CHEBI:28729 - α-D-mannose

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name α-D-mannose
ChEBI ID CHEBI:28729
ChEBI ASCII Name alpha-D-mannose
Definition D-Mannopyranose having α-configuration at the anomeric centre.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:43805, CHEBI:10260, CHEBI:22403
Supplier Information
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Formula C6H12O6
Net Charge 0
Average Mass 180.15588
Monoisotopic Mass 180.06339
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-PQMKYFCFSA-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 α-D-mannose (CHEBI:28729) has role epitope (CHEBI:53000)
α-D-mannose (CHEBI:28729) is a D-mannopyranose (CHEBI:4208)
α-D-mannose (CHEBI:28729) is enantiomer of α-L-mannose (CHEBI:37680)
Incoming α-D-mannose 1-phosphate (CHEBI:18205) has functional parent α-D-mannose (CHEBI:28729)
α-D-mannose 1-phosphate(2−) (CHEBI:58409) has functional parent α-D-mannose (CHEBI:28729)
β-D-Galf-(1→3)-α-D-Manp-OMe (CHEBI:62359) has functional parent α-D-mannose (CHEBI:28729)
β-D-Galf-(1→6)-α-D-Manp-OMe (CHEBI:62358) has functional parent α-D-mannose (CHEBI:28729)
16-α-D-mannopyranosyloxyisopimar-7-en-19-oic acid (CHEBI:68085) has functional parent α-D-mannose (CHEBI:28729)
2'-α-mannosyl-L-tryptophan (CHEBI:19232) has functional parent α-D-mannose (CHEBI:28729)
2-(α-D-mannosyl)-D-glyceric acid (CHEBI:15847) has functional parent α-D-mannose (CHEBI:28729)
2-deoxy-2-fluoro-α-D-mannose (CHEBI:49148) has functional parent α-D-mannose (CHEBI:28729)
4,6-dideoxy-4-(3-deoxy-L-glycero-tetronamido)-α-D-Manp2Me-(1→2)-4,6-dideoxy-4-(3-deoxy-L-glycero-tetronamido)-α-D-Manp-(1→2)-4,6-dideoxy-4-(3-deoxy-L-glycero-tetronamido)-α-D-Manp (CHEBI:52982) has functional parent α-D-mannose (CHEBI:28729)
4,6-dideoxy-4-(3-deoxy-L-glycero-tetronamido)-α-D-Manp2Me-(1→2)-4,6-dideoxy-4-(3-deoxy-L-glycero-tetronamido)-α-D-Manp-(1→2)-4,6-dideoxy-4-(3-deoxy-L-glycero-tetronamido)-α-D-Manp-(1→2)-4,6-dideoxy-4-(3-deoxy-L-glycero-tetronamido)-α-D-Manp (CHEBI:63135) has functional parent α-D-mannose (CHEBI:28729)
4,6-dideoxy-4-(3-deoxy-L-glycero-tetronamido)-α-D-Manp2Me-(1→2)-4,6-dideoxy-4-(3-deoxy-L-glycero-tetronamido)-α-D-Manp-(1→2)-4,6-dideoxy-4-(3-deoxy-L-glycero-tetronamido)-α-D-Manp-(1→2)-4,6-dideoxy-4-(3-deoxy-L-glycero-tetronamido)-α-D-Manp-(1→2)-4,6-dideoxy-4-(3-deoxy-L-glycero-tetronamido)-α-D-Manp (CHEBI:59267) has functional parent α-D-mannose (CHEBI:28729)
4,6-dideoxy-4-(3-deoxy-L-glycero-tetronamido)-α-D-Manp2Me-(1→2)-4,6-dideoxy-4-(3-deoxy-L-glycero-tetronamido)-α-D-ManpOMe (CHEBI:59241) has functional parent α-D-mannose (CHEBI:28729)
methyl 4,6-dideoxy-4-(3-deoxy-L-glycero-tetronamido)-2-O-methyl-α-D-mannopyranoside (CHEBI:43892) has functional parent α-D-mannose (CHEBI:28729)
α-L-mannose (CHEBI:37680) is enantiomer of α-D-mannose (CHEBI:28729)
IUPAC Name
α-D-mannopyranose
Synonyms Sources
α-D-Man JCBN
α-D-mannopyranose UniProt
alpha-D-Mannose KEGG COMPOUND
ALPHA-D-MANNOSE PDBeChem
Manual Xrefs Databases
C00001126 KNApSAcK
C00936 KEGG COMPOUND
DB02944
Note: (2016-12-31) Revoked entry. Revocation comment: Not an experimental drug.
DrugBank
MAN PDBeChem
View more database links
Registry Numbers Types Sources
1281606 Reaxys Registry Number Reaxys
1281606 Beilstein Registry Number Beilstein
185283 Gmelin Registry Number Gmelin
3458-28-4 CAS Registry Number KEGG COMPOUND
7296-15-3 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
19443021 PubMed citation Europe PMC
25568069 PubMed citation Europe PMC
Last Modified
13 September 2019