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CHEBI:18349 - N1-(5-phospho-D-ribosyl)glycinamide
| Formula | C7H15N2O8P |
| Net Charge | 0 |
| Average Mass | 286.177 |
| Monoisotopic Mass | 286.05660 |
| SMILES | NCC(=O)NC1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O |
| InChI | InChI=1S/C7H15N2O8P/c8-1-4(10)9-7-6(12)5(11)3(17-7)2-16-18(13,14)15/h3,5-7,11-12H,1-2,8H2,(H,9,10)(H2,13,14,15)/t3-,5-,6-,7?/m1/s1 |
| InChIKey | OBQMLSFOUZUIOB-HJZCUYRDSA-N |
| Species of Metabolite | Component | Source | Comments |
|---|---|---|---|
| Escherichia coli (ncbitaxon:562) | - | PubMed (21988831) | |
| Mus musculus (ncbitaxon:10090) | - | PubMed (19425150) | Source: BioModels - MODEL1507180067 |
| Roles Classification |
|---|
| Biological Roles: | 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). |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| N1-(5-phospho-D-ribosyl)glycinamide (CHEBI:18349) has role Escherichia coli metabolite (CHEBI:76971) |
| N1-(5-phospho-D-ribosyl)glycinamide (CHEBI:18349) has role mouse metabolite (CHEBI:75771) |
| N1-(5-phospho-D-ribosyl)glycinamide (CHEBI:18349) is a N-glycosyl compound (CHEBI:21731) |
| N1-(5-phospho-D-ribosyl)glycinamide (CHEBI:18349) is a ribose monophosphate (CHEBI:35159) |
| N1-(5-phospho-D-ribosyl)glycinamide (CHEBI:18349) is conjugate acid of N1-(5-phospho-D-ribosyl)glycinamide(1−) (CHEBI:58457) |
| Incoming Relation(s) |
| N1-(5-phospho-D-ribosyl)glycinamide(1−) (CHEBI:58457) is conjugate base of N1-(5-phospho-D-ribosyl)glycinamide (CHEBI:18349) |
| IUPAC Name |
|---|
| N-glycyl-D-ribofuranosylamine 5-(dihydrogen phosphate) |
| Synonyms | Source |
|---|---|
| 5'-Phosphoribosylglycinamide | KEGG COMPOUND |
| 5'-Phosphoribosylglycineamide | ChemIDplus |
| N-glycyl-5-O-phosphono-D-ribofuranosylamine | ChEBI |
| GAR | KEGG COMPOUND |
| Glycinamide ribonucleotide | KEGG COMPOUND |
| Glycineamide ribonucleotide | ChemIDplus |