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

2018-06-07 00:54:40 UTC

Update Date

2022-03-07 03:18:15 UTC

HMDB ID

HMDB0240284

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Hydroxystilbamidine

Description

Hydroxystilbamidine belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids. Hydroxystilbamidine is considered to be a practically insoluble (in water) and relatively neutral molecule.

Structure

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

HMDB0240284
     RDKit          3D
Hydroxystilbamidine
 37 38  0  0  0  0  0  0  0  0999 V2000
    6.5884   -1.7811    0.5629 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1271   -0.6327    0.2573 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1070    0.3867   -0.0263 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7137   -0.3300    0.1881 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7900   -1.2968    0.4570 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4150   -1.0149    0.3931 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9447    0.2175    0.0648 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5267    0.5489   -0.0121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4066   -0.3270    0.2324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8353   -0.1113    0.1868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6828   -1.1598    0.4771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0425   -1.0686    0.4645 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6360    0.1398    0.1438 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0969    0.1950    0.1418 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7042    1.2886   -0.1479 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8115   -0.9881    0.4672 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8291    1.1969   -0.1485 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4308    1.0754   -0.1280 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7375    2.2128   -0.4409 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9113    1.1960   -0.2076 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2573    0.9452   -0.1518 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0902   -2.6378    0.7984 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0470    1.2390    0.5504 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8273    0.2527   -0.7750 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1216   -2.2841    0.7205 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7676   -1.8286    0.6183 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2596    1.5836   -0.2888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0570   -1.3439    0.5037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2695   -2.1476    0.7399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6480   -1.9430    0.7057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2542    2.1630   -0.3877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9175   -1.2868    1.4467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2251   -1.5472   -0.2937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2860    2.1436   -0.3998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1797    3.0730   -0.6691 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5478    2.1731   -0.4680 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0080    1.6984   -0.3616 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  3
 14 16  1  0
 13 17  1  0
 17 18  2  0
 18 19  1  0
  7 20  1  0
 20 21  2  0
 21  4  1  0
 18 10  1  0
  1 22  1  0
  3 23  1  0
  3 24  1  0
  5 25  1  0
  6 26  1  0
  8 27  1  0
  9 28  1  0
 11 29  1  0
 12 30  1  0
 15 31  1  0
 16 32  1  0
 16 33  1  0
 17 34  1  0
 19 35  1  0
 20 36  1  0
 21 37  1  0
M  END


  Mrv1652306071803302D          

 21 22  0  0  0  0            999 V2000
    3.3001   -2.8601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7086   -2.1450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3001   -1.4301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4751   -1.4301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0586   -2.1450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4751   -2.8601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0586   -3.5751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4751   -4.2822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0586   -4.9973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2336   -4.9973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -5.7123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2336   -6.4273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0586   -6.4273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4751   -5.7123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3001   -5.7123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -7.1423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -7.1423    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2336   -7.8573    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7086   -0.7150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5337   -0.7150    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3001    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  2  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3 19  1  0  0  0  0
  4  5  2  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  1  0  0  0  0
  9 14  2  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 16  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0240284

> <DATABASE_NAME>
hmdb

> <SMILES>
NC(=N)C1=CC=C(\C=C\C2=C(O)C=C(C=C2)C(N)=N)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C16H16N4O/c17-15(18)12-5-2-10(3-6-12)1-4-11-7-8-13(16(19)20)9-14(11)21/h1-9,21H,(H3,17,18)(H3,19,20)/b4-1+

> <INCHI_KEY>
TUESWZZJYCLFNL-DAFODLJHSA-N

> <FORMULA>
C16H16N4O

> <MOLECULAR_WEIGHT>
280.331

> <EXACT_MASS>
280.132411151

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
30.998220709651267

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-[(E)-2-(4-carbamimidoylphenyl)ethenyl]-3-hydroxybenzene-1-carboximidamide

> <ALOGPS_LOGP>
1.44

> <JCHEM_LOGP>
1.243840055523608

> <ALOGPS_LOGS>
-3.64

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.21761460388819

> <JCHEM_PKA_STRONGEST_BASIC>
12.136800456905494

> <JCHEM_POLAR_SURFACE_AREA>
119.96999999999998

> <JCHEM_REFRACTIVITY>
106.8387

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.44e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
hydroxystilbamidine

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0240284
     RDKit          3D
Hydroxystilbamidine
 37 38  0  0  0  0  0  0  0  0999 V2000
    6.5884   -1.7811    0.5629 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1271   -0.6327    0.2573 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1070    0.3867   -0.0263 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7137   -0.3300    0.1881 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7900   -1.2968    0.4570 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4150   -1.0149    0.3931 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9447    0.2175    0.0648 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5267    0.5489   -0.0121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4066   -0.3270    0.2324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8353   -0.1113    0.1868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6828   -1.1598    0.4771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0425   -1.0686    0.4645 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6360    0.1398    0.1438 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0969    0.1950    0.1418 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7042    1.2886   -0.1479 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8115   -0.9881    0.4672 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8291    1.1969   -0.1485 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4308    1.0754   -0.1280 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7375    2.2128   -0.4409 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9113    1.1960   -0.2076 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2573    0.9452   -0.1518 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0902   -2.6378    0.7984 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0470    1.2390    0.5504 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8273    0.2527   -0.7750 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1216   -2.2841    0.7205 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7676   -1.8286    0.6183 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2596    1.5836   -0.2888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0570   -1.3439    0.5037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2695   -2.1476    0.7399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6480   -1.9430    0.7057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2542    2.1630   -0.3877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9175   -1.2868    1.4467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2251   -1.5472   -0.2937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2860    2.1436   -0.3998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1797    3.0730   -0.6691 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5478    2.1731   -0.4680 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0080    1.6984   -0.3616 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  3
 14 16  1  0
 13 17  1  0
 17 18  2  0
 18 19  1  0
  7 20  1  0
 20 21  2  0
 21  4  1  0
 18 10  1  0
  1 22  1  0
  3 23  1  0
  3 24  1  0
  5 25  1  0
  6 26  1  0
  8 27  1  0
  9 28  1  0
 11 29  1  0
 12 30  1  0
 15 31  1  0
 16 32  1  0
 16 33  1  0
 17 34  1  0
 19 35  1  0
 20 36  1  0
 21 37  1  0
M  END

HEADER    PROTEIN                                 07-JUN-18   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-JUN-18         0                                  
HETATM    1  C   UNK     0       6.160  -5.339   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.923  -4.004   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.160  -2.669   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.620  -2.669   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.843  -4.004   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.620  -5.339   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.843  -6.673   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.620  -7.994   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.843  -9.328   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.303  -9.328   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.540 -10.663   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.303 -11.998   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.843 -11.998   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.620 -10.663   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       6.160 -10.663   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       1.540 -13.332   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       0.000 -13.332   0.000  0.00  0.00           N+0
HETATM   18  N   UNK     0       2.303 -14.667   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0       6.923  -1.335   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       8.463  -1.335   0.000  0.00  0.00           N+0
HETATM   21  N   UNK     0       6.160   0.000   0.000  0.00  0.00           N+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   19                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    1    5    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   16                                                  
CONECT   13   12   14                                                       
CONECT   14    9   13   15                                                  
CONECT   15   14                                                            
CONECT   16   12   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19    3   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   44    0
END

COMPND    HMDB0240284
HETATM    1  N1  UNL     1       6.588  -1.781   0.563  1.00  0.00           N  
HETATM    2  C1  UNL     1       6.127  -0.633   0.257  1.00  0.00           C  
HETATM    3  N2  UNL     1       7.107   0.387  -0.026  1.00  0.00           N  
HETATM    4  C2  UNL     1       4.714  -0.330   0.188  1.00  0.00           C  
HETATM    5  C3  UNL     1       3.790  -1.297   0.457  1.00  0.00           C  
HETATM    6  C4  UNL     1       2.415  -1.015   0.393  1.00  0.00           C  
HETATM    7  C5  UNL     1       1.945   0.217   0.065  1.00  0.00           C  
HETATM    8  C6  UNL     1       0.527   0.549  -0.012  1.00  0.00           C  
HETATM    9  C7  UNL     1      -0.407  -0.327   0.232  1.00  0.00           C  
HETATM   10  C8  UNL     1      -1.835  -0.111   0.187  1.00  0.00           C  
HETATM   11  C9  UNL     1      -2.683  -1.160   0.477  1.00  0.00           C  
HETATM   12  C10 UNL     1      -4.043  -1.069   0.465  1.00  0.00           C  
HETATM   13  C11 UNL     1      -4.636   0.140   0.144  1.00  0.00           C  
HETATM   14  C12 UNL     1      -6.097   0.195   0.142  1.00  0.00           C  
HETATM   15  N3  UNL     1      -6.704   1.289  -0.148  1.00  0.00           N  
HETATM   16  N4  UNL     1      -6.812  -0.988   0.467  1.00  0.00           N  
HETATM   17  C13 UNL     1      -3.829   1.197  -0.148  1.00  0.00           C  
HETATM   18  C14 UNL     1      -2.431   1.075  -0.128  1.00  0.00           C  
HETATM   19  O1  UNL     1      -1.737   2.213  -0.441  1.00  0.00           O  
HETATM   20  C15 UNL     1       2.911   1.196  -0.208  1.00  0.00           C  
HETATM   21  C16 UNL     1       4.257   0.945  -0.152  1.00  0.00           C  
HETATM   22  H1  UNL     1       6.090  -2.638   0.798  1.00  0.00           H  
HETATM   23  H2  UNL     1       7.047   1.239   0.550  1.00  0.00           H  
HETATM   24  H3  UNL     1       7.827   0.253  -0.775  1.00  0.00           H  
HETATM   25  H4  UNL     1       4.122  -2.284   0.720  1.00  0.00           H  
HETATM   26  H5  UNL     1       1.768  -1.829   0.618  1.00  0.00           H  
HETATM   27  H6  UNL     1       0.260   1.584  -0.289  1.00  0.00           H  
HETATM   28  H7  UNL     1      -0.057  -1.344   0.504  1.00  0.00           H  
HETATM   29  H8  UNL     1      -2.270  -2.148   0.740  1.00  0.00           H  
HETATM   30  H9  UNL     1      -4.648  -1.943   0.706  1.00  0.00           H  
HETATM   31  H10 UNL     1      -6.254   2.163  -0.388  1.00  0.00           H  
HETATM   32  H11 UNL     1      -6.918  -1.287   1.447  1.00  0.00           H  
HETATM   33  H12 UNL     1      -7.225  -1.547  -0.294  1.00  0.00           H  
HETATM   34  H13 UNL     1      -4.286   2.144  -0.400  1.00  0.00           H  
HETATM   35  H14 UNL     1      -2.180   3.073  -0.669  1.00  0.00           H  
HETATM   36  H15 UNL     1       2.548   2.173  -0.468  1.00  0.00           H  
HETATM   37  H16 UNL     1       5.008   1.698  -0.362  1.00  0.00           H  
CONECT    1    2    2   22
CONECT    2    3    4
CONECT    3   23   24
CONECT    4    5    5   21
CONECT    5    6   25
CONECT    6    7    7   26
CONECT    7    8   20
CONECT    8    9    9   27
CONECT    9   10   28
CONECT   10   11   11   18
CONECT   11   12   29
CONECT   12   13   13   30
CONECT   13   14   17
CONECT   14   15   15   16
CONECT   15   31
CONECT   16   32   33
CONECT   17   18   18   34
CONECT   18   19
CONECT   19   35
CONECT   20   21   21   36
CONECT   21   37
END

HMDB0240284
     RDKit          3D
Hydroxystilbamidine
 37 38  0  0  0  0  0  0  0  0999 V2000
    6.5884   -1.7811    0.5629 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1271   -0.6327    0.2573 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1070    0.3867   -0.0263 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7137   -0.3300    0.1881 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7900   -1.2968    0.4570 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4150   -1.0149    0.3931 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9447    0.2175    0.0648 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5267    0.5489   -0.0121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4066   -0.3270    0.2324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8353   -0.1113    0.1868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6828   -1.1598    0.4771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0425   -1.0686    0.4645 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6360    0.1398    0.1438 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0969    0.1950    0.1418 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7042    1.2886   -0.1479 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8115   -0.9881    0.4672 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8291    1.1969   -0.1485 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4308    1.0754   -0.1280 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7375    2.2128   -0.4409 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9113    1.1960   -0.2076 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2573    0.9452   -0.1518 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0902   -2.6378    0.7984 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0470    1.2390    0.5504 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8273    0.2527   -0.7750 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1216   -2.2841    0.7205 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7676   -1.8286    0.6183 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2596    1.5836   -0.2888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0570   -1.3439    0.5037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2695   -2.1476    0.7399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6480   -1.9430    0.7057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2542    2.1630   -0.3877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9175   -1.2868    1.4467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2251   -1.5472   -0.2937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2860    2.1436   -0.3998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1797    3.0730   -0.6691 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5478    2.1731   -0.4680 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0080    1.6984   -0.3616 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  3
 14 16  1  0
 13 17  1  0
 17 18  2  0
 18 19  1  0
  7 20  1  0
 20 21  2  0
 21  4  1  0
 18 10  1  0
  1 22  1  0
  3 23  1  0
  3 24  1  0
  5 25  1  0
  6 26  1  0
  8 27  1  0
  9 28  1  0
 11 29  1  0
 12 30  1  0
 15 31  1  0
 16 32  1  0
 16 33  1  0
 17 34  1  0
 19 35  1  0
 20 36  1  0
 21 37  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
Hydroxystilbamidine hydrochloride	HMDB

Chemical Formula

C₁₆H₁₆N₄O

Average Molecular Weight

280.331

Monoisotopic Molecular Weight

280.132411151

IUPAC Name

4-[(E)-2-(4-carbamimidoylphenyl)ethenyl]-3-hydroxybenzene-1-carboximidamide

Traditional Name

hydroxystilbamidine

CAS Registry Number

Not Available

SMILES

NC(=N)C1=CC=C(\C=C\C2=C(O)C=C(C=C2)C(N)=N)C=C1

InChI Identifier

InChI=1S/C16H16N4O/c17-15(18)12-5-2-10(3-6-12)1-4-11-7-8-13(16(19)20)9-14(11)21/h1-9,21H,(H3,17,18)(H3,19,20)/b4-1+

InChI Key

TUESWZZJYCLFNL-DAFODLJHSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Stilbenes

Sub Class

Not Available

Direct Parent

Stilbenes

Alternative Parents

Substituents

Stilbene
Styrene
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Amidine
Carboxylic acid amidine
Carboximidamide
Organic nitrogen compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Exogenous (HMDB: HMDB0240284)

