N7764

Nicotinic acid mononucleotide

• Synonyme(s) : Nicotinate mononucleotide
• Formule empirique (notation de Hill) : C₁₁H₁₄NO₉P
• Numéro CAS: 321-02-8
• Poids moléculaire : 335.20
• NACRES: NA.79
• PubChem Substance ID: 24897839
• UNSPSC Code: 12352106
• MDL number: MFCD00070358
• Assay: ≥98.0% (HPLC)
• Biological source: animal
• Form: powder
• Storage temp.: −20°C

Propriétés

• biological source: animal
• Quality Segment: 200
• assay: ≥98.0% (HPLC)
• form: powder
• technique(s): HPLC: suitable
• color: white
• storage temp.: −20°C
• SMILES string: OC1C(O)C(OC1COP(O)(O)=O)[N]2=CC(=CC=C2)C(O)=O
• InChI: 1S/C11H15NO9P/c13-8-7(5-20-22(17,18)19)21-10(9(8)14)12-3-1-2-6(4-12)11(15)16/h1-4,7-10,13-14H,5H2,(H,15,16)(H2,17,18,19)
• InChI key: IUJWGLOJJKFASX-UHFFFAOYSA-N

Description

General description

Nicotinic acid mononucleotide (NaMN) is formed from nicotinic acid 5-phosphoribosyl-1-pyrophosphate (PRPP) in the Preiss-Handler pathway in the presence of enzyme phosphoribosyltransferase (NaPRT).

Application

Nicotinic acid mononucleotide has been used as a substrate for NMN/NaMN adenylyltransferase (NMNAT) during nicotinamide adenine dinucleotide (NAD) biosynthesis.

Biochem/physiol Actions

Nicotinic acid mononucleotide (NaMN) may be used to study the relationship between the phosphate-responsive signaling (PHO) pathway and nicotine adenine dinucleotide (NAD(+)) metabolism in yeast. Nicotinate mononucleotide is a substrate for NMN/NaMN adenylyltransferase (NMNAT) and nicotinate mononucleotide adenylyltransferase. NaMN amidation results in the synthesis of nicotinamide mononucleotide(NMN), which is further converted to NAD cofactor.

Informations sur la sécurité

• Classe de stockage: 11 - Combustible Solids
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)