ID Name Structure References (top 5) Molecular Target(s)
1ID:3601
ISOSTRYCHNINE


Aldrich#:S958883

Freqency:
in 1 ingredients:

  • 31
  • in 19 recipes:

  • 19
  • 118
  • 140
  • 144
  • 166
  • 185
  • 233
  • 235
  • 258
  • 284
  • 289
  • 351
  • 378
  • 395
  • 417
  • 427
  • 445
  • 465
  • 519

  • Properties
    C21H24N2O2    336.43





    1:  Braestrup C, Nielsen M, Krogsgaard-Larsen P.
    Glycine antagonists structurally related to 4,5,6,7-tetrahydroisoxazolo [5,4-c]pyridin-3-ol inhibit binding of [3H]strychnine to rat brain membranes.
    J Neurochem.    impact factor:   4.906
    1986;  47(3): 691-6

    2:  Eichberg MJ, Dorta RL, Lamottke K, Vollhardt KP.
    The formal total synthesis of (+/-)-strychnine via a cobalt-mediated [2 + 2 + 2]cycloaddition.
    Org Lett.    impact factor:   3.367
    2000;  2(16): 2479-81

    3:  Frederich M, De Pauw MC, Llabres G, Tits M, Hayette MP, Brandt V, Penelle J, De Mol P, Angenot L.
    New antimalarial and cytotoxic sungucine derivatives from Strychnos icaja roots.
    Planta Med.    impact factor:   1.438
    2000;  66(3): 262-9

    4:  Cai BC, Hattori M, Namba T.
    Processing of nux vomica. II. Changes in alkaloid composition of the seeds of Strychnos nux-vomica on traditional drug-processing.
    Chem Pharm Bull (Tokyo).    impact factor:   1.117
    1990;  38(5): 1295-8

    5:  Wu H, Cai BC, Zheng PX, Zhao CZ, Yuan ZR.
    [Effect of processing on the alkaloids in Strychnos nux-vomica L.]
    Zhongguo Zhong Yao Za Zhi.    impact factor:   0
    1994;  19(5): 277-9, 319

     
    Time used: 454 milliseconds.

    Webpage designed by Dr. Xueliang Fang, last updated on 3/10/2005