NP-MRD: Showing NP-Card for Elaiomycin F (NP0011123)

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Record Information

Version

2.0

Created at

2021-01-05 20:55:27 UTC

Updated at

2021-07-15 17:08:01 UTC

NP-MRD ID

NP0011123

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Elaiomycin F

Provided By

NPAtlas

Description

[(2S,3S)-3-hydroxy-1-methoxybutan-2-yl](octyl-oxo-λ⁵-azanylidene)amine belongs to the class of organic compounds known as azoxy compounds. These are organic compounds sharing a common functional group with the general structure RN=N+(O-)R. Elaiomycin F is found in Streptomyces. Elaiomycin F was first documented in 2012 (PMID: 23013356). Based on a literature review very few articles have been published on [(2S,3S)-3-hydroxy-1-methoxybutan-2-yl](octyl-oxo-λ⁵-azanylidene)amine.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242107443D          

 46 45  0  0  0  0            999 V2000
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M  CHG  2   9   1  10  -1
M  END

     RDKit          3D

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M  END


  Mrv1652306242107443D          

 46 45  0  0  0  0            999 V2000
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M  CHG  2   9   1  10  -1
M  END
> <DATABASE_ID>
NP0011123

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@@]([H])(C([H])([H])[H])[C@@]([H])(\N=[N+](/[O-])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H])C([H])([H])OC([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C13H28N2O3/c1-4-5-6-7-8-9-10-15(17)14-13(11-18-3)12(2)16/h12-13,16H,4-11H2,1-3H3/b15-14-/t12-,13-/m0/s1

> <INCHI_KEY>
WGHHPQYWXONJQE-ULNCKAKWSA-N

> <FORMULA>
C13H28N2O3

> <MOLECULAR_WEIGHT>
260.378

> <EXACT_MASS>
260.20999277

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
30.87868214612185

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(Z)-2-[(2S,3S)-3-hydroxy-1-methoxybutan-2-yl]-1-octyldiazen-1-ium-1-olate

