NP-MRD: Showing NP-Card for Camphosterol A (NP0011104)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

1.0

Created at

2021-01-05 20:54:46 UTC

Updated at

2021-07-15 17:07:58 UTC

NP-MRD ID

NP0011104

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Camphosterol A

Provided By

NPAtlas

Description

Camphosterol A is found in Antrodia and Taiwanofungus camphoratus. It was first documented in 2012 (PMID: 22999074). Based on a literature review very few articles have been published on Camphosterol A.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242107433D          

 56 58  0  0  0  0            999 V2000
   -4.1266    2.0707   -0.0152 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3198    0.7222   -0.6829 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.7998    0.5846   -0.9695 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.5522    0.6453    0.2108 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9421   -0.3675    0.2989 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1326   -1.7090   -0.3643 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5596   -0.1786    0.8179 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5860   -1.0536    0.7278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2260   -0.7334    1.2992 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0571   -1.8324    2.2914 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8214   -0.7649    0.2338 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4810    0.2600   -0.8782 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7962    0.3863   -1.6096 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8132   -0.3208   -0.8052 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1019    0.3920   -0.6522 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6616    1.4733   -1.1158 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9844    1.6015   -0.5403 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8095    2.5360   -0.7715 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1588    0.5132    0.2991 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0380   -0.2955    0.2596 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4134   -0.5835    1.6002 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0036   -1.1081    1.4844 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1695   -0.2711    0.6010 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1776    1.1879    1.0114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0637    2.3837   -0.1352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3727    1.9559    1.0490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8113    2.7872   -0.4984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7754    0.6504   -1.6280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0616   -0.3187   -1.5174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1165    1.5057   -1.5448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3347    1.4531    0.7281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6766   -0.3086    1.1383 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2210   -1.8668   -0.5118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5572   -1.7988   -1.2906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7500   -2.4758    0.3699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3415    0.7616    1.3113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7810   -1.9981    0.2387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2842    0.2151    1.8420 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3965   -1.4285    3.2714 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8006   -2.5158    1.8502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8499   -2.4980    2.4553 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9081   -1.7342   -0.2828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2957   -0.2510   -1.4874 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1106    1.1960   -0.4491 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0460    1.4259   -1.8807 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6737   -0.1670   -2.5832 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9143   -1.3728   -1.0817 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1908    2.1777   -1.8372 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3069   -1.2595   -0.2589 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0170   -1.3996    2.0682 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5048    0.2949    2.2320 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5918   -1.0930    2.5116 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0147   -2.1514    1.1087 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6675    1.8453    0.2785 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1615    1.5678    1.2498 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7457    1.2628    1.9556 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
  2  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 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  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 11  1  0  0  0  0
 23 14  1  0  0  0  0
 20 15  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
  2 28  1  6  0  0  0
  3 29  1  0  0  0  0
  3 30  1  0  0  0  0
  4 31  1  0  0  0  0
  5 32  1  1  0  0  0
  6 33  1  0  0  0  0
  6 34  1  0  0  0  0
  6 35  1  0  0  0  0
  7 36  1  0  0  0  0
  8 37  1  0  0  0  0
  9 38  1  1  0  0  0
 10 39  1  0  0  0  0
 10 40  1  0  0  0  0
 10 41  1  0  0  0  0
 11 42  1  6  0  0  0
 12 43  1  0  0  0  0
 12 44  1  0  0  0  0
 13 45  1  0  0  0  0
 13 46  1  0  0  0  0
 14 47  1  6  0  0  0
 16 48  1  0  0  0  0
 20 49  1  6  0  0  0
 21 50  1  0  0  0  0
 21 51  1  0  0  0  0
 22 52  1  0  0  0  0
 22 53  1  0  0  0  0
 24 54  1  0  0  0  0
 24 55  1  0  0  0  0
 24 56  1  0  0  0  0
M  END

