Pramipexole 2HCl Monohydrate

CAS No. 191217-81-9

Pramipexole 2HCl Monohydrate( Pramipexole Dihydrochloride Monohydrate | Pramipexole Dihydrochloride )

Catalog No. M18171 CAS No. 191217-81-9

Pramipexole Dihydrochloride is the hydrochloride salt of pramipexole, a benzothiazole derivative. As a nonergot dopamine agonist, pramipexole binds to D2 and D3 dopamine receptors in the striatum and substantia nigra of the brain.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 37 In Stock
10MG 37 In Stock
25MG 65 In Stock
50MG 113 In Stock
100MG 166 In Stock
200MG 249 In Stock
500MG 421 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Pramipexole 2HCl Monohydrate
  • Note
    Research use only, not for human use.
  • Brief Description
    Pramipexole Dihydrochloride is the hydrochloride salt of pramipexole, a benzothiazole derivative. As a nonergot dopamine agonist, pramipexole binds to D2 and D3 dopamine receptors in the striatum and substantia nigra of the brain.
  • Description
    Pramipexole Dihydrochloride is a D2/3 agonist. It acts by reducing mitochondrial ROS production and inhibiting the activation of apoptotic pathways.(In Vitro):Pramipexole dihydrochloride hydrate shows a low binding affinity for D1-type receptor, with an IC50 of >50,000 nM.Pramipexole dihydrochloride hydrate (0.01-10 μM; 72 hours) produces dose-dependent increases of dendritic arborization and soma size.Pramipexole dihydrochloride hydrate attenuates levodopa-induced toxicity in mesencephalic cultures.(In Vivo):Pramipexole dihydrochloride hydrate (0.25-1 mg/kg; i.p.) significantly reduces the infarction volume in animals.Pramipexole dihydrochloride hydrate improves neurological recovery.Pramipexole dihydrochloride hydrate prevents ischemic cell death via mitochondrial pathways in ischemic stroke.
  • In Vitro
    Pramipexole dihydrochloride hydrate shows a low binding affinity for D1-type receptor, with an IC50 of >50,000 nM.Pramipexole dihydrochloride hydrate (0.01-10?μM; 72 hours) produces dose-dependent increases of dendritic arborization and soma size.Pramipexole dihydrochloride hydrate attenuates levodopa-induced toxicity in mesencephalic cultures.
  • In Vivo
    Pramipexole dihydrochloride hydrate (0.25-1 mg/kg; i.p.) significantly reduces the infarction volume in animals.Pramipexole dihydrochloride hydrate improves neurological recovery.Pramipexole dihydrochloride hydrate prevents ischemic cell death via mitochondrial pathways in ischemic stroke. Animal Model:Male Wistar rats weighing 250-300 g (16-18 weeks old)Dosage:0.25 mg/kg, 1 mg/kg Administration:Intraperitoneal injection Result:Decreased infarction volume as compared to tMCAO (transient middle cerebral artery occlusion)-only animals.
  • Synonyms
    Pramipexole Dihydrochloride Monohydrate | Pramipexole Dihydrochloride
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    D2S|D2L|D3|D4
  • Research Area
    Neurological Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    191217-81-9
  • Formula Weight
    302.26
  • Molecular Formula
    C10H17N3S·2HCl·H2O
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?H2O : 100 mg/mL (330.84 mM)
  • SMILES
    O.Cl.CCCN[C@H]1CCc2c(C1)sc(N)n2.Cl
  • Chemical Name
    (S)-N6-propyl-4,5,6,7-tetrahydrobenzo[d]thiazole-2,6-diamine dihydrochloride hydrate

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Cassarino DS,etal..J Neurochem. 1998 Jul;71(1):295-301.
molnova catalog
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