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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 08:00:22 UTC

Update Date

2021-09-26 23:02:34 UTC

HMDB ID

HMDB0250859

Secondary Accession Numbers

None

Metabolite Identification

Common Name

4',6-Diamidino-2-phenylindole

Description

DAPI belongs to the class of organic compounds known as 2-phenylindoles. These are indoles substituted at the 2-position with a phenyl group. Based on a literature review a significant number of articles have been published on DAPI. This compound has been identified in human blood as reported by (PMID: 31557052 ). 4',6-diamidino-2-phenylindole is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 4',6-Diamidino-2-phenylindole is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

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

HMDB0250859
     RDKit          3D
4',6-Diamidino-2-phenylindole
 36 38  0  0  0  0  0  0  0  0999 V2000
   -6.4447   -0.8143    0.9521 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7993   -0.0210    0.2014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5532    0.8911   -0.6280 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3566   -0.0063    0.1551 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6213   -0.8670    0.9371 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2362   -0.7893    0.8338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5798    0.0898    0.0032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1301    0.1698   -0.1037 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5671    1.0320   -0.9195 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9069    0.7846   -0.7201 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0658    1.3212   -1.2441 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3269    0.8617   -0.8462 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3494   -0.1461    0.0885 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6463   -0.6623    0.5383 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7629   -0.2258    0.1080 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6444   -1.7022    1.5034 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1893   -0.6891    0.6185 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9700   -0.2279    0.2180 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7186   -0.6029    0.5942 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3774    0.9192   -0.7483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7471    0.9012   -0.7007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0665   -1.5193    1.5978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1535    1.5757   -0.1314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4845    0.8479   -1.6615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0824   -1.5900    1.6183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6393   -1.4548    1.4377 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1903    1.7861   -1.6107 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0044    2.1088   -1.9735 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2094    1.3093   -1.2814 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8947    0.5221   -0.5890 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5968   -1.4646    2.5021 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6907   -2.6809    1.1937 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2406   -1.4936    1.3638 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4991   -1.3502    1.2926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8613    1.6184   -1.4087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3402    1.5689   -1.3068 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
 19  8  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
  9 27  1  0
 11 28  1  0
 12 29  1  0
 15 30  1  0
 16 31  1  0
 16 32  1  0
 17 33  1  0
 19 34  1  0
 20 35  1  0
 21 36  1  0
M  END


  Mrv0541 05041402312D          

 21 23  0  0  0  0            999 V2000
   -1.8659    2.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8659    0.8085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6909    2.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6909    0.8085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    0.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4534    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1034    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9284    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3409    0.8085    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3409    2.2374    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    3.1729    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990    1.9354    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    2.1904    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  1  0  0  0  0
  4  2  2  0  0  0  0
  6  5  2  0  0  0  0
  9  1  2  0  0  0  0
  9  2  1  0  0  0  0
 10  3  2  0  0  0  0
 10  4  1  0  0  0  0
 11  5  1  0  0  0  0
 11  7  1  0  0  0  0
 12  6  1  0  0  0  0
 12  8  2  0  0  0  0
 13  7  2  0  0  0  0
 13  9  1  0  0  0  0
 14  8  1  0  0  0  0
 14 11  2  0  0  0  0
 15 10  1  0  0  0  0
 16 12  1  0  0  0  0
 17 15  1  0  0  0  0
 18 15  2  0  0  0  0
 19 16  2  0  0  0  0
 20 16  1  0  0  0  0
 21 13  1  0  0  0  0
 21 14  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0250859

> <DATABASE_NAME>
hmdb

> <SMILES>
NC(=N)C1=CC=C(C=C1)C1=CC2=C(N1)C=C(C=C2)C(N)=N

> <INCHI_IDENTIFIER>
InChI=1S/C16H15N5/c17-15(18)10-3-1-9(2-4-10)13-7-11-5-6-12(16(19)20)8-14(11)21-13/h1-8,21H,(H3,17,18)(H3,19,20)

> <INCHI_KEY>
FWBHETKCLVMNFS-UHFFFAOYSA-N

> <FORMULA>
C16H15N5

> <MOLECULAR_WEIGHT>
277.3238

> <EXACT_MASS>
277.132745505

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
31.47770773985444

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(4-carbamimidoylphenyl)-1H-indole-6-carboximidamide

> <ALOGPS_LOGP>
1.39

> <JCHEM_LOGP>
1.4801712433333332

> <ALOGPS_LOGS>
-3.87

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.501453452574275

> <JCHEM_PKA_STRONGEST_BASIC>
11.646783818685012

> <JCHEM_POLAR_SURFACE_AREA>
115.53

> <JCHEM_REFRACTIVITY>
105.5032

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.71e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
DAPI

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0250859
     RDKit          3D
4',6-Diamidino-2-phenylindole
 36 38  0  0  0  0  0  0  0  0999 V2000
   -6.4447   -0.8143    0.9521 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7993   -0.0210    0.2014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5532    0.8911   -0.6280 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3566   -0.0063    0.1551 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6213   -0.8670    0.9371 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2362   -0.7893    0.8338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5798    0.0898    0.0032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1301    0.1698   -0.1037 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5671    1.0320   -0.9195 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9069    0.7846   -0.7201 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0658    1.3212   -1.2441 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3269    0.8617   -0.8462 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3494   -0.1461    0.0885 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6463   -0.6623    0.5383 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7629   -0.2258    0.1080 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6444   -1.7022    1.5034 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1893   -0.6891    0.6185 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9700   -0.2279    0.2180 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7186   -0.6029    0.5942 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3774    0.9192   -0.7483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7471    0.9012   -0.7007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0665   -1.5193    1.5978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1535    1.5757   -0.1314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4845    0.8479   -1.6615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0824   -1.5900    1.6183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6393   -1.4548    1.4377 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1903    1.7861   -1.6107 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0044    2.1088   -1.9735 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2094    1.3093   -1.2814 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8947    0.5221   -0.5890 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5968   -1.4646    2.5021 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6907   -2.6809    1.1937 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2406   -1.4936    1.3638 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4991   -1.3502    1.2926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8613    1.6184   -1.4087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3402    1.5689   -1.3068 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
 19  8  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
  9 27  1  0
 11 28  1  0
 12 29  1  0
 15 30  1  0
 16 31  1  0
 16 32  1  0
 17 33  1  0
 19 34  1  0
 20 35  1  0
 21 36  1  0
M  END

HEADER    PROTEIN                                 04-MAY-14   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-MAY-14         0                                  
HETATM    1  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       0.000   0.000   0.000  0.00  0.00           N+0
HETATM   18  N   UNK     0       0.000   0.000   0.000  0.00  0.00           N+0
HETATM   19  N   UNK     0       0.000   0.000   0.000  0.00  0.00           N+0
HETATM   20  N   UNK     0       0.000   0.000   0.000  0.00  0.00           N+0
HETATM   21  N   UNK     0       0.000   0.000   0.000  0.00  0.00           N+0
CONECT    1    3    9                                                       
CONECT    2    4    9                                                       
CONECT    3    1   10                                                       
CONECT    4    2   10                                                       
CONECT    5    6   11                                                       
CONECT    6    5   12                                                       
CONECT    7   11   13                                                       
CONECT    8   12   14                                                       
CONECT    9    1    2   13                                                  
CONECT   10    3    4   15                                                  
CONECT   11    5    7   14                                                  
CONECT   12    6    8   16                                                  
CONECT   13    7    9   21                                                  
CONECT   14    8   11   21                                                  
CONECT   15   10   17   18                                                  
CONECT   16   12   19   20                                                  
CONECT   17   15                                                            
CONECT   18   15                                                            
CONECT   19   16                                                            
CONECT   20   16                                                            
CONECT   21   13   14                                                       
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

COMPND    HMDB0250859
HETATM    1  N1  UNL     1      -6.445  -0.814   0.952  1.00  0.00           N  
HETATM    2  C1  UNL     1      -5.799  -0.021   0.201  1.00  0.00           C  
HETATM    3  N2  UNL     1      -6.553   0.891  -0.628  1.00  0.00           N  
HETATM    4  C2  UNL     1      -4.357  -0.006   0.155  1.00  0.00           C  
HETATM    5  C3  UNL     1      -3.621  -0.867   0.937  1.00  0.00           C  
HETATM    6  C4  UNL     1      -2.236  -0.789   0.834  1.00  0.00           C  
HETATM    7  C5  UNL     1      -1.580   0.090   0.003  1.00  0.00           C  
HETATM    8  C6  UNL     1      -0.130   0.170  -0.104  1.00  0.00           C  
HETATM    9  C7  UNL     1       0.567   1.032  -0.919  1.00  0.00           C  
HETATM   10  C8  UNL     1       1.907   0.785  -0.720  1.00  0.00           C  
HETATM   11  C9  UNL     1       3.066   1.321  -1.244  1.00  0.00           C  
HETATM   12  C10 UNL     1       4.327   0.862  -0.846  1.00  0.00           C  
HETATM   13  C11 UNL     1       4.349  -0.146   0.088  1.00  0.00           C  
HETATM   14  C12 UNL     1       5.646  -0.662   0.538  1.00  0.00           C  
HETATM   15  N3  UNL     1       6.763  -0.226   0.108  1.00  0.00           N  
HETATM   16  N4  UNL     1       5.644  -1.702   1.503  1.00  0.00           N  
HETATM   17  C13 UNL     1       3.189  -0.689   0.618  1.00  0.00           C  
HETATM   18  C14 UNL     1       1.970  -0.228   0.218  1.00  0.00           C  
HETATM   19  N5  UNL     1       0.719  -0.603   0.594  1.00  0.00           N  
HETATM   20  C15 UNL     1      -2.377   0.919  -0.748  1.00  0.00           C  
HETATM   21  C16 UNL     1      -3.747   0.901  -0.701  1.00  0.00           C  
HETATM   22  H1  UNL     1      -6.067  -1.519   1.598  1.00  0.00           H  
HETATM   23  H2  UNL     1      -7.153   1.576  -0.131  1.00  0.00           H  
HETATM   24  H3  UNL     1      -6.485   0.848  -1.662  1.00  0.00           H  
HETATM   25  H4  UNL     1      -4.082  -1.590   1.618  1.00  0.00           H  
HETATM   26  H5  UNL     1      -1.639  -1.455   1.438  1.00  0.00           H  
HETATM   27  H6  UNL     1       0.190   1.786  -1.611  1.00  0.00           H  
HETATM   28  H7  UNL     1       3.004   2.109  -1.974  1.00  0.00           H  
HETATM   29  H8  UNL     1       5.209   1.309  -1.281  1.00  0.00           H  
HETATM   30  H9  UNL     1       6.895   0.522  -0.589  1.00  0.00           H  
HETATM   31  H10 UNL     1       5.597  -1.465   2.502  1.00  0.00           H  
HETATM   32  H11 UNL     1       5.691  -2.681   1.194  1.00  0.00           H  
HETATM   33  H12 UNL     1       3.241  -1.494   1.364  1.00  0.00           H  
HETATM   34  H13 UNL     1       0.499  -1.350   1.293  1.00  0.00           H  
HETATM   35  H14 UNL     1      -1.861   1.618  -1.409  1.00  0.00           H  
HETATM   36  H15 UNL     1      -4.340   1.569  -1.307  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   19
CONECT    9   10   27
CONECT   10   11   11   18
CONECT   11   12   28
CONECT   12   13   13   29
CONECT   13   14   17
CONECT   14   15   15   16
CONECT   15   30
CONECT   16   31   32
CONECT   17   18   18   33
CONECT   18   19
CONECT   19   34
CONECT   20   21   21   35
CONECT   21   36
END

