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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-10 23:38:47 UTC

Update Date

2021-09-26 22:55:49 UTC

HMDB ID

HMDB0246630

Secondary Accession Numbers

None

Metabolite Identification

Common Name

4'-Hydroxy Nimesulide

Description

4'-Hydroxy Nimesulide belongs to the class of organic compounds known as diphenylethers. These are aromatic compounds containing two benzene rings linked to each other through an ether group. Based on a literature review a small amount of articles have been published on 4'-Hydroxy Nimesulide. This compound has been identified in human blood as reported by (PMID: 31557052 ). 4'-hydroxy nimesulide is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 4'-Hydroxy Nimesulide is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

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

HMDB0246630
     RDKit          3D
4'-Hydroxy Nimesulide
 34 35  0  0  0  0  0  0  0  0999 V2000
   -4.6499   -1.4612    0.4933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7564   -1.7497   -1.0334 S   0  0  0  0  0  6  0  0  0  0  0  0
   -3.9677   -3.1876   -1.4072 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3861   -0.8404   -2.0666 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0957   -1.4064   -0.8159 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6259   -0.1126   -0.4618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4814    0.9332   -0.2777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9823    2.1720    0.0653 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6107    2.3920    0.2323 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0972    3.6584    0.5833 N   0  0  0  0  0  4  0  0  0  0  0  0
    1.1167    3.8162    0.7220 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9496    4.7054    0.7679 O   0  0  0  0  0  1  0  0  0  0  0  0
    0.2431    1.3232    0.0425 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2741    0.0984   -0.2986 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5966   -0.9916   -0.4922 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9539   -0.8882   -0.3548 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7648   -0.5564   -1.4215 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1304   -0.4635   -1.2358 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6820   -0.7006    0.0072 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0576   -0.6013    0.1698 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8739   -1.0341    1.0824 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5115   -1.1237    0.8840 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5679   -0.8817    0.3319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9213   -2.4267    0.9717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9602   -0.9284    1.1957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4201   -2.1923   -0.9537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5685    0.8263   -0.3937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6364    3.0418    0.2231 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3264    1.4346    0.1592 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3561   -0.3631   -2.4175 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7616   -0.1978   -2.0979 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4251    0.3146    0.4313 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2767   -1.2220    2.0530 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8752   -1.3867    1.7319 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  2  0
  2  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
  9 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  2  0
 14  6  1  0
 22 16  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  5 26  1  0
  7 27  1  0
  8 28  1  0
 13 29  1  0
 17 30  1  0
 18 31  1  0
 20 32  1  0
 21 33  1  0
 22 34  1  0
M  CHG  2  10   1  12  -1
M  END


  Mrv1652309112101392D          

 22 23  0  0  0  0            999 V2000
    0.7145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414    0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  2  0  0  0  0
  2  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  6 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
  7 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 16 21  1  0  0  0  0
 19 22  1  0  0  0  0
M  CHG  2  12   1  14  -1
M  END
> <DATABASE_ID>
HMDB0246630

> <DATABASE_NAME>
hmdb

> <SMILES>
CS(=O)(=O)NC1=C(OC2=CC=C(O)C=C2)C=C(C=C1)[N+]([O-])=O

> <INCHI_IDENTIFIER>
InChI=1S/C13H12N2O6S/c1-22(19,20)14-12-7-2-9(15(17)18)8-13(12)21-11-5-3-10(16)4-6-11/h2-8,14,16H,1H3

> <INCHI_KEY>
XYHFQSKAUPPPBY-UHFFFAOYSA-N

> <FORMULA>
C13H12N2O6S

> <MOLECULAR_WEIGHT>
324.31

> <EXACT_MASS>
324.041607288

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
29.94967805812442

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-[2-(4-hydroxyphenoxy)-4-nitrophenyl]methanesulfonamide

