NP-MRD: Showing NP-Card for (+)-(10R*)-cembra-1E,3E,7E,11Z,16-pentaen-20,10-olide (NP0036334)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

1.0

Created at

2021-06-20 19:32:04 UTC

Updated at

2021-06-30 00:07:56 UTC

NP-MRD ID

NP0036334

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-(10R*)-cembra-1E,3E,7E,11Z,16-pentaen-20,10-olide

Provided By

JEOL Database JEOL Logo

Description

(4E,6Z,10Z,13R)-7,11-dimethyl-4-(prop-1-en-2-yl)-14-oxabicyclo[11.2.1]Hexadeca-1(16),4,6,10-tetraen-15-one belongs to the class of organic compounds known as terpene lactones. (+)-(10R*)-cembra-1E,3E,7E,11Z,16-pentaen-20,10-olide is found in Croton gratissimus. It was first documented in 2011 (Langat, M. K., et al.). These are prenol lipids containing a lactone ring (4E,6Z,10Z,13R)-7,11-dimethyl-4-(prop-1-en-2-yl)-14-oxabicyclo[11.2.1]Hexadeca-1(16),4,6,10-tetraen-15-one is a strongly basic compound (based on its pKa).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202121323D          

 48 49  0  0  0  0            999 V2000
    1.5249   -0.8389   -4.3888 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3885   -0.8915   -3.0544 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5458   -0.6469   -2.1234 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0942   -1.1993   -2.4423 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0631   -2.3851   -1.8191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2755   -2.8797   -1.2038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3343   -3.7376   -0.1661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6686   -4.1981    0.3623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1256   -4.2964    0.5615 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5956   -3.2906    1.4792 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2518   -2.8116    2.6301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3766   -1.5552    3.1049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2785   -1.2846    4.2846 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3876   -0.3474    2.5918 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4725    0.7184    1.8933 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9426    0.3413    0.5412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4733    1.1701   -0.3913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6176    1.2092   -1.8759 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9728   -0.1207   -2.5668 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3526    2.1558    0.3214 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9575    3.0774   -0.1956 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3324    1.8801    1.6538 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4809   -0.6131   -4.8510 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6899   -1.0280   -5.0568 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4571   -0.3822   -2.6709 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7681   -1.5399   -1.5300 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3262    0.1775   -1.4377 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7903   -3.0605   -1.7746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2086   -2.5229   -1.6347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5075   -3.7638   -0.1920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7859   -3.9143    1.4125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7502   -5.2872    0.2842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4256   -5.1735    1.1506 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5923   -4.6859   -0.1714 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4749   -3.7922    1.9020 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9706   -2.4577    0.8785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8134   -3.6047    3.1249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1007   -0.6225    3.9970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7141   -0.8109    5.0945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7218   -2.2017    4.6873 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2147   -0.6391    1.9341 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8942    0.1212    3.4474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3148    1.0246    2.5226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5864   -0.5061    0.3616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4004    1.9398   -2.1174 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3041    1.6035   -2.3217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1462    0.0794   -3.6326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9408   -0.4603   -2.1843 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  2  1  0  0  0  0
 17 16  2  0  0  0  0
 19  4  1  0  0  0  0
  9 10  1  0  0  0  0
  2  3  1  0  0  0  0
 10 11  1  0  0  0  0
 18 19  1  0  0  0  0
 11 12  2  0  0  0  0
  2  1  2  0  0  0  0
 12 13  1  0  0  0  0
  4  5  2  0  0  0  0
 12 14  1  0  0  0  0
  6  7  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  5  6  1  0  0  0  0
 17 20  1  0  0  0  0
  7  9  1  0  0  0  0
 15 22  1  0  0  0  0
 22 20  1  0  0  0  0
 20 21  2  0  0  0  0
 18 17  1  0  0  0  0
  7  8  1  0  0  0  0
  6 29  1  0  0  0  0
 18 45  1  0  0  0  0
 18 46  1  0  0  0  0
 19 47  1  0  0  0  0
 19 48  1  0  0  0  0
  5 28  1  0  0  0  0
  3 25  1  0  0  0  0
  3 26  1  0  0  0  0
  3 27  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  9 33  1  0  0  0  0
  9 34  1  0  0  0  0
 16 44  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
 13 38  1  0  0  0  0
 13 39  1  0  0  0  0
 13 40  1  0  0  0  0
 14 41  1  0  0  0  0
 14 42  1  0  0  0  0
 15 43  1  1  0  0  0
  8 30  1  0  0  0  0
  8 31  1  0  0  0  0
  8 32  1  0  0  0  0
M  END