HMDB0250859
     RDKit          3D
4',6-Diamidino-2-phenylindole
 36 38  0  0  0  0  0  0  0  0999 V2000
   -6.4447   -0.8143    0.9521 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7993   -0.0210    0.2014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5532    0.8911   -0.6280 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3566   -0.0063    0.1551 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6213   -0.8670    0.9371 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2362   -0.7893    0.8338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5798    0.0898    0.0032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1301    0.1698   -0.1037 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5671    1.0320   -0.9195 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9069    0.7846   -0.7201 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0658    1.3212   -1.2441 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3269    0.8617   -0.8462 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3494   -0.1461    0.0885 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6463   -0.6623    0.5383 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7629   -0.2258    0.1080 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6444   -1.7022    1.5034 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1893   -0.6891    0.6185 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9700   -0.2279    0.2180 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7186   -0.6029    0.5942 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3774    0.9192   -0.7483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7471    0.9012   -0.7007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0665   -1.5193    1.5978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1535    1.5757   -0.1314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4845    0.8479   -1.6615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0824   -1.5900    1.6183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6393   -1.4548    1.4377 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1903    1.7861   -1.6107 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0044    2.1088   -1.9735 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2094    1.3093   -1.2814 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8947    0.5221   -0.5890 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5968   -1.4646    2.5021 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6907   -2.6809    1.1937 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2406   -1.4936    1.3638 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4991   -1.3502    1.2926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8613    1.6184   -1.4087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3402    1.5689   -1.3068 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
 19  8  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
  9 27  1  0
 11 28  1  0
 12 29  1  0
 15 30  1  0
 16 31  1  0
 16 32  1  0
 17 33  1  0
 19 34  1  0
 20 35  1  0
 21 36  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
2-(4-(Aminoiminomethyl)phenyl)-1H-indole-6-carboximidamide	ChEBI
4',6-Diamidino-2-phenylindole	ChEBI
4',6-Diamidinophenyl-indole	ChEBI
4,6-Diamidinophenylindole	MeSH
4,6-diamidino-2-Phenylindole	MeSH
DAPI hydrochloride	MeSH

Chemical Formula

C₁₆H₁₅N₅

Average Molecular Weight

277.3238

Monoisotopic Molecular Weight

277.132745505

IUPAC Name

2-(4-carbamimidoylphenyl)-1H-indole-6-carboximidamide

Traditional Name

DAPI

CAS Registry Number

Not Available

SMILES

NC(=N)C1=CC=C(C=C1)C1=CC2=C(N1)C=C(C=C2)C(N)=N

InChI Identifier

InChI=1S/C16H15N5/c17-15(18)10-3-1-9(2-4-10)13-7-11-5-6-12(16(19)20)8-14(11)21-13/h1-8,21H,(H3,17,18)(H3,19,20)

InChI Key

FWBHETKCLVMNFS-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2-phenylindoles. These are indoles substituted at the 2-position with a phenyl group.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indoles

