CHEBI:16905 - keto-D-fructose 1,6-bisphosphate

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name keto-D-fructose 1,6-bisphosphate
ChEBI ASCII Name keto-D-fructose 1,6-bisphosphate
Definition A ketohexose bisphosphate that is D-fructose substituted by phosphate groups at positions 1 and 6.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:4120, CHEBI:12924
Supplier Information
Download Molfile XML SDF
more structures >>
Formula C6H14O12P2
Net Charge 0
Average Mass 340.114
Monoisotopic Mass 339.99605
InChI InChI=1S/C6H14O12P2/c7-3(1-17-19(11,12)13)5(9)6(10)4(8)2-18-20(14,15)16/h3,5-7,9-10H,1-2H2,(H2,11,12,13)(H2,14,15,16)/t3-,5-,6-/m1/s1
SMILES O[C@H](COP(O)(O)=O)[C@@H](O)[C@H](O)C(=O)COP(O)(O)=O
Metabolite of Species Details
Saccharomyces cerevisiae (NCBI:txid4932) Source: See: PubMed
Homo sapiens (NCBI:txid9606) See: DOI
Roles Classification
Biological Role(s): Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
fundamental metabolite
Any metabolite produced by all living cells.
(via D-fructose 1,6-bisphosphate )
Application(s): anticonvulsant
A drug used to prevent seizures or reduce their severity.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing keto-D-fructose 1,6-bisphosphate (CHEBI:16905) has functional parent D-fructose (CHEBI:15824)
keto-D-fructose 1,6-bisphosphate (CHEBI:16905) has role Saccharomyces cerevisiae metabolite (CHEBI:75772)
keto-D-fructose 1,6-bisphosphate (CHEBI:16905) has role anticonvulsant (CHEBI:35623)
keto-D-fructose 1,6-bisphosphate (CHEBI:16905) is a D-fructose 1,6-bisphosphate (CHEBI:78682)
D-fructose 1,6-bis(dihydrogen phosphate)
Synonyms Sources
1,6-di-O-phosphono-D-fructose ChEBI
D-Fructose 1,6-bisphosphate KEGG COMPOUND
D-fructose-1,6-diphosphate ChEBI
fructose-1,6-diphosphate ChEBI
Harden-Young ester HMDB
Manual Xrefs Databases
76632 ChemSpider
C00007386 KNApSAcK
DB13863 DrugBank
HMDB0001058 HMDB
P6F PDBeChem
View more database links
Registry Numbers Types Sources
1729954 Reaxys Registry Number Reaxys
488-69-7 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
13150027 PubMed citation Europe PMC
16233003 PubMed citation Europe PMC
19049602 PubMed citation Europe PMC
19236002 PubMed citation Europe PMC
21983965 PubMed citation Europe PMC
25206915 PubMed citation Europe PMC
26011931 PubMed citation Europe PMC
28972169 PubMed citation Europe PMC
29593097 PubMed citation Europe PMC
4610358 PubMed citation Europe PMC
Last Modified
16 July 2021