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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

Expected but not Quantified

Creation Date

2008-09-15 16:53:13 UTC

Update Date

2021-09-14 15:39:01 UTC

HMDB ID

HMDB0010323

Secondary Accession Numbers

HMDB10323

Metabolite Identification

Common Name

Phenethylamine glucuronide

Description

Phenethylamine glucuronide is a natural human metabolite of Phenethylamine 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

HMDB0010323
     RDKit          3D
Phenethylamine glucuronide
 40 41  0  0  0  0  0  0  0  0999 V2000
    4.3717    2.1048    1.7801 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2477    1.9180    1.2550 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4755    3.0335    0.8680 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6870    0.5578    1.0210 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4273    0.6189    0.4431 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9055   -0.6457    0.3601 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4984   -0.6585    0.0043 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7953    0.0528   -1.1931 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2437   -0.1104   -1.5772 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2035    0.3858   -0.5716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6727    1.6789   -0.5901 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5931    2.1575    0.3327 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0759    1.3095    1.3311 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6132    0.0215    1.3559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7011   -0.4455    0.4376 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7377   -1.3801   -0.6943 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1175   -2.5626   -1.0317 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0722   -1.6607    0.0160 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8840   -2.4251   -0.8071 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6756   -0.2850    0.2700 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8052   -0.4059    1.0972 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3213    3.1060   -0.1447 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5618    0.0823    2.0235 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0566   -1.1602    1.3239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9064   -1.5995    0.0872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0924   -0.1073   -2.0390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7033    1.1573   -0.9209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3907    0.4232   -2.5623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4372   -1.2060   -1.7813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2959    2.3418   -1.3659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9178    3.1811    0.2584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7961    1.7343    2.0232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9984   -0.6182    2.1415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3701   -1.4809    0.5115 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9510   -0.7383   -1.5554 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2579   -2.3631   -1.4633 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8753   -2.1366    1.0063 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3337   -3.2067   -1.1298 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9958    0.1285   -0.6983 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5451   -0.7973    0.5953 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
  6 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20  4  1  0
 15 10  1  0
  3 22  1  0
  4 23  1  1
  6 24  1  1
  7 25  1  0
  8 26  1  0
  8 27  1  0
  9 28  1  0
  9 29  1  0
 11 30  1  0
 12 31  1  0
 13 32  1  0
 14 33  1  0
 15 34  1  0
 16 35  1  6
 17 36  1  0
 18 37  1  1
 19 38  1  0
 20 39  1  6
 21 40  1  0
M  END


  Mrv0541 02241200502D          

 21 22  0  0  1  0            999 V2000
   16.9793   -7.1594    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.4082   -8.8094    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.9793   -9.6344    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.5503   -8.8094    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.5503   -6.3345    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.8359   -7.5719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.4082   -7.1594    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   17.6937   -8.3969    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   16.9793   -8.8094    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.6937   -7.5719    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   16.2648   -8.3969    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   16.2648   -7.5719    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.4082   -6.3345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.5503   -7.1594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1227   -5.9220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1227   -5.0969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4082   -4.6844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.8371   -4.6844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4082   -3.8595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.8371   -3.8595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1227   -3.4470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1 10  1  0  0  0  0
  1 12  1  0  0  0  0
  8  2  1  6  0  0  0
  9  3  1  1  0  0  0
 11  4  1  6  0  0  0
  5 14  1  0  0  0  0
  6 14  2  0  0  0  0
 10  7  1  1  0  0  0
  7 13  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 14  1  1  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 17 19  1  0  0  0  0
 18 20  2  0  0  0  0
 19 21  2  0  0  0  0
 20 21  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0010323

> <DATABASE_NAME>
hmdb

> <SMILES>
O[C@@H]1[C@@H](O)[C@H](NCCC2=CC=CC=C2)O[C@@H]([C@H]1O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C14H19NO6/c16-9-10(17)12(14(19)20)21-13(11(9)18)15-7-6-8-4-2-1-3-5-8/h1-5,9-13,15-18H,6-7H2,(H,19,20)/t9-,10-,11+,12-,13+/m0/s1