> <ALOGPS_LOGP>
2.31

> <JCHEM_LOGP>
1.483091049

> <ALOGPS_LOGS>
-3.93

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.17591009198906

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.696510698910851

> <JCHEM_PKA_STRONGEST_BASIC>
-3.717609503702096

> <JCHEM_POLAR_SURFACE_AREA>
118.77000000000001

> <JCHEM_REFRACTIVITY>
77.28340000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.83e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-[2-(4-hydroxyphenoxy)-4-nitrophenyl]methanesulfonamide

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0246630
     RDKit          3D
4'-Hydroxy Nimesulide
 34 35  0  0  0  0  0  0  0  0999 V2000
   -4.6499   -1.4612    0.4933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7564   -1.7497   -1.0334 S   0  0  0  0  0  6  0  0  0  0  0  0
   -3.9677   -3.1876   -1.4072 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3861   -0.8404   -2.0666 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0957   -1.4064   -0.8159 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6259   -0.1126   -0.4618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4814    0.9332   -0.2777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9823    2.1720    0.0653 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6107    2.3920    0.2323 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0972    3.6584    0.5833 N   0  0  0  0  0  4  0  0  0  0  0  0
    1.1167    3.8162    0.7220 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9496    4.7054    0.7679 O   0  0  0  0  0  1  0  0  0  0  0  0
    0.2431    1.3232    0.0425 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2741    0.0984   -0.2986 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5966   -0.9916   -0.4922 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9539   -0.8882   -0.3548 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7648   -0.5564   -1.4215 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1304   -0.4635   -1.2358 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6820   -0.7006    0.0072 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0576   -0.6013    0.1698 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8739   -1.0341    1.0824 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5115   -1.1237    0.8840 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5679   -0.8817    0.3319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9213   -2.4267    0.9717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9602   -0.9284    1.1957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4201   -2.1923   -0.9537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5685    0.8263   -0.3937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6364    3.0418    0.2231 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3264    1.4346    0.1592 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3561   -0.3631   -2.4175 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7616   -0.1978   -2.0979 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4251    0.3146    0.4313 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2767   -1.2220    2.0530 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8752   -1.3867    1.7319 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  2  0
  2  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
  9 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  2  0
 14  6  1  0
 22 16  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  5 26  1  0
  7 27  1  0
  8 28  1  0
 13 29  1  0
 17 30  1  0
 18 31  1  0
 20 32  1  0
 21 33  1  0
 22 34  1  0
M  CHG  2  10   1  12  -1
M  END

HEADER    PROTEIN                                 11-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-21         0                                  
HETATM    1  C   UNK     0       1.334   0.770   0.000  0.00  0.00           C+0
HETATM    2  S   UNK     0       2.667   0.000   0.000  0.00  0.00           S+0
HETATM    3  O   UNK     0       1.897  -1.334   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       3.437   1.334   0.000  0.00  0.00           O+0
HETATM    5  N   UNK     0       4.001  -0.770   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       4.001  -6.930   0.000  0.00  0.00           N+1
HETATM   13  O   UNK     0       2.667  -7.700   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       5.335  -7.700   0.000  0.00  0.00           O-1
HETATM   15  O   UNK     0       6.668  -2.310   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      12.003  -5.390   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4    5                                             
CONECT    3    2                                                            
CONECT    4    2                                                            
CONECT    5    2    6                                                       
CONECT    6    5    7   11                                                  
CONECT    7    6    8   15                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10    6                                                       
CONECT   12    9   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15    7   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20   16                                                       
CONECT   22   19                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

COMPND    HMDB0246630
HETATM    1  C1  UNL     1      -4.650  -1.461   0.493  1.00  0.00           C  
HETATM    2  S1  UNL     1      -3.756  -1.750  -1.033  1.00  0.00           S  
HETATM    3  O1  UNL     1      -3.968  -3.188  -1.407  1.00  0.00           O  
HETATM    4  O2  UNL     1      -4.386  -0.840  -2.067  1.00  0.00           O  
HETATM    5  N1  UNL     1      -2.096  -1.406  -0.816  1.00  0.00           N  
HETATM    6  C2  UNL     1      -1.626  -0.113  -0.462  1.00  0.00           C  
HETATM    7  C3  UNL     1      -2.481   0.933  -0.278  1.00  0.00           C  
HETATM    8  C4  UNL     1      -1.982   2.172   0.065  1.00  0.00           C  
HETATM    9  C5  UNL     1      -0.611   2.392   0.232  1.00  0.00           C  
HETATM   10  N2  UNL     1      -0.097   3.658   0.583  1.00  0.00           N1+
HETATM   11  O3  UNL     1       1.117   3.816   0.722  1.00  0.00           O  
HETATM   12  O4  UNL     1      -0.950   4.705   0.768  1.00  0.00           O1-
HETATM   13  C6  UNL     1       0.243   1.323   0.042  1.00  0.00           C  
HETATM   14  C7  UNL     1      -0.274   0.098  -0.299  1.00  0.00           C  
HETATM   15  O5  UNL     1       0.597  -0.992  -0.492  1.00  0.00           O  
HETATM   16  C8  UNL     1       1.954  -0.888  -0.355  1.00  0.00           C  
HETATM   17  C9  UNL     1       2.765  -0.556  -1.421  1.00  0.00           C  
HETATM   18  C10 UNL     1       4.130  -0.464  -1.236  1.00  0.00           C  
HETATM   19  C11 UNL     1       4.682  -0.701   0.007  1.00  0.00           C  
HETATM   20  O6  UNL     1       6.058  -0.601   0.170  1.00  0.00           O  
HETATM   21  C12 UNL     1       3.874  -1.034   1.082  1.00  0.00           C  
HETATM   22  C13 UNL     1       2.512  -1.124   0.884  1.00  0.00           C  
HETATM   23  H1  UNL     1      -5.568  -0.882   0.332  1.00  0.00           H  
HETATM   24  H2  UNL     1      -4.921  -2.427   0.972  1.00  0.00           H  
HETATM   25  H3  UNL     1      -3.960  -0.928   1.196  1.00  0.00           H  
HETATM   26  H4  UNL     1      -1.420  -2.192  -0.954  1.00  0.00           H  
HETATM   27  H5  UNL     1      -3.569   0.826  -0.394  1.00  0.00           H  
HETATM   28  H6  UNL     1      -2.636   3.042   0.223  1.00  0.00           H  
HETATM   29  H7  UNL     1       1.326   1.435   0.159  1.00  0.00           H  
HETATM   30  H8  UNL     1       2.356  -0.363  -2.418  1.00  0.00           H  
HETATM   31  H9  UNL     1       4.762  -0.198  -2.098  1.00  0.00           H  
HETATM   32  H10 UNL     1       6.425   0.315   0.431  1.00  0.00           H  
HETATM   33  H11 UNL     1       4.277  -1.222   2.053  1.00  0.00           H  
HETATM   34  H12 UNL     1       1.875  -1.387   1.732  1.00  0.00           H  
CONECT    1    2   23   24   25
CONECT    2    3    3    4    4
CONECT    2    5
CONECT    5    6   26
CONECT    6    7    7   14
CONECT    7    8   27
CONECT    8    9    9   28
CONECT    9   10   13
CONECT   10   11   11   12
CONECT   13   14   14   29
CONECT   14   15
CONECT   15   16
CONECT   16   17   17   22
CONECT   17   18   30
CONECT   18   19   19   31
CONECT   19   20   21
CONECT   20   32
CONECT   21   22   22   33
CONECT   22   34
END

