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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 14:36:40 UTC

Update Date

2021-09-26 23:09:35 UTC

HMDB ID

HMDB0255075

Secondary Accession Numbers

None

Metabolite Identification

Common Name

N-Acetylsulfamethazine

Description

N-Acetylsulfamethazine, also known as N-acetylsulfadimidine, belongs to the class of organic compounds known as aminobenzenesulfonamides. These are organic compounds containing a benzenesulfonamide moiety with an amine group attached to the benzene ring. Based on a literature review a small amount of articles have been published on N-Acetylsulfamethazine. This compound has been identified in human blood as reported by (PMID: 31557052 ). N-acetylsulfamethazine is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically N-Acetylsulfamethazine 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

HMDB0255075
     RDKit          3D
N-Acetylsulfamethazine
 38 39  0  0  0  0  0  0  0  0999 V2000
   -0.3910   -1.6217   -2.0067 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3876   -1.0707   -0.8871 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6368   -1.2772   -0.8514 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2391   -0.3244    0.1323 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6453   -0.0640    0.1367 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4529   -0.9426    0.7537 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8002   -0.7642    0.8025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6546   -1.7635    1.5005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3004    0.3561    0.1910 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4833    1.2680   -0.4473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9780    2.4944   -1.1216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1679    1.0237   -0.4520 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6747    0.3206    1.4341 S   0  0  0  0  0  6  0  0  0  0  0  0
    0.4537   -0.5753    2.6254 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2988    1.7361    1.7301 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3812    0.2772    0.9933 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2075   -0.7721    1.3428 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5347   -0.7562    0.9679 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1034    0.2724    0.2440 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4822    0.2524   -0.1256 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2693    1.3173   -0.1018 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9430    1.3083    0.2697 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8671   -2.5920   -1.6965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2163   -0.8936   -2.2250 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2157   -1.8003   -2.9209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9538   -2.5279    0.7307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1001   -2.2632    2.3332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5494   -1.2471    1.8685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3490    0.5358    0.2083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9652    2.8056   -0.7251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2665    3.3413   -0.9332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0742    2.3641   -2.2235 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7748   -1.5997    1.9194 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1536   -1.6014    1.2648 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8182   -0.0908   -1.0461 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1797    0.5991    0.5608 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6827    2.1404   -0.6749 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2567    2.1347    0.0046 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
 10 11  1  0
 10 12  2  0
  4 13  1  0
 13 14  2  0
 13 15  2  0
 13 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
 12  5  1  0
 22 16  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  8 26  1  0
  8 27  1  0
  8 28  1  0
  9 29  1  0
 11 30  1  0
 11 31  1  0
 11 32  1  0
 17 33  1  0
 18 34  1  0
 20 35  1  0
 20 36  1  0
 21 37  1  0
 22 38  1  0
M  END

  Mrv1652309112116362D          

 22 23  0  0  0  0            999 V2000
    2.1434   -1.2375    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   -2.4750    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   -3.7125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 O   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   -3.3000    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125   -2.5855    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -4.0145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -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
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   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
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  8 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  2  0  0  0  0
 12 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 15 20  1  0  0  0  0
 18 21  1  0  0  0  0
  4 22  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0255075

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(=O)N(C1=NC(C)=CC(C)=N1)S(=O)(=O)C1=CC=C(N)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C14H16N4O3S/c1-9-8-10(2)17-14(16-9)18(11(3)19)22(20,21)13-6-4-12(15)5-7-13/h4-8H,15H2,1-3H3

> <INCHI_KEY>
VRYCOLRKKCBJJI-UHFFFAOYSA-N

> <FORMULA>
C14H16N4O3S

> <MOLECULAR_WEIGHT>
320.37

> <EXACT_MASS>
320.094311565

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
31.669571726542078

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-(4-aminobenzenesulfonyl)-N-(4,6-dimethylpyrimidin-2-yl)acetamide

> <ALOGPS_LOGP>
1.27

> <JCHEM_LOGP>
0.6386094516666667

> <ALOGPS_LOGS>
-3.07

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.395310669681074

> <JCHEM_PKA_STRONGEST_BASIC>
1.869879828880644

> <JCHEM_POLAR_SURFACE_AREA>
106.25

> <JCHEM_REFRACTIVITY>
82.94980000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.75e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-(4-aminobenzenesulfonyl)-N-(4,6-dimethylpyrimidin-2-yl)acetamide

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0255075
     RDKit          3D
N-Acetylsulfamethazine
 38 39  0  0  0  0  0  0  0  0999 V2000
   -0.3910   -1.6217   -2.0067 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3876   -1.0707   -0.8871 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6368   -1.2772   -0.8514 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2391   -0.3244    0.1323 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6453   -0.0640    0.1367 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4529   -0.9426    0.7537 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8002   -0.7642    0.8025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6546   -1.7635    1.5005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3004    0.3561    0.1910 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4833    1.2680   -0.4473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9780    2.4944   -1.1216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1679    1.0237   -0.4520 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6747    0.3206    1.4341 S   0  0  0  0  0  6  0  0  0  0  0  0
    0.4537   -0.5753    2.6254 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2988    1.7361    1.7301 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3812    0.2772    0.9933 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2075   -0.7721    1.3428 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5347   -0.7562    0.9679 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1034    0.2724    0.2440 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4822    0.2524   -0.1256 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2693    1.3173   -0.1018 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9430    1.3083    0.2697 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8671   -2.5920   -1.6965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2163   -0.8936   -2.2250 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2157   -1.8003   -2.9209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9538   -2.5279    0.7307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1001   -2.2632    2.3332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5494   -1.2471    1.8685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3490    0.5358    0.2083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9652    2.8056   -0.7251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2665    3.3413   -0.9332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0742    2.3641   -2.2235 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7748   -1.5997    1.9194 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1536   -1.6014    1.2648 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8182   -0.0908   -1.0461 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1797    0.5991    0.5608 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6827    2.1404   -0.6749 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2567    2.1347    0.0046 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
 10 11  1  0
 10 12  2  0
  4 13  1  0
 13 14  2  0
 13 15  2  0
 13 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
 12  5  1  0
 22 16  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  8 26  1  0
  8 27  1  0
  8 28  1  0
  9 29  1  0
 11 30  1  0
 11 31  1  0
 11 32  1  0
 17 33  1  0
 18 34  1  0
 20 35  1  0
 20 36  1  0
 21 37  1  0
 22 38  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       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.001  -3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335  -6.160   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       4.001  -6.930   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       2.667  -6.160   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       2.667  -4.620   0.000  0.00  0.00           N+0
HETATM    8  N   UNK     0       1.334  -6.930   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       1.334  -8.470   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       0.000  -9.240   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   12  S   UNK     0       0.000  -6.160   0.000  0.00  0.00           S+0
HETATM   13  O   UNK     0       0.770  -4.826   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      -0.770  -7.494   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.667  -6.160   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -4.001  -3.850   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.334  -3.850   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0      -5.335  -3.080   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   22                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6    2                                                       
CONECT    8    6    9   12                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    8   13   14   15                                             
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   12   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19   15                                                       
CONECT   21   18                                                            
CONECT   22    4                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

