CHEBI:28563 - β-D-mannose

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name β-D-mannose
ChEBI ID CHEBI:28563
ChEBI ASCII Name beta-D-mannose
Definition A D-mannopyranose in which the anomeric centre has β-configuration.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:10406, CHEBI:41167, CHEBI:22807
Supplier Information
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Formula C6H12O6
Net Charge 0
Average Mass 180.15588
Monoisotopic Mass 180.063
InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5+,6-/m1/s1
InChIKey WQZGKKKJIJFFOK-RWOPYEJCSA-N
SMILES OC[C@H]1O[C@@H](O)[C@@H](O)[C@@H](O)[C@@H]1O
Roles Classification
Biological Role(s): epitope
The biological role played by a material entity when bound by a receptor of the adaptive immune system. Specific site on an antigen to which an antibody binds.
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via D-mannopyranose )
Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
(via D-mannose )
fundamental metabolite
Any metabolite produced by all living cells.
(via mannose )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing β-D-mannose (CHEBI:28563) has role epitope (CHEBI:53000)
β-D-mannose (CHEBI:28563) is a D-mannopyranose (CHEBI:4208)
β-D-mannose (CHEBI:28563) is enantiomer of β-L-mannose (CHEBI:37679)
Incoming α-D-mannose 6-phosphate (CHEBI:43896) has functional parent β-D-mannose (CHEBI:28563)
2-deoxy-2-fluoro-β-D-mannose (CHEBI:49152) has functional parent β-D-mannose (CHEBI:28563)
β-L-mannose (CHEBI:37679) is enantiomer of β-D-mannose (CHEBI:28563)
IUPAC Name
β-D-mannopyranose
Synonyms Sources
BETA-D-MANNOSE PDBeChem
beta-D-Mannose KEGG COMPOUND
β-D-mannose UniProt
Database Links Databases
BMA PDBeChem
C02209 KEGG COMPOUND
CPD-12601 MetaCyc
DB02687 DrugBank
View more database links
Registry Numbers Types Sources
1680742 Beilstein Registry Number Beilstein
1680742 Reaxys Registry Number Reaxys
648640 Gmelin Registry Number Gmelin
7322-31-8 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
17157281 PubMed citation Europe PMC
25568069 PubMed citation Europe PMC
Last Modified
17 February 2015