ID Name Structure References (top 5) Molecular Target(s)
1ID:7096
CHELIRUBINE

Freqency:
in 2 ingredients:

  • 97
  • 609
  • in 4 recipes:

  • 6
  • 25
  • 210
  • 244

  • Properties
    C21H16NO5    362.36





    1:  Park SU, Yu M, Facchini PJ.
    Antisense RNA-mediated suppression of benzophenanthridine alkaloid biosynthesis in transgenic cell cultures of California poppy.
    Plant Physiol.    impact factor:   4.434
    2002;  128(2): 696-706

    2:  Cline SD, McHale RJ, Coscia CJ.
    Differential enhancement of benzophenanthridine alkaloid content in cell suspension cultures of Sanguinaria canadensis under conditions of combined hormonal deprivation and fungal elicitation.
    J Nat Prod.    impact factor:   1.652
    1993;  56(8): 1219-28

    3:  Tanahashi T, Zenk MH.
    New hydroxylated benzo[c]phenanthridine alkaloids from Eschscholtzia californica cell suspension cultures.
    J Nat Prod.    impact factor:   1.652
    1990;  53(3): 579-86

    4:  Ishii H, Ishikawa T.
    [Chemistry of benzo[c]phenanthridine alkaloids having antineoplastic activity (author's transl)]
    Yakugaku Zasshi.    impact factor:   .238
    1981;  101(8): 663-87

    5:  Rho D, Chauret N, Laberge N, Archambault J.
    Growth characteristics of Sanguinaria canadensis L. cell suspensions and immobilized cultures for production of benzophenanthridine alkaloids.
    Appl Microbiol Biotechnol.    impact factor:   0
    1992;  36(5): 611-7

     
    Time used: 125 milliseconds.

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