ID Name Structure References (top 5) Molecular Target(s)
1ID:4967
PANAXYTRIOL

Freqency:
in 1 ingredients:

  • 5
  • in 5 recipes:

  • 8
  • 107
  • 212
  • 308
  • 351

  • Properties
    C17H26O3    278.39





    1:  Mayer SF, Steinreiber A, Orru RV, Faber K.
    Chemoenzymatic Asymmetric Total Syntheses of Antitumor Agents (3R,9R,10R)- and (3S,9R,10R)-Panaxytriol and (R)- and (S)-Falcarinol from Panax ginseng Using an Enantioconvergent Enzyme-Triggered Cascade Reaction.
    J Org Chem.    impact factor:   3.44
    2002;  67(26): 9115-21

    2:  Matsunaga H, Saita T, Nagumo F, Mori M, Katano M.
    A possible mechanism for the cytotoxicity of a polyacetylenic alcohol, panaxytriol: inhibition of mitochondrial respiration.
    Cancer Chemother Pharmacol.    impact factor:   2.081
    1995;  35(4): 291-6

    3:  Matsunaga H, Katano M, Saita T, Yamamoto H, Mori M.
    Potentiation of cytotoxicity of mitomycin C by a polyacetylenic alcohol, panaxytriol.
    Cancer Chemother Pharmacol.    impact factor:   2.081
    1994;  33(4): 291-7

    4:  Jung HJ, Min BS, Park JY, Kim YH, Lee HK, Bae KH.
    Gymnasterkoreaynes A-F, cytotoxic polyacetylenes from Gymnaster koraiensis.
    J Nat Prod.    impact factor:   1.652
    2002;  65(6): 897-901

    5:  Kim JY, Lee KW, Kim SH, Wee JJ, Kim YS, Lee HJ.
    Inhibitory effect of tumor cell proliferation and induction of G2/M cell cycle arrest by panaxytriol.
    Planta Med.    impact factor:   1.438
    2002;  68(2): 119-22

     
    Time used: 109 milliseconds.

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