     RDKit          3D

 48 49  0  0  0  0  0  0  0  0999 V2000
    1.5249   -0.8389   -4.3888 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3885   -0.8915   -3.0544 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5458   -0.6469   -2.1234 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0942   -1.1993   -2.4423 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0631   -2.3851   -1.8191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2755   -2.8797   -1.2038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3343   -3.7376   -0.1661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6686   -4.1981    0.3623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1256   -4.2964    0.5615 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5956   -3.2906    1.4792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2518   -2.8116    2.6301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3766   -1.5552    3.1049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2785   -1.2846    4.2846 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3876   -0.3474    2.5918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4725    0.7184    1.8933 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9426    0.3413    0.5412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4733    1.1701   -0.3913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6176    1.2092   -1.8759 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9728   -0.1207   -2.5668 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3526    2.1558    0.3214 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9575    3.0774   -0.1956 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3324    1.8801    1.6538 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4809   -0.6131   -4.8510 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6899   -1.0280   -5.0568 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4571   -0.3822   -2.6709 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7681   -1.5399   -1.5300 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3262    0.1775   -1.4377 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7903   -3.0605   -1.7746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2086   -2.5229   -1.6347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5075   -3.7638   -0.1920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7859   -3.9143    1.4125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7502   -5.2872    0.2842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4256   -5.1735    1.1506 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5923   -4.6859   -0.1714 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4749   -3.7922    1.9020 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9706   -2.4577    0.8785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8134   -3.6047    3.1249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1007   -0.6225    3.9970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7141   -0.8109    5.0945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7218   -2.2017    4.6873 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2147   -0.6391    1.9341 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8942    0.1212    3.4474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3148    1.0246    2.5226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5864   -0.5061    0.3616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4004    1.9398   -2.1174 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3041    1.6035   -2.3217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1462    0.0794   -3.6326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9408   -0.4603   -2.1843 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  2  1  0
 17 16  2  0
 19  4  1  0
  9 10  1  0
  2  3  1  0
 10 11  1  0
 18 19  1  0
 11 12  2  0
  2  1  2  0
 12 13  1  0
  4  5  2  0
 12 14  1  0
  6  7  2  0
 14 15  1  0
 15 16  1  0
  5  6  1  0
 17 20  1  0
  7  9  1  0
 15 22  1  0
 22 20  1  0
 20 21  2  0
 18 17  1  0
  7  8  1  0
  6 29  1  0
 18 45  1  0
 18 46  1  0
 19 47  1  0
 19 48  1  0
  5 28  1  0
  3 25  1  0
  3 26  1  0
  3 27  1  0
  1 23  1  0
  1 24  1  0
  9 33  1  0
  9 34  1  0
 16 44  1  0
 10 35  1  0
 10 36  1  0
 11 37  1  0
 13 38  1  0
 13 39  1  0
 13 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  1
  8 30  1  0
  8 31  1  0
  8 32  1  0
M  END


  Mrv1652306202121323D          

 48 49  0  0  0  0            999 V2000
    1.5249   -0.8389   -4.3888 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3885   -0.8915   -3.0544 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5458   -0.6469   -2.1234 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0942   -1.1993   -2.4423 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0631   -2.3851   -1.8191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2755   -2.8797   -1.2038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3343   -3.7376   -0.1661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6686   -4.1981    0.3623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1256   -4.2964    0.5615 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5956   -3.2906    1.4792 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2518   -2.8116    2.6301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3766   -1.5552    3.1049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2785   -1.2846    4.2846 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3876   -0.3474    2.5918 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4725    0.7184    1.8933 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9426    0.3413    0.5412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4733    1.1701   -0.3913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6176    1.2092   -1.8759 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9728   -0.1207   -2.5668 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3526    2.1558    0.3214 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9575    3.0774   -0.1956 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3324    1.8801    1.6538 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4809   -0.6131   -4.8510 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6899   -1.0280   -5.0568 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4571   -0.3822   -2.6709 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7681   -1.5399   -1.5300 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3262    0.1775   -1.4377 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7903   -3.0605   -1.7746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2086   -2.5229   -1.6347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5075   -3.7638   -0.1920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7859   -3.9143    1.4125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7502   -5.2872    0.2842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4256   -5.1735    1.1506 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5923   -4.6859   -0.1714 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4749   -3.7922    1.9020 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9706   -2.4577    0.8785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8134   -3.6047    3.1249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1007   -0.6225    3.9970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7141   -0.8109    5.0945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7218   -2.2017    4.6873 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2147   -0.6391    1.9341 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8942    0.1212    3.4474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3148    1.0246    2.5226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5864   -0.5061    0.3616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4004    1.9398   -2.1174 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3041    1.6035   -2.3217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1462    0.0794   -3.6326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9408   -0.4603   -2.1843 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  2  1  0  0  0  0
 17 16  2  0  0  0  0
 19  4  1  0  0  0  0
  9 10  1  0  0  0  0
  2  3  1  0  0  0  0
 10 11  1  0  0  0  0
 18 19  1  0  0  0  0
 11 12  2  0  0  0  0
  2  1  2  0  0  0  0
 12 13  1  0  0  0  0
  4  5  2  0  0  0  0
 12 14  1  0  0  0  0
  6  7  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  5  6  1  0  0  0  0
 17 20  1  0  0  0  0
  7  9  1  0  0  0  0
 15 22  1  0  0  0  0
 22 20  1  0  0  0  0
 20 21  2  0  0  0  0
 18 17  1  0  0  0  0
  7  8  1  0  0  0  0
  6 29  1  0  0  0  0
 18 45  1  0  0  0  0
 18 46  1  0  0  0  0
 19 47  1  0  0  0  0
 19 48  1  0  0  0  0
  5 28  1  0  0  0  0
  3 25  1  0  0  0  0
  3 26  1  0  0  0  0
  3 27  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  9 33  1  0  0  0  0
  9 34  1  0  0  0  0
 16 44  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
 13 38  1  0  0  0  0
 13 39  1  0  0  0  0
 13 40  1  0  0  0  0
 14 41  1  0  0  0  0
 14 42  1  0  0  0  0
 15 43  1  1  0  0  0
  8 30  1  0  0  0  0
  8 31  1  0  0  0  0
  8 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0036334

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]C([H])=C(\C1=C(/[H])\C(\[H])=C(C([H])([H])[H])/C([H])([H])C([H])([H])\C([H])=C(C([H])([H])[H])/C([H])([H])[C@@]2([H])OC(=O)C(=C2[H])C([H])([H])C1([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C20H26O2/c1-14(2)17-9-8-15(3)6-5-7-16(4)12-19-13-18(11-10-17)20(21)22-19/h7-9,13,19H,1,5-6,10-12H2,2-4H3/b15-8-,16-7-,17-9+/t19-/m1/s1

> <INCHI_KEY>
KGUUUDYKWYRRMZ-CHWGSWCKSA-N

> <FORMULA>
C20H26O2

> <MOLECULAR_WEIGHT>
298.426

> <EXACT_MASS>
298.193280077

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
34.488697093912236

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4E,6Z,10Z,13R)-7,11-dimethyl-4-(prop-1-en-2-yl)-14-oxabicyclo[11.2.1]hexadeca-1(16),4,6,10-tetraen-15-one

> <ALOGPS_LOGP>
5.40

> <JCHEM_LOGP>
4.992347710333333

> <ALOGPS_LOGS>
-4.21

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.660516343326123

> <JCHEM_PKA_STRONGEST_BASIC>
-6.881970358558345

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
94.67599999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.86e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4E,6Z,10Z,13R)-7,11-dimethyl-4-(prop-1-en-2-yl)-14-oxabicyclo[11.2.1]hexadeca-1(16),4,6,10-tetraen-15-one