     RDKit          3D

 56 58  0  0  0  0  0  0  0  0999 V2000
   -4.1266    2.0707   -0.0152 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3198    0.7222   -0.6829 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.7998    0.5846   -0.9695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5522    0.6453    0.2108 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9421   -0.3675    0.2989 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1326   -1.7090   -0.3643 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5596   -0.1786    0.8179 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5860   -1.0536    0.7278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2260   -0.7334    1.2992 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0571   -1.8324    2.2914 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8214   -0.7649    0.2338 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4810    0.2600   -0.8782 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7962    0.3863   -1.6096 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8132   -0.3208   -0.8052 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1019    0.3920   -0.6522 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6616    1.4733   -1.1158 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9844    1.6015   -0.5403 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8095    2.5360   -0.7715 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1588    0.5132    0.2991 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0380   -0.2955    0.2596 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4134   -0.5835    1.6002 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0036   -1.1081    1.4844 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1695   -0.2711    0.6010 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1776    1.1879    1.0114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0637    2.3837   -0.1352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3727    1.9559    1.0490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8113    2.7872   -0.4984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7754    0.6504   -1.6280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0616   -0.3187   -1.5174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1165    1.5057   -1.5448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3347    1.4531    0.7281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6766   -0.3086    1.1383 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2210   -1.8668   -0.5118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5572   -1.7988   -1.2906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7500   -2.4758    0.3699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3415    0.7616    1.3113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7810   -1.9981    0.2387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2842    0.2151    1.8420 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3965   -1.4285    3.2714 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8006   -2.5158    1.8502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8499   -2.4980    2.4553 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9081   -1.7342   -0.2828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2957   -0.2510   -1.4874 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1106    1.1960   -0.4491 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0460    1.4259   -1.8807 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6737   -0.1670   -2.5832 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9143   -1.3728   -1.0817 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1908    2.1777   -1.8372 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3069   -1.2595   -0.2589 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0170   -1.3996    2.0682 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5048    0.2949    2.2320 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5918   -1.0930    2.5116 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0147   -2.1514    1.1087 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6675    1.8453    0.2785 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1615    1.5678    1.2498 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7457    1.2628    1.9556 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
  2  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  1
 23 11  1  0
 23 14  1  0
 20 15  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  6
  3 29  1  0
  3 30  1  0
  4 31  1  0
  5 32  1  1
  6 33  1  0
  6 34  1  0
  6 35  1  0
  7 36  1  0
  8 37  1  0
  9 38  1  1
 10 39  1  0
 10 40  1  0
 10 41  1  0
 11 42  1  6
 12 43  1  0
 12 44  1  0
 13 45  1  0
 13 46  1  0
 14 47  1  6
 16 48  1  0
 20 49  1  6
 21 50  1  0
 21 51  1  0
 22 52  1  0
 22 53  1  0
 24 54  1  0
 24 55  1  0
 24 56  1  0
M  END


  Mrv1652306242107433D          

 56 58  0  0  0  0            999 V2000
   -4.1266    2.0707   -0.0152 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3198    0.7222   -0.6829 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.7998    0.5846   -0.9695 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.5522    0.6453    0.2108 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9421   -0.3675    0.2989 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1326   -1.7090   -0.3643 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5596   -0.1786    0.8179 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5860   -1.0536    0.7278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2260   -0.7334    1.2992 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0571   -1.8324    2.2914 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8214   -0.7649    0.2338 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4810    0.2600   -0.8782 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7962    0.3863   -1.6096 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8132   -0.3208   -0.8052 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1019    0.3920   -0.6522 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6616    1.4733   -1.1158 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9844    1.6015   -0.5403 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8095    2.5360   -0.7715 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1588    0.5132    0.2991 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0380   -0.2955    0.2596 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4134   -0.5835    1.6002 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0036   -1.1081    1.4844 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1695   -0.2711    0.6010 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1776    1.1879    1.0114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0637    2.3837   -0.1352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3727    1.9559    1.0490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8113    2.7872   -0.4984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7754    0.6504   -1.6280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0616   -0.3187   -1.5174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1165    1.5057   -1.5448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3347    1.4531    0.7281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6766   -0.3086    1.1383 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2210   -1.8668   -0.5118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5572   -1.7988   -1.2906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7500   -2.4758    0.3699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3415    0.7616    1.3113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7810   -1.9981    0.2387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2842    0.2151    1.8420 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3965   -1.4285    3.2714 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8006   -2.5158    1.8502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8499   -2.4980    2.4553 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9081   -1.7342   -0.2828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2957   -0.2510   -1.4874 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1106    1.1960   -0.4491 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0460    1.4259   -1.8807 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6737   -0.1670   -2.5832 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9143   -1.3728   -1.0817 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1908    2.1777   -1.8372 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3069   -1.2595   -0.2589 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0170   -1.3996    2.0682 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5048    0.2949    2.2320 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5918   -1.0930    2.5116 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0147   -2.1514    1.1087 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6675    1.8453    0.2785 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1615    1.5678    1.2498 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7457    1.2628    1.9556 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
  2  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 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  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 11  1  0  0  0  0
 23 14  1  0  0  0  0
 20 15  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
  2 28  1  6  0  0  0
  3 29  1  0  0  0  0
  3 30  1  0  0  0  0
  4 31  1  0  0  0  0
  5 32  1  1  0  0  0
  6 33  1  0  0  0  0
  6 34  1  0  0  0  0
  6 35  1  0  0  0  0
  7 36  1  0  0  0  0
  8 37  1  0  0  0  0
  9 38  1  1  0  0  0
 10 39  1  0  0  0  0
 10 40  1  0  0  0  0
 10 41  1  0  0  0  0
 11 42  1  6  0  0  0
 12 43  1  0  0  0  0
 12 44  1  0  0  0  0
 13 45  1  0  0  0  0
 13 46  1  0  0  0  0
 14 47  1  6  0  0  0
 16 48  1  0  0  0  0
 20 49  1  6  0  0  0
 21 50  1  0  0  0  0
 21 51  1  0  0  0  0
 22 52  1  0  0  0  0
 22 53  1  0  0  0  0
 24 54  1  0  0  0  0
 24 55  1  0  0  0  0
 24 56  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0011104

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC([H])([H])[C@@]([H])(C([H])([H])[H])[C@]([H])(C(\[H])=C(/[H])[C@@]([H])(C([H])([H])[H])[C@@]1([H])C([H])([H])C([H])([H])[C@@]2([H])C3=C([H])C(=O)O[C@@]3([H])C([H])([H])C([H])([H])[C@]12C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C21H32O3/c1-13(15(3)12-22)5-6-14(2)17-7-8-18-16-11-20(23)24-19(16)9-10-21(17,18)4/h5-6,11,13-15,17-19,22H,7-10,12H2,1-4H3/b6-5+/t13-,14+,15+,17+,18-,19-,21+/m0/s1

> <INCHI_KEY>
KTECGYIRZKGESY-HQIHHQEMSA-N

> <FORMULA>
C21H32O3

> <MOLECULAR_WEIGHT>
332.484

> <EXACT_MASS>
332.23514489

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
39.04608140414393

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3aS,5aR,6R,8aR)-6-[(2R,3E,5S,6S)-7-hydroxy-5,6-dimethylhept-3-en-2-yl]-5a-methyl-2H,3aH,4H,5H,5aH,6H,7H,8H,8aH-indeno[5,4-b]furan-2-one

> <ALOGPS_LOGP>
4.49

> <JCHEM_LOGP>
4.205118284333332

> <ALOGPS_LOGS>
-4.72

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.7952076555928

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.778050224891879

> <JCHEM_PKA_STRONGEST_BASIC>
-1.576173766364183

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
97.80979999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.38e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3aS,5aR,6R,8aR)-6-[(2R,3E,5S,6S)-7-hydroxy-5,6-dimethylhept-3-en-2-yl]-5a-methyl-3aH,4H,5H,6H,7H,8H,8aH-indeno[5,4-b]furan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 56 58  0  0  0  0  0  0  0  0999 V2000
   -4.1266    2.0707   -0.0152 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3198    0.7222   -0.6829 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.7998    0.5846   -0.9695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5522    0.6453    0.2108 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9421   -0.3675    0.2989 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1326   -1.7090   -0.3643 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5596   -0.1786    0.8179 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5860   -1.0536    0.7278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2260   -0.7334    1.2992 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0571   -1.8324    2.2914 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8214   -0.7649    0.2338 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4810    0.2600   -0.8782 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7962    0.3863   -1.6096 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8132   -0.3208   -0.8052 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1019    0.3920   -0.6522 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6616    1.4733   -1.1158 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9844    1.6015   -0.5403 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8095    2.5360   -0.7715 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1588    0.5132    0.2991 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0380   -0.2955    0.2596 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4134   -0.5835    1.6002 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0036   -1.1081    1.4844 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1695   -0.2711    0.6010 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1776    1.1879    1.0114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0637    2.3837   -0.1352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3727    1.9559    1.0490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8113    2.7872   -0.4984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7754    0.6504   -1.6280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0616   -0.3187   -1.5174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1165    1.5057   -1.5448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3347    1.4531    0.7281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6766   -0.3086    1.1383 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2210   -1.8668   -0.5118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5572   -1.7988   -1.2906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7500   -2.4758    0.3699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3415    0.7616    1.3113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7810   -1.9981    0.2387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2842    0.2151    1.8420 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3965   -1.4285    3.2714 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8006   -2.5158    1.8502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8499   -2.4980    2.4553 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9081   -1.7342   -0.2828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2957   -0.2510   -1.4874 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1106    1.1960   -0.4491 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0460    1.4259   -1.8807 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6737   -0.1670   -2.5832 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9143   -1.3728   -1.0817 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1908    2.1777   -1.8372 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3069   -1.2595   -0.2589 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0170   -1.3996    2.0682 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5048    0.2949    2.2320 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5918   -1.0930    2.5116 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0147   -2.1514    1.1087 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6675    1.8453    0.2785 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1615    1.5678    1.2498 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7457    1.2628    1.9556 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
  2  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  1
 23 11  1  0
 23 14  1  0
 20 15  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  6
  3 29  1  0
  3 30  1  0
  4 31  1  0
  5 32  1  1
  6 33  1  0
  6 34  1  0
  6 35  1  0
  7 36  1  0
  8 37  1  0
  9 38  1  1
 10 39  1  0
 10 40  1  0
 10 41  1  0
 11 42  1  6
 12 43  1  0
 12 44  1  0
 13 45  1  0
 13 46  1  0
 14 47  1  6
 16 48  1  0
 20 49  1  6
 21 50  1  0
 21 51  1  0
 22 52  1  0
 22 53  1  0
 24 54  1  0
 24 55  1  0
 24 56  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      -4.127   2.071  -0.015  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.320   0.722  -0.683  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.800   0.585  -0.970  0.00  0.00           C+0
HETATM    4  O   UNK     0      -6.552   0.645   0.211  0.00  0.00           O+0
HETATM    5  C   UNK     0      -3.942  -0.368   0.299  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.133  -1.709  -0.364  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.560  -0.179   0.818  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.586  -1.054   0.728  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.226  -0.733   1.299  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.057  -1.832   2.291  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.821  -0.765   0.234  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.481   0.260  -0.878  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.796   0.386  -1.610  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.813  -0.321  -0.805  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.102   0.392  -0.652  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.662   1.473  -1.116  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.984   1.601  -0.540  0.00  0.00           C+0
HETATM   18  O   UNK     0       6.809   2.536  -0.772  0.00  0.00           O+0
HETATM   19  O   UNK     0       6.159   0.513   0.299  0.00  0.00           O+0
HETATM   20  C   UNK     0       5.038  -0.296   0.260  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.413  -0.584   1.600  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.004  -1.108   1.484  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.170  -0.271   0.601  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.178   1.188   1.011  0.00  0.00           C+0
HETATM   25  H   UNK     0      -3.064   2.384  -0.135  0.00  0.00           H+0
HETATM   26  H   UNK     0      -4.373   1.956   1.049  0.00  0.00           H+0
HETATM   27  H   UNK     0      -4.811   2.787  -0.498  0.00  0.00           H+0
HETATM   28  H   UNK     0      -3.775   0.650  -1.628  0.00  0.00           H+0
HETATM   29  H   UNK     0      -6.062  -0.319  -1.517  0.00  0.00           H+0
HETATM   30  H   UNK     0      -6.117   1.506  -1.545  0.00  0.00           H+0
HETATM   31  H   UNK     0      -6.335   1.453   0.728  0.00  0.00           H+0
HETATM   32  H   UNK     0      -4.677  -0.309   1.138  0.00  0.00           H+0
HETATM   33  H   UNK     0      -5.221  -1.867  -0.512  0.00  0.00           H+0
HETATM   34  H   UNK     0      -3.557  -1.799  -1.291  0.00  0.00           H+0
HETATM   35  H   UNK     0      -3.750  -2.476   0.370  0.00  0.00           H+0
HETATM   36  H   UNK     0      -2.341   0.762   1.311  0.00  0.00           H+0
HETATM   37  H   UNK     0      -1.781  -1.998   0.239  0.00  0.00           H+0
HETATM   38  H   UNK     0      -0.284   0.215   1.842  0.00  0.00           H+0
HETATM   39  H   UNK     0       0.397  -1.429   3.271  0.00  0.00           H+0
HETATM   40  H   UNK     0       0.801  -2.516   1.850  0.00  0.00           H+0
HETATM   41  H   UNK     0      -0.850  -2.498   2.455  0.00  0.00           H+0
HETATM   42  H   UNK     0       0.908  -1.734  -0.283  0.00  0.00           H+0
HETATM   43  H   UNK     0      -0.296  -0.251  -1.487  0.00  0.00           H+0
HETATM   44  H   UNK     0       0.111   1.196  -0.449  0.00  0.00           H+0
HETATM   45  H   UNK     0       2.046   1.426  -1.881  0.00  0.00           H+0
HETATM   46  H   UNK     0       1.674  -0.167  -2.583  0.00  0.00           H+0
HETATM   47  H   UNK     0       2.914  -1.373  -1.082  0.00  0.00           H+0
HETATM   48  H   UNK     0       4.191   2.178  -1.837  0.00  0.00           H+0
HETATM   49  H   UNK     0       5.307  -1.260  -0.259  0.00  0.00           H+0
HETATM   50  H   UNK     0       5.017  -1.400   2.068  0.00  0.00           H+0
HETATM   51  H   UNK     0       4.505   0.295   2.232  0.00  0.00           H+0
HETATM   52  H   UNK     0       2.592  -1.093   2.512  0.00  0.00           H+0
HETATM   53  H   UNK     0       3.015  -2.151   1.109  0.00  0.00           H+0
HETATM   54  H   UNK     0       2.668   1.845   0.279  0.00  0.00           H+0
HETATM   55  H   UNK     0       1.161   1.568   1.250  0.00  0.00           H+0
HETATM   56  H   UNK     0       2.746   1.263   1.956  0.00  0.00           H+0
CONECT    1    2   25   26   27                                             
CONECT    2    1    3    5   28                                             
CONECT    3    2    4   29   30                                             
CONECT    4    3   31                                                       
CONECT    5    2    6    7   32                                             
CONECT    6    5   33   34   35                                             
CONECT    7    5    8   36                                                  
CONECT    8    7    9   37                                                  
CONECT    9    8   10   11   38                                             
CONECT   10    9   39   40   41                                             
CONECT   11    9   12   23   42                                             
CONECT   12   11   13   43   44                                             
CONECT   13   12   14   45   46                                             
CONECT   14   13   15   23   47                                             
CONECT   15   14   16   20                                                  
CONECT   16   15   17   48                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   15   49                                             
CONECT   21   20   22   50   51                                             
CONECT   22   21   23   52   53                                             
CONECT   23   22   24   11   14                                             
CONECT   24   23   54   55   56                                             
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    2                                                            
CONECT   29    3                                                            
CONECT   30    3                                                            
CONECT   31    4                                                            
CONECT   32    5                                                            
CONECT   33    6                                                            
CONECT   34    6                                                            
CONECT   35    6                                                            
CONECT   36    7                                                            
CONECT   37    8                                                            
CONECT   38    9                                                            
CONECT   39   10                                                            
CONECT   40   10                                                            
CONECT   41   10                                                            
CONECT   42   11                                                            
CONECT   43   12                                                            
CONECT   44   12                                                            
CONECT   45   13                                                            
CONECT   46   13                                                            
CONECT   47   14                                                            
CONECT   48   16                                                            
CONECT   49   20                                                            
CONECT   50   21                                                            
CONECT   51   21                                                            
CONECT   52   22                                                            
CONECT   53   22                                                            
CONECT   54   24                                                            
CONECT   55   24                                                            
CONECT   56   24                                                            
MASTER        0    0    0    0    0    0    0    0   56    0  116    0
END

RDKit          3D

56 58  0  0  0  0  0  0  0  0999 V2000
   -4.1266    2.0707   -0.0152 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3198    0.7222   -0.6829 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.7998    0.5846   -0.9695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5522    0.6453    0.2108 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9421   -0.3675    0.2989 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1326   -1.7090   -0.3643 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5596   -0.1786    0.8179 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5860   -1.0536    0.7278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2260   -0.7334    1.2992 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0571   -1.8324    2.2914 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8214   -0.7649    0.2338 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4810    0.2600   -0.8782 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7962    0.3863   -1.6096 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8132   -0.3208   -0.8052 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1019    0.3920   -0.6522 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6616    1.4733   -1.1158 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9844    1.6015   -0.5403 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8095    2.5360   -0.7715 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1588    0.5132    0.2991 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0380   -0.2955    0.2596 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4134   -0.5835    1.6002 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0036   -1.1081    1.4844 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1695   -0.2711    0.6010 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1776    1.1879    1.0114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0637    2.3837   -0.1352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3727    1.9559    1.0490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8113    2.7872   -0.4984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7754    0.6504   -1.6280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0616   -0.3187   -1.5174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1165    1.5057   -1.5448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3347    1.4531    0.7281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6766   -0.3086    1.1383 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2210   -1.8668   -0.5118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5572   -1.7988   -1.2906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7500   -2.4758    0.3699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3415    0.7616    1.3113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7810   -1.9981    0.2387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2842    0.2151    1.8420 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3965   -1.4285    3.2714 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8006   -2.5158    1.8502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8499   -2.4980    2.4553 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9081   -1.7342   -0.2828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2957   -0.2510   -1.4874 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1106    1.1960   -0.4491 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0460    1.4259   -1.8807 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6737   -0.1670   -2.5832 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9143   -1.3728   -1.0817 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1908    2.1777   -1.8372 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3069   -1.2595   -0.2589 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0170   -1.3996    2.0682 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5048    0.2949    2.2320 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5918   -1.0930    2.5116 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0147   -2.1514    1.1087 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6675    1.8453    0.2785 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1615    1.5678    1.2498 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7457    1.2628    1.9556 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
  2  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  1
 23 11  1  0
 23 14  1  0
 20 15  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  6
  3 29  1  0
  3 30  1  0
  4 31  1  0
  5 32  1  1
  6 33  1  0
  6 34  1  0
  6 35  1  0
  7 36  1  0
  8 37  1  0
  9 38  1  1
 10 39  1  0
 10 40  1  0
 10 41  1  0
 11 42  1  6
 12 43  1  0
 12 44  1  0
 13 45  1  0
 13 46  1  0
 14 47  1  6
 16 48  1  0
 20 49  1  6
 21 50  1  0
 21 51  1  0
 22 52  1  0
 22 53  1  0
 24 54  1  0
 24 55  1  0
 24 56  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₂₁H₃₂O₃

Average Mass

332.4840 Da

Monoisotopic Mass

332.23514 Da

IUPAC Name

(3aS,5aR,6R,8aR)-6-[(2R,3E,5S,6S)-7-hydroxy-5,6-dimethylhept-3-en-2-yl]-5a-methyl-2H,3aH,4H,5H,5aH,6H,7H,8H,8aH-indeno[5,4-b]furan-2-one

Traditional Name

(3aS,5aR,6R,8aR)-6-[(2R,3E,5S,6S)-7-hydroxy-5,6-dimethylhept-3-en-2-yl]-5a-methyl-3aH,4H,5H,6H,7H,8H,8aH-indeno[5,4-b]furan-2-one

CAS Registry Number

Not Available

SMILES

CC(CO)[C@@H](C)\C=C\[C@@H](C)[C@H]1CC[C@H]2C3=CC(=O)O[C@H]3CC[C@]12C

InChI Identifier

InChI=1S/C21H32O3/c1-13(15(3)12-22)5-6-14(2)17-7-8-18-16-11-20(23)24-19(16)9-10-21(17,18)4/h5-6,11,13-15,17-19,22H,7-10,12H2,1-4H3/b6-5+/t13-,14+,15?,17+,18-,19-,21+/m0/s1

InChI Key

KTECGYIRZKGESY-HQIHHQEMSA-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
Antrodia	NPAtlas	22999074
Taiwanofungus camphoratus	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	4.49	ALOGPS
logP	4.21	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	7.78	ChemAxon
pKa (Strongest Basic)	-1.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	46.53 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	97.81 m³·mol⁻¹	ChemAxon
Polarizability	39.05 Å³	ChemAxon
Number of Rings	3	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

NPA005993

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78442299

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71511668

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Huang HC, Liaw CC, Yang HL, Hseu YC, Kuo HT, Tsai YC, Chien SC, Amagaya S, Chen YC, Kuo YH: Lanostane triterpenoids and sterols from Antrodia camphorata. Phytochemistry. 2012 Dec;84:177-83. doi: 10.1016/j.phytochem.2012.08.011. Epub 2012 Sep 18. [PubMed:22999074 ]

Showing NP-Card for Camphosterol A (NP0011104)

MOL for NP0011104 (Camphosterol A)

3D MOL for NP0011104 (Camphosterol A)

3D SDF for NP0011104 (Camphosterol A)

3D-SDF for NP0011104 (Camphosterol A)

PDB for NP0011104 (Camphosterol A)

3D PDB for NP0011104 (Camphosterol A)

SMILES for NP0011104 (Camphosterol A)

INCHI for NP0011104 (Camphosterol A)

Structure for NP0011104 (Camphosterol A)

3D Structure for NP0011104 (Camphosterol A)