CHEBI:15927 - N-ribosylnicotinamide

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ChEBI Name N-ribosylnicotinamide
ChEBI ASCII Name N-ribosylnicotinamide
Definition A pyridine nucleoside consisting of nicotinamide with a β-D-ribofuranosyl moiety at the 1-position.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:7337, CHEBI:47589, CHEBI:12527, CHEBI:21786
Supplier Information
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Formula C11H15N2O5
Net Charge +1
Average Mass 255.24728
Monoisotopic Mass 255.09755
InChI InChI=1S/C11H14N2O5/c12-10(17)6-2-1-3-13(4-6)11-9(16)8(15)7(5-14)18-11/h1-4,7-9,11,14-16H,5H2,(H-,12,17)/p+1/t7-,8-,9-,11-/m1/s1
SMILES NC(=O)c1ccc[n+](c1)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Metabolite of Species Details
Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed
Saccharomyces cerevisiae (NCBI:txid4932) Source: See: PubMed
Homo sapiens (NCBI:txid9606) See: DOI
Roles Classification
Biological Role(s): Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
Application(s): geroprotector
Any compound that supports healthy aging, slows the biological aging process, or extends lifespan.
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ChEBI Ontology
Outgoing N-ribosylnicotinamide (CHEBI:15927) has role Saccharomyces cerevisiae metabolite (CHEBI:75772)
N-ribosylnicotinamide (CHEBI:15927) has role geroprotector (CHEBI:176497)
N-ribosylnicotinamide (CHEBI:15927) has role human metabolite (CHEBI:77746)
N-ribosylnicotinamide (CHEBI:15927) has role mouse metabolite (CHEBI:75771)
N-ribosylnicotinamide (CHEBI:15927) is a N-glycosylnicotinamide (CHEBI:25526)
N-ribosylnicotinamide (CHEBI:15927) is a pyridine nucleoside (CHEBI:47896)
Synonyms Sources
1-(beta-D-Ribofuranosyl)nicotinamide KEGG COMPOUND
β-nicotinamide D-riboside UniProt
N-Ribosylnicotinamide KEGG COMPOUND
nicotinamide ribonucleoside ChemIDplus
nicotinamide ribose ChemIDplus
Nicotinamide riboside PDBeChem
nicotinamide-β-riboside ChemIDplus
Manual Xrefs Databases
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Registry Numbers Types Sources
1341-23-7 CAS Registry Number ChemIDplus
3912857 Beilstein Registry Number Beilstein
Citations Waiting for Citations Types Sources
15137942 PubMed citation Europe PMC
17482543 PubMed citation Europe PMC
18429699 PubMed citation Europe PMC
22682224 PubMed citation Europe PMC
Last Modified
26 October 2021