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Raclopride
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| Systematic (IUPAC) name | |
| 3,5-dichloro-N-[(1-ethylpyrrolidin-2-yl)methyl]- 2-hydroxy-6-methoxy-benzamide |
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| Identifiers | |
| CAS number | |
| ATC code | ? |
| PubChem | |
| Chemical data | |
| Formula | C15H20Cl2N2O3 |
| Mol. mass | 347.236 g/mol |
| Pharmacokinetic data | |
| Bioavailability | ? |
| Metabolism | ? |
| Half life | 30 min |
| Excretion | ? |
| Therapeutic considerations | |
| Pregnancy cat. |
? |
| Legal status | |
| Routes | ? |
Raclopride is a synthetic compound that acts as an antagonist on D2 dopamine receptors.[1] It can thus be used as a neuroleptic agent to treat schizophrenia. It can be radiolabelled with the carbon-11 radioisotope and used in positron emission tomography (PET) scanning to assess the degree of dopamine binding to the D2 neuroreceptor. For example, one study found decreasing binding with the personality trait detachment.[2]
References
- ^ C. Kohler, H. Hall, S. O. Ogren & L. Gawell (July 1985). "Specific in vitro and in vivo binding of 3H-raclopride. A potent substituted benzamide drug with high affinity for dopamine D-2 receptors in the rat brain". Biochemical Pharmacology 34 (13): 2251–2259. PMID 4015674.
- ^ Lars Farde, J. Petter Gustavsson & Erik Jönsson (February 1997). "D2 dopamine receptors and personality traits". Nature 385 (6617): 590. doi:. PMID 9024656.
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Wikipedia content modification information:
- This page was last modified on 24 July 2008, at 04:32.
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