pramipexole hydrochloride (CHEBI:51147)

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CHEBI:51147 - pramipexole hydrochloride

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ChEBI ID	CHEBI:51147
ChEBI Name	pramipexole hydrochloride
Stars
Definition	A hydrate that is the monohydrate of the dihydrochloride salt of pramiprexole.
Last Modified	18 November 2011
Submitter	Inma Spiteri
Downloads	Molfile

Formula	C10H17N3S.H2O.2HCl
Net Charge	0
Average Mass	302.271
Monoisotopic Mass	301.07824
SMILES	CCCN[C@H]1CCc2nc(N)sc2C1.Cl.Cl.O
InChI	InChI=1S/C10H17N3S.2ClH.H2O/c1-2-5-12-7-3-4-8-9(6-7)14-10(11)13-8;;;/h7,12H,2-6H2,1H3,(H2,11,13);2*1H;1H2/t7-;;;/m0.../s1
InChIKey	APVQOOKHDZVJEX-QTPLPEIMSA-N

Roles Classification

Biological Role:	dopamine agonist A drug that binds to and activates dopamine receptors.
Applications:	antipsychotic agent Antipsychotic drugs are agents that control agitated psychotic behaviour, alleviate acute psychotic states, reduce psychotic symptoms, and exert a quieting effect. antiparkinson drug A drug used in the treatment of Parkinson's disease. dopamine agonist A drug that binds to and activates dopamine receptors.

ChEBI Ontology

Outgoing Relation(s)
	pramipexole hydrochloride (CHEBI:51147) has part pramipexole hydrochloride anhydrous (CHEBI:51148)
	pramipexole hydrochloride (CHEBI:51147) has part pramipexole(2+) (CHEBI:63218)
	pramipexole hydrochloride (CHEBI:51147) has role antiparkinson drug (CHEBI:48407)
	pramipexole hydrochloride (CHEBI:51147) has role antipsychotic agent (CHEBI:35476)
	pramipexole hydrochloride (CHEBI:51147) has role dopamine agonist (CHEBI:51065)
	pramipexole hydrochloride (CHEBI:51147) is a hydrate (CHEBI:35505)

IUPAC Name
(6S)-N⁶-propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine dihydrochloride hydrate

Synonyms	Source
Daquiran	ChEMBL
(S)-2-Amino-4,5,6,7-tetrahydro-6-(propylamino)benzothiazole dihydrochloride monohydrate	ChemIDplus
PNU-98528E	ChEMBL
Pramipexole accord	ChEMBL
pramipexole dihydrochloride	ChEMBL
Pramipexole dihydrochloride anhydrous	ChEMBL

Brand Names	Source
Mirapex	ChEMBL
Mirapex er	ChEMBL

Manual Xrefs	Databases
D00559	KEGG DRUG
DB00413	DrugBank
US2010063116	Patent
WO2008052953	Patent
WO2008104847	Patent

Registry Numbers	Sources
Reaxys:14116907	Reaxys
CAS:191217-81-9	ChemIDplus

Citations