Direct Parent

2-phenylindoles

Alternative Parents

Substituents

2-phenylindole
2-phenylpyrrole
Monocyclic benzene moiety
Substituted pyrrole
Benzenoid
Pyrrole
Heteroaromatic compound
Amidine
Carboxylic acid amidine
Azacycle
Carboximidamide
Organonitrogen compound
Organopnictogen compound
Hydrocarbon derivative
Organic nitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

indoles (CHEBI:51231 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	1.39	ALOGPS
logP	1.48	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	14.5	ChemAxon
pKa (Strongest Basic)	11.65	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	115.53 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	105.5 m³·mol⁻¹	ChemAxon
Polarizability	31.48 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	166.765	30932474
DeepCCS	[M-H]-	164.407	30932474
DeepCCS	[M-2H]-	198.275	30932474
DeepCCS	[M+Na]+	173.503	30932474
AllCCS	[M+H]+	166.6	32859911
AllCCS	[M+H-H2O]+	162.9	32859911
AllCCS	[M+NH4]+	170.1	32859911
AllCCS	[M+Na]+	171.1	32859911
AllCCS	[M-H]-	169.2	32859911
AllCCS	[M+Na-2H]-	168.7	32859911
AllCCS	[M+HCOO]-	168.3	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
4',6-Diamidino-2-phenylindole	NC(=N)C1=CC=C(C=C1)C1=CC2=C(N1)C=C(C=C2)C(N)=N	4548.8	Standard polar	33892256
4',6-Diamidino-2-phenylindole	NC(=N)C1=CC=C(C=C1)C1=CC2=C(N1)C=C(C=C2)C(N)=N	3203.8	Standard non polar	33892256
4',6-Diamidino-2-phenylindole	NC(=N)C1=CC=C(C=C1)C1=CC2=C(N1)C=C(C=C2)C(N)=N	3761.1	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
4',6-Diamidino-2-phenylindole,1TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1	3596.8	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,1TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1	3243.1	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,1TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1	5216.4	Standard polar	33892256
4',6-Diamidino-2-phenylindole,1TMS,isomer #2	C[Si](C)(C)NC(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1	3578.6	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,1TMS,isomer #2	C[Si](C)(C)NC(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1	3234.7	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,1TMS,isomer #2	C[Si](C)(C)NC(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1	5215.8	Standard polar	33892256
4',6-Diamidino-2-phenylindole,1TMS,isomer #3	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1	3520.1	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,1TMS,isomer #3	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1	3233.5	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,1TMS,isomer #3	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1	5291.8	Standard polar	33892256
4',6-Diamidino-2-phenylindole,1TMS,isomer #4	C[Si](C)(C)N1C(C2=CC=C(C(=N)N)C=C2)=CC2=CC=C(C(=N)N)C=C21	3471.7	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,1TMS,isomer #4	C[Si](C)(C)N1C(C2=CC=C(C(=N)N)C=C2)=CC2=CC=C(C(=N)N)C=C21	3098.6	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,1TMS,isomer #4	C[Si](C)(C)N1C(C2=CC=C(C(=N)N)C=C2)=CC2=CC=C(C(=N)N)C=C21	5316.7	Standard polar	33892256
4',6-Diamidino-2-phenylindole,1TMS,isomer #5	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1	3487.6	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,1TMS,isomer #5	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1	3190.8	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,1TMS,isomer #5	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1	5291.5	Standard polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C)C=C3[NH]2)C=C1	3684.7	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C)C=C3[NH]2)C=C1	3322.6	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C)C=C3[NH]2)C=C1	4669.3	Standard polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #10	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(N)=N[Si](C)(C)C)C=C3[NH]2)C=C1	3503.4	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #10	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(N)=N[Si](C)(C)C)C=C3[NH]2)C=C1	3304.2	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #10	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(N)=N[Si](C)(C)C)C=C3[NH]2)C=C1	5059.7	Standard polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #11	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C)C=C1	3554.9	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #11	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C)C=C1	3203.9	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #11	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C)C=C1	4980.7	Standard polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #12	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C)C2=C1	3548.9	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #12	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C)C2=C1	3175.2	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #12	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C)C2=C1	4980.5	Standard polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #2	C[Si](C)(C)N(C(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1)[Si](C)(C)C	3624.2	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #2	C[Si](C)(C)N(C(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1)[Si](C)(C)C	3251.9	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #2	C[Si](C)(C)N(C(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1)[Si](C)(C)C	4954.4	Standard polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #3	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1	3513.7	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #3	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1	3305.4	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #3	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1	4802.5	Standard polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #4	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C)C=C3)[NH]C2=C1	3603.2	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #4	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C)C=C3)[NH]C2=C1	3320.2	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #4	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C)C=C3)[NH]C2=C1	4889.2	Standard polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #5	C[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C)C=C1	3626.1	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #5	C[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C)C=C1	3187.3	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #5	C[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C)C=C1	4760.0	Standard polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #6	C[Si](C)(C)N(C(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1)[Si](C)(C)C	3614.0	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #6	C[Si](C)(C)N(C(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1)[Si](C)(C)C	3251.6	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #6	C[Si](C)(C)N(C(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1)[Si](C)(C)C	4956.1	Standard polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #7	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1	3503.3	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #7	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1	3283.5	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #7	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1	4803.1	Standard polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #8	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C)C=C3[NH]2)C=C1	3610.0	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #8	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C)C=C3[NH]2)C=C1	3343.8	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #8	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C)C=C3[NH]2)C=C1	4891.4	Standard polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #9	C[Si](C)(C)NC(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C)C2=C1	3632.7	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #9	C[Si](C)(C)NC(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C)C2=C1	3180.7	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TMS,isomer #9	C[Si](C)(C)NC(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C)C2=C1	4757.9	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3)[NH]C2=C1	3644.8	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3)[NH]C2=C1	3379.8	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3)[NH]C2=C1	4417.7	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #10	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C)C=C1	3459.8	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #10	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C)C=C1	3258.9	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #10	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C)C=C1	4440.4	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #11	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1	3573.0	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #11	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1	3294.4	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #11	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1	4581.0	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #12	C[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1)N([Si](C)(C)C)[Si](C)(C)C	3480.1	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #12	C[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1)N([Si](C)(C)C)[Si](C)(C)C	3343.7	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #12	C[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1)N([Si](C)(C)C)[Si](C)(C)C	4447.0	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #13	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3[NH]2)C=C1	3569.2	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #13	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3[NH]2)C=C1	3402.4	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #13	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3[NH]2)C=C1	4728.5	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #14	C[Si](C)(C)N(C(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C)C2=C1)[Si](C)(C)C	3568.1	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #14	C[Si](C)(C)N(C(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C)C2=C1)[Si](C)(C)C	3262.6	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #14	C[Si](C)(C)N(C(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C)C2=C1)[Si](C)(C)C	4531.8	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #15	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C3[NH]2)C=C1	3410.7	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #15	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C3[NH]2)C=C1	3434.3	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #15	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C3[NH]2)C=C1	4630.3	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #16	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C)C2=C1	3457.5	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #16	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C)C2=C1	3239.9	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #16	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C)C2=C1	4436.8	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #17	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	3603.1	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #17	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	3301.3	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #17	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	4581.2	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #18	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(N)=N[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	3484.1	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #18	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(N)=N[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	3269.3	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #18	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(N)=N[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	4861.4	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #2	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C)C=C3[NH]2)C=C1	3500.5	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #2	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C)C=C3[NH]2)C=C1	3424.9	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #2	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C)C=C3[NH]2)C=C1	4341.2	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #3	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C)C=C3)[NH]C2=C1	3486.8	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #3	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C)C=C3)[NH]C2=C1	3421.3	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #3	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C)C=C3)[NH]C2=C1	4336.2	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #4	C[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3[NH]2)C=C1	3620.0	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #4	C[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3[NH]2)C=C1	3395.4	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #4	C[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3[NH]2)C=C1	4418.7	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #5	C[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	3678.7	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #5	C[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	3281.2	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #5	C[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	4263.4	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #6	C[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3512.1	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #6	C[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3375.8	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #6	C[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	4442.9	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #7	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3)[NH]C2=C1	3551.2	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #7	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3)[NH]C2=C1	3375.2	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #7	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3)[NH]C2=C1	4725.1	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #8	C[Si](C)(C)N(C(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C)C=C1)[Si](C)(C)C	3565.3	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #8	C[Si](C)(C)N(C(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C)C=C1)[Si](C)(C)C	3262.1	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #8	C[Si](C)(C)N(C(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C)C=C1)[Si](C)(C)C	4531.3	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #9	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C3)[NH]C2=C1	3393.4	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #9	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C3)[NH]C2=C1	3423.1	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TMS,isomer #9	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C3)[NH]C2=C1	4629.2	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #1	C[Si](C)(C)N(C(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3[NH]2)C=C1)[Si](C)(C)C	3544.0	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #1	C[Si](C)(C)N(C(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3[NH]2)C=C1)[Si](C)(C)C	3534.9	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #1	C[Si](C)(C)N(C(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3[NH]2)C=C1)[Si](C)(C)C	4240.2	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #10	C[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	3585.4	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #10	C[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	3391.6	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #10	C[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	4103.1	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #11	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3)[NH]C2=C1	3422.2	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #11	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3)[NH]C2=C1	3513.4	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #11	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3)[NH]C2=C1	4383.0	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #12	C[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3452.3	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #12	C[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3339.3	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #12	C[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	4164.2	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #13	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1	3487.3	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #13	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1	3368.3	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #13	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1	4471.8	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #14	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1	3389.5	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #14	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1	3358.1	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #14	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1	4407.2	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #15	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3[NH]2)C=C1	3428.3	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #15	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3[NH]2)C=C1	3511.0	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #15	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3[NH]2)C=C1	4387.4	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #16	C[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C)C2=C1)N([Si](C)(C)C)[Si](C)(C)C	3435.2	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #16	C[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C)C2=C1)N([Si](C)(C)C)[Si](C)(C)C	3318.1	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #16	C[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C)C2=C1)N([Si](C)(C)C)[Si](C)(C)C	4165.9	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #17	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	3515.8	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #17	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	3386.4	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #17	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	4474.1	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #18	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	3405.2	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #18	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	3363.5	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #18	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	4404.5	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #2	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3)[NH]C2=C1	3447.4	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #2	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3)[NH]C2=C1	3485.6	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #2	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3)[NH]C2=C1	4165.0	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #3	C[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C)C=C3[NH]2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3497.5	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #3	C[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C)C=C3[NH]2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3497.0	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #3	C[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C)C=C3[NH]2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	4003.7	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #4	C[Si](C)(C)NC(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1	3586.7	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #4	C[Si](C)(C)NC(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1	3371.8	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #4	C[Si](C)(C)NC(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1	4101.7	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #5	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C3[NH]2)C=C1	3395.1	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #5	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C3[NH]2)C=C1	3551.8	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #5	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C3[NH]2)C=C1	4110.1	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #6	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3[NH]2)C=C1	3465.2	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #6	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3[NH]2)C=C1	3501.0	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #6	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3[NH]2)C=C1	4171.3	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #7	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	3500.5	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #7	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	3362.2	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #7	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	4051.6	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #8	C[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C)C=C3)[NH]C2=C1)N([Si](C)(C)C)[Si](C)(C)C	3457.1	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #8	C[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C)C=C3)[NH]C2=C1)N([Si](C)(C)C)[Si](C)(C)C	3492.6	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #8	C[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C)C=C3)[NH]C2=C1)N([Si](C)(C)C)[Si](C)(C)C	3999.9	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #9	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1	3480.2	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #9	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1	3370.2	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TMS,isomer #9	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1	4045.4	Standard polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #1	C[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3[NH]2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3474.2	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #1	C[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3[NH]2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3603.4	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #1	C[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3[NH]2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3883.3	Standard polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #10	C[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1)N([Si](C)(C)C)[Si](C)(C)C	3479.7	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #10	C[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1)N([Si](C)(C)C)[Si](C)(C)C	3455.7	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #10	C[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1)N([Si](C)(C)C)[Si](C)(C)C	3778.3	Standard polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #11	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1	3429.9	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #11	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1	3449.2	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #11	C[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1	4207.4	Standard polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #12	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	3425.4	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #12	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	3449.4	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #12	C[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	4209.1	Standard polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #2	C[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3)[NH]C2=C1)N([Si](C)(C)C)[Si](C)(C)C	3457.4	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #2	C[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3)[NH]C2=C1)N([Si](C)(C)C)[Si](C)(C)C	3594.9	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #2	C[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3)[NH]C2=C1)N([Si](C)(C)C)[Si](C)(C)C	3878.0	Standard polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #3	C[Si](C)(C)N(C(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1)[Si](C)(C)C	3558.5	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #3	C[Si](C)(C)N(C(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1)[Si](C)(C)C	3505.4	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #3	C[Si](C)(C)N(C(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1)[Si](C)(C)C	3991.4	Standard polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #4	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3)[NH]C2=C1	3410.1	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #4	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3)[NH]C2=C1	3638.1	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #4	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3)[NH]C2=C1	3832.1	Standard polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #5	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1	3480.2	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #5	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1	3433.3	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #5	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1	3933.5	Standard polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #6	C[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3510.9	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #6	C[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3445.0	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #6	C[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3780.5	Standard polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #7	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3[NH]2)C=C1	3393.4	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #7	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3[NH]2)C=C1	3639.3	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #7	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3[NH]2)C=C1	3835.3	Standard polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #8	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	3429.5	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #8	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	3455.0	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #8	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	3886.9	Standard polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #9	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	3502.2	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #9	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	3440.1	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TMS,isomer #9	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	3941.9	Standard polar	33892256
4',6-Diamidino-2-phenylindole,6TMS,isomer #1	C[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3[NH]2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3438.6	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,6TMS,isomer #1	C[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3[NH]2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3728.0	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,6TMS,isomer #1	C[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3[NH]2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3594.3	Standard polar	33892256
4',6-Diamidino-2-phenylindole,6TMS,isomer #2	C[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3529.2	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,6TMS,isomer #2	C[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3532.7	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,6TMS,isomer #2	C[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3677.4	Standard polar	33892256
4',6-Diamidino-2-phenylindole,6TMS,isomer #3	C[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1)N([Si](C)(C)C)[Si](C)(C)C	3511.4	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,6TMS,isomer #3	C[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1)N([Si](C)(C)C)[Si](C)(C)C	3542.6	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,6TMS,isomer #3	C[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1)N([Si](C)(C)C)[Si](C)(C)C	3670.6	Standard polar	33892256
4',6-Diamidino-2-phenylindole,6TMS,isomer #4	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1	3461.9	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,6TMS,isomer #4	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1	3540.3	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,6TMS,isomer #4	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3)N([Si](C)(C)C)C2=C1	3664.8	Standard polar	33892256
4',6-Diamidino-2-phenylindole,6TMS,isomer #5	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	3451.6	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,6TMS,isomer #5	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	3545.6	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,6TMS,isomer #5	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1	3669.6	Standard polar	33892256
4',6-Diamidino-2-phenylindole,7TMS,isomer #1	C[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3505.2	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,7TMS,isomer #1	C[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3643.8	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,7TMS,isomer #1	C[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C3N2[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3456.0	Standard polar	33892256
4',6-Diamidino-2-phenylindole,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1	3877.2	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1	3413.9	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1	5034.3	Standard polar	33892256
4',6-Diamidino-2-phenylindole,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1	3854.2	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1	3398.3	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1	5034.4	Standard polar	33892256
4',6-Diamidino-2-phenylindole,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1	3736.5	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1	3418.2	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1	5167.2	Standard polar	33892256
4',6-Diamidino-2-phenylindole,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N1C(C2=CC=C(C(=N)N)C=C2)=CC2=CC=C(C(=N)N)C=C21	3755.9	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N1C(C2=CC=C(C(=N)N)C=C2)=CC2=CC=C(C(=N)N)C=C21	3278.5	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N1C(C2=CC=C(C(=N)N)C=C2)=CC2=CC=C(C(=N)N)C=C21	5181.2	Standard polar	33892256
4',6-Diamidino-2-phenylindole,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1	3714.5	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1	3373.7	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1	5166.3	Standard polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	4243.5	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	3706.8	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	4470.1	Standard polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(N)=N[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	3944.6	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(N)=N[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	3712.4	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(N)=N[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	4969.1	Standard polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4027.1	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	3585.2	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4864.1	Standard polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	4041.2	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	3556.2	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	4863.3	Standard polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1)[Si](C)(C)C(C)(C)C	4100.7	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1)[Si](C)(C)C(C)(C)C	3626.5	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1)[Si](C)(C)C(C)(C)C	4710.8	Standard polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1	4030.7	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1	3716.9	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1	4629.2	Standard polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3)[NH]C2=C1	4076.5	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3)[NH]C2=C1	3711.3	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3)[NH]C2=C1	4734.7	Standard polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4161.7	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	3593.1	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4585.1	Standard polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1)[Si](C)(C)C(C)(C)C	4098.4	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1)[Si](C)(C)C(C)(C)C	3625.6	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1)[Si](C)(C)C(C)(C)C	4712.6	Standard polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1	4018.7	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1	3687.6	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1	4628.6	Standard polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	4086.7	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	3724.2	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	4738.9	Standard polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	4179.3	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	3577.9	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	4584.6	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3)[NH]C2=C1	4333.5	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3)[NH]C2=C1	3975.5	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3)[NH]C2=C1	4314.5	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4163.8	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	3853.5	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4419.2	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	4249.4	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	3880.3	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	4554.7	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4136.2	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3950.5	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)[NH]C2=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4378.9	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	4191.2	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	3976.0	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	4628.3	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1)[Si](C)(C)C(C)(C)C	4248.4	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1)[Si](C)(C)C(C)(C)C	3841.5	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1)[Si](C)(C)C(C)(C)C	4441.3	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	4038.8	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	4056.6	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	4593.1	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	4169.5	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	3834.6	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	4415.1	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4266.9	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	3877.4	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4556.6	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(N)=N[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4136.5	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(N)=N[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	3851.4	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(N)=N[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4865.0	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	4178.8	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	4044.0	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	4280.5	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3)[NH]C2=C1	4162.7	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3)[NH]C2=C1	4036.1	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3)[NH]C2=C1	4274.2	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	4311.8	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	3984.9	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	4314.2	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4420.7	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	3906.4	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4234.3	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4178.3	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3970.1	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3[NH]2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4376.9	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3)[NH]C2=C1	4189.7	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3)[NH]C2=C1	3960.0	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3)[NH]C2=C1	4623.9	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C	4235.3	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C	3846.8	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C	4439.8	Standard polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C3)[NH]C2=C1	4041.9	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C3)[NH]C2=C1	4055.9	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C3)[NH]C2=C1	4593.0	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1)[Si](C)(C)C(C)(C)C	4350.6	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1)[Si](C)(C)C(C)(C)C	4275.4	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1)[Si](C)(C)C(C)(C)C	4208.5	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4424.9	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4173.1	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4154.7	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=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=C3)[NH]C2=C1	4219.1	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=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=C3)[NH]C2=C1	4306.6	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=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=C3)[NH]C2=C1	4447.9	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4276.9	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4104.9	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N)C=C3N2[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4271.9	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	4321.7	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	4131.1	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	4510.1	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	4209.9	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	4141.9	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	4496.2	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=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=C3[NH]2)C=C1	4206.6	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=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=C3[NH]2)C=C1	4310.2	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=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=C3[NH]2)C=C1	4450.5	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4280.6	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4108.1	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4272.2	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4342.5	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4124.9	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4512.7	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4220.1	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4137.8	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4493.6	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3)[NH]C2=C1	4228.9	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3)[NH]C2=C1	4276.9	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3)[NH]C2=C1	4197.4	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4299.6	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4286.6	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4099.6	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	4421.1	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	4162.5	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	4153.6	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	4094.1	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	4382.2	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	4193.7	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	4236.9	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	4284.6	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1	4203.8	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4292.1	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4143.9	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4150.6	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3)[NH]C2=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4278.8	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3)[NH]C2=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4287.7	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3)[NH]C2=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4096.2	Standard polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	4297.4	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	4152.3	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	4144.5	Standard polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4381.2	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4488.6	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3[NH]2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4026.1	Standard polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4454.9	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4390.5	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4000.3	Standard polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=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=C3)N([Si](C)(C)C(C)(C)C)C2=C1	4393.3	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=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=C3)N([Si](C)(C)C(C)(C)C)C2=C1	4359.5	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C2C=C(C3=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=C3)N([Si](C)(C)C(C)(C)C)C2=C1	4415.9	Standard polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=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=C3N2[Si](C)(C)C(C)(C)C)C=C1	4409.2	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=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=C3N2[Si](C)(C)C(C)(C)C)C=C1	4372.8	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(C2=CC3=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=C3N2[Si](C)(C)C(C)(C)C)C=C1	4416.3	Standard polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3)[NH]C2=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4385.3	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3)[NH]C2=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4506.0	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N=C(C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3)[NH]C2=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4019.3	Standard polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C	4492.9	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C	4400.7	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C	4056.1	Standard polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C2C=C(C3=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=C3)[NH]C2=C1	4284.7	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C2C=C(C3=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=C3)[NH]C2=C1	4581.5	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C2C=C(C3=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=C3)[NH]C2=C1	4062.2	Standard polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	4387.8	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	4367.7	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C2C=C(C3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3)N([Si](C)(C)C(C)(C)C)C2=C1	4093.0	Standard polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4449.0	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4359.8	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(C2=CC3=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4007.7	Standard polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=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=C3[NH]2)C=C1	4292.6	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=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=C3[NH]2)C=C1	4598.2	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=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=C3[NH]2)C=C1	4064.5	Standard polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4266.2	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4410.0	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4132.8	Standard polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4404.5	Semi standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4352.3	Standard non polar	33892256
4',6-Diamidino-2-phenylindole,5TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(C2=CC3=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C3N2[Si](C)(C)C(C)(C)C)C=C1	4102.7	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 4',6-Diamidino-2-phenylindole GC-MS (Non-derivatized) - 70eV, Positive	splash10-03fr-1390000000-2f5a31aa26e0b4809372	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4',6-Diamidino-2-phenylindole 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 - 4',6-Diamidino-2-phenylindole 10V, Positive-QTOF	splash10-01t9-0090000000-dffeea135e875cf6e26e	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4',6-Diamidino-2-phenylindole 20V, Positive-QTOF	splash10-03di-0090000000-0468593f61eb51b2fe8a	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4',6-Diamidino-2-phenylindole 40V, Positive-QTOF	splash10-00kf-0090000000-3c4eb2622cbcf16bd4d7	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4',6-Diamidino-2-phenylindole 10V, Negative-QTOF	splash10-004i-0090000000-bc8a2a69fce2c248472e	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4',6-Diamidino-2-phenylindole 20V, Negative-QTOF	splash10-0059-0090000000-422139cea7d2f13efa0b	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4',6-Diamidino-2-phenylindole 40V, Negative-QTOF	splash10-016r-0090000000-26fda039e1a193bcc9e4	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

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

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

C00027717

Chemspider ID

2848

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

DAPI

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

51231

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for 4',6-Diamidino-2-phenylindole (HMDB0250859)

MOL for HMDB0250859 (4',6-Diamidino-2-phenylindole)

3D MOL for HMDB0250859 (4',6-Diamidino-2-phenylindole)

3D SDF for HMDB0250859 (4',6-Diamidino-2-phenylindole)

3D-SDF for HMDB0250859 (4',6-Diamidino-2-phenylindole)

PDB for HMDB0250859 (4',6-Diamidino-2-phenylindole)

3D PDB for HMDB0250859 (4',6-Diamidino-2-phenylindole)

SMILES for HMDB0250859 (4',6-Diamidino-2-phenylindole)

INCHI for HMDB0250859 (4',6-Diamidino-2-phenylindole)

Structure for HMDB0250859 (4',6-Diamidino-2-phenylindole)

3D Structure for HMDB0250859 (4',6-Diamidino-2-phenylindole)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra