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Submit ReviewGuanabenz acetate is a α2-adrenergic agonist and IGRS (imidazoline I2 binding site) selective ligand.
M. Wt | 291.14 |
Formula | C8H8Cl2N4.CH3CO2H |
Storage | Store at RT |
Purity | ≥98% (HPLC) |
CAS Number | 23256-50-0 |
PubChem ID | 5702062 |
InChI Key | MCSPBPXATWBACD-GAYQJXMFSA-N |
Smiles | CC(O)=O.ClC1=C(/C=N/NC(N)=N)C(Cl)=CC=C1 |
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Solvent | Max Conc. mg/mL | Max Conc. mM | |
---|---|---|---|
Solubility | |||
DMSO | 21.84 | 75 |
The following data is based on the product molecular weight 291.14. Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
---|---|---|---|
0.75 mM | 4.58 mL | 22.9 mL | 45.8 mL |
3.75 mM | 0.92 mL | 4.58 mL | 9.16 mL |
7.5 mM | 0.46 mL | 2.29 mL | 4.58 mL |
37.5 mM | 0.09 mL | 0.46 mL | 0.92 mL |
References are publications that support the biological activity of the product.
Evans and Anderson (1995) Renal effects of infusion of rilmenidine and guan. in conscious dogs: contribution of peripheral and central nervous system α2-adrenoceptors. Br.J.Pharmacol. 116 1557 PMID: 8564219
Holmes et al (1983) Guanabenz. A review of its pharmacodynamic properties and therapeutic efficacy in hypertension. Drugs 26 212 PMID: 6352237
Michel and Insel (1989) Are there multiple imidazoline binding sites? Trends Pharmacol.Sci. 10 342 PMID: 2690423
Merck Index 12 4585
If you know of a relevant reference for Guanabenz acetate, please let us know.
Keywords: Guanabenz acetate, Guanabenz acetate supplier, α2-adrenoceptor, alpha2-adrenoceptor, α2-Adrenergic, alpha2-Adrenergic, a2-adrenoceptor, a2-adrenergic, agonists, I2, selective, ligands, Adrenoceptors, Imidazoline, Adrenergic, Alpha-2, Receptors, 0885, Tocris Bioscience
Citations are publications that use Tocris products. Selected citations for Guanabenz acetate include:
Ye et al (2013) Pharmaceutically controlled designer circuit for the treatment of the metabolic syndrome. J Korean Med Sci 110 141 PMID: 23248313
Nevin et al (2017) Modeling the Mutational and Phenotypic Landscapes of Pelizaeus-Merzbacher Disease with Human iPSC-Derived Oligodendrocytes. Am J Hum Genet 100 617 PMID: 28366443
Wan et al (2014) Distinctive subcellular inhibition of cytokine-induced SRC by salubrinal and fluid flow. PLoS One 9 e105699 PMID: 25157407
Hamamura et al (2015) Chondroprotective effects of Salubrinal in a mouse model of osteoarthritis. Proc Natl Acad Sci U S A 4 84 PMID: 25977571
Cardin and Schmidt (2004) Noradrenergic inputs mediate state dependence of auditory responses in the avian song system. Bone Joint Res 24 7745 PMID: 15342742
Do you know of a great paper that uses Guanabenz acetate from Tocris? Please let us know.
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Tocris offers the following scientific literature in this area to showcase our products. We invite you to request* your copy today!
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Major depressive disorder is characterized by depressed mood and a loss of interest and/or pleasure. Updated in 2015 this poster highlights presynaptic and postsynaptic targets for the potential treatment of major depressive disorder, as well as outlining the pharmacology of currently approved antidepressant drugs.
Parkinson's disease (PD) causes chronic disability and is the second most common neurodegenerative condition. This poster outlines the neurobiology of the disease, as well as highlighting current therapeutic treatments for symptomatic PD, and emerging therapeutic strategies to delay PD onset and progression.