CAS 321-02-8: Nicotinic acid mononucleotide

Description: Nicotinic acid mononucleotide (NAMN), with the CAS number 321-02-8, is a nucleotide that plays a crucial role in cellular metabolism and is a precursor to nicotinamide adenine dinucleotide (NAD+), an essential coenzyme in redox reactions. It consists of a nicotinic acid moiety linked to a ribose sugar and a phosphate group. NAMN is typically found in biological systems and is involved in various biochemical pathways, including those related to energy production and DNA repair. The substance is soluble in water, which facilitates its biological functions. Its structure allows it to participate in phosphorylation reactions, contributing to the synthesis of NAD+ and influencing cellular processes such as energy metabolism, signaling, and stress responses. Additionally, nicotinic acid mononucleotide has garnered interest in research related to aging and metabolic disorders, as NAD+ levels are known to decline with age, impacting cellular health and function. Overall, NAMN is a vital compound in biochemistry, linking vitamin B3 metabolism to essential cellular functions.

Formula: C₁₁H₁₄NO₉P

InChI: InChI=1S/C11H14NO9P/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,(H2-,15,16,17,18,19)/t7-,8-,9-,10-/m1/s1

InChI key: InChIKey=JOUIQRNQJGXQDC-ZYUZMQFOSA-N

SMILES: O=C([O-])C1=CC=C[N+](=C1)C2OC(COP(=O)(O)O)C(O)C2O

Synonyms:

• 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
• Pyridinium, 3-carboxy-1-(5-O-phosphono-β-D-ribofuranosyl)-, inner salt
• Nicotinic acid mononucleotide
• Pyridinium, 3-carboxy-1-β-D-ribofuranosyl-, hydroxide, 5′-(dihydrogen phosphate), inner salt
• 3-Carboxy-1-β-D-ribofuranosylpyridinium hydroxide, 5′-phosphate, inner salt
• Nicotinic acid mononucleotide

NICOTINIC ACID MONONUCLEOTIDE

CAS: 321-02-8

• Formula: C₁₁H₁₄NO₉P
• Purity: 98%
• Color and Shape: Solid
• Molecular weight: 335.2039

Nicotinic acid mononucleotide

CAS: 321-02-8

• Molecular weight: 335.20

Nicotinic acid mononucleotide

CAS: 321-02-8

Nicotinic acid mononucleotide is formed from nicotinic acid (NA) via the nicotinic acid phosphoribosyltransferase in …

• Formula: C₁₁H₁₄NO₉P
• Purity: 98%
• Color and Shape: Solid
• Molecular weight: 335.2

β-Nicotinic Acid Mononucleotide

CAS: 321-02-8

Stability Hygroscopic Applications A nucleotide of nicotinic acid which is produced from quinolinic acid by …

• Formula: C₁₁H₁₄NO₉P
• Color and Shape: Neat
• Molecular weight: 335.2

β-Nicotinic Acid Mononucleotide-d4

CAS: 321-02-8

Stability Hygroscopic Applications β-Nicotinic Acid Mononucleotide-d4 is the isotope labelled analog of β-Nicotinic Acid Mononucleotide …

• Formula: C₁₁H₁₀D₄NO₉P
• Purity: >90%
• Color and Shape: Neat
• Molecular weight: 339.23

²-Nicotinic Acid Mononucleotide-d4

CAS: 321-02-8

²-Nicotinic Acid Mononucleotide-d4 (NAMN) is a nicotinamide riboside analog that has been shown to inhibit …

• Formula: C₁₁H₁₀D₄NO₉P
• Purity: Min. 95%
• Molecular weight: 339.23 g/mol