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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 16:12:14 UTC

Update Date

2021-09-26 23:11:17 UTC

HMDB ID

HMDB0255976

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Oxdralazine

Description

2-[(6-hydrazinylidene-1,6-dihydropyridazin-3-yl)(2-hydroxyethyl)amino]ethan-1-ol belongs to the class of organic compounds known as dialkylarylamines. These are aliphatic aromatic amines in which the amino group is linked to two aliphatic chains and one aromatic group. Based on a literature review very few articles have been published on 2-[(6-hydrazinylidene-1,6-dihydropyridazin-3-yl)(2-hydroxyethyl)amino]ethan-1-ol. This compound has been identified in human blood as reported by (PMID: 31557052 ). Oxdralazine is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Oxdralazine 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

HMDB0255976
     RDKit          3D
Oxdralazine
 30 30  0  0  0  0  0  0  0  0999 V2000
    4.9942   -0.7087    0.4894 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3512    0.1999   -0.3308 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9376    0.1325   -0.3888 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1648    1.0296    0.3490 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7802    0.9834    0.3468 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1566   -0.0165   -0.4265 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2714   -0.0687   -0.3616 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9216   -1.1315    0.4137 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9687   -2.2976    0.5482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6010   -3.2898    1.2814 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1038    0.9422   -0.9552 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7159    1.9082    0.0009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5015    2.7984   -0.7642 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9395   -0.8427   -1.1066 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2831   -0.7905   -1.1047 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8510   -1.7114    0.1604 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6282   -0.7150    1.4855 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8723    0.8869   -0.8654 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6456    1.7892    0.9317 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1768    1.6661    0.9143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8496   -1.4995   -0.0602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2259   -0.7493    1.4256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0045   -1.9745    0.9067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9061   -2.7104   -0.5092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4700   -3.4966    0.8681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4809    1.4827   -1.6789 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9559    0.4615   -1.5127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9533    2.5727    0.4855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3677    1.4443    0.7589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4833    3.7051   -0.3702 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  7 11  1  0
 11 12  1  0
 12 13  1  0
  6 14  1  0
 14 15  2  0
 15  3  1  0
  1 16  1  0
  1 17  1  0
  2 18  1  0
  4 19  1  0
  5 20  1  0
  8 21  1  0
  8 22  1  0
  9 23  1  0
  9 24  1  0
 10 25  1  0
 11 26  1  0
 11 27  1  0
 12 28  1  0
 12 29  1  0
 13 30  1  0
M  END


  Mrv1652309112118122D          

 15 15  0  0  0  0            999 V2000
   -2.1434   -2.0625    0.0000 C   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   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.0625    0.0000 N   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   -3.3000    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
   -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
   -2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    1.6500    0.0000 O   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
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  3  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  9 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0255976

> <DATABASE_NAME>
hmdb

> <SMILES>
NNC1=NN=C(C=C1)N(CCO)CCO

> <INCHI_IDENTIFIER>
InChI=1S/C8H15N5O2/c9-10-7-1-2-8(12-11-7)13(3-5-14)4-6-15/h1-2,14-15H,3-6,9H2,(H,10,11)

> <INCHI_KEY>
POFDNYKJHWKGDU-UHFFFAOYSA-N

> <FORMULA>
C8H15N5O2

> <MOLECULAR_WEIGHT>
213.241

> <EXACT_MASS>
213.122574743

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
30

> <JCHEM_AVERAGE_POLARIZABILITY>
22.03921011058066

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(6-hydrazinylpyridazin-3-yl)(2-hydroxyethyl)amino]ethan-1-ol

