ID Name Structure References (top 5) Molecular Target(s)
1ID:6
ACACETIN


NSC#:76061
Aldrich#:00017

Freqency:
in 4 ingredients:

  • 302
  • 904
  • 925
  • 926
  • in 3 recipes:

  • 212
  • 233
  • 247

  • Properties
    C16H12O5    284.27





    1:  Boege F, Straub T, Kehr A, Boesenberg C, Christiansen K, Andersen A, Jakob F, Kohrle J.
    Selected novel flavones inhibit the DNA binding or the DNA religation step of eukaryotic topoisomerase I.
    J Biol Chem.    impact factor:   7.666
    1996;  271(4): 2262-70

    2:  Fiorani M, De Sanctis R, De Bellis R, Dacha M.
    Intracellular flavonoids as electron donors for extracellular ferricyanide reduction in human erythrocytes.
    Free Radic Biol Med.    impact factor:   4.116
    2002;  32(1): 64-72

    3:  Chen YT, Zheng RL, Jia ZJ, Ju Y.
    Flavonoids as superoxide scavengers and antioxidants.
    Free Radic Biol Med.    impact factor:   4.116
    1990;  9(1): 19-21

    4:  Wenzel U, Kuntz S, Daniel H.
    Flavonoids with epidermal growth factor-receptor tyrosine kinase inhibitory activity stimulate PEPT1-mediated cefixime uptake into human intestinal epithelial cells.
    J Pharmacol Exp Ther.    impact factor:   3.3
    2001;  299(1): 351-7

    5:  Bylka W, Franski R, Stobiecki M.
    Differentiation between isomeric acacetin-6-C-(6"-O-malonyl)glucoside and acacetin-8-C-(6"-O-malonyl)glucoside by using low-energy CID mass spectra.
    J Mass Spectrom.    impact factor:   3.167
    2002;  37(6): 648-50

    EGFR-1
    EGFR-2
    P450
    STEP
     
    Time used: 156 milliseconds.

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