CHEBI:21398 - L-altraric acid

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ChEBI Name L-altraric acid
ChEBI ID CHEBI:21398
ChEBI ASCII Name L-altraric acid
Definition Altraric acid of L-configuration.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C6H10O8
Net Charge 0
Average Mass 210.13880
Monoisotopic Mass 210.03757
InChI InChI=1S/C6H10O8/c7-1(3(9)5(11)12)2(8)4(10)6(13)14/h1-4,7-10H,(H,11,12)(H,13,14)/t1-,2+,3-,4-/m1/s1
InChIKey DSLZVSRJTYRBFB-GJPGBQJBSA-N
SMILES O[C@@H]([C@@H](O)[C@@H](O)C(O)=O)[C@@H](O)C(O)=O
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.
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ChEBI Ontology
Outgoing L-altraric acid (CHEBI:21398) has role bacterial metabolite (CHEBI:76969)
L-altraric acid (CHEBI:21398) is a altraric acid (CHEBI:26847)
L-altraric acid (CHEBI:21398) is conjugate acid of L-altrarate(1−) (CHEBI:21397)
L-altraric acid (CHEBI:21398) is enantiomer of D-altraric acid (CHEBI:21101)
Incoming L-altrarate(1−) (CHEBI:21397) is conjugate base of L-altraric acid (CHEBI:21398)
D-altraric acid (CHEBI:21101) is enantiomer of L-altraric acid (CHEBI:21398)
IUPAC Name
L-altraric acid
Synonyms Sources
(2R,3R,4S,5R)-2,3,4,5-tetrahydroxyhexanedioic acid IUPAC
L-talaric acid ChEBI
Registry Numbers Types Sources
1728118 Beilstein Registry Number Beilstein
1728118 Reaxys Registry Number Reaxys
Last Modified
08 July 2014