Jump To Section:

Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References XML

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2013-07-04 18:59:15 UTC

Update Date

2019-07-23 07:15:05 UTC

HMDB ID

HMDB0060785

Secondary Accession Numbers

HMDB60785

Metabolite Identification

Common Name

6-Hydroxyemedastine

Description

6-Hydroxyemedastine belongs to the class of organic compounds known as benzimidazoles. These are organic compounds containing a benzene ring fused to an imidazole ring (five member ring containing a nitrogen atom, 4 carbon atoms, and two double bonds). 6-Hydroxyemedastine is a very strong basic compound (based on its pKa). 6-Hydroxyemedastine is a metabolite of emedastine. Emedastine difumarate (Emadine) is a second generation antihistamine used in eye drops to treat allergic conjunctivitis. It's mechanism of action is a H1 receptor antagonist.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

HMDB0060785
     RDKit          3D
6-Hydroxyemedastine
 49 51  0  0  0  0  0  0  0  0999 V2000
    4.9742   -3.4200   -0.0434 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0445   -2.4775    0.6944 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3448   -1.7410   -0.2282 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4605   -0.8417    0.3211 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7598   -0.1008   -0.8096 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8124    0.8640   -0.3440 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4873    0.7113   -0.0850 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2041   -0.4945   -0.2311 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2411   -1.3295    0.9372 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6094   -1.9423    1.1559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7283   -1.0612    0.7113 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0036   -1.1889   -0.7160 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4322   -0.9862   -0.9044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2276   -0.2162   -1.4582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7858   -0.6979   -1.5285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0125    1.8976    0.3408 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0164    2.7996    0.3444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0294    4.1464    0.6939 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1743    4.8113    0.5887 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3418    4.2099    0.1660 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5277    4.9056    0.0727 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3142    2.8699   -0.1725 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1273    2.1571   -0.0835 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9110   -3.5709    0.5385 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2709   -3.0133   -1.0317 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4652   -4.4125   -0.1578 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3810   -3.0243    1.3951 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6888   -1.8197    1.3470 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0482   -0.0453    0.8668 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7552   -1.2517    1.0417 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5244    0.3341   -1.4881 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2661   -0.9107   -1.4224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4715   -2.1288    0.9022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0325   -0.6979    1.8346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7019   -2.9180    0.6355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7159   -2.1377    2.2403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5565   -0.0002    1.0054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6555   -1.4145    1.2496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6802    0.0726   -1.0985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9908   -1.2869    0.0141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7682   -1.6016   -1.7641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6229   -0.1281   -2.4923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3040    0.7743   -0.9762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8230   -1.7830   -1.7451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2621   -0.1214   -2.3203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9287    4.6469    1.0292 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1867    5.8708    0.8585 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7235    5.3579   -0.8190 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1886    2.3350   -0.5109 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  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
  7 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 20 22  1  0
 22 23  2  0
 23  6  1  0
 15  8  1  0
 23 17  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  9 33  1  0
  9 34  1  0
 10 35  1  0
 10 36  1  0
 11 37  1  0
 11 38  1  0
 13 39  1  0
 13 40  1  0
 13 41  1  0
 14 42  1  0
 14 43  1  0
 15 44  1  0
 15 45  1  0
 18 46  1  0
 19 47  1  0
 21 48  1  0
 22 49  1  0
M  END

  Mrv0541 07041311592D          

 23 25  0  0  0  0            999 V2000
   -3.9109    0.5756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1964    0.9881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4820    0.5756    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7675    0.9881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0530    0.5756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3386    0.9881    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4151    0.6526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9671    1.2657    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5546    1.9802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2523    1.8086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8044    2.4217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5494    3.2063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1015    3.8194    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2575    3.3779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8096    2.7648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5866   -0.1544    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3881   -0.3500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7349   -1.0985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3659   -1.8364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5589   -2.0079    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3633   -2.8094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0783   -1.4840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0660   -0.6591    0.0000 C   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  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  6 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
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
  9 15  1  0  0  0  0
  7 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 16 23  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0060785

