CHEBI:52794 - β-L-aspartylhydroxamic acid

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name β-L-aspartylhydroxamic acid
ChEBI ID CHEBI:52794
ChEBI ASCII Name beta-L-aspartylhydroxamic acid
Definition A non-proteinogenic L-α-amino acid that is L-asparagine hydroxylated at N-4.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
more structures >>
Formula C4H8N2O4
Net Charge 0
Average Mass 148.118
Monoisotopic Mass 148.04841
InChI InChI=1S/C4H8N2O4/c5-2(4(8)9)1-3(7)6-10/h2,10H,1,5H2,(H,6,7)(H,8,9)/t2-/m0/s1
InChIKey ZBYVTTSIVDYQSO-REOHCLBHSA-N
SMILES OC([C@H](CC(NO)=O)N)=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): mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
(via L-alpha-amino acid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing β-L-aspartylhydroxamic acid (CHEBI:52794) is a L-asparagine derivative (CHEBI:52987)
β-L-aspartylhydroxamic acid (CHEBI:52794) is a hydroxamic acid (CHEBI:24650)
β-L-aspartylhydroxamic acid (CHEBI:52794) is a non-proteinogenic L-α-amino acid (CHEBI:83822)
β-L-aspartylhydroxamic acid (CHEBI:52794) is tautomer of β-L-aspartylhydroxamic acid zwitterion (CHEBI:58902)
Incoming β-L-aspartylhydroxamic acid zwitterion (CHEBI:58902) is tautomer of β-L-aspartylhydroxamic acid (CHEBI:52794)
IUPAC Names
(2S)-2-amino-4-(hydroxyamino)-4-oxobutanoic acid
N4-hydroxy-L-asparagine
Synonyms Sources
β-aspartohydroxamic acid ChEBI
beta-L-Aspartylhydroxamate KEGG COMPOUND
L-Asparaginsäure-4-hydroxyamid ChEBI
L-aspartic acid β-hydroxamate ChEBI
Manual Xrefs Databases
C03124 KEGG COMPOUND
SD4 PDBeChem
View more database links
Registry Number Type Source
1725124 Beilstein Registry Number Beilstein
Last Modified
21 November 2019