Nicotinic acid mononucleotide

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Names

[ CAS No. ]:
321-02-8

[ Name ]:
Nicotinic acid mononucleotide

[Synonym ]:
3-Carboxy-1-methylpyridiniumiodid
Pyridinium,3-carboxy-1-methyl-,iodide
Trigonelline hydriodide
trigonelline hydroiodide
nicotinic acid mononucleotide
Nicotinsaeure-iodmethylat
Nicotinsaeure-mononucleotid
nicotinic acid methiodide
nicotinate adenine mononucleotide
3-Carboxy-1-methyl-pyridinium,Jodid
3-carboxy-1-methyl-pyridinium,iodide

Chemical & Physical Properties

[ Molecular Formula ]:
C11H14NO9P

[ Molecular Weight ]:
336.21200

[ Exact Mass ]:
336.04800

[ PSA ]:
167.44000

[ Storage condition ]:
20°C

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Precursor & DownStream

Precursor

  • Quinolinic acid
  • 5-PHOSPHORYLRIBOSE-1-PYROPHOSPHATE

DownStream

Articles

ArsAB, a novel enzyme from Sporomusa ovata activates phenolic bases for adenosylcobamide biosynthesis.

Mol. Microbiol. 81(4) , 952-67, (2011)

In the homoacetogenic bacterium Sporomusa ovata, phenol and p-cresol are converted into α-ribotides, which are incorporated into biologically active cobamides (Cbas) whose lower ligand bases do not fo...

Dissecting cobamide diversity through structural and functional analyses of the base-activating CobT enzyme of Salmonella enterica.

Biochim. Biophys. Acta 1840(1) , 464-75, (2014)

Cobamide diversity arises from the nature of the nucleotide base. Nicotinate mononucleotide (NaMN):base phosphoribosyltransferases (CobT) synthesize α-linked riboside monophosphates from diverse nucle...

Characterization of human nicotinate phosphoribosyltransferase: Kinetic studies, structure prediction and functional analysis by site-directed mutagenesis.

Biochimie 94(2) , 300-9, (2012)

Nicotinate phosphoribosyltransferase (NaPRT, EC 2.4.2.11) catalyzes the conversion of nicotinate (Na) to nicotinate mononucleotide, the first reaction of the Preiss-Handler pathway for the biosynthesi...


More Articles

Related Compounds

  • Nicotinic Acid-d4
  • nicotinic acid pyrimidin-2-ylamide
  • Nicotinic Acid Acyl--D-glucuronide
  • nicotinic acid, compound with 3,7-dihydro-1,3-dimethyl-7-[2-[(3-pyridylmethyl)amino]ethyl]-1H-purine-2,6-dione (1:1)
  • Nicotinic acid 1-(4-chloro-phenoxymethyl)-2-(methoxycarbonylmethyl-phenyl-amino)-ethyl ester
  • Nicotinic acid, 5-ethoxy-1,6-dihydro-6-oxo-, ethyl ester (6CI)
  • 2-Amino-3-(2-chloro-6-methoxyphenyl)-3-hydroxypropanoic acid
  • 1-(2-Chloropyridin-3-yl)-2,2,2-trifluoroethanol
  • 2-Ethoxy-5-phenyl-[1,2,4]triazolo[1,5-a]pyrimidine-7-carboxylic acid
  • 2-((1-(m-Tolyl)pyrrolidin-3-yl)oxy)ethanamine
  • 2-(2-Chloro-6-methoxyphenyl)-1,3-thiazole-4-carboxylic acid
  • 6-Bromo-2-ethoxy-[1,2,4]triazolo[1,5-a]pyrimidine
  • N-[(3-aminocyclopentyl)methyl]propane-1-sulfonamide
  • 1-(2-Chloro-6-methoxyphenyl)-2,2,2-trifluoroethan-1-ol
  • N-[(3-aminocyclopentyl)methyl]cyclopropanesulfonamide
  • 6-Chloro-7-cyclopropyl-2-(tetrahydrofuran-2-yl)-7H-purine
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