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β-Nicotinamide Mononucleotide

CAS No.
1094-61-7
Chemical Name:
β-Nicotinamide Mononucleotide
Synonyms
NMN;NICOTINAMIDE MONONUCLEOTIDE;NICOTINAMIDE RIBOTIDE;BETA-NICOTINAMIDE MONONUCLEOTIDE;BETA-NMN;β-NMN;B-NICOTINAMIDE MONONUCLEOTIDE;NMN powder;NicotinaMide Ribonucleotide;β-Nicotinamide Mononucleotide(NMN)
CBNumber:
CB6281591
Molecular Formula:
C11H15N2O8P
Molecular Weight:
334.22
MDL Number:
MFCD00038748
MOL File:
1094-61-7.mol
MSDS File:
SDS
Last updated:2024-11-20 15:18:15

β-Nicotinamide Mononucleotide Properties

Melting point 166 °C(dec.)
storage temp. -20°C
solubility DMSO (Slightly, Heated), Methanol (Slightly), Water (Slightly)
form Solid
color White to Yellow
Merck 13,6697
BRN 3570187
Stability Very Hygroscopic
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-/s3
InChIKey DAYLJWODMCOQEW-TURQNECASA-N
SMILES O[C@@H]1[C@@H]([C@@H](COP(O)([O-])=O)O[C@H]1[N+]1=CC=CC(C(=O)N)=C1)O |&1:1,2,3,11,r|
FDA UNII 2KG6QX4W0V

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P305+P351+P338
WGK Germany  3
8-10-21
HS Code  2934999090

β-Nicotinamide Mononucleotide price More Price(66)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich N3501 β-Nicotinamide mononucleotide ≥95% (HPLC) 1094-61-7 25mg $141 2024-03-01 Buy
Sigma-Aldrich N3501 β-Nicotinamide mononucleotide ≥95% (HPLC) 1094-61-7 100mg $423 2024-03-01 Buy
TCI Chemical N1123 β-Nicotinamide Mononucleotide 1094-61-7 50MG $128 2024-03-01 Buy
TCI Chemical N1123 β-Nicotinamide Mononucleotide 1094-61-7 250MG $394 2024-03-01 Buy
TCI Chemical N1123 β-Nicotinamide Mononucleotide 1094-61-7 1G $975 2024-03-01 Buy
Product number Packaging Price Buy
N3501 25mg $141 Buy
N3501 100mg $423 Buy
N1123 50MG $128 Buy
N1123 250MG $394 Buy
N1123 1G $975 Buy

β-Nicotinamide Mononucleotide Chemical Properties,Uses,Production

Description

Nicotinamide mononucleotide (NMN), a product of the NAMPT reaction and a key NAD+ intermediate, ameliorates glucose intolerance by restoring NAD+ levels in HFD-induced T2D mice. NMN also enhances hepatic insulin sensitivity and restores gene expression related to oxidative stress, inflammatory response, and circadian rhythm, partly through SIRT1 activation. NMN is used for studying binding motifs within RNA aptamers and ribozyme activation processes involving β-nicotinamide mononucleotide (β-NMN)-activated RNA fragments.
β-Nicotinamide mononucleotide (β-NMN) is an intermediate in the nicotinamide phosphoribosyltransferase (NAMPT)-catalyzed biosynthesis of nicotinamide adenine dinucleotide (NAD+). NAMPT mediates the condensation of nicotinamide with 5-phosphoribosyl-1-pyrophosphate to produce β-NMN. β-NMN adenyltransferase subsequently converts β-NMN to NAD+.

Chemical Properties

White to Yellowish lyophilized powder

Uses

β-Nicotinamide mononucleotide (NMN) is used to study binding motifs within RNA aptamers and ribozyme activation processes involving β-nicotinamide mononucleotide (β-NMN)-activated RNA fragments. NMN is a nucleotide derived from ribose and nicotinamide. Niacinamide (nicotinamide,) is a derivative of vitamin B3, also known as niacin.) As a biochemical precursor of NAD+, it may be useful in the prevention of pellagra.
β-Nicotinamide mononucleotide is an intermediate in the biosynthesis of nicotinamide adenine dinucleotide (NAD+). Nicotinamide phosphoribosyltransferase (Nampt) catalyzes the condensation of nicotinamide with 5-phosphoribosyl-1-pyrophosphate to generate β-NMN, which is subsequently converted to NAD+ by β-NMN adenyltransferase.At 50-100 μM, β-NMN has been used to enhance NAD biosynthesis and glucose-stimulated insulin secretion in a Nampt+/- mouse model of metabolic disease, demonstrating a role for Nampt in β cell function.Furthermore, at 500 mg/kg/day, it has been shown to ameliorate glucose intolerance in high-fat diet-induced type 2 diabetes mice by restoring NAD+ levels.

Preparation

β-Nicotinamide mononucleotide is a NAD+intermediate. In recent years, the relation of NAD+metabolism and aging-associated disease is attracting attention from various research fields.
Synthesis of β-nicotinamide mononucleotide (NMN)
A solution of NAD (3.5 g, 5.28 mmol) and ZrCl4(6.15 g, 26.4 mmol) in 500 ml water was stirred at 50°C for 30 min. The hydrolysis was monitored by TLC (SiO2EtOH/ 1 M NH4Ac [7 : 3]). The reaction was quenched with 245mL of a 0.5 M solution of Na3PO4. After adjusting to pH 7 with a 2 M solution of HCl, a white precipitate was formed. The suspension was centrifuged 8 min,1,000rpm, the supernatant was collected and the pellet was washed two times with 200 mL water. The combined supernatants wereconcentrated to 1/3 of its volume on a rotary evaporator. The remaining solution was purified with a column filled with Dowex 50WX8 (100-200 mesh, H+-Form, column-material: 2.5 x 30 cm). The column was loaded with 1.5 L5 % HCl and equilibrated with1.5L millipore water until pH 5 was reached. 100 mL of the concentrated solution was loaded on the ion exchange column and eluted with Milliporewater. The first cleavage product eluted was NMN (615 mg, 1.84 mmol,yield:35 %) and yielded a colorless solid after evaporation of the solvent, followed by AMP.
1H NMR (500MHz, D2O)δ: 9.48 (s, 1 H), 9.31 (d,J= 6.2 Hz, 1 H), 9.00 (d,J= 8.2 Hz, 1 H), 8.32 (dd,J= 8.2, 6.2 Hz, 1 H), 6.24 (d,J=5.4 Hz, 1 H), 4.68-4.64 (m, 1 H), 4.58 (t, 1 H), 4.48-4.45 (m, 1 H), 4.36–4.14 (m,J= 12.0, 2 H).
13C NMR (75 MHz, d2o) δ: 165.50, 145.65, 142.15, 139.53, 133.62, 128.19, 99.65, 87.18, 87.06, 77.42, 70.71, 63.89, 63.82.
31P NMR (202 MHz, D2O)δ:-0.03

Definition

ChEBI: β-Nicotinamide Mononucleotide is a condensation product of nicotinamide and ribose 5-phosphate, in which the nitrogen of nicotinamide is linked to the (β) c-l of the ribose. NMN zwitterion is a nicotinamide mononucleotide. It has a role as an Escherichia coli metabolite and a mouse metabolite. It is a conjugate base of a NMN(+). It is a conjugate acid of a NMN(-).

Application

β-Nicotinamide mononucleotide (NMN) is 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. It is used to study binding motifs within RNA aptamers and ribozyme activation processes involving β-nicotinamide mononucleotide (β-NMN)-activated RNA fragments.

benefits

As one of the primary precursors of NAD+ and intermediaries in NAD+ biosynthesis, NMN is as essential as NAD+ in the body’s proper functioning of cells.  NAD helps cells regulate a number of essential functions that help keep your cells running smoothly, including:energy metabolism, DNA repair, gene expression, and cellular stress responses.

General Description

β-Nicotinamide mononucleotide (β-NMN) is an intermediate in the nicotinamide phosphoribosyltransferase (NAMPT)-catalyzed biosynthesis of nicotinamide adenine dinucleotide (NAD+). NAMPT mediates the condensation of nicotinamide with 5-phosphoribosyl-1-pyrophosphate to produce β-NMN. β-NMN adenyltransferase subsequently converts β-NMN to NAD+.

