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Name |
Pyridinium,3-(aminocarbonyl)-1-(5-O-phosphono-b-D-ribofuranosyl)-, inner salt |
EINECS | N/A |
CAS No. | 1094-61-7 | Density | g/cm3 |
PSA | 176.06000 | LogP | -1.06000 |
Solubility | N/A | Melting Point |
166 °C(dec.) |
Formula | C11H15 N2 O8 P | Boiling Point | °Cat760mmHg |
Molecular Weight | 334.222 | Flash Point | °C |
Transport Information | N/A | Appearance | N/A |
Safety | Risk Codes | N/A | |
Molecular Structure | Hazard Symbols | N/A | |
Synonyms |
3-Carbamoyl-1-b-D-ribofuranosylpyridiniumhydroxide, 5'-phosphate, inner salt (6CI,7CI); Pyridinium,3-(aminocarbonyl)-1-(5-O-phosphono-b-D-ribofuranosyl)-, hydroxide, inner salt; Pyridinium, 3-carbamoyl-1-b-D-ribofuranosyl-, hydroxide,5'-(dihydrogen phosphate), inner salt (8CI); NMN; NMN (mononucleotide);Nicotinamide mononucleotide; Nicotinamide ribonucleoside 5'-phosphate;Nicotinamide ribonucleotide; Nicotinamide ribotide; b-D-NMN; b-NMN |
Article Data | 31 |
3-carbamoyl-1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyridin-1-ium (β-D-nicotinamide riboside)
nicotinamide mononucleotide
Conditions | Yield |
---|---|
With trimethyl phosphite; trichlorophosphate at 0℃; for 12h; Inert atmosphere; | 88.27% |
Stage #1: 3-carbamoyl-1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyridin-1-ium (β-D-nicotinamide riboside) With Sodium trimetaphosphate; sodium hydroxide In water at 30℃; for 4h; pH=9; Stage #2: With hydrogenchloride In water at 10℃; Reagent/catalyst; | 68% |
With nitromethane; water; trichlorophosphate |
3-carbamoyl-1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyridin-1-ium bromide
nicotinamide mononucleotide
Conditions | Yield |
---|---|
With trimethyl phosphite; trichlorophosphate at -5 - 0℃; for 7h; | 80% |
With trimethyl phosphite; trichlorophosphate at 0℃; for 4h; | 64% |
nicotinamide mononucleotide
Conditions | Yield |
---|---|
With ammonia In acetonitrile at -5 - 5℃; for 1h; | 80% |
Conditions | Yield |
---|---|
With ethylenediaminetetraacetic acid; ammonium acetate; zirconium(IV) chloride In ethanol at 50℃; for 0.5h; pH 5; | 70% |
With water; zirconium(IV) chloride at 80℃; for 0.5h; Reagent/catalyst; |
nicotinamide mononucleotide
Conditions | Yield |
---|---|
With platinum(IV) oxide; hydrogen In deuteromethanol for 12h; Reagent/catalyst; | 64% |
Conditions | Yield |
---|---|
With trichlorophosphate In tetrahydrofuran at 0 - 20℃; for 12h; | 56% |
3-carbamoyl-1-(2,4-dinitrophenyl)pyridinium chloride
ribose 5-phosphate bis(cyclohexylammonium) salt
nicotinamide mononucleotide
Conditions | Yield |
---|---|
With ammonia 1.) -60 deg C, 36 h; r.t., 1 h; 2.) methanol, ethylene glycol (1:1), 4 deg C, 11 h; | 35% |
nicotinamide
5-phosphoribosyl-1-pyrophosphate
nicotinamide mononucleotide
Conditions | Yield |
---|---|
Enzym aus Erythrocyten; |
3-carbamoyl-1-(2,4-dinitrophenyl)pyridinium chloride
phosphoribosylamine
A
nicotinamide mononucleotide
B
α-nicotinamide mononucleotide
C
2,4-Dinitroanilin
Conditions | Yield |
---|---|
In methanol at 5℃; for 14h; Yield given; | |
In methanol at 5℃; for 14h; |
nicotinamide mononucleotide
Conditions | Yield |
---|---|
enzymatische Spaltung; |