CHEBI:5832 - hypaphorine

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ChEBI Name hypaphorine
ChEBI ID CHEBI:5832
Definition An amino acid betaine obtaine by exhaustive methylation of the α-amino group of L-tryptophan with concomitant deprotonation of the carboxy group.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C14H18N2O2
Net Charge 0
Average Mass 246.305
Monoisotopic Mass 246.13683
InChI InChI=1S/C14H18N2O2/c1-16(2,3)13(14(17)18)8-10-9-15-12-7-5-4-6-11(10)12/h4-7,9,13,15H,8H2,1-3H3/t13-/m0/s1
InChIKey AOHCBEAZXHZMOR-ZDUSSCGKSA-N
SMILES C1(=CNC2=C1C=CC=C2)C[C@@H](C(=O)[O-])[N+](C)(C)C
Metabolite of Species Details
Erythrina suberosa (NCBI:txid1288013) Found in seed (BTO:0001226). See: PubMed
Pisolithus microcarpus (NCBI:txid178872) See: PubMed
Pisolithus tinctorius (NCBI:txid37468) 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.
xenobiotic
A xenobiotic (Greek, xenos "foreign"; bios "life") is a compound that is foreign to a living organism. Principal xenobiotics include: drugs, carcinogens and various compounds that have been introduced into the environment by artificial means.
fungal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in fungi, the kingdom that includes microorganisms such as the yeasts and moulds.
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 hypaphorine (CHEBI:5832) has role fungal metabolite (CHEBI:76946)
hypaphorine (CHEBI:5832) has role plant metabolite (CHEBI:76924)
hypaphorine (CHEBI:5832) has role xenobiotic (CHEBI:35703)
hypaphorine (CHEBI:5832) is a L-tryptophan derivative (CHEBI:47994)
hypaphorine (CHEBI:5832) is a amino-acid betaine (CHEBI:22860)
hypaphorine (CHEBI:5832) is a indole alkaloid (CHEBI:38958)
IUPAC Name
(2S)-3-(1H-indol-3-yl)-2-(trimethylazaniumyl)propanoate
Synonyms Sources
(+)-Hypaphorine ChemIDplus
Glyyunnanenine ChemIDplus
Hypaphorine KEGG COMPOUND
L-Hypaphorine ChemIDplus
L-tryptophan betaine ChEBI
Lenticin KEGG COMPOUND
N,N,N-trimethyltryptophan betaine ChEBI
Tryptophan betaine ChemIDplus
Manual Xrefs Databases
C00001740 KNApSAcK
C09213 KEGG COMPOUND
HMDB0061115 HMDB
View more database links
Registry Numbers Types Sources
3558356 Reaxys Registry Number Reaxys
487-58-1 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
10659705 PubMed citation Europe PMC
11089686 PubMed citation Europe PMC
11676477 PubMed citation Europe PMC
12056802 PubMed citation Europe PMC
12236599 PubMed citation Europe PMC
12710900 PubMed citation Europe PMC
14504925 PubMed citation Europe PMC
15032848 PubMed citation Europe PMC
16547865 PubMed citation Europe PMC
17370110 PubMed citation Europe PMC
18404567 PubMed citation Europe PMC
18571406 PubMed citation Europe PMC
18968328 PubMed citation Europe PMC
23855762 PubMed citation Europe PMC
5348524 PubMed citation Europe PMC
9951730 PubMed citation Europe PMC
IND20800355 Agricola citation Europe PMC
Last Modified
04 August 2016