CHEBI:32826 - D-allothreonine

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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
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Formula C4H9NO3
Net Charge 0
Average Mass 119.11920
Monoisotopic Mass 119.058
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 (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): 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 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
(2R,3R)-2-amino-3-hydroxybutanoic acid IUPAC
(2R,3R)-allothreonine ChemIDplus
(R)-allothreonine ChemIDplus
D-allo-Threonine KEGG COMPOUND
D-Allothreonine KEGG COMPOUND
Database Links Databases
2TL PDBeChem
C12317 KEGG COMPOUND
CPD-10303 MetaCyc
View more database links
Registry Numbers Types Sources
1721644 Reaxys Registry Number Reaxys
1721644 Beilstein Registry Number ChemIDplus
24830-94-2 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
13717442 PubMed citation Europe PMC
21190106 PubMed citation Europe PMC
7410203 PubMed citation Europe PMC
Last Modified
28 July 2014