> <DATABASE_NAME>
hmdb

> <SMILES>
CCOCCN1C(=NC2=C1C=C(O)C=C2)N1CCCN(C)CC1

> <INCHI_IDENTIFIER>
InChI=1S/C17H26N4O2/c1-3-23-12-11-21-16-13-14(22)5-6-15(16)18-17(21)20-8-4-7-19(2)9-10-20/h5-6,13,22H,3-4,7-12H2,1-2H3

> <INCHI_KEY>
YDYQGSLFCJVMNN-UHFFFAOYSA-N

> <FORMULA>
C17H26N4O2

> <MOLECULAR_WEIGHT>
318.4139

> <EXACT_MASS>
318.205576096

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
36.16111155918045

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-(2-ethoxyethyl)-2-(4-methyl-1,4-diazepan-1-yl)-1H-1,3-benzodiazol-6-ol

> <ALOGPS_LOGP>
2.39

> <JCHEM_LOGP>
1.864685755756753

> <ALOGPS_LOGS>
-2.14

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.443174723442384

> <JCHEM_PKA_STRONGEST_BASIC>
8.599490006833326

> <JCHEM_POLAR_SURFACE_AREA>
53.760000000000005

> <JCHEM_REFRACTIVITY>
92.45559999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.29e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-(2-ethoxyethyl)-2-(4-methyl-1,4-diazepan-1-yl)-1,3-benzodiazol-5-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0060785
     RDKit          3D
6-Hydroxyemedastine
 49 51  0  0  0  0  0  0  0  0999 V2000
    4.9742   -3.4200   -0.0434 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0445   -2.4775    0.6944 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3448   -1.7410   -0.2282 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4605   -0.8417    0.3211 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7598   -0.1008   -0.8096 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8124    0.8640   -0.3440 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4873    0.7113   -0.0850 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2041   -0.4945   -0.2311 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2411   -1.3295    0.9372 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6094   -1.9423    1.1559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7283   -1.0612    0.7113 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0036   -1.1889   -0.7160 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4322   -0.9862   -0.9044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2276   -0.2162   -1.4582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7858   -0.6979   -1.5285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0125    1.8976    0.3408 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0164    2.7996    0.3444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0294    4.1464    0.6939 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1743    4.8113    0.5887 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3418    4.2099    0.1660 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5277    4.9056    0.0727 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3142    2.8699   -0.1725 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1273    2.1571   -0.0835 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9110   -3.5709    0.5385 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2709   -3.0133   -1.0317 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4652   -4.4125   -0.1578 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3810   -3.0243    1.3951 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6888   -1.8197    1.3470 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0482   -0.0453    0.8668 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7552   -1.2517    1.0417 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5244    0.3341   -1.4881 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2661   -0.9107   -1.4224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4715   -2.1288    0.9022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0325   -0.6979    1.8346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7019   -2.9180    0.6355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7159   -2.1377    2.2403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5565   -0.0002    1.0054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6555   -1.4145    1.2496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6802    0.0726   -1.0985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9908   -1.2869    0.0141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7682   -1.6016   -1.7641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6229   -0.1281   -2.4923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3040    0.7743   -0.9762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8230   -1.7830   -1.7451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2621   -0.1214   -2.3203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9287    4.6469    1.0292 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1867    5.8708    0.8585 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7235    5.3579   -0.8190 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1886    2.3350   -0.5109 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  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
  7 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 20 22  1  0
 22 23  2  0
 23  6  1  0
 15  8  1  0
 23 17  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  9 33  1  0
  9 34  1  0
 10 35  1  0
 10 36  1  0
 11 37  1  0
 11 38  1  0
 13 39  1  0
 13 40  1  0
 13 41  1  0
 14 42  1  0
 14 43  1  0
 15 44  1  0
 15 45  1  0
 18 46  1  0
 19 47  1  0
 21 48  1  0
 22 49  1  0
M  END