> <ALOGPS_LOGP>
2.69

> <JCHEM_LOGP>
0.6064446261949208

> <ALOGPS_LOGS>
-3.41

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.463023537417065

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.719763691666174

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0607612183780626

> <JCHEM_POLAR_SURFACE_AREA>
67.89

> <JCHEM_REFRACTIVITY>
72.23960000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.02e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(Z)-2-[(2S,3S)-3-hydroxy-1-methoxybutan-2-yl]-1-octyldiazen-1-ium-1-olate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 46 45  0  0  0  0  0  0  0  0999 V2000
   -6.3890   -1.6831   -1.1366 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2937   -0.6504   -1.3037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3958   -0.7366   -0.1064 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2619    0.2328   -0.1366 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4486    0.0183    1.1429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2612    0.9881    1.1764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5183    0.7155    2.4547 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6811    1.5628    2.6818 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7162    1.4675    1.7037 N   0  0  0  0  0  4  0  0  0  0  0  0
    2.8304    2.2817    1.9215 O   0  0  0  0  0  1  0  0  0  0  0  0
    1.7038    0.7157    0.6771 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8325    0.7468   -0.2032 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0493    0.0974    0.4083 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0805    0.1944   -0.5524 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1941   -0.3992    0.0055 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5529    0.0930   -1.5367 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2674   -1.3839   -1.3812 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7338    0.1946   -2.2920 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2337   -1.5276   -1.8375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7191   -1.6114   -0.0714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9131   -2.6767   -1.2589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7538    0.3496   -1.4282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7344   -0.8651   -2.2464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0061   -0.5242    0.7899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9710   -1.7619   -0.0838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5583    0.0190   -0.9755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5632    1.2824   -0.2444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1052   -1.0253    1.2204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0472    0.2395    2.0488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6556    2.0164    1.1444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6211    0.8335    0.2940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2380    0.9484    3.2891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3086   -0.3714    2.5278 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1055    1.2931    3.6789 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3490    2.6217    2.7763 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0560    1.8215   -0.4184 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3790    0.6366    1.3111 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8034   -0.9577    0.6178 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0270   -1.4755    0.2641 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4652    0.1696    0.9229 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0834   -0.3036   -0.6690 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7614    0.5848   -2.1118 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6256   -1.5606   -0.4876 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7499   -1.7647   -2.2867 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1910   -1.9887   -1.2616 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7582    1.1430   -2.6045 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 12 16  1  0
 16 17  1  0
 16 18  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  0
  2 23  1  0
  3 24  1  0
  3 25  1  0
  4 26  1  0
  4 27  1  0
  5 28  1  0
  5 29  1  0
  6 30  1  0
  6 31  1  0
  7 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
 12 36  1  6
 13 37  1  0
 13 38  1  0
 15 39  1  0
 15 40  1  0
 15 41  1  0
 16 42  1  6
 17 43  1  0
 17 44  1  0
 17 45  1  0
 18 46  1  0
M  CHG  2   9   1  10  -1
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0      -6.389  -1.683  -1.137  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.294  -0.650  -1.304  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.396  -0.737  -0.106  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.262   0.233  -0.137  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.449   0.018   1.143  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.261   0.988   1.176  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.518   0.716   2.455  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.681   1.563   2.682  0.00  0.00           C+0
HETATM    9  N   UNK     0       1.716   1.468   1.704  0.00  0.00           N+1
HETATM   10  O   UNK     0       2.830   2.282   1.922  0.00  0.00           O-1
HETATM   11  N   UNK     0       1.704   0.716   0.677  0.00  0.00           N+0
HETATM   12  C   UNK     0       2.833   0.747  -0.203  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.049   0.097   0.408  0.00  0.00           C+0
HETATM   14  O   UNK     0       5.080   0.194  -0.552  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.194  -0.399   0.006  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.553   0.093  -1.537  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.267  -1.384  -1.381  0.00  0.00           C+0
HETATM   18  O   UNK     0       3.734   0.195  -2.292  0.00  0.00           O+0
HETATM   19  H   UNK     0      -7.234  -1.528  -1.837  0.00  0.00           H+0
HETATM   20  H   UNK     0      -6.719  -1.611  -0.071  0.00  0.00           H+0
HETATM   21  H   UNK     0      -5.913  -2.677  -1.259  0.00  0.00           H+0
HETATM   22  H   UNK     0      -5.754   0.350  -1.428  0.00  0.00           H+0
HETATM   23  H   UNK     0      -4.734  -0.865  -2.246  0.00  0.00           H+0
HETATM   24  H   UNK     0      -5.006  -0.524   0.790  0.00  0.00           H+0
HETATM   25  H   UNK     0      -3.971  -1.762  -0.084  0.00  0.00           H+0
HETATM   26  H   UNK     0      -2.558   0.019  -0.976  0.00  0.00           H+0
HETATM   27  H   UNK     0      -3.563   1.282  -0.244  0.00  0.00           H+0
HETATM   28  H   UNK     0      -2.105  -1.025   1.220  0.00  0.00           H+0
HETATM   29  H   UNK     0      -3.047   0.240   2.049  0.00  0.00           H+0
HETATM   30  H   UNK     0      -1.656   2.016   1.144  0.00  0.00           H+0
HETATM   31  H   UNK     0      -0.621   0.834   0.294  0.00  0.00           H+0
HETATM   32  H   UNK     0      -1.238   0.948   3.289  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.309  -0.371   2.528  0.00  0.00           H+0
HETATM   34  H   UNK     0       1.105   1.293   3.679  0.00  0.00           H+0
HETATM   35  H   UNK     0       0.349   2.622   2.776  0.00  0.00           H+0
HETATM   36  H   UNK     0       3.056   1.821  -0.418  0.00  0.00           H+0
HETATM   37  H   UNK     0       4.379   0.637   1.311  0.00  0.00           H+0
HETATM   38  H   UNK     0       3.803  -0.958   0.618  0.00  0.00           H+0
HETATM   39  H   UNK     0       6.027  -1.476   0.264  0.00  0.00           H+0
HETATM   40  H   UNK     0       6.465   0.170   0.923  0.00  0.00           H+0
HETATM   41  H   UNK     0       7.083  -0.304  -0.669  0.00  0.00           H+0
HETATM   42  H   UNK     0       1.761   0.585  -2.112  0.00  0.00           H+0
HETATM   43  H   UNK     0       1.626  -1.561  -0.488  0.00  0.00           H+0
HETATM   44  H   UNK     0       1.750  -1.765  -2.287  0.00  0.00           H+0
HETATM   45  H   UNK     0       3.191  -1.989  -1.262  0.00  0.00           H+0
HETATM   46  H   UNK     0       3.758   1.143  -2.604  0.00  0.00           H+0
CONECT    1    2   19   20   21                                             
CONECT    2    1    3   22   23                                             
CONECT    3    2    4   24   25                                             
CONECT    4    3    5   26   27                                             
CONECT    5    4    6   28   29                                             
CONECT    6    5    7   30   31                                             
CONECT    7    6    8   32   33                                             
CONECT    8    7    9   34   35                                             
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   16   36                                             
CONECT   13   12   14   37   38                                             
CONECT   14   13   15                                                       
CONECT   15   14   39   40   41                                             
CONECT   16   12   17   18   42                                             
CONECT   17   16   43   44   45                                             
CONECT   18   16   46                                                       
CONECT   19    1                                                            
CONECT   20    1                                                            
CONECT   21    1                                                            
CONECT   22    2                                                            
CONECT   23    2                                                            
CONECT   24    3                                                            
CONECT   25    3                                                            
CONECT   26    4                                                            
CONECT   27    4                                                            
CONECT   28    5                                                            
CONECT   29    5                                                            
CONECT   30    6                                                            
CONECT   31    6                                                            
CONECT   32    7                                                            
CONECT   33    7                                                            
CONECT   34    8                                                            
CONECT   35    8                                                            
CONECT   36   12                                                            
CONECT   37   13                                                            
CONECT   38   13                                                            
CONECT   39   15                                                            
CONECT   40   15                                                            
CONECT   41   15                                                            
CONECT   42   16                                                            
CONECT   43   17                                                            
CONECT   44   17                                                            
CONECT   45   17                                                            
CONECT   46   18                                                            
MASTER        0    0    0    0    0    0    0    0   46    0   90    0
END

