CHEBI:132125 - 2,4-didehydro-3-deoxy-L-rhamnonic acid

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name 2,4-didehydro-3-deoxy-L-rhamnonic acid
ChEBI ID CHEBI:132125
ChEBI ASCII Name 2,4-didehydro-3-deoxy-L-rhamnonic acid
Definition A ketoaldonic acid that is rhamnonic acid which is lacking the 3-hydroxy group, while those at positions 2 and 4 have been oxidised to the corresponding ketones.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C6H8O5
Net Charge 0
Average Mass 160.125
Monoisotopic Mass 160.03717
InChI InChI=1S/C6H8O5/c1-3(7)4(8)2-5(9)6(10)11/h3,7H,2H2,1H3,(H,10,11)/t3-/m0/s1
InChIKey CQZFXXYDOLONCO-VKHMYHEASA-N
SMILES OC(C(CC([C@H](C)O)=O)=O)=O
Metabolite of Species Details
Sulfobacillus thermosulfidooxidans (NCBI:txid28034) See: PubMed
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): bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 2,4-didehydro-3-deoxy-L-rhamnonic acid (CHEBI:132125) has functional parent rhamnonic acid (CHEBI:21376)
2,4-didehydro-3-deoxy-L-rhamnonic acid (CHEBI:132125) has role bacterial metabolite (CHEBI:76969)
2,4-didehydro-3-deoxy-L-rhamnonic acid (CHEBI:132125) is a hexonic acid (CHEBI:33752)
2,4-didehydro-3-deoxy-L-rhamnonic acid (CHEBI:132125) is a ketoaldonic acid (CHEBI:24963)
2,4-didehydro-3-deoxy-L-rhamnonic acid (CHEBI:132125) is conjugate acid of 2,4-didehydro-3-deoxy-L-rhamnonate (CHEBI:131847)
Incoming 2,4-didehydro-3-deoxy-L-rhamnonate (CHEBI:131847) is conjugate base of 2,4-didehydro-3-deoxy-L-rhamnonic acid (CHEBI:132125)
IUPAC Name
(5S)-5-hydroxy-2,4-dioxohexanoic acid
Synonym Source
L-2,4-diketo-3-deoxyrhamnonic acid MetaCyc
Manual Xref Database
CPD-13044 MetaCyc
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Citation Waiting for Citations Type Source
25617114 PubMed citation Europe PMC
Last Modified
02 June 2016