CHEBI:131603 - sucrose 6G-phosphate

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ChEBI Name sucrose 6G-phosphate
ChEBI ID CHEBI:131603
ChEBI ASCII Name sucrose 6(G)-phosphate
Definition A disaccharide phosphate that is sucrose carrying a single monophosphate substituent at position 6 on the glucose ring.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C12H23O14P
Net Charge 0
Average Mass 422.277
Monoisotopic Mass 422.083
InChI InChI=1S/C12H23O14P/c13-1-4-7(16)10(19)12(3-14,25-4)26-11-9(18)8(17)6(15)5(24-11)2-23-27(20,21)22/h4-11,13-19H,1-3H2,(H2,20,21,22)/t4-,5-,6-,7-,8+,9-,10+,11-,12+/m1/s1
InChIKey WQQSIXKPRAUZJL-UGDNZRGBSA-N
SMILES [C@H]1([C@](O[C@@H]([C@H]1O)CO)(CO)O[C@@H]2[C@@H]([C@H]([C@@H]([C@H](O2)COP(=O)(O)O)O)O)O)O
Metabolite of Species Details
Methylomicrobium alcaliphilum 20Z (NCBI:txid1091494) See: PubMed
Escherichia coli (NCBI:txid562) 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 sucrose 6G-phosphate (CHEBI:131603) has functional parent sucrose (CHEBI:17992)
sucrose 6G-phosphate (CHEBI:131603) has role Escherichia coli metabolite (CHEBI:76971)
sucrose 6G-phosphate (CHEBI:131603) is a disaccharide phosphate (CHEBI:23843)
sucrose 6G-phosphate (CHEBI:131603) is conjugate acid of sucrose 6G-phosphate(2−) (CHEBI:91002)
Incoming sucrose 6G-phosphate(2−) (CHEBI:91002) is conjugate base of sucrose 6G-phosphate (CHEBI:131603)
Synonyms Sources
6-O-Phosphonosucrose KEGG COMPOUND
6-Phosphosucrose KEGG COMPOUND
α-D-glucopyranosyl-(1↔2)-β-D-fructofuranoside 6-phosphate MetaCyc
β-D-fructofuranosyl-(1↔2)-α-D-glucopyranoside 6-phosphate MetaCyc
beta-D-Fructofuranosyl-6-O-phosphono-alpha-D-glucopyranoside KEGG COMPOUND
Sucrose 6-phosphate KEGG COMPOUND
Sucrose-6-phosphate ChemIDplus
Manual Xrefs Databases
C00007452 KNApSAcK
C16688 KEGG COMPOUND
CPD-15716 MetaCyc
View more database links
Registry Numbers Types Sources
22372-29-8 CAS Registry Number KNApSAcK
22372-29-8 CAS Registry Number ChemIDplus
8136715 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
25577257 PubMed citation Europe PMC
26826371 PubMed citation Europe PMC
Last Modified
23 March 2016