NP-MRD: Showing NP-Card for Isoepipolone (NP0025517)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

1.0

Created at

2021-06-19 17:37:20 UTC

Updated at

2021-06-29 23:50:32 UTC

NP-MRD ID

NP0025517

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Isoepipolone

Provided By

JEOL Database JEOL Logo

Description

Isoepipolone is found in Epipolasis reiswigi. It was first documented in 2002 (PMID: 33651529). Based on a literature review very few articles have been published on hydroxy-isopropyl-dimethyl-methylene-[?]One (PMID: 33079503) (PMID: 26389513) (PMID: 26389498) (PMID: 26389454) (PMID: 26389451) (PMID: 26389436).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192119373D          

 52 54  0  0  0  0            999 V2000
    2.5368   -2.0077    2.3977 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8479   -1.7798    1.2645 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3913   -1.4214    1.2945 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1746    0.0911    1.2586 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3402    0.8105   -0.1057 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0568    2.3494    0.0696 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4133    2.6521    0.3553 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9893    2.6556    1.7499 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1263    4.0892    2.2713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3352    1.9308    1.8320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0505    3.0210   -0.7686 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1108    3.1304   -1.9255 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2540    3.2056   -1.2150 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5828    4.6691   -0.8227 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3456    2.7153   -2.1493 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9454    3.4809   -2.9081 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6036    1.2370   -2.2306 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6992    0.5539   -0.8461 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9106    1.1297   -0.0833 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9138   -0.9562   -1.1680 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5006   -1.8655   -0.0836 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3635   -3.2088   -0.5487 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5926   -2.2627    2.3819 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0635   -1.9407    3.3733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0535   -1.8059    2.2226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1564   -1.9197    0.4863 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8032    0.5780    2.0151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8599    0.2270    1.5862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4513    0.4016   -0.7530 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6821    2.7464    0.8796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2956    2.1440    2.4255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8300    4.6745    1.6689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4894    4.0906    3.3049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1599    4.6054    2.2588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2593    0.9109    1.4398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1162    2.4531    1.2687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6697    1.8623    2.8730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0918    3.3081   -0.8319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3124    4.0313   -2.5144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2132    2.2598   -2.5821 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6171    5.3199   -1.7043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1540    5.0965   -0.1347 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5638    4.7270   -0.3365 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8011    0.7953   -2.8341 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5401    1.0965   -2.7861 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8449    0.8962   -0.6070 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9916    0.7300    0.9306 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8622    2.2189    0.0126 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9719   -1.3840   -1.5418 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5937   -1.0486   -2.0288 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5757   -1.6661    0.0025 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5699   -3.7913    0.2021 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  3  1  0  0  0  0
 20 21  1  0  0  0  0
  3  2  1  0  0  0  0
 21  2  1  0  0  0  0
 21 22  1  0  0  0  0
 13 15  1  0  0  0  0
  6  7  1  0  0  0  0
  7 11  2  0  0  0  0
 11 12  1  0  0  0  0
 13 14  1  1  0  0  0
 12 13  1  0  0  0  0
 18 19  1  1  0  0  0
 13  6  1  0  0  0  0
 21 51  1  1  0  0  0
  2  1  2  3  0  0  0
 18  5  1  0  0  0  0
  6 30  1  1  0  0  0
 17 18  1  0  0  0  0
  7  8  1  0  0  0  0
  5  4  1  0  0  0  0
  8  9  1  0  0  0  0
 17 15  1  0  0  0  0
  8 10  1  0  0  0  0
 18 20  1  0  0  0  0
  5 29  1  6  0  0  0
  5  6  1  0  0  0  0
 15 16  2  0  0  0  0
 17 44  1  0  0  0  0
 17 45  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
  4 27  1  0  0  0  0
  4 28  1  0  0  0  0
 20 49  1  0  0  0  0
 20 50  1  0  0  0  0
  3 25  1  0  0  0  0
  3 26  1  0  0  0  0
 22 52  1  0  0  0  0
 14 41  1  0  0  0  0
 14 42  1  0  0  0  0
 14 43  1  0  0  0  0
 19 46  1  0  0  0  0
 19 47  1  0  0  0  0
 19 48  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  8 31  1  1  0  0  0
  9 32  1  0  0  0  0
  9 33  1  0  0  0  0
  9 34  1  0  0  0  0
 10 35  1  0  0  0  0
 10 36  1  0  0  0  0
 10 37  1  0  0  0  0
M  END

