CHEBI:81200 - (S)-corytuberine

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ChEBI Name (S)-corytuberine
ChEBI ID CHEBI:81200
ChEBI ASCII Name (S)-corytuberine
Definition An aporphine alkaloid that is aporphine which is substituted by hydroxy groups at positions 1 and 11, and by methoxy groups at positions 2 and 10 (the S enantiomer).
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C19H21NO4
Net Charge 0
Average Mass 327.375
Monoisotopic Mass 327.14706
InChI InChI=1S/C19H21NO4/c1-20-7-6-11-9-14(24-3)19(22)17-15(11)12(20)8-10-4-5-13(23-2)18(21)16(10)17/h4-5,9,12,21-22H,6-8H2,1-3H3/t12-/m0/s1
InChIKey WHFUDAOCYRYAKQ-LBPRGKRZSA-N
SMILES C1=2C=3[C@@](N(CC1)C)(CC4=C(C3C(=C(C2)OC)O)C(=C(C=C4)OC)O)[H]
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
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.
metabolite
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)-corytuberine (CHEBI:81200) has role plant metabolite (CHEBI:76924)
(S)-corytuberine (CHEBI:81200) is a aporphine alkaloid (CHEBI:134209)
(S)-corytuberine (CHEBI:81200) is a aromatic ether (CHEBI:35618)
(S)-corytuberine (CHEBI:81200) is a organic heterotetracyclic compound (CHEBI:38163)
(S)-corytuberine (CHEBI:81200) is a polyphenol (CHEBI:26195)
(S)-corytuberine (CHEBI:81200) is a tertiary amino compound (CHEBI:50996)
Incoming (S)-magnoflorine (CHEBI:6641) has functional parent (S)-corytuberine (CHEBI:81200)
IUPAC Name
(6aS)-2,10-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-1,11-diol
Synonyms Sources
(+)-corytuberine KNApSAcK
(S)-corytuberine UniProt
Manual Xrefs Databases
C00025655 KNApSAcK
C17591 KEGG COMPOUND
CPD-9935 MetaCyc
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Registry Numbers Types Sources
517-56-6 CAS Registry Number ChemIDplus
94033 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
14090 PubMed citation Europe PMC
16413022 PubMed citation Europe PMC
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24963327 PubMed citation Europe PMC
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2907279 PubMed citation Europe PMC
300084 Chinese Abstracts citation Europe PMC
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Last Modified
04 January 2017