CHEBI:21077 - D-ribonic acid

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ChEBI Name D-ribonic acid
ChEBI ASCII Name D-ribonic acid
Definition The D-enantiomer ribonic acid.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C5H10O6
Net Charge 0
Average Mass 166.12930
Monoisotopic Mass 166.04774
InChI InChI=1S/C5H10O6/c6-1-2(7)3(8)4(9)5(10)11/h2-4,6-9H,1H2,(H,10,11)/t2-,3-,4-/m1/s1
SMILES OC[C@@H](O)[C@@H](O)[C@@H](O)C(O)=O
Metabolite of Species Details
Daphnia magna (NCBI:txid35525) See: Mixtures of similarly acting compounds in Daphnia magna: From gene to metabolite and beyondTine Vandenbrouck, Oliver A.H. Jones, Nathalie Dom, Julian L. Griffin, Wim De CoenEnvironment International 36 (2010) 254-268
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): Daphnia magna metabolite
A Daphnia metabolite produced by the species Daphnia magna.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing D-ribonic acid (CHEBI:21077) has role Daphnia magna metabolite (CHEBI:83056)
D-ribonic acid (CHEBI:21077) is a ribonic acid (CHEBI:33511)
D-ribonic acid (CHEBI:21077) is conjugate acid of D-ribonate (CHEBI:17773)
D-ribonic acid (CHEBI:21077) is enantiomer of L-ribonic acid (CHEBI:87765)
Incoming 2-carboxy-D-arabinitol 1,5-bisphosphate (CHEBI:41351) has functional parent D-ribonic acid (CHEBI:21077)
2-carboxy-D-arabinitol 1-phosphate (CHEBI:17541) has functional parent D-ribonic acid (CHEBI:21077)
2-deoxy-D-ribonic acid (CHEBI:86350) has functional parent D-ribonic acid (CHEBI:21077)
2-deoxy-D-ribono-1,4-lactone (CHEBI:17281) has functional parent D-ribonic acid (CHEBI:21077)
D-ribono-1,4-lactone (CHEBI:74168) has functional parent D-ribonic acid (CHEBI:21077)
D-ribonate (CHEBI:17773) is conjugate base of D-ribonic acid (CHEBI:21077)
L-ribonic acid (CHEBI:87765) is enantiomer of D-ribonic acid (CHEBI:21077)
(2R,3R,4R)-2,3,4,5-tetrahydroxypentanoic acid
D-ribonic acid
Synonym Source
D-Ribonic acid KEGG COMPOUND
Manual Xrefs Databases
HMDB0000867 HMDB
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Registry Numbers Types Sources
1724264 Reaxys Registry Number Reaxys
1724264 Beilstein Registry Number Beilstein
Citation Waiting for Citations Type Source
22770225 PubMed citation Europe PMC
Last Modified
23 October 2015