CHEBI:60897 - (3R)-3-hydroxy-D-aspartic acid

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ChEBI Name (3R)-3-hydroxy-D-aspartic acid
ChEBI ID CHEBI:60897
ChEBI ASCII Name (3R)-3-hydroxy-D-aspartic acid
Definition A 3-hydroxy-D-aspartic acid in which the carbon bearing the hydroxy substituent has R configuration.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C4H7NO5
Net Charge 0
Average Mass 149.10210
Monoisotopic Mass 149.03242
InChI InChI=1S/C4H7NO5/c5-1(3(7)8)2(6)4(9)10/h1-2,6H,5H2,(H,7,8)(H,9,10)/t1-,2-/m1/s1
InChIKey YYLQUHNPNCGKJQ-JCYAYHJZSA-N
SMILES N[C@H]([C@@H](O)C(O)=O)C(O)=O
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): fungal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in fungi, the kingdom that includes microorganisms such as the yeasts and moulds.
(via 3-hydroxy-D-aspartic acid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (3R)-3-hydroxy-D-aspartic acid (CHEBI:60897) is a 3-hydroxy-D-aspartic acid (CHEBI:60887)
(3R)-3-hydroxy-D-aspartic acid (CHEBI:60897) is conjugate acid of (3R)-3-hydroxy-D-aspartate(1−) (CHEBI:60898)
(3R)-3-hydroxy-D-aspartic acid (CHEBI:60897) is enantiomer of (3S)-3-hydroxy-L-aspartic acid (CHEBI:10696)
Incoming (3R)-3-hydroxy-D-aspartate(1−) (CHEBI:60898) is conjugate base of (3R)-3-hydroxy-D-aspartic acid (CHEBI:60897)
(3S)-3-hydroxy-L-aspartic acid (CHEBI:10696) is enantiomer of (3R)-3-hydroxy-D-aspartic acid (CHEBI:60897)
IUPAC Name
(3R)-3-hydroxy-D-aspartic acid
Synonyms Sources
(2R,3R)-2-amino-3-hydroxybutanedioic acid IUPAC
(2R,3R)-2-amino-3-hydroxysuccinic acid ChEBI
(R,R)-3-hydroxyaspartic acid ChEBI
D-threo-3-hydroxyaspartic acid ChEBI
D-threo-β-hydroxyaspartic acid ChEBI
threo-3-hydroxy-D-aspartic acid ChEBI
threo-β-hydroxy-D-aspartic acid ChEBI
threo-D-3-hydroxyaspartic acid ChEBI
Registry Number Type Source
2046211 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
12835921 PubMed citation Europe PMC
Last Modified
04 September 2014