     RDKit          3D

 52 54  0  0  0  0  0  0  0  0999 V2000
    2.5368   -2.0077    2.3977 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8479   -1.7798    1.2645 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3913   -1.4214    1.2945 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1746    0.0911    1.2586 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3402    0.8105   -0.1057 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0568    2.3494    0.0696 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4133    2.6521    0.3553 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9893    2.6556    1.7499 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1263    4.0892    2.2713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3352    1.9308    1.8320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0505    3.0210   -0.7686 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1108    3.1304   -1.9255 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2540    3.2056   -1.2150 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5828    4.6691   -0.8227 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3456    2.7153   -2.1493 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9454    3.4809   -2.9081 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6036    1.2370   -2.2306 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6992    0.5539   -0.8461 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9106    1.1297   -0.0833 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9138   -0.9562   -1.1680 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5006   -1.8655   -0.0836 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3635   -3.2088   -0.5487 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5926   -2.2627    2.3819 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0635   -1.9407    3.3733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0535   -1.8059    2.2226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1564   -1.9197    0.4863 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8032    0.5780    2.0151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8599    0.2270    1.5862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4513    0.4016   -0.7530 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6821    2.7464    0.8796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2956    2.1440    2.4255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8300    4.6745    1.6689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4894    4.0906    3.3049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1599    4.6054    2.2588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2593    0.9109    1.4398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1162    2.4531    1.2687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6697    1.8623    2.8730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0918    3.3081   -0.8319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3124    4.0313   -2.5144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2132    2.2598   -2.5821 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6171    5.3199   -1.7043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1540    5.0965   -0.1347 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5638    4.7270   -0.3365 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8011    0.7953   -2.8341 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5401    1.0965   -2.7861 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8449    0.8962   -0.6070 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9916    0.7300    0.9306 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8622    2.2189    0.0126 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9719   -1.3840   -1.5418 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5937   -1.0486   -2.0288 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5757   -1.6661    0.0025 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5699   -3.7913    0.2021 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  3  1  0
 20 21  1  0
  3  2  1  0
 21  2  1  0
 21 22  1  0
 13 15  1  0
  6  7  1  0
  7 11  2  0
 11 12  1  0
 13 14  1  1
 12 13  1  0
 18 19  1  1
 13  6  1  0
 21 51  1  1
  2  1  2  3
 18  5  1  0
  6 30  1  1
 17 18  1  0
  7  8  1  0
  5  4  1  0
  8  9  1  0
 17 15  1  0
  8 10  1  0
 18 20  1  0
  5 29  1  6
  5  6  1  0
 15 16  2  0
 17 44  1  0
 17 45  1  0
 11 38  1  0
 12 39  1  0
 12 40  1  0
  4 27  1  0
  4 28  1  0
 20 49  1  0
 20 50  1  0
  3 25  1  0
  3 26  1  0
 22 52  1  0
 14 41  1  0
 14 42  1  0
 14 43  1  0
 19 46  1  0
 19 47  1  0
 19 48  1  0
  1 23  1  0
  1 24  1  0
  8 31  1  1
  9 32  1  0
  9 33  1  0
  9 34  1  0
 10 35  1  0
 10 36  1  0
 10 37  1  0
M  END