> <INCHI_KEY>
OYNLGXUYULDVEJ-IEECTRCBSA-N

> <FORMULA>
C14H19NO6

> <MOLECULAR_WEIGHT>
297.3038

> <EXACT_MASS>
297.121237345

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_AVERAGE_POLARIZABILITY>
29.883497616878774

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[(2-phenylethyl)amino]oxane-2-carboxylic acid

> <ALOGPS_LOGP>
-1.46

> <JCHEM_LOGP>
-2.7472955778617694

> <ALOGPS_LOGS>
-1.16

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.48279345703823

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.3003963509938026

> <JCHEM_PKA_STRONGEST_BASIC>
7.809081648360088

> <JCHEM_POLAR_SURFACE_AREA>
119.25

> <JCHEM_REFRACTIVITY>
71.59050000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.07e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
phenethylamine glucuronide

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0010323
     RDKit          3D
Phenethylamine glucuronide
 40 41  0  0  0  0  0  0  0  0999 V2000
    4.3717    2.1048    1.7801 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2477    1.9180    1.2550 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4755    3.0335    0.8680 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6870    0.5578    1.0210 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4273    0.6189    0.4431 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9055   -0.6457    0.3601 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4984   -0.6585    0.0043 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7953    0.0528   -1.1931 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2437   -0.1104   -1.5772 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2035    0.3858   -0.5716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6727    1.6789   -0.5901 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5931    2.1575    0.3327 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0759    1.3095    1.3311 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6132    0.0215    1.3559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7011   -0.4455    0.4376 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7377   -1.3801   -0.6943 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1175   -2.5626   -1.0317 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0722   -1.6607    0.0160 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8840   -2.4251   -0.8071 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6756   -0.2850    0.2700 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8052   -0.4059    1.0972 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3213    3.1060   -0.1447 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5618    0.0823    2.0235 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0566   -1.1602    1.3239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9064   -1.5995    0.0872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0924   -0.1073   -2.0390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7033    1.1573   -0.9209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3907    0.4232   -2.5623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4372   -1.2060   -1.7813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2959    2.3418   -1.3659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9178    3.1811    0.2584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7961    1.7343    2.0232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9984   -0.6182    2.1415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3701   -1.4809    0.5115 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9510   -0.7383   -1.5554 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2579   -2.3631   -1.4633 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8753   -2.1366    1.0063 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3337   -3.2067   -1.1298 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9958    0.1285   -0.6983 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5451   -0.7973    0.5953 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
  6 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20  4  1  0
 15 10  1  0
  3 22  1  0
  4 23  1  1
  6 24  1  1
  7 25  1  0
  8 26  1  0
  8 27  1  0
  9 28  1  0
  9 29  1  0
 11 30  1  0
 12 31  1  0
 13 32  1  0
 14 33  1  0
 15 34  1  0
 16 35  1  6
 17 36  1  0
 18 37  1  1
 19 38  1  0
 20 39  1  6
 21 40  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      31.695 -13.364   0.000  0.00  0.00           O+0
HETATM    2  O   UNK     0      34.362 -16.444   0.000  0.00  0.00           O+0
HETATM    3  O   UNK     0      31.695 -17.984   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      29.027 -16.444   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      29.027 -11.824   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      27.694 -14.134   0.000  0.00  0.00           O+0
HETATM    7  N   UNK     0      34.362 -13.364   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0      33.028 -15.674   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      31.695 -16.444   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      33.028 -14.134   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      30.361 -15.674   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      30.361 -14.134   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      34.362 -11.824   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      29.027 -13.364   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      35.696 -11.054   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      35.696  -9.514   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      34.362  -8.744   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      37.029  -8.744   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      34.362  -7.204   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      37.029  -7.204   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      35.696  -6.434   0.000  0.00  0.00           C+0
CONECT    1   10   12                                                       
CONECT    2    8                                                            
CONECT    3    9                                                            
CONECT    4   11                                                            
CONECT    5   14                                                            
CONECT    6   14                                                            
CONECT    7   10   13                                                       
CONECT    8    2    9   10                                                  
CONECT    9    3    8   11                                                  
CONECT   10    1    7    8                                                  
CONECT   11    4    9   12                                                  
CONECT   12    1   11   14                                                  
CONECT   13    7   15                                                       
CONECT   14    5    6   12                                                  
CONECT   15   13   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16   19                                                       
CONECT   18   16   20                                                       
CONECT   19   17   21                                                       
CONECT   20   18   21                                                       
CONECT   21   19   20                                                       
MASTER        0    0    0    0    0    0    0    0   21    0   44    0
END

