5′-Phosphoribosyl-4-carboxy-5-aminoimidazole
Appearance
Names | |
---|---|
IUPAC name
5-Amino-1-(5-O-phosphono-β-D-ribofuranosyl)-1H-imidazole-4-carboxylic acid
| |
Systematic IUPAC name
5-Amino-1-{(2R,3R,4S,5R)-3,4-dihydroxy-5-[(phosphonooxy)methyl]oxolan-2-yl}-1H-imidazole-4-carboxylic acid | |
Other names
Carboxyaminoimidazole ribotide,
Carboxyaminoimidazole ribonucleotide, CAIR, | |
Identifiers | |
3D model (JSmol)
|
|
ChEBI | |
ChemSpider | |
PubChem CID
|
|
UNII | |
CompTox Dashboard (EPA)
|
|
| |
| |
Properties | |
C9H14N3O9P | |
Molar mass | 339.196 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
5′-Phosphoribosyl-4-carboxy-5-aminoimidazole (or CAIR) is an intermediate in the formation of purines.
It is formed by phosphoribosylaminoimidazole carboxylase.