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	1.44	ALOGPS
logP	1.24	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	8.22	ChemAxon
pKa (Strongest Basic)	12.14	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	119.97 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	106.84 m³·mol⁻¹	ChemAxon
Polarizability	31 Å³	ChemAxon
Number of Rings	2	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
AllCCS	[M+H]+	167.363	31661259
AllCCS	[M-H]-	168.109	31661259
DeepCCS	[M+H]+	171.797	30932474
DeepCCS	[M-H]-	169.439	30932474
DeepCCS	[M-2H]-	203.513	30932474
DeepCCS	[M+Na]+	178.882	30932474
AllCCS	[M+H]+	167.4	32859911
AllCCS	[M+H-H2O]+	163.7	32859911
AllCCS	[M+NH4]+	170.8	32859911
AllCCS	[M+Na]+	171.8	32859911
AllCCS	[M-H]-	168.1	32859911
AllCCS	[M+Na-2H]-	168.0	32859911
AllCCS	[M+HCOO]-	167.9	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Hydroxystilbamidine	NC(=N)C1=CC=C(\C=C\C2=C(O)C=C(C=C2)C(N)=N)C=C1	4785.2	Standard polar	33892256
Hydroxystilbamidine	NC(=N)C1=CC=C(\C=C\C2=C(O)C=C(C=C2)C(N)=N)C=C1	3011.1	Standard non polar	33892256
Hydroxystilbamidine	NC(=N)C1=CC=C(\C=C\C2=C(O)C=C(C=C2)C(N)=N)C=C1	3613.3	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Hydroxystilbamidine,1TMS,isomer #1	C[Si](C)(C)OC1=CC(C(=N)N)=CC=C1/C=C/C1=CC=C(C(=N)N)C=C1	3409.7	Semi standard non polar	33892256
Hydroxystilbamidine,1TMS,isomer #2	C[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O)C=C1	3473.1	Semi standard non polar	33892256
Hydroxystilbamidine,1TMS,isomer #3	C[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O)=C1	3479.7	Semi standard non polar	33892256
Hydroxystilbamidine,1TMS,isomer #4	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O)C=C1	3464.5	Semi standard non polar	33892256
Hydroxystilbamidine,1TMS,isomer #5	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O)=C1	3455.4	Semi standard non polar	33892256
Hydroxystilbamidine,2TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O[Si](C)(C)C)=C1	3531.4	Semi standard non polar	33892256
Hydroxystilbamidine,2TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O[Si](C)(C)C)=C1	3186.1	Standard non polar	33892256
Hydroxystilbamidine,2TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O[Si](C)(C)C)=C1	4634.8	Standard polar	33892256
Hydroxystilbamidine,2TMS,isomer #10	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O)=C1	3424.5	Semi standard non polar	33892256
Hydroxystilbamidine,2TMS,isomer #10	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O)=C1	3277.1	Standard non polar	33892256
Hydroxystilbamidine,2TMS,isomer #10	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O)=C1	4768.8	Standard polar	33892256
Hydroxystilbamidine,2TMS,isomer #11	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2O)C=C1	3544.0	Semi standard non polar	33892256
Hydroxystilbamidine,2TMS,isomer #11	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2O)C=C1	3314.5	Standard non polar	33892256
Hydroxystilbamidine,2TMS,isomer #11	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2O)C=C1	4861.2	Standard polar	33892256
Hydroxystilbamidine,2TMS,isomer #12	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(N)=N[Si](C)(C)C)C=C2O)C=C1	3445.0	Semi standard non polar	33892256
Hydroxystilbamidine,2TMS,isomer #12	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(N)=N[Si](C)(C)C)C=C2O)C=C1	3212.3	Standard non polar	33892256
Hydroxystilbamidine,2TMS,isomer #12	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(N)=N[Si](C)(C)C)C=C2O)C=C1	5000.5	Standard polar	33892256
Hydroxystilbamidine,2TMS,isomer #2	C[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O[Si](C)(C)C)C=C1	3529.1	Semi standard non polar	33892256
Hydroxystilbamidine,2TMS,isomer #2	C[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O[Si](C)(C)C)C=C1	3161.8	Standard non polar	33892256
Hydroxystilbamidine,2TMS,isomer #2	C[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O[Si](C)(C)C)C=C1	4638.4	Standard polar	33892256
Hydroxystilbamidine,2TMS,isomer #3	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O[Si](C)(C)C)=C1	3448.1	Semi standard non polar	33892256
Hydroxystilbamidine,2TMS,isomer #3	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O[Si](C)(C)C)=C1	3120.3	Standard non polar	33892256
Hydroxystilbamidine,2TMS,isomer #3	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O[Si](C)(C)C)=C1	4847.7	Standard polar	33892256
Hydroxystilbamidine,2TMS,isomer #4	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O[Si](C)(C)C)C=C1	3446.4	Semi standard non polar	33892256
Hydroxystilbamidine,2TMS,isomer #4	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O[Si](C)(C)C)C=C1	3118.4	Standard non polar	33892256
Hydroxystilbamidine,2TMS,isomer #4	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O[Si](C)(C)C)C=C1	4849.5	Standard polar	33892256
Hydroxystilbamidine,2TMS,isomer #5	C[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2O)C=C1	3571.6	Semi standard non polar	33892256
Hydroxystilbamidine,2TMS,isomer #5	C[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2O)C=C1	3363.2	Standard non polar	33892256
Hydroxystilbamidine,2TMS,isomer #5	C[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2O)C=C1	4708.2	Standard polar	33892256
Hydroxystilbamidine,2TMS,isomer #6	C[Si](C)(C)N(C(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O)C=C1)[Si](C)(C)C	3563.8	Semi standard non polar	33892256
Hydroxystilbamidine,2TMS,isomer #6	C[Si](C)(C)N(C(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O)C=C1)[Si](C)(C)C	3238.9	Standard non polar	33892256
Hydroxystilbamidine,2TMS,isomer #6	C[Si](C)(C)N(C(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O)C=C1)[Si](C)(C)C	4956.4	Standard polar	33892256
Hydroxystilbamidine,2TMS,isomer #7	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O)C=C1	3425.1	Semi standard non polar	33892256
Hydroxystilbamidine,2TMS,isomer #7	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O)C=C1	3278.1	Standard non polar	33892256
Hydroxystilbamidine,2TMS,isomer #7	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O)C=C1	4768.0	Standard polar	33892256
Hydroxystilbamidine,2TMS,isomer #8	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C(O)=C1	3532.1	Semi standard non polar	33892256
Hydroxystilbamidine,2TMS,isomer #8	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C(O)=C1	3299.1	Standard non polar	33892256
Hydroxystilbamidine,2TMS,isomer #8	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C(O)=C1	4863.9	Standard polar	33892256
Hydroxystilbamidine,2TMS,isomer #9	C[Si](C)(C)N(C(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O)=C1)[Si](C)(C)C	3576.8	Semi standard non polar	33892256
Hydroxystilbamidine,2TMS,isomer #9	C[Si](C)(C)N(C(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O)=C1)[Si](C)(C)C	3250.0	Standard non polar	33892256
Hydroxystilbamidine,2TMS,isomer #9	C[Si](C)(C)N(C(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O)=C1)[Si](C)(C)C	4949.5	Standard polar	33892256
Hydroxystilbamidine,3TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	3569.0	Semi standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	3312.9	Standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	4245.6	Standard polar	33892256
Hydroxystilbamidine,3TMS,isomer #10	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2O)C=C1	3468.4	Semi standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #10	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2O)C=C1	3448.1	Standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #10	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2O)C=C1	4359.4	Standard polar	33892256
Hydroxystilbamidine,3TMS,isomer #11	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C(O)=C1	3474.1	Semi standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #11	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C(O)=C1	3439.3	Standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #11	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C(O)=C1	4362.2	Standard polar	33892256
Hydroxystilbamidine,3TMS,isomer #12	C[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O)C=C1	3598.0	Semi standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #12	C[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O)C=C1	3409.5	Standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #12	C[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O)C=C1	4476.0	Standard polar	33892256
Hydroxystilbamidine,3TMS,isomer #13	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3472.7	Semi standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #13	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3309.7	Standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #13	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O)C=C1)N([Si](C)(C)C)[Si](C)(C)C	4426.4	Standard polar	33892256
Hydroxystilbamidine,3TMS,isomer #14	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O)=C1	3523.5	Semi standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #14	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O)=C1	3363.6	Standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #14	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O)=C1	4717.4	Standard polar	33892256
Hydroxystilbamidine,3TMS,isomer #15	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2)C(O)=C1	3385.3	Semi standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #15	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2)C(O)=C1	3387.3	Standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #15	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2)C(O)=C1	4595.6	Standard polar	33892256
Hydroxystilbamidine,3TMS,isomer #16	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O)=C1)N([Si](C)(C)C)[Si](C)(C)C	3464.4	Semi standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #16	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O)=C1)N([Si](C)(C)C)[Si](C)(C)C	3306.6	Standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #16	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O)=C1)N([Si](C)(C)C)[Si](C)(C)C	4434.3	Standard polar	33892256
Hydroxystilbamidine,3TMS,isomer #17	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O)C=C1	3530.6	Semi standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #17	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O)C=C1	3375.1	Standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #17	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O)C=C1	4714.9	Standard polar	33892256
Hydroxystilbamidine,3TMS,isomer #18	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2O)C=C1	3397.6	Semi standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #18	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2O)C=C1	3391.2	Standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #18	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2O)C=C1	4597.9	Standard polar	33892256
Hydroxystilbamidine,3TMS,isomer #2	C[Si](C)(C)OC1=CC(C(=N)N([Si](C)(C)C)[Si](C)(C)C)=CC=C1/C=C/C1=CC=C(C(=N)N)C=C1	3537.3	Semi standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #2	C[Si](C)(C)OC1=CC(C(=N)N([Si](C)(C)C)[Si](C)(C)C)=CC=C1/C=C/C1=CC=C(C(=N)N)C=C1	3243.6	Standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #2	C[Si](C)(C)OC1=CC(C(=N)N([Si](C)(C)C)[Si](C)(C)C)=CC=C1/C=C/C1=CC=C(C(=N)N)C=C1	4453.7	Standard polar	33892256
Hydroxystilbamidine,3TMS,isomer #3	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O[Si](C)(C)C)=C1	3419.2	Semi standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #3	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O[Si](C)(C)C)=C1	3259.7	Standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #3	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O[Si](C)(C)C)=C1	4358.1	Standard polar	33892256
Hydroxystilbamidine,3TMS,isomer #4	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	3495.4	Semi standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #4	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	3293.8	Standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #4	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	4500.1	Standard polar	33892256
Hydroxystilbamidine,3TMS,isomer #5	C[Si](C)(C)OC1=CC(C(=N)N)=CC=C1/C=C/C1=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C1	3536.2	Semi standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #5	C[Si](C)(C)OC1=CC(C(=N)N)=CC=C1/C=C/C1=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C1	3236.0	Standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #5	C[Si](C)(C)OC1=CC(C(=N)N)=CC=C1/C=C/C1=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C1	4455.0	Standard polar	33892256
Hydroxystilbamidine,3TMS,isomer #6	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O[Si](C)(C)C)C=C1	3418.9	Semi standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #6	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O[Si](C)(C)C)C=C1	3244.0	Standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #6	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O[Si](C)(C)C)C=C1	4358.5	Standard polar	33892256
Hydroxystilbamidine,3TMS,isomer #7	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1	3494.3	Semi standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #7	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1	3281.3	Standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #7	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1	4501.7	Standard polar	33892256
Hydroxystilbamidine,3TMS,isomer #8	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(N)=N[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	3423.1	Semi standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #8	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(N)=N[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	3239.3	Standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #8	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(N)=N[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	4759.8	Standard polar	33892256
Hydroxystilbamidine,3TMS,isomer #9	C[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O)=C1	3593.2	Semi standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #9	C[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O)=C1	3409.0	Standard non polar	33892256
Hydroxystilbamidine,3TMS,isomer #9	C[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O)=C1	4474.8	Standard polar	33892256
Hydroxystilbamidine,4TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1	3565.3	Semi standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1	3380.4	Standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1	4122.1	Standard polar	33892256
Hydroxystilbamidine,4TMS,isomer #10	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1	3385.4	Semi standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #10	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1	3369.9	Standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #10	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1	4347.3	Standard polar	33892256
Hydroxystilbamidine,4TMS,isomer #11	C[Si](C)(C)N(C(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O)C=C1)[Si](C)(C)C	3602.6	Semi standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #11	C[Si](C)(C)N(C(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O)C=C1)[Si](C)(C)C	3519.0	Standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #11	C[Si](C)(C)N(C(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O)C=C1)[Si](C)(C)C	4293.2	Standard polar	33892256
Hydroxystilbamidine,4TMS,isomer #12	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O)=C1	3479.4	Semi standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #12	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O)=C1	3500.5	Standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #12	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O)=C1	4203.9	Standard polar	33892256
Hydroxystilbamidine,4TMS,isomer #13	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2O)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3497.6	Semi standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #13	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2O)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3479.9	Standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #13	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2O)C=C1)N([Si](C)(C)C)[Si](C)(C)C	4053.3	Standard polar	33892256
Hydroxystilbamidine,4TMS,isomer #14	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2O)C=C1	3406.5	Semi standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #14	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2O)C=C1	3575.8	Standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #14	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2O)C=C1	4128.9	Standard polar	33892256
Hydroxystilbamidine,4TMS,isomer #15	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O)C=C1	3488.4	Semi standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #15	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O)C=C1	3509.2	Standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #15	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O)C=C1	4205.4	Standard polar	33892256
Hydroxystilbamidine,4TMS,isomer #16	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C(O)=C1)N([Si](C)(C)C)[Si](C)(C)C	3480.6	Semi standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #16	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C(O)=C1)N([Si](C)(C)C)[Si](C)(C)C	3472.1	Standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #16	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C(O)=C1)N([Si](C)(C)C)[Si](C)(C)C	4060.1	Standard polar	33892256
Hydroxystilbamidine,4TMS,isomer #17	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O)=C1	3427.8	Semi standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #17	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O)=C1	3438.9	Standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #17	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O)=C1	4362.9	Standard polar	33892256
Hydroxystilbamidine,4TMS,isomer #18	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2O)C=C1	3434.4	Semi standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #18	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2O)C=C1	3442.1	Standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #18	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2O)C=C1	4370.8	Standard polar	33892256
Hydroxystilbamidine,4TMS,isomer #2	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	3504.4	Semi standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #2	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	3390.0	Standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #2	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	4053.4	Standard polar	33892256
Hydroxystilbamidine,4TMS,isomer #3	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1	3498.2	Semi standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #3	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1	3396.0	Standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #3	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1	4054.2	Standard polar	33892256
Hydroxystilbamidine,4TMS,isomer #4	C[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	3557.5	Semi standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #4	C[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	3380.3	Standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #4	C[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	4124.4	Standard polar	33892256
Hydroxystilbamidine,4TMS,isomer #5	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C	3436.2	Semi standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #5	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C	3308.7	Standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #5	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C	4119.8	Standard polar	33892256
Hydroxystilbamidine,4TMS,isomer #6	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	3491.6	Semi standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #6	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	3356.7	Standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #6	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	4419.4	Standard polar	33892256
Hydroxystilbamidine,4TMS,isomer #7	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	3383.9	Semi standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #7	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	3384.3	Standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #7	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	4348.2	Standard polar	33892256
Hydroxystilbamidine,4TMS,isomer #8	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1	3491.8	Semi standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #8	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1	3353.6	Standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #8	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1	4418.8	Standard polar	33892256
Hydroxystilbamidine,4TMS,isomer #9	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3447.9	Semi standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #9	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3309.6	Standard non polar	33892256
Hydroxystilbamidine,4TMS,isomer #9	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	4115.1	Standard polar	33892256
Hydroxystilbamidine,5TMS,isomer #1	C[Si](C)(C)OC1=CC(C(=N)N([Si](C)(C)C)[Si](C)(C)C)=CC=C1/C=C/C1=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C1	3598.5	Semi standard non polar	33892256
Hydroxystilbamidine,5TMS,isomer #1	C[Si](C)(C)OC1=CC(C(=N)N([Si](C)(C)C)[Si](C)(C)C)=CC=C1/C=C/C1=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C1	3471.5	Standard non polar	33892256
Hydroxystilbamidine,5TMS,isomer #1	C[Si](C)(C)OC1=CC(C(=N)N([Si](C)(C)C)[Si](C)(C)C)=CC=C1/C=C/C1=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C1	4030.7	Standard polar	33892256
Hydroxystilbamidine,5TMS,isomer #10	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O)=C1)N([Si](C)(C)C)[Si](C)(C)C	3512.0	Semi standard non polar	33892256
Hydroxystilbamidine,5TMS,isomer #10	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O)=C1)N([Si](C)(C)C)[Si](C)(C)C	3564.4	Standard non polar	33892256
Hydroxystilbamidine,5TMS,isomer #10	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O)=C1)N([Si](C)(C)C)[Si](C)(C)C	3946.4	Standard polar	33892256
Hydroxystilbamidine,5TMS,isomer #11	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O)=C1	3424.7	Semi standard non polar	33892256
Hydroxystilbamidine,5TMS,isomer #11	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O)=C1	3602.1	Standard non polar	33892256
Hydroxystilbamidine,5TMS,isomer #11	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O)=C1	3879.7	Standard polar	33892256
Hydroxystilbamidine,5TMS,isomer #12	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2O)C=C1	3410.7	Semi standard non polar	33892256
Hydroxystilbamidine,5TMS,isomer #12	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2O)C=C1	3602.1	Standard non polar	33892256
Hydroxystilbamidine,5TMS,isomer #12	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2O)C=C1	3887.5	Standard polar	33892256
Hydroxystilbamidine,5TMS,isomer #2	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1	3511.3	Semi standard non polar	33892256
Hydroxystilbamidine,5TMS,isomer #2	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1	3449.3	Standard non polar	33892256
Hydroxystilbamidine,5TMS,isomer #2	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1	3962.5	Standard polar	33892256
Hydroxystilbamidine,5TMS,isomer #3	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3527.8	Semi standard non polar	33892256
Hydroxystilbamidine,5TMS,isomer #3	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3452.3	Standard non polar	33892256
Hydroxystilbamidine,5TMS,isomer #3	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3813.4	Standard polar	33892256
Hydroxystilbamidine,5TMS,isomer #4	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	3460.2	Semi standard non polar	33892256
Hydroxystilbamidine,5TMS,isomer #4	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	3513.4	Standard non polar	33892256
Hydroxystilbamidine,5TMS,isomer #4	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	3901.5	Standard polar	33892256
Hydroxystilbamidine,5TMS,isomer #5	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	3519.8	Semi standard non polar	33892256
Hydroxystilbamidine,5TMS,isomer #5	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	3437.1	Standard non polar	33892256
Hydroxystilbamidine,5TMS,isomer #5	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	3965.5	Standard polar	33892256
Hydroxystilbamidine,5TMS,isomer #6	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C	3515.3	Semi standard non polar	33892256
Hydroxystilbamidine,5TMS,isomer #6	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C	3452.3	Standard non polar	33892256
Hydroxystilbamidine,5TMS,isomer #6	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C	3817.9	Standard polar	33892256
Hydroxystilbamidine,5TMS,isomer #7	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	3442.5	Semi standard non polar	33892256
Hydroxystilbamidine,5TMS,isomer #7	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	3435.0	Standard non polar	33892256
Hydroxystilbamidine,5TMS,isomer #7	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	4171.6	Standard polar	33892256
Hydroxystilbamidine,5TMS,isomer #8	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1	3438.0	Semi standard non polar	33892256
Hydroxystilbamidine,5TMS,isomer #8	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1	3434.1	Standard non polar	33892256
Hydroxystilbamidine,5TMS,isomer #8	C[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1	4167.4	Standard polar	33892256
Hydroxystilbamidine,5TMS,isomer #9	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3520.0	Semi standard non polar	33892256
Hydroxystilbamidine,5TMS,isomer #9	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3566.6	Standard non polar	33892256
Hydroxystilbamidine,5TMS,isomer #9	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3944.5	Standard polar	33892256
Hydroxystilbamidine,6TMS,isomer #1	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C	3540.4	Semi standard non polar	33892256
Hydroxystilbamidine,6TMS,isomer #1	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C	3506.9	Standard non polar	33892256
Hydroxystilbamidine,6TMS,isomer #1	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C	3736.8	Standard polar	33892256
Hydroxystilbamidine,6TMS,isomer #2	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3542.6	Semi standard non polar	33892256
Hydroxystilbamidine,6TMS,isomer #2	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3497.5	Standard non polar	33892256
Hydroxystilbamidine,6TMS,isomer #2	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3739.3	Standard polar	33892256
Hydroxystilbamidine,6TMS,isomer #3	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1	3467.7	Semi standard non polar	33892256
Hydroxystilbamidine,6TMS,isomer #3	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1	3566.0	Standard non polar	33892256
Hydroxystilbamidine,6TMS,isomer #3	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C(O[Si](C)(C)C)=C1	3710.0	Standard polar	33892256
Hydroxystilbamidine,6TMS,isomer #4	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	3472.4	Semi standard non polar	33892256
Hydroxystilbamidine,6TMS,isomer #4	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	3556.5	Standard non polar	33892256
Hydroxystilbamidine,6TMS,isomer #4	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1	3713.0	Standard polar	33892256
Hydroxystilbamidine,6TMS,isomer #5	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2O)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3448.2	Semi standard non polar	33892256
Hydroxystilbamidine,6TMS,isomer #5	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2O)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3650.9	Standard non polar	33892256