> <ALOGPS_LOGP>
-0.70

> <JCHEM_LOGP>
-0.9157990583333332

> <ALOGPS_LOGS>
-1.27

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
15.87761055469619

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.275339107100184

> <JCHEM_PKA_STRONGEST_BASIC>
8.917246483024487

> <JCHEM_POLAR_SURFACE_AREA>
107.53

> <JCHEM_REFRACTIVITY>
61.1113

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.13e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[(6-hydrazinylpyridazin-3-yl)(2-hydroxyethyl)amino]ethanol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0255976
     RDKit          3D
Oxdralazine
 30 30  0  0  0  0  0  0  0  0999 V2000
    4.9942   -0.7087    0.4894 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3512    0.1999   -0.3308 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9376    0.1325   -0.3888 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1648    1.0296    0.3490 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7802    0.9834    0.3468 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1566   -0.0165   -0.4265 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2714   -0.0687   -0.3616 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9216   -1.1315    0.4137 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9687   -2.2976    0.5482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6010   -3.2898    1.2814 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1038    0.9422   -0.9552 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7159    1.9082    0.0009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5015    2.7984   -0.7642 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9395   -0.8427   -1.1066 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2831   -0.7905   -1.1047 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8510   -1.7114    0.1604 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6282   -0.7150    1.4855 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8723    0.8869   -0.8654 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6456    1.7892    0.9317 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1768    1.6661    0.9143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8496   -1.4995   -0.0602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2259   -0.7493    1.4256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0045   -1.9745    0.9067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9061   -2.7104   -0.5092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4700   -3.4966    0.8681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4809    1.4827   -1.6789 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9559    0.4615   -1.5127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9533    2.5727    0.4855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3677    1.4443    0.7589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4833    3.7051   -0.3702 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  7 11  1  0
 11 12  1  0
 12 13  1  0
  6 14  1  0
 14 15  2  0
 15  3  1  0
  1 16  1  0
  1 17  1  0
  2 18  1  0
  4 19  1  0
  5 20  1  0
  8 21  1  0
  8 22  1  0
  9 23  1  0
  9 24  1  0
 10 25  1  0
 11 26  1  0
 11 27  1  0
 12 28  1  0
 12 29  1  0
 13 30  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  -3.850   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.667  -1.540   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0      -1.334  -2.310   0.000  0.00  0.00           N+0
HETATM    5  N   UNK     0      -1.334  -3.850   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0      -2.667  -6.160   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  N   UNK     0      -2.667   0.000   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0      -4.001   0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -5.335   3.080   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -1.334   0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       0.000   3.080   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    3   10   13                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13    9   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14                                                            
MASTER        0    0    0    0    0    0    0    0   15    0   30    0
END

COMPND    HMDB0255976
HETATM    1  N1  UNL     1       4.994  -0.709   0.489  1.00  0.00           N  
HETATM    2  N2  UNL     1       4.351   0.200  -0.331  1.00  0.00           N  
HETATM    3  C1  UNL     1       2.938   0.132  -0.389  1.00  0.00           C  
HETATM    4  C2  UNL     1       2.165   1.030   0.349  1.00  0.00           C  
HETATM    5  C3  UNL     1       0.780   0.983   0.347  1.00  0.00           C  
HETATM    6  C4  UNL     1       0.157  -0.016  -0.427  1.00  0.00           C  
HETATM    7  N3  UNL     1      -1.271  -0.069  -0.362  1.00  0.00           N  
HETATM    8  C5  UNL     1      -1.922  -1.131   0.414  1.00  0.00           C  
HETATM    9  C6  UNL     1      -0.969  -2.298   0.548  1.00  0.00           C  
HETATM   10  O1  UNL     1      -1.601  -3.290   1.281  1.00  0.00           O  
HETATM   11  C7  UNL     1      -2.104   0.942  -0.955  1.00  0.00           C  
HETATM   12  C8  UNL     1      -2.716   1.908   0.001  1.00  0.00           C  
HETATM   13  O2  UNL     1      -3.501   2.798  -0.764  1.00  0.00           O  
HETATM   14  N4  UNL     1       0.940  -0.843  -1.107  1.00  0.00           N  
HETATM   15  N5  UNL     1       2.283  -0.790  -1.105  1.00  0.00           N  
HETATM   16  H1  UNL     1       4.851  -1.711   0.160  1.00  0.00           H  
HETATM   17  H2  UNL     1       4.628  -0.715   1.486  1.00  0.00           H  
HETATM   18  H3  UNL     1       4.872   0.887  -0.865  1.00  0.00           H  
HETATM   19  H4  UNL     1       2.646   1.789   0.932  1.00  0.00           H  
HETATM   20  H5  UNL     1       0.177   1.666   0.914  1.00  0.00           H  
HETATM   21  H6  UNL     1      -2.850  -1.500  -0.060  1.00  0.00           H  
HETATM   22  H7  UNL     1      -2.226  -0.749   1.426  1.00  0.00           H  
HETATM   23  H8  UNL     1      -0.005  -1.975   0.907  1.00  0.00           H  
HETATM   24  H9  UNL     1      -0.906  -2.710  -0.509  1.00  0.00           H  
HETATM   25  H10 UNL     1      -2.470  -3.497   0.868  1.00  0.00           H  
HETATM   26  H11 UNL     1      -1.481   1.483  -1.679  1.00  0.00           H  
HETATM   27  H12 UNL     1      -2.956   0.461  -1.513  1.00  0.00           H  
HETATM   28  H13 UNL     1      -1.953   2.573   0.486  1.00  0.00           H  
HETATM   29  H14 UNL     1      -3.368   1.444   0.759  1.00  0.00           H  
HETATM   30  H15 UNL     1      -3.483   3.705  -0.370  1.00  0.00           H  
CONECT    1    2   16   17
CONECT    2    3   18
CONECT    3    4    4   15
CONECT    4    5   19
CONECT    5    6    6   20
CONECT    6    7   14
CONECT    7    8   11
CONECT    8    9   21   22
CONECT    9   10   23   24
CONECT   10   25
CONECT   11   12   26   27
CONECT   12   13   28   29
CONECT   13   30
CONECT   14   15   15
END

