ID Name Structure References (top 5) Molecular Target(s)
1ID:2368
FISETIN


NSC#:407010
NSC#:656275
Aldrich#:46340

Freqency:
in 2 ingredients:

  • 312
  • 468
  • in 14 recipes:

  • 8
  • 37
  • 50
  • 167
  • 212
  • 236
  • 268
  • 281
  • 339
  • 352
  • 466
  • 469
  • 492
  • 506

  • Properties
    C15H10O6    286.24





    1:  Fotsis T, Pepper MS, Aktas E, Breit S, Rasku S, Adlercreutz H, Wahala K, Montesano R, Schweigerer L.
    Flavonoids, dietary-derived inhibitors of cell proliferation and in vitro angiogenesis.
    Cancer Res.    impact factor:   8.614
    1997;  57(14): 2916-21

    2:  Sarno S, Moro S, Meggio F, Zagotto G, Dal Ben D, Ghisellini P, Battistutta R, Zanotti G, Pinna LA.
    Toward the rational design of protein kinase casein kinase-2 inhibitors.
    Pharmacol Ther.    impact factor:   7.711
    2002;  93(2-3): 159-68

    3:  Zhu BT, Liehr JG.
    Inhibition of catechol O-methyltransferase-catalyzed O-methylation of 2- and 4-hydroxyestradiol by quercetin. Possible role in estradiol-induced tumorigenesis.
    J Biol Chem.    impact factor:   7.666
    1996;  271(3): 1357-63

    4:  Zhu BT, Ezell EL, Liehr JG.
    Catechol-O-methyltransferase-catalyzed rapid O-methylation of mutagenic flavonoids. Metabolic inactivation as a possible reason for their lack of carcinogenicity in vivo.
    J Biol Chem.    impact factor:   7.666
    1994;  269(1): 292-9

    5:  Huckle WR, Earp HS.
    Synergistic activation of tyrosine phosphorylation by o-vanadate plus calcium ionophore A23187 or aromatic 1,2-diols.
    Biochemistry.    impact factor:   4.493
    1994;  33(6): 1518-25

     
    Time used: 109 milliseconds.

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