RDKit          3D

46 45  0  0  0  0  0  0  0  0999 V2000
   -6.3890   -1.6831   -1.1366 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2937   -0.6504   -1.3037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3958   -0.7366   -0.1064 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2619    0.2328   -0.1366 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4486    0.0183    1.1429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2612    0.9881    1.1764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5183    0.7155    2.4547 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6811    1.5628    2.6818 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7162    1.4675    1.7037 N   0  0  0  0  0  4  0  0  0  0  0  0
    2.8304    2.2817    1.9215 O   0  0  0  0  0  1  0  0  0  0  0  0
    1.7038    0.7157    0.6771 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8325    0.7468   -0.2032 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0493    0.0974    0.4083 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0805    0.1944   -0.5524 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1941   -0.3992    0.0055 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5529    0.0930   -1.5367 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2674   -1.3839   -1.3812 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7338    0.1946   -2.2920 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2337   -1.5276   -1.8375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7191   -1.6114   -0.0714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9131   -2.6767   -1.2589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7538    0.3496   -1.4282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7344   -0.8651   -2.2464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0061   -0.5242    0.7899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9710   -1.7619   -0.0838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5583    0.0190   -0.9755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5632    1.2824   -0.2444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1052   -1.0253    1.2204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0472    0.2395    2.0488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6556    2.0164    1.1444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6211    0.8335    0.2940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2380    0.9484    3.2891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3086   -0.3714    2.5278 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1055    1.2931    3.6789 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3490    2.6217    2.7763 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0560    1.8215   -0.4184 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3790    0.6366    1.3111 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8034   -0.9577    0.6178 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0270   -1.4755    0.2641 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4652    0.1696    0.9229 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0834   -0.3036   -0.6690 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7614    0.5848   -2.1118 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6256   -1.5606   -0.4876 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7499   -1.7647   -2.2867 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1910   -1.9887   -1.2616 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7582    1.1430   -2.6045 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 12 16  1  0
 16 17  1  0
 16 18  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  0
  2 23  1  0
  3 24  1  0
  3 25  1  0
  4 26  1  0
  4 27  1  0
  5 28  1  0
  5 29  1  0
  6 30  1  0
  6 31  1  0
  7 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
 12 36  1  6
 13 37  1  0
 13 38  1  0
 15 39  1  0
 15 40  1  0
 15 41  1  0
 16 42  1  6
 17 43  1  0
 17 44  1  0
 17 45  1  0
 18 46  1  0
M  CHG  2   9   1  10  -1
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₃H₂₈N₂O₃

