Ropinirole hydrochloride
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Ropinirole hydrochloride ??
- ???
- 241-243°C
- ?? ??
- 2-8°C
- ???
- H2O: >10mg/mL
- ??? ??
- ??
- ??
- ???
- InChI
- InChI=1S/C16H24N2O.ClH/c1-3-9-18(10-4-2)11-8-13-6-5-7-15-14(13)12-16(19)17-15;/h5-7H,3-4,8-12H2,1-2H3,(H,17,19);1H
- InChIKey
- XDXHAEQXIBQUEZ-UHFFFAOYSA-N
- SMILES
- C12CC(=O)NC=1C=CC=C2CCN(CCC)CCC.Cl
- CAS ??????
- 91374-20-8(CAS DataBase Reference)
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- ?? ? ?? ??
- ?? ? ???? ?? (GHS)
??? ?? | Xn,N,Xi | ||
---|---|---|---|
?? ???? ?? | 22-50/53-36/38 | ||
????? | 36-60-61-37/39-26 | ||
????(UN No.) | UN 3077 9/PG 3 | ||
WGK ?? | 3 | ||
RTECS ?? | NM3288250 | ||
HS ?? | 2933790002 |
Ropinirole hydrochloride C??? ??, ??, ??
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ReQuip was launched in the UK as a monotherapy or in combination with low-dose levodopa for the treatment of early-stage idiopathic Parkinson's disease. An eight step (24% overall yield) synthesis from isochroman provides access to ropinirole. It is a non-ergot postsynaptic dopamine D2 agonist with activity in the extrapyramidal system. It has weak or no significant activity at α2-adrenergic, 5-HT2 receptors and is inactive at 5-HT1, benzodiazepine, GABA, α1 and β adrenoreceptors. Thus it has essentially no CNS side effects, fewer dyskinesias and on-off fluctuations. In animals, it was able to reverse all motor deficits induced by MPTP. Tolerance is not developed and ropinirole has similar postsynaptic potency to apomorphine but with significantly less stereotyped behavior.??? ??
Off-White Solid??
An antiparkinsonian agent. A selective dopamine D2-receptor agonist?? ??
Ropinirole hydrochloride,4-(2-(dipropylamino)ethyl)indolin-2-one hydrochloride(Requip), is a white to pale greenish yellow powder that isvery soluble in water. Ropinirole is rapidly absorbed afteroral administration with maximal plasma concentrationsgenerally reached after about 1.5 hours, and the eliminationhalf-life appears to be approximately 3 hours. Ropinirole isalso rapidly and extensively distributed from the vascularcompartment and shows low plasma protein binding that isindependent of its plasma concentration. This drug iscleared by metabolism in the liver, with only 10% being excretedunchanged. The main metabolite of ropinirole is theN-despropyl metabolite. The glucuronide of this metaboliteand the carboxylic acid metabolite, 4-carboxymethylindolin-2-one, account only for 10% of the administered dose.None of the metabolites is pharmacologically active, and theexcretion of ropinirole-derived products is mainly via theurine. The main CYP450 isozyme involved in the metabolismof ropinirole is CYP1A2. Inhibitors or inducers ofthis enzyme have been shown to alter the clearance ofropinirole.Ropinirole is believed to act as an agonist atpostsynaptic D2 receptors. Ropinirole is indicated for thetreatment of the signs and symptoms of idiopathic PD andmoderate to severe primary RLS.???? ??
Selective D 2 -like receptor agonist (D 3 > D 2 > D 4 ). Causes biphasic spontaneous locomotor activity and contralateral circling in 6-OHDA-lesioned mice. Displays antiParkinsonian activity.Ropinirole hydrochloride ?? ?? ? ???
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Ropinirole hydrochloride ?? ??
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Ropinirole hydrochloride ?? ??:
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