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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2017-11-16 21:45:41 UTC

Update Date

2022-09-22 18:34:31 UTC

HMDB ID

HMDB0240215

Secondary Accession Numbers

None

Metabolite Identification

Common Name

2-Methoxyacetaminophen glucuronide

Description

2-Methoxyacetaminophen glucuronide is classified as a member of the class of compounds known as phenolic glycosides. Phenolic glycosides 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. 2-Methoxyacetaminophen glucuronide is considered to be soluble (in water) and a moderately acidic compound.

Structure

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

HMDB0240215
     RDKit          3D
2-Methoxyacetaminophen glucuronide
 44 45  0  0  0  0  0  0  0  0999 V2000
    3.7996   -2.5878    1.8834 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9904   -1.5004    1.0262 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9483   -0.7891    0.4517 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6343   -1.0811    0.6669 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5753   -0.3642    0.0878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7141   -0.7345    0.3651 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8848   -0.1483   -0.1120 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5279    0.4140    0.9785 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7475    0.9732    0.6387 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2470    1.8747    1.6803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5723    2.0497    2.7185 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4593    2.5244    1.5077 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6797   -0.2162    0.4108 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.9859    0.1946    0.2837 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1853   -0.9141   -0.8096 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8636   -2.1533   -0.8823 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7266   -1.1007   -0.8959 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3535   -1.0397   -2.2535 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9404    0.6610   -0.7181 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2811    1.0122   -0.9798 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2800    0.2910   -0.3980 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6299    0.5709   -0.6032 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.1391    1.5918   -1.4040 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6530    1.7420   -1.5048 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4530    2.3958   -2.0474 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3762   -2.2638    2.8687 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2358   -3.4175    1.4471 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8207   -2.9882    2.1407 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3626   -1.9045    1.3145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6278    0.6948   -0.7753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6214    1.5160   -0.3223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5096    3.3910    0.9916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5194   -0.8954    1.2900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3520    0.3627    1.2073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5684   -0.3354   -1.7014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0841   -2.4676    0.0316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4650   -2.1294   -0.5684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5164   -1.5382   -2.4110 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1944    1.2713   -1.2093 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4684    1.8361   -1.6288 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3457   -0.0601   -0.0962 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1537    1.0199   -0.8296 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9601    2.7673   -1.2899 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9700    1.4750   -2.5325 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  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
 10 12  1  0
  9 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
  5 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  2  0
 21  3  1  0
 17  7  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  4 29  1  0
  7 30  1  6
  9 31  1  6
 12 32  1  0
 13 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  0
 20 40  1  0
 22 41  1  0
 24 42  1  0
 24 43  1  0
 24 44  1  0
M  END

      
  Mrv1652311171717002D          

 25 26  0  0  1  0            999 V2000
    8.6677   -6.0748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9531   -5.6623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3821   -4.8372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6677   -4.4248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3821   -5.6623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9531   -4.8372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3821   -3.1871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6677   -3.5997    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.3821   -2.3621    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0965   -3.5997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6677   -6.8998    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0966   -4.4248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8111   -4.8372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9533   -7.3122    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.9533   -8.1373    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.2388   -6.8999    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2390   -8.5498    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.5244   -7.3124    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5244   -8.1373    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.6678   -8.5498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2390   -9.3749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8099   -8.5498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8099   -6.8999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0955   -7.3124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8098   -6.0749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1 11  1  0  0  0  0
  2  1  1  0  0  0  0
  4  3  2  0  0  0  0
  4  8  1  0  0  0  0
  5  3  1  0  0  0  0
  1  5  2  0  0  0  0
  2  6  2  0  0  0  0
  6  4  1  0  0  0  0
 10  7  1  0  0  0  0
  8  7  1  0  0  0  0
  9  7  2  0  0  0  0
  3 12  1  0  0  0  0
 12 13  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 15 17  1  0  0  0  0
 16 18  1  0  0  0  0
 17 19  1  0  0  0  0
 18 19  1  0  0  0  0
 14 11  1  1  0  0  0
 15 20  1  6  0  0  0
 17 21  1  1  0  0  0
 19 22  1  6  0  0  0
 18 23  1  1  0  0  0
 24 23  1  0  0  0  0
 25 23  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0240215

> <DATABASE_NAME>
hmdb

> <SMILES>
COC1=C(NC(C)=O)C=CC(O[C@@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)C(O)=O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C15H19NO9/c1-6(17)16-8-4-3-7(5-9(8)23-2)24-15-12(20)10(18)11(19)13(25-15)14(21)22/h3-5,10-13,15,18-20H,1-2H3,(H,16,17)(H,21,22)/t10-,11-,12+,13-,15+/m0/s1

> <INCHI_KEY>
GDCCQRYSPGZVPX-DKBOKBLXSA-N

> <FORMULA>
C15H19NO9

> <MOLECULAR_WEIGHT>
357.315

> <EXACT_MASS>
357.105981196

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
33.33139386035292

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3S,4S,5R,6S)-6-(4-acetamido-3-methoxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid

> <ALOGPS_LOGP>
-0.69

> <JCHEM_LOGP>
-1.1980739593333336

> <ALOGPS_LOGS>
-1.32

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.129910208896796

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.9181416205985893

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6868267697442434

> <JCHEM_POLAR_SURFACE_AREA>
154.78

> <JCHEM_REFRACTIVITY>
81.37689999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.70e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3S,4S,5R,6S)-6-(4-acetamido-3-methoxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0240215
     RDKit          3D
2-Methoxyacetaminophen glucuronide
 44 45  0  0  0  0  0  0  0  0999 V2000
    3.7996   -2.5878    1.8834 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9904   -1.5004    1.0262 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9483   -0.7891    0.4517 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6343   -1.0811    0.6669 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5753   -0.3642    0.0878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7141   -0.7345    0.3651 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8848   -0.1483   -0.1120 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5279    0.4140    0.9785 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7475    0.9732    0.6387 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2470    1.8747    1.6803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5723    2.0497    2.7185 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4593    2.5244    1.5077 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6797   -0.2162    0.4108 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.9859    0.1946    0.2837 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1853   -0.9141   -0.8096 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8636   -2.1533   -0.8823 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7266   -1.1007   -0.8959 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3535   -1.0397   -2.2535 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9404    0.6610   -0.7181 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2811    1.0122   -0.9798 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2800    0.2910   -0.3980 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6299    0.5709   -0.6032 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.1391    1.5918   -1.4040 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6530    1.7420   -1.5048 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4530    2.3958   -2.0474 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3762   -2.2638    2.8687 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2358   -3.4175    1.4471 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8207   -2.9882    2.1407 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3626   -1.9045    1.3145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6278    0.6948   -0.7753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6214    1.5160   -0.3223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5096    3.3910    0.9916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5194   -0.8954    1.2900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3520    0.3627    1.2073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5684   -0.3354   -1.7014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0841   -2.4676    0.0316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4650   -2.1294   -0.5684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5164   -1.5382   -2.4110 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1944    1.2713   -1.2093 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4684    1.8361   -1.6288 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3457   -0.0601   -0.0962 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1537    1.0199   -0.8296 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9601    2.7673   -1.2899 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9700    1.4750   -2.5325 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  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
 10 12  1  0
  9 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
  5 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  2  0
 21  3  1  0
 17  7  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  4 29  1  0
  7 30  1  6
  9 31  1  6
 12 32  1  0
 13 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  0
 20 40  1  0
 22 41  1  0
 24 42  1  0
 24 43  1  0
 24 44  1  0
M  END

HEADER    PROTEIN                                 17-NOV-17   NONE
TITLE     NULL                                                        
COMPND    MOLECULE:                                                   
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-NOV-17         0                                  
HETATM    1  C   UNK     0      16.180 -11.340   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.846 -10.570   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      17.513  -9.029   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      16.180  -8.260   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      17.513 -10.570   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      14.846  -9.029   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      17.513  -5.949   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0      16.180  -6.719   0.000  0.00  0.00           N+0
HETATM    9  O   UNK     0      17.513  -4.409   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      18.847  -6.719   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      16.180 -12.880   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0      18.847  -8.260   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      20.181  -9.029   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.846 -13.649   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.846 -15.190   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      13.512 -12.880   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      13.513 -15.960   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.179 -13.650   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      12.179 -15.190   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      16.180 -15.960   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      13.513 -17.500   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      10.845 -15.960   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      10.845 -12.880   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       9.512 -13.650   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      10.845 -11.340   0.000  0.00  0.00           O+0
CONECT    1   11    2    5                                                  
CONECT    2    1    6                                                       
CONECT    3    4    5   12                                                  
CONECT    4    3    8    6                                                  
CONECT    5    3    1                                                       
CONECT    6    2    4                                                       
CONECT    7   10    8    9                                                  
CONECT    8    4    7                                                       
CONECT    9    7                                                            
CONECT   10    7                                                            
CONECT   11    1   14                                                       
CONECT   12    3   13                                                       
CONECT   13   12                                                            
CONECT   14   15   16   11                                                  
CONECT   15   14   17   20                                                  
CONECT   16   14   18                                                       
CONECT   17   15   19   21                                                  
CONECT   18   16   19   23                                                  
CONECT   19   17   18   22                                                  
CONECT   20   15                                                            
CONECT   21   17                                                            
CONECT   22   19                                                            
CONECT   23   18   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   52    0
END