HMDB0246630
     RDKit          3D
4'-Hydroxy Nimesulide
 34 35  0  0  0  0  0  0  0  0999 V2000
   -4.6499   -1.4612    0.4933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7564   -1.7497   -1.0334 S   0  0  0  0  0  6  0  0  0  0  0  0
   -3.9677   -3.1876   -1.4072 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3861   -0.8404   -2.0666 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0957   -1.4064   -0.8159 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6259   -0.1126   -0.4618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4814    0.9332   -0.2777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9823    2.1720    0.0653 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6107    2.3920    0.2323 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0972    3.6584    0.5833 N   0  0  0  0  0  4  0  0  0  0  0  0
    1.1167    3.8162    0.7220 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9496    4.7054    0.7679 O   0  0  0  0  0  1  0  0  0  0  0  0
    0.2431    1.3232    0.0425 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2741    0.0984   -0.2986 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5966   -0.9916   -0.4922 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9539   -0.8882   -0.3548 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7648   -0.5564   -1.4215 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1304   -0.4635   -1.2358 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6820   -0.7006    0.0072 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0576   -0.6013    0.1698 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8739   -1.0341    1.0824 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5115   -1.1237    0.8840 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5679   -0.8817    0.3319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9213   -2.4267    0.9717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9602   -0.9284    1.1957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4201   -2.1923   -0.9537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5685    0.8263   -0.3937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6364    3.0418    0.2231 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3264    1.4346    0.1592 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3561   -0.3631   -2.4175 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7616   -0.1978   -2.0979 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4251    0.3146    0.4313 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2767   -1.2220    2.0530 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8752   -1.3867    1.7319 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  2  0
  2  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
  9 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  2  0
 14  6  1  0
 22 16  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  5 26  1  0
  7 27  1  0
  8 28  1  0
 13 29  1  0
 17 30  1  0
 18 31  1  0
 20 32  1  0
 21 33  1  0
 22 34  1  0
M  CHG  2  10   1  12  -1
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
N-[2-(4-Hydroxyphenoxy)-4-nitrophenyl]methanesulphonamide	HMDB
4-Hydroxynimesulide	HMDB
4-Nitro-2-(4'-hydroxyphenoxy)methanesulfonanilide	HMDB
Hydroxynimesulide	HMDB

Chemical Formula

C₁₃H₁₂N₂O₆S

Average Molecular Weight

324.31

Monoisotopic Molecular Weight

324.041607288

IUPAC Name

N-[2-(4-hydroxyphenoxy)-4-nitrophenyl]methanesulfonamide

Traditional Name

N-[2-(4-hydroxyphenoxy)-4-nitrophenyl]methanesulfonamide

CAS Registry Number

Not Available

SMILES

CS(=O)(=O)NC1=C(OC2=CC=C(O)C=C2)C=C(C=C1)[N+]([O-])=O

InChI Identifier

InChI=1S/C13H12N2O6S/c1-22(19,20)14-12-7-2-9(15(17)18)8-13(12)21-11-5-3-10(16)4-6-11/h2-8,14,16H,1H3

InChI Key

XYHFQSKAUPPPBY-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diphenylethers. These are aromatic compounds containing two benzene rings linked to each other through an ether group.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Diphenylethers

Direct Parent

Diphenylethers

Alternative Parents

Substituents

Diphenylether
Diaryl ether
Sulfanilide
Nitrobenzene
Phenoxy compound
Nitroaromatic compound
Phenol ether
1-hydroxy-2-unsubstituted benzenoid
Phenol
Organic sulfonic acid amide
Organosulfonic acid amide
Organic sulfonic acid or derivatives
Organosulfonic acid or derivatives
Sulfonyl
Aminosulfonyl compound
Organic nitro compound
C-nitro compound
Ether
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Allyl-type 1,3-dipolar organic compound
Organic oxoazanium
Organic nitrogen compound
Organopnictogen compound
Organosulfur compound
Organooxygen compound
Organonitrogen compound
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
Organic zwitterion
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Source

Exogenous

Exogenous (PMID: 31557052)

