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 |
10MG | 35 | In Stock |
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25MG | 61 | In Stock |
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50MG | 110 | In Stock |
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100MG | 160 | In Stock |
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200MG | 241 | In Stock |
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500MG | Get Quote | In Stock |
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1G | Get Quote | In Stock |
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Biological Information
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Product NamePramipexole 2HCl Monohydrate
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NoteResearch use only, not for human use.
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Brief DescriptionPramipexole 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.
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DescriptionPramipexole 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.
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In VitroPramipexole 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.
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In VivoPramipexole 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.
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SynonymsPramipexole Dihydrochloride Monohydrate | Pramipexole Dihydrochloride
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PathwayOthers
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TargetOther Targets
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RecptorD2S|D2L|D3|D4
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Research AreaNeurological Disease
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Indication——
Chemical Information
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CAS Number191217-81-9
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Formula Weight302.26
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Molecular FormulaC10H17N3S·2HCl·H2O
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Purity>98% (HPLC)
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SolubilityIn Vitro:?H2O : 100 mg/mL (330.84 mM)
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SMILESO.Cl.CCCN[C@H]1CCc2c(C1)sc(N)n2.Cl
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Chemical Name(S)-N6-propyl-4,5,6,7-tetrahydrobenzo[d]thiazole-2,6-diamine dihydrochloride hydrate
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Cassarino DS,etal..J Neurochem. 1998 Jul;71(1):295-301.
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