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 48 49  0  0  0  0  0  0  0  0999 V2000
    1.5249   -0.8389   -4.3888 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3885   -0.8915   -3.0544 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5458   -0.6469   -2.1234 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0942   -1.1993   -2.4423 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0631   -2.3851   -1.8191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2755   -2.8797   -1.2038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3343   -3.7376   -0.1661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6686   -4.1981    0.3623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1256   -4.2964    0.5615 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5956   -3.2906    1.4792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2518   -2.8116    2.6301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3766   -1.5552    3.1049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2785   -1.2846    4.2846 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3876   -0.3474    2.5918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4725    0.7184    1.8933 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9426    0.3413    0.5412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4733    1.1701   -0.3913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6176    1.2092   -1.8759 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9728   -0.1207   -2.5668 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3526    2.1558    0.3214 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9575    3.0774   -0.1956 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3324    1.8801    1.6538 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4809   -0.6131   -4.8510 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6899   -1.0280   -5.0568 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4571   -0.3822   -2.6709 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7681   -1.5399   -1.5300 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3262    0.1775   -1.4377 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7903   -3.0605   -1.7746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2086   -2.5229   -1.6347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5075   -3.7638   -0.1920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7859   -3.9143    1.4125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7502   -5.2872    0.2842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4256   -5.1735    1.1506 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5923   -4.6859   -0.1714 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4749   -3.7922    1.9020 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9706   -2.4577    0.8785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8134   -3.6047    3.1249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1007   -0.6225    3.9970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7141   -0.8109    5.0945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7218   -2.2017    4.6873 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2147   -0.6391    1.9341 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8942    0.1212    3.4474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3148    1.0246    2.5226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5864   -0.5061    0.3616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4004    1.9398   -2.1174 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3041    1.6035   -2.3217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1462    0.0794   -3.6326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9408   -0.4603   -2.1843 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  2  1  0
 17 16  2  0
 19  4  1  0
  9 10  1  0
  2  3  1  0
 10 11  1  0
 18 19  1  0
 11 12  2  0
  2  1  2  0
 12 13  1  0
  4  5  2  0
 12 14  1  0
  6  7  2  0
 14 15  1  0
 15 16  1  0
  5  6  1  0
 17 20  1  0
  7  9  1  0
 15 22  1  0
 22 20  1  0
 20 21  2  0
 18 17  1  0
  7  8  1  0
  6 29  1  0
 18 45  1  0
 18 46  1  0
 19 47  1  0
 19 48  1  0
  5 28  1  0
  3 25  1  0
  3 26  1  0
  3 27  1  0
  1 23  1  0
  1 24  1  0
  9 33  1  0
  9 34  1  0
 16 44  1  0
 10 35  1  0
 10 36  1  0
 11 37  1  0
 13 38  1  0
 13 39  1  0
 13 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  1
  8 30  1  0
  8 31  1  0
  8 32  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0       1.525  -0.839  -4.389  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.389  -0.892  -3.054  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.546  -0.647  -2.123  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.094  -1.199  -2.442  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.063  -2.385  -1.819  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.276  -2.880  -1.204  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.334  -3.738  -0.166  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.669  -4.198   0.362  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.126  -4.296   0.562  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.596  -3.291   1.479  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.252  -2.812   2.630  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.377  -1.555   3.105  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.278  -1.285   4.285  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.388  -0.347   2.592  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.473   0.718   1.893  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.943   0.341   0.541  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.473   1.170  -0.391  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.618   1.209  -1.876  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.973  -0.121  -2.567  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.353   2.156   0.321  0.00  0.00           C+0
HETATM   21  O   UNK     0       0.958   3.077  -0.196  0.00  0.00           O+0
HETATM   22  O   UNK     0       0.332   1.880   1.654  0.00  0.00           O+0
HETATM   23  H   UNK     0       2.481  -0.613  -4.851  0.00  0.00           H+0
HETATM   24  H   UNK     0       0.690  -1.028  -5.057  0.00  0.00           H+0
HETATM   25  H   UNK     0       3.457  -0.382  -2.671  0.00  0.00           H+0
HETATM   26  H   UNK     0       2.768  -1.540  -1.530  0.00  0.00           H+0
HETATM   27  H   UNK     0       2.326   0.178  -1.438  0.00  0.00           H+0
HETATM   28  H   UNK     0       0.790  -3.061  -1.775  0.00  0.00           H+0
HETATM   29  H   UNK     0      -2.209  -2.523  -1.635  0.00  0.00           H+0
HETATM   30  H   UNK     0      -3.507  -3.764  -0.192  0.00  0.00           H+0
HETATM   31  H   UNK     0      -2.786  -3.914   1.413  0.00  0.00           H+0
HETATM   32  H   UNK     0      -2.750  -5.287   0.284  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.426  -5.173   1.151  0.00  0.00           H+0
HETATM   34  H   UNK     0       0.592  -4.686  -0.171  0.00  0.00           H+0
HETATM   35  H   UNK     0       1.475  -3.792   1.902  0.00  0.00           H+0
HETATM   36  H   UNK     0       0.971  -2.458   0.879  0.00  0.00           H+0
HETATM   37  H   UNK     0      -0.813  -3.605   3.125  0.00  0.00           H+0
HETATM   38  H   UNK     0      -2.101  -0.623   3.997  0.00  0.00           H+0
HETATM   39  H   UNK     0      -0.714  -0.811   5.095  0.00  0.00           H+0
HETATM   40  H   UNK     0      -1.722  -2.202   4.687  0.00  0.00           H+0
HETATM   41  H   UNK     0       1.215  -0.639   1.934  0.00  0.00           H+0
HETATM   42  H   UNK     0       0.894   0.121   3.447  0.00  0.00           H+0
HETATM   43  H   UNK     0      -1.315   1.025   2.523  0.00  0.00           H+0
HETATM   44  H   UNK     0      -1.586  -0.506   0.362  0.00  0.00           H+0
HETATM   45  H   UNK     0      -1.400   1.940  -2.117  0.00  0.00           H+0
HETATM   46  H   UNK     0       0.304   1.603  -2.322  0.00  0.00           H+0
HETATM   47  H   UNK     0      -1.146   0.079  -3.633  0.00  0.00           H+0
HETATM   48  H   UNK     0      -1.941  -0.460  -2.184  0.00  0.00           H+0
CONECT    1    2   23   24                                                  
CONECT    2    4    3    1                                                  
CONECT    3    2   25   26   27                                             
CONECT    4    2   19    5                                                  
CONECT    5    4    6   28                                                  
CONECT    6    7    5   29                                                  
CONECT    7    6    9    8                                                  
CONECT    8    7   30   31   32                                             
CONECT    9   10    7   33   34                                             
CONECT   10    9   11   35   36                                             
CONECT   11   10   12   37                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12   38   39   40                                             
CONECT   14   12   15   41   42                                             
CONECT   15   14   16   22   43                                             
CONECT   16   17   15   44                                                  
CONECT   17   16   20   18                                                  
CONECT   18   19   17   45   46                                             
CONECT   19    4   18   47   48                                             
CONECT   20   17   22   21                                                  
CONECT   21   20                                                            
CONECT   22   15   20                                                       
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    3                                                            
CONECT   26    3                                                            
CONECT   27    3                                                            
CONECT   28    5                                                            
CONECT   29    6                                                            
CONECT   30    8                                                            
CONECT   31    8                                                            
CONECT   32    8                                                            
CONECT   33    9                                                            
CONECT   34    9                                                            
CONECT   35   10                                                            
CONECT   36   10                                                            
CONECT   37   11                                                            
CONECT   38   13                                                            
CONECT   39   13                                                            
CONECT   40   13                                                            
CONECT   41   14                                                            
CONECT   42   14                                                            
CONECT   43   15                                                            
CONECT   44   16                                                            
CONECT   45   18                                                            
CONECT   46   18                                                            
CONECT   47   19                                                            
CONECT   48   19                                                            
MASTER        0    0    0    0    0    0    0    0   48    0   98    0
END

RDKit          3D

48 49  0  0  0  0  0  0  0  0999 V2000
    1.5249   -0.8389   -4.3888 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3885   -0.8915   -3.0544 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5458   -0.6469   -2.1234 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0942   -1.1993   -2.4423 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0631   -2.3851   -1.8191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2755   -2.8797   -1.2038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3343   -3.7376   -0.1661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6686   -4.1981    0.3623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1256   -4.2964    0.5615 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5956   -3.2906    1.4792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2518   -2.8116    2.6301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3766   -1.5552    3.1049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2785   -1.2846    4.2846 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3876   -0.3474    2.5918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4725    0.7184    1.8933 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9426    0.3413    0.5412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4733    1.1701   -0.3913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6176    1.2092   -1.8759 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9728   -0.1207   -2.5668 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3526    2.1558    0.3214 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9575    3.0774   -0.1956 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3324    1.8801    1.6538 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4809   -0.6131   -4.8510 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6899   -1.0280   -5.0568 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4571   -0.3822   -2.6709 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7681   -1.5399   -1.5300 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3262    0.1775   -1.4377 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7903   -3.0605   -1.7746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2086   -2.5229   -1.6347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5075   -3.7638   -0.1920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7859   -3.9143    1.4125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7502   -5.2872    0.2842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4256   -5.1735    1.1506 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5923   -4.6859   -0.1714 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4749   -3.7922    1.9020 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9706   -2.4577    0.8785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8134   -3.6047    3.1249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1007   -0.6225    3.9970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7141   -0.8109    5.0945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7218   -2.2017    4.6873 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2147   -0.6391    1.9341 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8942    0.1212    3.4474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3148    1.0246    2.5226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5864   -0.5061    0.3616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4004    1.9398   -2.1174 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3041    1.6035   -2.3217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1462    0.0794   -3.6326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9408   -0.4603   -2.1843 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  2  1  0
 17 16  2  0
 19  4  1  0
  9 10  1  0
  2  3  1  0
 10 11  1  0
 18 19  1  0
 11 12  2  0
  2  1  2  0
 12 13  1  0
  4  5  2  0
 12 14  1  0
  6  7  2  0
 14 15  1  0
 15 16  1  0
  5  6  1  0
 17 20  1  0
  7  9  1  0
 15 22  1  0
 22 20  1  0
 20 21  2  0
 18 17  1  0
  7  8  1  0
  6 29  1  0
 18 45  1  0
 18 46  1  0
 19 47  1  0
 19 48  1  0
  5 28  1  0
  3 25  1  0
  3 26  1  0
  3 27  1  0
  1 23  1  0
  1 24  1  0
  9 33  1  0
  9 34  1  0
 16 44  1  0
 10 35  1  0
 10 36  1  0
 11 37  1  0
 13 38  1  0
 13 39  1  0
 13 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  1
  8 30  1  0
  8 31  1  0
  8 32  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₆O₂

Average Mass

298.4260 Da

Monoisotopic Mass

298.19328 Da

IUPAC Name

(4E,6Z,10Z,13R)-7,11-dimethyl-4-(prop-1-en-2-yl)-14-oxabicyclo[11.2.1]hexadeca-1(16),4,6,10-tetraen-15-one

Traditional Name

(4E,6Z,10Z,13R)-7,11-dimethyl-4-(prop-1-en-2-yl)-14-oxabicyclo[11.2.1]hexadeca-1(16),4,6,10-tetraen-15-one

CAS Registry Number

Not Available

SMILES

[H]C([H])=C(\C1=C(/[H])\C(\[H])=C(C([H])([H])[H])/C([H])([H])C([H])([H])\C([H])=C(C([H])([H])[H])/C([H])([H])[C@@]2([H])OC(=O)C(=C2[H])C([H])([H])C1([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C20H26O2/c1-14(2)17-9-8-15(3)6-5-7-16(4)12-19-13-18(11-10-17)20(21)22-19/h7-9,13,19H,1,5-6,10-12H2,2-4H3/b15-8-,16-7-,17-9+/t19-/m1/s1

InChI Key

KGUUUDYKWYRRMZ-CHWGSWCKSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
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, 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, 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, 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, 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

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Croton gratissimus	JEOL database	Langat, M. K., et al, J. Nat. Prod. 74, 2349 (2011)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Terpene lactones

Alternative Parents

Substituents

Terpene lactone
Sesquiterpenoid
2-furanone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Dihydrofuran
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	5.4	ALOGPS
logP	4.99	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	13.66	ChemAxon
pKa (Strongest Basic)	-6.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	26.3 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	94.68 m³·mol⁻¹	ChemAxon
Polarizability	34.49 Å³	ChemAxon
Number of Rings	2	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

76962732

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Langat, M. K., et al. (2011). Langat, M. K., et al, J. Nat. Prod. 74, 2349 (2011). J. Nat. Prod..

Showing NP-Card for (+)-(10R*)-cembra-1E,3E,7E,11Z,16-pentaen-20,10-olide (NP0036334)

MOL for NP0036334 ((+)-(10R*)-cembra-1E,3E,7E,11Z,16-pentaen-20,10-olide)

3D MOL for NP0036334 ((+)-(10R*)-cembra-1E,3E,7E,11Z,16-pentaen-20,10-olide)

3D SDF for NP0036334 ((+)-(10R*)-cembra-1E,3E,7E,11Z,16-pentaen-20,10-olide)

3D-SDF for NP0036334 ((+)-(10R*)-cembra-1E,3E,7E,11Z,16-pentaen-20,10-olide)

PDB for NP0036334 ((+)-(10R*)-cembra-1E,3E,7E,11Z,16-pentaen-20,10-olide)

3D PDB for NP0036334 ((+)-(10R*)-cembra-1E,3E,7E,11Z,16-pentaen-20,10-olide)

SMILES for NP0036334 ((+)-(10R*)-cembra-1E,3E,7E,11Z,16-pentaen-20,10-olide)

INCHI for NP0036334 ((+)-(10R*)-cembra-1E,3E,7E,11Z,16-pentaen-20,10-olide)

Structure for NP0036334 ((+)-(10R*)-cembra-1E,3E,7E,11Z,16-pentaen-20,10-olide)

3D Structure for NP0036334 ((+)-(10R*)-cembra-1E,3E,7E,11Z,16-pentaen-20,10-olide)