Process

Not Available

Role

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	2.31	ALOGPS
logP	1.48	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	6.7	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	118.77 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	77.28 m³·mol⁻¹	ChemAxon
Polarizability	29.95 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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
DeepCCS	[M+H]+	162.59	30932474
DeepCCS	[M-H]-	160.232	30932474
DeepCCS	[M-2H]-	193.117	30932474
DeepCCS	[M+Na]+	168.683	30932474
AllCCS	[M+H]+	170.6	32859911
AllCCS	[M+H-H2O]+	167.3	32859911
AllCCS	[M+NH4]+	173.5	32859911
AllCCS	[M+Na]+	174.4	32859911
AllCCS	[M-H]-	165.8	32859911
AllCCS	[M+Na-2H]-	165.2	32859911
AllCCS	[M+HCOO]-	164.7	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Predicted by Siyang on May 30, 2022	12.2683 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	1.31 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	1834.7 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	315.9 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	153.4 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	186.9 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	133.1 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	464.6 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	474.1 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	133.9 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	1077.9 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	419.6 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	1217.0 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	343.3 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	377.0 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	357.6 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	212.1 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	81.5 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
4'-Hydroxy Nimesulide	CS(=O)(=O)NC1=C(OC2=CC=C(O)C=C2)C=C(C=C1)[N+]([O-])=O	4775.9	Standard polar	33892256
4'-Hydroxy Nimesulide	CS(=O)(=O)NC1=C(OC2=CC=C(O)C=C2)C=C(C=C1)[N+]([O-])=O	2982.5	Standard non polar	33892256
4'-Hydroxy Nimesulide	CS(=O)(=O)NC1=C(OC2=CC=C(O)C=C2)C=C(C=C1)[N+]([O-])=O	3031.7	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
4'-Hydroxy Nimesulide,2TMS,isomer #1	C[Si](C)(C)OC1=CC=C(OC2=CC([N+](=O)[O-])=CC=C2N([Si](C)(C)C)S(C)(=O)=O)C=C1	2791.0	Semi standard non polar	33892256
4'-Hydroxy Nimesulide,2TMS,isomer #1	C[Si](C)(C)OC1=CC=C(OC2=CC([N+](=O)[O-])=CC=C2N([Si](C)(C)C)S(C)(=O)=O)C=C1	2908.2	Standard non polar	33892256
4'-Hydroxy Nimesulide,2TMS,isomer #1	C[Si](C)(C)OC1=CC=C(OC2=CC([N+](=O)[O-])=CC=C2N([Si](C)(C)C)S(C)(=O)=O)C=C1	3614.0	Standard polar	33892256
4'-Hydroxy Nimesulide,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC=C(OC2=CC([N+](=O)[O-])=CC=C2N([Si](C)(C)C(C)(C)C)S(C)(=O)=O)C=C1	3297.4	Semi standard non polar	33892256
4'-Hydroxy Nimesulide,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC=C(OC2=CC([N+](=O)[O-])=CC=C2N([Si](C)(C)C(C)(C)C)S(C)(=O)=O)C=C1	3412.7	Standard non polar	33892256
4'-Hydroxy Nimesulide,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC=C(OC2=CC([N+](=O)[O-])=CC=C2N([Si](C)(C)C(C)(C)C)S(C)(=O)=O)C=C1	3662.3	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 4'-Hydroxy Nimesulide GC-MS (Non-derivatized) - 70eV, Positive	splash10-0561-4982000000-7eb8a1a08faeb93b6244	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4'-Hydroxy Nimesulide GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4'-Hydroxy Nimesulide GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4'-Hydroxy Nimesulide GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4'-Hydroxy Nimesulide GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4'-Hydroxy Nimesulide GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	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

Not Available

KNApSAcK ID

Not Available

Chemspider ID

115831

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

130995

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

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for 4'-Hydroxy Nimesulide (HMDB0246630)

MOL for HMDB0246630 (4'-Hydroxy Nimesulide)

3D MOL for HMDB0246630 (4'-Hydroxy Nimesulide)

3D SDF for HMDB0246630 (4'-Hydroxy Nimesulide)

3D-SDF for HMDB0246630 (4'-Hydroxy Nimesulide)

PDB for HMDB0246630 (4'-Hydroxy Nimesulide)

3D PDB for HMDB0246630 (4'-Hydroxy Nimesulide)

SMILES for HMDB0246630 (4'-Hydroxy Nimesulide)

INCHI for HMDB0246630 (4'-Hydroxy Nimesulide)

Structure for HMDB0246630 (4'-Hydroxy Nimesulide)

3D Structure for HMDB0246630 (4'-Hydroxy Nimesulide)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra