CHEBI:136598 - 3-amino-D-alanine

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ChEBI Name 3-amino-D-alanine
ChEBI ID CHEBI:136598
ChEBI ASCII Name 3-amino-D-alanine
Definition A 3-aminoalanine that has R configuration.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Anne Morgat
Supplier Information
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Formula C3H8N2O2
Net Charge 0
Average Mass 104.109
Monoisotopic Mass 104.05858
InChI InChI=1S/C3H8N2O2/c4-1-2(5)3(6)7/h2H,1,4-5H2,(H,6,7)/t2-/m1/s1
InChIKey PECYZEOJVXMISF-UWTATZPHSA-N
SMILES [C@@H](N)(CN)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): Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
(via 3-aminoalanine )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 3-amino-D-alanine (CHEBI:136598) is a 3-aminoalanine (CHEBI:18383)
3-amino-D-alanine (CHEBI:136598) is a D-alanine derivative (CHEBI:83944)
3-amino-D-alanine (CHEBI:136598) is enantiomer of 3-amino-L-alanine (CHEBI:16303)
3-amino-D-alanine (CHEBI:136598) is tautomer of 3-amino-D-alanine zwitterion (CHEBI:136599)
Incoming 3-amino-L-alanine (CHEBI:16303) is enantiomer of 3-amino-D-alanine (CHEBI:136598)
3-amino-D-alanine zwitterion (CHEBI:136599) is tautomer of 3-amino-D-alanine (CHEBI:136598)
IUPAC Name
3-amino-D-alanine
Synonyms Sources
(2R)-2,3-bis(azanyl)propanoic acid PDBeChem
(2R)-2,3-diaminopropanoic acid IUPAC
(2R)-2,3-diaminopropionic acid ChEBI
(R)-2,3-diaminopropanoic acid ChEBI
(R)-2,3-diaminopropionic acid ChEBI
D-2,3-diaminopropanoic acid ChEBI
D-2,3-diaminopropionic acid ChEBI
D-DAP ChEBI
D-Dap-OH ChEBI
Manual Xref Database
2RA PDBeChem
View more database links
Registry Numbers Types Sources
1721399 Reaxys Registry Number Reaxys
1915-96-4 CAS Registry Number ChEBI
Citation Waiting for Citations Type Source
6814950 PubMed citation Europe PMC
Last Modified
25 November 2019