CHEBI:48000 - 5-carboxyamino-1-(5-phospho-D-ribosyl)imidazole

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name 5-carboxyamino-1-(5-phospho-D-ribosyl)imidazole
ChEBI ID CHEBI:48000
ChEBI ASCII Name 5-carboxyamino-1-(5-phospho-D-ribosyl)imidazole
Definition A 1-(phosphoribosyl)imidazole having the phospho group at the 5'-position and a carboxyamino group at the 5-position on the imidazole ring.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Save molfile Download Molfile
Formula C9H14N3O9P
Net Charge 0
Average Mass 339.19604
Monoisotopic Mass 339.047
InChI InChI=1S/C9H14N3O9P/c13-6-4(2-20-22(17,18)19)21-8(7(6)14)12-3-10-1-5(12)11-9(15)16/h1,3-4,6-8,11,13-14H,2H2,(H,15,16)(H2,17,18,19)/t4-,6-,7-,8-/m1/s1
InChIKey JHLXDWGVSYMXPL-XVFCMESISA-N
SMILES O[C@@H]1[C@@H](COP(O)(O)=O)O[C@H]([C@@H]1O)n1cncc1NC(O)=O
Metabolite of Species Details
Escherichia coli (NCBI:562) See: PubMed
Roles Classification
Biological Role(s): Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 5-carboxyamino-1-(5-phospho-D-ribosyl)imidazole (CHEBI:48000) has functional parent carbamic acid (CHEBI:28616)
5-carboxyamino-1-(5-phospho-D-ribosyl)imidazole (CHEBI:48000) has role Escherichia coli metabolite (CHEBI:76971)
5-carboxyamino-1-(5-phospho-D-ribosyl)imidazole (CHEBI:48000) is a 1-(phosphoribosyl)imidazole (CHEBI:37292)
5-carboxyamino-1-(5-phospho-D-ribosyl)imidazole (CHEBI:48000) is conjugate acid of 5-carboxylatoamino-1-(5-O-phosphonato-D-ribosyl)imidazole(3−) (CHEBI:58730)
Incoming 5-carboxylatoamino-1-(5-O-phosphonato-D-ribosyl)imidazole(3−) (CHEBI:58730) is conjugate base of 5-carboxyamino-1-(5-phospho-D-ribosyl)imidazole (CHEBI:48000)
IUPAC Name
N-carboxy-1-(5-O-phosphono-β-D-ribofuranosyl)-1H-imidazol-5-amine
Synonym Source
5-carboxyamino-1-(5-phospho-D-ribosyl)imidazole KEGG COMPOUND
Database Link Database
C15667 KEGG COMPOUND
View more database links
Last Modified
25 January 2016