HMDB0255976
     RDKit          3D
Oxdralazine
 30 30  0  0  0  0  0  0  0  0999 V2000
    4.9942   -0.7087    0.4894 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3512    0.1999   -0.3308 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9376    0.1325   -0.3888 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1648    1.0296    0.3490 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7802    0.9834    0.3468 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1566   -0.0165   -0.4265 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2714   -0.0687   -0.3616 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9216   -1.1315    0.4137 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9687   -2.2976    0.5482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6010   -3.2898    1.2814 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1038    0.9422   -0.9552 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7159    1.9082    0.0009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5015    2.7984   -0.7642 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9395   -0.8427   -1.1066 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2831   -0.7905   -1.1047 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8510   -1.7114    0.1604 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6282   -0.7150    1.4855 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8723    0.8869   -0.8654 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6456    1.7892    0.9317 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1768    1.6661    0.9143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8496   -1.4995   -0.0602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2259   -0.7493    1.4256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0045   -1.9745    0.9067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9061   -2.7104   -0.5092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4700   -3.4966    0.8681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4809    1.4827   -1.6789 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9559    0.4615   -1.5127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9533    2.5727    0.4855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3677    1.4443    0.7589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4833    3.7051   -0.3702 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  7 11  1  0
 11 12  1  0
 12 13  1  0
  6 14  1  0
 14 15  2  0
 15  3  1  0
  1 16  1  0
  1 17  1  0
  2 18  1  0
  4 19  1  0
  5 20  1  0
  8 21  1  0
  8 22  1  0
  9 23  1  0
  9 24  1  0
 10 25  1  0
 11 26  1  0
 11 27  1  0
 12 28  1  0
 12 29  1  0
 13 30  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
3-(Bis(2-hydroxyethyl)amino)-6-hydrazinopyridazine	MeSH
3-Hydrazino-6-(N,N-bis(2-hydroxyethyl)amino)pyridazine dihydrochloride	MeSH
DL 150 IT	MeSH
Hydrazinopyridazine	MeSH
Oxdralazine dihydrochloride	MeSH

Chemical Formula

C₈H₁₅N₅O₂

Average Molecular Weight

213.241

Monoisotopic Molecular Weight

213.122574743

IUPAC Name

2-[(6-hydrazinylpyridazin-3-yl)(2-hydroxyethyl)amino]ethan-1-ol

Traditional Name

2-[(6-hydrazinylpyridazin-3-yl)(2-hydroxyethyl)amino]ethanol

CAS Registry Number

Not Available

SMILES

NNC1=NN=C(C=C1)N(CCO)CCO

InChI Identifier

InChI=1S/C8H15N5O2/c9-10-7-1-2-8(12-11-7)13(3-5-14)4-6-15/h1-2,14-15H,3-6,9H2,(H,10,11)

InChI Key

POFDNYKJHWKGDU-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dialkylarylamines. These are aliphatic aromatic amines in which the amino group is linked to two aliphatic chains and one aromatic group.

Kingdom

Organic compounds

Super Class

Organic nitrogen compounds

Class

Organonitrogen compounds

Sub Class

Amines

Direct Parent

Dialkylarylamines

Alternative Parents

Substituents

Dialkylarylamine
Aminopyridazine
Pyridazine
Imidolactam
Heteroaromatic compound
Organoheterocyclic compound
Alkanolamine
Azacycle
Alcohol
Hydrocarbon derivative
Organopnictogen compound
Primary alcohol
Organooxygen compound
Hydrazine derivative
Organic oxygen compound
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)

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	-0.7	ALOGPS
logP	-0.92	ChemAxon
logS	-1.3	ALOGPS
pKa (Strongest Acidic)	15.28	ChemAxon
pKa (Strongest Basic)	8.92	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	107.53 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	61.11 m³·mol⁻¹	ChemAxon
Polarizability	22.04 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	145.334	30932474
DeepCCS	[M-H]-	142.953	30932474
DeepCCS	[M-2H]-	178.285	30932474
DeepCCS	[M+Na]+	152.885	30932474
AllCCS	[M+H]+	148.2	32859911
AllCCS	[M+H-H2O]+	144.5	32859911
AllCCS	[M+NH4]+	151.8	32859911
AllCCS	[M+Na]+	152.8	32859911
AllCCS	[M-H]-	147.8	32859911
AllCCS	[M+Na-2H]-	148.5	32859911
AllCCS	[M+HCOO]-	149.3	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Oxdralazine	NNC1=NN=C(C=C1)N(CCO)CCO	3098.1	Standard polar	33892256
Oxdralazine	NNC1=NN=C(C=C1)N(CCO)CCO	2353.5	Standard non polar	33892256
Oxdralazine	NNC1=NN=C(C=C1)N(CCO)CCO	2456.6	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Oxdralazine,3TMS,isomer #1	C[Si](C)(C)NNC1=CC=C(N(CCO[Si](C)(C)C)CCO[Si](C)(C)C)N=N1	2392.7	Semi standard non polar	33892256
Oxdralazine,3TMS,isomer #1	C[Si](C)(C)NNC1=CC=C(N(CCO[Si](C)(C)C)CCO[Si](C)(C)C)N=N1	2325.0	Standard non polar	33892256
Oxdralazine,3TMS,isomer #1	C[Si](C)(C)NNC1=CC=C(N(CCO[Si](C)(C)C)CCO[Si](C)(C)C)N=N1	3438.5	Standard polar	33892256
Oxdralazine,3TMS,isomer #2	C[Si](C)(C)OCCN(CCO[Si](C)(C)C)C1=CC=C(N(N)[Si](C)(C)C)N=N1	2279.3	Semi standard non polar	33892256
Oxdralazine,3TMS,isomer #2	C[Si](C)(C)OCCN(CCO[Si](C)(C)C)C1=CC=C(N(N)[Si](C)(C)C)N=N1	2335.5	Standard non polar	33892256
Oxdralazine,3TMS,isomer #2	C[Si](C)(C)OCCN(CCO[Si](C)(C)C)C1=CC=C(N(N)[Si](C)(C)C)N=N1	3512.0	Standard polar	33892256
Oxdralazine,3TMS,isomer #3	C[Si](C)(C)OCCN(CCO)C1=CC=C(NN([Si](C)(C)C)[Si](C)(C)C)N=N1	2454.5	Semi standard non polar	33892256
Oxdralazine,3TMS,isomer #3	C[Si](C)(C)OCCN(CCO)C1=CC=C(NN([Si](C)(C)C)[Si](C)(C)C)N=N1	2421.2	Standard non polar	33892256
Oxdralazine,3TMS,isomer #3	C[Si](C)(C)OCCN(CCO)C1=CC=C(NN([Si](C)(C)C)[Si](C)(C)C)N=N1	3395.4	Standard polar	33892256
Oxdralazine,3TMS,isomer #4	C[Si](C)(C)NN(C1=CC=C(N(CCO)CCO[Si](C)(C)C)N=N1)[Si](C)(C)C	2384.1	Semi standard non polar	33892256
Oxdralazine,3TMS,isomer #4	C[Si](C)(C)NN(C1=CC=C(N(CCO)CCO[Si](C)(C)C)N=N1)[Si](C)(C)C	2332.2	Standard non polar	33892256
Oxdralazine,3TMS,isomer #4	C[Si](C)(C)NN(C1=CC=C(N(CCO)CCO[Si](C)(C)C)N=N1)[Si](C)(C)C	3138.1	Standard polar	33892256
Oxdralazine,3TMS,isomer #5	C[Si](C)(C)N(C1=CC=C(N(CCO)CCO)N=N1)N([Si](C)(C)C)[Si](C)(C)C	2382.3	Semi standard non polar	33892256
Oxdralazine,3TMS,isomer #5	C[Si](C)(C)N(C1=CC=C(N(CCO)CCO)N=N1)N([Si](C)(C)C)[Si](C)(C)C	2355.1	Standard non polar	33892256
Oxdralazine,3TMS,isomer #5	C[Si](C)(C)N(C1=CC=C(N(CCO)CCO)N=N1)N([Si](C)(C)C)[Si](C)(C)C	3098.7	Standard polar	33892256
Oxdralazine,4TMS,isomer #1	C[Si](C)(C)OCCN(CCO[Si](C)(C)C)C1=CC=C(NN([Si](C)(C)C)[Si](C)(C)C)N=N1	2405.7	Semi standard non polar	33892256
Oxdralazine,4TMS,isomer #1	C[Si](C)(C)OCCN(CCO[Si](C)(C)C)C1=CC=C(NN([Si](C)(C)C)[Si](C)(C)C)N=N1	2434.9	Standard non polar	33892256
Oxdralazine,4TMS,isomer #1	C[Si](C)(C)OCCN(CCO[Si](C)(C)C)C1=CC=C(NN([Si](C)(C)C)[Si](C)(C)C)N=N1	3213.9	Standard polar	33892256
Oxdralazine,4TMS,isomer #2	C[Si](C)(C)NN(C1=CC=C(N(CCO[Si](C)(C)C)CCO[Si](C)(C)C)N=N1)[Si](C)(C)C	2387.3	Semi standard non polar	33892256
Oxdralazine,4TMS,isomer #2	C[Si](C)(C)NN(C1=CC=C(N(CCO[Si](C)(C)C)CCO[Si](C)(C)C)N=N1)[Si](C)(C)C	2319.6	Standard non polar	33892256
Oxdralazine,4TMS,isomer #2	C[Si](C)(C)NN(C1=CC=C(N(CCO[Si](C)(C)C)CCO[Si](C)(C)C)N=N1)[Si](C)(C)C	2942.5	Standard polar	33892256
Oxdralazine,4TMS,isomer #3	C[Si](C)(C)OCCN(CCO)C1=CC=C(N(N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)N=N1	2403.5	Semi standard non polar	33892256
Oxdralazine,4TMS,isomer #3	C[Si](C)(C)OCCN(CCO)C1=CC=C(N(N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)N=N1	2420.8	Standard non polar	33892256
Oxdralazine,4TMS,isomer #3	C[Si](C)(C)OCCN(CCO)C1=CC=C(N(N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)N=N1	2866.4	Standard polar	33892256
Oxdralazine,5TMS,isomer #1	C[Si](C)(C)OCCN(CCO[Si](C)(C)C)C1=CC=C(N(N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)N=N1	2421.0	Semi standard non polar	33892256
Oxdralazine,5TMS,isomer #1	C[Si](C)(C)OCCN(CCO[Si](C)(C)C)C1=CC=C(N(N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)N=N1	2418.3	Standard non polar	33892256
Oxdralazine,5TMS,isomer #1	C[Si](C)(C)OCCN(CCO[Si](C)(C)C)C1=CC=C(N(N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)N=N1	2703.6	Standard polar	33892256
Oxdralazine,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NNC1=CC=C(N(CCO[Si](C)(C)C(C)(C)C)CCO[Si](C)(C)C(C)(C)C)N=N1	3008.9	Semi standard non polar	33892256
Oxdralazine,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NNC1=CC=C(N(CCO[Si](C)(C)C(C)(C)C)CCO[Si](C)(C)C(C)(C)C)N=N1	2996.4	Standard non polar	33892256
Oxdralazine,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NNC1=CC=C(N(CCO[Si](C)(C)C(C)(C)C)CCO[Si](C)(C)C(C)(C)C)N=N1	3569.8	Standard polar	33892256
Oxdralazine,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCCN(CCO[Si](C)(C)C(C)(C)C)C1=CC=C(N(N)[Si](C)(C)C(C)(C)C)N=N1	2875.8	Semi standard non polar	33892256
Oxdralazine,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCCN(CCO[Si](C)(C)C(C)(C)C)C1=CC=C(N(N)[Si](C)(C)C(C)(C)C)N=N1	2948.7	Standard non polar	33892256
Oxdralazine,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCCN(CCO[Si](C)(C)C(C)(C)C)C1=CC=C(N(N)[Si](C)(C)C(C)(C)C)N=N1	3594.6	Standard polar	33892256
Oxdralazine,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCCN(CCO)C1=CC=C(NN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=N1	3003.9	Semi standard non polar	33892256
Oxdralazine,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCCN(CCO)C1=CC=C(NN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=N1	3045.9	Standard non polar	33892256
Oxdralazine,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCCN(CCO)C1=CC=C(NN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=N1	3518.2	Standard polar	33892256
Oxdralazine,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NN(C1=CC=C(N(CCO)CCO[Si](C)(C)C(C)(C)C)N=N1)[Si](C)(C)C(C)(C)C	2949.4	Semi standard non polar	33892256
Oxdralazine,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NN(C1=CC=C(N(CCO)CCO[Si](C)(C)C(C)(C)C)N=N1)[Si](C)(C)C(C)(C)C	2992.5	Standard non polar	33892256
Oxdralazine,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NN(C1=CC=C(N(CCO)CCO[Si](C)(C)C(C)(C)C)N=N1)[Si](C)(C)C(C)(C)C	3287.8	Standard polar	33892256
Oxdralazine,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N(C1=CC=C(N(CCO)CCO)N=N1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2974.8	Semi standard non polar	33892256
Oxdralazine,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N(C1=CC=C(N(CCO)CCO)N=N1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2993.5	Standard non polar	33892256
Oxdralazine,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N(C1=CC=C(N(CCO)CCO)N=N1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3189.0	Standard polar	33892256
Oxdralazine,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCCN(CCO[Si](C)(C)C(C)(C)C)C1=CC=C(NN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=N1	3146.4	Semi standard non polar	33892256
Oxdralazine,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCCN(CCO[Si](C)(C)C(C)(C)C)C1=CC=C(NN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=N1	3201.2	Standard non polar	33892256
Oxdralazine,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCCN(CCO[Si](C)(C)C(C)(C)C)C1=CC=C(NN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=N1	3449.4	Standard polar	33892256
Oxdralazine,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NN(C1=CC=C(N(CCO[Si](C)(C)C(C)(C)C)CCO[Si](C)(C)C(C)(C)C)N=N1)[Si](C)(C)C(C)(C)C	3133.9	Semi standard non polar	33892256
Oxdralazine,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NN(C1=CC=C(N(CCO[Si](C)(C)C(C)(C)C)CCO[Si](C)(C)C(C)(C)C)N=N1)[Si](C)(C)C(C)(C)C	3126.8	Standard non polar	33892256
Oxdralazine,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NN(C1=CC=C(N(CCO[Si](C)(C)C(C)(C)C)CCO[Si](C)(C)C(C)(C)C)N=N1)[Si](C)(C)C(C)(C)C	3240.8	Standard polar	33892256
Oxdralazine,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCCN(CCO)C1=CC=C(N(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=N1	3137.2	Semi standard non polar	33892256
Oxdralazine,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCCN(CCO)C1=CC=C(N(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=N1	3194.3	Standard non polar	33892256
Oxdralazine,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCCN(CCO)C1=CC=C(N(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=N1	3134.2	Standard polar	33892256
Oxdralazine,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCCN(CCO[Si](C)(C)C(C)(C)C)C1=CC=C(N(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=N1	3312.9	Semi standard non polar	33892256
Oxdralazine,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCCN(CCO[Si](C)(C)C(C)(C)C)C1=CC=C(N(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=N1	3334.1	Standard non polar	33892256
Oxdralazine,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCCN(CCO[Si](C)(C)C(C)(C)C)C1=CC=C(N(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=N1	3088.5	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Oxdralazine GC-MS (Non-derivatized) - 70eV, Positive	splash10-00lr-2900000000-4d41d7038a08f4bf9b3d	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Oxdralazine GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Oxdralazine GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Oxdralazine GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Oxdralazine GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Oxdralazine GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Oxdralazine GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Oxdralazine GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Oxdralazine GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Oxdralazine GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Oxdralazine GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Oxdralazine GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Oxdralazine GC-MS (TBDMS_1_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Oxdralazine GC-MS (TBDMS_2_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Oxdralazine GC-MS (TBDMS_2_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Oxdralazine GC-MS (TBDMS_2_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Oxdralazine GC-MS (TBDMS_2_4) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Oxdralazine GC-MS (TBDMS_2_5) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-25	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

26452

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 Oxdralazine (HMDB0255976)

MOL for HMDB0255976 (Oxdralazine)

3D MOL for HMDB0255976 (Oxdralazine)

3D SDF for HMDB0255976 (Oxdralazine)

3D-SDF for HMDB0255976 (Oxdralazine)

PDB for HMDB0255976 (Oxdralazine)

3D PDB for HMDB0255976 (Oxdralazine)

SMILES for HMDB0255976 (Oxdralazine)

INCHI for HMDB0255976 (Oxdralazine)

Structure for HMDB0255976 (Oxdralazine)

3D Structure for HMDB0255976 (Oxdralazine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

NMR Spectra