COMPND    HMDB0240215
HETATM    1  C1  UNL     1       3.800  -2.588   1.883  1.00  0.00           C  
HETATM    2  O1  UNL     1       3.990  -1.500   1.026  1.00  0.00           O  
HETATM    3  C2  UNL     1       2.948  -0.789   0.452  1.00  0.00           C  
HETATM    4  C3  UNL     1       1.634  -1.081   0.667  1.00  0.00           C  
HETATM    5  C4  UNL     1       0.575  -0.364   0.088  1.00  0.00           C  
HETATM    6  O2  UNL     1      -0.714  -0.734   0.365  1.00  0.00           O  
HETATM    7  C5  UNL     1      -1.885  -0.148  -0.112  1.00  0.00           C  
HETATM    8  O3  UNL     1      -2.528   0.414   0.978  1.00  0.00           O  
HETATM    9  C6  UNL     1      -3.748   0.973   0.639  1.00  0.00           C  
HETATM   10  C7  UNL     1      -4.247   1.875   1.680  1.00  0.00           C  
HETATM   11  O4  UNL     1      -3.572   2.050   2.719  1.00  0.00           O  
HETATM   12  O5  UNL     1      -5.459   2.524   1.508  1.00  0.00           O  
HETATM   13  C8  UNL     1      -4.680  -0.216   0.411  1.00  0.00           C  
HETATM   14  O6  UNL     1      -5.986   0.195   0.284  1.00  0.00           O  
HETATM   15  C9  UNL     1      -4.185  -0.914  -0.810  1.00  0.00           C  
HETATM   16  O7  UNL     1      -4.864  -2.153  -0.882  1.00  0.00           O  
HETATM   17  C10 UNL     1      -2.727  -1.101  -0.896  1.00  0.00           C  
HETATM   18  O8  UNL     1      -2.354  -1.040  -2.254  1.00  0.00           O  
HETATM   19  C11 UNL     1       0.940   0.661  -0.718  1.00  0.00           C  
HETATM   20  C12 UNL     1       2.281   1.012  -0.980  1.00  0.00           C  
HETATM   21  C13 UNL     1       3.280   0.291  -0.398  1.00  0.00           C  
HETATM   22  N1  UNL     1       4.630   0.571  -0.603  1.00  0.00           N  
HETATM   23  C14 UNL     1       5.139   1.592  -1.404  1.00  0.00           C  
HETATM   24  C15 UNL     1       6.653   1.742  -1.505  1.00  0.00           C  
HETATM   25  O9  UNL     1       4.453   2.396  -2.047  1.00  0.00           O  
HETATM   26  H1  UNL     1       3.376  -2.264   2.869  1.00  0.00           H  
HETATM   27  H2  UNL     1       3.236  -3.418   1.447  1.00  0.00           H  
HETATM   28  H3  UNL     1       4.821  -2.988   2.141  1.00  0.00           H  
HETATM   29  H4  UNL     1       1.363  -1.905   1.314  1.00  0.00           H  
HETATM   30  H5  UNL     1      -1.628   0.695  -0.775  1.00  0.00           H  
HETATM   31  H6  UNL     1      -3.621   1.516  -0.322  1.00  0.00           H  
HETATM   32  H7  UNL     1      -5.510   3.391   0.992  1.00  0.00           H  
HETATM   33  H8  UNL     1      -4.519  -0.895   1.290  1.00  0.00           H  
HETATM   34  H9  UNL     1      -6.352   0.363   1.207  1.00  0.00           H  
HETATM   35  H10 UNL     1      -4.568  -0.335  -1.701  1.00  0.00           H  
HETATM   36  H11 UNL     1      -5.084  -2.468   0.032  1.00  0.00           H  
HETATM   37  H12 UNL     1      -2.465  -2.129  -0.568  1.00  0.00           H  
HETATM   38  H13 UNL     1      -1.516  -1.538  -2.411  1.00  0.00           H  
HETATM   39  H14 UNL     1       0.194   1.271  -1.209  1.00  0.00           H  
HETATM   40  H15 UNL     1       2.468   1.836  -1.629  1.00  0.00           H  
HETATM   41  H16 UNL     1       5.346  -0.060  -0.096  1.00  0.00           H  
HETATM   42  H17 UNL     1       7.154   1.020  -0.830  1.00  0.00           H  
HETATM   43  H18 UNL     1       6.960   2.767  -1.290  1.00  0.00           H  
HETATM   44  H19 UNL     1       6.970   1.475  -2.533  1.00  0.00           H  
CONECT    1    2   26   27   28
CONECT    2    3
CONECT    3    4    4   21
CONECT    4    5   29
CONECT    5    6   19   19
CONECT    6    7
CONECT    7    8   17   30
CONECT    8    9
CONECT    9   10   13   31
CONECT   10   11   11   12
CONECT   12   32
CONECT   13   14   15   33
CONECT   14   34
CONECT   15   16   17   35
CONECT   16   36
CONECT   17   18   37
CONECT   18   38
CONECT   19   20   39
CONECT   20   21   21   40
CONECT   21   22
CONECT   22   23   41
CONECT   23   24   25   25
CONECT   24   42   43   44
END

HMDB0240215
     RDKit          3D
2-Methoxyacetaminophen glucuronide
 44 45  0  0  0  0  0  0  0  0999 V2000
    3.7996   -2.5878    1.8834 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9904   -1.5004    1.0262 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9483   -0.7891    0.4517 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6343   -1.0811    0.6669 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5753   -0.3642    0.0878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7141   -0.7345    0.3651 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8848   -0.1483   -0.1120 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5279    0.4140    0.9785 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7475    0.9732    0.6387 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2470    1.8747    1.6803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5723    2.0497    2.7185 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4593    2.5244    1.5077 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6797   -0.2162    0.4108 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.9859    0.1946    0.2837 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1853   -0.9141   -0.8096 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8636   -2.1533   -0.8823 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7266   -1.1007   -0.8959 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3535   -1.0397   -2.2535 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9404    0.6610   -0.7181 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2811    1.0122   -0.9798 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2800    0.2910   -0.3980 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6299    0.5709   -0.6032 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.1391    1.5918   -1.4040 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6530    1.7420   -1.5048 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4530    2.3958   -2.0474 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3762   -2.2638    2.8687 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2358   -3.4175    1.4471 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8207   -2.9882    2.1407 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3626   -1.9045    1.3145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6278    0.6948   -0.7753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6214    1.5160   -0.3223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5096    3.3910    0.9916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5194   -0.8954    1.2900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3520    0.3627    1.2073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5684   -0.3354   -1.7014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0841   -2.4676    0.0316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4650   -2.1294   -0.5684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5164   -1.5382   -2.4110 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1944    1.2713   -1.2093 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4684    1.8361   -1.6288 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3457   -0.0601   -0.0962 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1537    1.0199   -0.8296 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9601    2.7673   -1.2899 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9700    1.4750   -2.5325 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  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
 10 12  1  0
  9 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
  5 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  2  0
 21  3  1  0
 17  7  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  4 29  1  0
  7 30  1  6
  9 31  1  6
 12 32  1  0
 13 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  0
 20 40  1  0
 22 41  1  0
 24 42  1  0
 24 43  1  0
 24 44  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
2-Methoxyacetaminophen beta-D-glucuronide	ChEBI
2-Methoxyacetaminophen O-beta-D-glucosiduronic acid	ChEBI
2-Methoxyacetaminophen b-D-glucuronide	Generator
2-Methoxyacetaminophen β-D-glucuronide	Generator
2-Methoxyacetaminophen O-b-D-glucosiduronate	Generator
2-Methoxyacetaminophen O-b-D-glucosiduronic acid	Generator
2-Methoxyacetaminophen O-beta-D-glucosiduronate	Generator
2-Methoxyacetaminophen O-β-D-glucosiduronate	Generator
2-Methoxyacetaminophen O-β-D-glucosiduronic acid	Generator
2-Methoxy-4-glucuronideacetanilide	HMDB

Chemical Formula

C₁₅H₁₉NO₉

Average Molecular Weight

357.315

Monoisotopic Molecular Weight

357.105981196

IUPAC Name

(2S,3S,4S,5R,6S)-6-(4-acetamido-3-methoxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid

Traditional Name

(2S,3S,4S,5R,6S)-6-(4-acetamido-3-methoxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid

CAS Registry Number

53446-12-1

SMILES

COC1=C(NC(C)=O)C=CC(O[C@@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)C(O)=O)=C1

InChI Identifier

InChI=1S/C15H19NO9/c1-6(17)16-8-4-3-7(5-9(8)23-2)24-15-12(20)10(18)11(19)13(25-15)14(21)22/h3-5,10-13,15,18-20H,1-2H3,(H,16,17)(H,21,22)/t10-,11-,12+,13-,15+/m0/s1

InChI Key

GDCCQRYSPGZVPX-DKBOKBLXSA-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
O-glucuronide
1-o-glucuronide
Glucuronic acid or derivatives
O-glycosyl compound
Methoxyaniline
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
Alkyl aryl ether
Beta-hydroxy acid
Monocyclic benzene moiety
Benzenoid
Pyran
Monosaccharide
Hydroxy acid
Oxane
Secondary alcohol
Acetal
Carboximidic acid
Carboximidic acid derivative
Carboxylic acid derivative
Carboxylic acid
Ether
Oxacycle
Organoheterocyclic compound
Polyol
Propargyl-type 1,3-dipolar organic compound
Organic 1,3-dipolar compound
Monocarboxylic acid or derivatives
Organic oxide
Hydrocarbon derivative
Carbonyl group
Alcohol
Organic nitrogen compound
Organopnictogen compound
Organonitrogen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Physical Properties

State

Not Available

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
logP	-0.69	ALOGPS
logP	-1.2	ChemAxon
logS	-1.3	ALOGPS
pKa (Strongest Acidic)	2.92	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	154.78 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	81.38 m³·mol⁻¹	ChemAxon
Polarizability	33.33 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
AllCCS	[M+H]+	182.325	31661259
AllCCS	[M-H]-	179.304	31661259
DeepCCS	[M+H]+	182.181	30932474
DeepCCS	[M-H]-	179.785	30932474
DeepCCS	[M-2H]-	212.668	30932474
DeepCCS	[M+Na]+	188.2	30932474
AllCCS	[M+H]+	182.3	32859911
AllCCS	[M+H-H2O]+	179.5	32859911
AllCCS	[M+NH4]+	185.0	32859911
AllCCS	[M+Na]+	185.7	32859911
AllCCS	[M-H]-	179.3	32859911
AllCCS	[M+Na-2H]-	179.4	32859911
AllCCS	[M+HCOO]-	179.7	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.	3.22 minutes	32390414
Predicted by Siyang on May 30, 2022	10.5981 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	6.57 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	1245.4 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	221.4 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	77.7 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	175.5 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	57.3 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	264.8 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	320.8 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	450.1 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	651.0 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	163.1 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	995.0 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	225.7 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	220.3 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	471.4 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	436.8 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	241.8 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
2-Methoxyacetaminophen glucuronide	COC1=C(NC(C)=O)C=CC(O[C@@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)C(O)=O)=C1	4649.4	Standard polar	33892256
2-Methoxyacetaminophen glucuronide	COC1=C(NC(C)=O)C=CC(O[C@@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)C(O)=O)=C1	2931.5	Standard non polar	33892256
2-Methoxyacetaminophen glucuronide	COC1=C(NC(C)=O)C=CC(O[C@@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)C(O)=O)=C1	3187.9	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
2-Methoxyacetaminophen glucuronide,1TMS,isomer #1	COC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)=CC=C1NC(C)=O	3082.2	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,1TMS,isomer #2	COC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)=CC=C1NC(C)=O	3089.1	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,1TMS,isomer #3	COC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)=CC=C1NC(C)=O	3102.1	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,1TMS,isomer #4	COC1=CC(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)=CC=C1NC(C)=O	3096.0	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,1TMS,isomer #5	COC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)=CC=C1N(C(C)=O)[Si](C)(C)C	2911.3	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,2TMS,isomer #1	COC1=CC(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)=CC=C1NC(C)=O	3064.6	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,2TMS,isomer #10	COC1=CC(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)=CC=C1N(C(C)=O)[Si](C)(C)C	2831.6	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,2TMS,isomer #2	COC1=CC(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)=CC=C1NC(C)=O	3081.5	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,2TMS,isomer #3	COC1=CC(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)=CC=C1NC(C)=O	3084.2	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,2TMS,isomer #4	COC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)=CC=C1N(C(C)=O)[Si](C)(C)C	2858.2	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,2TMS,isomer #5	COC1=CC(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)=CC=C1NC(C)=O	3070.6	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,2TMS,isomer #6	COC1=CC(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)=CC=C1NC(C)=O	3088.7	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,2TMS,isomer #7	COC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)=CC=C1N(C(C)=O)[Si](C)(C)C	2867.4	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,2TMS,isomer #8	COC1=CC(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)=CC=C1NC(C)=O	3071.0	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,2TMS,isomer #9	COC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)=CC=C1N(C(C)=O)[Si](C)(C)C	2860.7	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,3TMS,isomer #1	COC1=CC(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)=CC=C1NC(C)=O	3059.8	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,3TMS,isomer #10	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C	2844.5	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,3TMS,isomer #2	COC1=CC(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)=CC=C1NC(C)=O	3063.8	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,3TMS,isomer #3	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C	2848.9	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,3TMS,isomer #4	COC1=CC(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)=CC=C1NC(C)=O	3071.6	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,3TMS,isomer #5	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C	2871.7	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,3TMS,isomer #6	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C	2879.7	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,3TMS,isomer #7	COC1=CC(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)=CC=C1NC(C)=O	3055.8	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,3TMS,isomer #8	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C	2866.4	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,3TMS,isomer #9	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C	2876.0	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,4TMS,isomer #1	COC1=CC(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)=CC=C1NC(C)=O	3095.3	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,4TMS,isomer #2	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C	2890.3	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,4TMS,isomer #3	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C	2916.8	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,4TMS,isomer #4	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C	2910.3	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,4TMS,isomer #5	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C	2890.5	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,5TMS,isomer #1	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C	2939.1	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,5TMS,isomer #1	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C	2830.6	Standard non polar	33892256
2-Methoxyacetaminophen glucuronide,5TMS,isomer #1	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C	3201.0	Standard polar	33892256
2-Methoxyacetaminophen glucuronide,1TBDMS,isomer #1	COC1=CC(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)=CC=C1NC(C)=O	3348.3	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,1TBDMS,isomer #2	COC1=CC(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)=CC=C1NC(C)=O	3364.4	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,1TBDMS,isomer #3	COC1=CC(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)=CC=C1NC(C)=O	3375.0	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,1TBDMS,isomer #4	COC1=CC(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)=CC=C1NC(C)=O	3385.3	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,1TBDMS,isomer #5	COC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)=CC=C1N(C(C)=O)[Si](C)(C)C(C)(C)C	3140.7	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,2TBDMS,isomer #1	COC1=CC(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)=CC=C1NC(C)=O	3571.2	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,2TBDMS,isomer #10	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C(C)(C)C	3312.5	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,2TBDMS,isomer #2	COC1=CC(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)=CC=C1NC(C)=O	3538.3	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,2TBDMS,isomer #3	COC1=CC(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)=CC=C1NC(C)=O	3554.5	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,2TBDMS,isomer #4	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C(C)(C)C	3328.0	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,2TBDMS,isomer #5	COC1=CC(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)=CC=C1NC(C)=O	3560.3	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,2TBDMS,isomer #6	COC1=CC(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)=CC=C1NC(C)=O	3551.6	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,2TBDMS,isomer #7	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C(C)(C)C	3329.0	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,2TBDMS,isomer #8	COC1=CC(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)=CC=C1NC(C)=O	3576.6	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,2TBDMS,isomer #9	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C(C)(C)C	3333.4	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,3TBDMS,isomer #1	COC1=CC(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)=CC=C1NC(C)=O	3729.0	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,3TBDMS,isomer #10	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C(C)(C)C	3515.0	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,3TBDMS,isomer #2	COC1=CC(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)=CC=C1NC(C)=O	3759.4	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,3TBDMS,isomer #3	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C(C)(C)C	3507.0	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,3TBDMS,isomer #4	COC1=CC(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)=CC=C1NC(C)=O	3733.4	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,3TBDMS,isomer #5	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C(C)(C)C	3502.7	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,3TBDMS,isomer #6	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C(C)(C)C	3523.3	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,3TBDMS,isomer #7	COC1=CC(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)=CC=C1NC(C)=O	3727.8	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,3TBDMS,isomer #8	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C(C)(C)C	3505.1	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,3TBDMS,isomer #9	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C(C)(C)C	3507.8	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,4TBDMS,isomer #1	COC1=CC(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)=CC=C1NC(C)=O	3909.2	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,4TBDMS,isomer #2	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C(C)(C)C	3678.7	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,4TBDMS,isomer #3	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C(C)(C)C	3720.9	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,4TBDMS,isomer #4	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C(C)(C)C	3693.8	Semi standard non polar	33892256
2-Methoxyacetaminophen glucuronide,4TBDMS,isomer #5	COC1=CC(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)=CC=C1N(C(C)=O)[Si](C)(C)C(C)(C)C	3678.4	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 - 2-Methoxyacetaminophen glucuronide GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-Methoxyacetaminophen 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 - 2-Methoxyacetaminophen glucuronide 10V, Positive-QTOF	splash10-053u-0918000000-5d5a4831ccd75dee010e	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Methoxyacetaminophen glucuronide 20V, Positive-QTOF	splash10-001r-0900000000-033a1ff898505a194e9f	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Methoxyacetaminophen glucuronide 40V, Positive-QTOF	splash10-01q3-2900000000-3c182a347ae754aed09e	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Methoxyacetaminophen glucuronide 10V, Negative-QTOF	splash10-0bu0-1519000000-7020d9404c68db3d6a8b	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Methoxyacetaminophen glucuronide 20V, Negative-QTOF	splash10-01q9-2922000000-dd86d7470b54665b4cb2	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Methoxyacetaminophen glucuronide 40V, Negative-QTOF	splash10-06sr-5900000000-73759157c2a5638b3197	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Methoxyacetaminophen glucuronide 10V, Negative-QTOF	splash10-0a70-0907000000-eaaf047f466ff41b58b2	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Methoxyacetaminophen glucuronide 20V, Negative-QTOF	splash10-08gr-5911000000-224feb3028550a239a6d	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Methoxyacetaminophen glucuronide 40V, Negative-QTOF	splash10-0pb9-9703000000-899d68501a5c9fa478ed	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Methoxyacetaminophen glucuronide 10V, Positive-QTOF	splash10-053u-0709000000-90e52dd403356120aae4	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Methoxyacetaminophen glucuronide 20V, Positive-QTOF	splash10-008l-0954000000-a85fe99e5ec73381c8dc	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Methoxyacetaminophen glucuronide 40V, Positive-QTOF	splash10-001l-4910000000-98eee2a457fd7d4f89b9	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

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Expected but not Quantified	Not Quantified	Not Specified	Not Specified	Cancer patients undergoing total body irradiation	31424920	details
Urine	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Cancer patients undergoing total body irradiation	31424920	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

Not Available

KNApSAcK ID

Not Available

Chemspider ID

58163585

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

121596203

PDB ID

Not Available

ChEBI ID

133005

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

Showing metabocard for 2-Methoxyacetaminophen glucuronide (HMDB0240215)

MOL for HMDB0240215 (2-Methoxyacetaminophen glucuronide)

3D MOL for HMDB0240215 (2-Methoxyacetaminophen glucuronide)

3D SDF for HMDB0240215 (2-Methoxyacetaminophen glucuronide)

3D-SDF for HMDB0240215 (2-Methoxyacetaminophen glucuronide)

PDB for HMDB0240215 (2-Methoxyacetaminophen glucuronide)

3D PDB for HMDB0240215 (2-Methoxyacetaminophen glucuronide)

SMILES for HMDB0240215 (2-Methoxyacetaminophen glucuronide)

INCHI for HMDB0240215 (2-Methoxyacetaminophen glucuronide)

Structure for HMDB0240215 (2-Methoxyacetaminophen glucuronide)

3D Structure for HMDB0240215 (2-Methoxyacetaminophen glucuronide)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra