NP-MRD: Showing NP-Card for oligomycin d (NP0247688)

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Record Information

Version

2.0

Created at

2022-09-07 09:37:38 UTC

Updated at

2022-09-07 09:37:38 UTC

NP-MRD ID

NP0247688

Secondary Accession Numbers

None

Natural Product Identification

Common Name

oligomycin d

Description

Oligomycin D, also known as rutamycin, belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members. oligomycin d is found in Kitasatospora aureofaciens. oligomycin d was first documented in 2013 (PMID: 23448552). Based on a literature review very few articles have been published on Oligomycin D (PMID: 29741854).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072211372D          

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M  END

     RDKit          3D

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    6.0104    1.7515    5.2685 H   0  0  0  0  0  0  0  0  0  0  0  0
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  6 64  1  0
  5 63  1  0
  4 62  1  0
 54124  1  1
 55125  1  0
 55126  1  0
 55127  1  0
M  END


  Mrv1652309072211372D          

 55 57  0  0  1  0            999 V2000
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    4.6961   -1.4808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8989   -1.6932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3164   -1.1091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5192   -1.3215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.1394   -0.9497    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -0.0257    0.2186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    1.7833    1.4400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5687    0.6434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.7951    2.4491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1631    1.0683    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9484    0.2717    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9603    1.2807    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1749    2.0773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5428    0.6966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3400    0.9090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9225    0.3248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7079   -0.4718    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7197    0.5372    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3023   -0.0469    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.0995    0.1655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6820   -0.4187    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.8967    0.3779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6938    0.5903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2764    0.0062    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.0736    0.2186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0618   -0.7904    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.6443   -1.3746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4415   -1.1622    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.6561   -0.3656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0241   -1.7463    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    7.4556   -2.2243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6584   -2.4367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0877   -0.8435    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2905   -1.0559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  6  0  0  0
 13 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 30 31  1  6  0  0  0
 30 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  6  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  1  0  0  0
 42 44  1  0  0  0  0
 44 45  1  1  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  1  6  0  0  0
 44 49  1  0  0  0  0
 39 49  1  1  0  0  0
 39 50  1  0  0  0  0
 51 50  1  6  0  0  0
 51 52  1  0  0  0  0
 52 53  1  0  0  0  0
  3 53  1  0  0  0  0
 51 54  1  0  0  0  0
 37 54  1  0  0  0  0
 54 55  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0247688

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H]1CC[C@H]2O[C@@]3(CC[C@@H](C)[C@@H](C[C@H](C)O)O3)C[C@@H](OC(=O)\C=C\[C@@H](C)[C@H](O)[C@@H](C)C(=O)[C@@H](C)[C@H](O)[C@@H](C)C(=O)[C@@](C)(O)[C@H](O)[C@@H](C)C\C=C\C=C\1)[C@H]2C

> <INCHI_IDENTIFIER>
InChI=1S/C44H72O11/c1-11-33-16-14-12-13-15-27(4)41(50)43(10,52)42(51)32(9)40(49)31(8)39(48)30(7)38(47)26(3)17-20-37(46)53-36-24-44(54-34(19-18-33)29(36)6)22-21-25(2)35(55-44)23-28(5)45/h12-14,16-17,20,25-36,38,40-41,45,47,49-50,52H,11,15,18-19,21-24H2,1-10H3/b13-12+,16-14+,20-17+/t25-,26-,27+,28+,29+,30-,31-,32-,33-,34-,35-,36-,38+,40+,41-,43+,44-/m1/s1

> <INCHI_KEY>
LVWVMRBMGDJZLM-WXPRFNGZSA-N

> <FORMULA>
C44H72O11

> <MOLECULAR_WEIGHT>
777.049

> <EXACT_MASS>
776.507463138

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
127

> <JCHEM_AVERAGE_POLARIZABILITY>
88.0653498783474

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,4E,5'R,6R,6'R,7S,8R,10S,11S,12R,14S,15R,16S,18E,20E,22S,25R,27S,29S)-22-ethyl-7,11,14,15-tetrahydroxy-6'-[(2S)-2-hydroxypropyl]-5',6,8,10,12,14,16,29-octamethyl-2,26-dioxaspiro[bicyclo[23.3.1]nonacosane-27,2'-oxane]-4,18,20-triene-3,9,13-trione

> <JCHEM_LOGP>
7.07347488633333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.70521013012052

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.26452980612247

> <JCHEM_PKA_STRONGEST_BASIC>
-2.545429960303193

> <JCHEM_POLAR_SURFACE_AREA>
180.04999999999998

> <JCHEM_REFRACTIVITY>
214.6046

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
rutamycin

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      12.028  -6.036   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.941  -4.945   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.342  -3.458   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.854  -3.855   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.766  -2.764   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.278  -3.161   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.191  -2.070   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.702  -2.467   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.615  -1.376   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.016   0.111   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.127  -1.773   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       1.726  -3.260   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       1.040  -0.682   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.355  -0.030   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       0.154  -1.943   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       1.440   0.805   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -0.048   0.408   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.353   1.895   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.135   1.499   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.753   3.382   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.334   4.472   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.241   3.779   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.642   5.266   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.329   2.688   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       2.928   1.201   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       4.817   3.085   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.218   4.572   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.904   1.994   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       5.504   0.507   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       7.392   2.391   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.793   3.878   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.480   1.300   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       9.968   1.697   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      11.055   0.606   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      10.655  -0.881   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      12.543   1.003   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      13.631  -0.088   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      15.119   0.309   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      16.206  -0.782   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      16.607   0.705   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      18.095   1.102   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      19.183   0.012   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      20.671   0.408   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      18.782  -1.475   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      19.869  -2.566   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      21.357  -2.169   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      21.758  -0.682   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      22.445  -3.260   0.000  0.00  0.00           O+0
HETATM   49  O   UNK     0      17.294  -1.872   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0      15.806  -2.269   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0      14.318  -2.665   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      13.917  -4.152   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      12.429  -4.549   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      13.230  -1.575   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      11.742  -1.971   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   53                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15   16                                             
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   13   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36   38   54                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40   49   50                                             
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   45   49                                                  
CONECT   45   44   46                                                       
CONECT   46   45   47   48                                                  
CONECT   47   46                                                            
CONECT   48   46                                                            
CONECT   49   44   39                                                       
CONECT   50   39   51                                                       
CONECT   51   50   52   54                                                  
CONECT   52   51   53                                                       
CONECT   53   52    3                                                       
CONECT   54   51   37   55                                                  
CONECT   55   54                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  114    0
END

View in JSmol

Synonyms

Value	Source
Rutamycin	Kegg

Chemical Formula

C₄₄H₇₂O₁₁

Average Mass

777.0490 Da

Monoisotopic Mass

776.50746 Da

IUPAC Name

(1R,4E,5'R,6R,6'R,7S,8R,10S,11S,12R,14S,15R,16S,18E,20E,22S,25R,27S,29S)-22-ethyl-7,11,14,15-tetrahydroxy-6'-[(2S)-2-hydroxypropyl]-5',6,8,10,12,14,16,29-octamethyl-2,26-dioxaspiro[bicyclo[23.3.1]nonacosane-27,2'-oxane]-4,18,20-triene-3,9,13-trione

Traditional Name

rutamycin

CAS Registry Number

Not Available

SMILES

CC[C@H]1CC[C@H]2O[C@@]3(CC[C@@H](C)[C@@H](C[C@H](C)O)O3)C[C@@H](OC(=O)\C=C\[C@@H](C)[C@H](O)[C@@H](C)C(=O)[C@@H](C)[C@H](O)[C@@H](C)C(=O)[C@@](C)(O)[C@H](O)[C@@H](C)C\C=C\C=C\1)[C@H]2C

InChI Identifier

InChI=1S/C44H72O11/c1-11-33-16-14-12-13-15-27(4)41(50)43(10,52)42(51)32(9)40(49)31(8)39(48)30(7)38(47)26(3)17-20-37(46)53-36-24-44(54-34(19-18-33)29(36)6)22-21-25(2)35(55-44)23-28(5)45/h12-14,16-17,20,25-36,38,40-41,45,47,49-50,52H,11,15,18-19,21-24H2,1-10H3/b13-12+,16-14+,20-17+/t25-,26-,27+,28+,29+,30-,31-,32-,33-,34-,35-,36-,38+,40+,41-,43+,44-/m1/s1

InChI Key

LVWVMRBMGDJZLM-WXPRFNGZSA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Kitasatospora aureofaciens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Sub Class

Not Available

Direct Parent

Macrolides and analogues

Alternative Parents

Substituents

Macrolide
Ketal
Acyloin
Oxane
Tertiary alcohol
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Cyclic ketone
Secondary alcohol
Carboxylic acid ester
Lactone
Ketone
Oxacycle
Acetal
Polyol
Organoheterocyclic compound
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Organic oxygen compound
Organic oxide
Organooxygen compound
Carbonyl group
Alcohol
Hydrocarbon derivative
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

macrolide (CHEBI:7753 )
oligomycin (CHEBI:7753 )

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	7.07	ChemAxon
pKa (Strongest Acidic)	12.26	ChemAxon
pKa (Strongest Basic)	-2.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	180.05 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	214.6 m³·mol⁻¹	ChemAxon
Polarizability	88.07 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

16735943

KEGG Compound ID

C11314

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5281902

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Duan X, Zhao F, Yan X, Xue Q, Li X, Wen B, Jia L, Yan H: [Construction of SPA7074-deficient mutant of biocontrol strain Streptomyces pactum Act12 and characterization of its secondary metabolites]. Wei Sheng Wu Xue Bao. 2016 Dec 4;56(12):1883-91. [PubMed:29741854 ]
Starovoytova AN, Sorokin MI, Sokolov SS, Severin FF, Knorre DA: Mitochondrial signaling in Saccharomyces cerevisiae pseudohyphae formation induced by butanol. FEMS Yeast Res. 2013 Jun;13(4):367-74. doi: 10.1111/1567-1364.12039. Epub 2013 Mar 19. [PubMed:23448552 ]
LOTUS database [Link]

Showing NP-Card for oligomycin d (NP0247688)

MOL for NP0247688 (oligomycin d)

3D MOL for NP0247688 (oligomycin d)

3D SDF for NP0247688 (oligomycin d)

3D-SDF for NP0247688 (oligomycin d)

PDB for NP0247688 (oligomycin d)

3D PDB for NP0247688 (oligomycin d)

SMILES for NP0247688 (oligomycin d)

INCHI for NP0247688 (oligomycin d)

Structure for NP0247688 (oligomycin d)

3D Structure for NP0247688 (oligomycin d)