NP-MRD: Showing NP-Card for Epohelmin A (NP0005603)

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Record Information

Version

2.0

Created at

2020-12-09 02:48:47 UTC

Updated at

2021-07-15 16:52:28 UTC

NP-MRD ID

NP0005603

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Epohelmin A

Provided By

NPAtlas

Description

(E)-1-[(1R,3R,8R)-9-Oxa-4-azabicyclo[6.1.0]Nonane-3-yl]-5-undecene-4-one belongs to the class of organic compounds known as enones. Enones are compounds containing the enone functional group, with the structure RC(=O)CR'. Epohelmin A is found in bacterium. Epohelmin A was first documented in 2004 (PMID: 15580956). Based on a literature review very few articles have been published on (E)-1-[(1R,3R,8R)-9-Oxa-4-azabicyclo[6.1.0]Nonane-3-yl]-5-undecene-4-one.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118213D          

 52 53  0  0  0  0            999 V2000
    7.0970    0.9260    1.2006 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6492   -0.0458    0.1144 C   0  0  1  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652306242118213D          

 52 53  0  0  0  0            999 V2000
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   -5.2418   -1.0215    1.8547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5445    0.4602    0.4751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5628    0.9961    1.8636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2098    1.4000   -1.1010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1359    2.5604    0.2357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9578    1.1057   -1.0568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8913    2.4619    0.0739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4350    1.1177    1.8474 H   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  1  0  0  0  0
  4  5  1  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  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 13  1  0  0  0  0
 17 15  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  2 25  1  0  0  0  0
  2 26  1  0  0  0  0
  3 27  1  0  0  0  0
  3 28  1  0  0  0  0
  4 29  1  0  0  0  0
  4 30  1  0  0  0  0
  5 31  1  0  0  0  0
  5 32  1  0  0  0  0
  6 33  1  0  0  0  0
  7 34  1  0  0  0  0
 10 35  1  0  0  0  0
 10 36  1  0  0  0  0
 11 37  1  0  0  0  0
 11 38  1  0  0  0  0
 12 39  1  0  0  0  0
 12 40  1  0  0  0  0
 13 41  1  1  0  0  0
 14 42  1  0  0  0  0
 14 43  1  0  0  0  0
 15 44  1  6  0  0  0
 17 45  1  1  0  0  0
 18 46  1  0  0  0  0
 18 47  1  0  0  0  0
 19 48  1  0  0  0  0
 19 49  1  0  0  0  0
 20 50  1  0  0  0  0
 20 51  1  0  0  0  0
 21 52  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0005603

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]N1C([H])([H])C([H])([H])C([H])([H])[C@@]2([H])O[C@]2([H])C([H])([H])[C@@]1([H])C([H])([H])C([H])([H])C([H])([H])C(=O)C(\[H])=C(/[H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C18H31NO2/c1-2-3-4-5-6-10-16(20)11-7-9-15-14-18-17(21-18)12-8-13-19-15/h6,10,15,17-19H,2-5,7-9,11-14H2,1H3/b10-6+/t15-,17-,18-/m1/s1

> <INCHI_KEY>
CFZBYEMAQOZSHS-KFCNSJSKSA-N

> <FORMULA>
C18H31NO2

> <MOLECULAR_WEIGHT>
293.451

> <EXACT_MASS>
293.235479242

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
35.532961884794396

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5E)-1-[(1R,3R,8R)-9-oxa-4-azabicyclo[6.1.0]nonan-3-yl]undec-5-en-4-one

> <ALOGPS_LOGP>
3.83

> <JCHEM_LOGP>
3.9327335913333332

> <ALOGPS_LOGS>
-5.01

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
10.633816908780656

> <JCHEM_POLAR_SURFACE_AREA>
41.63

> <JCHEM_REFRACTIVITY>
87.60119999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.89e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5E)-1-[(1R,3R,8R)-9-oxa-4-azabicyclo[6.1.0]nonan-3-yl]undec-5-en-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 52 53  0  0  0  0  0  0  0  0999 V2000
    7.0970    0.9260    1.2006 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6492   -0.0458    0.1144 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5534    0.6005   -0.7436 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1280   -0.3571   -1.7987 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5496   -1.6434   -1.3253 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2477   -1.5164   -0.6577 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5564   -0.4121   -0.5534 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2589   -0.4185    0.1509 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8273   -1.4810    0.6446 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5045    0.8188    0.2569 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8417    0.5885    0.8767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6983   -0.2975    0.0562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0623   -0.5476    0.6615 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8227   -1.4492   -0.2560 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2676   -1.1250   -0.4045 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.2517   -1.8646    0.2400 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8226   -0.7708    0.9493 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4853    0.5646    0.8417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7861    1.5286   -0.0628 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2866    1.4097   -0.0431 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7593    0.6343    1.0127 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.0933    0.5711    1.5574 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4139    0.8730    2.0566 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2070    1.9445    0.7871 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4871   -0.3870   -0.4931 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1937   -0.9053    0.6305 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7739    0.9535   -0.1004 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0468    1.4635   -1.2636 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0215   -0.5334   -2.4743 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3365    0.1674   -2.4197 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2391   -2.1864   -0.6275 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3983   -2.3222   -2.2171 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7761   -2.4037   -0.1904 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8714    0.4976   -0.9910 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4292    1.3778   -0.7090 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0564    1.5364    0.9306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6519    0.1917    1.9003 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3105    1.6186    0.9431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8636    0.2376   -0.9299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1976   -1.2315   -0.2201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8722   -1.1255    1.6071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7593   -2.5344    0.0517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3533   -1.4441   -1.2837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6448   -0.5813   -1.2824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2418   -1.0215    1.8547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5445    0.4602    0.4751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5628    0.9961    1.8636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2098    1.4000   -1.1010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1359    2.5604    0.2357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9578    1.1057   -1.0568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8913    2.4619    0.0739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4350    1.1177    1.8474 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  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 13  1  0
 17 15  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  0
  7 34  1  0
 10 35  1  0
 10 36  1  0
 11 37  1  0
 11 38  1  0
 12 39  1  0
 12 40  1  0
 13 41  1  1
 14 42  1  0
 14 43  1  0
 15 44  1  6
 17 45  1  1
 18 46  1  0
 18 47  1  0
 19 48  1  0
 19 49  1  0
 20 50  1  0
 20 51  1  0
 21 52  1  0
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       7.097   0.926   1.201  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.649  -0.046   0.114  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.553   0.601  -0.744  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.128  -0.357  -1.799  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.550  -1.643  -1.325  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.248  -1.516  -0.658  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.556  -0.412  -0.553  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.259  -0.419   0.151  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.827  -1.481   0.645  0.00  0.00           O+0
HETATM   10  C   UNK     0       0.504   0.819   0.257  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.842   0.589   0.877  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.698  -0.298   0.056  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.062  -0.548   0.662  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.823  -1.449  -0.256  0.00  0.00           C+0
HETATM   15  C   UNK     0      -5.268  -1.125  -0.405  0.00  0.00           C+0
HETATM   16  O   UNK     0      -6.252  -1.865   0.240  0.00  0.00           O+0
HETATM   17  C   UNK     0      -5.823  -0.771   0.949  0.00  0.00           C+0
HETATM   18  C   UNK     0      -6.485   0.565   0.842  0.00  0.00           C+0
HETATM   19  C   UNK     0      -5.786   1.529  -0.063  0.00  0.00           C+0
HETATM   20  C   UNK     0      -4.287   1.410  -0.043  0.00  0.00           C+0
HETATM   21  N   UNK     0      -3.759   0.634   1.013  0.00  0.00           N+0
HETATM   22  H   UNK     0       8.093   0.571   1.557  0.00  0.00           H+0
HETATM   23  H   UNK     0       6.414   0.873   2.057  0.00  0.00           H+0
HETATM   24  H   UNK     0       7.207   1.944   0.787  0.00  0.00           H+0
HETATM   25  H   UNK     0       7.487  -0.387  -0.493  0.00  0.00           H+0
HETATM   26  H   UNK     0       6.194  -0.905   0.631  0.00  0.00           H+0
HETATM   27  H   UNK     0       4.774   0.954  -0.100  0.00  0.00           H+0
HETATM   28  H   UNK     0       6.047   1.464  -1.264  0.00  0.00           H+0
HETATM   29  H   UNK     0       6.021  -0.533  -2.474  0.00  0.00           H+0
HETATM   30  H   UNK     0       4.337   0.167  -2.420  0.00  0.00           H+0
HETATM   31  H   UNK     0       5.239  -2.186  -0.628  0.00  0.00           H+0
HETATM   32  H   UNK     0       4.398  -2.322  -2.217  0.00  0.00           H+0
HETATM   33  H   UNK     0       2.776  -2.404  -0.190  0.00  0.00           H+0
HETATM   34  H   UNK     0       2.871   0.498  -0.991  0.00  0.00           H+0
HETATM   35  H   UNK     0       0.429   1.378  -0.709  0.00  0.00           H+0
HETATM   36  H   UNK     0       1.056   1.536   0.931  0.00  0.00           H+0
HETATM   37  H   UNK     0      -0.652   0.192   1.900  0.00  0.00           H+0
HETATM   38  H   UNK     0      -1.311   1.619   0.943  0.00  0.00           H+0
HETATM   39  H   UNK     0      -1.864   0.238  -0.930  0.00  0.00           H+0
HETATM   40  H   UNK     0      -1.198  -1.232  -0.220  0.00  0.00           H+0
HETATM   41  H   UNK     0      -2.872  -1.125   1.607  0.00  0.00           H+0
HETATM   42  H   UNK     0      -3.759  -2.534   0.052  0.00  0.00           H+0
HETATM   43  H   UNK     0      -3.353  -1.444  -1.284  0.00  0.00           H+0
HETATM   44  H   UNK     0      -5.645  -0.581  -1.282  0.00  0.00           H+0
HETATM   45  H   UNK     0      -5.242  -1.022   1.855  0.00  0.00           H+0
HETATM   46  H   UNK     0      -7.545   0.460   0.475  0.00  0.00           H+0
HETATM   47  H   UNK     0      -6.563   0.996   1.864  0.00  0.00           H+0
HETATM   48  H   UNK     0      -6.210   1.400  -1.101  0.00  0.00           H+0
HETATM   49  H   UNK     0      -6.136   2.560   0.236  0.00  0.00           H+0
HETATM   50  H   UNK     0      -3.958   1.106  -1.057  0.00  0.00           H+0
HETATM   51  H   UNK     0      -3.891   2.462   0.074  0.00  0.00           H+0
HETATM   52  H   UNK     0      -3.435   1.118   1.847  0.00  0.00           H+0
CONECT    1    2   22   23   24                                             
CONECT    2    1    3   25   26                                             
CONECT    3    2    4   27   28                                             
CONECT    4    3    5   29   30                                             
CONECT    5    4    6   31   32                                             
CONECT    6    5    7   33                                                  
CONECT    7    6    8   34                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   35   36                                             
CONECT   11   10   12   37   38                                             
CONECT   12   11   13   39   40                                             
CONECT   13   12   14   21   41                                             
CONECT   14   13   15   42   43                                             
CONECT   15   14   16   17   44                                             
CONECT   16   15   17                                                       
CONECT   17   16   18   15   45                                             
CONECT   18   17   19   46   47                                             
CONECT   19   18   20   48   49                                             
CONECT   20   19   21   50   51                                             
CONECT   21   20   13   52                                                  
CONECT   22    1                                                            
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    2                                                            
CONECT   26    2                                                            
CONECT   27    3                                                            
CONECT   28    3                                                            
CONECT   29    4                                                            
CONECT   30    4                                                            
CONECT   31    5                                                            
CONECT   32    5                                                            
CONECT   33    6                                                            
CONECT   34    7                                                            
CONECT   35   10                                                            
CONECT   36   10                                                            
CONECT   37   11                                                            
CONECT   38   11                                                            
CONECT   39   12                                                            
CONECT   40   12                                                            
CONECT   41   13                                                            
CONECT   42   14                                                            
CONECT   43   14                                                            
CONECT   44   15                                                            
CONECT   45   17                                                            
CONECT   46   18                                                            
CONECT   47   18                                                            
CONECT   48   19                                                            
CONECT   49   19                                                            
CONECT   50   20                                                            
CONECT   51   20                                                            
CONECT   52   21                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  106    0
END

RDKit          3D

52 53  0  0  0  0  0  0  0  0999 V2000
    7.0970    0.9260    1.2006 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6492   -0.0458    0.1144 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5534    0.6005   -0.7436 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1280   -0.3571   -1.7987 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5496   -1.6434   -1.3253 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2477   -1.5164   -0.6577 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5564   -0.4121   -0.5534 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2589   -0.4185    0.1509 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8273   -1.4810    0.6446 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5045    0.8188    0.2569 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8417    0.5885    0.8767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6983   -0.2975    0.0562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0623   -0.5476    0.6615 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8227   -1.4492   -0.2560 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2676   -1.1250   -0.4045 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.2517   -1.8646    0.2400 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8226   -0.7708    0.9493 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4853    0.5646    0.8417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7861    1.5286   -0.0628 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2866    1.4097   -0.0431 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7593    0.6343    1.0127 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.0933    0.5711    1.5574 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4139    0.8730    2.0566 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2070    1.9445    0.7871 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4871   -0.3870   -0.4931 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1937   -0.9053    0.6305 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7739    0.9535   -0.1004 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0468    1.4635   -1.2636 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0215   -0.5334   -2.4743 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3365    0.1674   -2.4197 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2391   -2.1864   -0.6275 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3983   -2.3222   -2.2171 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7761   -2.4037   -0.1904 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8714    0.4976   -0.9910 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4292    1.3778   -0.7090 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0564    1.5364    0.9306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6519    0.1917    1.9003 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3105    1.6186    0.9431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8636    0.2376   -0.9299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1976   -1.2315   -0.2201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8722   -1.1255    1.6071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7593   -2.5344    0.0517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3533   -1.4441   -1.2837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6448   -0.5813   -1.2824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2418   -1.0215    1.8547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5445    0.4602    0.4751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5628    0.9961    1.8636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2098    1.4000   -1.1010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1359    2.5604    0.2357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9578    1.1057   -1.0568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8913    2.4619    0.0739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4350    1.1177    1.8474 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  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 13  1  0
 17 15  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  0
  7 34  1  0
 10 35  1  0
 10 36  1  0
 11 37  1  0
 11 38  1  0
 12 39  1  0
 12 40  1  0
 13 41  1  1
 14 42  1  0
 14 43  1  0
 15 44  1  6
 17 45  1  1
 18 46  1  0
 18 47  1  0
 19 48  1  0
 19 49  1  0
 20 50  1  0
 20 51  1  0
 21 52  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₈H₃₁NO₂

Average Mass

293.4510 Da

Monoisotopic Mass

293.23548 Da

IUPAC Name

(5E)-1-[(1R,3R,8R)-9-oxa-4-azabicyclo[6.1.0]nonan-3-yl]undec-5-en-4-one

Traditional Name

(5E)-1-[(1R,3R,8R)-9-oxa-4-azabicyclo[6.1.0]nonan-3-yl]undec-5-en-4-one

CAS Registry Number

Not Available

SMILES

CCCCC\C=C\C(=O)CCC[C@@H]1C[C@H]2O[C@@H]2CCCN1

InChI Identifier

InChI=1S/C18H31NO2/c1-2-3-4-5-6-10-16(20)11-7-9-15-14-18-17(21-18)12-8-13-19-15/h6,10,15,17-19H,2-5,7-9,11-14H2,1H3/b10-6+/t15-,17-,18-/m1/s1

InChI Key

CFZBYEMAQOZSHS-KFCNSJSKSA-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
Bacterium; sewage; soil	NPAtlas	15580956

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as enones. Enones are compounds containing the enone functional group, with the structure RC(=O)CR'.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Enones

Alternative Parents

Substituents

Acryloyl-group
Enone
Ketone
Dialkyl ether
Secondary aliphatic amine
Oxirane
Ether
Secondary amine
Organoheterocyclic compound
Oxacycle
Azacycle
Hydrocarbon derivative
Organonitrogen compound
Organic oxide
Amine
Organic nitrogen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	3.83	ALOGPS
logP	3.93	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Basic)	10.63	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	41.63 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	87.6 m³·mol⁻¹	ChemAxon
Polarizability	35.53 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA006713

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

8238545

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10063004

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Sakano Y, Shibuya M, Yamaguchi Y, Masuma R, Tomoda H, Omura S, Ebizuka Y: Epohelmins A and B, novel lanosterol synthase inhibitors from a fungal strain FKI-0929. J Antibiot (Tokyo). 2004 Sep;57(9):564-8. doi: 10.7164/antibiotics.57.564. [PubMed:15580956 ]

Showing NP-Card for Epohelmin A (NP0005603)

MOL for NP0005603 (Epohelmin A)

3D MOL for NP0005603 (Epohelmin A)

3D SDF for NP0005603 (Epohelmin A)

3D-SDF for NP0005603 (Epohelmin A)

PDB for NP0005603 (Epohelmin A)

3D PDB for NP0005603 (Epohelmin A)

SMILES for NP0005603 (Epohelmin A)

INCHI for NP0005603 (Epohelmin A)

Structure for NP0005603 (Epohelmin A)

3D Structure for NP0005603 (Epohelmin A)