CHEBI:28413 - 5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxylic acid

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name 5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxylic acid
ChEBI ID CHEBI:28413
ChEBI ASCII Name 5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxylic acid
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:12103, CHEBI:18968, CHEBI:575
Supplier Information
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Formula C9H14N3O9P
Net Charge 0
Average Mass 339.19604
Monoisotopic Mass 339.047
InChI InChI=1S/C9H14N3O9P/c10-7-4(9(15)16)11-2-12(7)8-6(14)5(13)3(21-8)1-20-22(17,18)19/h2-3,5-6,8,13-14H,1,10H2,(H,15,16)(H2,17,18,19)/t3-,5-,6-,8-/m1/s1
InChIKey XFVULMDJZXYMSG-ZIYNGMLESA-N
SMILES Nc1c(ncn1[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O)C(O)=O
Metabolite of Species Details
Mus musculus (NCBI:10090) Source: BioModels - MODEL1507180067 See: PubMed
Escherichia coli (NCBI:562) See: PubMed
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxylic acid (CHEBI:28413) has role Escherichia coli metabolite (CHEBI:76971)
5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxylic acid (CHEBI:28413) has role mouse metabolite (CHEBI:75771)
5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxylic acid (CHEBI:28413) is a 1-(phosphoribosyl)imidazole (CHEBI:37292)
5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxylic acid (CHEBI:28413) is a aminoimidazole (CHEBI:22512)
5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxylic acid (CHEBI:28413) is a imidazole-4-carboxylic acid (CHEBI:38306)
5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxylic acid (CHEBI:28413) is conjugate acid of 5-amino-1-(5-phosphonato-D-ribosyl)imidazole-4-carboxylate (CHEBI:58564)
5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxylic acid (CHEBI:28413) is conjugate acid of 5-amino-1-(5-phosphonato-D-ribosyl)imidazolium-4-carboxylate(2−) (CHEBI:77657)
Incoming 5-amino-1-(5-phosphonato-D-ribosyl)imidazole-4-carboxylate (CHEBI:58564) is conjugate base of 5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxylic acid (CHEBI:28413)
5-amino-1-(5-phosphonato-D-ribosyl)imidazolium-4-carboxylate(2−) (CHEBI:77657) is conjugate base of 5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxylic acid (CHEBI:28413)
IUPAC Name
5-amino-1-(5-O-phosphono-β-D-ribofuranosyl)-1H-imidazole-4-carboxylic acid
Synonyms Sources
1-(5'-Phosphoribosyl)-4-carboxy-5-aminoimidazole KEGG COMPOUND
1-(5'-Phosphoribosyl)-5-amino-4-carboxyimidazole KEGG COMPOUND
1-(5'-Phosphoribosyl)-5-amino-4-imidazolecarboxylate KEGG COMPOUND
1-(5-Phospho-D-ribosyl)-5-amino-4-imidazolecarboxylate KEGG COMPOUND
5'-Phosphoribosyl-4-carboxy-5-aminoimidazole KEGG COMPOUND
5'-Phosphoribosyl-5-amino-4-imidazolecarboxylate KEGG COMPOUND
5-Amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxylate KEGG COMPOUND
5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxylic acid UniProt
Database Links Databases
C04751 KEGG COMPOUND
C2R PDBeChem
View more database links
Last Modified
27 January 2016