Home > Name List By p > Pyridinium,3-(aminocarbonyl)-1-(5-O-phosphono-b-D-ribofuranosyl)-, inner salt

CAS No 1094-61-7 , Pyridinium,3-(aminocarbonyl)-1-(5-O-phosphono-b-D-ribofuranosyl)-, inner salt

  • Name: Pyridinium,3-(aminocarbonyl)-1-(5-O-phosphono-b-D-ribofuranosyl)-, inner salt
  • Synonyms: Nicotinamide ribotide;Nicotinamide mononucleotide;Nicotinamide ribonucleotide;3-Carbamoyl-1-b-D-ribofuranosylpyridiniumhydroxide, 5'-phosphate, inner salt (6CI,7CI); b-D-NMN; Nicotinamide ribonucleoside 5'-phosphate; b-NMN; Pyridinium,3-(aminocarbonyl)-1-(5-O-phosphono-b-D-ribofuranosyl)-, hydroxide, inner salt;Pyridinium,3-(aminocarbonyl)-1-(5-O-phosphono-b-D-ribofuranosyl)-, inner salt; NMN; NMN (mononucleotide); Pyridinium, 3-carbamoyl-1-b-D-ribofuranosyl-, hydroxide,5'-(dihydrogen phosphate), inner salt (8CI);
  • CAS Registry Number:
  • Flash Point: °C
  • Boiling Point: °Cat760mmHg
  • Density: g/cm3
  • Flash Point: °C
  • EINECS: 214-136-5
  • Molecular Weight: 335.2266
  • 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
  • Molecular Formula: C11H15 N2 O8 P
  • Molecular Structure:CAS No:1094-61-7 Pyridinium,3-(aminocarbonyl)-1-(5-O-phosphono-b-D-ribofuranosyl)-, inner salt

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References of Pyridinium,3-(aminocarbonyl)-1-(5-O-phosphono-b-D-ribofuranosyl)-, inner salt
Title: NMN
CAS Registry Number: 1094-61-7
CAS Name: 3-(Aminocarbonyl)-1-(5-O-phosphono-b-D-ribofuranosyl)pyridinium inner salt
Synonyms: 3-carbamoyl-1-b-D-ribofuranosylpyridinium hydroxide 5￠-(dihydrogen phosphate) inner salt; nicotinamide mononucleotide
Molecular Formula: C11H15N2O8P
Molecular Weight: 334.22
Percent Composition: C 39.53%, H 4.52%, N 8.38%, O 38.30%, P 9.27%
Literature References: Prepd by incubation of NAD with potato pyrophosphatase in a non-phosphate buffer and in the presence of fluoride: Plaut, Plaut, Arch. Biochem. Biophys. 48, 189 (1954); Biochem. Prep. 5, 55 (1957). Enzymatic synthesis from nicotinamide by human erythrocytes and hemolyzates: Preiss, Handler, J. Biol. Chem. 225, 759 (1957). Prepn by hydrolysis of NAD by a yeast enzyme: Takei, Agric. Biol. Chem. 34, 23 (1970); by cleavage of NAD with crude rattlesnake venom: Apps, FEBS Lett. 15, 277 (1971); R. Jeck, C. W?nckhaus, Methods Enzymol. 66, 62 (1980). NMR studies and conformation of a- and b-nicotinamide nucleotide: N. J. Oppenheimer, N. O. Kaplan, Biochemistry 15, 3981 (1976).
Properties: Can be precipitated from slightly acidic aq soln by a large vol of acetone. Freely sol in water, practically insol in acetone. More stable when stored frozen in soln, than when in dry form.