Jump To Section:

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

Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-10 21:34:36 UTC

Update Date

2021-09-26 22:52:08 UTC

HMDB ID

HMDB0244416

Secondary Accession Numbers

None

Metabolite Identification

Common Name

2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine

Description

2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine, also known as DEGBG, belongs to the class of organic compounds known as guanidines. Guanidines are compounds containing a guanidine moiety, with the general structure (R1R2N)(R3R4N)C=N-R5. Based on a literature review very few articles have been published on 2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine. This compound has been identified in human blood as reported by (PMID: 31557052 ). 2-[(z)-[(4z)-4-(diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine 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

HMDB0244416
     RDKit          3D
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guani...
 34 33  0  0  0  0  0  0  0  0999 V2000
    2.1561   -1.7660   -1.3045 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7323   -1.3660   -1.0609 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5851   -0.2558   -0.0989 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5255    0.3498    0.5023 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8288    0.0603    0.3493 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8630    0.1445    1.0392 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0970   -0.2879    0.4905 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8103    0.6741    2.3550 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8145    0.1939    0.1991 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0310    1.2712    1.1695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4768    1.6043    1.3355 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7117   -0.4037   -0.4068 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0552   -0.2244   -0.3494 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7168   -0.0836   -1.4475 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0236   -0.1214   -2.6782 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1082    0.1046   -1.3891 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7712   -0.9768   -1.7753 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1274   -2.5952   -2.0756 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6456   -2.1709   -0.3960 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2349   -2.2645   -0.5972 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2526   -1.1450   -2.0372 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3939   -1.2739    0.5746 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7011    0.3945    0.0011 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2481    1.5831    2.6155 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3021    0.1034    3.0674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5514    1.0375    2.1540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5000    2.1804    0.7785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9488    1.9511    0.3930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5480    2.4387    2.1050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0334    0.7582    1.7593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5058   -0.3241   -3.6017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9767    0.0535   -2.7210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7126    0.0133   -2.2279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5607    0.3429   -0.4874 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  3
  4  5  1  0
  5  6  2  3
  6  7  1  0
  6  8  1  0
  3  9  1  0
  9 10  1  0
 10 11  1  0
  9 12  2  3
 12 13  1  0
 13 14  2  3
 14 15  1  0
 14 16  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  2 21  1  0
  7 22  1  0
  7 23  1  0
  8 24  1  0
  8 25  1  0
 10 26  1  0
 10 27  1  0
 11 28  1  0
 11 29  1  0
 11 30  1  0
 15 31  1  0
 15 32  1  0
 16 33  1  0
 16 34  1  0
M  END

  Mrv1652309102123342D          

 16 15  0  0  0  0            999 V2000
    1.2375    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    1.4289    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    2.1434    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    2.8579    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    1.4289    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    0.7145    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -0.7145    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    0.7145    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  4  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  3  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  4  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0244416

> <DATABASE_NAME>
hmdb

> <SMILES>
CCC(=NN=C(N)N)C(CC)=NN=C(N)N

> <INCHI_IDENTIFIER>
InChI=1S/C8H18N8/c1-3-5(13-15-7(9)10)6(4-2)14-16-8(11)12/h3-4H2,1-2H3,(H4,9,10,15)(H4,11,12,16)

> <INCHI_KEY>
HXWLLFLQUZOBFF-UHFFFAOYSA-N

> <FORMULA>
C8H18N8

> <MOLECULAR_WEIGHT>
226.288

> <EXACT_MASS>
226.165442612

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
24.179232529459682

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N''-[(4-{[(diaminomethylidene)amino]imino}hexan-3-ylidene)amino]guanidine

> <ALOGPS_LOGP>
1.54

> <JCHEM_LOGP>
-0.564905914666667

> <ALOGPS_LOGS>
-3.15

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA>
19.43053327824504

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.87420354051963

> <JCHEM_PKA_STRONGEST_BASIC>
7.465588005245606

> <JCHEM_POLAR_SURFACE_AREA>
153.51999999999998

> <JCHEM_REFRACTIVITY>
62.5966

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.62e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N''-[(4-{[(diaminomethylidene)amino]imino}hexan-3-ylidene)amino]guanidine