Hydroxystilbamidine,6TMS,isomer #5	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2O)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3676.8	Standard polar	33892256
Hydroxystilbamidine,7TMS,isomer #1	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3488.1	Semi standard non polar	33892256
Hydroxystilbamidine,7TMS,isomer #1	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3612.8	Standard non polar	33892256
Hydroxystilbamidine,7TMS,isomer #1	C[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3511.4	Standard polar	33892256
Hydroxystilbamidine,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC(C(=N)N)=CC=C1/C=C/C1=CC=C(C(=N)N)C=C1	3714.0	Semi standard non polar	33892256
Hydroxystilbamidine,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O)C=C1	3784.3	Semi standard non polar	33892256
Hydroxystilbamidine,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O)=C1	3787.4	Semi standard non polar	33892256
Hydroxystilbamidine,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O)C=C1	3726.9	Semi standard non polar	33892256
Hydroxystilbamidine,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O)=C1	3718.7	Semi standard non polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	4083.8	Semi standard non polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	3604.2	Standard non polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	4543.9	Standard polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O)=C1	3949.0	Semi standard non polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O)=C1	3692.3	Standard non polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O)=C1	4606.0	Standard polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4050.7	Semi standard non polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2O)C=C1	3707.0	Standard non polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4722.2	Standard polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(N)=N[Si](C)(C)C(C)(C)C)C=C2O)C=C1	3942.9	Semi standard non polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(N)=N[Si](C)(C)C(C)(C)C)C=C2O)C=C1	3621.2	Standard non polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(N)=N[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4932.3	Standard polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4092.1	Semi standard non polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O[Si](C)(C)C(C)(C)C)C=C1	3586.9	Standard non polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4547.4	Standard polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	3957.4	Semi standard non polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	3546.8	Standard non polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	4792.5	Standard polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O[Si](C)(C)C(C)(C)C)C=C1	3970.3	Semi standard non polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O[Si](C)(C)C(C)(C)C)C=C1	3545.8	Standard non polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4793.9	Standard polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4113.6	Semi standard non polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2O)C=C1	3740.5	Standard non polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4509.7	Standard polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O)C=C1)[Si](C)(C)C(C)(C)C	4025.5	Semi standard non polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O)C=C1)[Si](C)(C)C(C)(C)C	3620.3	Standard non polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O)C=C1)[Si](C)(C)C(C)(C)C	4715.5	Standard polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O)C=C1	3947.0	Semi standard non polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O)C=C1	3694.6	Standard non polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O)C=C1	4607.6	Standard polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1	4046.6	Semi standard non polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1	3688.8	Standard non polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1	4726.2	Standard polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O)=C1)[Si](C)(C)C(C)(C)C	4034.9	Semi standard non polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O)=C1)[Si](C)(C)C(C)(C)C	3629.3	Standard non polar	33892256
Hydroxystilbamidine,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O)=C1)[Si](C)(C)C(C)(C)C	4711.6	Standard polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4303.0	Semi standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	3945.4	Standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4259.3	Standard polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4156.4	Semi standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4050.9	Standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4308.8	Standard polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1	4165.2	Semi standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1	4041.7	Standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1	4307.3	Standard polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4283.5	Semi standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)C=C1	3975.0	Standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4341.4	Standard polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4115.2	Semi standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3904.8	Standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4371.4	Standard polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1	4166.0	Semi standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1	3928.8	Standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1	4617.9	Standard polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1	4056.0	Semi standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1	4009.4	Standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1	4580.3	Standard polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O)=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4124.6	Semi standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O)=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3899.9	Standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O)=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4374.6	Standard polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4180.1	Semi standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)C=C1	3940.6	Standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4616.4	Standard polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4065.4	Semi standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4014.9	Standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4578.3	Standard polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC=C1/C=C/C1=CC=C(C(=N)N)C=C1	4199.6	Semi standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC=C1/C=C/C1=CC=C(C(=N)N)C=C1	3843.2	Standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC=C1/C=C/C1=CC=C(C(=N)N)C=C1	4420.1	Standard polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	4092.3	Semi standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	3886.9	Standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	4389.4	Standard polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4193.1	Semi standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	3910.8	Standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4529.8	Standard polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1=CC(C(=N)N)=CC=C1/C=C/C1=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1	4204.7	Semi standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1=CC(C(=N)N)=CC=C1/C=C/C1=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1	3839.1	Standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1=CC(C(=N)N)=CC=C1/C=C/C1=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1	4421.1	Standard polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4104.5	Semi standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O[Si](C)(C)C(C)(C)C)C=C1	3879.1	Standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4391.7	Standard polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	4186.4	Semi standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	3902.3	Standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	4531.7	Standard polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(N)=N[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4096.9	Semi standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(N)=N[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	3862.7	Standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(N)=N[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4813.0	Standard polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1	4273.5	Semi standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1	3975.3	Standard non polar	33892256
