at a dose of 25 mg/kg, while phellopterin and oxypeucedanin had no effect.

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