Raclopride

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Raclopride
Raclopride.svg
Systematic (IUPAC) name
3,5-dichloro-N-[[(2S)-1-ethylpyrrolidin-2-yl]methyl]-2-hydroxy-6-methoxybenzamide
Pharmacokinetic data
Biological half-life 20 min
Identifiers
CAS Number 84225-95-6 N
ATC code none
PubChem CID: 3033769
IUPHAR/BPS 94
ChemSpider 2298373 YesY
UNII 430K3SOZ7G YesY
ChEMBL CHEMBL8809 YesY
Chemical data
Formula C15H20Cl2N2O3
Molecular mass 347.236 g/mol
  • Clc1c(O)c(c(OC)c(Cl)c1)C(=O)NC[C@H]2N(CC)CCC2
  • InChI=1S/C15H20Cl2N2O3/c1-3-19-6-4-5-9(19)8-18-15(21)12-13(20)10(16)7-11(17)14(12)22-2/h7,9,20H,3-6,8H2,1-2H3,(H,18,21)/t9-/m0/s1 YesY
  • Key:WAOQONBSWFLFPE-VIFPVBQESA-N YesY
 NYesY (what is this?)  (verify)

Raclopride is a synthetic compound that acts as a selective antagonist on D2 dopamine receptors.[1]

Its selectivity to the cerebral D2 receptors is characterized by its respective Ki-values, which are as follows: 1.8, 3.5, 2400 and 18000 nM for D2, D3, D4 and D1 receptors respectively.

It can be radiolabelled with radioisotopes, e.g. 3H or 11C and used as a tracer for in vitro imaging (autoradiography) as well as in vivo imaging positron emission tomography (PET). Images obtained by cerebral PET scanning (e.g. PET/CT or PET/MRI) allow the non-invasive assessment of the binding capacity of the cerebral D2 dopamine receptor, which can be useful for the diagnosis of movement disorders. In particular, cerebral D2 receptor binding as measured by carbon-11-raclopride (11C-raclopride) has shown to reflect disease severity of Huntington's disease, a genetical disease characterized by selective degeneration of cerebral D2 receptors.[2]

Other studies have investigated the relationship of D2 receptor binding capacity and personality disorders. For example, one study found decreasing binding with the personality trait detachment.[3] Radiolabelled raclopride is also commonly used to determine the efficacy and neurotoxicity of dopaminergic drugs.

References

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