Hydroxystilbamidine,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1	4339.5	Standard polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	4409.2	Semi standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	4167.2	Standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	4170.3	Standard polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	4226.6	Semi standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	4195.0	Standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	4471.5	Standard polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)C=C1)[Si](C)(C)C(C)(C)C	4400.9	Semi standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)C=C1)[Si](C)(C)C(C)(C)C	4243.8	Standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)C=C1)[Si](C)(C)C(C)(C)C	4229.7	Standard polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1	4305.4	Semi standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1	4257.4	Standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1	4218.1	Standard polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4339.1	Semi standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4243.7	Standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4124.8	Standard polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4197.2	Semi standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4374.8	Standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4213.1	Standard polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4310.1	Semi standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4262.7	Standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4225.1	Standard polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4339.7	Semi standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4239.4	Standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4124.2	Standard polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1	4250.7	Semi standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1	4222.7	Standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1	4443.2	Standard polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4256.1	Semi standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4227.0	Standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4442.2	Standard polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4310.1	Semi standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4208.8	Standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4167.2	Standard polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	4307.4	Semi standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	4213.3	Standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	4165.2	Standard polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4415.3	Semi standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4162.3	Standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4172.8	Standard polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4257.6	Semi standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4096.3	Standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4252.9	Standard polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4332.5	Semi standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4124.3	Standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4490.0	Standard polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4225.9	Semi standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4204.2	Standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4468.6	Standard polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	4321.0	Semi standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	4125.2	Standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	4490.5	Standard polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4277.3	Semi standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4093.4	Standard non polar	33892256
Hydroxystilbamidine,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N)C=C2O[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4254.3	Standard polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC=C1/C=C/C1=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1	4544.2	Semi standard non polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC=C1/C=C/C1=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1	4366.9	Standard non polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC=C1/C=C/C1=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1	4079.8	Standard polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4484.2	Semi standard non polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4461.7	Standard non polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4058.3	Standard polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1	4389.2	Semi standard non polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1	4555.6	Standard non polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O)=C1	4085.3	Standard polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4387.6	Semi standard non polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4556.2	Standard non polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)C=C1	4093.1	Standard polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	4452.8	Semi standard non polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	4388.3	Standard non polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	4114.0	Standard polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4493.4	Semi standard non polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4393.2	Standard non polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4023.6	Standard polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4337.2	Semi standard non polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4493.5	Standard non polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4146.9	Standard polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4465.7	Semi standard non polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4372.9	Standard non polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4119.2	Standard polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4480.1	Semi standard non polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4394.0	Standard non polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4022.9	Standard polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4418.2	Semi standard non polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4383.8	Standard non polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)C=C1	4393.5	Standard polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	4429.8	Semi standard non polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	4382.2	Standard non polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/C=C/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C(O[Si](C)(C)C(C)(C)C)=C1	4395.6	Standard polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4486.2	Semi standard non polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4463.5	Standard non polar	33892256
Hydroxystilbamidine,5TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/C=C/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4059.5	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Hydroxystilbamidine 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 - Hydroxystilbamidine 10V, Positive-QTOF	splash10-001i-0190000000-4e3e0c161221ec42fe79	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hydroxystilbamidine 20V, Positive-QTOF	splash10-03ea-0690000000-d75b21ad2c8b40a35aa8	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hydroxystilbamidine 40V, Positive-QTOF	splash10-015d-1910000000-93a6bc364592f9baa9aa	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hydroxystilbamidine 10V, Negative-QTOF	splash10-004i-0090000000-28453818cabb0a561889	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hydroxystilbamidine 20V, Negative-QTOF	splash10-004i-0090000000-888bccbcc2804735d203	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hydroxystilbamidine 40V, Negative-QTOF	splash10-000f-9550000000-356cc2761d4a794e01d2	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hydroxystilbamidine 10V, Negative-QTOF	splash10-004i-0090000000-43beeb311509a104aab7	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hydroxystilbamidine 20V, Negative-QTOF	splash10-002u-0390000000-cc55153110adcd8a6083	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hydroxystilbamidine 40V, Negative-QTOF	splash10-0006-9380000000-8eec3f68ab21ec6ed077	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hydroxystilbamidine 10V, Positive-QTOF	splash10-01q9-0090000000-4e47158248bdb108ae25	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hydroxystilbamidine 20V, Positive-QTOF	splash10-03di-0090000000-a0d8e190b28a4b714bb7	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Hydroxystilbamidine 40V, Positive-QTOF	splash10-00dj-0290000000-fd907089f6377d00d53e	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

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

10612853

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Hydroxystilbamidine

METLIN ID

Not Available

PubChem Compound

5284571

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 Hydroxystilbamidine (HMDB0240284)

MOL for HMDB0240284 (Hydroxystilbamidine)

3D MOL for HMDB0240284 (Hydroxystilbamidine)

3D SDF for HMDB0240284 (Hydroxystilbamidine)

3D-SDF for HMDB0240284 (Hydroxystilbamidine)

PDB for HMDB0240284 (Hydroxystilbamidine)

3D PDB for HMDB0240284 (Hydroxystilbamidine)

SMILES for HMDB0240284 (Hydroxystilbamidine)

INCHI for HMDB0240284 (Hydroxystilbamidine)

Structure for HMDB0240284 (Hydroxystilbamidine)

3D Structure for HMDB0240284 (Hydroxystilbamidine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra