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Showing metabocard for Dopaquinone (HMDB0001229)

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enzymes (1) Show 1 protein
Record Information
Version5.0
StatusDetected but not Quantified
Creation Date2005-11-16 15:48:42 UTC
Update Date2023-02-21 17:15:32 UTC
HMDB IDHMDB0001229
Secondary Accession Numbers
  • HMDB01229
Metabolite Identification
Common NameDopaquinone
DescriptionDopaquinone, also known as o-dopaquinone or L-dopaquinone, is a member of the class of compounds known as L-alpha-amino acids. L-alpha-amino acids are alpha-amino acids which have the L-configuration of the alpha-carbon atom. Dopaquinone is slightly soluble (in water) and a moderately acidic compound (based on its pKa). L-Dopaquinone is a metabolite of L-DOPA and a precursor of melanin. Melanin is synthesized from tyrosine by hydroxylation to dihydroxyphenylalanine (DOPA) and subsequent oxidation to dopaquinone. Both reactions are catalyzed by the enzyme tyrosinase, which is the rate-limiting step. Dopaquinone has an ortho-quinone ring, which is known to be neurotoxic and highly reactive with many other compounds (PMID: 413870 ). Dopaquinone typically combines with cysteine to form pheomelanin (a pigment-polymer). Alternatively, dopaquinone can be converted to leucodopachrome and eventually to eumelanin (also a pigment-polymer). Dopaquinone can be found in skin and feces. Within the cell, dopaquinone is primarily located in the cytoplasm. Dopaquinone is involved in several metabolic disorders, some of which include transient tyrosinemia, hawkinsinuria, tyrosinemia type I, and alkaptonuria. Chronically high levels of dopaquinone are associated with Parkinson's disease (PD). Many Parkinson's patients are treated with L-DOPA. However, long-term treatment with L-DOPA may actually worsen symptoms or result in neurotic and psychotic symptoms. These may be due to dopachrome and dopaquinone accumulating in the brain of L-DOPA treated patients (PMID: 19131041 , PMID: 12373519 ).
Structure
Data?1676999732
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0001229 (Dopaquinone)

ChEBI
  Mrv1652309042000192D          

 14 14  0  0  1  0            999 V2000
    7.7084   -2.5947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4245   -3.0214    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9924   -3.0016    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.7310   -1.7673    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9699   -3.8291    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.2763   -2.5749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5520   -2.9675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5520   -3.8011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7972   -4.1731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1179   -3.7445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8727   -2.5388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3937   -4.1368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1323   -2.9026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4177   -2.4901    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  3  1  1  0  0  0  0
  4  1  2  0  0  0  0
  3  5  1  1  0  0  0
  6  3  1  0  0  0  0
  7  6  1  0  0  0  0
  8  7  1  0  0  0  0
 11  7  2  0  0  0  0
  9  8  2  0  0  0  0
 10  9  1  0  0  0  0
 13 10  1  0  0  0  0
 12 10  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
M  END
Download

3D MOL for HMDB0001229 (Dopaquinone)

HMDB0001229
     RDKit          3D
Dopaquinone
 23 23  0  0  0  0  0  0  0  0999 V2000
   -1.8238   -1.4433    0.4865 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9287   -0.0009    0.5539 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7513    0.6463    1.1874 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5390    0.4249    0.5311 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2356    1.4739    0.0619 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5260    1.2803   -0.5966 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2120    2.2320   -1.0510 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0601   -0.0673   -0.7437 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1807   -0.2689   -1.3123 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2573   -1.1579   -0.2140 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0787   -0.9129    0.3805 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1859    0.4733   -0.8277 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3110    1.7124   -0.9895 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2944   -0.3435   -1.9251 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4253   -1.8480   -0.2642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0093   -1.8549    1.4277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8719    0.2024    1.1195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9982    1.7446    1.2777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7200    0.3073    2.2652 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8283    2.4664    0.1780 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5980   -2.1767   -0.2920 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4853   -1.7419    0.7788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6813   -1.1474   -2.0322 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  2  0
  2 12  1  0
 12 13  2  0
 12 14  1  0
 11  4  1  0
  1 15  1  0
  1 16  1  0
  2 17  1  1
  3 18  1  0
  3 19  1  0
  5 20  1  0
 10 21  1  0
 11 22  1  0
 14 23  1  0
M  END
Download

