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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:28159 -
D
-asparagine
Main
ChEBI Ontology
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ChEBI Name
D
-asparagine
ChEBI ID
CHEBI:28159
ChEBI ASCII Name
D-asparagine
Definition
An optically active form of asparagine having
D
-configuration.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:4107, CHEBI:20918
Supplier Information
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Molfile
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Formula
C4H8N2O3
Net Charge
0
Average Mass
132.119
Monoisotopic Mass
132.05349
InChI
InChI=1S/C4H8N2O3/c5-2(4(8)9)1-3(6)7/h2H,1,5H2,(H2,6,7)(H,8,9)/t2-/m1/s1
InChIKey
DCXYFEDJOCDNAF-UWTATZPHSA-N
SMILES
OC([C@@H](CC(N)=O)N)=O
Metabolite of Species
Details
Saccharomyces cerevisiae
(NCBI:txid4932)
See:
PubMed
Roles Classification
Chemical Role
(s):
Bronsted base
A molecular entity capable of accepting a hydron from a donor (Br
o
nsted acid).
(via
organic amino compound
)
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Br
o
nsted base).
(via
oxoacid
)
Biological Role
(s):
algal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in algae including unicellular organisms like chlorella and diatoms to multicellular organisms like giant kelps and brown algae.
(via
asparagine
)
Daphnia magna metabolite
A
Daphnia
metabolite produced by the species
Daphnia magna
.
(via
asparagine
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
D
-asparagine (
CHEBI:28159
)
is a
D
-α-amino acid (
CHEBI:16733
)
D
-asparagine (
CHEBI:28159
)
is a
asparagine (
CHEBI:22653
)
D
-asparagine (
CHEBI:28159
)
is conjugate acid of
D
-asparaginate (
CHEBI:32656
)
D
-asparagine (
CHEBI:28159
)
is conjugate base of
D
-asparaginium (
CHEBI:32657
)
D
-asparagine (
CHEBI:28159
)
is enantiomer of
L
-asparagine (
CHEBI:17196
)
D
-asparagine (
CHEBI:28159
)
is tautomer of
D
-asparagine zwitterion (
CHEBI:74337
)
Incoming
D
-asparagine derivative (
CHEBI:83975
)
has functional parent
D
-asparagine (
CHEBI:28159
)
D
-asparaginium (
CHEBI:32657
)
is conjugate acid of
D
-asparagine (
CHEBI:28159
)
D
-asparaginate (
CHEBI:32656
)
is conjugate base of
D
-asparagine (
CHEBI:28159
)
L
-asparagine (
CHEBI:17196
)
is enantiomer of
D
-asparagine (
CHEBI:28159
)
N
2
-
D
-asparagino group (
CHEBI:32658
)
is substituent group from
D
-asparagine (
CHEBI:28159
)
N
4
-
D
-asparagino group (
CHEBI:32659
)
is substituent group from
D
-asparagine (
CHEBI:28159
)
D
-asparagine residue (
CHEBI:50349
)
is substituent group from
D
-asparagine (
CHEBI:28159
)
D
-asparaginyl group (
CHEBI:32653
)
is substituent group from
D
-asparagine (
CHEBI:28159
)
D
-asparagine zwitterion (
CHEBI:74337
)
is tautomer of
D
-asparagine (
CHEBI:28159
)
IUPAC Name
D
-asparagine
Synonyms
Sources
(2
R
)-2,4-diamino-4-oxobutanoic acid
IUPAC
(2
R
)-2-amino-3-carbamoylpropanoic acid
JCBN
(
R
)-2-amino-3-carbamoylpropanoic acid
ChEBI
D
-2-aminosuccinamic acid
ChEBI
D
-Asparagin
ChEBI
D-Asparagine
KEGG COMPOUND
D
-aspartic acid β-amide
ChEBI
DSG
PDBeChem
Manual Xrefs
Databases
C01905
KEGG COMPOUND
CN101333175
Patent
CPD-3633
MetaCyc
DB03943
DrugBank
DSG
PDBeChem
HMDB0033780
HMDB
YMDB00849
YMDB
View more database links
Registry Numbers
Types
Sources
101784
Gmelin Registry Number
Gmelin
1723526
Beilstein Registry Number
Beilstein
1723526
Reaxys Registry Number
Reaxys
2058-58-4
CAS Registry Number
KEGG COMPOUND
2058-58-4
CAS Registry Number
ChemIDplus
Citation
Type
Source
767332
PubMed citation
Europe PMC
Last Modified
25 November 2019