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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 03:24:10 UTC

Update Date

2022-11-23 21:48:33 UTC

HMDB ID

HMDB0248938

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Bemoradan

Description

7-(6-hydroxy-4-methyl-4,5-dihydropyridazin-3-yl)-2H-1,4-benzoxazin-3-ol belongs to the class of organic compounds known as benzoxazinones. These are organic compounds containing a benzene fused to an oxazine ring (a six-member aliphatic ring with four carbon atoms, one oxygen atom, and one nitrogen atom) bearing a ketone group. Based on a literature review a significant number of articles have been published on 7-(6-hydroxy-4-methyl-4,5-dihydropyridazin-3-yl)-2H-1,4-benzoxazin-3-ol. This compound has been identified in human blood as reported by (PMID: 31557052 ). Bemoradan is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Bemoradan 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

HMDB0248938
     RDKit          3D
BEMORADAN
 32 34  0  0  0  0  0  0  0  0999 V2000
   -2.4406    1.8173    0.2834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6664    0.4653   -0.3933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9092   -0.0957    0.2506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1343   -1.4968   -0.1147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2022   -2.0202   -0.4732 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9667   -2.3429   -0.0409 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7314   -1.7229   -0.1533 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5409   -0.4383   -0.3188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1099   -0.0577   -0.4204 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2864    1.1995   -0.7581 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6266    1.5747   -0.8219 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5907    0.6490   -0.5366 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2312   -0.6327   -0.1923 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9036   -0.9686   -0.1384 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2270   -1.5466    0.0900 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5792   -1.3595   -0.2760 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9445    0.0791   -0.3058 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1228    0.4793   -0.0695 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9558    1.0544   -0.6068 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5824    1.8354    0.9580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5237    2.6516   -0.4357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3282    1.9889    0.9735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9316    0.6935   -1.4675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8595    0.0198    1.3588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7679    0.5495   -0.1174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1192   -3.3611    0.0898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4029    1.9718   -1.0217 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8999    2.5836   -1.0932 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6111   -1.9711    0.1308 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1984   -1.8415    0.5256 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8365   -1.7998   -1.2371 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2034    2.0431   -0.8734 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
  8  2  1  0
 14  9  1  0
 19 12  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  2 23  1  0
  3 24  1  0
  3 25  1  0
  6 26  1  0
 10 27  1  0
 11 28  1  0
 14 29  1  0
 16 30  1  0
 16 31  1  0
 19 32  1  0
M  END


  Mrv1533004241522582D          

 19 21  0  0  0  0            999 V2000
   -0.7145   -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
   -2.1434   -2.8875    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
   -3.5724   -2.8875    0.0000 O   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
   -2.1434   -1.2375    0.0000 N   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   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -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 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 O   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
    1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  2  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 11 19  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0248938

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1CC(=O)NN=C1C1=CC2=C(NC(=O)CO2)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C13H13N3O3/c1-7-4-11(17)15-16-13(7)8-2-3-9-10(5-8)19-6-12(18)14-9/h2-3,5,7H,4,6H2,1H3,(H,14,18)(H,15,17)

> <INCHI_KEY>
XZPGINPFWXLYNW-UHFFFAOYSA-N

> <FORMULA>
C13H13N3O3

> <MOLECULAR_WEIGHT>
259.265

> <EXACT_MASS>
259.095691291

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
32

> <JCHEM_AVERAGE_POLARIZABILITY>
26.149765401350013

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7-(4-methyl-6-oxo-1,4,5,6-tetrahydropyridazin-3-yl)-3,4-dihydro-2H-1,4-benzoxazin-3-one

> <ALOGPS_LOGP>
1.61

> <JCHEM_LOGP>
0.3266683433333334

> <ALOGPS_LOGS>
-3.08

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.96880143745521

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.321222851550893

> <JCHEM_PKA_STRONGEST_BASIC>
1.0532219028322343

> <JCHEM_POLAR_SURFACE_AREA>
79.79

> <JCHEM_REFRACTIVITY>
68.97500000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.15e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-(4-methyl-6-oxo-4,5-dihydro-1H-pyridazin-3-yl)-2,4-dihydro-1,4-benzoxazin-3-one

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0248938
     RDKit          3D
BEMORADAN
 32 34  0  0  0  0  0  0  0  0999 V2000
   -2.4406    1.8173    0.2834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6664    0.4653   -0.3933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9092   -0.0957    0.2506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1343   -1.4968   -0.1147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2022   -2.0202   -0.4732 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9667   -2.3429   -0.0409 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7314   -1.7229   -0.1533 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5409   -0.4383   -0.3188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1099   -0.0577   -0.4204 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2864    1.1995   -0.7581 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6266    1.5747   -0.8219 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5907    0.6490   -0.5366 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2312   -0.6327   -0.1923 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9036   -0.9686   -0.1384 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2270   -1.5466    0.0900 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5792   -1.3595   -0.2760 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9445    0.0791   -0.3058 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1228    0.4793   -0.0695 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9558    1.0544   -0.6068 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5824    1.8354    0.9580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5237    2.6516   -0.4357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3282    1.9889    0.9735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9316    0.6935   -1.4675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8595    0.0198    1.3588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7679    0.5495   -0.1174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1192   -3.3611    0.0898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4029    1.9718   -1.0217 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8999    2.5836   -1.0932 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6111   -1.9711    0.1308 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1984   -1.8415    0.5256 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8365   -1.7998   -1.2371 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2034    2.0431   -0.8734 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
  8  2  1  0
 14  9  1  0
 19 12  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  2 23  1  0
  3 24  1  0
  3 25  1  0
  6 26  1  0
 10 27  1  0
 11 28  1  0
 14 29  1  0
 16 30  1  0
 16 31  1  0
 19 32  1  0
M  END

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -6.668  -5.390   0.000  0.00  0.00           O+0
HETATM    6  N   UNK     0      -5.335  -3.080   0.000  0.00  0.00           N+0
HETATM    7  N   UNK     0      -4.001  -2.310   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0       2.667  -0.000   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.335  -0.000   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    8                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    2    9                                                  
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   19                                                  
CONECT   12   11   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13    9                                                       
CONECT   15   12   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   11                                                       
MASTER        0    0    0    0    0    0    0    0   19    0   42    0
END

COMPND    HMDB0248938
HETATM    1  C1  UNL     1      -2.441   1.817   0.283  1.00  0.00           C  
HETATM    2  C2  UNL     1      -2.666   0.465  -0.393  1.00  0.00           C  
HETATM    3  C3  UNL     1      -3.909  -0.096   0.251  1.00  0.00           C  
HETATM    4  C4  UNL     1      -4.134  -1.497  -0.115  1.00  0.00           C  
HETATM    5  O1  UNL     1      -5.202  -2.020  -0.473  1.00  0.00           O  
HETATM    6  N1  UNL     1      -2.967  -2.343  -0.041  1.00  0.00           N  
HETATM    7  N2  UNL     1      -1.731  -1.723  -0.153  1.00  0.00           N  
HETATM    8  C5  UNL     1      -1.541  -0.438  -0.319  1.00  0.00           C  
HETATM    9  C6  UNL     1      -0.110  -0.058  -0.420  1.00  0.00           C  
HETATM   10  C7  UNL     1       0.286   1.199  -0.758  1.00  0.00           C  
HETATM   11  C8  UNL     1       1.627   1.575  -0.822  1.00  0.00           C  
HETATM   12  C9  UNL     1       2.591   0.649  -0.537  1.00  0.00           C  
HETATM   13  C10 UNL     1       2.231  -0.633  -0.192  1.00  0.00           C  
HETATM   14  C11 UNL     1       0.904  -0.969  -0.138  1.00  0.00           C  
HETATM   15  O2  UNL     1       3.227  -1.547   0.090  1.00  0.00           O  
HETATM   16  C12 UNL     1       4.579  -1.360  -0.276  1.00  0.00           C  
HETATM   17  C13 UNL     1       4.944   0.079  -0.306  1.00  0.00           C  
HETATM   18  O3  UNL     1       6.123   0.479  -0.070  1.00  0.00           O  
HETATM   19  N3  UNL     1       3.956   1.054  -0.607  1.00  0.00           N  
HETATM   20  H1  UNL     1      -1.582   1.835   0.958  1.00  0.00           H  
HETATM   21  H2  UNL     1      -2.524   2.652  -0.436  1.00  0.00           H  
HETATM   22  H3  UNL     1      -3.328   1.989   0.974  1.00  0.00           H  
HETATM   23  H4  UNL     1      -2.932   0.693  -1.468  1.00  0.00           H  
HETATM   24  H5  UNL     1      -3.859   0.020   1.359  1.00  0.00           H  
HETATM   25  H6  UNL     1      -4.768   0.549  -0.117  1.00  0.00           H  
HETATM   26  H7  UNL     1      -3.119  -3.361   0.090  1.00  0.00           H  
HETATM   27  H8  UNL     1      -0.403   1.972  -1.022  1.00  0.00           H  
HETATM   28  H9  UNL     1       1.900   2.584  -1.093  1.00  0.00           H  
HETATM   29  H10 UNL     1       0.611  -1.971   0.131  1.00  0.00           H  
HETATM   30  H11 UNL     1       5.198  -1.842   0.526  1.00  0.00           H  
HETATM   31  H12 UNL     1       4.836  -1.800  -1.237  1.00  0.00           H  
HETATM   32  H13 UNL     1       4.203   2.043  -0.873  1.00  0.00           H  
CONECT    1    2   20   21   22
CONECT    2    3    8   23
CONECT    3    4   24   25
CONECT    4    5    5    6
CONECT    6    7   26
CONECT    7    8    8
CONECT    8    9
CONECT    9   10   10   14
CONECT   10   11   27
CONECT   11   12   12   28
CONECT   12   13   19
CONECT   13   14   14   15
CONECT   14   29
CONECT   15   16
CONECT   16   17   30   31
CONECT   17   18   18   19
CONECT   19   32
END

HMDB0248938
     RDKit          3D
BEMORADAN
 32 34  0  0  0  0  0  0  0  0999 V2000
   -2.4406    1.8173    0.2834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6664    0.4653   -0.3933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9092   -0.0957    0.2506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1343   -1.4968   -0.1147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2022   -2.0202   -0.4732 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9667   -2.3429   -0.0409 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7314   -1.7229   -0.1533 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5409   -0.4383   -0.3188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1099   -0.0577   -0.4204 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2864    1.1995   -0.7581 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6266    1.5747   -0.8219 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5907    0.6490   -0.5366 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2312   -0.6327   -0.1923 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9036   -0.9686   -0.1384 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2270   -1.5466    0.0900 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5792   -1.3595   -0.2760 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9445    0.0791   -0.3058 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1228    0.4793   -0.0695 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9558    1.0544   -0.6068 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5824    1.8354    0.9580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5237    2.6516   -0.4357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3282    1.9889    0.9735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9316    0.6935   -1.4675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8595    0.0198    1.3588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7679    0.5495   -0.1174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1192   -3.3611    0.0898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4029    1.9718   -1.0217 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8999    2.5836   -1.0932 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6111   -1.9711    0.1308 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1984   -1.8415    0.5256 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8365   -1.7998   -1.2371 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2034    2.0431   -0.8734 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
  8  2  1  0
 14  9  1  0
 19 12  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  2 23  1  0
  3 24  1  0
  3 25  1  0
  6 26  1  0
 10 27  1  0
 11 28  1  0
 14 29  1  0
 16 30  1  0
 16 31  1  0
 19 32  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
ORF 22867	ChEMBL

Chemical Formula

C₁₃H₁₃N₃O₃

Average Molecular Weight

259.265

Monoisotopic Molecular Weight

259.095691291

IUPAC Name

7-(4-methyl-6-oxo-1,4,5,6-tetrahydropyridazin-3-yl)-3,4-dihydro-2H-1,4-benzoxazin-3-one

Traditional Name

7-(4-methyl-6-oxo-4,5-dihydro-1H-pyridazin-3-yl)-2,4-dihydro-1,4-benzoxazin-3-one

CAS Registry Number

Not Available

SMILES

CC1CC(=O)NN=C1C1=CC2=C(NC(=O)CO2)C=C1

InChI Identifier

InChI=1S/C13H13N3O3/c1-7-4-11(17)15-16-13(7)8-2-3-9-10(5-8)19-6-12(18)14-9/h2-3,5,7H,4,6H2,1H3,(H,14,18)(H,15,17)

InChI Key

XZPGINPFWXLYNW-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzoxazinones. These are organic compounds containing a benzene fused to an oxazine ring (a six-member aliphatic ring with four carbon atoms, one oxygen atom, and one nitrogen atom) bearing a ketone group.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzoxazines

Sub Class

Benzoxazinones

Direct Parent

Benzoxazinones

Alternative Parents

Substituents

Benzoxazinone
Benzomorpholine
Alkyl aryl ether
Pyridazinone
Oxazinane
Pyridazine
Benzenoid
Carboxamide group
Lactam
Secondary carboxylic acid amide
Ether
Carboxylic acid derivative
Oxacycle
Azacycle
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Carbonyl group
Organic oxide
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	1.61	ALOGPS
logP	0.33	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	11.32	ChemAxon
pKa (Strongest Basic)	1.05	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	79.79 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	68.98 m³·mol⁻¹	ChemAxon
Polarizability	26.15 Å³	ChemAxon
Number of Rings	3	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]+	162.741	30932474
DeepCCS	[M-H]-	160.383	30932474
DeepCCS	[M-2H]-	193.269	30932474
DeepCCS	[M+Na]+	168.834	30932474

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Predicted by Siyang on May 30, 2022	10.8183 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	2.13 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	1817.9 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	269.8 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	113.2 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	167.6 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	61.5 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	302.7 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	537.0 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	111.4 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	811.6 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	298.2 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	1234.9 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	262.6 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	265.7 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	386.5 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	246.2 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	159.5 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
BEMORADAN	CC1CC(=O)NN=C1C1=CC2=C(NC(=O)CO2)C=C1	3563.6	Standard polar	33892256
BEMORADAN	CC1CC(=O)NN=C1C1=CC2=C(NC(=O)CO2)C=C1	2291.9	Standard non polar	33892256
BEMORADAN	CC1CC(=O)NN=C1C1=CC2=C(NC(=O)CO2)C=C1	2852.9	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
BEMORADAN,1TMS,isomer #1	CC1CC(=O)N([Si](C)(C)C)N=C1C1=CC=C2NC(=O)COC2=C1	2698.8	Semi standard non polar	33892256
BEMORADAN,1TMS,isomer #1	CC1CC(=O)N([Si](C)(C)C)N=C1C1=CC=C2NC(=O)COC2=C1	2708.3	Standard non polar	33892256
BEMORADAN,1TMS,isomer #1	CC1CC(=O)N([Si](C)(C)C)N=C1C1=CC=C2NC(=O)COC2=C1	4242.2	Standard polar	33892256
BEMORADAN,1TMS,isomer #2	CC1CC(=O)NN=C1C1=CC=C2C(=C1)OCC(=O)N2[Si](C)(C)C	2609.2	Semi standard non polar	33892256
BEMORADAN,1TMS,isomer #2	CC1CC(=O)NN=C1C1=CC=C2C(=C1)OCC(=O)N2[Si](C)(C)C	2718.5	Standard non polar	33892256
BEMORADAN,1TMS,isomer #2	CC1CC(=O)NN=C1C1=CC=C2C(=C1)OCC(=O)N2[Si](C)(C)C	4264.2	Standard polar	33892256
BEMORADAN,2TMS,isomer #1	CC1CC(=O)N([Si](C)(C)C)N=C1C1=CC=C2C(=C1)OCC(=O)N2[Si](C)(C)C	2493.5	Semi standard non polar	33892256
BEMORADAN,2TMS,isomer #1	CC1CC(=O)N([Si](C)(C)C)N=C1C1=CC=C2C(=C1)OCC(=O)N2[Si](C)(C)C	2753.4	Standard non polar	33892256
BEMORADAN,2TMS,isomer #1	CC1CC(=O)N([Si](C)(C)C)N=C1C1=CC=C2C(=C1)OCC(=O)N2[Si](C)(C)C	4022.7	Standard polar	33892256
BEMORADAN,1TBDMS,isomer #1	CC1CC(=O)N([Si](C)(C)C(C)(C)C)N=C1C1=CC=C2NC(=O)COC2=C1	2926.5	Semi standard non polar	33892256
BEMORADAN,1TBDMS,isomer #1	CC1CC(=O)N([Si](C)(C)C(C)(C)C)N=C1C1=CC=C2NC(=O)COC2=C1	2924.7	Standard non polar	33892256
BEMORADAN,1TBDMS,isomer #1	CC1CC(=O)N([Si](C)(C)C(C)(C)C)N=C1C1=CC=C2NC(=O)COC2=C1	4334.4	Standard polar	33892256
BEMORADAN,1TBDMS,isomer #2	CC1CC(=O)NN=C1C1=CC=C2C(=C1)OCC(=O)N2[Si](C)(C)C(C)(C)C	2851.3	Semi standard non polar	33892256
BEMORADAN,1TBDMS,isomer #2	CC1CC(=O)NN=C1C1=CC=C2C(=C1)OCC(=O)N2[Si](C)(C)C(C)(C)C	2959.0	Standard non polar	33892256
BEMORADAN,1TBDMS,isomer #2	CC1CC(=O)NN=C1C1=CC=C2C(=C1)OCC(=O)N2[Si](C)(C)C(C)(C)C	4346.0	Standard polar	33892256
BEMORADAN,2TBDMS,isomer #1	CC1CC(=O)N([Si](C)(C)C(C)(C)C)N=C1C1=CC=C2C(=C1)OCC(=O)N2[Si](C)(C)C(C)(C)C	2967.0	Semi standard non polar	33892256
BEMORADAN,2TBDMS,isomer #1	CC1CC(=O)N([Si](C)(C)C(C)(C)C)N=C1C1=CC=C2C(=C1)OCC(=O)N2[Si](C)(C)C(C)(C)C	3205.2	Standard non polar	33892256
BEMORADAN,2TBDMS,isomer #1	CC1CC(=O)N([Si](C)(C)C(C)(C)C)N=C1C1=CC=C2C(=C1)OCC(=O)N2[Si](C)(C)C(C)(C)C	4026.0	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Bemoradan GC-MS (Non-derivatized) - 70eV, Positive	splash10-0gc3-1390000000-7785252ec72ce23251f5	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Bemoradan 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 - Bemoradan 10V, Negative-QTOF	splash10-0a4i-0090000000-940ab321673f0205ccea	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Bemoradan 20V, Negative-QTOF	splash10-0a4i-0090000000-0bb2f1bf6bf4586ac6a1	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Bemoradan 40V, Negative-QTOF	splash10-01ox-6890000000-a2605962406971f9cd4d	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Bemoradan 10V, Positive-QTOF	splash10-03di-0090000000-3aacaf02559e63725696	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Bemoradan 20V, Positive-QTOF	splash10-03di-0090000000-7c24f982eb36c34d5530	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Bemoradan 40V, Positive-QTOF	splash10-0j4i-0980000000-c836246b4db9aa764815	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

4515029

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5362399

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 Bemoradan (HMDB0248938)

MOL for HMDB0248938 (Bemoradan)

3D MOL for HMDB0248938 (Bemoradan)

3D SDF for HMDB0248938 (Bemoradan)

3D-SDF for HMDB0248938 (Bemoradan)

PDB for HMDB0248938 (Bemoradan)

3D PDB for HMDB0248938 (Bemoradan)

SMILES for HMDB0248938 (Bemoradan)

INCHI for HMDB0248938 (Bemoradan)

Structure for HMDB0248938 (Bemoradan)

3D Structure for HMDB0248938 (Bemoradan)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra