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Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References enzymes (18) Show 18 proteins XML

Record Information

Version

5.0

Status

Detected and Quantified

Creation Date

2008-09-15 17:06:35 UTC

Update Date

2021-09-14 14:57:35 UTC

HMDB ID

HMDB0010329

Secondary Accession Numbers

HMDB10329

Metabolite Identification

Common Name

Dopamine glucuronide

Description

Dopamine glucuronide is a natural human metabolite of Dopamine generated in the liver by UDP glucuonyltransferase. Glucuronidation is used to assist in the excretion of toxic substances, drugs or other substances that cannot be used as an energy source. Glucuronic acid is attached via a glycosidic bond to the substance, and the resulting glucuronide, which has a much higher water solubility than the original substance, is eventually excreted by the kidneys.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

HMDB0010329
     RDKit          3D
Dopamine glucuronide
 42 43  0  0  0  0  0  0  0  0999 V2000
    6.9930    0.0924   -1.0316 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.5738    0.4074   -0.9136 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8518   -0.9090   -0.7391 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3775   -0.7078   -0.6067 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8542   -0.5261    0.6394 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4912   -0.3373    0.7927 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6241   -0.3246   -0.2758 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7233   -0.1417   -0.1637 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4852    0.0611    0.9829 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3931   -0.9672    1.1049 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6851   -0.6699    0.7605 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4449   -1.9260    0.5586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9106   -3.0478    0.7028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7756   -1.8867    0.2024 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6174    0.1404   -0.5357 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8466    0.1274   -1.1903 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2146    1.5389   -0.1231 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7507    2.2688   -1.2175 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1253    1.4265    0.9068 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7197    1.6752    2.1650 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1743   -0.5106   -1.5315 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4126   -0.5199   -2.6926 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5436   -0.7003   -1.6867 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4971    0.2075   -0.1237 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1165   -0.8698   -1.4303 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4607    1.0160    0.0046 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2752    0.9458   -1.8134 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9913   -1.5623   -1.6222 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2606   -1.4449    0.1265 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5287   -0.5335    1.4934 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1292   -0.1996    1.7844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8710    0.0680    1.9320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1570   -0.0547    1.5508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4756   -1.8256    0.9399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8137   -0.2620   -1.1856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0302    1.0749   -1.4691 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1113    2.0663    0.2741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0637    3.2201   -1.1733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3752    2.2079    0.6928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9707    2.6269    2.2440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5726   -0.3972   -2.7322 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9777   -0.8468   -2.6754 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
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 11 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
  7 21  1  0
 21 22  1  0
 21 23  2  0
 23  4  1  0
 19  9  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  2 27  1  0
  3 28  1  0
  3 29  1  0
  5 30  1  0
  6 31  1  0
  9 32  1  1
 11 33  1  1
 14 34  1  0
 15 35  1  6
 16 36  1  0
 17 37  1  1
 18 38  1  0
 19 39  1  6
 20 40  1  0
 22 41  1  0
 23 42  1  0
M  END


  Mrv0541 02241200502D          

 23 24  0  0  1  0            999 V2000
   17.5597   -7.7273    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.1308   -7.7273    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.5597  -10.2023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.1308   -9.3773    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.9887   -9.3773    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.7031   -8.1398    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.9887   -6.9023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.5597   -6.9023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.4163   -3.1898    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   17.5597   -9.3773    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   16.8453   -8.9648    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   18.2742   -8.9648    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.2742   -8.1398    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   16.8453   -8.1398    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.9887   -7.7273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1308   -6.9023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8453   -6.4898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4163   -6.4898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1308   -5.2523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8453   -5.6648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4163   -5.6648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1308   -4.4273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4163   -4.0148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1 13  1  0  0  0  0
  1 14  1  0  0  0  0
 14  2  1  6  0  0  0
  2 16  1  0  0  0  0
 10  3  1  6  0  0  0
 11  4  1  1  0  0  0
 12  5  1  1  0  0  0
  6 15  1  0  0  0  0
  7 15  2  0  0  0  0
  8 17  1  0  0  0  0
  9 23  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 11 14  1  0  0  0  0
 12 13  1  0  0  0  0
 13 15  1  6  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 17 20  1  0  0  0  0
 18 21  2  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0010329

> <DATABASE_NAME>
hmdb

> <SMILES>
NCCC1=CC(O)=C(O[C@@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)C(O)=O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C14H19NO8/c15-4-3-6-1-2-8(7(16)5-6)22-14-11(19)9(17)10(18)12(23-14)13(20)21/h1-2,5,9-12,14,16-19H,3-4,15H2,(H,20,21)/t9-,10-,11+,12-,14+/m0/s1

> <INCHI_KEY>
CQASRCDNLNMIJY-BYNIDDHOSA-N

> <FORMULA>
C14H19NO8

> <MOLECULAR_WEIGHT>
329.3026

> <EXACT_MASS>
329.111066589

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_AVERAGE_POLARIZABILITY>
31.44788217315186

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3S,4S,5R,6S)-6-[4-(2-aminoethyl)-2-hydroxyphenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid

> <ALOGPS_LOGP>
-2.12

> <JCHEM_LOGP>
-3.4301786993281453

> <ALOGPS_LOGS>
-1.29

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.151323648968098

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.7901423350033108

> <JCHEM_PKA_STRONGEST_BASIC>
9.5045522004217

> <JCHEM_POLAR_SURFACE_AREA>
162.70000000000002

> <JCHEM_REFRACTIVITY>
75.26

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.70e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
dopamine glucuronide

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0010329
     RDKit          3D
Dopamine glucuronide
 42 43  0  0  0  0  0  0  0  0999 V2000
    6.9930    0.0924   -1.0316 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.5738    0.4074   -0.9136 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8518   -0.9090   -0.7391 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3775   -0.7078   -0.6067 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8542   -0.5261    0.6394 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4912   -0.3373    0.7927 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6241   -0.3246   -0.2758 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7233   -0.1417   -0.1637 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4852    0.0611    0.9829 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3931   -0.9672    1.1049 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6851   -0.6699    0.7605 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4449   -1.9260    0.5586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9106   -3.0478    0.7028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7756   -1.8867    0.2024 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6174    0.1404   -0.5357 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8466    0.1274   -1.1903 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2146    1.5389   -0.1231 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7507    2.2688   -1.2175 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1253    1.4265    0.9068 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7197    1.6752    2.1650 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1743   -0.5106   -1.5315 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4126   -0.5199   -2.6926 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5436   -0.7003   -1.6867 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4971    0.2075   -0.1237 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1165   -0.8698   -1.4303 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4607    1.0160    0.0046 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2752    0.9458   -1.8134 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9913   -1.5623   -1.6222 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2606   -1.4449    0.1265 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5287   -0.5335    1.4934 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1292   -0.1996    1.7844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8710    0.0680    1.9320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1570   -0.0547    1.5508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4756   -1.8256    0.9399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8137   -0.2620   -1.1856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0302    1.0749   -1.4691 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1113    2.0663    0.2741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0637    3.2201   -1.1733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3752    2.2079    0.6928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9707    2.6269    2.2440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5726   -0.3972   -2.7322 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9777   -0.8468   -2.6754 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
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 11 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
  7 21  1  0
 21 22  1  0
 21 23  2  0
 23  4  1  0
 19  9  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  2 27  1  0
  3 28  1  0
  3 29  1  0
  5 30  1  0
  6 31  1  0
  9 32  1  1
 11 33  1  1
 14 34  1  0
 15 35  1  6
 16 36  1  0
 17 37  1  1
 18 38  1  0
 19 39  1  6
 20 40  1  0
 22 41  1  0
 23 42  1  0
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  O   UNK     0      32.778 -14.424   0.000  0.00  0.00           O+0
HETATM    2  O   UNK     0      30.111 -14.424   0.000  0.00  0.00           O+0
HETATM    3  O   UNK     0      32.778 -19.044   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      30.111 -17.504   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      35.446 -17.504   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      36.779 -15.194   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      35.446 -12.884   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0      32.778 -12.884   0.000  0.00  0.00           O+0
HETATM    9  N   UNK     0      28.777  -5.954   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0      32.778 -17.504   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      31.445 -16.734   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      34.112 -16.734   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      34.112 -15.194   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      31.445 -15.194   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      35.446 -14.424   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      30.111 -12.884   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      31.445 -12.114   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      28.777 -12.114   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      30.111  -9.804   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      31.445 -10.574   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      28.777 -10.574   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      30.111  -8.264   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      28.777  -7.494   0.000  0.00  0.00           C+0
CONECT    1   13   14                                                       
CONECT    2   14   16                                                       
CONECT    3   10                                                            
CONECT    4   11                                                            
CONECT    5   12                                                            
CONECT    6   15                                                            
CONECT    7   15                                                            
CONECT    8   17                                                            
CONECT    9   23                                                            
CONECT   10    3   11   12                                                  
CONECT   11    4   10   14                                                  
CONECT   12    5   10   13                                                  
CONECT   13    1   12   15                                                  
CONECT   14    1    2   11                                                  
CONECT   15    6    7   13                                                  
CONECT   16    2   17   18                                                  
CONECT   17    8   16   20                                                  
CONECT   18   16   21                                                       
CONECT   19   20   21   22                                                  
CONECT   20   17   19                                                       
CONECT   21   18   19                                                       
CONECT   22   19   23                                                       
CONECT   23    9   22                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

COMPND    HMDB0010329
HETATM    1  N1  UNL     1       6.993   0.092  -1.032  1.00  0.00           N  
HETATM    2  C1  UNL     1       5.574   0.407  -0.914  1.00  0.00           C  
HETATM    3  C2  UNL     1       4.852  -0.909  -0.739  1.00  0.00           C  
HETATM    4  C3  UNL     1       3.378  -0.708  -0.607  1.00  0.00           C  
HETATM    5  C4  UNL     1       2.854  -0.526   0.639  1.00  0.00           C  
HETATM    6  C5  UNL     1       1.491  -0.337   0.793  1.00  0.00           C  
HETATM    7  C6  UNL     1       0.624  -0.325  -0.276  1.00  0.00           C  
HETATM    8  O1  UNL     1      -0.723  -0.142  -0.164  1.00  0.00           O  
HETATM    9  C7  UNL     1      -1.485   0.061   0.983  1.00  0.00           C  
HETATM   10  O2  UNL     1      -2.393  -0.967   1.105  1.00  0.00           O  
HETATM   11  C8  UNL     1      -3.685  -0.670   0.760  1.00  0.00           C  
HETATM   12  C9  UNL     1      -4.445  -1.926   0.559  1.00  0.00           C  
HETATM   13  O3  UNL     1      -3.911  -3.048   0.703  1.00  0.00           O  
HETATM   14  O4  UNL     1      -5.776  -1.887   0.202  1.00  0.00           O  
HETATM   15  C10 UNL     1      -3.617   0.140  -0.536  1.00  0.00           C  
HETATM   16  O5  UNL     1      -4.847   0.127  -1.190  1.00  0.00           O  
HETATM   17  C11 UNL     1      -3.215   1.539  -0.123  1.00  0.00           C  
HETATM   18  O6  UNL     1      -2.751   2.269  -1.218  1.00  0.00           O  
HETATM   19  C12 UNL     1      -2.125   1.427   0.907  1.00  0.00           C  
HETATM   20  O7  UNL     1      -2.720   1.675   2.165  1.00  0.00           O  
HETATM   21  C13 UNL     1       1.174  -0.511  -1.531  1.00  0.00           C  
HETATM   22  O8  UNL     1       0.413  -0.520  -2.693  1.00  0.00           O  
HETATM   23  C14 UNL     1       2.544  -0.700  -1.687  1.00  0.00           C  
HETATM   24  H1  UNL     1       7.497   0.207  -0.124  1.00  0.00           H  
HETATM   25  H2  UNL     1       7.117  -0.870  -1.430  1.00  0.00           H  
HETATM   26  H3  UNL     1       5.461   1.016   0.005  1.00  0.00           H  
HETATM   27  H4  UNL     1       5.275   0.946  -1.813  1.00  0.00           H  
HETATM   28  H5  UNL     1       4.991  -1.562  -1.622  1.00  0.00           H  
HETATM   29  H6  UNL     1       5.261  -1.445   0.126  1.00  0.00           H  
HETATM   30  H7  UNL     1       3.529  -0.533   1.493  1.00  0.00           H  
HETATM   31  H8  UNL     1       1.129  -0.200   1.784  1.00  0.00           H  
HETATM   32  H9  UNL     1      -0.871   0.068   1.932  1.00  0.00           H  
HETATM   33  H10 UNL     1      -4.157  -0.055   1.551  1.00  0.00           H  
HETATM   34  H11 UNL     1      -6.476  -1.826   0.940  1.00  0.00           H  
HETATM   35  H12 UNL     1      -2.814  -0.262  -1.186  1.00  0.00           H  
HETATM   36  H13 UNL     1      -5.030   1.075  -1.469  1.00  0.00           H  
HETATM   37  H14 UNL     1      -4.111   2.066   0.274  1.00  0.00           H  
HETATM   38  H15 UNL     1      -3.064   3.220  -1.173  1.00  0.00           H  
HETATM   39  H16 UNL     1      -1.375   2.208   0.693  1.00  0.00           H  
HETATM   40  H17 UNL     1      -2.971   2.627   2.244  1.00  0.00           H  
HETATM   41  H18 UNL     1      -0.573  -0.397  -2.732  1.00  0.00           H  
HETATM   42  H19 UNL     1       2.978  -0.847  -2.675  1.00  0.00           H  
CONECT    1    2   24   25
CONECT    2    3   26   27
CONECT    3    4   28   29
CONECT    4    5    5   23
CONECT    5    6   30
CONECT    6    7    7   31
CONECT    7    8   21
CONECT    8    9
CONECT    9   10   19   32
CONECT   10   11
CONECT   11   12   15   33
CONECT   12   13   13   14
CONECT   14   34
CONECT   15   16   17   35
CONECT   16   36
CONECT   17   18   19   37
CONECT   18   38
CONECT   19   20   39
CONECT   20   40
CONECT   21   22   23   23
CONECT   22   41
CONECT   23   42
END

HMDB0010329
     RDKit          3D
Dopamine glucuronide
 42 43  0  0  0  0  0  0  0  0999 V2000
    6.9930    0.0924   -1.0316 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.5738    0.4074   -0.9136 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8518   -0.9090   -0.7391 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3775   -0.7078   -0.6067 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8542   -0.5261    0.6394 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4912   -0.3373    0.7927 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6241   -0.3246   -0.2758 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7233   -0.1417   -0.1637 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4852    0.0611    0.9829 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3931   -0.9672    1.1049 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6851   -0.6699    0.7605 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4449   -1.9260    0.5586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9106   -3.0478    0.7028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7756   -1.8867    0.2024 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6174    0.1404   -0.5357 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8466    0.1274   -1.1903 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2146    1.5389   -0.1231 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7507    2.2688   -1.2175 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1253    1.4265    0.9068 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7197    1.6752    2.1650 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1743   -0.5106   -1.5315 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4126   -0.5199   -2.6926 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5436   -0.7003   -1.6867 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4971    0.2075   -0.1237 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1165   -0.8698   -1.4303 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4607    1.0160    0.0046 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2752    0.9458   -1.8134 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9913   -1.5623   -1.6222 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2606   -1.4449    0.1265 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5287   -0.5335    1.4934 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1292   -0.1996    1.7844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8710    0.0680    1.9320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1570   -0.0547    1.5508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4756   -1.8256    0.9399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8137   -0.2620   -1.1856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0302    1.0749   -1.4691 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1113    2.0663    0.2741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0637    3.2201   -1.1733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3752    2.2079    0.6928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9707    2.6269    2.2440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5726   -0.3972   -2.7322 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9777   -0.8468   -2.6754 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
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 11 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
  7 21  1  0
 21 22  1  0
 21 23  2  0
 23  4  1  0
 19  9  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  2 27  1  0
  3 28  1  0
  3 29  1  0
  5 30  1  0
  6 31  1  0
  9 32  1  1
 11 33  1  1
 14 34  1  0
 15 35  1  6
 16 36  1  0
 17 37  1  1
 18 38  1  0
 19 39  1  6
 20 40  1  0
 22 41  1  0
 23 42  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
4-(2-Aminoethyl)-2-hydroxyphenyl beta-D-glucopyranosiduronate	HMDB
4-(2-Aminoethyl)-2-hydroxyphenyl beta-D-glucopyranosiduronic acid	HMDB
4-(2-Aminoethyl)-2-hydroxyphenyl beta-delta-glucopyranosiduronate	HMDB
4-(2-Aminoethyl)-2-hydroxyphenyl beta-delta-glucopyranosiduronic acid	HMDB
Dopamine-4-O-glucuronide	HMDB
(2S,3S,4S,5R,6S)-6-[4-(2-Aminoethyl)-2-hydroxyphenoxy]-3,4,5-trihydroxyoxane-2-carboxylate	HMDB
Dopamine glucuronide	MeSH

Chemical Formula

C₁₄H₁₉NO₈

Average Molecular Weight

329.3026

Monoisotopic Molecular Weight

329.111066589

IUPAC Name

(2S,3S,4S,5R,6S)-6-[4-(2-aminoethyl)-2-hydroxyphenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid

Traditional Name

dopamine glucuronide

CAS Registry Number

38632-24-5

SMILES

NCCC1=CC(O)=C(O[C@@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)C(O)=O)C=C1

InChI Identifier

InChI=1S/C14H19NO8/c15-4-3-6-1-2-8(7(16)5-6)22-14-11(19)9(17)10(18)12(23-14)13(20)21/h1-2,5,9-12,14,16-19H,3-4,15H2,(H,20,21)/t9-,10-,11+,12-,14+/m0/s1

InChI Key

CQASRCDNLNMIJY-BYNIDDHOSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Phenolic glycosides

Alternative Parents

Substituents

Phenolic glycoside
1-o-glucuronide
O-glucuronide
Glucuronic acid or derivatives
Hexose monosaccharide
O-glycosyl compound
Phenethylamine
Phenol ether
2-arylethylamine
Phenoxy compound
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Phenol
Beta-hydroxy acid
Aralkylamine
Pyran
Hydroxy acid
Oxane
Benzenoid
Monosaccharide
Monocyclic benzene moiety
Amino acid or derivatives
Secondary alcohol
Amino acid
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Carboxylic acid
Polyol
Monocarboxylic acid or derivatives
Acetal
Organic nitrogen compound
Hydrocarbon derivative
Amine
Carbonyl group
Primary amine
Primary aliphatic amine
Organic oxide
Alcohol
Organonitrogen compound
Organopnictogen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Blood (HMDB: HMDB0010329)
Urine (HMDB: HMDB0010329)

Organ

Liver (HMDB: HMDB0010329)
Kidney (HMDB: HMDB0010329)

Excreta

Biofluid or Excreta

Urine (PMID: 8320494)

Non-excretory biofluid

Biofluid or Excreta

Blood (HMDB: HMDB0010329)

Cellular substructure

Cytoplasm (HMDB: HMDB0010329)

Source

Endogenous

Endogenous (HMDB: HMDB0010329)

Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)
Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)

Equine

Horse (FooDB: FOOD00378)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Process