HEADER    PROTEIN                                 04-JUL-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-JUL-13         0                                  
HETATM    1  C   UNK     0      -7.300   1.074   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.967   1.844   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -4.633   1.074   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -3.299   1.844   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.966   1.074   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      -0.632   1.844   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0       0.775   1.218   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       1.805   2.363   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       1.035   3.696   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.471   3.376   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.502   4.521   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.026   5.985   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -2.056   7.130   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       0.481   6.305   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.511   5.161   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       1.095  -0.288   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       2.591  -0.653   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.238  -2.051   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.550  -3.428   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       1.043  -3.748   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       0.678  -5.244   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.146  -2.770   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.123  -1.230   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   10                                                  
CONECT    7    6    8   16                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   15                                                  
CONECT   10    9    6   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14    9                                                       
CONECT   16    7   17   23                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   16                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

COMPND    HMDB0060785
HETATM    1  C1  UNL     1       4.974  -3.420  -0.043  1.00  0.00           C  
HETATM    2  C2  UNL     1       4.045  -2.478   0.694  1.00  0.00           C  
HETATM    3  O1  UNL     1       3.345  -1.741  -0.228  1.00  0.00           O  
HETATM    4  C3  UNL     1       2.461  -0.842   0.321  1.00  0.00           C  
HETATM    5  C4  UNL     1       1.760  -0.101  -0.810  1.00  0.00           C  
HETATM    6  N1  UNL     1       0.812   0.864  -0.344  1.00  0.00           N  
HETATM    7  C5  UNL     1      -0.487   0.711  -0.085  1.00  0.00           C  
HETATM    8  N2  UNL     1      -1.204  -0.494  -0.231  1.00  0.00           N  
HETATM    9  C6  UNL     1      -1.241  -1.329   0.937  1.00  0.00           C  
HETATM   10  C7  UNL     1      -2.609  -1.942   1.156  1.00  0.00           C  
HETATM   11  C8  UNL     1      -3.728  -1.061   0.711  1.00  0.00           C  
HETATM   12  N3  UNL     1      -4.004  -1.189  -0.716  1.00  0.00           N  
HETATM   13  C9  UNL     1      -5.432  -0.986  -0.904  1.00  0.00           C  
HETATM   14  C10 UNL     1      -3.228  -0.216  -1.458  1.00  0.00           C  
HETATM   15  C11 UNL     1      -1.786  -0.698  -1.529  1.00  0.00           C  
HETATM   16  N4  UNL     1      -1.013   1.898   0.341  1.00  0.00           N  
HETATM   17  C12 UNL     1      -0.016   2.800   0.344  1.00  0.00           C  
HETATM   18  C13 UNL     1      -0.029   4.146   0.694  1.00  0.00           C  
HETATM   19  C14 UNL     1       1.174   4.811   0.589  1.00  0.00           C  
HETATM   20  C15 UNL     1       2.342   4.210   0.166  1.00  0.00           C  
HETATM   21  O2  UNL     1       3.528   4.906   0.073  1.00  0.00           O  
HETATM   22  C16 UNL     1       2.314   2.870  -0.173  1.00  0.00           C  
HETATM   23  C17 UNL     1       1.127   2.157  -0.084  1.00  0.00           C  
HETATM   24  H1  UNL     1       5.911  -3.571   0.538  1.00  0.00           H  
HETATM   25  H2  UNL     1       5.271  -3.013  -1.032  1.00  0.00           H  
HETATM   26  H3  UNL     1       4.465  -4.413  -0.158  1.00  0.00           H  
HETATM   27  H4  UNL     1       3.381  -3.024   1.395  1.00  0.00           H  
HETATM   28  H5  UNL     1       4.689  -1.820   1.347  1.00  0.00           H  
HETATM   29  H6  UNL     1       3.048  -0.045   0.867  1.00  0.00           H  
HETATM   30  H7  UNL     1       1.755  -1.252   1.042  1.00  0.00           H  
HETATM   31  H8  UNL     1       2.524   0.334  -1.488  1.00  0.00           H  
HETATM   32  H9  UNL     1       1.266  -0.911  -1.422  1.00  0.00           H  
HETATM   33  H10 UNL     1      -0.471  -2.129   0.902  1.00  0.00           H  
HETATM   34  H11 UNL     1      -1.033  -0.698   1.835  1.00  0.00           H  
HETATM   35  H12 UNL     1      -2.702  -2.918   0.635  1.00  0.00           H  
HETATM   36  H13 UNL     1      -2.716  -2.138   2.240  1.00  0.00           H  
HETATM   37  H14 UNL     1      -3.556  -0.000   1.005  1.00  0.00           H  
HETATM   38  H15 UNL     1      -4.656  -1.414   1.250  1.00  0.00           H  
HETATM   39  H16 UNL     1      -5.680   0.073  -1.099  1.00  0.00           H  
HETATM   40  H17 UNL     1      -5.991  -1.287   0.014  1.00  0.00           H  
HETATM   41  H18 UNL     1      -5.768  -1.602  -1.764  1.00  0.00           H  
HETATM   42  H19 UNL     1      -3.623  -0.128  -2.492  1.00  0.00           H  
HETATM   43  H20 UNL     1      -3.304   0.774  -0.976  1.00  0.00           H  
HETATM   44  H21 UNL     1      -1.823  -1.783  -1.745  1.00  0.00           H  
HETATM   45  H22 UNL     1      -1.262  -0.121  -2.320  1.00  0.00           H  
HETATM   46  H23 UNL     1      -0.929   4.647   1.029  1.00  0.00           H  
HETATM   47  H24 UNL     1       1.187   5.871   0.858  1.00  0.00           H  
HETATM   48  H25 UNL     1       3.724   5.358  -0.819  1.00  0.00           H  
HETATM   49  H26 UNL     1       3.189   2.335  -0.511  1.00  0.00           H  
CONECT    1    2   24   25   26
CONECT    2    3   27   28
CONECT    3    4
CONECT    4    5   29   30
CONECT    5    6   31   32
CONECT    6    7   23
CONECT    7    8   16   16
CONECT    8    9   15
CONECT    9   10   33   34
CONECT   10   11   35   36
CONECT   11   12   37   38
CONECT   12   13   14
CONECT   13   39   40   41
CONECT   14   15   42   43
CONECT   15   44   45
CONECT   16   17
CONECT   17   18   18   23
CONECT   18   19   46
CONECT   19   20   20   47
CONECT   20   21   22
CONECT   21   48
CONECT   22   23   23   49
END

