(3R)-3-hydroxy-L-aspartic acid (CHEBI:17576)

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ChEBI Name	(3R)-3-hydroxy-L-aspartic acid

ChEBI ID	CHEBI:17576

ChEBI ASCII Name	(3R)-3-hydroxy-L-aspartic acid

Stars	This entity has been manually annotated by the ChEBI Team.

Secondary ChEBI IDs	CHEBI:10557, CHEBI:21287, CHEBI:676808

Supplier Information

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Formula

C4H7NO5

Net Charge

Average Mass

149.10212

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+/m0/s1

InChIKey

YYLQUHNPNCGKJQ-NHYDCYSISA-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 )

ChEBI Ontology
Outgoing	(3R)-3-hydroxy-L-aspartic acid (CHEBI:17576) is a 3-hydroxy-L-aspartic acid (CHEBI:48423) (3R)-3-hydroxy-L-aspartic acid (CHEBI:17576) is conjugate acid of (3R)-3-hydroxy-L-aspartate(1−) (CHEBI:58196) (3R)-3-hydroxy-L-aspartic acid (CHEBI:17576) is conjugate acid of (3R)-3-hydroxy-L-aspartate(2−) (CHEBI:33196) (3R)-3-hydroxy-L-aspartic acid (CHEBI:17576) is enantiomer of (3S)-3-hydroxy-D-aspartic acid (CHEBI:60893)

Incoming	(3R)-3-hydroxy-L-aspartate(1−) (CHEBI:58196) is conjugate base of (3R)-3-hydroxy-L-aspartic acid (CHEBI:17576) (3R)-3-hydroxy-L-aspartate(2−) (CHEBI:33196) is conjugate base of (3R)-3-hydroxy-L-aspartic acid (CHEBI:17576) (3S)-3-hydroxy-D-aspartic acid (CHEBI:60893) is enantiomer of (3R)-3-hydroxy-L-aspartic acid (CHEBI:17576)

IUPAC Names

(2S,3R)-2-amino-3-hydroxybutanedioic acid

(3R)-3-hydroxy-L-aspartic acid

Synonyms	Sources
(2S,3R)-2-amino-3-hydroxysuccinic acid	ChEBI
(3R)-3-hydroxy-L-aspartic acid	ChEBI
erythro-3-Hydroxy-L-aspartate	KEGG COMPOUND
erythro-3-Hydroxy-L-aspartic acid	KEGG COMPOUND
erythro-3-Hydroxy-Ls-aspartic acid	KEGG COMPOUND
erythro-β-hydroxy-L-aspartic acid	ChEBI
L-erythro-beta-hydroxyaspartic acid	ChEBI

Registry Number	Type	Source
2046210	Beilstein Registry Number	Beilstein

Citation	Type	Source
19791805	PubMed citation	ChEMBL

Last Modified

07 January 2019