ID Name Structure References (top 5) Molecular Target(s)
1ID:4125
MATRINE


NSC#:143088
NSC#:146051
NSC#:318810
Aldrich#:R260584

Freqency:
in 3 ingredients:

  • 18
  • 152
  • 434
  • in 46 recipes:

  • 19
  • 36
  • 51
  • 91
  • 195
  • 204
  • 206
  • 221
  • 223
  • 239
  • 252
  • 267
  • 280
  • 281
  • 284
  • 288
  • 291
  • 296
  • 299
  • 303
  • 315
  • 321
  • 327
  • 331
  • 339
  • 344
  • 346
  • 348
  • 356
  • 361
  • 366
  • 371
  • 390
  • 392
  • 398
  • 411
  • 435
  • 443
  • 446
  • 455
  • 473
  • 488
  • 491
  • 493
  • 518
  • 524

  • Properties
    C15H24N2O    248.37





    1:  Mandell L, Singh KP, Gresham JT, Freeman WJ.
    The total syntheses of d,l-matrine and d,l-leontine.
    J Am Chem Soc.    impact factor:   5.537
    1965;  87(22): 5234-6

    2:  Michael JP.
    Indolizidine and quinolizidine alkaloids.
    Nat Prod Rep.    impact factor:   4.373
    2001;  18(5): 520-42

    3:  Ishida M, Shinozaki H.
    Glutamate inhibitory action of matrine at the crayfish neuromuscular junction.
    Br J Pharmacol.    impact factor:   3.722
    1984;  82(2): 523-31

    4:  Song JZ, Xu HX, Tian SJ, But PP.
    Determination of quinolizidine alkaloids in traditional Chinese herbal drugs by nonaqueous capillary electrophoresis.
    J Chromatogr A.    impact factor:   2.52
    1999;  857(1-2): 303-11

    5:  Yang F, Quan J, Zhang T, Ito Y.
    Preparative separation of alkaloids from the root of Sophora flavescens Ait by pH-zone-refining counter-current chromatography.
    J Chromatogr A.    impact factor:   2.52
    1998;  822(2): 316-20

     
    Time used: 125 milliseconds.

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