Name | pramipexole hydrochloride anhydrous |
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Synonyms |
2,6-Benzothiazolediamine, 4,5,6,7-tetrahydro-N-propyl-, (6S)-, hydrochloride (1:2)
(6S)-4,5,6,7-Tetrahydro-N6-propyl-2,6-benzothiazolediamine Dihydrochloride (S)-2-Amino-4,5,6,7-tetrahydro-6-(propylamino)benzothiazole dihydrochloride Pramipexole hydrochloride Pramipexole dihydrochloride MFCD00876894 (S)-Pramipexole Dihydrochloride (6S)-N-Propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine dihydrochloride (S)-N6-Propyl-4,5,6,7-tetrahydrobenzo[d]thiazole-2,6-diamine dihydrochloride Pramipexole (dihydrochloride) |
Description | Pramipexole 2Hcl 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. IC50 Value: 3.9 nM(D2S); 2.2 nM(D2L); 0.5 nM(D3); 5.1 nM(D4)Target: Dopamine ReceptorPramipexole dihydrochloride is a dopamine receptor agonist with selectivity for the D3 receptor (Ki values are 3.9, 3.3, 0.5 and 3.9 nM for D2L, D2S, D3 and D4 receptors respectively). Pramipexole dihydrochloride exhibits negligable affinity for D1 and D5 receptors. Pramipexole has been found to have neuroprotective effects independent of its dopamine receptor agonism. It reduces mitochondrial reactive oxygen species (ROS) production and inhibits the activation of apoptotic pathways. Pramipexole displays activity in the treatment of Parkinson's disease (PD) and restless legs syndrome (RLS). |
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Related Catalog | |
References |
Boiling Point | 378ºC at 760 mmHg |
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Melting Point | 288-290ºC |
Molecular Formula | C10H19Cl2N3S |
Molecular Weight | 284.249 |
Flash Point | 182.4ºC |
Exact Mass | 283.067688 |
PSA | 79.18000 |
LogP | 4.15830 |
Vapour Pressure | 6.49E-06mmHg at 25°C |
Storage condition | Desiccate at RT |
Hazard Codes | Xi |
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RIDADR | NONH for all modes of transport |
HS Code | 2934999090 |
~84% 104632-25-9 |
Literature: INSTYTUT FARMACEUTYCZNY Patent: WO2007/75095 A1, 2007 ; Location in patent: Page/Page column 7 ; |
~72% 104632-25-9 |
Literature: Ravinder; Rajeswar Reddy; Panasa Reddy; Bandichhor, Rakeshwar Tetrahedron Letters, 2013 , vol. 54, # 36 p. 4908 - 4913 |
~98% 104632-25-9 |
Literature: Helm AG; CF Pharma Gyogyszergyarto Kft. Patent: EP1878731 A1, 2008 ; Location in patent: Page/Page column 11 ; |
~85% 104632-25-9 |
Literature: Helm AG; CF Pharma Gyogyszergyarto Kft. Patent: EP1878731 A1, 2008 ; Location in patent: Page/Page column 11 ; |
~% 104632-25-9 |
Literature: WO2011/21214 A2, ; |
~% 104632-25-9 |
Literature: WO2011/21214 A2, ; |
~% 104632-25-9 |
Literature: WO2011/21214 A2, ; |
~% 104632-25-9 |
Literature: WO2011/21214 A2, ; |
~% 104632-25-9 |
Literature: WO2011/21214 A2, ; |
Precursor 8 | |
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DownStream 1 | |
HS Code | 2934999090 |
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Summary | 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |