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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:32826 -
D
-allothreonine
Main
ChEBI Ontology
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ChEBI Name
D
-allothreonine
ChEBI ID
CHEBI:32826
ChEBI ASCII Name
D-allothreonine
Definition
The
D
-enantiomer of allothreonine. It occurs as a component of peptido-lipids in certain bacteria.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:31452, CHEBI:29378
Supplier Information
Download
Molfile
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Molfile
Formula
C4H9NO3
Net Charge
0
Average Mass
119.11920
Monoisotopic Mass
119.05824
InChI
InChI=1S/C4H9NO3/c1-2(6)3(5)4(7)8/h2-3,6H,5H2,1H3,(H,7,8)/t2-,3-/m1/s1
InChIKey
AYFVYJQAPQTCCC-PWNYCUMCSA-N
SMILES
C[C@@H](O)[C@@H](N)C(O)=O
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):
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
(via
2-amino-3-hydroxybutanoic acid
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
D
-allothreonine (
CHEBI:32826
)
has role
bacterial metabolite (
CHEBI:76969
)
D
-allothreonine (
CHEBI:32826
)
is a
D
-α-amino acid (
CHEBI:16733
)
D
-allothreonine (
CHEBI:32826
)
is a
allothreonine (
CHEBI:38262
)
D
-allothreonine (
CHEBI:32826
)
is enantiomer of
L
-allothreonine (
CHEBI:28718
)
D
-allothreonine (
CHEBI:32826
)
is tautomer of
D
-allothreonine zwitterion (
CHEBI:58645
)
Incoming
L
-allothreonine (
CHEBI:28718
)
is enantiomer of
D
-allothreonine (
CHEBI:32826
)
D
-allothreonine zwitterion (
CHEBI:58645
)
is tautomer of
D
-allothreonine (
CHEBI:32826
)
IUPAC Name
D
-allothreonine
Synonyms
Sources
(2
R
,3
R
)-2-amino-3-hydroxybutanoic acid
IUPAC
(2
R
,3
R
)-allothreonine
ChemIDplus
(
R
)-allothreonine
ChemIDplus
D-allo-Threonine
KEGG COMPOUND
D-Allothreonine
KEGG COMPOUND
Manual Xrefs
Databases
2TL
PDBeChem
C12317
KEGG COMPOUND
CPD-10303
MetaCyc
View more database links
Registry Numbers
Types
Sources
1721644
Reaxys Registry Number
Reaxys
24830-94-2
CAS Registry Number
ChemIDplus
Citations
Types
Sources
13717442
PubMed citation
Europe PMC
21190106
PubMed citation
Europe PMC
7410203
PubMed citation
Europe PMC
Last Modified
28 August 2020