Biochem/physiol Actions

In light of metabolic control mechanisms and many reports on β-Nicotinamide Mononucleotide (β-NMN), β-NMN is likely to be more effective as an NAD+ precursor than Nam. Research has compared the blood total NAD (NAD++NADH) and urinary excretion amounts of NAD+ catabolites in β-NMN- and Nam-administered rats. The concentration of blood total NAD and liver total NAD showed no significant differences among the three groups. However, when examining the kinetics of the urinary excretion, the urinary excretion of the SUM was lower in the β-NMN group than in the Nam group at 3-6 h after the administration. Moreover, the percentage of the urinary SUM was much lower in the β-NMN group than in the Nam group at 3-6 h. This result suggests that β-NMN is retained in the body for longer than Nam is. In addition, this result means that β-NMN has a higher turnover of salvage biosynthesis of NAD+ than Nam does. The resulting phenomenon accelerates the turnover of salvage biosynthesis of NAD+, which activates the SIRT1 reaction because SIRT1 (histone deacetylase) needs NAD+. Deacetylated histone molecules induce DNA silencing, contributing to anti-aging and longevity. When β-NMN is intraperitoneally injected, β-NMN is dephosphorylated in the blood to form Nam riboside (NR), which is then transported into the cells. NR is re-phosphorylated to form β-NMN, which is then synthesized to NAD+ in the nucleus. In contrast to Nam, which is controlled at the Nam→β-NMN reaction, the β-NMN biosynthesis pathway is not regulated[1]. 

Side effects

NMN studies to date suggest mostly beneficial effects with minimal side effects. However, though generally well tolerated, nicotinamide can have ill effects on the kidneys, liver, and beta-cells in the pancreas (which makes insulin) and can lead to gastrointestinal upset and headaches. These effects seem to be dose-dependent, with higher doses causing negative effects and lower doses having more protective effects.

in vitro

β-nicotinamide mononucleotide has several beneficial pharmacological activities. Mostly mediated by its involvement in NAD+ biosynthesis, the pharmacological activities of NMN include its role in cellular biochemical functions, cardioprotection, diabetes, Alzheimer's disease, and complications associated with obesity.The intracellular NAD+ levels are significantly decreased by knockdown or knockout of Nampt (Nampt KD or Nampt KO) or treatment with Nampt inhibitor FK866, whereas NAD+ levels are dramatically increased by supplement of NAD+ precursors NAM or NMN (0.5–1 mM). NAD+ precursor NMN treatment inhibited CD8+ T cells activation and function.

in vivo

β-Nicotinamide mononucleotide (500 mg/kg; i.p.; 3 times per week for 7-10 week) prevents mtDNA damage and Dox-induced cardiac dysfunction.Nampt KO markedly inhibits tumor progression, whereas Nampt metabolite β-Nicotinamide mononucleotide (300 mg/kg body weight; i.p.; once every two days for 2 weeks) significantly promotes tumor growth in C57BL/6 mice (bearing wildtype Hepa1-6 cells). The reduction and increase in NAD+ level of respective Nampt KO and β-Nicotinamide mononucleotide-treated tumors are confirmed.β-nicotinamide mononucleotide ameliorates glucose intolerance by restoring NAD(+) levels in HFD-induced T2D mice. β-nicotinamide mononucleotide also enhances hepatic insulin sensitivity and restores gene expression related to oxidative stress, inflammatory response, and circadian rhythm, partly through SIRT1 activation.

Purification Methods

Purify NMN by passage through a column of Dowex-1 (Clform) and washing with H2O until no absorbance is observed at 260 nm. The tubes containing NMN are pooled, adjusted to pH 5.5-6 and evaporated in vacuo to a small volume. This is adjusted to pH 3 with dilute HNO3 in an ice-bath and treated with 20volumes of Me2CO at 0-5o. The heavy white precipitate is collected by centrifugation at 0o. It is best stored wet and frozen or it can be dried to give a gummy residue. It has max 266nm ( 4,600) and min 249nm ( 3600) at pH 7.0 (i.e. no absorption at 340nm). It can be estimated by reaction with CNor hydrosulfite which form the 4-adducts (equivalent to NADH) which have UV max 340nm ( 6,200). Thus after reaction, an OD340 of one is obtained from a 0.1612mM solution in a 1cm path cuvette. [Plaut & Plaut Biochemical Preparations 5 56 1957, Maplan & Stolzenbach Methods Enzymol 3 899 1957, Kaplan et al. J Am Chem Soc 77 815 1955, Beilstein 22/2 V 168.]

References

[1] Kawamura T., et al. "β-Nicotinamide Mononucleotide, an Anti-Aging Candidate Compound, Is Retained in the Body for Longer than Nicotinamide in Rats." Journal of nutritional science and vitaminology 62(2016): 272-276.

23111-00-4
1094-61-7
Synthesis of β-Nicotinamide Mononucleotide from Nicotinamide riboside chloride

β-Nicotinamide Mononucleotide Preparation Products And Raw materials

Raw materials

Preparation Products

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β-Nicotinamide Mononucleotide Spectrum

3-(aminocarbonyl)-1-(5-O-phosphonato-beta-D-ribofuranosyl)pyridinium NICOTINAMIDE-1-IUM-1-BETA-D-RIBOFURANOSIDE 5'-PHOSPHATE 1-[3,4-dihydroxy-5-[(hydroxy-oxido-phosphoryl)oxymethyl]oxolan-2-yl]pyridine-5-carboxamide β-Nicotinamide ribose monophosphate, β-NMN, Nicotinamide ribotide, NMN, Nicotinamide-1-ium-1-β-D-ribofuranoside 5μ-phosphate 1-Deoxy-1-(3-carbamoylpyridinio)-5-O-oxylatophosphonyl-β-D-ribofuranose Nicotinamide ribonucleoside 5'-phosphate β-D-NMN 3-(AMinocarbonyl)-1-(5-O-phosphono-β-D-ribofuranosyl)pyridiniuM Inner Salt 3-CarbaMoyl-1-β-D-ribofuranosylpyridiniuM Hydroxide, 5'-Phosphate Inner Salt NMN zwitterion ((2R,3S,4R,5R)-5-(3-Carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl hydrogen phosphate Nicotinamide-1-ium-1-β-D-ribofuranoside 5′-phosphate Beta-Nicotinamide mononucleotide (NMN) beta-D-NMN NicotinaMide ribonucleotide SynonyMs NicotinaMide Mononucleotide NMN(β-Nicotinamide mononucleotide) BETA-NMN , Beta-Nicotinamide Mononucleotide β-nicotinamide D-ribonucleotide Nicotinamide Mononucleotide(NMN) β-NMN,BETA-Nicotinamide Mononucleotide 3-(Aminocarbonyl)-1-(5-O-phosphonato-β-D-ribofuranosyl)pyridinium Beta-nicotinamide single nucleotide Nicotinamide ribonucleotide (NMN) β-Nicotinamidse Mononucleotide Nicotimide mononucleotide BETA-NICOTINAMIDE MONONUCLEOTIDE1094-61-7 3-(Aminocarbonyl)-1-(5-O-phosphono-beta-D-ribofuranosyl)pyridinium Inner Salt BETA-NICOTINAMIDE MONONUCLEOTIDE 99 Nicotinamide ribonucleotide/NMN Quality Gurantee fast-shipping Nicotinamide ribonucleotide/NMN β-Nicotinamide Mononucleotide,95% C:C&B65 Nicotinamide Mononucleotide NMN powder β-Nicotinamide ononucleotide BEITA-Nicotinamide mononucleotide β-Nicotinamide Mononucleotide Pyridinium,3-(aminocarbonyl)-1-(5-O-phosphono-b-D-ribofuranosyl)-, inner salt β-Nicotinamide Moonucleotide NMN/β-Nicotinamide Mononucleotide NMN/ Nicotinamide Mononucleotide /β-Nicotinamide Mononucleotide beta-Nicotinamide Moonucleotide (NMN Beta-Nicotinamide mononucle (2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl hydrogen phosphate β-Nicotinamide Mononucleotide Basic information β-Nicotinamide Mononucleotide USP/EP/BP nicotinamide mononucleotide 99% NMN API β-Nicotinamide Mononucleotide 99% NMN CAS 1094 61 7 β-Nicotinamide Mononucleotide,0.95 BETA-NMN POWDER NMN / β-D-NMN / BETA-NMN / Nicotinamide nucleotide / Nicotinamide mononuclotide β-Nicotinamide Mononucleotid β-NMN, Beta-Nicotinamide Mononucleotide Nmn CAS No.?1094-61-7?Beta-Nicotinamide Mononucleotide NMN Synonyms:Beta-Nicotinamide Mononucleotide β-Nicotinamide Mononucleotide (β-NMN) extrapure, 95% β-Nicotinamide Mononucleotide (β-NMN) for cell culture, 99% BETA-NMN