HMDB0060785
     RDKit          3D
6-Hydroxyemedastine
 49 51  0  0  0  0  0  0  0  0999 V2000
    4.9742   -3.4200   -0.0434 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0445   -2.4775    0.6944 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3448   -1.7410   -0.2282 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4605   -0.8417    0.3211 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7598   -0.1008   -0.8096 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8124    0.8640   -0.3440 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4873    0.7113   -0.0850 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2041   -0.4945   -0.2311 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2411   -1.3295    0.9372 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6094   -1.9423    1.1559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7283   -1.0612    0.7113 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0036   -1.1889   -0.7160 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4322   -0.9862   -0.9044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2276   -0.2162   -1.4582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7858   -0.6979   -1.5285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0125    1.8976    0.3408 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0164    2.7996    0.3444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0294    4.1464    0.6939 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1743    4.8113    0.5887 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3418    4.2099    0.1660 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5277    4.9056    0.0727 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3142    2.8699   -0.1725 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1273    2.1571   -0.0835 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9110   -3.5709    0.5385 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2709   -3.0133   -1.0317 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4652   -4.4125   -0.1578 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3810   -3.0243    1.3951 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6888   -1.8197    1.3470 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0482   -0.0453    0.8668 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7552   -1.2517    1.0417 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5244    0.3341   -1.4881 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2661   -0.9107   -1.4224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4715   -2.1288    0.9022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0325   -0.6979    1.8346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7019   -2.9180    0.6355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7159   -2.1377    2.2403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5565   -0.0002    1.0054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6555   -1.4145    1.2496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6802    0.0726   -1.0985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9908   -1.2869    0.0141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7682   -1.6016   -1.7641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6229   -0.1281   -2.4923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3040    0.7743   -0.9762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8230   -1.7830   -1.7451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2621   -0.1214   -2.3203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9287    4.6469    1.0292 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1867    5.8708    0.8585 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7235    5.3579   -0.8190 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1886    2.3350   -0.5109 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  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
  7 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 20 22  1  0
 22 23  2  0
 23  6  1  0
 15  8  1  0
 23 17  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  9 33  1  0
  9 34  1  0
 10 35  1  0
 10 36  1  0
 11 37  1  0
 11 38  1  0
 13 39  1  0
 13 40  1  0
 13 41  1  0
 14 42  1  0
 14 43  1  0
 15 44  1  0
 15 45  1  0
 18 46  1  0
 19 47  1  0
 21 48  1  0
 22 49  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₁₇H₂₆N₄O₂

Average Molecular Weight

318.4139

Monoisotopic Molecular Weight

318.205576096

IUPAC Name

1-(2-ethoxyethyl)-2-(4-methyl-1,4-diazepan-1-yl)-1H-1,3-benzodiazol-6-ol

Traditional Name

3-(2-ethoxyethyl)-2-(4-methyl-1,4-diazepan-1-yl)-1,3-benzodiazol-5-ol

CAS Registry Number

Not Available

SMILES

CCOCCN1C(=NC2=C1C=C(O)C=C2)N1CCCN(C)CC1

InChI Identifier

InChI=1S/C17H26N4O2/c1-3-23-12-11-21-16-13-14(22)5-6-15(16)18-17(21)20-8-4-7-19(2)9-10-20/h5-6,13,22H,3-4,7-12H2,1-2H3

InChI Key

YDYQGSLFCJVMNN-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzimidazoles. These are organic compounds containing a benzene ring fused to an imidazole ring (five member ring containing a nitrogen atom, 4 carbon atoms, and two double bonds).

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzimidazoles

Sub Class

Not Available

Direct Parent

Benzimidazoles

Alternative Parents

Substituents

Benzimidazole
Dialkylarylamine
1,4-diazepane
1-hydroxy-2-unsubstituted benzenoid
Diazepane
Aminoimidazole
Benzenoid
N-substituted imidazole
Azole
Heteroaromatic compound
Imidazole
Tertiary aliphatic amine
Tertiary amine
Dialkyl ether
Azacycle
Ether
Amine
Organic nitrogen compound
Hydrocarbon derivative
Organopnictogen compound
Organic oxygen compound
Organooxygen compound
Organonitrogen 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 (HMDB: HMDB0060785)

Organ

Kidney (HMDB: HMDB0060785)
Liver (HMDB: HMDB0060785)

Excreta

Biofluid or Excreta

Urine (HMDB: HMDB0060785)

Cellular substructure

Cytoplasm (HMDB: HMDB0060785)

Source

Endogenous

Endogenous (HMDB: HMDB0060785)

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
Water Solubility	2.29 g/L	ALOGPS
logP	2.39	ALOGPS
logP	1.86	ChemAxon
logS	-2.1	ALOGPS
pKa (Strongest Acidic)	9.44	ChemAxon
pKa (Strongest Basic)	8.6	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	53.76 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	92.46 m³·mol⁻¹	ChemAxon
Polarizability	36.16 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
DarkChem	[M+H]+	174.137	31661259
DarkChem	[M-H]-	175.057	31661259
DeepCCS	[M+H]+	176.321	30932474
DeepCCS	[M-H]-	173.963	30932474
DeepCCS	[M-2H]-	206.849	30932474
DeepCCS	[M+Na]+	182.415	30932474
AllCCS	[M+H]+	175.5	32859911
AllCCS	[M+H-H2O]+	172.4	32859911
AllCCS	[M+NH4]+	178.3	32859911
AllCCS	[M+Na]+	179.1	32859911
AllCCS	[M-H]-	178.4	32859911
AllCCS	[M+Na-2H]-	178.5	32859911
AllCCS	[M+HCOO]-	178.7	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
6-Hydroxyemedastine	CCOCCN1C(=NC2=C1C=C(O)C=C2)N1CCCN(C)CC1	3677.0	Standard polar	33892256
6-Hydroxyemedastine	CCOCCN1C(=NC2=C1C=C(O)C=C2)N1CCCN(C)CC1	2599.0	Standard non polar	33892256
6-Hydroxyemedastine	CCOCCN1C(=NC2=C1C=C(O)C=C2)N1CCCN(C)CC1	2766.5	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
6-Hydroxyemedastine,1TMS,isomer #1	CCOCCN1C(N2CCCN(C)CC2)=NC2=CC=C(O[Si](C)(C)C)C=C21	2665.0	Semi standard non polar	33892256
6-Hydroxyemedastine,1TBDMS,isomer #1	CCOCCN1C(N2CCCN(C)CC2)=NC2=CC=C(O[Si](C)(C)C(C)(C)C)C=C21	2858.9	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 - 6-Hydroxyemedastine GC-MS (Non-derivatized) - 70eV, Positive	splash10-0adi-6490000000-00f107ce84743f5b094c	2017-09-20	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Hydroxyemedastine GC-MS (1 TMS) - 70eV, Positive	splash10-00or-6309000000-7f9bcdbdd8dc48b99391	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Hydroxyemedastine 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 - 6-Hydroxyemedastine 10V, Positive-QTOF	splash10-014i-0029000000-712b48aa878c5924d96c	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxyemedastine 20V, Positive-QTOF	splash10-00xs-1093000000-ddd5f98e4d4c4ba1ee3c	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxyemedastine 40V, Positive-QTOF	splash10-05ai-9260000000-c53b0783030474713f13	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxyemedastine 10V, Negative-QTOF	splash10-014i-0039000000-6a63d634202dc093770d	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxyemedastine 20V, Negative-QTOF	splash10-00kb-1093000000-4d898d9f2064c4ec3996	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxyemedastine 40V, Negative-QTOF	splash10-0101-2590000000-900be4be1f4159d15c88	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxyemedastine 10V, Positive-QTOF	splash10-014i-0009000000-0cb8fa1317b9e645f171	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxyemedastine 20V, Positive-QTOF	splash10-014i-0059000000-4207c3259cd8ac3a1104	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxyemedastine 40V, Positive-QTOF	splash10-03di-1930000000-7e4f66014feb9340bcbc	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxyemedastine 10V, Negative-QTOF	splash10-014i-0029000000-b867ed4329eea230dd26	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxyemedastine 20V, Negative-QTOF	splash10-0cdj-0392000000-c51a9d4e950ecf7daec5	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Hydroxyemedastine 40V, Negative-QTOF	splash10-0571-0980000000-2a540f2f3463298a950e	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm

Biospecimen Locations

Blood
Urine

Tissue Locations

Kidney
Liver

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Expected but not Quantified	Not Quantified	Not Available	Not Available	Normal	Not Available	details
Urine	Expected but not Quantified	Not Quantified	Not Available	Not Available	Normal	Not Available	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14356145

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

Not Available

Showing metabocard for 6-Hydroxyemedastine (HMDB0060785)

MOL for HMDB0060785 (6-Hydroxyemedastine)

3D MOL for HMDB0060785 (6-Hydroxyemedastine)

3D SDF for HMDB0060785 (6-Hydroxyemedastine)

3D-SDF for HMDB0060785 (6-Hydroxyemedastine)

PDB for HMDB0060785 (6-Hydroxyemedastine)

3D PDB for HMDB0060785 (6-Hydroxyemedastine)

SMILES for HMDB0060785 (6-Hydroxyemedastine)

INCHI for HMDB0060785 (6-Hydroxyemedastine)

Structure for HMDB0060785 (6-Hydroxyemedastine)

3D Structure for HMDB0060785 (6-Hydroxyemedastine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra