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About This Item
Empirical Formula (Hill Notation):
C11H15N2O8P
CAS Number:
Molecular Weight:
334.22
UNSPSC Code:
41106305
NACRES:
NA.51
PubChem Substance ID:
EC Number:
214-136-5
Beilstein/REAXYS Number:
3570187
MDL number:
Form:
powder
Assay:
≥95% (HPLC), ≥95% (spectrophotometric assay)
Solubility:
H2O: soluble-50 mg/mL to clear, colorless to faintly yellow
Quality Level
assay
≥95% (HPLC), ≥95% (spectrophotometric assay)
form
powder
solubility
H2O: soluble-50 mg/mL to clear, colorless to faintly yellow
storage temp.
−20°C
SMILES string
C[C@H]1[C@@H](C)[C@@H](O[C@@H]1COP(O)([O-])=O)[n+]2cccc(c2)C(N)=O
InChI
1S/C13H19N2O6P/c1-8-9(2)13(21-11(8)7-20-22(17,18)19)15-5-3-4-10(6-15)12(14)16/h3-6,8-9,11,13H,7H2,1-2H3,(H3-,14,16,17,18,19)/t8-,9+,11+,13+/m0/s1
InChI key
YYNOOWWEYJELSF-SEMCEJNYSA-N
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+.
Application
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.
Other Notes
Note: This is the common form of NMN. Do not confuse it with α-NMN.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Zheng-Hu Shi et al.
Scientific reports, 7(1), 8041-8041 (2017-08-16)
Metanephrines (MNs) were suggested as a potential first-line biochemical index for the diagnosis of phaeochromocytomas (PHEO). In this study, we developed a simple electrochemical method for the quantitative measurement of MNs in spot urine samples. As MNs contain a hydroxyphenyl
Jun Yoshino et al.
Cell metabolism, 14(4), 528-536 (2011-10-11)
Type 2 diabetes (T2D) has become epidemic in our modern lifestyle, likely due to calorie-rich diets overwhelming our adaptive metabolic pathways. One such pathway is mediated by nicotinamide phosphoribosyltransferase (NAMPT), the rate-limiting enzyme in mammalian NAD(+) biosynthesis, and the NAD(+)-dependent
Zhe Wei et al.
Nature communications, 11(1), 3393-3393 (2020-07-09)
Meiotic divisions in oocytes are extremely asymmetric and require pre- and post-anaphase-onset phases of spindle migration. The latter induces membrane protrusion that is moulded around the spindle thereby reducing cytoplasmic loss. Here, we find that depleting the NAD biosynthetic enzyme
Global Trade Item Number
| SKU | GTIN |
|---|---|
| N3501-500MG | 04061834116110 |
| N3501-100MG | 04061834116080 |
| N3501-250MG | 04061834116097 |
| N3501-25MG | 04061834116103 |