  Mrv1652306192119373D          

 52 54  0  0  0  0            999 V2000
    2.5368   -2.0077    2.3977 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8479   -1.7798    1.2645 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3913   -1.4214    1.2945 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1746    0.0911    1.2586 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3402    0.8105   -0.1057 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0568    2.3494    0.0696 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4133    2.6521    0.3553 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9893    2.6556    1.7499 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1263    4.0892    2.2713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3352    1.9308    1.8320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0505    3.0210   -0.7686 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1108    3.1304   -1.9255 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2540    3.2056   -1.2150 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5828    4.6691   -0.8227 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3456    2.7153   -2.1493 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9454    3.4809   -2.9081 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6036    1.2370   -2.2306 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6992    0.5539   -0.8461 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9106    1.1297   -0.0833 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9138   -0.9562   -1.1680 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5006   -1.8655   -0.0836 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3635   -3.2088   -0.5487 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5926   -2.2627    2.3819 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0635   -1.9407    3.3733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0535   -1.8059    2.2226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1564   -1.9197    0.4863 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8032    0.5780    2.0151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8599    0.2270    1.5862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4513    0.4016   -0.7530 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6821    2.7464    0.8796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2956    2.1440    2.4255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8300    4.6745    1.6689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4894    4.0906    3.3049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1599    4.6054    2.2588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2593    0.9109    1.4398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1162    2.4531    1.2687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6697    1.8623    2.8730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0918    3.3081   -0.8319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3124    4.0313   -2.5144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2132    2.2598   -2.5821 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6171    5.3199   -1.7043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1540    5.0965   -0.1347 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5638    4.7270   -0.3365 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8011    0.7953   -2.8341 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5401    1.0965   -2.7861 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8449    0.8962   -0.6070 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9916    0.7300    0.9306 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8622    2.2189    0.0126 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9719   -1.3840   -1.5418 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5937   -1.0486   -2.0288 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5757   -1.6661    0.0025 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5699   -3.7913    0.2021 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  3  1  0  0  0  0
 20 21  1  0  0  0  0
  3  2  1  0  0  0  0
 21  2  1  0  0  0  0
 21 22  1  0  0  0  0
 13 15  1  0  0  0  0
  6  7  1  0  0  0  0
  7 11  2  0  0  0  0
 11 12  1  0  0  0  0
 13 14  1  1  0  0  0
 12 13  1  0  0  0  0
 18 19  1  1  0  0  0
 13  6  1  0  0  0  0
 21 51  1  1  0  0  0
  2  1  2  3  0  0  0
 18  5  1  0  0  0  0
  6 30  1  1  0  0  0
 17 18  1  0  0  0  0
  7  8  1  0  0  0  0
  5  4  1  0  0  0  0
  8  9  1  0  0  0  0
 17 15  1  0  0  0  0
  8 10  1  0  0  0  0
 18 20  1  0  0  0  0
  5 29  1  6  0  0  0
  5  6  1  0  0  0  0
 15 16  2  0  0  0  0
 17 44  1  0  0  0  0
 17 45  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
  4 27  1  0  0  0  0
  4 28  1  0  0  0  0
 20 49  1  0  0  0  0
 20 50  1  0  0  0  0
  3 25  1  0  0  0  0
  3 26  1  0  0  0  0
 22 52  1  0  0  0  0
 14 41  1  0  0  0  0
 14 42  1  0  0  0  0
 14 43  1  0  0  0  0
 19 46  1  0  0  0  0
 19 47  1  0  0  0  0
 19 48  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  8 31  1  1  0  0  0
  9 32  1  0  0  0  0
  9 33  1  0  0  0  0
  9 34  1  0  0  0  0
 10 35  1  0  0  0  0
 10 36  1  0  0  0  0
 10 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0025517

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@]1([H])C(=C([H])[H])C([H])([H])C([H])([H])[C@@]2([H])[C@]3([H])C(=C([H])C([H])([H])[C@@]3(C(=O)C([H])([H])[C@]2(C([H])([H])[H])C1([H])[H])C([H])([H])[H])C([H])(C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O2/c1-12(2)14-8-9-20(5)17(22)11-19(4)10-16(21)13(3)6-7-15(19)18(14)20/h8,12,15-16,18,21H,3,6-7,9-11H2,1-2,4-5H3/t15-,16-,18-,19-,20+/m0/s1

> <INCHI_KEY>
YBQUCTGYBPMQDP-CZKCSJLSSA-N

> <FORMULA>
C20H30O2

> <MOLECULAR_WEIGHT>
302.458

> <EXACT_MASS>
302.224580206

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
35.73786138623553

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3aS,5aS,7S,10aS,10bR)-7-hydroxy-3a,5a-dimethyl-8-methylidene-1-(propan-2-yl)-3H,3aH,4H,5H,5aH,6H,7H,8H,9H,10H,10aH,10bH-cyclohepta[e]inden-4-one

> <ALOGPS_LOGP>
3.96

> <JCHEM_LOGP>
3.920711703333334

> <ALOGPS_LOGS>
-4.17

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.86482275695185

> <JCHEM_PKA_STRONGEST_BASIC>
-1.1083263488009734

> <JCHEM_POLAR_SURFACE_AREA>
37.3

> <JCHEM_REFRACTIVITY>
90.63319999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.05e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3aS,5aS,7S,10aS,10bR)-7-hydroxy-1-isopropyl-3a,5a-dimethyl-8-methylidene-3H,5H,6H,7H,9H,10H,10aH,10bH-cyclohepta[e]inden-4-one

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 52 54  0  0  0  0  0  0  0  0999 V2000
    2.5368   -2.0077    2.3977 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8479   -1.7798    1.2645 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3913   -1.4214    1.2945 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1746    0.0911    1.2586 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3402    0.8105   -0.1057 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0568    2.3494    0.0696 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4133    2.6521    0.3553 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9893    2.6556    1.7499 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1263    4.0892    2.2713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3352    1.9308    1.8320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0505    3.0210   -0.7686 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1108    3.1304   -1.9255 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2540    3.2056   -1.2150 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5828    4.6691   -0.8227 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3456    2.7153   -2.1493 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9454    3.4809   -2.9081 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6036    1.2370   -2.2306 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6992    0.5539   -0.8461 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9106    1.1297   -0.0833 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9138   -0.9562   -1.1680 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5006   -1.8655   -0.0836 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3635   -3.2088   -0.5487 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5926   -2.2627    2.3819 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0635   -1.9407    3.3733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0535   -1.8059    2.2226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1564   -1.9197    0.4863 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8032    0.5780    2.0151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8599    0.2270    1.5862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4513    0.4016   -0.7530 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6821    2.7464    0.8796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2956    2.1440    2.4255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8300    4.6745    1.6689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4894    4.0906    3.3049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1599    4.6054    2.2588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2593    0.9109    1.4398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1162    2.4531    1.2687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6697    1.8623    2.8730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0918    3.3081   -0.8319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3124    4.0313   -2.5144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2132    2.2598   -2.5821 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6171    5.3199   -1.7043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1540    5.0965   -0.1347 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5638    4.7270   -0.3365 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8011    0.7953   -2.8341 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5401    1.0965   -2.7861 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8449    0.8962   -0.6070 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9916    0.7300    0.9306 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8622    2.2189    0.0126 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9719   -1.3840   -1.5418 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5937   -1.0486   -2.0288 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5757   -1.6661    0.0025 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5699   -3.7913    0.2021 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  3  1  0
 20 21  1  0
  3  2  1  0
 21  2  1  0
 21 22  1  0
 13 15  1  0
  6  7  1  0
  7 11  2  0
 11 12  1  0
 13 14  1  1
 12 13  1  0
 18 19  1  1
 13  6  1  0
 21 51  1  1
  2  1  2  3
 18  5  1  0
  6 30  1  1
 17 18  1  0
  7  8  1  0
  5  4  1  0
  8  9  1  0
 17 15  1  0
  8 10  1  0
 18 20  1  0
  5 29  1  6
  5  6  1  0
 15 16  2  0
 17 44  1  0
 17 45  1  0
 11 38  1  0
 12 39  1  0
 12 40  1  0
  4 27  1  0
  4 28  1  0
 20 49  1  0
 20 50  1  0
  3 25  1  0
  3 26  1  0
 22 52  1  0
 14 41  1  0
 14 42  1  0
 14 43  1  0
 19 46  1  0
 19 47  1  0
 19 48  1  0
  1 23  1  0
  1 24  1  0
  8 31  1  1
  9 32  1  0
  9 33  1  0
  9 34  1  0
 10 35  1  0
 10 36  1  0
 10 37  1  0
M  END

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  C   UNK     0       2.537  -2.008   2.398  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.848  -1.780   1.264  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.391  -1.421   1.295  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.175   0.091   1.259  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.340   0.811  -0.106  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.057   2.349   0.070  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.413   2.652   0.355  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.989   2.656   1.750  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.126   4.089   2.271  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.335   1.931   1.832  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.050   3.021  -0.769  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.111   3.130  -1.926  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.254   3.206  -1.215  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.583   4.669  -0.823  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.346   2.715  -2.149  0.00  0.00           C+0
HETATM   16  O   UNK     0       1.945   3.481  -2.908  0.00  0.00           O+0
HETATM   17  C   UNK     0       1.604   1.237  -2.231  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.699   0.554  -0.846  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.911   1.130  -0.083  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.914  -0.956  -1.168  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.501  -1.865  -0.084  0.00  0.00           C+0
HETATM   22  O   UNK     0       2.364  -3.209  -0.549  0.00  0.00           O+0
HETATM   23  H   UNK     0       3.593  -2.263   2.382  0.00  0.00           H+0
HETATM   24  H   UNK     0       2.063  -1.941   3.373  0.00  0.00           H+0
HETATM   25  H   UNK     0      -0.054  -1.806   2.223  0.00  0.00           H+0
HETATM   26  H   UNK     0      -0.156  -1.920   0.486  0.00  0.00           H+0
HETATM   27  H   UNK     0       0.803   0.578   2.015  0.00  0.00           H+0
HETATM   28  H   UNK     0      -0.860   0.227   1.586  0.00  0.00           H+0
HETATM   29  H   UNK     0      -0.451   0.402  -0.753  0.00  0.00           H+0
HETATM   30  H   UNK     0       0.682   2.746   0.880  0.00  0.00           H+0
HETATM   31  H   UNK     0      -1.296   2.144   2.426  0.00  0.00           H+0
HETATM   32  H   UNK     0      -2.830   4.675   1.669  0.00  0.00           H+0
HETATM   33  H   UNK     0      -2.489   4.091   3.305  0.00  0.00           H+0
HETATM   34  H   UNK     0      -1.160   4.605   2.259  0.00  0.00           H+0
HETATM   35  H   UNK     0      -3.259   0.911   1.440  0.00  0.00           H+0
HETATM   36  H   UNK     0      -4.116   2.453   1.269  0.00  0.00           H+0
HETATM   37  H   UNK     0      -3.670   1.862   2.873  0.00  0.00           H+0
HETATM   38  H   UNK     0      -3.092   3.308  -0.832  0.00  0.00           H+0
HETATM   39  H   UNK     0      -1.312   4.031  -2.514  0.00  0.00           H+0
HETATM   40  H   UNK     0      -1.213   2.260  -2.582  0.00  0.00           H+0
HETATM   41  H   UNK     0       0.617   5.320  -1.704  0.00  0.00           H+0
HETATM   42  H   UNK     0      -0.154   5.096  -0.135  0.00  0.00           H+0
HETATM   43  H   UNK     0       1.564   4.727  -0.337  0.00  0.00           H+0
HETATM   44  H   UNK     0       0.801   0.795  -2.834  0.00  0.00           H+0
HETATM   45  H   UNK     0       2.540   1.097  -2.786  0.00  0.00           H+0
HETATM   46  H   UNK     0       3.845   0.896  -0.607  0.00  0.00           H+0
HETATM   47  H   UNK     0       2.992   0.730   0.931  0.00  0.00           H+0
HETATM   48  H   UNK     0       2.862   2.219   0.013  0.00  0.00           H+0
HETATM   49  H   UNK     0       0.972  -1.384  -1.542  0.00  0.00           H+0
HETATM   50  H   UNK     0       2.594  -1.049  -2.029  0.00  0.00           H+0
HETATM   51  H   UNK     0       3.576  -1.666   0.003  0.00  0.00           H+0
HETATM   52  H   UNK     0       2.570  -3.791   0.202  0.00  0.00           H+0
CONECT    1    2   23   24                                                  
CONECT    2    3   21    1                                                  
CONECT    3    4    2   25   26                                             
CONECT    4    3    5   27   28                                             
CONECT    5   18    4   29    6                                             
CONECT    6    7   13   30    5                                             
CONECT    7    6   11    8                                                  
CONECT    8    7    9   10   31                                             
CONECT    9    8   32   33   34                                             
CONECT   10    8   35   36   37                                             
CONECT   11    7   12   38                                                  
CONECT   12   11   13   39   40                                             
CONECT   13   15   14   12    6                                             
CONECT   14   13   41   42   43                                             
CONECT   15   13   17   16                                                  
CONECT   16   15                                                            
CONECT   17   18   15   44   45                                             
CONECT   18   19    5   17   20                                             
CONECT   19   18   46   47   48                                             
CONECT   20   21   18   49   50                                             
CONECT   21   20    2   22   51                                             
CONECT   22   21   52                                                       
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    3                                                            
CONECT   26    3                                                            
CONECT   27    4                                                            
CONECT   28    4                                                            
CONECT   29    5                                                            
CONECT   30    6                                                            
CONECT   31    8                                                            
CONECT   32    9                                                            
CONECT   33    9                                                            
CONECT   34    9                                                            
CONECT   35   10                                                            
CONECT   36   10                                                            
CONECT   37   10                                                            
CONECT   38   11                                                            
CONECT   39   12                                                            
CONECT   40   12                                                            
CONECT   41   14                                                            
CONECT   42   14                                                            
CONECT   43   14                                                            
CONECT   44   17                                                            
CONECT   45   17                                                            
CONECT   46   19                                                            
CONECT   47   19                                                            
CONECT   48   19                                                            
CONECT   49   20                                                            
CONECT   50   20                                                            
CONECT   51   21                                                            
CONECT   52   22                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  108    0
END