Not Available

Role

Biological role

Drug metabolite (HMDB: HMDB0010329)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	17 g/L	ALOGPS
logP	-2.1	ALOGPS
logP	-3.4	ChemAxon
logS	-1.3	ALOGPS
pKa (Strongest Acidic)	2.79	ChemAxon
pKa (Strongest Basic)	9.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	162.7 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	75.26 m³·mol⁻¹	ChemAxon
Polarizability	31.45 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	176.42	31661259
DarkChem	[M-H]-	175.238	31661259
DeepCCS	[M+H]+	179.49	30932474
DeepCCS	[M-H]-	177.094	30932474
DeepCCS	[M-2H]-	210.013	30932474
DeepCCS	[M+Na]+	185.403	30932474
AllCCS	[M+H]+	175.8	32859911
AllCCS	[M+H-H2O]+	172.8	32859911
AllCCS	[M+NH4]+	178.5	32859911
AllCCS	[M+Na]+	179.3	32859911
AllCCS	[M-H]-	172.8	32859911
AllCCS	[M+Na-2H]-	172.8	32859911
AllCCS	[M+HCOO]-	173.0	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Dopamine glucuronide	NCCC1=CC(O)=C(O[C@@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)C(O)=O)C=C1	4074.8	Standard polar	33892256
Dopamine glucuronide	NCCC1=CC(O)=C(O[C@@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)C(O)=O)C=C1	3384.2	Standard non polar	33892256
Dopamine glucuronide	NCCC1=CC(O)=C(O[C@@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)C(O)=O)C=C1	2995.4	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Dopamine glucuronide,1TMS,isomer #1	C[Si](C)(C)OC1=CC(CCN)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]1O	2895.4	Semi standard non polar	33892256
Dopamine glucuronide,1TMS,isomer #2	C[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC=C(CCN)C=C2O)[C@H](O)[C@H]1O	2834.2	Semi standard non polar	33892256
Dopamine glucuronide,1TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC=C(CCN)C=C2O)O[C@H](C(=O)O)[C@H]1O	2859.3	Semi standard non polar	33892256
Dopamine glucuronide,1TMS,isomer #4	C[Si](C)(C)O[C@H]1[C@H](OC2=CC=C(CCN)C=C2O)O[C@H](C(=O)O)[C@@H](O)[C@@H]1O	2869.5	Semi standard non polar	33892256
Dopamine glucuronide,1TMS,isomer #5	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O)[C@H](O)[C@@H](O)[C@@H]1O	2818.6	Semi standard non polar	33892256
Dopamine glucuronide,1TMS,isomer #6	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C1	2938.2	Semi standard non polar	33892256
Dopamine glucuronide,2TMS,isomer #1	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	2827.3	Semi standard non polar	33892256
Dopamine glucuronide,2TMS,isomer #10	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](C(=O)O)O[C@@H](OC2=CC=C(CCN)C=C2O)[C@@H]1O[Si](C)(C)C	2855.3	Semi standard non polar	33892256
Dopamine glucuronide,2TMS,isomer #11	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2819.8	Semi standard non polar	33892256
Dopamine glucuronide,2TMS,isomer #12	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C1	2901.9	Semi standard non polar	33892256
Dopamine glucuronide,2TMS,isomer #13	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2811.8	Semi standard non polar	33892256
Dopamine glucuronide,2TMS,isomer #14	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C1	2915.1	Semi standard non polar	33892256
Dopamine glucuronide,2TMS,isomer #15	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C1	2885.9	Semi standard non polar	33892256
Dopamine glucuronide,2TMS,isomer #16	C[Si](C)(C)N(CCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C1)[Si](C)(C)C	3130.1	Semi standard non polar	33892256
Dopamine glucuronide,2TMS,isomer #2	C[Si](C)(C)OC1=CC(CCN)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2853.6	Semi standard non polar	33892256
Dopamine glucuronide,2TMS,isomer #3	C[Si](C)(C)OC1=CC(CCN)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2874.6	Semi standard non polar	33892256
Dopamine glucuronide,2TMS,isomer #4	C[Si](C)(C)OC1=CC(CCN)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	2872.2	Semi standard non polar	33892256
Dopamine glucuronide,2TMS,isomer #5	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C1	2914.7	Semi standard non polar	33892256
Dopamine glucuronide,2TMS,isomer #6	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2808.2	Semi standard non polar	33892256
Dopamine glucuronide,2TMS,isomer #7	C[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC=C(CCN)C=C2O)[C@H](O[Si](C)(C)C)[C@H]1O	2856.5	Semi standard non polar	33892256
Dopamine glucuronide,2TMS,isomer #8	C[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC=C(CCN)C=C2O)[C@H](O)[C@H]1O[Si](C)(C)C	2842.6	Semi standard non polar	33892256
Dopamine glucuronide,2TMS,isomer #9	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C1	2896.3	Semi standard non polar	33892256
Dopamine glucuronide,3TMS,isomer #1	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2834.9	Semi standard non polar	33892256
Dopamine glucuronide,3TMS,isomer #10	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C1	2878.0	Semi standard non polar	33892256
Dopamine glucuronide,3TMS,isomer #11	C[Si](C)(C)OC1=CC(CCN([Si](C)(C)C)[Si](C)(C)C)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]1O	3075.2	Semi standard non polar	33892256
Dopamine glucuronide,3TMS,isomer #12	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2838.5	Semi standard non polar	33892256
Dopamine glucuronide,3TMS,isomer #13	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2813.0	Semi standard non polar	33892256
Dopamine glucuronide,3TMS,isomer #14	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C1	2866.0	Semi standard non polar	33892256
Dopamine glucuronide,3TMS,isomer #15	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=CC=C(CCN)C=C2O)O[C@H](C(=O)O)[C@H]1O[Si](C)(C)C	2848.7	Semi standard non polar	33892256
Dopamine glucuronide,3TMS,isomer #16	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C1	2889.6	Semi standard non polar	33892256
Dopamine glucuronide,3TMS,isomer #17	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C1	2872.7	Semi standard non polar	33892256
Dopamine glucuronide,3TMS,isomer #18	C[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O)[C@H](O)[C@H]1O	3054.2	Semi standard non polar	33892256
Dopamine glucuronide,3TMS,isomer #19	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2809.3	Semi standard non polar	33892256
Dopamine glucuronide,3TMS,isomer #2	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2840.8	Semi standard non polar	33892256
Dopamine glucuronide,3TMS,isomer #20	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C1	2879.5	Semi standard non polar	33892256
Dopamine glucuronide,3TMS,isomer #21	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C1	2869.9	Semi standard non polar	33892256
Dopamine glucuronide,3TMS,isomer #22	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O)O[C@H](C(=O)O)[C@H]1O	3054.6	Semi standard non polar	33892256
Dopamine glucuronide,3TMS,isomer #23	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C1	2871.0	Semi standard non polar	33892256
Dopamine glucuronide,3TMS,isomer #24	C[Si](C)(C)O[C@H]1[C@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O)O[C@H](C(=O)O)[C@@H](O)[C@@H]1O	3064.5	Semi standard non polar	33892256
Dopamine glucuronide,3TMS,isomer #25	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O)[C@H](O)[C@@H](O)[C@@H]1O	3039.5	Semi standard non polar	33892256
Dopamine glucuronide,3TMS,isomer #3	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2829.0	Semi standard non polar	33892256
Dopamine glucuronide,3TMS,isomer #4	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C1	2869.2	Semi standard non polar	33892256
Dopamine glucuronide,3TMS,isomer #5	C[Si](C)(C)OC1=CC(CCN)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2851.4	Semi standard non polar	33892256
Dopamine glucuronide,3TMS,isomer #6	C[Si](C)(C)OC1=CC(CCN)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2859.7	Semi standard non polar	33892256
Dopamine glucuronide,3TMS,isomer #7	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C1	2876.0	Semi standard non polar	33892256
Dopamine glucuronide,3TMS,isomer #8	C[Si](C)(C)OC1=CC(CCN)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2850.9	Semi standard non polar	33892256
Dopamine glucuronide,3TMS,isomer #9	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C1	2885.5	Semi standard non polar	33892256
Dopamine glucuronide,4TMS,isomer #1	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2851.8	Semi standard non polar	33892256
Dopamine glucuronide,4TMS,isomer #10	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C1	2892.8	Semi standard non polar	33892256
Dopamine glucuronide,4TMS,isomer #11	C[Si](C)(C)OC1=CC(CCN([Si](C)(C)C)[Si](C)(C)C)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	3052.9	Semi standard non polar	33892256
Dopamine glucuronide,4TMS,isomer #12	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C1	2874.5	Semi standard non polar	33892256
Dopamine glucuronide,4TMS,isomer #13	C[Si](C)(C)OC1=CC(CCN([Si](C)(C)C)[Si](C)(C)C)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	3056.3	Semi standard non polar	33892256
Dopamine glucuronide,4TMS,isomer #14	C[Si](C)(C)OC1=CC(CCN([Si](C)(C)C)[Si](C)(C)C)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	3049.4	Semi standard non polar	33892256
Dopamine glucuronide,4TMS,isomer #15	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2859.0	Semi standard non polar	33892256
Dopamine glucuronide,4TMS,isomer #16	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C1	2903.5	Semi standard non polar	33892256
Dopamine glucuronide,4TMS,isomer #17	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C1	2877.3	Semi standard non polar	33892256
Dopamine glucuronide,4TMS,isomer #18	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3025.4	Semi standard non polar	33892256
Dopamine glucuronide,4TMS,isomer #19	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C1	2881.1	Semi standard non polar	33892256
Dopamine glucuronide,4TMS,isomer #2	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2876.8	Semi standard non polar	33892256
Dopamine glucuronide,4TMS,isomer #20	C[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O)[C@H](O[Si](C)(C)C)[C@H]1O	3036.7	Semi standard non polar	33892256
Dopamine glucuronide,4TMS,isomer #21	C[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O)[C@H](O)[C@H]1O[Si](C)(C)C	3032.6	Semi standard non polar	33892256
Dopamine glucuronide,4TMS,isomer #22	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C1	2877.4	Semi standard non polar	33892256
Dopamine glucuronide,4TMS,isomer #23	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](C(=O)O)O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O)[C@@H]1O[Si](C)(C)C	3025.0	Semi standard non polar	33892256
Dopamine glucuronide,4TMS,isomer #24	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3028.3	Semi standard non polar	33892256
Dopamine glucuronide,4TMS,isomer #25	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3029.5	Semi standard non polar	33892256
Dopamine glucuronide,4TMS,isomer #3	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C1	2891.4	Semi standard non polar	33892256
Dopamine glucuronide,4TMS,isomer #4	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2849.0	Semi standard non polar	33892256
Dopamine glucuronide,4TMS,isomer #5	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C1	2889.8	Semi standard non polar	33892256
Dopamine glucuronide,4TMS,isomer #6	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C1	2896.1	Semi standard non polar	33892256
Dopamine glucuronide,4TMS,isomer #7	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3049.0	Semi standard non polar	33892256
Dopamine glucuronide,4TMS,isomer #8	C[Si](C)(C)OC1=CC(CCN)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2857.5	Semi standard non polar	33892256
Dopamine glucuronide,4TMS,isomer #9	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C1	2878.2	Semi standard non polar	33892256
Dopamine glucuronide,5TMS,isomer #1	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2879.7	Semi standard non polar	33892256
Dopamine glucuronide,5TMS,isomer #10	C[Si](C)(C)OC1=CC(CCN([Si](C)(C)C)[Si](C)(C)C)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3066.6	Semi standard non polar	33892256
Dopamine glucuronide,5TMS,isomer #11	C[Si](C)(C)OC1=CC(CCN([Si](C)(C)C)[Si](C)(C)C)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3054.8	Semi standard non polar	33892256
Dopamine glucuronide,5TMS,isomer #12	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C1	2919.5	Semi standard non polar	33892256
Dopamine glucuronide,5TMS,isomer #13	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3070.4	Semi standard non polar	33892256
Dopamine glucuronide,5TMS,isomer #14	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3044.9	Semi standard non polar	33892256
Dopamine glucuronide,5TMS,isomer #15	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O)O[C@H](C(=O)O)[C@H]1O[Si](C)(C)C	3042.8	Semi standard non polar	33892256
Dopamine glucuronide,5TMS,isomer #16	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3045.5	Semi standard non polar	33892256
Dopamine glucuronide,5TMS,isomer #2	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C1	2909.0	Semi standard non polar	33892256
Dopamine glucuronide,5TMS,isomer #3	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C1	2944.2	Semi standard non polar	33892256
Dopamine glucuronide,5TMS,isomer #4	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3082.3	Semi standard non polar	33892256
Dopamine glucuronide,5TMS,isomer #5	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C1	2915.6	Semi standard non polar	33892256
Dopamine glucuronide,5TMS,isomer #6	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3084.9	Semi standard non polar	33892256
Dopamine glucuronide,5TMS,isomer #7	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3085.7	Semi standard non polar	33892256
Dopamine glucuronide,5TMS,isomer #8	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C1	2901.3	Semi standard non polar	33892256
Dopamine glucuronide,5TMS,isomer #9	C[Si](C)(C)OC1=CC(CCN([Si](C)(C)C)[Si](C)(C)C)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3063.5	Semi standard non polar	33892256
Dopamine glucuronide,6TMS,isomer #1	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C1	2956.7	Semi standard non polar	33892256
Dopamine glucuronide,6TMS,isomer #1	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C1	2927.0	Standard non polar	33892256
Dopamine glucuronide,6TMS,isomer #1	C[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C1	3099.9	Standard polar	33892256
Dopamine glucuronide,6TMS,isomer #2	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3116.0	Semi standard non polar	33892256
Dopamine glucuronide,6TMS,isomer #2	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3009.4	Standard non polar	33892256
Dopamine glucuronide,6TMS,isomer #2	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3227.3	Standard polar	33892256
Dopamine glucuronide,6TMS,isomer #3	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3140.6	Semi standard non polar	33892256
Dopamine glucuronide,6TMS,isomer #3	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3024.7	Standard non polar	33892256
Dopamine glucuronide,6TMS,isomer #3	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3210.5	Standard polar	33892256
Dopamine glucuronide,6TMS,isomer #4	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3116.7	Semi standard non polar	33892256
Dopamine glucuronide,6TMS,isomer #4	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2993.8	Standard non polar	33892256
Dopamine glucuronide,6TMS,isomer #4	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3221.7	Standard polar	33892256
Dopamine glucuronide,6TMS,isomer #5	C[Si](C)(C)OC1=CC(CCN([Si](C)(C)C)[Si](C)(C)C)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3094.3	Semi standard non polar	33892256
Dopamine glucuronide,6TMS,isomer #5	C[Si](C)(C)OC1=CC(CCN([Si](C)(C)C)[Si](C)(C)C)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2980.6	Standard non polar	33892256
Dopamine glucuronide,6TMS,isomer #5	C[Si](C)(C)OC1=CC(CCN([Si](C)(C)C)[Si](C)(C)C)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3217.9	Standard polar	33892256
Dopamine glucuronide,6TMS,isomer #6	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3089.1	Semi standard non polar	33892256
Dopamine glucuronide,6TMS,isomer #6	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3041.3	Standard non polar	33892256
Dopamine glucuronide,6TMS,isomer #6	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3217.1	Standard polar	33892256
Dopamine glucuronide,7TMS,isomer #1	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3147.2	Semi standard non polar	33892256
Dopamine glucuronide,7TMS,isomer #1	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3033.5	Standard non polar	33892256
Dopamine glucuronide,7TMS,isomer #1	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3113.3	Standard polar	33892256
Dopamine glucuronide,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC(CCN)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]1O	3163.4	Semi standard non polar	33892256
Dopamine glucuronide,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC=C(CCN)C=C2O)[C@H](O)[C@H]1O	3099.0	Semi standard non polar	33892256
Dopamine glucuronide,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC=C(CCN)C=C2O)O[C@H](C(=O)O)[C@H]1O	3122.9	Semi standard non polar	33892256
Dopamine glucuronide,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](OC2=CC=C(CCN)C=C2O)O[C@H](C(=O)O)[C@@H](O)[C@@H]1O	3136.4	Semi standard non polar	33892256
Dopamine glucuronide,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O)[C@H](O)[C@@H](O)[C@@H]1O	3100.0	Semi standard non polar	33892256
Dopamine glucuronide,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C1	3197.5	Semi standard non polar	33892256
Dopamine glucuronide,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3338.5	Semi standard non polar	33892256
Dopamine glucuronide,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](C(=O)O)O[C@@H](OC2=CC=C(CCN)C=C2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3314.1	Semi standard non polar	33892256
Dopamine glucuronide,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3307.9	Semi standard non polar	33892256
Dopamine glucuronide,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(O)=C1	3408.4	Semi standard non polar	33892256
Dopamine glucuronide,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3316.2	Semi standard non polar	33892256
Dopamine glucuronide,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(O)=C1	3419.9	Semi standard non polar	33892256
Dopamine glucuronide,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C1	3402.0	Semi standard non polar	33892256
Dopamine glucuronide,2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N(CCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C1)[Si](C)(C)C(C)(C)C	3551.5	Semi standard non polar	33892256
Dopamine glucuronide,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC(CCN)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3344.1	Semi standard non polar	33892256
Dopamine glucuronide,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=CC(CCN)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3364.4	Semi standard non polar	33892256
Dopamine glucuronide,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1=CC(CCN)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3364.3	Semi standard non polar	33892256
Dopamine glucuronide,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C(C)(C)C)=C1	3415.3	Semi standard non polar	33892256
Dopamine glucuronide,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3304.7	Semi standard non polar	33892256
Dopamine glucuronide,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC=C(CCN)C=C2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3310.0	Semi standard non polar	33892256
Dopamine glucuronide,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC=C(CCN)C=C2O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3297.4	Semi standard non polar	33892256
Dopamine glucuronide,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)C(O)=C1	3396.6	Semi standard non polar	33892256
Dopamine glucuronide,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3530.3	Semi standard non polar	33892256
Dopamine glucuronide,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1	3617.4	Semi standard non polar	33892256
Dopamine glucuronide,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC1=CC(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]1O	3755.4	Semi standard non polar	33892256
Dopamine glucuronide,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3532.3	Semi standard non polar	33892256
Dopamine glucuronide,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3496.7	Semi standard non polar	33892256
Dopamine glucuronide,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)C(O)=C1	3595.8	Semi standard non polar	33892256
Dopamine glucuronide,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](OC2=CC=C(CCN)C=C2O)O[C@H](C(=O)O)[C@H]1O[Si](C)(C)C(C)(C)C	3507.5	Semi standard non polar	33892256
Dopamine glucuronide,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(O)=C1	3594.3	Semi standard non polar	33892256
Dopamine glucuronide,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(O)=C1	3575.4	Semi standard non polar	33892256
Dopamine glucuronide,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC=C(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)[C@H](O)[C@H]1O	3746.2	Semi standard non polar	33892256
Dopamine glucuronide,3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3499.2	Semi standard non polar	33892256
Dopamine glucuronide,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3518.9	Semi standard non polar	33892256
Dopamine glucuronide,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C(O)=C1	3588.3	Semi standard non polar	33892256
Dopamine glucuronide,3TBDMS,isomer #21	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(O)=C1	3589.5	Semi standard non polar	33892256
Dopamine glucuronide,3TBDMS,isomer #22	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC=C(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)O[C@H](C(=O)O)[C@H]1O	3753.0	Semi standard non polar	33892256
Dopamine glucuronide,3TBDMS,isomer #23	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(O)=C1	3609.7	Semi standard non polar	33892256
Dopamine glucuronide,3TBDMS,isomer #24	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](OC2=CC=C(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)O[C@H](C(=O)O)[C@@H](O)[C@@H]1O	3768.8	Semi standard non polar	33892256
Dopamine glucuronide,3TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)[C@H](O)[C@@H](O)[C@@H]1O	3747.3	Semi standard non polar	33892256
Dopamine glucuronide,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3515.4	Semi standard non polar	33892256
Dopamine glucuronide,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C(C)(C)C)=C1	3614.2	Semi standard non polar	33892256
Dopamine glucuronide,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1=CC(CCN)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3522.9	Semi standard non polar	33892256
Dopamine glucuronide,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1=CC(CCN)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3535.4	Semi standard non polar	33892256
Dopamine glucuronide,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C(C)(C)C)=C1	3603.5	Semi standard non polar	33892256
Dopamine glucuronide,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1=CC(CCN)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3532.6	Semi standard non polar	33892256
Dopamine glucuronide,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(O[Si](C)(C)C(C)(C)C)=C1	3626.1	Semi standard non polar	33892256
Dopamine glucuronide,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3701.5	Semi standard non polar	33892256
Dopamine glucuronide,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1	3782.6	Semi standard non polar	33892256
Dopamine glucuronide,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC1=CC(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3950.1	Semi standard non polar	33892256
Dopamine glucuronide,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1	3769.2	Semi standard non polar	33892256
Dopamine glucuronide,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1=CC(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3955.8	Semi standard non polar	33892256
Dopamine glucuronide,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC1=CC(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3960.2	Semi standard non polar	33892256
Dopamine glucuronide,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3718.3	Semi standard non polar	33892256
Dopamine glucuronide,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(O)=C1	3796.5	Semi standard non polar	33892256
Dopamine glucuronide,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(O)=C1	3759.5	Semi standard non polar	33892256
Dopamine glucuronide,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3929.1	Semi standard non polar	33892256
Dopamine glucuronide,4TBDMS,isomer #19	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C(O)=C1	3757.6	Semi standard non polar	33892256
Dopamine glucuronide,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3727.3	Semi standard non polar	33892256
Dopamine glucuronide,4TBDMS,isomer #20	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC=C(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3937.1	Semi standard non polar	33892256
Dopamine glucuronide,4TBDMS,isomer #21	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC=C(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3920.4	Semi standard non polar	33892256
Dopamine glucuronide,4TBDMS,isomer #22	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C(O)=C1	3760.3	Semi standard non polar	33892256
Dopamine glucuronide,4TBDMS,isomer #23	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](C(=O)O)O[C@@H](OC2=CC=C(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3924.7	Semi standard non polar	33892256
Dopamine glucuronide,4TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3910.2	Semi standard non polar	33892256
Dopamine glucuronide,4TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3947.2	Semi standard non polar	33892256
Dopamine glucuronide,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1	3791.5	Semi standard non polar	33892256
Dopamine glucuronide,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3694.7	Semi standard non polar	33892256
Dopamine glucuronide,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(O[Si](C)(C)C(C)(C)C)=C1	3779.1	Semi standard non polar	33892256
Dopamine glucuronide,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C(C)(C)C)=C1	3786.3	Semi standard non polar	33892256
Dopamine glucuronide,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3951.8	Semi standard non polar	33892256
Dopamine glucuronide,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1=CC(CCN)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3714.9	Semi standard non polar	33892256
Dopamine glucuronide,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(O[Si](C)(C)C(C)(C)C)=C1	3770.6	Semi standard non polar	33892256
Dopamine glucuronide,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN)C=C2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3915.1	Semi standard non polar	33892256
Dopamine glucuronide,5TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1=CC(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4140.6	Semi standard non polar	33892256
Dopamine glucuronide,5TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC1=CC(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	4127.8	Semi standard non polar	33892256
Dopamine glucuronide,5TBDMS,isomer #12	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C(O)=C1	3959.4	Semi standard non polar	33892256
Dopamine glucuronide,5TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4126.6	Semi standard non polar	33892256
Dopamine glucuronide,5TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	4096.2	Semi standard non polar	33892256
Dopamine glucuronide,5TBDMS,isomer #15	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](OC2=CC=C(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)O[C@H](C(=O)O)[C@H]1O[Si](C)(C)C(C)(C)C	4121.5	Semi standard non polar	33892256
Dopamine glucuronide,5TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4099.4	Semi standard non polar	33892256
Dopamine glucuronide,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1	3926.3	Semi standard non polar	33892256
Dopamine glucuronide,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1	3971.9	Semi standard non polar	33892256
Dopamine glucuronide,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	4132.1	Semi standard non polar	33892256
Dopamine glucuronide,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(O[Si](C)(C)C(C)(C)C)=C1	3927.3	Semi standard non polar	33892256
Dopamine glucuronide,5TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4117.4	Semi standard non polar	33892256
Dopamine glucuronide,5TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4126.8	Semi standard non polar	33892256
Dopamine glucuronide,5TBDMS,isomer #8	CC(C)(C)[Si](C)(C)NCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1	3946.9	Semi standard non polar	33892256
Dopamine glucuronide,5TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1=CC(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4133.9	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Dopamine glucuronide GC-MS (Non-derivatized) - 70eV, Positive	splash10-06wc-9352000000-343bd0f0b87468777501	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Dopamine glucuronide GC-MS (5 TMS) - 70eV, Positive	splash10-00fr-2211019000-6cb50bef6a04950150ac	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Dopamine glucuronide GC-MS (TBDMS_5_2) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Dopamine glucuronide GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Dopamine glucuronide GC-MS ("Dopamine glucuronide,5TBDMS,#2" TMS) - 70eV, Positive	Not Available	2021-10-14	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dopamine glucuronide 10V, Positive-QTOF	splash10-0w39-0905000000-973b514d779787c1ed35	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dopamine glucuronide 20V, Positive-QTOF	splash10-0udr-0900000000-b39ce9a39c0704f826ab	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dopamine glucuronide 40V, Positive-QTOF	splash10-0f7c-4900000000-1ca8c1f80f365afab9e8	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dopamine glucuronide 10V, Negative-QTOF	splash10-0fb9-2936000000-d4215ec6d1b1a5c32e9d	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dopamine glucuronide 20V, Negative-QTOF	splash10-0udi-1910000000-e44be480655e1eab22b7	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dopamine glucuronide 40V, Negative-QTOF	splash10-0udi-3900000000-6faf5b2447d959a4e90a	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dopamine glucuronide 10V, Positive-QTOF	splash10-03di-0569000000-aea0886f18677f86e9a5	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dopamine glucuronide 20V, Positive-QTOF	splash10-000i-0942000000-b7dd21b08c387d6f2712	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dopamine glucuronide 40V, Positive-QTOF	splash10-014i-0900000000-ecc68c9736f744bb1d28	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dopamine glucuronide 10V, Negative-QTOF	splash10-004i-0009000000-196d0448ff8008bd804b	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dopamine glucuronide 20V, Negative-QTOF	splash10-0fbi-5926000000-297592c1f05e46b2074d	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dopamine glucuronide 40V, Negative-QTOF	splash10-05g0-6900000000-2b7c940ded815fa31547	2021-09-23	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm

Biospecimen Locations

Blood
Urine

Tissue Locations

Kidney
Liver

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Expected but not Quantified	Not Quantified	Not Available	Not Available	Normal	Not Available	details

Abnormal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Urine	Detected and Quantified	0.0055 +/- 0.00035 umol/mmol creatinine	Adult (>18 years old)	Both	Increased dietary phosphate intake	8320494	details

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB027481

KNApSAcK ID

Not Available

Chemspider ID

2339915

KEGG Compound ID

Not Available

BioCyc ID

Beta-D-Glucuronides

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

3082490

PDB ID

Not Available

ChEBI ID

88776

Food Biomarker Ontology

Not Available

VMH ID

DOPA4GLCUR

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Not Available

Only showing the first 10 proteins. There are 18 proteins in total.

Show all enzymes and transporters

Enzymes

Enzyme Details

1. UDP-glucuronosyltransferase 2B28

General function:: Involved in transferase activity, transferring hexosyl groups
Specific function:: UDPGTs are of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. This isozyme has glucuronidating capacity with steroid substrates such as 5-beta-androstane 3-alpha,17-beta-diol, estradiol, ADT, eugenol and bile acids. Only isoform 1 seems to be active.
Gene Name:: UGT2B28
Uniprot ID:: Q9BY64
Molecular weight:: 38742.9

Enzyme Details

2. UDP-glucuronosyltransferase 2B4

General function:: Involved in transferase activity, transferring hexosyl groups
Specific function:: UDPGTs are of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. This isozyme is active on polyhydroxylated estrogens (such as estriol, 4-hydroxyestrone and 2-hydroxyestriol) and xenobiotics (such as 4-methylumbelliferone, 1-naphthol, 4-nitrophenol, 2-aminophenol, 4-hydroxybiphenyl and menthol). It is capable of 6 alpha-hydroxyglucuronidation of hyodeoxycholic acid.
Gene Name:: UGT2B4
Uniprot ID:: P06133
Molecular weight:: 60512.035

Enzyme Details

3. UDP-glucuronosyltransferase 1-4

General function:: Involved in transferase activity, transferring hexosyl groups
Specific function:: UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. This isoform glucuronidates bilirubin IX-alpha to form both the IX-alpha-C8 and IX-alpha-C12 monoconjugates and diconjugate.
Gene Name:: UGT1A4
Uniprot ID:: P22310
Molecular weight:: 60024.535

Enzyme Details

4. UDP-glucuronosyltransferase 2B7

General function:: Involved in transferase activity, transferring hexosyl groups
Specific function:: UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. Its unique specificity for 3,4-catechol estrogens and estriol suggests it may play an important role in regulating the level and activity of these potent and active estrogen metabolites. Is also active with androsterone, hyodeoxycholic acid and tetrachlorocatechol (in vitro).
Gene Name:: UGT2B7
Uniprot ID:: P16662
Molecular weight:: 60720.15

Enzyme Details

5. UDP-glucuronosyltransferase 2B15

General function:: Involved in transferase activity, transferring hexosyl groups
Specific function:: UDPGTs are of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. This isozyme displays activity toward several classes of xenobiotic substrates, including simple phenolic compounds, 7-hydroxylated coumarins, flavonoids, anthraquinones, and certain drugs and their hydroxylated metabolites. It also catalyzes the glucuronidation of endogenous estrogens and androgens.
Gene Name:: UGT2B15
Uniprot ID:: P54855
Molecular weight:: 61035.815

Enzyme Details

6. UDP-glucuronosyltransferase 2A1

General function:: Involved in transferase activity, transferring hexosyl groups
Specific function:: UDP-glucuronosyltransferases catalyze phase II biotransformation reactions in which lipophilic substrates are conjugated with glucuronic acid to increase water solubility and enhance excretion. They are of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. Active on odorants and seems to be involved in olfaction; it could help clear lipophilic odorant molecules from the sensory epithelium.
Gene Name:: UGT2A1
Uniprot ID:: Q9Y4X1
Molecular weight:: 60771.605

Enzyme Details

7. UDP-glucuronosyltransferase 1-1

General function:: Involved in transferase activity, transferring hexosyl groups
Specific function:: UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. This isoform glucuronidates bilirubin IX-alpha to form both the IX-alpha-C8 and IX-alpha-C12 monoconjugates and diconjugate. Is also able to catalyze the glucuronidation of 17beta-estradiol, 17alpha-ethinylestradiol, 1-hydroxypyrene, 4-methylumbelliferone, 1-naphthol, paranitrophenol, scopoletin, and umbelliferone.
Gene Name:: UGT1A1
Uniprot ID:: P22309
Molecular weight:: 59590.91

Enzyme Details

8. UDP-glucuronosyltransferase 1-9

General function:: Involved in transferase activity, transferring hexosyl groups
Specific function:: UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. This isoform has specificity for phenols.
Gene Name:: UGT1A9
Uniprot ID:: O60656
Molecular weight:: 59940.495

Enzyme Details

9. UDP-glucuronosyltransferase 1-3

General function:: Involved in transferase activity, transferring hexosyl groups
Specific function:: UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds.
Gene Name:: UGT1A3
Uniprot ID:: P35503
Molecular weight:: 60337.835

Enzyme Details

10. UDP-glucuronosyltransferase 2B17

General function:: Involved in transferase activity, transferring hexosyl groups
Specific function:: UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. The major substrates of this isozyme are eugenol > 4-methylumbelliferone > dihydrotestosterone (DHT) > androstane-3-alpha,17-beta-diol (3-alpha-diol) > testosterone > androsterone (ADT).
Gene Name:: UGT2B17
Uniprot ID:: O75795
Molecular weight:: 61094.915

Only showing the first 10 proteins. There are 18 proteins in total.

Show all enzymes and transporters

Showing metabocard for Dopamine glucuronide (HMDB0010329)

MOL for HMDB0010329 (Dopamine glucuronide)

3D MOL for HMDB0010329 (Dopamine glucuronide)

3D SDF for HMDB0010329 (Dopamine glucuronide)

3D-SDF for HMDB0010329 (Dopamine glucuronide)

PDB for HMDB0010329 (Dopamine glucuronide)

3D PDB for HMDB0010329 (Dopamine glucuronide)

SMILES for HMDB0010329 (Dopamine glucuronide)

INCHI for HMDB0010329 (Dopamine glucuronide)

Structure for HMDB0010329 (Dopamine glucuronide)

3D Structure for HMDB0010329 (Dopamine glucuronide)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

Enzymes