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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 20:16:53 UTC

Update Date

2021-09-26 23:15:39 UTC

HMDB ID

HMDB0258624

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Sultosilic acid

Description

2-hydroxy-5-[(4-methylbenzenesulfonyl)oxy]benzene-1-sulfonic acid belongs to the class of organic compounds known as benzenesulfonate esters. These are arenesulfonate esters that result from the formal condensation of the hydroxy group of an alcohol, enol, phenol or heteroarenol with benzenesulfonic acid. Based on a literature review very few articles have been published on 2-hydroxy-5-[(4-methylbenzenesulfonyl)oxy]benzene-1-sulfonic acid. This compound has been identified in human blood as reported by (PMID: 31557052 ). Sultosilic acid is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Sultosilic acid 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

HMDB0258624
     RDKit          3D
Sultosilic acid
 34 35  0  0  0  0  0  0  0  0999 V2000
   -6.0374    1.4051    0.2831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7299    0.6939    0.1948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5274   -0.3042   -0.7329 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3068   -0.9625   -0.8096 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2572   -0.6490    0.0300 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7084   -1.4723   -0.0549 S   0  0  0  0  0  6  0  0  0  0  0  0
   -0.0519   -1.5119    1.3027 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8689   -2.8733   -0.5787 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3168   -0.6526   -1.1393 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6805   -0.6917   -0.8805 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5141   -1.6714   -1.3764 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8619   -1.6717   -1.0943 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3922   -0.6723   -0.2993 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7450   -0.6253    0.0162 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5813    0.3171    0.2079 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2270    1.5921    1.2157 S   0  0  0  0  0  6  0  0  0  0  0  0
    4.8062    1.0648    2.4915 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1312    2.5503    1.5872 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3875    2.4381    0.3471 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2378    0.2835   -0.0964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4643    0.3514    0.9578 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6807    1.0053    1.0320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5688    1.4527   -0.6705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6754    0.8972    1.0429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8317    2.4312    0.7006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3541   -0.5528   -1.3960 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1470   -1.7452   -1.5366 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0977   -2.4443   -1.9925 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5497   -2.4202   -1.4625 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3472   -1.3621   -0.3619 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2286    2.3210   -0.6377 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5763    1.0638    0.2991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6386    0.6149    1.6356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8327    1.8005    1.7758 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  6  8  2  0
  6  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  2  0
 16 19  1  0
 15 20  2  0
  5 21  1  0
 21 22  2  0
 22  2  1  0
 20 10  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  3 26  1  0
  4 27  1  0
 11 28  1  0
 12 29  1  0
 14 30  1  0
 19 31  1  0
 20 32  1  0
 21 33  1  0
 22 34  1  0
M  END


  Mrv1652309112122172D          

 22 23  0  0  0  0            999 V2000
    2.8579   -0.8250    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
    3.5724   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -3.3000    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
    2.1434   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -7.4250    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -8.2500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -7.4250    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
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  2  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  2  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
 15 18  1  0  0  0  0
 14 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  2  0  0  0  0
 19 22  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0258624

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1=CC=C(C=C1)S(=O)(=O)OC1=CC(=C(O)C=C1)S(O)(=O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C13H12O7S2/c1-9-2-5-11(6-3-9)22(18,19)20-10-4-7-12(14)13(8-10)21(15,16)17/h2-8,14H,1H3,(H,15,16,17)

> <INCHI_KEY>
SVXZTCUBEFUKRQ-UHFFFAOYSA-N

> <FORMULA>
C13H12O7S2

> <MOLECULAR_WEIGHT>
344.35

> <EXACT_MASS>
344.002445074

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
30.79090894697174

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-hydroxy-5-[(4-methylbenzenesulfonyl)oxy]benzene-1-sulfonic acid

> <ALOGPS_LOGP>
-0.22

> <JCHEM_LOGP>
3.2308344883333326

> <ALOGPS_LOGS>
-3.11

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
11.308196497278098

> <JCHEM_PKA_STRONGEST_ACIDIC>
-2.784702098837708

> <JCHEM_PKA_STRONGEST_BASIC>
-6.4707349258862275

> <JCHEM_POLAR_SURFACE_AREA>
117.97000000000001

> <JCHEM_REFRACTIVITY>
78.585

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.68e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
sultosilic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0258624
     RDKit          3D
Sultosilic acid
 34 35  0  0  0  0  0  0  0  0999 V2000
   -6.0374    1.4051    0.2831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7299    0.6939    0.1948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5274   -0.3042   -0.7329 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3068   -0.9625   -0.8096 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2572   -0.6490    0.0300 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7084   -1.4723   -0.0549 S   0  0  0  0  0  6  0  0  0  0  0  0
   -0.0519   -1.5119    1.3027 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8689   -2.8733   -0.5787 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3168   -0.6526   -1.1393 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6805   -0.6917   -0.8805 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5141   -1.6714   -1.3764 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8619   -1.6717   -1.0943 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3922   -0.6723   -0.2993 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7450   -0.6253    0.0162 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5813    0.3171    0.2079 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2270    1.5921    1.2157 S   0  0  0  0  0  6  0  0  0  0  0  0
    4.8062    1.0648    2.4915 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1312    2.5503    1.5872 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3875    2.4381    0.3471 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2378    0.2835   -0.0964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4643    0.3514    0.9578 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6807    1.0053    1.0320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5688    1.4527   -0.6705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6754    0.8972    1.0429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8317    2.4312    0.7006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3541   -0.5528   -1.3960 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1470   -1.7452   -1.5366 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0977   -2.4443   -1.9925 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5497   -2.4202   -1.4625 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3472   -1.3621   -0.3619 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2286    2.3210   -0.6377 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5763    1.0638    0.2991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6386    0.6149    1.6356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8327    1.8005    1.7758 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  6  8  2  0
  6  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  2  0
 16 19  1  0
 15 20  2  0
  5 21  1  0
 21 22  2  0
 22  2  1  0
 20 10  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  3 26  1  0
  4 27  1  0
 11 28  1  0
 12 29  1  0
 14 30  1  0
 19 31  1  0
 20 32  1  0
 21 33  1  0
 22 34  1  0
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       5.335  -1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.668  -3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.335  -6.160   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001  -3.850   0.000  0.00  0.00           C+0
HETATM    8  S   UNK     0       5.335  -7.700   0.000  0.00  0.00           S+0
HETATM    9  O   UNK     0       3.795  -7.700   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       6.875  -7.700   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       5.335  -9.240   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001 -11.550   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667 -12.320   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334 -11.550   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -0.000 -12.320   0.000  0.00  0.00           O+0
HETATM   19  S   UNK     0       2.667 -13.860   0.000  0.00  0.00           S+0
HETATM   20  O   UNK     0       2.667 -15.400   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       1.127 -13.860   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       4.207 -13.860   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    8                                                  
CONECT    6    5    7                                                       
CONECT    7    6    2                                                       
CONECT    8    5    9   10   11                                             
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    8   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   19                                                  
CONECT   15   14   16   18                                                  
CONECT   16   15   17                                                       
CONECT   17   16   12                                                       
CONECT   18   15                                                            
CONECT   19   14   20   21   22                                             
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   19                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

COMPND    HMDB0258624
HETATM    1  C1  UNL     1      -6.037   1.405   0.283  1.00  0.00           C  
HETATM    2  C2  UNL     1      -4.730   0.694   0.195  1.00  0.00           C  
HETATM    3  C3  UNL     1      -4.527  -0.304  -0.733  1.00  0.00           C  
HETATM    4  C4  UNL     1      -3.307  -0.963  -0.810  1.00  0.00           C  
HETATM    5  C5  UNL     1      -2.257  -0.649   0.030  1.00  0.00           C  
HETATM    6  S1  UNL     1      -0.708  -1.472  -0.055  1.00  0.00           S  
HETATM    7  O1  UNL     1      -0.052  -1.512   1.303  1.00  0.00           O  
HETATM    8  O2  UNL     1      -0.869  -2.873  -0.579  1.00  0.00           O  
HETATM    9  O3  UNL     1       0.317  -0.653  -1.139  1.00  0.00           O  
HETATM   10  C6  UNL     1       1.680  -0.692  -0.881  1.00  0.00           C  
HETATM   11  C7  UNL     1       2.514  -1.671  -1.376  1.00  0.00           C  
HETATM   12  C8  UNL     1       3.862  -1.672  -1.094  1.00  0.00           C  
HETATM   13  C9  UNL     1       4.392  -0.672  -0.299  1.00  0.00           C  
HETATM   14  O4  UNL     1       5.745  -0.625   0.016  1.00  0.00           O  
HETATM   15  C10 UNL     1       3.581   0.317   0.208  1.00  0.00           C  
HETATM   16  S2  UNL     1       4.227   1.592   1.216  1.00  0.00           S  
HETATM   17  O5  UNL     1       4.806   1.065   2.492  1.00  0.00           O  
HETATM   18  O6  UNL     1       3.131   2.550   1.587  1.00  0.00           O  
HETATM   19  O7  UNL     1       5.388   2.438   0.347  1.00  0.00           O  
HETATM   20  C11 UNL     1       2.238   0.283  -0.096  1.00  0.00           C  
HETATM   21  C12 UNL     1      -2.464   0.351   0.958  1.00  0.00           C  
HETATM   22  C13 UNL     1      -3.681   1.005   1.032  1.00  0.00           C  
HETATM   23  H1  UNL     1      -6.569   1.453  -0.670  1.00  0.00           H  
HETATM   24  H2  UNL     1      -6.675   0.897   1.043  1.00  0.00           H  
HETATM   25  H3  UNL     1      -5.832   2.431   0.701  1.00  0.00           H  
HETATM   26  H4  UNL     1      -5.354  -0.553  -1.396  1.00  0.00           H  
HETATM   27  H5  UNL     1      -3.147  -1.745  -1.537  1.00  0.00           H  
HETATM   28  H6  UNL     1       2.098  -2.444  -1.993  1.00  0.00           H  
HETATM   29  H7  UNL     1       4.550  -2.420  -1.463  1.00  0.00           H  
HETATM   30  H8  UNL     1       6.347  -1.362  -0.362  1.00  0.00           H  
HETATM   31  H9  UNL     1       5.229   2.321  -0.638  1.00  0.00           H  
HETATM   32  H10 UNL     1       1.576   1.064   0.299  1.00  0.00           H  
HETATM   33  H11 UNL     1      -1.639   0.615   1.636  1.00  0.00           H  
HETATM   34  H12 UNL     1      -3.833   1.801   1.776  1.00  0.00           H  
CONECT    1    2   23   24   25
CONECT    2    3    3   22
CONECT    3    4   26
CONECT    4    5    5   27
CONECT    5    6   21
CONECT    6    7    7    8    8
CONECT    6    9
CONECT    9   10
CONECT   10   11   11   20
CONECT   11   12   28
CONECT   12   13   13   29
CONECT   13   14   15
CONECT   14   30
CONECT   15   16   20   20
CONECT   16   17   17   18   18
CONECT   16   19
CONECT   19   31
CONECT   20   32
CONECT   21   22   22   33
CONECT   22   34
END

HMDB0258624
     RDKit          3D
Sultosilic acid
 34 35  0  0  0  0  0  0  0  0999 V2000
   -6.0374    1.4051    0.2831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7299    0.6939    0.1948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5274   -0.3042   -0.7329 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3068   -0.9625   -0.8096 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2572   -0.6490    0.0300 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7084   -1.4723   -0.0549 S   0  0  0  0  0  6  0  0  0  0  0  0
   -0.0519   -1.5119    1.3027 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8689   -2.8733   -0.5787 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3168   -0.6526   -1.1393 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6805   -0.6917   -0.8805 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5141   -1.6714   -1.3764 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8619   -1.6717   -1.0943 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3922   -0.6723   -0.2993 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7450   -0.6253    0.0162 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5813    0.3171    0.2079 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2270    1.5921    1.2157 S   0  0  0  0  0  6  0  0  0  0  0  0
    4.8062    1.0648    2.4915 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1312    2.5503    1.5872 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3875    2.4381    0.3471 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2378    0.2835   -0.0964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4643    0.3514    0.9578 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6807    1.0053    1.0320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5688    1.4527   -0.6705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6754    0.8972    1.0429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8317    2.4312    0.7006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3541   -0.5528   -1.3960 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1470   -1.7452   -1.5366 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0977   -2.4443   -1.9925 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5497   -2.4202   -1.4625 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3472   -1.3621   -0.3619 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2286    2.3210   -0.6377 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5763    1.0638    0.2991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6386    0.6149    1.6356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8327    1.8005    1.7758 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  6  8  2  0
  6  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  2  0
 16 19  1  0
 15 20  2  0
  5 21  1  0
 21 22  2  0
 22  2  1  0
 20 10  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  3 26  1  0
  4 27  1  0
 11 28  1  0
 12 29  1  0
 14 30  1  0
 19 31  1  0
 20 32  1  0
 21 33  1  0
 22 34  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
2-Hydroxy-5-[(4-methylbenzenesulfonyl)oxy]benzene-1-sulfonate	Generator
2-Hydroxy-5-[(4-methylbenzenesulphonyl)oxy]benzene-1-sulphonate	Generator
2-Hydroxy-5-[(4-methylbenzenesulphonyl)oxy]benzene-1-sulphonic acid	Generator
Sultosilate	Generator
5-Tosyloxy-2-hydroxy-benzenesulfonate piperazine	MeSH
Mimedran	MeSH
Piperazine sultosylate	MeSH

Chemical Formula

C₁₃H₁₂O₇S₂

Average Molecular Weight

344.35

Monoisotopic Molecular Weight

344.002445074

IUPAC Name

2-hydroxy-5-[(4-methylbenzenesulfonyl)oxy]benzene-1-sulfonic acid

Traditional Name

sultosilic acid

CAS Registry Number

Not Available

SMILES

CC1=CC=C(C=C1)S(=O)(=O)OC1=CC(=C(O)C=C1)S(O)(=O)=O

InChI Identifier

InChI=1S/C13H12O7S2/c1-9-2-5-11(6-3-9)22(18,19)20-10-4-7-12(14)13(8-10)21(15,16)17/h2-8,14H,1H3,(H,15,16,17)

InChI Key

SVXZTCUBEFUKRQ-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzenesulfonate esters. These are arenesulfonate esters that result from the formal condensation of the hydroxy group of an alcohol, enol, phenol or heteroarenol with benzenesulfonic acid.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzenesulfonic acids and derivatives

Direct Parent

Benzenesulfonate esters

Alternative Parents

Substituents

Benzenesulfonate ester
P-methylbenzenesulfonate
Tosyl compound
Arylsulfonic acid or derivatives
1-sulfo,2-unsubstituted aromatic compound
Benzenesulfonyl group
Phenoxy compound
1-hydroxy-2-unsubstituted benzenoid
Phenol
Toluene
Organosulfonic acid ester
Sulfonyl
Organosulfonic acid
Organosulfonic acid or derivatives
Organic sulfonic acid or derivatives
Organooxygen compound
Organosulfur compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
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)

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	-0.22	ALOGPS
logP	3.23	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	-2.8	ChemAxon
pKa (Strongest Basic)	-6.5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	117.97 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	78.58 m³·mol⁻¹	ChemAxon
Polarizability	30.79 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]+	173.131	30932474
DeepCCS	[M-H]-	170.773	30932474
DeepCCS	[M-2H]-	204.072	30932474
DeepCCS	[M+Na]+	179.299	30932474
AllCCS	[M+H]+	175.3	32859911
AllCCS	[M+H-H2O]+	172.1	32859911
AllCCS	[M+NH4]+	178.2	32859911
AllCCS	[M+Na]+	179.1	32859911
AllCCS	[M-H]-	167.3	32859911
AllCCS	[M+Na-2H]-	166.9	32859911
AllCCS	[M+HCOO]-	166.7	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Sultosilic acid	CC1=CC=C(C=C1)S(=O)(=O)OC1=CC(=C(O)C=C1)S(O)(=O)=O	4937.6	Standard polar	33892256
Sultosilic acid	CC1=CC=C(C=C1)S(=O)(=O)OC1=CC(=C(O)C=C1)S(O)(=O)=O	2545.7	Standard non polar	33892256
Sultosilic acid	CC1=CC=C(C=C1)S(=O)(=O)OC1=CC(=C(O)C=C1)S(O)(=O)=O	2856.6	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Sultosilic acid,2TMS,isomer #1	CC1=CC=C(S(=O)(=O)OC2=CC=C(O[Si](C)(C)C)C(S(=O)(=O)O[Si](C)(C)C)=C2)C=C1	2856.9	Semi standard non polar	33892256
Sultosilic acid,2TMS,isomer #1	CC1=CC=C(S(=O)(=O)OC2=CC=C(O[Si](C)(C)C)C(S(=O)(=O)O[Si](C)(C)C)=C2)C=C1	2918.9	Standard non polar	33892256
Sultosilic acid,2TMS,isomer #1	CC1=CC=C(S(=O)(=O)OC2=CC=C(O[Si](C)(C)C)C(S(=O)(=O)O[Si](C)(C)C)=C2)C=C1	3684.5	Standard polar	33892256
Sultosilic acid,2TBDMS,isomer #1	CC1=CC=C(S(=O)(=O)OC2=CC=C(O[Si](C)(C)C(C)(C)C)C(S(=O)(=O)O[Si](C)(C)C(C)(C)C)=C2)C=C1	3366.9	Semi standard non polar	33892256
Sultosilic acid,2TBDMS,isomer #1	CC1=CC=C(S(=O)(=O)OC2=CC=C(O[Si](C)(C)C(C)(C)C)C(S(=O)(=O)O[Si](C)(C)C(C)(C)C)=C2)C=C1	3406.0	Standard non polar	33892256
Sultosilic acid,2TBDMS,isomer #1	CC1=CC=C(S(=O)(=O)OC2=CC=C(O[Si](C)(C)C(C)(C)C)C(S(=O)(=O)O[Si](C)(C)C(C)(C)C)=C2)C=C1	3734.6	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Sultosilic acid GC-MS (Non-derivatized) - 70eV, Positive	splash10-052f-4912000000-746f17a21a28532feb2c	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Sultosilic acid GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Sultosilic acid GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Sultosilic acid GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Sultosilic acid GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Sultosilic acid GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-05	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

62018

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

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 Sultosilic acid (HMDB0258624)

MOL for HMDB0258624 (Sultosilic acid)

3D MOL for HMDB0258624 (Sultosilic acid)

3D SDF for HMDB0258624 (Sultosilic acid)

3D-SDF for HMDB0258624 (Sultosilic acid)

PDB for HMDB0258624 (Sultosilic acid)

3D PDB for HMDB0258624 (Sultosilic acid)

SMILES for HMDB0258624 (Sultosilic acid)

INCHI for HMDB0258624 (Sultosilic acid)

Structure for HMDB0258624 (Sultosilic acid)

3D Structure for HMDB0258624 (Sultosilic acid)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra