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Postion:Product Catalog >API>Nervous system drugs>Parkinson's disease drugs>Pramipexole
Pramipexole
  • Pramipexole
  • Pramipexole
  • Pramipexole

Pramipexole

Price $10
Package 1kg
Min. Order: 1kg
Supply Ability: Ex 20 tons
Update Time: 2022-09-27

Product Details

Product Name: Pramipexole CAS No.: 104632-26-0
EC-No.: 600-593-1 Min. Order: 1kg
Purity: 99% Supply Ability: Ex 20 tons
Release date: 2022/09/27

Use of Pramipexole


Pramipexole is a dopamine agonist of the non-ergoline class indicated for treating Parkinson's disease (PD) and restless legs syndrome (RLS).Target: Dopamine Receptor Pramipexole also possesses low/insignificant affinity (500-10,000 nM) for the 5-HT1A, 5-HT1B, 5-HT1D, and α2-adrenergic receptors. It has negligible affinity (>10,000 nM) for the D1, D5, 5-HT2, α1-adrenergic, β-adrenergic, H1, and mACh receptors. All sites assayed were done using human tissues. While pramipexole is used clinically, its D3-preferring receptor binding profile has made it a popular tool compound for preclinical research. Pramipexole has been used (in combination with D2- and or D3-preferring antagonists) to interrogate the role of D3 receptor function in rodent models and tasks for neuropsychiatric disorders [1-3].

Pramipexole Biological Activity

DescriptionPramipexole is a dopamine agonist of the non-ergoline class indicated for treating Parkinson's disease (PD) and restless legs syndrome (RLS).Target: Dopamine Receptor Pramipexole also possesses low/insignificant affinity (500-10,000 nM) for the 5-HT1A, 5-HT1B, 5-HT1D, and α2-adrenergic receptors. It has negligible affinity (>10,000 nM) for the D1, D5, 5-HT2, α1-adrenergic, β-adrenergic, H1, and mACh receptors. All sites assayed were done using human tissues. While pramipexole is used clinically, its D3-preferring receptor binding profile has made it a popular tool compound for preclinical research. Pramipexole has been used (in combination with D2- and or D3-preferring antagonists) to interrogate the role of D3 receptor function in rodent models and tasks for neuropsychiatric disorders [1-3].
Related Catalog
Signaling Pathways >> GPCR/G Protein >> Dopamine Receptor
Signaling Pathways >> Neuronal Signaling >> Dopamine Receptor
Research Areas >> Neurological Disease
Solvent
In Vitro:

10 mM in DMSO

Solubility1 mM4.7319 mL23.6597 mL47.3194 mL5 mM0.9464 mL4.7319 mL9.4639 mL10 mM0.4732 mL2.3660 mL4.7319 mL
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

ShippingRoom temperature in continental US; may vary elsewhere
SMILESNC1=NC(CC[C@H](NCCC)C2)=C2S1
References

[1]. Kvernmo, T., S. Hartter, and E. Burger, A review of the receptor-binding and pharmacokinetic properties of dopamine agonists. Clin Ther, 2006. 28(8): p. 1065-78.

[2]. Millan, M.J., et al., Differential actions of antiparkinson agents at multiple classes of monoaminergic receptor. I. A multivariate analysis of the binding profiles of 14 drugs at 21 native and cloned human receptor subtypes. J Pharmacol Exp Ther, 2002. 3

[3]. Weber, M., et al., Heritable strain differences in sensitivity to the startle gating-disruptive effects of D2 but not D3 receptor stimulation. Behav Pharmacol, 2008. 19(8): p. 786-95.

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