CHEBI:16733 - D-α-amino acid

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name D-α-amino acid
ChEBI ID CHEBI:16733
ChEBI ASCII Name D-alpha-amino acid
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:4097, CHEBI:13625, CHEBI:12909, CHEBI:20906
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Formulae C2H4NO2R
C2H4NO2R
Net Charge 0
Average Mass (excl. R groups) 74.05870
Monoisotopic Mass (excl. R groups) 74.02420
SMILES N[C@H]([*])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 )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing D-α-amino acid (CHEBI:16733) is a non-proteinogenic α-amino acid (CHEBI:83925)
D-α-amino acid (CHEBI:16733) is conjugate acid of D-α-amino acid anion (CHEBI:60895)
D-α-amino acid (CHEBI:16733) is tautomer of D-α-amino acid zwitterion (CHEBI:59871)
Incoming pradimicin (CHEBI:83230) has functional parent D-α-amino acid (CHEBI:16733)
β-(2-thienyl)-D-alanine (CHEBI:77819) is a D-α-amino acid (CHEBI:16733)
γ-D-glutamyl-meso-diaminopimelic acid (CHEBI:59271) is a D-α-amino acid (CHEBI:16733)
(1S,2S)-2-[(1S)-1-amino-1-carboxyethyl]-1-cyclopropanecarboxylic acid (CHEBI:125551) is a D-α-amino acid (CHEBI:16733)
(2R)-2-amino-6-hydroxy-4-hexynoic acid (CHEBI:204524) is a D-α-amino acid (CHEBI:16733)
(3R)-3-methyl-D-ornithine (CHEBI:64693) is a D-α-amino acid (CHEBI:16733)
(3R,5R)-5-amino-3-methyl-D-proline (CHEBI:46486) is a D-α-amino acid (CHEBI:16733)
(R)-1-Methylpiperidine-2-carboxylic acid (CHEBI:230033) is a D-α-amino acid (CHEBI:16733)
2-Amino-8-oxo-9,10-epoxy-decanoic acid (CHEBI:165431) is a D-α-amino acid (CHEBI:16733)
2-methyl-L-arginine (CHEBI:223950) is a D-α-amino acid (CHEBI:16733)
2R-amino-4S-hydroxy-5-hexynoic acid (CHEBI:203879) is a D-α-amino acid (CHEBI:16733)
3-fluoro-D-tyrosine (CHEBI:32770) is a D-α-amino acid (CHEBI:16733)
3-hydroxy-D-aspartic acid (CHEBI:60887) is a D-α-amino acid (CHEBI:16733)
3-nitro-D-tyrosine (CHEBI:86270) is a D-α-amino acid (CHEBI:16733)
4-methylene-D-glutamic acid (CHEBI:48032) is a D-α-amino acid (CHEBI:16733)
5-hydroxy-D-tryptophan (CHEBI:43186) is a D-α-amino acid (CHEBI:16733)
6-chloro-D-tryptophan (CHEBI:140515) is a D-α-amino acid (CHEBI:16733)
7-chloro-D-tryptophan (CHEBI:55355) is a D-α-amino acid (CHEBI:16733)
N-(5'-phosphopyridoxyl)-D-alanine (CHEBI:44743) is a D-α-amino acid (CHEBI:16733)
N-formyl-D-kynurenine (CHEBI:55476) is a D-α-amino acid (CHEBI:16733)
N-methyl-D-aspartic acid (CHEBI:31882) is a D-α-amino acid (CHEBI:16733)
N6-[(2-amino-4-oxo-3,4-dihydropteridin-6-yl)methyl]-D-lysine (CHEBI:76630) is a D-α-amino acid (CHEBI:16733)
O-ureido-D-serine (CHEBI:74212) is a D-α-amino acid (CHEBI:16733)
O4-phospho-D-tyrosine (CHEBI:74959) is a D-α-amino acid (CHEBI:16733)
p-N,N-bis(2-chloroethyl)amino-D-phenylalanine (CHEBI:25814) is a D-α-amino acid (CHEBI:16733)
Se-methyl-D-selenocysteine (CHEBI:53125) is a D-α-amino acid (CHEBI:16733)
Se-methyl-D-selenomethionine (CHEBI:156247) is a D-α-amino acid (CHEBI:16733)