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0244416
     RDKit          3D
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guani...
 34 33  0  0  0  0  0  0  0  0999 V2000
    2.1561   -1.7660   -1.3045 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7323   -1.3660   -1.0609 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5851   -0.2558   -0.0989 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5255    0.3498    0.5023 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8288    0.0603    0.3493 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8630    0.1445    1.0392 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0970   -0.2879    0.4905 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8103    0.6741    2.3550 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8145    0.1939    0.1991 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0310    1.2712    1.1695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4768    1.6043    1.3355 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7117   -0.4037   -0.4068 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0552   -0.2244   -0.3494 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7168   -0.0836   -1.4475 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0236   -0.1214   -2.6782 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1082    0.1046   -1.3891 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7712   -0.9768   -1.7753 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1274   -2.5952   -2.0756 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6456   -2.1709   -0.3960 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2349   -2.2645   -0.5972 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2526   -1.1450   -2.0372 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3939   -1.2739    0.5746 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7011    0.3945    0.0011 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2481    1.5831    2.6155 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3021    0.1034    3.0674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5514    1.0375    2.1540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5000    2.1804    0.7785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9488    1.9511    0.3930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5480    2.4387    2.1050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0334    0.7582    1.7593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5058   -0.3241   -3.6017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9767    0.0535   -2.7210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7126    0.0133   -2.2279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5607    0.3429   -0.4874 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  3
  4  5  1  0
  5  6  2  3
  6  7  1  0
  6  8  1  0
  3  9  1  0
  9 10  1  0
 10 11  1  0
  9 12  2  3
 12 13  1  0
 13 14  2  3
 14 15  1  0
 14 16  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  2 21  1  0
  7 22  1  0
  7 23  1  0
  8 24  1  0
  8 25  1  0
 10 26  1  0
 10 27  1  0
 11 28  1  0
 11 29  1  0
 11 30  1  0
 15 31  1  0
 15 32  1  0
 16 33  1  0
 16 34  1  0
M  END

HEADER    PROTEIN                                 10-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-21         0                                  
HETATM    1  C   UNK     0       2.310   4.001   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.850   4.001   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.620   2.667   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0       6.160   2.667   0.000  0.00  0.00           N+0
HETATM    5  N   UNK     0       6.930   4.001   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       8.470   4.001   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       9.240   5.335   0.000  0.00  0.00           N+0
HETATM    8  N   UNK     0       9.240   2.667   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       3.850   1.334   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       2.310   1.334   0.000  0.00  0.00           N+0
HETATM   11  N   UNK     0       1.540   0.000   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      -0.770  -1.334   0.000  0.00  0.00           N+0
HETATM   14  N   UNK     0      -0.770   1.334   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       4.620   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.850  -1.334   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    3   10   15                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15    9   16                                                       
CONECT   16   15                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   30    0
END

COMPND    HMDB0244416
HETATM    1  C1  UNL     1       2.156  -1.766  -1.305  1.00  0.00           C  
HETATM    2  C2  UNL     1       0.732  -1.366  -1.061  1.00  0.00           C  
HETATM    3  C3  UNL     1       0.585  -0.256  -0.099  1.00  0.00           C  
HETATM    4  N1  UNL     1       1.525   0.350   0.502  1.00  0.00           N  
HETATM    5  N2  UNL     1       2.829   0.060   0.349  1.00  0.00           N  
HETATM    6  C4  UNL     1       3.863   0.144   1.039  1.00  0.00           C  
HETATM    7  N3  UNL     1       5.097  -0.288   0.490  1.00  0.00           N  
HETATM    8  N4  UNL     1       3.810   0.674   2.355  1.00  0.00           N  
HETATM    9  C5  UNL     1      -0.814   0.194   0.199  1.00  0.00           C  
HETATM   10  C6  UNL     1      -1.031   1.271   1.169  1.00  0.00           C  
HETATM   11  C7  UNL     1      -2.477   1.604   1.336  1.00  0.00           C  
HETATM   12  N5  UNL     1      -1.712  -0.404  -0.407  1.00  0.00           N  
HETATM   13  N6  UNL     1      -3.055  -0.224  -0.349  1.00  0.00           N  
HETATM   14  C8  UNL     1      -3.717  -0.084  -1.447  1.00  0.00           C  
HETATM   15  N7  UNL     1      -3.024  -0.121  -2.678  1.00  0.00           N  
HETATM   16  N8  UNL     1      -5.108   0.105  -1.389  1.00  0.00           N  
HETATM   17  H1  UNL     1       2.771  -0.977  -1.775  1.00  0.00           H  
HETATM   18  H2  UNL     1       2.127  -2.595  -2.076  1.00  0.00           H  
HETATM   19  H3  UNL     1       2.646  -2.171  -0.396  1.00  0.00           H  
HETATM   20  H4  UNL     1       0.235  -2.265  -0.597  1.00  0.00           H  
HETATM   21  H5  UNL     1       0.253  -1.145  -2.037  1.00  0.00           H  
HETATM   22  H6  UNL     1       5.394  -1.274   0.575  1.00  0.00           H  
HETATM   23  H7  UNL     1       5.701   0.395   0.001  1.00  0.00           H  
HETATM   24  H8  UNL     1       4.248   1.583   2.616  1.00  0.00           H  
HETATM   25  H9  UNL     1       3.302   0.103   3.067  1.00  0.00           H  
HETATM   26  H10 UNL     1      -0.551   1.038   2.154  1.00  0.00           H  
HETATM   27  H11 UNL     1      -0.500   2.180   0.779  1.00  0.00           H  
HETATM   28  H12 UNL     1      -2.949   1.951   0.393  1.00  0.00           H  
HETATM   29  H13 UNL     1      -2.548   2.439   2.105  1.00  0.00           H  
HETATM   30  H14 UNL     1      -3.033   0.758   1.759  1.00  0.00           H  
HETATM   31  H15 UNL     1      -3.506  -0.324  -3.602  1.00  0.00           H  
HETATM   32  H16 UNL     1      -1.977   0.053  -2.721  1.00  0.00           H  
HETATM   33  H17 UNL     1      -5.713   0.013  -2.228  1.00  0.00           H  
HETATM   34  H18 UNL     1      -5.561   0.343  -0.487  1.00  0.00           H  
CONECT    1    2   17   18   19
CONECT    2    3   20   21
CONECT    3    4    4    9
CONECT    4    5
CONECT    5    6    6
CONECT    6    7    8
CONECT    7   22   23
CONECT    8   24   25
CONECT    9   10   12   12
CONECT   10   11   26   27
CONECT   11   28   29   30
CONECT   12   13
CONECT   13   14   14
CONECT   14   15   16
CONECT   15   31   32
CONECT   16   33   34
END

HMDB0244416
     RDKit          3D
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guani...
 34 33  0  0  0  0  0  0  0  0999 V2000
    2.1561   -1.7660   -1.3045 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7323   -1.3660   -1.0609 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5851   -0.2558   -0.0989 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5255    0.3498    0.5023 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8288    0.0603    0.3493 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8630    0.1445    1.0392 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0970   -0.2879    0.4905 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8103    0.6741    2.3550 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8145    0.1939    0.1991 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0310    1.2712    1.1695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4768    1.6043    1.3355 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7117   -0.4037   -0.4068 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0552   -0.2244   -0.3494 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7168   -0.0836   -1.4475 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0236   -0.1214   -2.6782 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1082    0.1046   -1.3891 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7712   -0.9768   -1.7753 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1274   -2.5952   -2.0756 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6456   -2.1709   -0.3960 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2349   -2.2645   -0.5972 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2526   -1.1450   -2.0372 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3939   -1.2739    0.5746 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7011    0.3945    0.0011 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2481    1.5831    2.6155 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3021    0.1034    3.0674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5514    1.0375    2.1540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5000    2.1804    0.7785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9488    1.9511    0.3930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5480    2.4387    2.1050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0334    0.7582    1.7593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5058   -0.3241   -3.6017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9767    0.0535   -2.7210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7126    0.0133   -2.2279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5607    0.3429   -0.4874 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  3
  4  5  1  0
  5  6  2  3
  6  7  1  0
  6  8  1  0
  3  9  1  0
  9 10  1  0
 10 11  1  0
  9 12  2  3
 12 13  1  0
 13 14  2  3
 14 15  1  0
 14 16  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  2 21  1  0
  7 22  1  0
  7 23  1  0
  8 24  1  0
  8 25  1  0
 10 26  1  0
 10 27  1  0
 11 28  1  0
 11 29  1  0
 11 30  1  0
 15 31  1  0
 15 32  1  0
 16 33  1  0
 16 34  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
DEGBG	HMDB

