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nicotinamide ribotide

Structure via PubChem · Public domain (PubChem)

EntityQ21547155· pop 15· linked from 23 articles

nicotinamide ribotide

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Also known as 3-(aminocarbonyl)-1-(5-O-phosphono-beta-D-ribofuranosyl)pyridinium, inner salt, 3-(aminocarbonyl)-1-(5-O-phosphonato-beta-D-ribofuranosyl)pyridinium, 1-[(2R,3R,4S,5S)-3,4-dihydroxy-5-[(hydroxy-oxido-phosphoryl)oxymethyl]tetrahydrofuran-2-yl]pyridine-5-carboxamide, 1-[(2R,3R,4S,5S)-3,4-dihydroxy-5-[(hydroxy-oxido-phosphoryl)oxymethyl]oxolan-2-yl]pyridine-5-carboxamide, 3-(Aminocarbonyl)-1-(5-O-phosphono-beta-delta-ribofuranosyl)-Pyridinium hydroxide inner salt, 3-carbamoyl-1-[(2R,3R,4S,5R)-5-[(hydrogen phosphonatooxy)methyl]-3,4-dihydroxyoxolan-2-yl]-1$l^{5}-pyridin-1-ylium, 3-(Aminocarbonyl)-1-(5-O-phosphono-b-D-ribofuranosyl)-Pyridinium hydroxide inner salt, 3-Carbamoyl-1-b-D-ribofuranosylpyridinium hydroxide 5'-phosphate inner salt

chemical compound

In the Vinony graph

Within Vinony's link graph, nicotinamide ribotide is referenced by 23 other articles, and connects out to mitochondrion, Cucumis sativus and Aguacate.

It is catalogued under topics including Anti-aging substances, Chembox image size set and ECHA InfoCard ID from Wikidata.

Its subject is documented across 14 Wikipedia language editions.

Chemical data

Formula
C11H15N2O8P
Molecular weight
334.22 g/mol
IUPAC name
[(2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl hydrogen phosphate
SMILES
C1=CC(=C[N+](=C1)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)(O)[O-])O)O)C(=O)N
InChIKey
DAYLJWODMCOQEW-TURQNECASA-N
XLogP
-3.5
Polar surface area
166 Ų
H-bond donors
4
H-bond acceptors
8
Formal charge
0

via PubChem

Drug data · ChEMBL

Molecule type
Small molecule

via ChEMBL · EBI

Wikidata facts

Has part
phosphorus
Mass
334.056602
Show 5 more facts
isomeric SMILES
C1=CC(=C[N+](=C1)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)(O)[O-])O)O)C(=O)N
chemical formula
C₁₁H₁₅N₂O₈P
canonical SMILES
C1=CC(=C[N+](=C1)C2C(C(C(O2)COP(=O)(O)[O-])O)O)C(=O)N
Commons category
Nicotinamide mononucleotide
Sources (4)

via Wikidata · CC0

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