Nicotinic acid mononucleotide

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Company Name: Maintain Biotech Co., Ltd.  Gold
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Nicotinic acid mononucleotide manufacturers

Nicotinic acid mononucleotide Basic information
Product Name:Nicotinic acid mononucleotide
Synonyms:nicotinatemononucleotide;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
CAS:321-02-8
MF:C11H14NO9P
MW:335.2
EINECS:
Product Categories:Cofactors;Enzymes, Inhibitors, and Substrates;Oxidation-Reduction;Amines;Aromatics;Bases & Related Reagents;Intermediates & Fine Chemicals;Nicotine Derivatives;Nucleotides;Pharmaceuticals
Mol File:321-02-8.mol
Nicotinic acid mononucleotide Structure
Nicotinic acid mononucleotide Chemical Properties
Melting point >115°C (dec.)
storage temp. −20°C
solubility Methanol (Slightly, Heated), Water(Slightly)
form Solid
pka1.856±0.10(predicted)
color White to Off-White
biological sourceanimal
Stability:Hygroscopic
InChIInChI=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
InChIKeyJOUIQRNQJGXQDC-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|
Safety Information
WGK Germany 3
Storage Class11 - Combustible Solids
MSDS Information
ProviderLanguage
SigmaAldrich English
Nicotinic acid mononucleotide Usage And Synthesis
UsesA 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 ActivityNicotinic 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.
SynthesisNicotinic 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 synthesis
Nicotinic acid mononucleotide Preparation Products And Raw materials
Tag:Nicotinic acid mononucleotide(321-02-8) Related Product Information
Nicotinic-d4 acid Nicotinic acid hydrazide Methylenediphosphonic acid Cyanuric acid β-Nicotinamide Adenine Dinucleotide Sodium Salt Hydrate β-Nicotinamide Mononucleotide Nicotinic Acid Riboside SODIUM NICOTINATE Ethyl nicotinate Nicotinic acid Methyl nicotinate DIAMOND Nicotinic acid mononucleotide nicotinic acid mononucleotide adenylyltransferase DEAMIDO NAD SODIUM SALT