CAS 1094-61-7
:beta-nicotinamide mononucleotide
Description:
Beta-nicotinamide mononucleotide (NMN) is a nucleotide derived from ribose, nicotinamide, and phosphate. It plays a crucial role in cellular metabolism as a precursor to nicotinamide adenine dinucleotide (NAD+), a vital coenzyme involved in redox reactions and energy production within cells. NMN is recognized for its potential health benefits, particularly in aging research, as it may help enhance NAD+ levels, which tend to decline with age. This compound is typically found in small amounts in various foods, including vegetables and fruits. NMN is water-soluble, allowing for easy absorption in biological systems. Its stability can be influenced by factors such as pH and temperature, which are important considerations in storage and formulation. Research into NMN has expanded, focusing on its implications for metabolic health, neuroprotection, and overall longevity. However, while promising, further studies are necessary to fully understand its mechanisms and therapeutic potential.
Formula:C11H15N2O8P
InChI:InChI=1/C11H15N2O8P/c12-10(16)6-2-1-3-13(4-6)11-9(15)8(14)7(21-11)5-20-22(17,18)19/h1-4,7-9,11,14-15H,5H2,(H3-,12,16,17,18,19)/t7-,8-,9-,11-/m1/s1
InChI key:InChIKey=DAYLJWODMCOQEW-TURQNECASA-N
SMILES:O[C@H]1[C@@H](O[C@H](COP(=O)([O-])O)[C@H]1O)[N+]=2C=C(C(N)=O)C=CC2
Synonyms:- 3-(Aminocarbonyl)-1-(5-O-phosphonato-beta-D-ribofuranosyl)pyridinium
- 3-Carbamoyl-1-β-<span class="text-smallcaps">D</span>-ribofuranosylpyridinium hydroxide, 5′-phosphate, inner salt
- 3-carbamoyl-1-(5-O-phosphonopentofuranosyl)pyridinium
- 3-carbamoyl-1-[5-O-(hydroxyphosphinato)-beta-D-ribofuranosyl]pyridinium
- NMN
- NMN (mononucleotide)
- Nicotinamide mononucleotide
- Nicotinamide ribonucleoside 5′-phosphate
- Nicotinamide ribonucleotide
- Nicotinamide ribotide
- Pyridinium, 3-(aminocarbonyl)-1-(5-O-phosphono-beta-D-ribofuranosyl)-, inner salt
- Pyridinium, 3-(aminocarbonyl)-1-(5-O-phosphono-β-<span class="text-smallcaps">D</span>-ribofuranosyl)-, hydroxide, inner salt
- Pyridinium, 3-(aminocarbonyl)-1-(5-O-phosphono-β-<span class="text-smallcaps">D</span>-ribofuranosyl)-, inner salt
- Pyridinium, 3-carbamoyl-1-β-<span class="text-smallcaps">D</span>-ribofuranosyl-, hydroxide, 5′-(dihydrogen phosphate), inner salt
- coenzyme NMN
- β-<span class="text-smallcaps">D</span>-NMN
- β-NMN
- β-Nicotinamide mononucleotide
- Pyridinium, 3-(aminocarbonyl)-1-(5-O-phosphono-β-D-ribofuranosyl)-, inner salt
- Pyridinium, 3-(aminocarbonyl)-1-(5-O-phosphono-β-D-ribofuranosyl)-, hydroxide, inner salt
- 3-Carbamoyl-1-β-D-ribofuranosylpyridinium hydroxide, 5′-phosphate, inner salt
- Pyridinium, 3-carbamoyl-1-β-D-ribofuranosyl-, hydroxide, 5′-(dihydrogen phosphate), inner salt
- β-Nicotinamide ononucleotide
- beta-D-NMN
- Nicotinamide nucleotide
- β-nicotinamide D-ribonucleotide
- NMN zwitterion
- β-Nicotinamide Moonucleotide
- Nicotimide mononucleotide
- 99% NMN CAS 1094 61 7
- β-Nicotinamide Mononucleotid
- Nicotinamide mononuclotide
- β-Nicotinamidse Mononucleotide
- β-D-NMN
- beta-Nicotinamide Moonucleotide
- NMN powder
- BETA-NMN POWDER
- See more synonyms
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β-Nicotinamide mononucleotide
CAS:((2R,3S,4R,5R)-5-(3-Carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl hydrogen phosphateFormula:C11H15N2O8PPurity:97%Molecular weight:334.22ß-Nicotinamide Mononucleotide (ß-NMN) for cell culture, 99%, Endotoxin (BET) 0.05EU/mg
CAS:Formula:C11H15N2O8PPurity:min. 99.0%Color and Shape:White, Crystalline powder.Molecular weight:334.22ß-Nicotinamide Mononucleotide (ß-NMN) extrapure, 98%
CAS:Formula:C11H15N2O8PPurity:min. 98.0%Color and Shape:White, Crystalline powderMolecular weight:334.22β-Nicotinamide Mononucleotide-13C5
CAS:Controlled ProductApplications The labelled analogue of a product of the extracellular Nicotinamide phosphoribosyltransferase (eNAMPT) reaction and a key NAD+ intermediate. It ameliorates glucose intolerance by restoring NAD+ levels in HFD-induced T2D mice. It also enhances hepatic insulin sensitivity and restores gene expression related to oxidative stress, inflammatory response, and circadian rhythm, partly through SIRT1 activation.
References Yoshino, J. et al.: Cell Metab., 14, 528 (2011); Caton, P.W. et al.: Diabetologia, 54, 3083 (2011); Formentini, L. et al.: BIochem. Pharmacol., 77, 1612 (2009);Formula:C5C6H15N2O8PColor and Shape:NeatMolecular weight:339.182



