CHEBI:134213 - (S)-1,2,9,10-tetramethoxy-6-methylaporphine(1+)

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ChEBI Name (S)-1,2,9,10-tetramethoxy-6-methylaporphine(1+)
ChEBI ASCII Name (S)-1,2,9,10-tetramethoxy-6-methylaporphine(1+)
Definition A aporphine alkaloid that is the quaternary ammonium ion obtained by methylation of the tertiary amino group of (S)-glaucine.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Kristian Axelsen
Supplier Information
Download Molfile XML SDF
Formula C22H28NO4
Net Charge +1
Average Mass 370.463
Monoisotopic Mass 370.20128
InChI InChI=1S/C22H28NO4/c1-23(2)8-7-13-10-19(26-5)22(27-6)21-15-12-18(25-4)17(24-3)11-14(15)9-16(23)20(13)21/h10-12,16H,7-9H2,1-6H3/q+1/t16-/m0/s1
SMILES C12=C3[C@](CC4=C1C=C(OC)C(=C4)OC)([N+](CCC3=CC(=C2OC)OC)(C)C)[H]
Metabolite of Species Details
Isopyrum thalictroides (NCBI:txid432643) Found in rhizome (BTO:0001181). See: PubMed
Isopyrum thalictroides (NCBI:txid432643) Found in root (BTO:0001188). See: PubMed
Roles Classification
Biological Role(s): plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via alkaloid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (S)-1,2,9,10-tetramethoxy-6-methylaporphine(1+) (CHEBI:134213) has functional parent (S)-glaucine (CHEBI:5373)
(S)-1,2,9,10-tetramethoxy-6-methylaporphine(1+) (CHEBI:134213) has role plant metabolite (CHEBI:76924)
(S)-1,2,9,10-tetramethoxy-6-methylaporphine(1+) (CHEBI:134213) is a aporphine alkaloid (CHEBI:134209)
(S)-1,2,9,10-tetramethoxy-6-methylaporphine(1+) (CHEBI:134213) is a quaternary ammonium ion (CHEBI:35267)
Synonyms Sources
(S)-1,2,9,10-tetramethoxy-6-methylaporphinium ChEBI
(S)-N-methylglaucine UniProt
(S)-N-methylglaucine(1+) ChEBI
1,2-dimethoxy-N,O,O-trimethylapomorphinium ChEBI
N-methyl-(S)-glaucine(1+) ChEBI
N-Methylglaucine KNApSAcK
Manual Xref Database
C00028700 KNApSAcK
View more database links
Registry Numbers Types Sources
1555014 Reaxys Registry Number Reaxys
2533-94-0 CAS Registry Number KNApSAcK
Citations Waiting for Citations Types Sources
15143837 PubMed citation Europe PMC
27573242 PubMed citation SUBMITTER
Last Modified
06 April 2017