COMPND    HMDB0010323
HETATM    1  O1  UNL     1       4.372   2.105   1.780  1.00  0.00           O  
HETATM    2  C1  UNL     1       3.248   1.918   1.255  1.00  0.00           C  
HETATM    3  O2  UNL     1       2.475   3.034   0.868  1.00  0.00           O  
HETATM    4  C2  UNL     1       2.687   0.558   1.021  1.00  0.00           C  
HETATM    5  O3  UNL     1       1.427   0.619   0.443  1.00  0.00           O  
HETATM    6  C3  UNL     1       0.905  -0.646   0.360  1.00  0.00           C  
HETATM    7  N1  UNL     1      -0.498  -0.658   0.004  1.00  0.00           N  
HETATM    8  C4  UNL     1      -0.795   0.053  -1.193  1.00  0.00           C  
HETATM    9  C5  UNL     1      -2.244  -0.110  -1.577  1.00  0.00           C  
HETATM   10  C6  UNL     1      -3.204   0.386  -0.572  1.00  0.00           C  
HETATM   11  C7  UNL     1      -3.673   1.679  -0.590  1.00  0.00           C  
HETATM   12  C8  UNL     1      -4.593   2.158   0.333  1.00  0.00           C  
HETATM   13  C9  UNL     1      -5.076   1.310   1.331  1.00  0.00           C  
HETATM   14  C10 UNL     1      -4.613   0.021   1.356  1.00  0.00           C  
HETATM   15  C11 UNL     1      -3.701  -0.445   0.438  1.00  0.00           C  
HETATM   16  C12 UNL     1       1.738  -1.380  -0.694  1.00  0.00           C  
HETATM   17  O4  UNL     1       1.118  -2.563  -1.032  1.00  0.00           O  
HETATM   18  C13 UNL     1       3.072  -1.661   0.016  1.00  0.00           C  
HETATM   19  O5  UNL     1       3.884  -2.425  -0.807  1.00  0.00           O  
HETATM   20  C14 UNL     1       3.676  -0.285   0.270  1.00  0.00           C  
HETATM   21  O6  UNL     1       4.805  -0.406   1.097  1.00  0.00           O  
HETATM   22  H1  UNL     1       2.321   3.106  -0.145  1.00  0.00           H  
HETATM   23  H2  UNL     1       2.562   0.082   2.024  1.00  0.00           H  
HETATM   24  H3  UNL     1       1.057  -1.160   1.324  1.00  0.00           H  
HETATM   25  H4  UNL     1      -0.906  -1.599   0.087  1.00  0.00           H  
HETATM   26  H5  UNL     1      -0.092  -0.107  -2.039  1.00  0.00           H  
HETATM   27  H6  UNL     1      -0.703   1.157  -0.921  1.00  0.00           H  
HETATM   28  H7  UNL     1      -2.391   0.423  -2.562  1.00  0.00           H  
HETATM   29  H8  UNL     1      -2.437  -1.206  -1.781  1.00  0.00           H  
HETATM   30  H9  UNL     1      -3.296   2.342  -1.366  1.00  0.00           H  
HETATM   31  H10 UNL     1      -4.918   3.181   0.258  1.00  0.00           H  
HETATM   32  H11 UNL     1      -5.796   1.734   2.023  1.00  0.00           H  
HETATM   33  H12 UNL     1      -4.998  -0.618   2.142  1.00  0.00           H  
HETATM   34  H13 UNL     1      -3.370  -1.481   0.511  1.00  0.00           H  
HETATM   35  H14 UNL     1       1.951  -0.738  -1.555  1.00  0.00           H  
HETATM   36  H15 UNL     1       0.258  -2.363  -1.463  1.00  0.00           H  
HETATM   37  H16 UNL     1       2.875  -2.137   1.006  1.00  0.00           H  
HETATM   38  H17 UNL     1       3.334  -3.207  -1.130  1.00  0.00           H  
HETATM   39  H18 UNL     1       3.996   0.129  -0.698  1.00  0.00           H  
HETATM   40  H19 UNL     1       5.545  -0.797   0.595  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3    4
CONECT    3   22
CONECT    4    5   20   23
CONECT    5    6
CONECT    6    7   16   24
CONECT    7    8   25
CONECT    8    9   26   27
CONECT    9   10   28   29
CONECT   10   11   11   15
CONECT   11   12   30
CONECT   12   13   13   31
CONECT   13   14   32
CONECT   14   15   15   33
CONECT   15   34
CONECT   16   17   18   35
CONECT   17   36
CONECT   18   19   20   37
CONECT   19   38
CONECT   20   21   39
CONECT   21   40
END

HMDB0010323
     RDKit          3D
Phenethylamine glucuronide
 40 41  0  0  0  0  0  0  0  0999 V2000
    4.3717    2.1048    1.7801 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2477    1.9180    1.2550 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4755    3.0335    0.8680 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6870    0.5578    1.0210 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4273    0.6189    0.4431 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9055   -0.6457    0.3601 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4984   -0.6585    0.0043 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7953    0.0528   -1.1931 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2437   -0.1104   -1.5772 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2035    0.3858   -0.5716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6727    1.6789   -0.5901 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5931    2.1575    0.3327 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0759    1.3095    1.3311 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6132    0.0215    1.3559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7011   -0.4455    0.4376 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7377   -1.3801   -0.6943 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1175   -2.5626   -1.0317 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0722   -1.6607    0.0160 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8840   -2.4251   -0.8071 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6756   -0.2850    0.2700 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8052   -0.4059    1.0972 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3213    3.1060   -0.1447 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5618    0.0823    2.0235 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0566   -1.1602    1.3239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9064   -1.5995    0.0872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0924   -0.1073   -2.0390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7033    1.1573   -0.9209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3907    0.4232   -2.5623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4372   -1.2060   -1.7813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2959    2.3418   -1.3659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9178    3.1811    0.2584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7961    1.7343    2.0232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9984   -0.6182    2.1415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3701   -1.4809    0.5115 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9510   -0.7383   -1.5554 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2579   -2.3631   -1.4633 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8753   -2.1366    1.0063 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3337   -3.2067   -1.1298 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9958    0.1285   -0.6983 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5451   -0.7973    0.5953 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
  6 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20  4  1  0
 15 10  1  0
  3 22  1  0
  4 23  1  1
  6 24  1  1
  7 25  1  0
  8 26  1  0
  8 27  1  0
  9 28  1  0
  9 29  1  0
 11 30  1  0
 12 31  1  0
 13 32  1  0
 14 33  1  0
 15 34  1  0
 16 35  1  6
 17 36  1  0
 18 37  1  1
 19 38  1  0
 20 39  1  6
 21 40  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
2-Phenylethylamine glucuronide	HMDB
(2S,3S,4S,5R,6R)-3,4,5-Trihydroxy-6-[(2-phenylethyl)amino]oxane-2-carboxylate	HMDB

Chemical Formula

C₁₄H₁₉NO₆

Average Molecular Weight

297.3038

Monoisotopic Molecular Weight

297.121237345

IUPAC Name

(2S,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[(2-phenylethyl)amino]oxane-2-carboxylic acid

Traditional Name

phenethylamine glucuronide

CAS Registry Number

Not Available

SMILES

O[C@@H]1[C@@H](O)[C@H](NCCC2=CC=CC=C2)O[C@@H]([C@H]1O)C(O)=O

InChI Identifier

InChI=1S/C14H19NO6/c16-9-10(17)12(14(19)20)21-13(11(9)18)15-7-6-8-4-2-1-3-5-8/h1-5,9-13,15-18H,6-7H2,(H,19,20)/t9-,10-,11+,12-,13+/m0/s1

InChI Key

OYNLGXUYULDVEJ-IEECTRCBSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as n-glucuronides. These are glucuronides in which the aglycone is linked to the carbohydrate unit through a N-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

N-glucuronides

Alternative Parents

Substituents

N-glucuronide
1-n-glucuronide
Glycosyl compound
N-glycosyl compound
Beta-hydroxy acid
Monocyclic benzene moiety
Hydroxy acid
Monosaccharide
Oxane
Pyran
Benzenoid
Amino acid
Amino acid or derivatives
Secondary alcohol
Hemiaminal
Polyol
Oxacycle
Organoheterocyclic compound
Secondary amine
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Carboxylic acid
Secondary aliphatic amine
Organonitrogen compound
Organopnictogen compound
Organic oxide
Carbonyl group
Alcohol
Amine
Hydrocarbon derivative
Organic nitrogen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Not Available

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	20.7 g/L	ALOGPS
logP	-1.5	ALOGPS
logP	-2.7	ChemAxon
logS	-1.2	ALOGPS
pKa (Strongest Acidic)	3.3	ChemAxon
pKa (Strongest Basic)	7.81	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	119.25 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	71.59 m³·mol⁻¹	ChemAxon
Polarizability	29.88 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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]+	171.912	31661259
DarkChem	[M-H]-	165.471	31661259
DeepCCS	[M+H]+	168.772	30932474
DeepCCS	[M-H]-	166.414	30932474
DeepCCS	[M-2H]-	200.532	30932474
DeepCCS	[M+Na]+	175.453	30932474
AllCCS	[M+H]+	170.9	32859911
AllCCS	[M+H-H2O]+	167.6	32859911
AllCCS	[M+NH4]+	174.0	32859911
AllCCS	[M+Na]+	174.9	32859911
AllCCS	[M-H]-	167.7	32859911
AllCCS	[M+Na-2H]-	167.7	32859911
AllCCS	[M+HCOO]-	167.9	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.	2.14 minutes	32390414
Predicted by Siyang on May 30, 2022	11.29 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	6.03 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	1036.6 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	238.0 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	79.8 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	176.0 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	94.9 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	288.5 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	315.6 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	529.4 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	680.4 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	328.5 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	1113.1 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	207.7 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	239.3 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	434.4 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	258.1 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	160.7 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Phenethylamine glucuronide	O[C@@H]1[C@@H](O)[C@H](NCCC2=CC=CC=C2)O[C@@H]([C@H]1O)C(O)=O	4139.8	Standard polar	33892256
Phenethylamine glucuronide	O[C@@H]1[C@@H](O)[C@H](NCCC2=CC=CC=C2)O[C@@H]([C@H]1O)C(O)=O	2572.6	Standard non polar	33892256
Phenethylamine glucuronide	O[C@@H]1[C@@H](O)[C@H](NCCC2=CC=CC=C2)O[C@@H]([C@H]1O)C(O)=O	2606.0	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Phenethylamine glucuronide,1TMS,isomer #1	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](C(=O)O)O[C@@H](NCCC2=CC=CC=C2)[C@@H]1O	2524.2	Semi standard non polar	33892256
Phenethylamine glucuronide,1TMS,isomer #2	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](C(=O)O)O[C@H]1NCCC1=CC=CC=C1	2518.0	Semi standard non polar	33892256
Phenethylamine glucuronide,1TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](NCCC2=CC=CC=C2)[C@H](O)[C@H]1O	2526.9	Semi standard non polar	33892256
Phenethylamine glucuronide,1TMS,isomer #4	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](NCCC2=CC=CC=C2)[C@H](O)[C@@H](O)[C@@H]1O	2509.0	Semi standard non polar	33892256
Phenethylamine glucuronide,1TMS,isomer #5	C[Si](C)(C)N(CCC1=CC=CC=C1)[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]1O	2492.1	Semi standard non polar	33892256
Phenethylamine glucuronide,2TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](NCCC2=CC=CC=C2)[C@H](O)[C@H]1O[Si](C)(C)C	2536.6	Semi standard non polar	33892256
Phenethylamine glucuronide,2TMS,isomer #10	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](N(CCC2=CC=CC=C2)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	2463.5	Semi standard non polar	33892256
Phenethylamine glucuronide,2TMS,isomer #2	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](NCCC2=CC=CC=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2513.3	Semi standard non polar	33892256
Phenethylamine glucuronide,2TMS,isomer #3	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](C(=O)O)O[C@@H](NCCC2=CC=CC=C2)[C@@H]1O[Si](C)(C)C	2518.0	Semi standard non polar	33892256
Phenethylamine glucuronide,2TMS,isomer #4	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](C(=O)O)O[C@@H](N(CCC2=CC=CC=C2)[Si](C)(C)C)[C@@H]1O	2491.5	Semi standard non polar	33892256
Phenethylamine glucuronide,2TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](NCCC2=CC=CC=C2)[C@H](O[Si](C)(C)C)[C@H]1O	2515.4	Semi standard non polar	33892256
Phenethylamine glucuronide,2TMS,isomer #6	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](NCCC2=CC=CC=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2502.7	Semi standard non polar	33892256
Phenethylamine glucuronide,2TMS,isomer #7	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](C(=O)O)O[C@H]1N(CCC1=CC=CC=C1)[Si](C)(C)C	2495.7	Semi standard non polar	33892256
Phenethylamine glucuronide,2TMS,isomer #8	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](NCCC2=CC=CC=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2513.9	Semi standard non polar	33892256
Phenethylamine glucuronide,2TMS,isomer #9	C[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](N(CCC2=CC=CC=C2)[Si](C)(C)C)[C@H](O)[C@H]1O	2481.9	Semi standard non polar	33892256
Phenethylamine glucuronide,3TMS,isomer #1	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](NCCC2=CC=CC=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2534.4	Semi standard non polar	33892256
Phenethylamine glucuronide,3TMS,isomer #10	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](N(CCC2=CC=CC=C2)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2517.9	Semi standard non polar	33892256
Phenethylamine glucuronide,3TMS,isomer #2	C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](C(=O)O)O[C@@H](NCCC2=CC=CC=C2)[C@@H]1O[Si](C)(C)C	2527.5	Semi standard non polar	33892256
Phenethylamine glucuronide,3TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](N(CCC2=CC=CC=C2)[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2531.2	Semi standard non polar	33892256
Phenethylamine glucuronide,3TMS,isomer #4	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](NCCC2=CC=CC=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2512.9	Semi standard non polar	33892256
Phenethylamine glucuronide,3TMS,isomer #5	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](N(CCC2=CC=CC=C2)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2520.8	Semi standard non polar	33892256
Phenethylamine glucuronide,3TMS,isomer #6	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](C(=O)O)O[C@@H](N(CCC2=CC=CC=C2)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2527.7	Semi standard non polar	33892256
Phenethylamine glucuronide,3TMS,isomer #7	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](NCCC2=CC=CC=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2521.1	Semi standard non polar	33892256
Phenethylamine glucuronide,3TMS,isomer #8	C[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](N(CCC2=CC=CC=C2)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2534.5	Semi standard non polar	33892256
Phenethylamine glucuronide,3TMS,isomer #9	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](N(CCC2=CC=CC=C2)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2514.9	Semi standard non polar	33892256
Phenethylamine glucuronide,4TMS,isomer #1	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](NCCC2=CC=CC=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2547.5	Semi standard non polar	33892256
Phenethylamine glucuronide,4TMS,isomer #2	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](N(CCC2=CC=CC=C2)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2576.8	Semi standard non polar	33892256
Phenethylamine glucuronide,4TMS,isomer #3	C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](C(=O)O)O[C@@H](N(CCC2=CC=CC=C2)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2588.0	Semi standard non polar	33892256
Phenethylamine glucuronide,4TMS,isomer #4	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](N(CCC2=CC=CC=C2)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2570.8	Semi standard non polar	33892256
Phenethylamine glucuronide,4TMS,isomer #5	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](N(CCC2=CC=CC=C2)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2576.0	Semi standard non polar	33892256
Phenethylamine glucuronide,5TMS,isomer #1	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](N(CCC2=CC=CC=C2)[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	2622.4	Semi standard non polar	33892256
Phenethylamine glucuronide,5TMS,isomer #1	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](N(CCC2=CC=CC=C2)[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	2645.1	Standard non polar	33892256
Phenethylamine glucuronide,5TMS,isomer #1	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](N(CCC2=CC=CC=C2)[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	2750.5	Standard polar	33892256
Phenethylamine glucuronide,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](C(=O)O)O[C@@H](NCCC2=CC=CC=C2)[C@@H]1O	2790.2	Semi standard non polar	33892256
Phenethylamine glucuronide,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](C(=O)O)O[C@H]1NCCC1=CC=CC=C1	2779.0	Semi standard non polar	33892256
Phenethylamine glucuronide,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](NCCC2=CC=CC=C2)[C@H](O)[C@H]1O	2780.5	Semi standard non polar	33892256
Phenethylamine glucuronide,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](NCCC2=CC=CC=C2)[C@H](O)[C@@H](O)[C@@H]1O	2789.0	Semi standard non polar	33892256
Phenethylamine glucuronide,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N(CCC1=CC=CC=C1)[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]1O	2751.7	Semi standard non polar	33892256
Phenethylamine glucuronide,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](NCCC2=CC=CC=C2)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	2980.9	Semi standard non polar	33892256
Phenethylamine glucuronide,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](N(CCC2=CC=CC=C2)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	2981.8	Semi standard non polar	33892256
Phenethylamine glucuronide,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](NCCC2=CC=CC=C2)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3003.5	Semi standard non polar	33892256
Phenethylamine glucuronide,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](C(=O)O)O[C@@H](NCCC2=CC=CC=C2)[C@@H]1O[Si](C)(C)C(C)(C)C	2962.0	Semi standard non polar	33892256
Phenethylamine glucuronide,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](C(=O)O)O[C@@H](N(CCC2=CC=CC=C2)[Si](C)(C)C(C)(C)C)[C@@H]1O	2996.9	Semi standard non polar	33892256
Phenethylamine glucuronide,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](NCCC2=CC=CC=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	2961.5	Semi standard non polar	33892256
Phenethylamine glucuronide,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](NCCC2=CC=CC=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	2991.4	Semi standard non polar	33892256
Phenethylamine glucuronide,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](C(=O)O)O[C@H]1N(CCC1=CC=CC=C1)[Si](C)(C)C(C)(C)C	2993.6	Semi standard non polar	33892256
Phenethylamine glucuronide,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](NCCC2=CC=CC=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	2997.7	Semi standard non polar	33892256
Phenethylamine glucuronide,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](N(CCC2=CC=CC=C2)[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	2990.4	Semi standard non polar	33892256
Phenethylamine glucuronide,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](NCCC2=CC=CC=C2)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3162.7	Semi standard non polar	33892256
Phenethylamine glucuronide,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](N(CCC2=CC=CC=C2)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3212.6	Semi standard non polar	33892256
Phenethylamine glucuronide,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)O)O[C@@H](NCCC2=CC=CC=C2)[C@@H]1O[Si](C)(C)C(C)(C)C	3140.5	Semi standard non polar	33892256
Phenethylamine glucuronide,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](N(CCC2=CC=CC=C2)[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3209.0	Semi standard non polar	33892256
Phenethylamine glucuronide,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](NCCC2=CC=CC=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3134.9	Semi standard non polar	33892256
Phenethylamine glucuronide,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](N(CCC2=CC=CC=C2)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3210.3	Semi standard non polar	33892256
Phenethylamine glucuronide,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](C(=O)O)O[C@@H](N(CCC2=CC=CC=C2)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3205.4	Semi standard non polar	33892256
Phenethylamine glucuronide,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](NCCC2=CC=CC=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3119.2	Semi standard non polar	33892256
Phenethylamine glucuronide,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](N(CCC2=CC=CC=C2)[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3203.7	Semi standard non polar	33892256
Phenethylamine glucuronide,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](N(CCC2=CC=CC=C2)[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3209.6	Semi standard non polar	33892256
Phenethylamine glucuronide,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](NCCC2=CC=CC=C2)[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	3304.8	Semi standard non polar	33892256
