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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 03:32:53 UTC

Update Date

2021-09-26 22:59:40 UTC

HMDB ID

HMDB0249062

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Benzydamine N-oxide

Description

Benzydamine N-oxide belongs to the class of organic compounds known as indazoles. Indazoles are compounds containing an indazole, which is structurally characterized by a pyrazole fused to a benzene. Based on a literature review a significant number of articles have been published on Benzydamine N-oxide. This compound has been identified in human blood as reported by (PMID: 31557052 ). Benzydamine n-oxide is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Benzydamine N-oxide 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

HMDB0249062
     RDKit          3D
Benzydamine N-oxide
 47 49  0  0  0  0  0  0  0  0999 V2000
   -3.4998   -1.2863    3.0740 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4167   -1.8574    2.1366 N   0  0  0  0  0  4  0  0  0  0  0  0
   -5.5490   -0.8646    2.1268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0521   -2.9411    2.7802 O   0  0  0  0  0  1  0  0  0  0  0  0
   -4.0338   -2.1470    0.8335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6501   -2.4141    0.3592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6885   -1.2917    0.4242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5322   -1.0083    0.0459 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6907   -0.7112   -0.4219 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2473   -0.5929   -1.6032 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4874   -0.2394   -1.5036 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3982    0.1693   -2.5996 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0557    1.5635   -2.9716 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4556    1.7532   -4.3310 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9710    2.9854   -4.6418 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0451    4.0146   -3.7140 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5626    3.9282   -2.5049 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0588    2.6467   -2.1959 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8454   -0.1076   -0.1877 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9662    0.2120    0.4878 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0072    0.2470    1.8635 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8400   -0.0651    2.5984 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6592   -0.4089    1.8862 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7026   -0.4122    0.5297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6099   -1.8686    3.3208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0309   -1.2534    4.1212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2727   -0.2560    2.8015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3890   -1.3378    1.6262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8244   -0.7675    3.2019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1780    0.0704    1.7079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7264   -2.9374    0.3510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3506   -1.2118    0.1853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2474   -3.3490    0.9518 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6622   -2.8004   -0.6639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5538   -1.2998    1.6680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3487   -0.2906    0.3898 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4245    0.0399   -2.3018 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1354   -0.4913   -3.4390 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4669    0.8886   -4.9159 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5258    3.1428   -5.6147 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6134    4.9609   -4.0860 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6136    4.7583   -1.8029 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4863    2.5893   -1.1809 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8989    0.4288   -0.0331 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8611    0.4480    2.4903 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8359   -0.0246    3.6650 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7613   -0.6110    2.4396 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
  2  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 11 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24  9  1  0
 18 13  1  0
 24 19  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  0
  6 34  1  0
  7 35  1  0
  7 36  1  0
 12 37  1  0
 12 38  1  0
 14 39  1  0
 15 40  1  0
 16 41  1  0
 17 42  1  0
 18 43  1  0
 20 44  1  0
 21 45  1  0
 22 46  1  0
 23 47  1  0
M  CHG  2   2   1   4  -1
M  END

  Mrv1652309112105332D          

 24 26  0  0  0  0            999 V2000
    1.2230   -5.7301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4780   -4.9454    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
    2.2626   -5.2004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7329   -4.1608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1809   -3.5477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4358   -2.7631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838   -2.1500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838    0.7541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4358    1.3672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1809    2.1518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7329    2.7649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5399    2.5934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7948    1.8088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2428    1.1957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6933   -4.6905    0.0000 O   0  5  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  2  0  0  0  0
  9 10  1  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
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
  8 16  1  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 18 23  1  0  0  0  0
  2 24  1  0  0  0  0
M  CHG  2   2   1  24  -1
M  END
> <DATABASE_ID>
HMDB0249062

> <DATABASE_NAME>
hmdb

> <SMILES>
C[N+](C)([O-])CCCOC1=NN(CC2=CC=CC=C2)C2=CC=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C19H23N3O2/c1-22(2,23)13-8-14-24-19-17-11-6-7-12-18(17)21(20-19)15-16-9-4-3-5-10-16/h3-7,9-12H,8,13-15H2,1-2H3

> <INCHI_KEY>
VHKKEFPZHPEYJK-UHFFFAOYSA-N

> <FORMULA>
C19H23N3O2

> <MOLECULAR_WEIGHT>
325.412

> <EXACT_MASS>
325.179026993

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
36.68327586122125

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-[(1-benzyl-1H-indazol-3-yl)oxy]-N,N-dimethylpropanamine oxide

> <ALOGPS_LOGP>
1.29

> <JCHEM_LOGP>
2.535472213666667

> <ALOGPS_LOGS>
-4.78

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
4.450866396321852

> <JCHEM_POLAR_SURFACE_AREA>
50.11

> <JCHEM_REFRACTIVITY>
107.6078

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.35e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-[(1-benzylindazol-3-yl)oxy]-N,N-dimethylpropanamine oxide

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0249062
     RDKit          3D
Benzydamine N-oxide
 47 49  0  0  0  0  0  0  0  0999 V2000
   -3.4998   -1.2863    3.0740 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4167   -1.8574    2.1366 N   0  0  0  0  0  4  0  0  0  0  0  0
   -5.5490   -0.8646    2.1268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0521   -2.9411    2.7802 O   0  0  0  0  0  1  0  0  0  0  0  0
   -4.0338   -2.1470    0.8335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6501   -2.4141    0.3592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6885   -1.2917    0.4242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5322   -1.0083    0.0459 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6907   -0.7112   -0.4219 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2473   -0.5929   -1.6032 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4874   -0.2394   -1.5036 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3982    0.1693   -2.5996 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0557    1.5635   -2.9716 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4556    1.7532   -4.3310 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9710    2.9854   -4.6418 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0451    4.0146   -3.7140 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5626    3.9282   -2.5049 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0588    2.6467   -2.1959 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8454   -0.1076   -0.1877 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9662    0.2120    0.4878 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0072    0.2470    1.8635 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8400   -0.0651    2.5984 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6592   -0.4089    1.8862 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7026   -0.4122    0.5297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6099   -1.8686    3.3208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0309   -1.2534    4.1212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2727   -0.2560    2.8015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3890   -1.3378    1.6262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8244   -0.7675    3.2019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1780    0.0704    1.7079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7264   -2.9374    0.3510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3506   -1.2118    0.1853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2474   -3.3490    0.9518 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6622   -2.8004   -0.6639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5538   -1.2998    1.6680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3487   -0.2906    0.3898 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4245    0.0399   -2.3018 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1354   -0.4913   -3.4390 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4669    0.8886   -4.9159 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5258    3.1428   -5.6147 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6134    4.9609   -4.0860 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6136    4.7583   -1.8029 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4863    2.5893   -1.1809 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8989    0.4288   -0.0331 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8611    0.4480    2.4903 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8359   -0.0246    3.6650 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7613   -0.6110    2.4396 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
  2  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 11 19  1  0
 19 20  2  0
 20 21  1  0
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 23 24  2  0
 24  9  1  0
 18 13  1  0
 24 19  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  0
  6 34  1  0
  7 35  1  0
  7 36  1  0
 12 37  1  0
 12 38  1  0
 14 39  1  0
 15 40  1  0
 16 41  1  0
 17 42  1  0
 18 43  1  0
 20 44  1  0
 21 45  1  0
 22 46  1  0
 23 47  1  0
M  CHG  2   2   1   4  -1
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       2.283 -10.696   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0       2.759  -9.231   0.000  0.00  0.00           N+1
HETATM    3  C   UNK     0       4.224  -9.707   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.235  -7.767   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.204  -6.622   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.680  -5.158   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.650  -4.013   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.126  -2.549   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       1.220  -1.303   0.000  0.00  0.00           N+0
HETATM   10  N   UNK     0       2.126  -0.057   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.650   1.408   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.680   2.552   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.204   4.017   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.235   5.161   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.741   4.841   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.217   3.376   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.187   2.232   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       1.294  -8.756   0.000  0.00  0.00           O-1
CONECT    1    2                                                            
CONECT    2    1    3    4   24                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   16                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   17                                                  
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   11    8                                                  
CONECT   17   10   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   18                                                       
CONECT   24    2                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

COMPND    HMDB0249062
HETATM    1  C1  UNL     1      -3.500  -1.286   3.074  1.00  0.00           C  
HETATM    2  N1  UNL     1      -4.417  -1.857   2.137  1.00  0.00           N1+
HETATM    3  C2  UNL     1      -5.549  -0.865   2.127  1.00  0.00           C  
HETATM    4  O1  UNL     1      -5.052  -2.941   2.780  1.00  0.00           O1-
HETATM    5  C3  UNL     1      -4.034  -2.147   0.833  1.00  0.00           C  
HETATM    6  C4  UNL     1      -2.650  -2.414   0.359  1.00  0.00           C  
HETATM    7  C5  UNL     1      -1.689  -1.292   0.424  1.00  0.00           C  
HETATM    8  O2  UNL     1      -0.532  -1.008   0.046  1.00  0.00           O  
HETATM    9  C6  UNL     1       0.691  -0.711  -0.422  1.00  0.00           C  
HETATM   10  N2  UNL     1       1.247  -0.593  -1.603  1.00  0.00           N  
HETATM   11  N3  UNL     1       2.487  -0.239  -1.504  1.00  0.00           N  
HETATM   12  C7  UNL     1       3.398   0.169  -2.600  1.00  0.00           C  
HETATM   13  C8  UNL     1       3.056   1.563  -2.972  1.00  0.00           C  
HETATM   14  C9  UNL     1       2.456   1.753  -4.331  1.00  0.00           C  
HETATM   15  C10 UNL     1       1.971   2.985  -4.642  1.00  0.00           C  
HETATM   16  C11 UNL     1       2.045   4.015  -3.714  1.00  0.00           C  
HETATM   17  C12 UNL     1       2.563   3.928  -2.505  1.00  0.00           C  
HETATM   18  C13 UNL     1       3.059   2.647  -2.196  1.00  0.00           C  
HETATM   19  C14 UNL     1       2.845  -0.108  -0.188  1.00  0.00           C  
HETATM   20  C15 UNL     1       3.966   0.212   0.488  1.00  0.00           C  
HETATM   21  C16 UNL     1       4.007   0.247   1.864  1.00  0.00           C  
HETATM   22  C17 UNL     1       2.840  -0.065   2.598  1.00  0.00           C  
HETATM   23  C18 UNL     1       1.659  -0.409   1.886  1.00  0.00           C  
HETATM   24  C19 UNL     1       1.703  -0.412   0.530  1.00  0.00           C  
HETATM   25  H1  UNL     1      -2.610  -1.869   3.321  1.00  0.00           H  
HETATM   26  H2  UNL     1      -4.031  -1.253   4.121  1.00  0.00           H  
HETATM   27  H3  UNL     1      -3.273  -0.256   2.801  1.00  0.00           H  
HETATM   28  H4  UNL     1      -6.389  -1.338   1.626  1.00  0.00           H  
HETATM   29  H5  UNL     1      -5.824  -0.768   3.202  1.00  0.00           H  
HETATM   30  H6  UNL     1      -5.178   0.070   1.708  1.00  0.00           H  
HETATM   31  H7  UNL     1      -4.726  -2.937   0.351  1.00  0.00           H  
HETATM   32  H8  UNL     1      -4.351  -1.212   0.185  1.00  0.00           H  
HETATM   33  H9  UNL     1      -2.247  -3.349   0.952  1.00  0.00           H  
HETATM   34  H10 UNL     1      -2.662  -2.800  -0.664  1.00  0.00           H  
HETATM   35  H11 UNL     1      -1.554  -1.300   1.668  1.00  0.00           H  
HETATM   36  H12 UNL     1      -2.349  -0.291   0.390  1.00  0.00           H  
HETATM   37  H13 UNL     1       4.424   0.040  -2.302  1.00  0.00           H  
HETATM   38  H14 UNL     1       3.135  -0.491  -3.439  1.00  0.00           H  
HETATM   39  H15 UNL     1       2.467   0.889  -4.916  1.00  0.00           H  
HETATM   40  H16 UNL     1       1.526   3.143  -5.615  1.00  0.00           H  
HETATM   41  H17 UNL     1       1.613   4.961  -4.086  1.00  0.00           H  
HETATM   42  H18 UNL     1       2.614   4.758  -1.803  1.00  0.00           H  
HETATM   43  H19 UNL     1       3.486   2.589  -1.181  1.00  0.00           H  
HETATM   44  H20 UNL     1       4.899   0.429  -0.033  1.00  0.00           H  
HETATM   45  H21 UNL     1       4.861   0.448   2.490  1.00  0.00           H  
HETATM   46  H22 UNL     1       2.836  -0.025   3.665  1.00  0.00           H  
HETATM   47  H23 UNL     1       0.761  -0.611   2.440  1.00  0.00           H  
CONECT    1    2   25   26   27
CONECT    2    3    4    5
CONECT    3   28   29   30
CONECT    5    6   31   32
CONECT    6    7   33   34
CONECT    7    8   35   36
CONECT    8    9
CONECT    9   10   10   24
CONECT   10   11
CONECT   11   12   19
CONECT   12   13   37   38
CONECT   13   14   14   18
CONECT   14   15   39
CONECT   15   16   16   40
CONECT   16   17   41
CONECT   17   18   18   42
CONECT   18   43
CONECT   19   20   20   24
CONECT   20   21   44
CONECT   21   22   22   45
CONECT   22   23   46
CONECT   23   24   24   47
END

