ID Name Structure References (top 5) Molecular Target(s)
1ID:8412
RINDERINE


NSC#:89937
NSC#:136052

Freqency:
in 1 ingredients:

  • 702
  • in 4 recipes:

  • 10
  • 48
  • 215
  • 279

  • Properties
    C15H25NO5    299.36





    1:  Zalkow LH, Glinski JA, Gelbaum LT, Fleischmann TJ, McGowan LS, Gordon MM.
    Synthesis of pyrrolizidine alkaloids indicine, intermedine, lycopsamine, and analogues and their N-oxides. Potential antitumor agents.
    J Med Chem.    impact factor:   4.079
    1985;  28(6): 687-94

    2:  Ayabe S, Udagawa A, Furuya T.
    NAD(P)H-dependent 6'-deoxychalcone synthase activity in Glycyrrhiza echinata cells induced by yeast extract.
    Arch Biochem Biophys.    impact factor:   2.386
    1988;  261(2): 458-62

    3:  Ames MM, Miser JS, Smithson WA, Coccia PF, Hughes CS, Davis DM.
    Pharmacokinetic study of indicine N-oxide in pediatric cancer patients.
    Cancer Chemother Pharmacol.    impact factor:   2.081
    1982;  10(1): 43-6

    4:  Reina M, Gonzalez-Coloma A, Gutierrez C, Cabrera R, Henriquez J, Villarroel L.
    Pyrrolizidine alkaloids from Heliotropium megalanthum.
    J Nat Prod.    impact factor:   1.652
    1998;  61(11): 1418-20

    5:  Asibal CF, Glinski JA, Gelbaum LT, Zalkow LH.
    Pyrrolizidine alkaloids from Cynoglossum creticum. Synthesis of the pyrrolizidine alkaloids echinatine, rinderine, and analogues.
    J Nat Prod.    impact factor:   1.652
    1989;  52(1): 109-18

     
    Time used: 125 milliseconds.

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