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Details

Stereochemistry ABSOLUTE
Molecular Formula C9H9NO4
Molecular Weight 195.1721
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DOPAQUINONE

SMILES

N[C@@H](CC1=CC(=O)C(=O)C=C1)C(O)=O

InChI

InChIKey=AHMIDUVKSGCHAU-LURJTMIESA-N
InChI=1S/C9H9NO4/c10-6(9(13)14)3-5-1-2-7(11)8(12)4-5/h1-2,4,6H,3,10H2,(H,13,14)/t6-/m0/s1

HIDE SMILES / InChI

Molecular Formula C9H9NO4
Molecular Weight 195.1721
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Biochemical observations in UV-induced pigmentation.
1988 Feb
Generalized melanosis in metastatic malignant melanoma: the possible role of DOPAquinone metabolites.
1998
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 19:50:19 GMT 2023
Edited
by admin
on Fri Dec 15 19:50:19 GMT 2023
Record UNII
8F09Y50AX6
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DOPAQUINONE
Common Name English
1,5-CYCLOHEXADIENE-1-PROPIONIC ACID, .ALPHA.-AMINO-3,4-DIOXO-, L-
Common Name English
(.ALPHA.S)-.ALPHA.-AMINO-3,4-DIOXO-1,5-CYCLOHEXADIENE-1-PROPANOIC ACID
Common Name English
L-DOPA SEMIQUINONE
Common Name English
1,5-CYCLOHEXADIENE-1-PROPANOIC ACID, .ALPHA.-AMINO-3,4-DIOXO-, (.ALPHA.S)-
Common Name English
1,5-CYCLOHEXADIENE-1-PROPIONIC ACID, .ALPHA.-AMINO-3,4-DIOXO-, S-
Common Name English
Code System Code Type Description
WIKIPEDIA
Dopaquinone
Created by admin on Fri Dec 15 19:50:19 GMT 2023 , Edited by admin on Fri Dec 15 19:50:19 GMT 2023
PRIMARY
CHEBI
16852
Created by admin on Fri Dec 15 19:50:19 GMT 2023 , Edited by admin on Fri Dec 15 19:50:19 GMT 2023
PRIMARY
CAS
25520-73-4
Created by admin on Fri Dec 15 19:50:19 GMT 2023 , Edited by admin on Fri Dec 15 19:50:19 GMT 2023
PRIMARY
PUBCHEM
439316
Created by admin on Fri Dec 15 19:50:19 GMT 2023 , Edited by admin on Fri Dec 15 19:50:19 GMT 2023
PRIMARY
FDA UNII
8F09Y50AX6
Created by admin on Fri Dec 15 19:50:19 GMT 2023 , Edited by admin on Fri Dec 15 19:50:19 GMT 2023
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER