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25635-88-5

25635-88-5 Structure

25635-88-5 Structure
IdentificationBack Directory
[Name]

[5-(5-aminoimidazol-1-yl)-3,4-dihydroxy-oxolan-2-yl]methoxyphosphonic acid
[CAS]

25635-88-5
[Synonyms]

AIR【nucleotide】
aminoimidazole ribotide
5-Aminoimidazole ribonucleotide
5'-Phosphoribosyl-5-aminoimidazole
1-(5-O-Phosphono-β-D-ribofuranosyl)-1H-imidazol-5-amine
(2-Amino-1H-imidazol-1-yl)β-D-ribofuranoside 5-phosphate
1H-IMidazol-5-aMine, 1-(5-O-phosphono-b-D-ribofuranosyl)-
1H-Imidazol-5-amine, 1-(5-O-phosphono-β-D-ribofuranosyl)-
1-(5-Amino-1H-imidazole-1-yl)-1-deoxy-β-D-ribofuranose 5-phosphoric acid
[5-(5-aminoimidazol-1-yl)-3,4-dihydroxy-oxolan-2-yl]methoxyphosphonic acid
Phosphoric acid [[(2R)-3β,4β-dihydroxy-5α-(5-amino-1H-imidazole-1-yl)tetrahydrofuran]-2α-yl]methyl ester
[Molecular Formula]

C8H14N3O7P
[MOL File]

25635-88-5.mol
[Molecular Weight]

295.19
Hazard InformationBack Directory
[Description]

Aminoimidazole ribotide is an intermediate in the formation of purines.
[Uses]

5-Aminoimidazole ribonucleotide is an intermediate of purine nucleotide biosynthesis. 5-Aminoimidazole ribonucleotide is a precursor to 4-amino-2-methyl-5-hydroxymethylpyrimidine (HMP) used in the biosynthesis of the thiamin pyrimidine in Escherichia coli.
[Definition]

ChEBI: 5-amino-1-(5-phospho-beta-D-ribosyl)imidazole is a 1-(phosphoribosyl)imidazole that is 5-aminoimidazole in which the proton at position 1 has been replaced by a 5-phospho-beta-D-ribofuranosyl group. It has a role as a bacterial metabolite. It is a 1-(phosphoribosyl)imidazole and an aminoimidazole. It is a conjugate acid of a 5-amino-1-(5-phosphonato-beta-D-ribosyl)imidazol-3-ium.
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