ID Name Structure References (top 5) Molecular Target(s)
1ID:1643
DEOXYHARRINGTONINE


NSC#:142196

Freqency:
in 3 ingredients:

  • 9
  • 429
  • 459

  • Properties
    C28H37NO8    515.6





    1:  Parry RJ, Sternbach DD, Cabelli MD.
    Biosynthesis of Cephalotaxus alkaloids. 2. Biosynthesis of the acyl portion of deoxyharringtonine.
    J Am Chem Soc.    impact factor:   5.537
    1976;  98(20): 6380-2

    2:  Mikolajczak KL, Powell RG, Smith CR Jr.
    Preparation and antitumor activity of a rearranged ester of cephalotaxine.
    J Med Chem.    impact factor:   4.079
    1975;  18(1): 63-6

    3:  Wang DZ, Ma GE, Xu RS.
    [Studies on the alkaloids of Cephalotaxus. VII. Structures and semi-synthesis of two anticancer cephalotaxine esters]
    Yao Xue Xue Bao.    impact factor:   0
    1992;  27(3): 173-7

    4:  Wang DZ, Ma GE, Xu RS.
    [Studies on the alkaloids of Cephalotaxus. IX. Semi-synthesis of cephalotaxine esters and their anti-leukemic activity]
    Yao Xue Xue Bao.    impact factor:   0
    1992;  27(3): 178-84

    5:  Whaun JM, Brown ND.
    Treatment of chloroquine-resistant malaria with esters of cephalotaxine: homoharringtonine.
    Ann Trop Med Parasitol.    impact factor:   0
    1990;  84(3): 229-37

     
    Time used: 109 milliseconds.

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