D-α-aminobutyric acid (CHEBI:28797) is a D-α-amino acid (CHEBI:16733)
D-2-aminopentanoic acid (CHEBI:28804) is a D-α-amino acid (CHEBI:16733)
D-alanine (CHEBI:15570) is a D-α-amino acid (CHEBI:16733)
D-alloisoleucine (CHEBI:20899) is a D-α-amino acid (CHEBI:16733)
D-allothreonine (CHEBI:32826) is a D-α-amino acid (CHEBI:16733)
D-arginine (CHEBI:15816) is a D-α-amino acid (CHEBI:16733)
D-asparagine (CHEBI:28159) is a D-α-amino acid (CHEBI:16733)
D-aspartic acid (CHEBI:17364) is a D-α-amino acid (CHEBI:16733)
D-cysteine (CHEBI:16375) is a D-α-amino acid (CHEBI:16733)
D-glutamic acid (CHEBI:15966) is a D-α-amino acid (CHEBI:16733)
D-glutamine (CHEBI:17061) is a D-α-amino acid (CHEBI:16733)
D-histidine (CHEBI:27947) is a D-α-amino acid (CHEBI:16733)
D-homoserine (CHEBI:30654) is a D-α-amino acid (CHEBI:16733)
D-isoleucine (CHEBI:27730) is a D-α-amino acid (CHEBI:16733)
D-kynurenine (CHEBI:86262) is a D-α-amino acid (CHEBI:16733)
D-leucine (CHEBI:28225) is a D-α-amino acid (CHEBI:16733)
D-lysine (CHEBI:16855) is a D-α-amino acid (CHEBI:16733)
D-methionine (CHEBI:16867) is a D-α-amino acid (CHEBI:16733)
D-ornithine (CHEBI:16176) is a D-α-amino acid (CHEBI:16733)
D-phenylalanine (CHEBI:16998) is a D-α-amino acid (CHEBI:16733)
D-proline (CHEBI:16313) is a D-α-amino acid (CHEBI:16733)
D-selenocysteine (CHEBI:30001) is a D-α-amino acid (CHEBI:16733)
D-serine (CHEBI:16523) is a D-α-amino acid (CHEBI:16733)
D-thioproline (CHEBI:64562) is a D-α-amino acid (CHEBI:16733)
D-threonine (CHEBI:16398) is a D-α-amino acid (CHEBI:16733)
D-tryptophan (CHEBI:16296) is a D-α-amino acid (CHEBI:16733)
D-tyrosine (CHEBI:28479) is a D-α-amino acid (CHEBI:16733)
D-valine (CHEBI:27477) is a D-α-amino acid (CHEBI:16733)
alpha-methylmethionine (CHEBI:191230) is a D-α-amino acid (CHEBI:16733)
D-4-dihydroxyphenylglycine (CHEBI:20892) is a D-α-amino acid (CHEBI:16733)
D-Capreomycidin (CHEBI:220901) is a D-α-amino acid (CHEBI:16733)
delta-Citryl-d-ornithine (CHEBI:181938) is a D-α-amino acid (CHEBI:16733)
DL-threo-beta-Methylaspartate (CHEBI:194704) is a D-α-amino acid (CHEBI:16733)
Enantiopyochelin (CHEBI:219599) is a D-α-amino acid (CHEBI:16733)
LSM-12459 (CHEBI:101088) is a D-α-amino acid (CHEBI:16733)
Muscazone (CHEBI:221476) is a D-α-amino acid (CHEBI:16733)
nocardicin A (CHEBI:17711) is a D-α-amino acid (CHEBI:16733)
nocardicin C (CHEBI:81021) is a D-α-amino acid (CHEBI:16733)
O-Benzyl-D-serine (CHEBI:229987) is a D-α-amino acid (CHEBI:16733)
tauropine (CHEBI:16461) is a D-α-amino acid (CHEBI:16733)
D-α-amino acid anion (CHEBI:60895) is conjugate base of D-α-amino acid (CHEBI:16733)
D-α-amino acid residue (CHEBI:142417) is substituent group from D-α-amino acid (CHEBI:16733)
D-α-amino acid zwitterion (CHEBI:59871) is tautomer of D-α-amino acid (CHEBI:16733)
IUPAC Name
D-α-amino acids
Synonyms Sources
D-α-amino acid ChEBI
D-α-amino acids ChEBI
D-Amino acid KEGG COMPOUND
Manual Xref Database
C00405 KEGG COMPOUND
View more database links
Last Modified
28 August 2020