CHEBI:47006 - D-ribopyranose

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ChEBI Name D-ribopyranose
ChEBI ID CHEBI:47006
ChEBI ASCII Name D-ribopyranose
Definition A D-ribose and the D-enantiomer of ribopyranose.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C5H10O5
Net Charge 0
Average Mass 150.12990
Monoisotopic Mass 150.05282
InChI InChI=1S/C5H10O5/c6-2-1-10-5(9)4(8)3(2)7/h2-9H,1H2/t2-,3-,4-,5?/m1/s1
InChIKey SRBFZHDQGSBBOR-SOOFDHNKSA-N
SMILES O[C@@H]1COC(O)[C@H](O)[C@@H]1O
Roles Classification
Biological Role(s): human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
(via D-ribose )
fundamental metabolite
Any metabolite produced by all living cells.
(via D-ribose )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing D-ribopyranose (CHEBI:47006) is a D-ribose (CHEBI:16988)
D-ribopyranose (CHEBI:47006) is a ribopyranose (CHEBI:47007)
D-ribopyranose (CHEBI:47006) is enantiomer of L-ribopyranose (CHEBI:47010)
Incoming α-D-ribopyranose (CHEBI:47008) is a D-ribopyranose (CHEBI:47006)
β-D-ribopyranose (CHEBI:27476) is a D-ribopyranose (CHEBI:47006)
L-ribopyranose (CHEBI:47010) is enantiomer of D-ribopyranose (CHEBI:47006)
IUPAC Name
D-ribopyranose
Synonyms Sources
(3R,4R,5R)-tetrahydro-2H-pyran-2,3,4,5-tetrol IUPAC
WURCS=2.0/1,1,0/[a222h-1x_1-5]/1/ GlyTouCan
Manual Xrefs Databases
G75380KK GlyTouCan
G75380KK GlyGen
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Registry Numbers Types Sources
1560983 Reaxys Registry Number Reaxys
1560983 Beilstein Registry Number Beilstein
Citations Waiting for Citations Types Sources
24643482 PubMed citation Europe PMC
25108762 PubMed citation Europe PMC
Last Modified
07 April 2021