ID Name Structure References (top 5) Molecular Target(s)


in 4 ingredients:

  • 123
  • 470
  • 477
  • 568
  • in 4 recipes:

  • 10
  • 113
  • 215
  • 381

  • Properties
    C37H40N2O6    608.73

    1:  Shen YC, Chou CJ, Chiou WF, Chen CF.
    Anti-inflammatory effects of the partially purified extract of radix Stephaniae tetrandrae: comparative studies of its active principles tetrandrine and fangchinoline on human polymorphonuclear leukocyte functions.
    Mol Pharmacol.    impact factor:   5.465
    2001;  60(5): 1083-90

    2:  Frappier F, Jossang A, Soudon J, Calvo F, Rasoanaivo P, Ratsimamanga-Urverg S, Saez J, Schrevel J, Grellier P.
    Bisbenzylisoquinolines as modulators of chloroquine resistance in Plasmodium falciparum and multidrug resistance in tumor cells.
    Antimicrob Agents Chemother.    impact factor:   3.969
    1996;  40(6): 1476-81

    3:  Sridar C, Kent UM, Notley LM, Gillam EM, Hollenberg PF.
    Effect of tamoxifen on the enzymatic activity of human cytochrome CYP2B6.
    J Pharmacol Exp Ther.    impact factor:   3.3
    2002;  301(3): 945-52

    4:  Dong GZ, Kameyama K, Rinken A, Haga T.
    Ligand binding properties of muscarinic acetylcholine receptor subtypes (m1-m5) expressed in baculovirus-infected insect cells.
    J Pharmacol Exp Ther.    impact factor:   3.3
    1995;  274(1): 378-84

    5:  Yu XC, Wu S, Wang GY, Shan J, Wong TM, Chen CF, Pang KT.
    Cardiac effects of the extract and active components of radix stephaniae tetrandrae. II. Myocardial infarct, arrhythmias, coronary arterial flow and heart rate in the isolated perfused rat heart.
    Life Sci.    impact factor:   1.774
    2001;  68(25): 2863-72

    Time used: 140 milliseconds.

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