CHEBI:49169 - D-dopa

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ChEBI Name D-dopa ChEBI ID CHEBI:49169 ChEBI ASCII Name D-dopa Definition The D-enantiomer of dopa. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Wikipedia License Read full article at Wikipedia Formula C9H11NO4 Net Charge 0 Average Mass 197.18798 Monoisotopic Mass 197.06881 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 InChIKey WTDRDQBEARUVNC-ZCFIWIBFSA-N 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) D-dopa (CHEBI:49169) is tautomer of D-dopa zwitterion (CHEBI:149689) Incoming N-methyl-D-dopa (CHEBI:167647) has functional parent D-dopa (CHEBI:49169) L-dopa (CHEBI:15765) is enantiomer of D-dopa (CHEBI:49169) D-dopa zwitterion (CHEBI:149689) is tautomer of D-dopa (CHEBI:49169) IUPAC Names (2R)-2-amino-3-(3,4-dihydroxyphenyl)propanoic acid D-dopa 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 View more database links 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 Types Sources 21210766 PubMed citation Europe PMC 22454242 PubMed citation Europe PMC 24190293 PubMed citation Europe PMC 3129126 PubMed citation Europe PMC Last Modified 12 March 2021