CHEBI:119 - D-synephrine

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name D-synephrine
ChEBI ID CHEBI:119
ChEBI ASCII Name D-synephrine
Definition The D-enantiomer of synephrine.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C9H13NO2
Net Charge 0
Average Mass 167.20500
Monoisotopic Mass 167.09463
InChI InChI=1S/C9H13NO2/c1-10-6-9(12)7-2-4-8(11)5-3-7/h2-5,9-12H,6H2,1H3/t9-/m0/s1
InChIKey YRCWQPVGYLYSOX-VIFPVBQESA-N
SMILES CNC[C@H](O)c1ccc(O)cc1
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.
(via synephrine )
alpha-adrenergic agonist
An agent that selectively binds to and activates alpha-adrenergic receptors.
(via synephrine )
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via alkaloid )
Application(s): alpha-adrenergic agonist
An agent that selectively binds to and activates alpha-adrenergic receptors.
(via synephrine )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing D-synephrine (CHEBI:119) is a synephrine (CHEBI:29081)
D-synephrine (CHEBI:119) is conjugate base of D-synephrine(1+) (CHEBI:63694)
Incoming D-synephrine(1+) (CHEBI:63694) is conjugate acid of D-synephrine (CHEBI:119)
IUPAC Name
4-[(1R)-1-hydroxy-2-(methylamino)ethyl]phenol
Synonyms Sources
(−)-4-hydroxy-α-[(methylamino)methyl]benzenemethanol ChemIDplus
(−)-Oxedrine ChemIDplus
(−)-p-hydroxy-α-[(methylamino)methyl]benzyl alcohol ChemIDplus
(−)-Synephrine ChemIDplus
(-)-Sympatol KEGG COMPOUND
(-)-Synephrine KEGG COMPOUND
D(−)-Synephrine ChemIDplus
Manual Xrefs Databases
1-4-HYDROXYPHENYL-2-METHYLAMINOETHAN MetaCyc
C01869 KEGG COMPOUND
HMDB0004826 HMDB
View more database links
Registry Numbers Types Sources
3198818 Beilstein Registry Number Beilstein
3198818 Reaxys Registry Number Reaxys
614-35-7 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
8255371 PubMed citation Europe PMC
8833327 PubMed citation Europe PMC
Last Modified
23 October 2015