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CHEBI:28602 - β-D-fructofuranose 2,6-bisphosphate
| Formula | C6H14O12P2 |
| Net Charge | 0 |
| Average Mass | 340.114 |
| Monoisotopic Mass | 339.99605 |
| SMILES | O=P(O)(O)OC[C@H]1O[C@@](CO)(OP(=O)(O)O)[C@@H](O)[C@@H]1O |
| InChI | InChI=1S/C6H14O12P2/c7-2-6(18-20(13,14)15)5(9)4(8)3(17-6)1-16-19(10,11)12/h3-5,7-9H,1-2H2,(H2,10,11,12)(H2,13,14,15)/t3-,4-,5+,6+/m1/s1 |
| InChIKey | YXWOAJXNVLXPMU-ZXXMMSQZSA-N |
| Wikipedia |
|---|
| Species of Metabolite | Component | Source | Comments |
|---|---|---|---|
| Mus musculus (ncbitaxon:10090) | - | PubMed (19425150) | Source: BioModels - MODEL1507180067 |
| Roles Classification |
|---|
| Biological Roles: | human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). mouse metabolite Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus). |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| β-D-fructofuranose 2,6-bisphosphate (CHEBI:28602) has functional parent β-D-fructofuranose (CHEBI:28645) |
| β-D-fructofuranose 2,6-bisphosphate (CHEBI:28602) has role human metabolite (CHEBI:77746) |
| β-D-fructofuranose 2,6-bisphosphate (CHEBI:28602) has role mouse metabolite (CHEBI:75771) |
| β-D-fructofuranose 2,6-bisphosphate (CHEBI:28602) is a D-fructofuranose 2,6-bisphosphate (CHEBI:78687) |
| β-D-fructofuranose 2,6-bisphosphate (CHEBI:28602) is conjugate acid of β-D-fructofuranose 2,6-bisphosphate(4−) (CHEBI:58579) |
| Incoming Relation(s) |
| β-D-fructofuranose 2,6-bisphosphate(4−) (CHEBI:58579) is conjugate base of β-D-fructofuranose 2,6-bisphosphate (CHEBI:28602) |
| IUPAC Name |
|---|
| β-D-fructofuranose 2,6-bis(dihydrogen phosphate) |
| Synonyms | Source |
|---|---|
| D-Fructose 2,6-bisphosphate | KEGG COMPOUND |
| 2,6-di-O-phosphono-β-D-fructofuranose | IUPAC |
| D-Fructose 2,6-bisphosphate | KEGG COMPOUND |
| Manual Xrefs | Databases |
|---|---|
| C00665 | KEGG COMPOUND |
| FDP | PDBeChem |
| HMDB0001047 | HMDB |
| Fructose_2,6-bisphosphate | Wikipedia |
| C00007441 | KNApSAcK |
| Registry Numbers | Sources |
|---|---|
| Reaxys:15436010 | Reaxys |
| CAS:79082-92-1 | ChemIDplus |