COMPND    HMDB0255075
HETATM    1  C1  UNL     1      -0.391  -1.622  -2.007  1.00  0.00           C  
HETATM    2  C2  UNL     1       0.388  -1.071  -0.887  1.00  0.00           C  
HETATM    3  O1  UNL     1       1.637  -1.277  -0.851  1.00  0.00           O  
HETATM    4  N1  UNL     1      -0.239  -0.324   0.132  1.00  0.00           N  
HETATM    5  C3  UNL     1      -1.645  -0.064   0.137  1.00  0.00           C  
HETATM    6  N2  UNL     1      -2.453  -0.943   0.754  1.00  0.00           N  
HETATM    7  C4  UNL     1      -3.800  -0.764   0.802  1.00  0.00           C  
HETATM    8  C5  UNL     1      -4.655  -1.763   1.500  1.00  0.00           C  
HETATM    9  C6  UNL     1      -4.300   0.356   0.191  1.00  0.00           C  
HETATM   10  C7  UNL     1      -3.483   1.268  -0.447  1.00  0.00           C  
HETATM   11  C8  UNL     1      -3.978   2.494  -1.122  1.00  0.00           C  
HETATM   12  N3  UNL     1      -2.168   1.024  -0.452  1.00  0.00           N  
HETATM   13  S1  UNL     1       0.675   0.321   1.434  1.00  0.00           S  
HETATM   14  O2  UNL     1       0.454  -0.575   2.625  1.00  0.00           O  
HETATM   15  O3  UNL     1       0.299   1.736   1.730  1.00  0.00           O  
HETATM   16  C9  UNL     1       2.381   0.277   0.993  1.00  0.00           C  
HETATM   17  C10 UNL     1       3.207  -0.772   1.343  1.00  0.00           C  
HETATM   18  C11 UNL     1       4.535  -0.756   0.968  1.00  0.00           C  
HETATM   19  C12 UNL     1       5.103   0.272   0.244  1.00  0.00           C  
HETATM   20  N4  UNL     1       6.482   0.252  -0.126  1.00  0.00           N  
HETATM   21  C13 UNL     1       4.269   1.317  -0.102  1.00  0.00           C  
HETATM   22  C14 UNL     1       2.943   1.308   0.270  1.00  0.00           C  
HETATM   23  H1  UNL     1      -0.867  -2.592  -1.696  1.00  0.00           H  
HETATM   24  H2  UNL     1      -1.216  -0.894  -2.225  1.00  0.00           H  
HETATM   25  H3  UNL     1       0.216  -1.800  -2.921  1.00  0.00           H  
HETATM   26  H4  UNL     1      -4.954  -2.528   0.731  1.00  0.00           H  
HETATM   27  H5  UNL     1      -4.100  -2.263   2.333  1.00  0.00           H  
HETATM   28  H6  UNL     1      -5.549  -1.247   1.869  1.00  0.00           H  
HETATM   29  H7  UNL     1      -5.349   0.536   0.208  1.00  0.00           H  
HETATM   30  H8  UNL     1      -4.965   2.806  -0.725  1.00  0.00           H  
HETATM   31  H9  UNL     1      -3.267   3.341  -0.933  1.00  0.00           H  
HETATM   32  H10 UNL     1      -4.074   2.364  -2.224  1.00  0.00           H  
HETATM   33  H11 UNL     1       2.775  -1.600   1.919  1.00  0.00           H  
HETATM   34  H12 UNL     1       5.154  -1.601   1.265  1.00  0.00           H  
HETATM   35  H13 UNL     1       6.818  -0.091  -1.046  1.00  0.00           H  
HETATM   36  H14 UNL     1       7.180   0.599   0.561  1.00  0.00           H  
HETATM   37  H15 UNL     1       4.683   2.140  -0.675  1.00  0.00           H  
HETATM   38  H16 UNL     1       2.257   2.135   0.005  1.00  0.00           H  
CONECT    1    2   23   24   25
CONECT    2    3    3    4
CONECT    4    5   13
CONECT    5    6    6   12
CONECT    6    7
CONECT    7    8    9    9
CONECT    8   26   27   28
CONECT    9   10   29
CONECT   10   11   12   12
CONECT   11   30   31   32
CONECT   13   14   14   15   15
CONECT   13   16
CONECT   16   17   17   22
CONECT   17   18   33
CONECT   18   19   19   34
CONECT   19   20   21
CONECT   20   35   36
CONECT   21   22   22   37
CONECT   22   38
END

HMDB0255075
     RDKit          3D
N-Acetylsulfamethazine
 38 39  0  0  0  0  0  0  0  0999 V2000
   -0.3910   -1.6217   -2.0067 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3876   -1.0707   -0.8871 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6368   -1.2772   -0.8514 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2391   -0.3244    0.1323 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6453   -0.0640    0.1367 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4529   -0.9426    0.7537 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8002   -0.7642    0.8025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6546   -1.7635    1.5005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3004    0.3561    0.1910 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4833    1.2680   -0.4473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9780    2.4944   -1.1216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1679    1.0237   -0.4520 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6747    0.3206    1.4341 S   0  0  0  0  0  6  0  0  0  0  0  0
    0.4537   -0.5753    2.6254 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2988    1.7361    1.7301 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3812    0.2772    0.9933 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2075   -0.7721    1.3428 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5347   -0.7562    0.9679 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1034    0.2724    0.2440 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4822    0.2524   -0.1256 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2693    1.3173   -0.1018 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9430    1.3083    0.2697 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8671   -2.5920   -1.6965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2163   -0.8936   -2.2250 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2157   -1.8003   -2.9209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9538   -2.5279    0.7307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1001   -2.2632    2.3332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5494   -1.2471    1.8685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3490    0.5358    0.2083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9652    2.8056   -0.7251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2665    3.3413   -0.9332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0742    2.3641   -2.2235 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7748   -1.5997    1.9194 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1536   -1.6014    1.2648 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8182   -0.0908   -1.0461 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1797    0.5991    0.5608 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6827    2.1404   -0.6749 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2567    2.1347    0.0046 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
 10 11  1  0
 10 12  2  0
  4 13  1  0
 13 14  2  0
 13 15  2  0
 13 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
 12  5  1  0
 22 16  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  8 26  1  0
  8 27  1  0
  8 28  1  0
  9 29  1  0
 11 30  1  0
 11 31  1  0
 11 32  1  0
 17 33  1  0
 18 34  1  0
 20 35  1  0
 20 36  1  0
 21 37  1  0
 22 38  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
N-Acetylsulphamethazine	Generator
N-Acetylsulfadimidine	HMDB

Chemical Formula

C₁₄H₁₆N₄O₃S

Average Molecular Weight

320.37

Monoisotopic Molecular Weight

320.094311565

IUPAC Name

N-(4-aminobenzenesulfonyl)-N-(4,6-dimethylpyrimidin-2-yl)acetamide

Traditional Name

N-(4-aminobenzenesulfonyl)-N-(4,6-dimethylpyrimidin-2-yl)acetamide

CAS Registry Number

Not Available

SMILES

CC(=O)N(C1=NC(C)=CC(C)=N1)S(=O)(=O)C1=CC=C(N)C=C1

InChI Identifier

InChI=1S/C14H16N4O3S/c1-9-8-10(2)17-14(16-9)18(11(3)19)22(20,21)13-6-4-12(15)5-7-13/h4-8H,15H2,1-3H3

InChI Key

VRYCOLRKKCBJJI-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aminobenzenesulfonamides. These are organic compounds containing a benzenesulfonamide moiety with an amine group attached to the benzene ring.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzenesulfonamides

Direct Parent

Aminobenzenesulfonamides

Alternative Parents

Substituents

Aminobenzenesulfonamide
Benzenesulfonyl group
Aniline or substituted anilines
Pyrimidine
Organic sulfonic acid or derivatives
Organosulfonic acid or derivatives
Sulfonyl
Aminosulfonyl compound
Acetamide
Heteroaromatic compound
Amino acid or derivatives
Organoheterocyclic compound
Azacycle
Carboxylic acid derivative
Organic nitrogen compound
Amine
Organic oxygen compound
Primary amine
Organosulfur compound
Organooxygen compound
Organonitrogen compound
Carbonyl group
Organopnictogen compound
Hydrocarbon derivative
Organic oxide
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	1.27	ALOGPS
logP	0.64	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	19.4	ChemAxon
pKa (Strongest Basic)	1.87	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	106.25 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	82.95 m³·mol⁻¹	ChemAxon
Polarizability	31.67 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]+	175.208	30932474
DeepCCS	[M-H]-	172.85	30932474
DeepCCS	[M-2H]-	206.959	30932474
DeepCCS	[M+Na]+	182.187	30932474
AllCCS	[M+H]+	173.6	32859911
AllCCS	[M+H-H2O]+	170.4	32859911
AllCCS	[M+NH4]+	176.7	32859911
AllCCS	[M+Na]+	177.5	32859911
AllCCS	[M-H]-	171.6	32859911
AllCCS	[M+Na-2H]-	171.6	32859911
AllCCS	[M+HCOO]-	171.8	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
N-Acetylsulfamethazine	CC(=O)N(C1=NC(C)=CC(C)=N1)S(=O)(=O)C1=CC=C(N)C=C1	4185.9	Standard polar	33892256
N-Acetylsulfamethazine	CC(=O)N(C1=NC(C)=CC(C)=N1)S(=O)(=O)C1=CC=C(N)C=C1	2748.2	Standard non polar	33892256
N-Acetylsulfamethazine	CC(=O)N(C1=NC(C)=CC(C)=N1)S(=O)(=O)C1=CC=C(N)C=C1	2754.7	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
N-Acetylsulfamethazine,1TMS,isomer #1	CC(=O)N(C1=NC(C)=CC(C)=N1)S(=O)(=O)C1=CC=C(N[Si](C)(C)C)C=C1	2902.5	Semi standard non polar	33892256
N-Acetylsulfamethazine,1TMS,isomer #1	CC(=O)N(C1=NC(C)=CC(C)=N1)S(=O)(=O)C1=CC=C(N[Si](C)(C)C)C=C1	2795.6	Standard non polar	33892256
N-Acetylsulfamethazine,1TMS,isomer #1	CC(=O)N(C1=NC(C)=CC(C)=N1)S(=O)(=O)C1=CC=C(N[Si](C)(C)C)C=C1	3926.2	Standard polar	33892256
N-Acetylsulfamethazine,2TMS,isomer #1	CC(=O)N(C1=NC(C)=CC(C)=N1)S(=O)(=O)C1=CC=C(N([Si](C)(C)C)[Si](C)(C)C)C=C1	2712.5	Semi standard non polar	33892256
N-Acetylsulfamethazine,2TMS,isomer #1	CC(=O)N(C1=NC(C)=CC(C)=N1)S(=O)(=O)C1=CC=C(N([Si](C)(C)C)[Si](C)(C)C)C=C1	2890.5	Standard non polar	33892256
N-Acetylsulfamethazine,2TMS,isomer #1	CC(=O)N(C1=NC(C)=CC(C)=N1)S(=O)(=O)C1=CC=C(N([Si](C)(C)C)[Si](C)(C)C)C=C1	3688.3	Standard polar	33892256
N-Acetylsulfamethazine,1TBDMS,isomer #1	CC(=O)N(C1=NC(C)=CC(C)=N1)S(=O)(=O)C1=CC=C(N[Si](C)(C)C(C)(C)C)C=C1	3066.1	Semi standard non polar	33892256
N-Acetylsulfamethazine,1TBDMS,isomer #1	CC(=O)N(C1=NC(C)=CC(C)=N1)S(=O)(=O)C1=CC=C(N[Si](C)(C)C(C)(C)C)C=C1	3002.5	Standard non polar	33892256
N-Acetylsulfamethazine,1TBDMS,isomer #1	CC(=O)N(C1=NC(C)=CC(C)=N1)S(=O)(=O)C1=CC=C(N[Si](C)(C)C(C)(C)C)C=C1	3943.6	Standard polar	33892256
N-Acetylsulfamethazine,2TBDMS,isomer #1	CC(=O)N(C1=NC(C)=CC(C)=N1)S(=O)(=O)C1=CC=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1	3192.3	Semi standard non polar	33892256
N-Acetylsulfamethazine,2TBDMS,isomer #1	CC(=O)N(C1=NC(C)=CC(C)=N1)S(=O)(=O)C1=CC=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1	3331.2	Standard non polar	33892256
N-Acetylsulfamethazine,2TBDMS,isomer #1	CC(=O)N(C1=NC(C)=CC(C)=N1)S(=O)(=O)C1=CC=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1	3728.5	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - N-Acetylsulfamethazine GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a4l-5921000000-0f1954d277097c500c4a	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-Acetylsulfamethazine GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	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

97127

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

108015

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 N-Acetylsulfamethazine (HMDB0255075)

MOL for HMDB0255075 (N-Acetylsulfamethazine)

3D MOL for HMDB0255075 (N-Acetylsulfamethazine)

3D SDF for HMDB0255075 (N-Acetylsulfamethazine)

3D-SDF for HMDB0255075 (N-Acetylsulfamethazine)

PDB for HMDB0255075 (N-Acetylsulfamethazine)

3D PDB for HMDB0255075 (N-Acetylsulfamethazine)

SMILES for HMDB0255075 (N-Acetylsulfamethazine)

INCHI for HMDB0255075 (N-Acetylsulfamethazine)

Structure for HMDB0255075 (N-Acetylsulfamethazine)

3D Structure for HMDB0255075 (N-Acetylsulfamethazine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra