ID Name Structure References (top 5) Molecular Target(s)
1ID:1103
CIRSILIOL

Freqency:
in 1 ingredients:

  • 715
  • in 7 recipes:

  • 6
  • 39
  • 210
  • 269
  • 287
  • 312
  • 334

  • Properties
    C17H14O7    330.29





    1:  Horie T, Tsukayama M, Kourai H, Yokoyama C, Furukawa M, Yoshimoto T, Yamamoto S, Watanabe-Kohno S, Ohata K.
    Syntheses of 5,6,7- and 5,7,8-trioxygenated 3',4'-dihydroxyflavones having alkoxy groups and their inhibitory activities against arachidonate 5-lipoxygenase.
    J Med Chem.    impact factor:   4.079
    1986;  29(11): 2256-62

    2:  Forstermann U, Alheid U, Frolich JC, Mulsch A.
    Mechanisms of action of lipoxygenase and cytochrome P-450-mono-oxygenase inhibitors in blocking endothelium-dependent vasodilatation.
    Br J Pharmacol.    impact factor:   3.722
    1988;  93(3): 569-78

    3:  Tsukada T, Nakashima K, Shirakawa S.
    Arachidonate 5-lipoxygenase inhibitors show potent antiproliferative effects on human leukemia cell lines.
    Biochem Biophys Res Commun.    impact factor:   3.161
    1986;  140(3): 832-6

    4:  Yoshimoto T, Furukawa M, Yamamoto S, Horie T, Watanabe-Kohno S.
    Flavonoids: potent inhibitors of arachidonate 5-lipoxygenase.
    Biochem Biophys Res Commun.    impact factor:   3.161
    1983;  116(2): 612-8

    5:  Furukawa M, Yoshimoto T, Ochi K, Yamamoto S.
    Studies on arachidonate 5-lipoxygenase of rat basophilic leukemia cells.
    Biochim Biophys Acta.    impact factor:   2.59
    1984;  795(3): 458-65

     
    Time used: 93 milliseconds.

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