CHEBI:14649 - NMN

ChEBI IDCHEBI:14649
ChEBI NameNMN
Stars
ASCII NameNMN(-)
Last Modified21 January 2016
DownloadsMolfile
FormulaC11H14N2O8P
Net Charge-1
Average Mass333.213
Monoisotopic Mass333.04933
SMILESNC(=O)c1ccc[n+]([C@@H]2O[C@H](COP(=O)([O-])[O-])[C@@H](O)[C@H]2O)c1
InChIInChI=1S/C11H15N2O8P/c12-10(16)6-2-1-3-13(4-6)11-9(15)8(14)7(21-11)5-20-22(17,18)19/h1-4,7-9,11,14-15H,5H2,(H3-,12,16,17,18,19)/p-1/t7-,8-,9-,11-/m1/s1
InChIKeyDAYLJWODMCOQEW-TURQNECASA-M
Species of MetaboliteComponentSourceComments
Homo sapiens (ncbitaxon:9606) - DOI (10.1038/nbt.2488)
Saccharomyces cerevisiae (ncbitaxon:4932) - PubMed (24678285) Source: yeast.sf.net
Roles Classification
Biological Roles:
human metabolite  Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
Saccharomyces cerevisiae metabolite  Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
ChEBI Ontology
Outgoing Relation(s)
NMN (CHEBI:14649) has role Saccharomyces cerevisiae metabolite (CHEBI:75772)
NMN (CHEBI:14649) has role human metabolite (CHEBI:77746)
NMN (CHEBI:14649) is a nicotinamide mononucleotide (CHEBI:50383)
NMN (CHEBI:14649) is conjugate base of NMN zwitterion (CHEBI:16171)
Incoming Relation(s)
NMN zwitterion (CHEBI:16171) is conjugate acid of NMN (CHEBI:14649)
IUPAC Name 
3-carbamoyl-1-(5-O-phosphonato-β-D-ribofuranosyl)pyridinium
UniProt Name  Source
β-nicotinamide D-ribonucleotideUniProt
Registry NumbersSources
Beilstein:5153835Beilstein