Chemical Formula

C₈H₁₈N₈

Average Molecular Weight

226.288

Monoisotopic Molecular Weight

226.165442612

IUPAC Name

N''-[(4-{[(diaminomethylidene)amino]imino}hexan-3-ylidene)amino]guanidine

Traditional Name

N''-[(4-{[(diaminomethylidene)amino]imino}hexan-3-ylidene)amino]guanidine

CAS Registry Number

Not Available

SMILES

CCC(=NN=C(N)N)C(CC)=NN=C(N)N

InChI Identifier

InChI=1S/C8H18N8/c1-3-5(13-15-7(9)10)6(4-2)14-16-8(11)12/h3-4H2,1-2H3,(H4,9,10,15)(H4,11,12,16)

InChI Key

HXWLLFLQUZOBFF-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as guanidines. Guanidines are compounds containing a guanidine moiety, with the general structure (R1R2N)(R3R4N)C=N-R5.

Kingdom

Organic compounds

Super Class

Organic nitrogen compounds

Class

Organonitrogen compounds

Sub Class

Guanidines

Direct Parent

Guanidines

Alternative Parents

Substituents

Guanidine
Organopnictogen compound
Hydrocarbon derivative
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Source

Exogenous

Exogenous (PMID: 31557052)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	1.54	ALOGPS
logP	-0.56	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	18.87	ChemAxon
pKa (Strongest Basic)	7.47	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	153.52 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	62.6 m³·mol⁻¹	ChemAxon
Polarizability	24.18 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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]+	155.353	30932474
DeepCCS	[M-H]-	152.995	30932474
DeepCCS	[M-2H]-	186.511	30932474
DeepCCS	[M+Na]+	161.478	30932474

