Catalog Number: 0885
Chemical Name: [(2,6-Dichlorobenzylidene)amino]guanidine acetate
Biological Activity
α2-adrenergic agonist and IGRS (imidazoline I2 binding site) selective ligand.
Technical Data
  • M.Wt:
    291.14
  • Formula:
    C8H8Cl2N4.CH3CO2H
  • Solubility:
    Soluble to 75 mM in DMSO
  • Purity:
    >98%
  • Storage:
    Store at RT
  • CAS No:
    23256-50-0
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis. All Tocris products are intended for laboratory research use only.
Background References

  1. Kishimoto T et al.
    Leucocyte Typing VI. Garland Publishing Inc. London.
  2. Guanabenz. A review of its pharmacodynamic properties and therapeutic efficacy in hypertension.
    Holmes et al.
    Drugs, 1983;26:212
  3. Renal effects of infusion of rilmenidine and guanabenz in conscious dogs: contribution of peripheral and central nervous system α2-adrenoceptors.
    Evans and Anderson
    Br.J.Pharmacol., 1995;116:1557
  4. Are there multiple imidazoline binding sites?
    Michel and Insel
    Trends Pharmacol.Sci., 1989;10:342
Citations:

The citations listed below are publications that use Tocris products. Selected citations for Guanabenz acetate include:

4 Citations: Showing 1 - 4
Filter your results:

  1. Chondroprotective effects of Salubrinal in a mouse model of osteoarthritis.
    Authors: Hamamura Et al.
    Proc Natl Acad Sci U S A 2015;4:84
  2. Distinctive subcellular inhibition of cytokine-induced SRC by salubrinal and fluid flow.
    Authors: Wan Et al.
    PLoS One 2014;9:e105699
  3. Pharmaceutically controlled designer circuit for the treatment of the metabolic syndrome.
    Authors: Ye Et al.
    J Korean Med Sci 2013;110:141
  4. Noradrenergic inputs mediate state dependence of auditory responses in the avian song system.
    Authors: Cardin and Schmidt
    Bone Joint Res 2004;24:7745

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