HMDB0249062
     RDKit          3D
Benzydamine N-oxide
 47 49  0  0  0  0  0  0  0  0999 V2000
   -3.4998   -1.2863    3.0740 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4167   -1.8574    2.1366 N   0  0  0  0  0  4  0  0  0  0  0  0
   -5.5490   -0.8646    2.1268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0521   -2.9411    2.7802 O   0  0  0  0  0  1  0  0  0  0  0  0
   -4.0338   -2.1470    0.8335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6501   -2.4141    0.3592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6885   -1.2917    0.4242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5322   -1.0083    0.0459 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6907   -0.7112   -0.4219 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2473   -0.5929   -1.6032 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4874   -0.2394   -1.5036 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3982    0.1693   -2.5996 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0557    1.5635   -2.9716 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4556    1.7532   -4.3310 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9710    2.9854   -4.6418 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0451    4.0146   -3.7140 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5626    3.9282   -2.5049 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0588    2.6467   -2.1959 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8454   -0.1076   -0.1877 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9662    0.2120    0.4878 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0072    0.2470    1.8635 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8400   -0.0651    2.5984 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6592   -0.4089    1.8862 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7026   -0.4122    0.5297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6099   -1.8686    3.3208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0309   -1.2534    4.1212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2727   -0.2560    2.8015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3890   -1.3378    1.6262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8244   -0.7675    3.2019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1780    0.0704    1.7079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7264   -2.9374    0.3510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3506   -1.2118    0.1853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2474   -3.3490    0.9518 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6622   -2.8004   -0.6639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5538   -1.2998    1.6680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3487   -0.2906    0.3898 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4245    0.0399   -2.3018 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1354   -0.4913   -3.4390 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4669    0.8886   -4.9159 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5258    3.1428   -5.6147 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6134    4.9609   -4.0860 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6136    4.7583   -1.8029 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4863    2.5893   -1.1809 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8989    0.4288   -0.0331 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8611    0.4480    2.4903 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8359   -0.0246    3.6650 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7613   -0.6110    2.4396 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
  2  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 11 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24  9  1  0
 18 13  1  0
 24 19  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  0
  6 34  1  0
  7 35  1  0
  7 36  1  0
 12 37  1  0
 12 38  1  0
 14 39  1  0
 15 40  1  0
 16 41  1  0
 17 42  1  0
 18 43  1  0
 20 44  1  0
 21 45  1  0
 22 46  1  0
 23 47  1  0
M  CHG  2   2   1   4  -1
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
Benzydamine N-oxide maleate	HMDB

Chemical Formula

C₁₉H₂₃N₃O₂

Average Molecular Weight

325.412

Monoisotopic Molecular Weight

325.179026993

IUPAC Name

3-[(1-benzyl-1H-indazol-3-yl)oxy]-N,N-dimethylpropanamine oxide

Traditional Name

3-[(1-benzylindazol-3-yl)oxy]-N,N-dimethylpropanamine oxide

CAS Registry Number

Not Available

SMILES

C[N+](C)([O-])CCCOC1=NN(CC2=CC=CC=C2)C2=CC=CC=C12

InChI Identifier

InChI=1S/C19H23N3O2/c1-22(2,23)13-8-14-24-19-17-11-6-7-12-18(17)21(20-19)15-16-9-4-3-5-10-16/h3-7,9-12H,8,13-15H2,1-2H3

InChI Key

VHKKEFPZHPEYJK-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as indazoles. Indazoles are compounds containing an indazole, which is structurally characterized by a pyrazole fused to a benzene.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrazoles

Sub Class

Indazoles

Direct Parent

Indazoles

Alternative Parents

Substituents

Benzopyrazole
Indazole
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Azole
Pyrazole
Trialkyl amine oxide
Heteroaromatic compound
Trisubstituted n-oxide
N-oxide
Ether
Azacycle
Organooxygen compound
Organonitrogen compound
Organic oxide
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
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	1.29	ALOGPS
logP	2.54	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Basic)	4.45	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	50.11 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	107.61 m³·mol⁻¹	ChemAxon
Polarizability	36.68 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	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M-2H]-	194.633	30932474
DeepCCS	[M+Na]+	169.862	30932474
AllCCS	[M+H]+	179.2	32859911
AllCCS	[M+H-H2O]+	176.2	32859911
AllCCS	[M+NH4]+	182.0	32859911
AllCCS	[M+Na]+	182.8	32859911
AllCCS	[M-H]-	185.7	32859911
AllCCS	[M+Na-2H]-	186.0	32859911
AllCCS	[M+HCOO]-	186.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Benzydamine N-oxide	C[N+](C)([O-])CCCOC1=NN(CC2=CC=CC=C2)C2=CC=CC=C12	3706.4	Standard polar	33892256
Benzydamine N-oxide	C[N+](C)([O-])CCCOC1=NN(CC2=CC=CC=C2)C2=CC=CC=C12	2252.8	Standard non polar	33892256
Benzydamine N-oxide	C[N+](C)([O-])CCCOC1=NN(CC2=CC=CC=C2)C2=CC=CC=C12	2565.0	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Benzydamine N-oxide GC-MS (Non-derivatized) - 70eV, Positive	splash10-000x-9321000000-7e4b0b5d369d5dedb5c6	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Benzydamine N-oxide 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

58918

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

65465

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 Benzydamine N-oxide (HMDB0249062)

MOL for HMDB0249062 (Benzydamine N-oxide)

3D MOL for HMDB0249062 (Benzydamine N-oxide)

3D SDF for HMDB0249062 (Benzydamine N-oxide)

3D-SDF for HMDB0249062 (Benzydamine N-oxide)

PDB for HMDB0249062 (Benzydamine N-oxide)

3D PDB for HMDB0249062 (Benzydamine N-oxide)

SMILES for HMDB0249062 (Benzydamine N-oxide)

INCHI for HMDB0249062 (Benzydamine N-oxide)

Structure for HMDB0249062 (Benzydamine N-oxide)

3D Structure for HMDB0249062 (Benzydamine N-oxide)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra