CHEBI:49169 - D-dopa

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ChEBI Name D-dopa
ChEBI ASCII Name D-dopa
Definition The D-enantiomer of dopa.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C9H11NO4
Net Charge 0
Average Mass 197.18798
Monoisotopic Mass 197.069
InChI InChI=1S/C9H11NO4/c10-6(9(13)14)3-5-1-2-7(11)8(12)4-5/h1-2,4,6,11-12H,3,10H2,(H,13,14)/t6-/m1/s1
SMILES N[C@H](Cc1ccc(O)c(O)c1)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): human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
(via dopa )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing D-dopa (CHEBI:49169) is a D-tyrosine derivative (CHEBI:84124)
D-dopa (CHEBI:49169) is a dopa (CHEBI:49168)
D-dopa (CHEBI:49169) is enantiomer of L-dopa (CHEBI:15765)
Incoming L-dopa (CHEBI:15765) is enantiomer of D-dopa (CHEBI:49169)
(2R)-2-amino-3-(3,4-dihydroxyphenyl)propanoic acid
Synonyms Sources
(+)-3,4-dihydroxyphenylalanine ChemIDplus
(+)-3-(3,4-dihydroxyphenyl)alanine ChemIDplus
3,4-dihydroxy-D-phenylalanine ChemIDplus
3-hydroxy-D-tyrosine ChemIDplus
D-3,4-dihydroxyphenylalanine ChemIDplus
D-3-(3,4-dihydroxyphenyl)alanine ChemIDplus
dopa D-form ChemIDplus
Manual Xref Database
D-DOPA Wikipedia
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Registry Numbers Types Sources
1862048 Gmelin Registry Number Gmelin
2417637 Reaxys Registry Number Reaxys
2417637 Beilstein Registry Number Beilstein
5796-17-8 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
21210766 PubMed citation Europe PMC
22454242 PubMed citation Europe PMC
24190293 PubMed citation Europe PMC
3129126 PubMed citation Europe PMC
Last Modified
17 December 2014