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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 20:28:48 UTC

Update Date

2021-09-26 23:15:53 UTC

HMDB ID

HMDB0258752

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Tazolol

Description

Tazolol belongs to the class of organic compounds known as alkyl aryl ethers. These are organic compounds containing the alkyl aryl ether functional group with the generic formula R-O-R' , where R is an alkyl group and R' is an aryl group. Based on a literature review a significant number of articles have been published on Tazolol. This compound has been identified in human blood as reported by (PMID: 31557052 ). Tazolol is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Tazolol 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

HMDB0258752
     RDKit          3D
Tazolol
 30 30  0  0  0  0  0  0  0  0999 V2000
   -3.5038    0.3311   -0.9220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6630   -0.8614   -0.5235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2388   -1.3996    0.7612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2738   -0.5097   -0.4077 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0157    0.4599    0.6088 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4624    0.8130    0.6902 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1918   -0.3324    0.9795 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8968    1.5071   -0.5616 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2085    1.9599   -0.5828 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2442    1.0129   -0.4337 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9376    0.3993   -1.3780 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8628   -0.4488   -1.0562 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0812   -0.6715    0.2828 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9280    0.3648    0.9991 S   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6526    0.9980   -0.0424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5091   -0.0309   -1.2056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0651    0.8440   -1.7797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7898   -1.6309   -1.3114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5467   -2.0304    1.3332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1479   -2.0139    0.5710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5944   -0.5519    1.4116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6574   -1.3345   -0.3645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5768    1.3867    0.3526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3158    0.1552    1.6265 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6451    1.5129    1.5572 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9028   -0.7285    1.8219 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6716    0.7950   -1.4117 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2073    2.3629   -0.7265 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4854   -1.0015   -1.8044 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8254   -1.3564    0.7251 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 10  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  2 18  1  0
  3 19  1  0
  3 20  1  0
  3 21  1  0
  4 22  1  0
  5 23  1  0
  5 24  1  0
  6 25  1  0
  7 26  1  0
  8 27  1  0
  8 28  1  0
 12 29  1  0
 13 30  1  0
M  END

  Mrv1652309112122292D          

 14 14  0  0  0  0            999 V2000
    1.7344   -2.9519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4489   -3.3644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4489   -4.1894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1634   -2.9519    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8779   -3.3644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5923   -2.9519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3068   -3.3644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0213   -2.9519    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7357   -3.3644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4894   -3.0288    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.0414   -3.6419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6289   -4.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8220   -4.1848    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    4.5923   -2.1269    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  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
  9 13  1  0  0  0  0
  6 14  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0258752

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)NCC(O)COC1=NC=CS1

> <INCHI_IDENTIFIER>
InChI=1S/C9H16N2O2S/c1-7(2)11-5-8(12)6-13-9-10-3-4-14-9/h3-4,7-8,11-12H,5-6H2,1-2H3

> <INCHI_KEY>
DREVJBVJBRSSDL-UHFFFAOYSA-N

> <FORMULA>
C9H16N2O2S

> <MOLECULAR_WEIGHT>
216.3

> <EXACT_MASS>
216.093248937

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
30

> <JCHEM_AVERAGE_POLARIZABILITY>
23.450743925691217

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-[(propan-2-yl)amino]-3-(1,3-thiazol-2-yloxy)propan-2-ol

> <ALOGPS_LOGP>
0.57

> <JCHEM_LOGP>
0.9372619580000003

> <ALOGPS_LOGS>
-2.22

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.083277184339181

> <JCHEM_PKA_STRONGEST_BASIC>
9.666095569432597

> <JCHEM_POLAR_SURFACE_AREA>
54.379999999999995

> <JCHEM_REFRACTIVITY>
55.057199999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.31e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
tazolol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0258752
     RDKit          3D
Tazolol
 30 30  0  0  0  0  0  0  0  0999 V2000
   -3.5038    0.3311   -0.9220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6630   -0.8614   -0.5235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2388   -1.3996    0.7612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2738   -0.5097   -0.4077 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0157    0.4599    0.6088 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4624    0.8130    0.6902 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1918   -0.3324    0.9795 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8968    1.5071   -0.5616 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2085    1.9599   -0.5828 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2442    1.0129   -0.4337 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9376    0.3993   -1.3780 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8628   -0.4488   -1.0562 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0812   -0.6715    0.2828 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9280    0.3648    0.9991 S   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6526    0.9980   -0.0424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5091   -0.0309   -1.2056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0651    0.8440   -1.7797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7898   -1.6309   -1.3114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5467   -2.0304    1.3332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1479   -2.0139    0.5710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5944   -0.5519    1.4116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6574   -1.3345   -0.3645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5768    1.3867    0.3526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3158    0.1552    1.6265 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6451    1.5129    1.5572 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9028   -0.7285    1.8219 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6716    0.7950   -1.4117 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2073    2.3629   -0.7265 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4854   -1.0015   -1.8044 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8254   -1.3564    0.7251 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 10  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  2 18  1  0
  3 19  1  0
  3 20  1  0
  3 21  1  0
  4 22  1  0
  5 23  1  0
  5 24  1  0
  6 25  1  0
  7 26  1  0
  8 27  1  0
  8 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       3.238  -5.510   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.571  -6.280   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.571  -7.820   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0       5.905  -5.510   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0       7.239  -6.280   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.572  -5.510   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.906  -6.280   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      11.240  -5.510   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      12.573  -6.280   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0      13.980  -5.654   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      15.011  -6.798   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.241  -8.132   0.000  0.00  0.00           C+0
HETATM   13  S   UNK     0      12.734  -7.812   0.000  0.00  0.00           S+0
HETATM   14  O   UNK     0       8.572  -3.970   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   14                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   13                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    9                                                       
CONECT   14    6                                                            
MASTER        0    0    0    0    0    0    0    0   14    0   28    0
END

COMPND    HMDB0258752
HETATM    1  C1  UNL     1      -3.504   0.331  -0.922  1.00  0.00           C  
HETATM    2  C2  UNL     1      -2.663  -0.861  -0.523  1.00  0.00           C  
HETATM    3  C3  UNL     1      -3.239  -1.400   0.761  1.00  0.00           C  
HETATM    4  N1  UNL     1      -1.274  -0.510  -0.408  1.00  0.00           N  
HETATM    5  C4  UNL     1      -1.016   0.460   0.609  1.00  0.00           C  
HETATM    6  C5  UNL     1       0.462   0.813   0.690  1.00  0.00           C  
HETATM    7  O1  UNL     1       1.192  -0.332   0.979  1.00  0.00           O  
HETATM    8  C6  UNL     1       0.897   1.507  -0.562  1.00  0.00           C  
HETATM    9  O2  UNL     1       2.208   1.960  -0.583  1.00  0.00           O  
HETATM   10  C7  UNL     1       3.244   1.013  -0.434  1.00  0.00           C  
HETATM   11  N2  UNL     1       3.938   0.399  -1.378  1.00  0.00           N  
HETATM   12  C8  UNL     1       4.863  -0.449  -1.056  1.00  0.00           C  
HETATM   13  C9  UNL     1       5.081  -0.672   0.283  1.00  0.00           C  
HETATM   14  S1  UNL     1       3.928   0.365   0.999  1.00  0.00           S  
HETATM   15  H1  UNL     1      -3.653   0.998  -0.042  1.00  0.00           H  
HETATM   16  H2  UNL     1      -4.509  -0.031  -1.206  1.00  0.00           H  
HETATM   17  H3  UNL     1      -3.065   0.844  -1.780  1.00  0.00           H  
HETATM   18  H4  UNL     1      -2.790  -1.631  -1.311  1.00  0.00           H  
HETATM   19  H5  UNL     1      -2.547  -2.030   1.333  1.00  0.00           H  
HETATM   20  H6  UNL     1      -4.148  -2.014   0.571  1.00  0.00           H  
HETATM   21  H7  UNL     1      -3.594  -0.552   1.412  1.00  0.00           H  
HETATM   22  H8  UNL     1      -0.657  -1.335  -0.364  1.00  0.00           H  
HETATM   23  H9  UNL     1      -1.577   1.387   0.353  1.00  0.00           H  
HETATM   24  H10 UNL     1      -1.316   0.155   1.626  1.00  0.00           H  
HETATM   25  H11 UNL     1       0.645   1.513   1.557  1.00  0.00           H  
HETATM   26  H12 UNL     1       0.903  -0.729   1.822  1.00  0.00           H  
HETATM   27  H13 UNL     1       0.672   0.795  -1.412  1.00  0.00           H  
HETATM   28  H14 UNL     1       0.207   2.363  -0.727  1.00  0.00           H  
HETATM   29  H15 UNL     1       5.485  -1.002  -1.804  1.00  0.00           H  
HETATM   30  H16 UNL     1       5.825  -1.356   0.725  1.00  0.00           H  
CONECT    1    2   15   16   17
CONECT    2    3    4   18
CONECT    3   19   20   21
CONECT    4    5   22
CONECT    5    6   23   24
CONECT    6    7    8   25
CONECT    7   26
CONECT    8    9   27   28
CONECT    9   10
CONECT   10   11   11   14
CONECT   11   12
CONECT   12   13   13   29
CONECT   13   14   30
END

HMDB0258752
     RDKit          3D
Tazolol
 30 30  0  0  0  0  0  0  0  0999 V2000
   -3.5038    0.3311   -0.9220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6630   -0.8614   -0.5235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2388   -1.3996    0.7612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2738   -0.5097   -0.4077 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0157    0.4599    0.6088 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4624    0.8130    0.6902 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1918   -0.3324    0.9795 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8968    1.5071   -0.5616 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2085    1.9599   -0.5828 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2442    1.0129   -0.4337 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9376    0.3993   -1.3780 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8628   -0.4488   -1.0562 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0812   -0.6715    0.2828 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9280    0.3648    0.9991 S   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6526    0.9980   -0.0424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5091   -0.0309   -1.2056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0651    0.8440   -1.7797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7898   -1.6309   -1.3114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5467   -2.0304    1.3332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1479   -2.0139    0.5710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5944   -0.5519    1.4116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6574   -1.3345   -0.3645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5768    1.3867    0.3526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3158    0.1552    1.6265 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6451    1.5129    1.5572 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9028   -0.7285    1.8219 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6716    0.7950   -1.4117 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2073    2.3629   -0.7265 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4854   -1.0015   -1.8044 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8254   -1.3564    0.7251 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 10  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  2 18  1  0
  3 19  1  0
  3 20  1  0
  3 21  1  0
  4 22  1  0
  5 23  1  0
  5 24  1  0
  6 25  1  0
  7 26  1  0
  8 27  1  0
  8 28  1  0
 12 29  1  0
 13 30  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
1-Isopropylamino-3-(2-thiazoloxy)-2-propanol	HMDB

Chemical Formula

C₉H₁₆N₂O₂S

Average Molecular Weight

216.3

Monoisotopic Molecular Weight

216.093248937

IUPAC Name

1-[(propan-2-yl)amino]-3-(1,3-thiazol-2-yloxy)propan-2-ol

Traditional Name

tazolol

CAS Registry Number

Not Available

SMILES

CC(C)NCC(O)COC1=NC=CS1

InChI Identifier

InChI=1S/C9H16N2O2S/c1-7(2)11-5-8(12)6-13-9-10-3-4-14-9/h3-4,7-8,11-12H,5-6H2,1-2H3

InChI Key

DREVJBVJBRSSDL-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alkyl aryl ethers. These are organic compounds containing the alkyl aryl ether functional group with the generic formula R-O-R' , where R is an alkyl group and R' is an aryl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Ethers

Direct Parent

Alkyl aryl ethers

Alternative Parents

Substituents

Alkyl aryl ether
Azole
Heteroaromatic compound
Thiazole
1,2-aminoalcohol
Secondary alcohol
Secondary aliphatic amine
Azacycle
Secondary amine
Organoheterocyclic compound
Organic nitrogen compound
Hydrocarbon derivative
Organonitrogen compound
Alcohol
Organopnictogen compound
Amine
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	0.57	ALOGPS
logP	0.94	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	14.08	ChemAxon
pKa (Strongest Basic)	9.67	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	54.38 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	55.06 m³·mol⁻¹	ChemAxon
Polarizability	23.45 Å³	ChemAxon
Number of Rings	1	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]+	148.328	30932474
DeepCCS	[M-H]-	145.97	30932474
DeepCCS	[M-2H]-	181.516	30932474
DeepCCS	[M+Na]+	156.589	30932474
AllCCS	[M+H]+	148.8	32859911
AllCCS	[M+H-H2O]+	145.2	32859911
AllCCS	[M+NH4]+	152.2	32859911
AllCCS	[M+Na]+	153.1	32859911
AllCCS	[M-H]-	149.1	32859911
AllCCS	[M+Na-2H]-	150.2	32859911
AllCCS	[M+HCOO]-	151.5	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Tazolol	CC(C)NCC(O)COC1=NC=CS1	2561.5	Standard polar	33892256
Tazolol	CC(C)NCC(O)COC1=NC=CS1	1625.1	Standard non polar	33892256
Tazolol	CC(C)NCC(O)COC1=NC=CS1	1610.2	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Tazolol,2TMS,isomer #1	CC(C)N(CC(COC1=NC=CS1)O[Si](C)(C)C)[Si](C)(C)C	1933.9	Semi standard non polar	33892256
Tazolol,2TMS,isomer #1	CC(C)N(CC(COC1=NC=CS1)O[Si](C)(C)C)[Si](C)(C)C	1983.2	Standard non polar	33892256
Tazolol,2TMS,isomer #1	CC(C)N(CC(COC1=NC=CS1)O[Si](C)(C)C)[Si](C)(C)C	2298.6	Standard polar	33892256
Tazolol,2TBDMS,isomer #1	CC(C)N(CC(COC1=NC=CS1)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2381.2	Semi standard non polar	33892256
Tazolol,2TBDMS,isomer #1	CC(C)N(CC(COC1=NC=CS1)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2432.9	Standard non polar	33892256
Tazolol,2TBDMS,isomer #1	CC(C)N(CC(COC1=NC=CS1)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2495.1	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Tazolol GC-MS (Non-derivatized) - 70eV, Positive	splash10-0knc-9200000000-3c9b57b12e7b894c32ed	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tazolol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tazolol GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tazolol GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tazolol GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tazolol GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

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

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

64770

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Tazolol

METLIN ID

Not Available

PubChem Compound

71721

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 Tazolol (HMDB0258752)

MOL for HMDB0258752 (Tazolol)

3D MOL for HMDB0258752 (Tazolol)

3D SDF for HMDB0258752 (Tazolol)

3D-SDF for HMDB0258752 (Tazolol)

PDB for HMDB0258752 (Tazolol)

3D PDB for HMDB0258752 (Tazolol)

SMILES for HMDB0258752 (Tazolol)

INCHI for HMDB0258752 (Tazolol)

Structure for HMDB0258752 (Tazolol)

3D Structure for HMDB0258752 (Tazolol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra