ID Name Structure References (top 5) Molecular Target(s)
1ID:1186
COLUMBAMINE

Freqency:
in 5 ingredients:

  • 10
  • 115
  • 234
  • 342
  • 880
  • in 49 recipes:

  • 2
  • 3
  • 8
  • 20
  • 36
  • 43
  • 123
  • 124
  • 140
  • 150
  • 153
  • 166
  • 205
  • 206
  • 212
  • 219
  • 221
  • 226
  • 228
  • 229
  • 236
  • 237
  • 241
  • 247
  • 248
  • 259
  • 267
  • 271
  • 274
  • 276
  • 286
  • 292
  • 293
  • 325
  • 335
  • 351
  • 352
  • 355
  • 362
  • 402
  • 403
  • 421
  • 438
  • 465
  • 485
  • 500
  • 502
  • 506
  • 521

  • Properties
    C20H21NO5    355.38





    1:  Cava MP, Reed TA.
    A synthesis of columbamine from berberine.
    J Org Chem.    impact factor:   3.44
    1967;  32(5): 1640-1

    2:  Morishige T, Dubouzet E, Choi KB, Yazaki K, Sato F.
    Molecular cloning of columbamine O-methyltransferase from cultured Coptis japonica cells.
    Eur J Biochem.    impact factor:   3.307
    2002;  269(22): 5659-67

    3:  Amann M, Nagakura N, Zenk MH.
    Purification and properties of (S)-tetrahydroprotoberberine oxidase from suspension-cultured cells of Berberis wilsoniae.
    Eur J Biochem.    impact factor:   3.307
    1988;  175(1): 17-25

    4:  Kupeli E, Kosar M, Yesilada E, Husnu K, Baser C.
    A comparative study on the anti-inflammatory, antinociceptive and antipyretic effects of isoquinoline alkaloids from the roots of Turkish Berberis species.
    Life Sci.    impact factor:   1.774
    2002;  72(6): 645-57

    5:  Wright CW, Marshall SJ, Russell PF, Anderson MM, Phillipson JD, Kirby GC, Warhurst DC, Schiff PL.
    In vitro antiplasmodial, antiamoebic, and cytotoxic activities of some monomeric isoquinoline alkaloids.
    J Nat Prod.    impact factor:   1.652
    2000;  63(12): 1638-40

     
    Time used: 125 milliseconds.

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