Average Mass

260.3780 Da

Monoisotopic Mass

260.20999 Da

IUPAC Name

(Z)-2-[(2S,3S)-3-hydroxy-1-methoxybutan-2-yl]-1-octyldiazen-1-ium-1-olate

Traditional Name

(Z)-2-[(2S,3S)-3-hydroxy-1-methoxybutan-2-yl]-1-octyldiazen-1-ium-1-olate

CAS Registry Number

Not Available

SMILES

CCCCCCCC\[N+]([O-])=N\[C@@H](COC)[C@H](C)O

InChI Identifier

InChI=1S/C13H28N2O3/c1-4-5-6-7-8-9-10-15(17)14-13(11-18-3)12(2)16/h12-13,16H,4-11H2,1-3H3/b15-14-/t12-,13-/m0/s1

InChI Key

WGHHPQYWXONJQE-ULNCKAKWSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Streptomyces	NPAtlas	23013356

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as azoxy compounds. These are organic compounds sharing a common functional group with the general structure RN=N+(O-)R.

Kingdom

Organic compounds

Super Class

Organic 1,3-dipolar compounds

Class

Allyl-type 1,3-dipolar organic compounds

Sub Class

Azoxy compounds

Direct Parent

Azoxy compounds

Alternative Parents

Substituents

Azoxy compound
Secondary alcohol
Ether
Dialkyl ether
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organic zwitterion
Organooxygen compound
Organonitrogen compound
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental 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

Predicted Properties

Property	Value	Source
logP	2.69	ALOGPS
logP	0.61	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	8.72	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	67.89 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	72.24 m³·mol⁻¹	ChemAxon
Polarizability	30.88 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA011788

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

28533909

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Ding L, Ndejouong Ble S, Maier A, Fiebig HH, Hertweck C: Elaiomycins D-F, antimicrobial and cytotoxic azoxides from Streptomyces sp. strain HKI0708. J Nat Prod. 2012 Oct 26;75(10):1729-34. doi: 10.1021/np300329m. Epub 2012 Sep 26. [PubMed:23013356 ]

Showing NP-Card for Elaiomycin F (NP0011123)

MOL for NP0011123 (Elaiomycin F)

3D MOL for NP0011123 (Elaiomycin F)

3D SDF for NP0011123 (Elaiomycin F)

3D-SDF for NP0011123 (Elaiomycin F)

PDB for NP0011123 (Elaiomycin F)

3D PDB for NP0011123 (Elaiomycin F)

SMILES for NP0011123 (Elaiomycin F)

INCHI for NP0011123 (Elaiomycin F)

Structure for NP0011123 (Elaiomycin F)

3D Structure for NP0011123 (Elaiomycin F)