321-02-8

321-02-8 structure

Name: Nicotinic acid mononucleotide
Chemical Name: 3-Carboxy-1-(5-O-phosphono-β-D-ribofuranosyl)pyridinium
CAS Number: 321-02-8
Molecular Formula: C₁₁H₁₄NO₉P
Molecular Weight: 336.21200
Catalog: Research Areas Others
Create Date: 2018-12-17 19:22:12
Modify Date: 2025-08-25 09:17:07
Nicotinic acid mononucleotide (NAMN) is formed from nicotinic acid (NA) via the nicotinic acid phosphoribosyltransferase in the biosynthesis of NAD+. Nicotinate mononucleotide is a substrate for nicotinamide mononucleotide/Nicotinic acid mononucleotide adenylyltransferase[1][2].

Name	3-Carboxy-1-(5-O-phosphono-β-D-ribofuranosyl)pyridinium
Synonyms	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

Description	Nicotinic acid mononucleotide (NAMN) is formed from nicotinic acid (NA) via the nicotinic acid phosphoribosyltransferase in the biosynthesis of NAD+. Nicotinate mononucleotide is a substrate for nicotinamide mononucleotide/Nicotinic acid mononucleotide adenylyltransferase[1][2].
Related Catalog	Research Areas >> Others Signaling Pathways >> Others >> Others
References	[1]. O'Hara JK, et al. Targeting NAD+ metabolism in the human malaria parasite Plasmodium falciparum. PLoS One. 2014 Apr 18;9(4):e94061. [2]. Khan JA, et al. Nicotinamide adenine dinucleotide metabolism as an attractive target for drug discovery. Expert Opin Ther Targets. 2007 May;11(5):695-705.

Personal Protective Equipment	Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
RIDADR	NONH for all modes of transport
WGK Germany	3

Precursor 2
89-00-9 97-55-2
DownStream 0