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Raclopride Dopamine Receptor antagonist

Cat.No.E0125

Raclopride is a selective dopamine D2/D3 receptor antagonist that discriminates between dopamine-mediated motor functions. This compound binds to D2 and D3 receptors with dissociation constants of between 1.8 nM and 3.5 nM, but has a very low affinity for D4 receptors.
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Quality Control

Batch: E012501 DMSO]69 mg/mL]false]Ethanol]69 mg/mL]false]Water]1 mg/mL]false Purity: 99.98%
99.98

Solubility

In vitro
Batch:

DMSO : 69 mg/mL (198.7 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 69 mg/mL

Water : 1 mg/mL

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In vivo
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In vivo Formulation Calculator (Clear solution)

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Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
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Chemical Information, Storage & Stability

Molecular Weight 347.24 Formula

C15H20Cl2N2O3

Storage (From the date of receipt) 3 years -20°C powder
CAS No. 84225-95-6 -- Storage of Stock Solutions

Read more about storage stability stock solution CAS number SMILES

Mechanism of Action

Targets/IC50/Ki
Dopamine D2 receptor
1.8 nM(Ki)
Dopamine D3 receptor
3.5 nM(Ki)
In vivo

Raclopride is an antagonist of central dopaminergic D2 receptors, possessing antiaggressive effect of this compound with very little motor impairment and some increase in exploratory behavior.

References

Clinical Trial Information

(data from https://clinicaltrials.gov, updated on 2026-07-28)

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT07559500 RECRUITING
Alcohol Use Disorder (AUD)
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
2026-05-20 PHASE1
NCT06977308 NOT_YET_RECRUITING
Clinical High Risk for Psychosis (CHR)
New York State Psychiatric Institute
2026-10-01 PHASE1
NCT05282277 RECRUITING
Depression; Psychosis; Anhedonia
University of North Carolina, Chapel Hill
2022-04-20 PHASE4
NCT03190954 COMPLETED
Normal Physiology; Opioid Use Disorders
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
2017-08-17 EARLY_PHASE1
NCT02169310 COMPLETED
Traumatic Brain Injury
National Institute of Neurological Disorders and Stroke (NINDS)
2014-11-18 PHASE1
NCT03637075 COMPLETED
Diabetes Mellitus, Type 2
University Hospital Tuebingen
2017-02-20

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