Phenethylamine glucuronide,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](N(CCC2=CC=CC=C2)[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	3427.7	Semi standard non polar	33892256
Phenethylamine glucuronide,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)O)O[C@@H](N(CCC2=CC=CC=C2)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3433.9	Semi standard non polar	33892256
Phenethylamine glucuronide,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](N(CCC2=CC=CC=C2)[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	3432.9	Semi standard non polar	33892256
Phenethylamine glucuronide,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](N(CCC2=CC=CC=C2)[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	3426.6	Semi standard non polar	33892256
Phenethylamine glucuronide,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](N(CCC2=CC=CC=C2)[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	3634.3	Semi standard non polar	33892256
Phenethylamine glucuronide,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](N(CCC2=CC=CC=C2)[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	3510.0	Standard non polar	33892256
Phenethylamine glucuronide,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](N(CCC2=CC=CC=C2)[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	3237.6	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Phenethylamine glucuronide GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a6r-9440000000-53feb5385bf85eb9990d	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Phenethylamine glucuronide GC-MS (4 TMS) - 70eV, Positive	splash10-00di-3122490000-d086a68a8f89f70181d7	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Phenethylamine glucuronide GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	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 - Phenethylamine glucuronide 10V, Positive-QTOF	splash10-008a-0390000000-c36c12c05b9bd705cc9c	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Phenethylamine glucuronide 20V, Positive-QTOF	splash10-0ab9-1920000000-b61f7b736af2bb008eac	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Phenethylamine glucuronide 40V, Positive-QTOF	splash10-0a4i-4900000000-749286a7ce9ce348b6d2	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Phenethylamine glucuronide 10V, Negative-QTOF	splash10-01ot-0890000000-3f93998103c3e2900a5b	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Phenethylamine glucuronide 20V, Negative-QTOF	splash10-00el-2920000000-98736ca1b61facb0441b	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Phenethylamine glucuronide 40V, Negative-QTOF	splash10-05fs-7900000000-ec5e4aa12a33ac96e57d	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Phenethylamine glucuronide 10V, Negative-QTOF	splash10-0032-0090000000-69ce0cdd12ed53cd0c9b	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Phenethylamine glucuronide 20V, Negative-QTOF	splash10-05bg-6490000000-80037d60a671c4948c93	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Phenethylamine glucuronide 40V, Negative-QTOF	splash10-0a4l-9610000000-1ada3099cf31a1833c57	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Phenethylamine glucuronide 10V, Positive-QTOF	splash10-059t-0960000000-76b0d6f4811f27fda574	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Phenethylamine glucuronide 20V, Positive-QTOF	splash10-0a59-1970000000-f7c4c059de3e872d1c62	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Phenethylamine glucuronide 40V, Positive-QTOF	splash10-054o-9600000000-4f079ef34b5091a692f8	2021-09-22	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

Not Available

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
Urine	Expected but not Quantified	Not Quantified	Not Available	Not Available	Normal	Not Available	details

Abnormal Concentrations

Not Available

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

FDB027475

KNApSAcK ID

Not Available

Chemspider ID

166036

KEGG Compound ID

C03033

BioCyc ID

Beta-D-Glucuronides

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

191195

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

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.

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Showing metabocard for Phenethylamine glucuronide (HMDB0010323)

MOL for HMDB0010323 (Phenethylamine glucuronide)

3D MOL for HMDB0010323 (Phenethylamine glucuronide)

3D SDF for HMDB0010323 (Phenethylamine glucuronide)

3D-SDF for HMDB0010323 (Phenethylamine glucuronide)

PDB for HMDB0010323 (Phenethylamine glucuronide)

3D PDB for HMDB0010323 (Phenethylamine glucuronide)

SMILES for HMDB0010323 (Phenethylamine glucuronide)

INCHI for HMDB0010323 (Phenethylamine glucuronide)

Structure for HMDB0010323 (Phenethylamine glucuronide)

3D Structure for HMDB0010323 (Phenethylamine glucuronide)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

Enzymes