NICOTINIC ACID MONONUCLEOTIDE
NICOTINIC ACID MONONUCLEOTIDE Basic information
- Product Name:
- NICOTINIC ACID MONONUCLEOTIDE
- Synonyms:
-
- 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
- CAS:
- 321-02-8
- MF:
- C11H14NO9P
- MW:
- 335.2
- 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 Chemical Properties
- Melting point:
- >115°C (dec.)
- storage temp.
- −20°C
- solubility
- Methanol (Slightly, Heated), Water(Slightly)
- form
- Solid
- 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|
MSDS
- Language:English Provider:SigmaAldrich
NICOTINIC ACID MONONUCLEOTIDE Usage And Synthesis
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.
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NICOTINIC ACID MONONUCLEOTIDE(321-02-8)Related Product Information
- β-Nicotinamide Adenine Dinucleotide Sodium Salt Hydrate
- β-Nicotinamide Mononucleotide
- Nicotinic Acid Riboside
- SODIUM NICOTINATE
- NICOTINIC ACID HYDRAZIDE
- NICOTINIC-D4 ACID
- Ethyl nicotinate
- Nicotinic acid
- METHYLENEDIPHOSPHONIC ACID
- Methyl nicotinate
- DIAMOND
- Cyanuric acid
- nicotinic acid mononucleotide adenylyltransferase
- DEAMIDO NAD SODIUM SALT
- NICOTINIC ACID MONONUCLEOTIDE