CHEBI:28718 - L-allothreonine

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ChEBI Name L-allothreonine
ChEBI ASCII Name L-allothreonine
Definition The L-enantiomer of allothreonine.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:40698, CHEBI:6174, CHEBI:21221
Supplier Information
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Formula C4H9NO3
Net Charge 0
Average Mass 119.120
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-/m0/s1
SMILES C([C@H]([C@@H](O)C)N)(=O)O
Metabolite of Species Details
Saccharomyces cerevisiae (NCBI:txid4932) Source: See: PubMed
Escherichia coli (NCBI:txid562) See: PubMed
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): Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
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 L-allothreonine (CHEBI:28718) has role Escherichia coli metabolite (CHEBI:76971)
L-allothreonine (CHEBI:28718) has role Saccharomyces cerevisiae metabolite (CHEBI:75772)
L-allothreonine (CHEBI:28718) is a L-α-amino acid (CHEBI:15705)
L-allothreonine (CHEBI:28718) is a allothreonine (CHEBI:38262)
L-allothreonine (CHEBI:28718) is enantiomer of D-allothreonine (CHEBI:32826)
L-allothreonine (CHEBI:28718) is tautomer of L-allothreonine zwitterion (CHEBI:58585)
Incoming D-allothreonine (CHEBI:32826) is enantiomer of L-allothreonine (CHEBI:28718)
L-allothreonine zwitterion (CHEBI:58585) is tautomer of L-allothreonine (CHEBI:28718)
Synonyms Sources
(2S,3S)-2-amino-3-hydroxybutanoic acid IUPAC
allo-L-threonine ChemIDplus
L-allo-Threonine KEGG COMPOUND
L-Allothreonine KEGG COMPOUND
Manual Xrefs Databases
HMDB0004041 HMDB
View more database links
Registry Numbers Types Sources
1721645 Beilstein Registry Number ChemIDplus
1721645 Reaxys Registry Number Reaxys
28954-12-3 CAS Registry Number KEGG COMPOUND
28954-12-3 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
15726349 PubMed citation Europe PMC
17597243 PubMed citation Europe PMC
9151955 PubMed citation Europe PMC
Last Modified
28 August 2020