Date published: 2026-2-1

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4-Hydroxy Clonidine (CAS 57101-48-1)

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Alternate Names:
3,5-dichloro-4-(4,5-dihydro-1h-imidazol-2-ylamino)phenol; para-Hydroxyclonidine
Application:
4-Hydroxy Clonidine is A metabolite of Clonidine
CAS Number:
57101-48-1
Molecular Weight:
246.09
Molecular Formula:
C9H9Cl2N3O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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4-Hydroxy Clonidine, also known as 4-OHClon, is a selective α2-adrenoceptor agonist and a metabolite of clonidine. It has gained significant attention in scientific research due to its usefulness in studying the role of α2-adrenoceptors in various physiological and pathological processes. Compared to clonidine, 4-Hydroxy clonidine exhibits higher selectivity and potency for α2-adrenoceptors. This characteristic makes it useful in investigating the specific functions of α2-adrenoceptors. Researchers have utilized 4-Hydroxy Clonidine in multiple research applications, focusing on pain modulation, cardiovascular function, and neuronal signaling mediated by α2-adrenoceptors. Additionally, it has been employed to explore the effects of α2-adrenoceptor agonists on the release of neurotransmitters like norepinephrine and dopamine. The mechanism of action of 4-Hydroxy clonidine involves its role as an agonist for α2-adrenoceptors. These receptors are G-protein-coupled receptors located on the presynaptic membrane of neurons. Upon activation, α2-adrenoceptors inhibit the release of neurotransmitters such as norepinephrine and dopamine. Consequently, sympathetic activity decreases, resulting in various physiological responses.


4-Hydroxy Clonidine (CAS 57101-48-1) References

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  2. Supersensitivity of analgesic responses to alpha 2-adrenergic agonists in genetically hypertensive rats.  |  Marwaha, J. 1984. Brain Res. 304: 363-6. PMID: 6331590
  3. Development of a RIA for clonidine and its comparison with the reference methods.  |  Arndts, D., et al. 1981. J Pharmacol Methods. 6: 295-307. PMID: 7334811
  4. Quantitative analyses of the structure-hydrophobicity relationship for N-acetyl di- and tripeptide amides.  |  Akamatsu, M., et al. 1994. J Pharm Sci. 83: 1026-33. PMID: 7965659
  5. Dissociation of hypertension and enhanced clonidine-induced antinociception in spontaneously hypertensive rats.  |  Lin, JC., et al. 1993. Pain. 53: 53-58. PMID: 8316390
  6. Clonidine and related analogues. Quantitative correlations.  |  Rouot, B., et al. 1976. J Med Chem. 19: 1049-54. PMID: 9510

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

4-Hydroxy Clonidine, 1 mg

sc-206887
1 mg
$398.00