β-Nicotinic Acid Mononucleotide

CAS : 321-02-8

Ref. TR-N429390

Informations sur le produit

• Nom: β-Nicotinic Acid Mononucleotide
• Synonymes: 3-Carboxy-1-(5-O-phosphono-beta-D-ribofuranosyl)pyridinium Inner Salt, 3-Carboxy-1-beta-D-ribofuranosylpyridinium Hydroxide 5'-Phosphate Inner Salt, Nicotinate Mononucleotide, Nicotinate Ribonucleotide, Nicotinic Acid Ribonucleotide, Nicotinic Acid Ribotide, Nicotinic Mononucleotide, beta-NaMN, 1-(5-O-phosphono-beta-D-ribofuranosyl)pyridinium-3-carboxylate, 3-Carboxy-1-β-<span class="text-smallcaps">D</span>-ribofuranosylpyridinium hydroxide, 5′-phosphate, inner salt, 3-Pyridinecarboxylic acid, mononucleotide, 3-carboxy-1-(5-O-phosphono-beta-D-ribofuranosyl)pyridinium, 3-carboxy-1-(5-O-phosphonopentofuranosyl)pyridinium, Deamido nicotinamide ribonucleotide, Deamido-NMN, Nicotinate mononucleotide, Nicotinate ribonucleotide, Nicotinic acid ribonucleotide, Nicotinic acid ribotide, Nicotinic mononucleotide, Pyridinium, 3-carboxy-1-(5-O-phosphono-beta-D-ribofuranosyl)-, inner salt, Pyridinium, 3-carboxy-1-(5-O-phosphono-β-<span class="text-smallcaps">D</span>-ribofuranosyl)-, inner salt, Pyridinium, 3-carboxy-1-β-<span class="text-smallcaps">D</span>-ribofuranosyl-, hydroxide, 5′-(dihydrogen phosphate), inner salt, cyclohexane-1,4-diylbis[N-(2-chlorobenzyl)methanamine] dihydrochloride, β-Nicotinic acid mononucleotide

Description

Stability Hygroscopic
Applications A nucleotide of nicotinic acid which is produced from quinolinic acid by quinolinate phosphoribosyltransferase via transfer of a phosphoribose group. It is an intermediate of nicotinic acid adenine dinucleotide (NaAD) which is then converted to NAD via amidation and in turn converted to NADPH.
References Petrelli, R. et al.: Curr. Med. Chem., 18, 1973 (2011); Shibata, K. et al.: J. Chrom. B Biomed. Sci. Appl., 749, 281 (2000); Evans, C. et al.: BMC Chem. Biol., 10, 2 (2010);

• Marque: TRC

Propriétés chimiques

• Masse moléculaire: 335.2
• Formule: C₁₁H₁₄NO₉P
• Couleur/Forme: Neat
• SMILES: O=C(O)c1ccc[n+]([C@@H]2O[C@H](COP(=O)([O-])O)[C@@H](O)[C@H]2O)c1