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Pramipexole Dopamine Receptor agonist

Cat.No.S2460

Pramipexole (SND 919,Mirapexin,Sifrol,Mirapex) is a partial/full D2S, D2L, D3, D4 receptor agonist with a Ki of 3.9, 2.2, 0.5 and 5.1 nM for D2S, D2L, D3, D4 receptor, respectively.
Pramipexole Dopamine Receptor agonist Chemical Structure

Chemical Structure

Molecular Weight: 211.33

Quality Control

Cell Culture, Treatment & Working Concentration

Cell Lines Assay Type Concentration Incubation Time Formulation Activity Description PMID
CHO cells Function assay High inhibition constant against [3H]spiperone binding to human Dopamine receptor D3 expressed in CHO cells, Ki=0.88 nM
Click to View More Cell Line Experimental Data

Chemical Information, Storage & Stability

Molecular Weight 211.33 Formula

C10H17N3S

Storage (From the date of receipt)
CAS No. 104632-26-0 Download SDF Storage of Stock Solutions

Synonyms SND 919,Mirapexin,Sifrol,Mirapex Smiles CCCNC1CCC2=C(C1)SC(=N2)N

Solubility

In vitro
Batch:

DMSO : 42 mg/mL (198.74 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 42 mg/mL

Water : Insoluble

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
Batch:

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
as vortex, ultrasound or hot water bath can be used to aid dissolving.

Mechanism of Action

Targets/IC50/Ki
D3 receptor [1]
0.5 nM(Ki)
D2L Receptor [1]
2.2 nM(Ki)
D2S Receptor [1]
3.9 nM(Ki)
D4 receptor [1]
5.1 nM(Ki)
References

Clinical Trial Information

(data from https://clinicaltrials.gov, updated on 2024-05-22)

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT06269146 Not yet recruiting
Anxiety Disorders|Anxiety|Depression|Social Disconnection
University of California San Diego|National Institute of Mental Health (NIMH)|New York State Psychiatric Institute
February 2024 Phase 2
NCT03683225 Active not recruiting
Idiopathic Parkinson Disease
Chase Therapeutics Corporation
April 1 2019 Phase 2
NCT03642964 Active not recruiting
Major Depressive Disorder (MDD)
Chase Therapeutics Corporation
September 10 2018 Phase 2
NCT02101138 Unknown status
Hypereosinophilic Syndrome
National Institute of Allergy and Infectious Diseases (NIAID)|Knopp Biosciences|National Institutes of Health Clinical Center (CC)
March 14 2014 Phase 2
NCT01733199 Completed
Parkinson''s Disease|Secondary Behavioural Addiction
Nantes University Hospital
October 2012 Phase 4
NCT01607034 Completed
Healthy Volunteers
Knopp Biosciences
June 2012 Phase 1

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