CHEBI:177381 - naxagolide hydrochloride

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name naxagolide hydrochloride
ChEBI ID CHEBI:177381
Definition The hydrochloride salt of naxagolide.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
more structures >>
Formula C15H21NO2.ClH
Net Charge 0
Average Mass 283.800
Monoisotopic Mass 283.13391
InChI InChI=1S/C15H21NO2.ClH/c1-2-7-16-8-9-18-15-13-10-12(17)5-3-11(13)4-6-14(15)16;/h3,5,10,14-15,17H,2,4,6-9H2,1H3;1H/t14-,15-;/m1./s1
InChIKey NNEACMQMRLNNIL-CTHHTMFSSA-N
SMILES Cl.[H][C@@]12CCC3=C(C=C(O)C=C3)[C@@]1([H])OCCN2CCC
Roles Classification
Biological Role(s): dopamine agonist
A drug that binds to and activates dopamine receptors.
Application(s): anticonvulsant
A drug used to prevent seizures or reduce their severity.
antiparkinson drug
A drug used in the treatment of Parkinson's disease.
dopamine agonist
A drug that binds to and activates dopamine receptors.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing naxagolide hydrochloride (CHEBI:177381) has part naxagolide(1+) (CHEBI:177380)
naxagolide hydrochloride (CHEBI:177381) has role anticonvulsant (CHEBI:35623)
naxagolide hydrochloride (CHEBI:177381) has role antiparkinson drug (CHEBI:48407)
naxagolide hydrochloride (CHEBI:177381) has role dopamine agonist (CHEBI:51065)
naxagolide hydrochloride (CHEBI:177381) is a hydrochloride (CHEBI:36807)
IUPAC Name
(4aR,10bR)-4-propyl-3,4,4a,5,6,10b-hexahydro-2H-naphtho[1,2-b][1,4]oxazin-9-ol hydrochloride
Synonyms Sources
(+)-PHNO hydrochloride ChEBI
(4aR,10bR)-9-hydroxy-4-propyl-3,4,4a,5,6,10b-hexahydro-2H-naphtho[1,2-b][1,4]oxazin-4-ium chloride ChEBI
(4aR-trans)-3,4,4a,5,6,10b-hexahydro-4-propyl-2H-naphth[1,2-b]-1,4-oxazin-9-ol hydrochloride ChEBI
L 647,339 ChemIDplus
L 647339 ChEBI
L-647,339 ChemIDplus
MK 458 ChemIDplus
MK-458 ChemIDplus
naxagolide HCl ChemIDplus
naxagolide monohydrochloride ChEBI
Manual Xrefs Databases
51862 ChemSpider
D05124 KEGG DRUG
View more database links
Registry Number Type Source
99705-65-4 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
1348452 PubMed citation Europe PMC
1580821 PubMed citation Europe PMC
15943487 PubMed citation Europe PMC
1676932 PubMed citation Europe PMC
1913699 PubMed citation Europe PMC
1979657 PubMed citation Europe PMC
2900065 PubMed citation Europe PMC
8363442 PubMed citation Europe PMC
Last Modified
13 August 2021