RDKit          3D

52 54  0  0  0  0  0  0  0  0999 V2000
    2.5368   -2.0077    2.3977 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8479   -1.7798    1.2645 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3913   -1.4214    1.2945 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1746    0.0911    1.2586 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3402    0.8105   -0.1057 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0568    2.3494    0.0696 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4133    2.6521    0.3553 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9893    2.6556    1.7499 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1263    4.0892    2.2713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3352    1.9308    1.8320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0505    3.0210   -0.7686 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1108    3.1304   -1.9255 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2540    3.2056   -1.2150 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5828    4.6691   -0.8227 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3456    2.7153   -2.1493 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9454    3.4809   -2.9081 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6036    1.2370   -2.2306 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6992    0.5539   -0.8461 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9106    1.1297   -0.0833 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9138   -0.9562   -1.1680 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5006   -1.8655   -0.0836 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3635   -3.2088   -0.5487 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5926   -2.2627    2.3819 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0635   -1.9407    3.3733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0535   -1.8059    2.2226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1564   -1.9197    0.4863 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8032    0.5780    2.0151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8599    0.2270    1.5862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4513    0.4016   -0.7530 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6821    2.7464    0.8796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2956    2.1440    2.4255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8300    4.6745    1.6689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4894    4.0906    3.3049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1599    4.6054    2.2588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2593    0.9109    1.4398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1162    2.4531    1.2687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6697    1.8623    2.8730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0918    3.3081   -0.8319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3124    4.0313   -2.5144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2132    2.2598   -2.5821 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6171    5.3199   -1.7043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1540    5.0965   -0.1347 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5638    4.7270   -0.3365 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8011    0.7953   -2.8341 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5401    1.0965   -2.7861 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8449    0.8962   -0.6070 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9916    0.7300    0.9306 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8622    2.2189    0.0126 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9719   -1.3840   -1.5418 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5937   -1.0486   -2.0288 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5757   -1.6661    0.0025 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5699   -3.7913    0.2021 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  3  1  0
 20 21  1  0
  3  2  1  0
 21  2  1  0
 21 22  1  0
 13 15  1  0
  6  7  1  0
  7 11  2  0
 11 12  1  0
 13 14  1  1
 12 13  1  0
 18 19  1  1
 13  6  1  0
 21 51  1  1
  2  1  2  3
 18  5  1  0
  6 30  1  1
 17 18  1  0
  7  8  1  0
  5  4  1  0
  8  9  1  0
 17 15  1  0
  8 10  1  0
 18 20  1  0
  5 29  1  6
  5  6  1  0
 15 16  2  0
 17 44  1  0
 17 45  1  0
 11 38  1  0
 12 39  1  0
 12 40  1  0
  4 27  1  0
  4 28  1  0
 20 49  1  0
 20 50  1  0
  3 25  1  0
  3 26  1  0
 22 52  1  0
 14 41  1  0
 14 42  1  0
 14 43  1  0
 19 46  1  0
 19 47  1  0
 19 48  1  0
  1 23  1  0
  1 24  1  0
  8 31  1  1
  9 32  1  0
  9 33  1  0
  9 34  1  0
 10 35  1  0
 10 36  1  0
 10 37  1  0
M  END

View in JSmol View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₂₀H₃₀O₂

Average Mass

302.4580 Da

Monoisotopic Mass

302.22458 Da

IUPAC Name

(3aS,5aS,7S,10aS,10bR)-7-hydroxy-3a,5a-dimethyl-8-methylidene-1-(propan-2-yl)-3H,3aH,4H,5H,5aH,6H,7H,8H,9H,10H,10aH,10bH-cyclohepta[e]inden-4-one

Traditional Name

(3aS,5aS,7S,10aS,10bR)-7-hydroxy-1-isopropyl-3a,5a-dimethyl-8-methylidene-3H,5H,6H,7H,9H,10H,10aH,10bH-cyclohepta[e]inden-4-one

CAS Registry Number

Not Available

SMILES

[H]O[C@]1([H])C(=C([H])[H])C([H])([H])C([H])([H])[C@@]2([H])[C@]3([H])C(=C([H])C([H])([H])[C@@]3(C(=O)C([H])([H])[C@]2(C([H])([H])[H])C1([H])[H])C([H])([H])[H])C([H])(C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C20H30O2/c1-12(2)14-8-9-20(5)17(22)11-19(4)10-16(21)13(3)6-7-15(19)18(14)20/h8,12,15-16,18,21H,3,6-7,9-11H2,1-2,4-5H3/t15-,16-,18-,19-,20+/m0/s1

InChI Key

YBQUCTGYBPMQDP-CZKCSJLSSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, chcl3, 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
Epipolasis reiswigi	JEOL database	Rodriguez, A. D., et al, J. Org. Chem. 66, 6364 (2001)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Cyclic alcohol
Secondary alcohol
Ketone
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	3.96	ALOGPS
logP	3.92	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	18.86	ChemAxon
pKa (Strongest Basic)	-1.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	37.3 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	90.63 m³·mol⁻¹	ChemAxon
Polarizability	35.74 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

8510567

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10335108

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Authors unspecified: Curcumin (Curcuma, Turmeric) and Cancer (PDQ(R)): Health Professional Version. 2002. [PubMed:33651529 ]
Authors unspecified: Cancer Therapy Interactions With Foods and Dietary Supplements (PDQ(R)): Health Professional Version. 2002. [PubMed:33079503 ]
Authors unspecified: Planning the Transition to End-of-Life Care in Advanced Cancer (PDQ(R)): Health Professional Version. 2002. [PubMed:26389513 ]
Authors unspecified: Childhood Central Nervous System Germ Cell Tumors Treatment (PDQ(R)): Health Professional Version. 2002. [PubMed:26389498 ]
Authors unspecified: Childhood Acute Myeloid Leukemia/Other Myeloid Malignancies Treatment (PDQ(R)): Health Professional Version. 2002. [PubMed:26389454 ]
Authors unspecified: Cancer Prevention Overview (PDQ(R)): Health Professional Version. 2002. [PubMed:26389451 ]
Authors unspecified: Spirituality in Cancer Care (PDQ(R)): Health Professional Version. 2002. [PubMed:26389436 ]
Authors unspecified: Oral Cavity, Oropharyngeal, Hypopharyngeal, and Laryngeal Cancer Prevention (PDQ(R)): Health Professional Version. 2002. [PubMed:26389416 ]
Authors unspecified: Adjustment to Cancer: Anxiety and Distress (PDQ(R)): Health Professional Version. 2002. [PubMed:26389397 ]
Authors unspecified: Cancer Pain (PDQ(R)): Health Professional Version. 2002. [PubMed:26389387 ]
Authors unspecified: Ovarian, Fallopian Tube, and Primary Peritoneal Cancer Screening (PDQ(R)): Health Professional Version. 2002. [PubMed:26389336 ]
Authors unspecified: Informal Caregivers in Cancer: Roles, Burden, and Support (PDQ(R)): Health Professional Version. 2002. [PubMed:26389284 ]
Authors unspecified: Neuroblastoma Treatment (PDQ(R)): Patient Version. 2002. [PubMed:26389278 ]
Authors unspecified: Late Effects of Treatment for Childhood Cancer (PDQ(R)): Health Professional Version. 2002. [PubMed:26389273 ]
Authors unspecified: Lip and Oral Cavity Cancer Treatment (Adult) (PDQ(R)): Health Professional Version. 2002. [PubMed:26389262 ]
Rodriguez, A. D., et al. (2001). Rodriguez, A. D., et al, J. Org. Chem. 66, 6364 (2001). J. Org. Chem..

Showing NP-Card for Isoepipolone (NP0025517)

MOL for NP0025517 (Isoepipolone)

3D MOL for NP0025517 (Isoepipolone)

3D SDF for NP0025517 (Isoepipolone)

3D-SDF for NP0025517 (Isoepipolone)

PDB for NP0025517 (Isoepipolone)

3D PDB for NP0025517 (Isoepipolone)

SMILES for NP0025517 (Isoepipolone)

INCHI for NP0025517 (Isoepipolone)

Structure for NP0025517 (Isoepipolone)

3D Structure for NP0025517 (Isoepipolone)