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NICOTINIC ACID MONONUCLEOTIDE

Product Name
NICOTINIC ACID MONONUCLEOTIDE
CAS No.
321-02-8
Chemical Name
NICOTINIC ACID MONONUCLEOTIDE
Synonyms
β-NaMN;β-Nicotinic Acid Mon;Nicotinic Acid Ribotide;Nicotinic Mononucleotide;nicotinatemononucleotide;Nicotinate Ribonucleotide;Nicotinic Acid Ribonucleotide;NICOTINIC ACID MONONUCLEOTIDE;β-NicotinicAcidMononucleotide;b-Nicotinic Acid Mononucleotide
CBNumber
CB9670381
Molecular Formula
C11H14NO9P
Formula Weight
335.2
MOL File
321-02-8.mol
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NICOTINIC ACID MONONUCLEOTIDE Property

Melting point:
>115°C (dec.)
storage temp. 
−20°C
solubility 
Methanol (Slightly, Heated), Water(Slightly)
form 
Solid
pka
1.856±0.10(predicted)
color 
White to Off-White
biological source
animal
Stability:
Hygroscopic
InChI
InChI=1/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-/s3
InChIKey
JOUIQRNQJGXQDC-NLNRFTKUNA-N
SMILES
[C@@H]1([C@H](O)[C@H](O)[C@@H](COP([O-])(=O)O)O1)[N+]1C=CC=C(C(=O)O)C=1 |&1:0,1,3,5,r|
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Safety

WGK Germany 
3
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
N7764
Product name
Nicotinic acid mononucleotide
Packaging
5mg
Price
$226
Updated
2025/07/31
Sigma-Aldrich
Product number
N7764
Product name
Nicotinic acid mononucleotide
Packaging
10mg
Price
$430
Updated
2025/07/31
Sigma-Aldrich
Product number
N7764
Product name
Nicotinic acid mononucleotide
Packaging
25mg
Price
$774.25
Updated
2025/07/31
Sigma-Aldrich
Product number
N7764
Product name
Nicotinic acid mononucleotide
Packaging
100mg
Price
$2420
Updated
2025/07/31
TRC
Product number
N429390
Product name
β-NicotinicAcidMononucleotide
Packaging
10mg
Price
$1455
Updated
2021/12/16
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NICOTINIC ACID MONONUCLEOTIDE Chemical Properties,Usage,Production

Uses

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.

Biological Activity

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.

Synthesis

Nicotinic acid mononucleotide is prepared by the reaction of 2,3-dicarboxypyridine and 5-phosphoribosyl-1-pyrophosphate. The steps are as follows:
With phosphoribosyl pyrophosphate-quinolinate phosphoribosyltransferase; magnesium chloride In aq. phosphate buffer at 37℃; for 6h; pH=7.0; Enzymatic reaction.

NICOTINIC ACID MONONUCLEOTIDE Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from NICOTINIC ACID MONONUCLEOTIDE manufacturers

Career Henan Chemical Co
Product
NICOTINIC ACID MONONUCLEOTIDE 321-02-8
Price
US $3.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
1000kg
Release date
2019-08-01

321-02-8, NICOTINIC ACID MONONUCLEOTIDERelated Search:


  • nicotinatemononucleotide
  • NICOTINIC ACID MONONUCLEOTIDE
  • 1-[3,4-dihydroxy-5-(phosphonooxymethyl)oxolan-2-yl]pyridine-5-carboxylate
  • 3-Carboxylato-1-(5-O-phosphono-β-D-ribofuranosyl)pyridinium
  • 3-Carboxy-1-(5-O-phosphono-β-D-ribofuranosyl)pyridiniuM Inner Salt
  • 3-Carboxy-1-β-D-ribofuranosylpyridiniuM Hydroxide 5'-Phosphate Inner Salt
  • Nicotinate Ribonucleotide
  • Nicotinic Acid Ribonucleotide
  • Nicotinic Acid Ribotide
  • Nicotinic Mononucleotide
  • β-NaMN
  • β-NicotinicAcidMononucleotide
  • 3-Carboxy-1-(5-O-phosphono-β-D-ribofuranosyl)pyridinium
  • 3-Carboxy-1-methylpyridiniumiodid
  • β-Nicotinic Acid Mon
  • b-Nicotinic Acid Mononucleotide
  • Pyridinium, 3-carboxy-1-(5-O-phosphono-β-D-ribofuranosyl)-, inner salt
  • 1-((2R,3R,4S,5R)-3,4-Dihydroxy-5-((phosphonooxy)methyl)tetrahydrofuran-2-yl)pyridin-1-ium-3-carboxylate
  • 321-02-8
  • C11H15NO9P
  • C11H14NO9P
  • Cofactors
  • Enzymes, Inhibitors, and Substrates
  • Oxidation-Reduction
  • Biochemicals and Reagents
  • BioChemical
  • Cofactors
  • Enzymes, Inhibitors, and Substrates
  • Oxidation-Reduction
  • Amines
  • Aromatics
  • Bases & Related Reagents
  • Intermediates & Fine Chemicals
  • Nicotine Derivatives
  • Nucleotides
  • Pharmaceuticals