CHEBI:27410 - N-methyl-6-pyridone-3-carboxamide

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name N-methyl-6-pyridone-3-carboxamide
ChEBI ID CHEBI:27410
ChEBI ASCII Name N-methyl-6-pyridone-3-carboxamide
Definition A pyridone that is 2-pyridone substituted with a carboxamide group at C-5 and a methyl group at N-1.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:7358, CHEBI:21800
Supplier Information
Download Molfile XML SDF
Formula C7H8N2O2
Net Charge 0
Average Mass 152.15060
Monoisotopic Mass 152.05858
InChI InChI=1S/C7H8N2O2/c1-9-4-5(7(8)11)2-3-6(9)10/h2-4H,1H3,(H2,8,11)
InChIKey JLQSXXWTCJPCBC-UHFFFAOYSA-N
SMILES Cn1cc(ccc1=O)C(N)=O
Metabolite of Species Details
Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed
Roles Classification
Biological Role(s): mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing N-methyl-6-pyridone-3-carboxamide (CHEBI:27410) has role metabolite (CHEBI:25212)
N-methyl-6-pyridone-3-carboxamide (CHEBI:27410) has role mouse metabolite (CHEBI:75771)
N-methyl-6-pyridone-3-carboxamide (CHEBI:27410) is a methylpyridines (CHEBI:25340)
N-methyl-6-pyridone-3-carboxamide (CHEBI:27410) is a pyridinecarboxamide (CHEBI:25529)
N-methyl-6-pyridone-3-carboxamide (CHEBI:27410) is a pyridone (CHEBI:38183)
Incoming 1-(methyl-d3)-2-pyridoxone-5-carboxamide (CHEBI:145118) is a N-methyl-6-pyridone-3-carboxamide (CHEBI:27410)
IUPAC Name
1-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide
Synonyms Sources
1-Methyl-5-carboxylamide-2-pyridone KEGG COMPOUND
3-Pyridinecarboxamide, 1,6-dihydro-1-methyl-6-oxo- ChemIDplus
N'-Methyl-2-pyridone-5-carboxamide KEGG COMPOUND
N(1)-methyl-2-pyridone-5-carboxamide HMDB
N-methyl-2-pyridone-5-carboxamide HMDB
Manual Xrefs Databases
C05842 KEGG COMPOUND
HMDB0004193 HMDB
View more database links
Registry Numbers Types Sources
124385 Reaxys Registry Number Reaxys
701-44-0 CAS Registry Number KEGG COMPOUND
701-44-0 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
10694697 PubMed citation Europe PMC
12694300 PubMed citation Europe PMC
13211649 PubMed citation Europe PMC
15663182 PubMed citation Europe PMC
16029944 PubMed citation Europe PMC
17190852 PubMed citation Europe PMC
20073472 PubMed citation Europe PMC
20853461 PubMed citation Europe PMC
Last Modified
27 January 2016