CHEBI:4208 - D-mannopyranose

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ChEBI Name D-mannopyranose
ChEBI ID CHEBI:4208
ChEBI ASCII Name D-mannopyranose
Definition D-Mannose in its six-membered ring form.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information ChemicalBook:CB6284800, eMolecules:478929, Selleckchem:Decitabine, ZINC000016929327
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Decitabine (i.e., 5-aza-2′-deoxycytidine), sold under the brand name Dacogen among others, acts as a nucleic acid synthesis inhibitor. It is a medication for the treatment of myelodysplastic syndromes, a class of conditions where certain blood cells are dysfunctional, and for acute myeloid leukemia (AML). Chemically, it is a cytidine analog.
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Formula C6H12O6
Net Charge 0
Average Mass 180.15590
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-QTVWNMPRSA-N
SMILES OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O
Roles Classification
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
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 )
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ChEBI Ontology
Outgoing D-mannopyranose (CHEBI:4208) has role metabolite (CHEBI:25212)
D-mannopyranose (CHEBI:4208) is a D-aldohexose (CHEBI:17608)
D-mannopyranose (CHEBI:4208) is a D-mannose (CHEBI:16024)
D-mannopyranose (CHEBI:4208) is a mannopyranose (CHEBI:37683)
Incoming α-D-Manp6P-(1→6)-D-Manp (CHEBI:150738) has functional parent D-mannopyranose (CHEBI:4208)
β-D-Arap-(1→2)-D-Manp (CHEBI:153582) has functional parent D-mannopyranose (CHEBI:4208)
β-D-Galf-(1→3)-D-Manp (CHEBI:150079) has functional parent D-mannopyranose (CHEBI:4208)
β-D-Galp-(1→3)-D-Manp (CHEBI:154815) has functional parent D-mannopyranose (CHEBI:4208)
β-D-Galp-(1→6)-D-Manp (CHEBI:154693) has functional parent D-mannopyranose (CHEBI:4208)
β-D-GclpNAc-(1→2)-[β-D-GlcpNAc-(1→3)]-D-Manp (CHEBI:146487) has functional parent D-mannopyranose (CHEBI:4208)
β-D-GlcpNAc-(1→4)-D-Manp (CHEBI:147602) has functional parent D-mannopyranose (CHEBI:4208)
(6S)-6-C-methyl-D-mannopyranose (CHEBI:64171) has functional parent D-mannopyranose (CHEBI:4208)
2-deoxy-2-fluoro-D-mannopyranose (CHEBI:49146) has functional parent D-mannopyranose (CHEBI:4208)
C-α-D-mannosyl-L-tryptophyl residue (CHEBI:195646) has functional parent D-mannopyranose (CHEBI:4208)
D-Manp-(1→2)-D-Araf (CHEBI:148278) has functional parent D-mannopyranose (CHEBI:4208)
D-Manp-(1→2)-D-Manp (CHEBI:151498) has functional parent D-mannopyranose (CHEBI:4208)
D-Manp-(1→3)-D-Manp (CHEBI:153986) has functional parent D-mannopyranose (CHEBI:4208)
D-Manp-(1→5)-D-Araf (CHEBI:151463) has functional parent D-mannopyranose (CHEBI:4208)
D-mannose 1-phosphate (CHEBI:35374) has functional parent D-mannopyranose (CHEBI:4208)
α-D-mannose (CHEBI:28729) is a D-mannopyranose (CHEBI:4208)
α-D-mannosyl-(1→4)-poly[3-O-methyl-α-D-mannosyl-(1→4)]-3-O-methyl-D-mannose (CHEBI:196962) is a D-mannopyranose (CHEBI:4208)
β-D-mannose (CHEBI:28563) is a D-mannopyranose (CHEBI:4208)
poly[3-O-methyl-α-D-mannosyl-(1→4)]-3-O-methyl-D-mannose (CHEBI:196967) is a D-mannopyranose (CHEBI:4208)
IUPAC Name
D-mannopyranose
Synonyms Sources
(3S,4S,5R,6R)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol IUPAC
(3S,4S,5R,6R)-6-(hydroxymethyl)tetrahydropyran-2,3,4,5-tetrol IUPAC
(3S,4S,5R,6R)-6-methyloltetrahydropyran-2,3,4,5-tetrol IUPAC
(3S,4S,5S,6R)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol HMDB
Carubinose KEGG COMPOUND
D-mannose UniProt
D-Mannose KEGG COMPOUND
mannopyranose MetaCyc
Seminose KEGG COMPOUND
WURCS=2.0/1,1,0/[a2122h-1x_1-5]/1/ GlyTouCan
Manual Xrefs Databases
C00001126 KNApSAcK
C00159 KEGG COMPOUND
G70323CJ GlyTouCan
G70323CJ GlyGen
HMDB0000169 HMDB
Mannose Wikipedia
MANNOSE MetaCyc
View more database links
Registry Numbers Types Sources
1423215 Reaxys Registry Number Reaxys
31103-86-3 CAS Registry Number KEGG COMPOUND
3458-28-4 CAS Registry Number KEGG COMPOUND
530-26-7 CAS Registry Number ChemIDplus
83255 Gmelin Registry Number Gmelin
Citations Types Sources
11414367 PubMed citation Europe PMC
16154739 PubMed citation Europe PMC
17336832 PubMed citation Europe PMC
17439666 PubMed citation Europe PMC
19913595 PubMed citation Europe PMC
23623960 PubMed citation Europe PMC
7504304 PubMed citation Europe PMC
7540499 PubMed citation Europe PMC
9488699 PubMed citation Europe PMC
Last Modified
07 April 2021