ID Name Structure References (top 5) Molecular Target(s)
1ID:5333
PROTOPANAXATRIOL

Freqency:
in 1 ingredients:

  • 5
  • in 5 recipes:

  • 8
  • 107
  • 212
  • 308
  • 351

  • Properties
    C30H52O4    476.74





    1:  Danieli B, Falcone L, Monti D, Riva S, Gebhardt S, Schubert-Zsilavecz M.
    Regioselective enzymatic glycosylation of natural polyhydroxylated compounds: galactosylation and glucosylation of protopanaxatriol ginsenosides.
    J Org Chem.    impact factor:   3.44
    2001;  66(1): 262-9

    2:  Miao XS, Metcalfe CD, Hao C, March RE.
    Electrospray ionization mass spectrometry of ginsenosides.
    J Mass Spectrom.    impact factor:   3.167
    2002;  37(5): 495-506

    3:  Gillis CN.
    Panax ginseng pharmacology: a nitric oxide link?
    Biochem Pharmacol.    impact factor:   2.755
    1997;  54(1): 1-8

    4:  Liu ZQ, Luo XY, Sun YX, Chen YP, Wang ZC.
    Can ginsenosides protect human erythrocytes against free-radical-induced hemolysis?
    Biochim Biophys Acta.    impact factor:   2.59
    2002;  1572(1): 58-66

    5:  Popovich DG, Kitts DD.
    Structure-function relationship exists for ginsenosides in reducing cell proliferation and inducing apoptosis in the human leukemia (THP-1) cell line.
    Arch Biochem Biophys.    impact factor:   2.386
    2002;  406(1): 1-8

     
    Time used: 47 milliseconds.

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