3D SDF for HMDB0001229 (Dopaquinone)

ChEBI
  Mrv1652309042000192D          

 14 14  0  0  1  0            999 V2000
    7.7084   -2.5947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4245   -3.0214    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9924   -3.0016    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.7310   -1.7673    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9699   -3.8291    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.2763   -2.5749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5520   -2.9675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5520   -3.8011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7972   -4.1731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1179   -3.7445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8727   -2.5388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3937   -4.1368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1323   -2.9026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4177   -2.4901    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  3  1  1  0  0  0  0
  4  1  2  0  0  0  0
  3  5  1  1  0  0  0
  6  3  1  0  0  0  0
  7  6  1  0  0  0  0
  8  7  1  0  0  0  0
 11  7  2  0  0  0  0
  9  8  2  0  0  0  0
 10  9  1  0  0  0  0
 13 10  1  0  0  0  0
 12 10  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0001229

> <DATABASE_NAME>
hmdb

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

> <INCHI_IDENTIFIER>
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

> <INCHI_KEY>
AHMIDUVKSGCHAU-LURJTMIESA-N

> <FORMULA>
C9H9NO4

> <MOLECULAR_WEIGHT>
195.1721

> <EXACT_MASS>
195.053157781

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
23

> <JCHEM_AVERAGE_POLARIZABILITY>
18.058114570835116

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-2-amino-3-(3,4-dioxocyclohexa-1,5-dien-1-yl)propanoic acid

> <ALOGPS_LOGP>
-1.86

> <JCHEM_LOGP>
-2.0996093301828904

> <ALOGPS_LOGS>
-2.09

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8696975640830837

> <JCHEM_PKA_STRONGEST_BASIC>
9.06375153550613

> <JCHEM_POLAR_SURFACE_AREA>
97.46000000000001

> <JCHEM_REFRACTIVITY>
49.478100000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.58e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
dopaquinone

> <JCHEM_VEBER_RULE>
0

$$$$
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3D-SDF for HMDB0001229 (Dopaquinone)

HMDB0001229
     RDKit          3D
Dopaquinone
 23 23  0  0  0  0  0  0  0  0999 V2000
   -1.8238   -1.4433    0.4865 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9287   -0.0009    0.5539 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7513    0.6463    1.1874 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5390    0.4249    0.5311 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2356    1.4739    0.0619 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5260    1.2803   -0.5966 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2120    2.2320   -1.0510 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0601   -0.0673   -0.7437 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1807   -0.2689   -1.3123 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2573   -1.1579   -0.2140 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0787   -0.9129    0.3805 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1859    0.4733   -0.8277 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3110    1.7124   -0.9895 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2944   -0.3435   -1.9251 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4253   -1.8480   -0.2642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0093   -1.8549    1.4277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8719    0.2024    1.1195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9982    1.7446    1.2777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7200    0.3073    2.2652 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8283    2.4664    0.1780 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5980   -2.1767   -0.2920 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4853   -1.7419    0.7788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6813   -1.1474   -2.0322 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  2  0
  2 12  1  0
 12 13  2  0
 12 14  1  0
 11  4  1  0
  1 15  1  0
  1 16  1  0
  2 17  1  1
  3 18  1  0
  3 19  1  0
  5 20  1  0
 10 21  1  0
 11 22  1  0
 14 23  1  0
M  END
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PDB for HMDB0001229 (Dopaquinone)

HEADER    PROTEIN                                 04-SEP-20   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: ChEBI                                             
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-20         0                                  
HETATM    1  C   UNK     0      14.389  -4.843   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      15.726  -5.640   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      13.052  -5.603   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      14.431  -3.299   0.000  0.00  0.00           O+0
HETATM    5  N   UNK     0      13.010  -7.148   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      11.716  -4.806   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.364  -5.539   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.364  -7.095   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.955  -7.790   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.687  -6.990   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.096  -4.739   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       6.335  -7.722   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       7.714  -5.418   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       6.380  -4.648   0.000  0.00  0.00           O+0
CONECT    1    2    3    4                                                  
CONECT    2    1                                                            
CONECT    3    1    5    6                                                  
CONECT    4    1                                                            
CONECT    5    3                                                            
CONECT    6    3    7                                                       
CONECT    7    6    8   11                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   13   12                                                  
CONECT   11    7   13                                                       
CONECT   12   10                                                            
CONECT   13   10   11   14                                                  
CONECT   14   13                                                            
MASTER        0    0    0    0    0    0    0    0   14    0   28    0
END
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3D PDB for HMDB0001229 (Dopaquinone)

COMPND    HMDB0001229
HETATM    1  N1  UNL     1      -1.824  -1.443   0.486  1.00  0.00           N  
HETATM    2  C1  UNL     1      -1.929  -0.001   0.554  1.00  0.00           C  
HETATM    3  C2  UNL     1      -0.751   0.646   1.187  1.00  0.00           C  
HETATM    4  C3  UNL     1       0.539   0.425   0.531  1.00  0.00           C  
HETATM    5  C4  UNL     1       1.236   1.474   0.062  1.00  0.00           C  
HETATM    6  C5  UNL     1       2.526   1.280  -0.597  1.00  0.00           C  
HETATM    7  O1  UNL     1       3.212   2.232  -1.051  1.00  0.00           O  
HETATM    8  C6  UNL     1       3.060  -0.067  -0.744  1.00  0.00           C  
HETATM    9  O2  UNL     1       4.181  -0.269  -1.312  1.00  0.00           O  
HETATM   10  C7  UNL     1       2.257  -1.158  -0.214  1.00  0.00           C  
HETATM   11  C8  UNL     1       1.079  -0.913   0.380  1.00  0.00           C  
HETATM   12  C9  UNL     1      -2.186   0.473  -0.828  1.00  0.00           C  
HETATM   13  O3  UNL     1      -2.311   1.712  -0.990  1.00  0.00           O  
HETATM   14  O4  UNL     1      -2.294  -0.344  -1.925  1.00  0.00           O  
HETATM   15  H1  UNL     1      -2.425  -1.848  -0.264  1.00  0.00           H  
HETATM   16  H2  UNL     1      -2.009  -1.855   1.428  1.00  0.00           H  
HETATM   17  H3  UNL     1      -2.872   0.202   1.120  1.00  0.00           H  
HETATM   18  H4  UNL     1      -0.998   1.745   1.278  1.00  0.00           H  
HETATM   19  H5  UNL     1      -0.720   0.307   2.265  1.00  0.00           H  
HETATM   20  H6  UNL     1       0.828   2.466   0.178  1.00  0.00           H  
HETATM   21  H7  UNL     1       2.598  -2.177  -0.292  1.00  0.00           H  
HETATM   22  H8  UNL     1       0.485  -1.742   0.779  1.00  0.00           H  
HETATM   23  H9  UNL     1      -1.681  -1.147  -2.032  1.00  0.00           H  
CONECT    1    2   15   16
CONECT    2    3   12   17
CONECT    3    4   18   19
CONECT    4    5    5   11
CONECT    5    6   20
CONECT    6    7    7    8
CONECT    8    9    9   10
CONECT   10   11   11   21
CONECT   11   22
CONECT   12   13   13   14
CONECT   14   23
END
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SMILES for HMDB0001229 (Dopaquinone)

N[C@@H](CC1=CC(=O)C(=O)C=C1)C(O)=O
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INCHI for HMDB0001229 (Dopaquinone)

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
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View in JSmolView NMR AssignmentsView Stereo Labels
Synonyms
ValueSource
(S)-2-Amino-3-(3,4-dioxocyclohexa-1,5-dien-1-yl)propanoateChEBI
(S)-2-Amino-3-(3,4-dioxocyclohexa-1,5-dien-1-yl)propanoic acidGenerator
O-DopaquinoneHMDB
4-(2-Carboxy-2-aminoethyl)-1,2-benzoquinoneHMDB
Dopaquinone, (S)-isomerHMDB
L-DopaquinoneHMDB
Chemical FormulaC9H9NO4
Average Molecular Weight195.1721
Monoisotopic Molecular Weight195.053157781
IUPAC Name(2S)-2-amino-3-(3,4-dioxocyclohexa-1,5-dien-1-yl)propanoic acid
Traditional Namedopaquinone
CAS Registry Number4430-97-1
SMILES
N[C@@H](CC1=CC(=O)C(=O)C=C1)C(O)=O
InChI Identifier
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
InChI KeyAHMIDUVKSGCHAU-LURJTMIESA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom.
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
Sub ClassAmino acids, peptides, and analogues
Direct ParentL-alpha-amino acids
Alternative Parents
Substituents
  • L-alpha-amino acid
  • O-benzoquinone
  • Quinone
  • Ketone
  • Amino acid
  • Cyclic ketone
  • Carboxylic acid
  • Monocarboxylic acid or derivatives
  • Amine
  • Hydrocarbon derivative
  • Primary amine
  • Organooxygen compound
  • Organonitrogen compound
  • Organic oxide
  • Organopnictogen compound
  • Primary aliphatic amine
  • Organic oxygen compound
  • Organic nitrogen compound
  • Carbonyl group
  • Aliphatic homomonocyclic compound
Molecular FrameworkAliphatic homomonocyclic compounds
External Descriptors
Ontology
Physiological effectNot Available
Disposition
Biological locationSource
Process
Naturally occurring process
RoleNot Available
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility1.58 g/LALOGPS
logP-1.9ALOGPS
logP-2.1ChemAxon
logS-2.1ALOGPS
pKa (Strongest Acidic)1.87ChemAxon
pKa (Strongest Basic)9.06ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count5ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area97.46 ŲChemAxon
Rotatable Bond Count3ChemAxon
Refractivity49.48 m³·mol⁻¹ChemAxon
Polarizability18.06 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+147.00431661259
DarkChem[M-H]-138.67931661259
AllCCS[M+H]+142.47732859911
AllCCS[M-H]-139.83232859911
DeepCCS[M+H]+144.99430932474
DeepCCS[M-H]-142.59830932474
DeepCCS[M-2H]-175.82630932474
DeepCCS[M+Na]+150.91330932474
AllCCS[M+H]+142.532859911
AllCCS[M+H-H2O]+138.432859911
AllCCS[M+NH4]+146.332859911
AllCCS[M+Na]+147.432859911
AllCCS[M-H]-139.832859911
AllCCS[M+Na-2H]-140.432859911
AllCCS[M+HCOO]-141.132859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
DopaquinoneN[C@@H](CC1=CC(=O)C(=O)C=C1)C(O)=O2992.9Standard polar33892256
DopaquinoneN[C@@H](CC1=CC(=O)C(=O)C=C1)C(O)=O1669.1Standard non polar33892256
DopaquinoneN[C@@H](CC1=CC(=O)C(=O)C=C1)C(O)=O2072.5Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Dopaquinone,1TMS,isomer #1C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(=O)C(=O)C=C12063.1Semi standard non polar33892256
Dopaquinone,1TMS,isomer #2C[Si](C)(C)N[C@@H](CC1=CC(=O)C(=O)C=C1)C(=O)O2136.6Semi standard non polar33892256
Dopaquinone,2TMS,isomer #1C[Si](C)(C)N[C@@H](CC1=CC(=O)C(=O)C=C1)C(=O)O[Si](C)(C)C2162.5Semi standard non polar33892256
Dopaquinone,2TMS,isomer #1C[Si](C)(C)N[C@@H](CC1=CC(=O)C(=O)C=C1)C(=O)O[Si](C)(C)C2039.3Standard non polar33892256
Dopaquinone,2TMS,isomer #1C[Si](C)(C)N[C@@H](CC1=CC(=O)C(=O)C=C1)C(=O)O[Si](C)(C)C3018.7Standard polar33892256
Dopaquinone,2TMS,isomer #2C[Si](C)(C)N([C@@H](CC1=CC(=O)C(=O)C=C1)C(=O)O)[Si](C)(C)C2268.6Semi standard non polar33892256
Dopaquinone,2TMS,isomer #2C[Si](C)(C)N([C@@H](CC1=CC(=O)C(=O)C=C1)C(=O)O)[Si](C)(C)C2106.1Standard non polar33892256
Dopaquinone,2TMS,isomer #2C[Si](C)(C)N([C@@H](CC1=CC(=O)C(=O)C=C1)C(=O)O)[Si](C)(C)C3121.6Standard polar33892256
Dopaquinone,3TMS,isomer #1C[Si](C)(C)OC(=O)[C@H](CC1=CC(=O)C(=O)C=C1)N([Si](C)(C)C)[Si](C)(C)C2276.6Semi standard non polar33892256
Dopaquinone,3TMS,isomer #1C[Si](C)(C)OC(=O)[C@H](CC1=CC(=O)C(=O)C=C1)N([Si](C)(C)C)[Si](C)(C)C2183.4Standard non polar33892256
Dopaquinone,3TMS,isomer #1C[Si](C)(C)OC(=O)[C@H](CC1=CC(=O)C(=O)C=C1)N([Si](C)(C)C)[Si](C)(C)C2949.5Standard polar33892256
Dopaquinone,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(=O)C(=O)C=C12328.9Semi standard non polar33892256
Dopaquinone,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(=O)C(=O)C=C1)C(=O)O2387.6Semi standard non polar33892256
Dopaquinone,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(=O)C(=O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C2642.8Semi standard non polar33892256
Dopaquinone,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(=O)C(=O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C2501.2Standard non polar33892256
Dopaquinone,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(=O)C(=O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C3149.8Standard polar33892256
Dopaquinone,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)N([C@@H](CC1=CC(=O)C(=O)C=C1)C(=O)O)[Si](C)(C)C(C)(C)C2772.2Semi standard non polar33892256
Dopaquinone,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)N([C@@H](CC1=CC(=O)C(=O)C=C1)C(=O)O)[Si](C)(C)C(C)(C)C2535.4Standard non polar33892256
Dopaquinone,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)N([C@@H](CC1=CC(=O)C(=O)C=C1)C(=O)O)[Si](C)(C)C(C)(C)C3226.8Standard polar33892256
Dopaquinone,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC1=CC(=O)C(=O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2996.1Semi standard non polar33892256
Dopaquinone,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC1=CC(=O)C(=O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2809.2Standard non polar33892256
Dopaquinone,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC1=CC(=O)C(=O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3101.0Standard polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Dopaquinone GC-MS (Non-derivatized) - 70eV, Positivesplash10-0fml-5900000000-3f77b48d5f42d89513242017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Dopaquinone GC-MS (1 TMS) - 70eV, Positivesplash10-00di-9570000000-5d835cfbd2b202044cb72017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Dopaquinone GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Dopaquinone 10V, Positive-QTOFsplash10-0ufs-0900000000-093c511b443d879169302017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Dopaquinone 20V, Positive-QTOFsplash10-0ue9-1900000000-fc3bdef4314080b351c12017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Dopaquinone 40V, Positive-QTOFsplash10-0uxr-9200000000-07d0c6318c984ef80e412017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Dopaquinone 10V, Negative-QTOFsplash10-0006-0900000000-7481c7c6fe6294da272c2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Dopaquinone 20V, Negative-QTOFsplash10-002f-0900000000-04347396e1171463fb622017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Dopaquinone 40V, Negative-QTOFsplash10-00di-7900000000-13ce3640966908fffe552017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Dopaquinone 10V, Negative-QTOFsplash10-0006-0900000000-c319fd057861dc7d7ad42021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Dopaquinone 20V, Negative-QTOFsplash10-00e9-3900000000-b64033d6c2ec2ca4314b2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Dopaquinone 40V, Negative-QTOFsplash10-00di-5900000000-cde5f7d52f36428ed06e2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Dopaquinone 10V, Positive-QTOFsplash10-0udj-0900000000-2ca1383c9487e79be90a2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Dopaquinone 20V, Positive-QTOFsplash10-0ff0-0900000000-92f4bf729acf4be5b6bf2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Dopaquinone 40V, Positive-QTOFsplash10-00e9-8900000000-d3972df871a20993fe052021-09-25Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum

IR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M-H]-)2023-02-03FELIX labView Spectrum
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+H]+)2023-02-03FELIX labView Spectrum
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+Na]+)2023-02-03FELIX labView Spectrum
Biological Properties
Cellular Locations
  • Cytoplasm
Biospecimen Locations
  • Feces
Tissue LocationsNot Available
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
FecesDetected but not QuantifiedNot QuantifiedAdult (>18 years old)BothNormal details
FecesDetected but not QuantifiedNot QuantifiedChildren (1-13 years old)BothNormal details
Abnormal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
FecesDetected but not QuantifiedNot QuantifiedAdult (>18 years old)BothCCD details
FecesDetected but not QuantifiedNot QuantifiedAdult (>18 years old)BothIleal Crohn's disease details
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB022501
KNApSAcK IDNot Available
Chemspider ID388447
KEGG Compound IDC00822
BioCyc IDDOPAQUINONE
BiGG ID36114
Wikipedia LinkL-Dopaquinone
METLIN ID354
PubChem Compound439316
PDB IDNot Available
ChEBI ID16852
Food Biomarker OntologyNot Available
VMH IDDOPAQN
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceLand E J; Riley P A Spontaneous redox reactions of dopaquinone and the balance between the eumelanic and phaeomelanic pathways. Pigment cell research / sponsored by the European Society for Pigment Cell Research and the International Pigment Cell Society (2000), 13(4), 273-7.
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Rorsman H, Tegner E: Biochemical observations in UV-induced pigmentation. Photodermatol. 1988 Feb;5(1):30-8. [PubMed:3281148 ]
  2. Tsukamoto K, Furue M, Sato Y, Takayama O, Akasu R, Ohtake N, Wakamatsu K, Ito S, Tamaki K, Shimada S: Generalized melanosis in metastatic malignant melanoma: the possible role of DOPAquinone metabolites. Dermatology. 1998;197(4):338-42. [PubMed:9873171 ]
  3. Graham DG, Tiffany SM, Vogel FS: The toxicity of melanin precursors. J Invest Dermatol. 1978 Feb;70(2):113-6. [PubMed:413870 ]
  4. Hattoria N, Wanga M, Taka H, Fujimura T, Yoritaka A, Kubo S, Mochizuki H: Toxic effects of dopamine metabolism in Parkinson's disease. Parkinsonism Relat Disord. 2009 Jan;15 Suppl 1:S35-8. doi: 10.1016/S1353-8020(09)70010-0. [PubMed:19131041 ]
  5. Kostrzewa RM, Kostrzewa JP, Brus R: Neuroprotective and neurotoxic roles of levodopa (L-DOPA) in neurodegenerative disorders relating to Parkinson's disease. Amino Acids. 2002;23(1-3):57-63. doi: 10.1007/s00726-001-0110-x. [PubMed:12373519 ]

Enzymes

Enzyme Details
1. Tyrosinase
General function:
Involved in oxidoreductase activity
Specific function:
This is a copper-containing oxidase that functions in the formation of pigments such as melanins and other polyphenolic compounds. Catalyzes the rate-limiting conversions of tyrosine to DOPA, DOPA to DOPA-quinone and possibly 5,6-dihydroxyindole to indole-5,6 quinone.
Gene Name:
TYR
Uniprot ID:
P14679
Molecular weight:
60392.69
Reactions
L-Dopa + Oxygen → Dopaquinone + Waterdetails
L-Tyrosine + Oxygen → Dopaquinone + Waterdetails
L-Dopa + L-Tyrosine + Oxygen → Dopaquinone + L-Dopa + Waterdetails