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine	CCC(=NN=C(N)N)C(CC)=NN=C(N)N	2984.8	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine	CCC(=NN=C(N)N)C(CC)=NN=C(N)N	1904.9	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine	CCC(=NN=C(N)N)C(CC)=NN=C(N)N	3211.7	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,1TMS,isomer #1	CCC(=NN=C(N)N)C(CC)=NN=C(N)N[Si](C)(C)C	2515.1	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,1TMS,isomer #1	CCC(=NN=C(N)N)C(CC)=NN=C(N)N[Si](C)(C)C	2146.9	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,1TMS,isomer #1	CCC(=NN=C(N)N)C(CC)=NN=C(N)N[Si](C)(C)C	5317.1	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,2TMS,isomer #1	CCC(=NN=C(N)N[Si](C)(C)C)C(CC)=NN=C(N)N[Si](C)(C)C	2470.8	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,2TMS,isomer #1	CCC(=NN=C(N)N[Si](C)(C)C)C(CC)=NN=C(N)N[Si](C)(C)C	2134.2	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,2TMS,isomer #1	CCC(=NN=C(N)N[Si](C)(C)C)C(CC)=NN=C(N)N[Si](C)(C)C	5402.6	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,2TMS,isomer #2	CCC(=NN=C(N)N)C(CC)=NN=C(N[Si](C)(C)C)N[Si](C)(C)C	2556.2	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,2TMS,isomer #2	CCC(=NN=C(N)N)C(CC)=NN=C(N[Si](C)(C)C)N[Si](C)(C)C	2070.3	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,2TMS,isomer #2	CCC(=NN=C(N)N)C(CC)=NN=C(N[Si](C)(C)C)N[Si](C)(C)C	5418.7	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,2TMS,isomer #3	CCC(=NN=C(N)N)C(CC)=NN=C(N)N([Si](C)(C)C)[Si](C)(C)C	2427.2	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,2TMS,isomer #3	CCC(=NN=C(N)N)C(CC)=NN=C(N)N([Si](C)(C)C)[Si](C)(C)C	2152.1	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,2TMS,isomer #3	CCC(=NN=C(N)N)C(CC)=NN=C(N)N([Si](C)(C)C)[Si](C)(C)C	5413.5	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,3TMS,isomer #1	CCC(=NN=C(N)N[Si](C)(C)C)C(CC)=NN=C(N[Si](C)(C)C)N[Si](C)(C)C	2510.0	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,3TMS,isomer #1	CCC(=NN=C(N)N[Si](C)(C)C)C(CC)=NN=C(N[Si](C)(C)C)N[Si](C)(C)C	2022.4	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,3TMS,isomer #1	CCC(=NN=C(N)N[Si](C)(C)C)C(CC)=NN=C(N[Si](C)(C)C)N[Si](C)(C)C	5466.0	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,3TMS,isomer #2	CCC(=NN=C(N)N[Si](C)(C)C)C(CC)=NN=C(N)N([Si](C)(C)C)[Si](C)(C)C	2492.9	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,3TMS,isomer #2	CCC(=NN=C(N)N[Si](C)(C)C)C(CC)=NN=C(N)N([Si](C)(C)C)[Si](C)(C)C	2125.8	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,3TMS,isomer #2	CCC(=NN=C(N)N[Si](C)(C)C)C(CC)=NN=C(N)N([Si](C)(C)C)[Si](C)(C)C	5440.8	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,3TMS,isomer #3	CCC(=NN=C(N)N)C(CC)=NN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2478.9	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,3TMS,isomer #3	CCC(=NN=C(N)N)C(CC)=NN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2085.7	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,3TMS,isomer #3	CCC(=NN=C(N)N)C(CC)=NN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	5284.0	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TMS,isomer #1	CCC(=NN=C(N[Si](C)(C)C)N[Si](C)(C)C)C(CC)=NN=C(N[Si](C)(C)C)N[Si](C)(C)C	2470.3	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TMS,isomer #1	CCC(=NN=C(N[Si](C)(C)C)N[Si](C)(C)C)C(CC)=NN=C(N[Si](C)(C)C)N[Si](C)(C)C	2048.1	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TMS,isomer #1	CCC(=NN=C(N[Si](C)(C)C)N[Si](C)(C)C)C(CC)=NN=C(N[Si](C)(C)C)N[Si](C)(C)C	5434.3	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TMS,isomer #2	CCC(=NN=C(N[Si](C)(C)C)N[Si](C)(C)C)C(CC)=NN=C(N)N([Si](C)(C)C)[Si](C)(C)C	2556.5	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TMS,isomer #2	CCC(=NN=C(N[Si](C)(C)C)N[Si](C)(C)C)C(CC)=NN=C(N)N([Si](C)(C)C)[Si](C)(C)C	2077.8	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TMS,isomer #2	CCC(=NN=C(N[Si](C)(C)C)N[Si](C)(C)C)C(CC)=NN=C(N)N([Si](C)(C)C)[Si](C)(C)C	5352.9	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TMS,isomer #3	CCC(=NN=C(N)N[Si](C)(C)C)C(CC)=NN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2503.2	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TMS,isomer #3	CCC(=NN=C(N)N[Si](C)(C)C)C(CC)=NN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2085.7	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TMS,isomer #3	CCC(=NN=C(N)N[Si](C)(C)C)C(CC)=NN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	5225.5	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TMS,isomer #4	CCC(=NN=C(N)N([Si](C)(C)C)[Si](C)(C)C)C(CC)=NN=C(N)N([Si](C)(C)C)[Si](C)(C)C	2609.3	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TMS,isomer #4	CCC(=NN=C(N)N([Si](C)(C)C)[Si](C)(C)C)C(CC)=NN=C(N)N([Si](C)(C)C)[Si](C)(C)C	2180.9	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TMS,isomer #4	CCC(=NN=C(N)N([Si](C)(C)C)[Si](C)(C)C)C(CC)=NN=C(N)N([Si](C)(C)C)[Si](C)(C)C	5407.5	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TMS,isomer #5	CCC(=NN=C(N)N)C(CC)=NN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2459.6	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TMS,isomer #5	CCC(=NN=C(N)N)C(CC)=NN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2244.4	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TMS,isomer #5	CCC(=NN=C(N)N)C(CC)=NN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	5004.6	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,5TMS,isomer #1	CCC(=NN=C(N[Si](C)(C)C)N[Si](C)(C)C)C(CC)=NN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2568.7	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,5TMS,isomer #1	CCC(=NN=C(N[Si](C)(C)C)N[Si](C)(C)C)C(CC)=NN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2118.5	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,5TMS,isomer #1	CCC(=NN=C(N[Si](C)(C)C)N[Si](C)(C)C)C(CC)=NN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	5099.1	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,5TMS,isomer #2	CCC(=NN=C(N)N([Si](C)(C)C)[Si](C)(C)C)C(CC)=NN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2635.8	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,5TMS,isomer #2	CCC(=NN=C(N)N([Si](C)(C)C)[Si](C)(C)C)C(CC)=NN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2186.2	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,5TMS,isomer #2	CCC(=NN=C(N)N([Si](C)(C)C)[Si](C)(C)C)C(CC)=NN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	5099.4	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,5TMS,isomer #3	CCC(=NN=C(N)N[Si](C)(C)C)C(CC)=NN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2573.1	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,5TMS,isomer #3	CCC(=NN=C(N)N[Si](C)(C)C)C(CC)=NN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2223.7	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,5TMS,isomer #3	CCC(=NN=C(N)N[Si](C)(C)C)C(CC)=NN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	4909.7	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,6TMS,isomer #1	CCC(=NN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC)=NN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2633.4	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,6TMS,isomer #1	CCC(=NN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC)=NN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2228.0	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,6TMS,isomer #1	CCC(=NN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC)=NN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	4769.9	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,6TMS,isomer #2	CCC(=NN=C(N[Si](C)(C)C)N[Si](C)(C)C)C(CC)=NN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2683.1	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,6TMS,isomer #2	CCC(=NN=C(N[Si](C)(C)C)N[Si](C)(C)C)C(CC)=NN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2251.2	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,6TMS,isomer #2	CCC(=NN=C(N[Si](C)(C)C)N[Si](C)(C)C)C(CC)=NN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	4656.2	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,6TMS,isomer #3	CCC(=NN=C(N)N([Si](C)(C)C)[Si](C)(C)C)C(CC)=NN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2749.0	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,6TMS,isomer #3	CCC(=NN=C(N)N([Si](C)(C)C)[Si](C)(C)C)C(CC)=NN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2332.2	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,6TMS,isomer #3	CCC(=NN=C(N)N([Si](C)(C)C)[Si](C)(C)C)C(CC)=NN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	4779.4	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,7TMS,isomer #1	CCC(=NN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC)=NN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2756.8	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,7TMS,isomer #1	CCC(=NN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC)=NN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2372.2	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,7TMS,isomer #1	CCC(=NN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC)=NN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	4202.1	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,8TMS,isomer #1	CCC(=NN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC)=NN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2909.5	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,8TMS,isomer #1	CCC(=NN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC)=NN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2522.6	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,8TMS,isomer #1	CCC(=NN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC)=NN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3465.0	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,1TBDMS,isomer #1	CCC(=NN=C(N)N)C(CC)=NN=C(N)N[Si](C)(C)C(C)(C)C	2626.9	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,1TBDMS,isomer #1	CCC(=NN=C(N)N)C(CC)=NN=C(N)N[Si](C)(C)C(C)(C)C	2278.6	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,1TBDMS,isomer #1	CCC(=NN=C(N)N)C(CC)=NN=C(N)N[Si](C)(C)C(C)(C)C	5426.1	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,2TBDMS,isomer #1	CCC(=NN=C(N)N[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N)N[Si](C)(C)C(C)(C)C	2753.1	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,2TBDMS,isomer #1	CCC(=NN=C(N)N[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N)N[Si](C)(C)C(C)(C)C	2419.2	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,2TBDMS,isomer #1	CCC(=NN=C(N)N[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N)N[Si](C)(C)C(C)(C)C	5551.4	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,2TBDMS,isomer #2	CCC(=NN=C(N)N)C(CC)=NN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C	2804.0	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,2TBDMS,isomer #2	CCC(=NN=C(N)N)C(CC)=NN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C	2346.6	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,2TBDMS,isomer #2	CCC(=NN=C(N)N)C(CC)=NN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C	5469.9	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,2TBDMS,isomer #3	CCC(=NN=C(N)N)C(CC)=NN=C(N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2711.9	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,2TBDMS,isomer #3	CCC(=NN=C(N)N)C(CC)=NN=C(N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2508.9	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,2TBDMS,isomer #3	CCC(=NN=C(N)N)C(CC)=NN=C(N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5578.6	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,3TBDMS,isomer #1	CCC(=NN=C(N)N[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C	2937.1	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,3TBDMS,isomer #1	CCC(=NN=C(N)N[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C	2436.8	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,3TBDMS,isomer #1	CCC(=NN=C(N)N[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C	5529.7	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,3TBDMS,isomer #2	CCC(=NN=C(N)N[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2887.9	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,3TBDMS,isomer #2	CCC(=NN=C(N)N[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2599.5	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,3TBDMS,isomer #2	CCC(=NN=C(N)N[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5583.7	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,3TBDMS,isomer #3	CCC(=NN=C(N)N)C(CC)=NN=C(N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2839.8	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,3TBDMS,isomer #3	CCC(=NN=C(N)N)C(CC)=NN=C(N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2633.3	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,3TBDMS,isomer #3	CCC(=NN=C(N)N)C(CC)=NN=C(N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5319.1	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TBDMS,isomer #1	CCC(=NN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C	3094.4	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TBDMS,isomer #1	CCC(=NN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C	2618.3	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TBDMS,isomer #1	CCC(=NN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C	5418.2	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TBDMS,isomer #2	CCC(=NN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3108.1	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TBDMS,isomer #2	CCC(=NN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2716.8	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TBDMS,isomer #2	CCC(=NN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5464.6	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TBDMS,isomer #3	CCC(=NN=C(N)N[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3021.4	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TBDMS,isomer #3	CCC(=NN=C(N)N[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2729.9	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TBDMS,isomer #3	CCC(=NN=C(N)N[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5337.2	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TBDMS,isomer #4	CCC(=NN=C(N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3148.0	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TBDMS,isomer #4	CCC(=NN=C(N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2838.4	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TBDMS,isomer #4	CCC(=NN=C(N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5604.5	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TBDMS,isomer #5	CCC(=NN=C(N)N)C(CC)=NN=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3039.7	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TBDMS,isomer #5	CCC(=NN=C(N)N)C(CC)=NN=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2888.3	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,4TBDMS,isomer #5	CCC(=NN=C(N)N)C(CC)=NN=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5091.2	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,5TBDMS,isomer #1	CCC(=NN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3264.5	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,5TBDMS,isomer #1	CCC(=NN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2927.4	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,5TBDMS,isomer #1	CCC(=NN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5132.3	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,5TBDMS,isomer #2	CCC(=NN=C(N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3313.7	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,5TBDMS,isomer #2	CCC(=NN=C(N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3017.6	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,5TBDMS,isomer #2	CCC(=NN=C(N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5245.3	Standard polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,5TBDMS,isomer #3	CCC(=NN=C(N)N[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3289.7	Semi standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,5TBDMS,isomer #3	CCC(=NN=C(N)N[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3015.2	Standard non polar	33892256
2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine,5TBDMS,isomer #3	CCC(=NN=C(N)N[Si](C)(C)C(C)(C)C)C(CC)=NN=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5022.2	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine GC-MS (Non-derivatized) - 70eV, Positive	splash10-03dm-9810000000-aa9ad71a8fdb75def36d	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine 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 - 2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine 10V, Positive-QTOF	splash10-004i-0190000000-f72451dc95978537c967	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine 20V, Positive-QTOF	splash10-066r-1910000000-441fc14c86669864a5d1	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine 40V, Positive-QTOF	splash10-03l1-9400000000-8f433201fa6cd9f59058	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine 10V, Negative-QTOF	splash10-002f-8090000000-19d6124d67c66a979f32	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine 20V, Negative-QTOF	splash10-0a4l-9200000000-c282059f67e78b2fe983	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine 40V, Negative-QTOF	splash10-0a4i-9800000000-4e94cc8ba4bf4a8d881d	2021-10-12	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

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

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

109337

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

122633

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

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

Showing metabocard for 2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine (HMDB0244416)

MOL for HMDB0244416 (2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine)

3D MOL for HMDB0244416 (2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine)

3D SDF for HMDB0244416 (2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine)

3D-SDF for HMDB0244416 (2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine)

PDB for HMDB0244416 (2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine)

3D PDB for HMDB0244416 (2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine)

SMILES for HMDB0244416 (2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine)

INCHI for HMDB0244416 (2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine)

Structure for HMDB0244416 (2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine)

3D Structure for HMDB0244416 (2-[(Z)-[(4Z)-4-(Diaminomethylidenehydrazinylidene)hexan-3-ylidene]amino]guanidine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra