Jump To Section:

Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References XML

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2021-09-23 23:11:06 UTC

Update Date

2021-09-23 23:11:06 UTC

HMDB ID

HMDB0303083

Secondary Accession Numbers

None

Metabolite Identification

Common Name

trans-24-Methyl-23-dehydrolophenol

Description

trans-24-Methyl-23-dehydrolophenol belongs to the class of organic compounds known as ergosterols and derivatives. These are steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton. trans-24-Methyl-23-dehydrolophenol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI


  Mrv0541 02241212332D          

 31 34  0  0  0  0            999 V2000
   -2.3977   -1.5105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1122   -1.9230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1122   -2.7480    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3977   -3.1605    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6833   -2.7480    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6833   -1.9230    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9688   -1.5105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9688   -3.1605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2543   -2.7480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2543   -1.9230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2543   -0.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9688   -0.6855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1746   -0.2730    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4601   -0.6855    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4601   -1.5105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8890   -1.5105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8890   -0.6855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8267   -3.1605    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6833   -1.0980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4601    0.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8891    0.9645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1746    0.5520    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6035    0.5520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3180    0.9645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0325    0.5520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7469    0.9645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0325   -0.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4601    0.9645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3977   -3.9855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6833   -3.5730    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3180    1.7895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3 18  1  1  0  0  0
  4  5  1  0  0  0  0
  6  5  1  0  0  0  0
  5  8  1  0  0  0  0
  7  6  1  0  0  0  0
  6 19  1  1  0  0  0
 12  7  1  0  0  0  0
  7 10  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 15  1  0  0  0  0
 11 12  1  0  0  0  0
 11 14  1  0  0  0  0
 13 14  1  0  0  0  0
 13 17  1  0  0  0  0
 14 15  1  0  0  0  0
 14 20  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 22 28  1  6  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
  4 29  1  6  0  0  0
  5 30  1  6  0  0  0
 13 22  1  1  0  0  0
 24 31  1  4  0  0  0
M  END

HMDB0303083
     RDKit          3D
trans-24-Methyl-23-dehydrolophenol
 78 81  0  0  0  0  0  0  0  0999 V2000
    5.7209   -0.9996   -1.3473 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9477   -0.6158    0.0767 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8799   -0.4967    0.8521 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4922   -0.7291    0.3556 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6769    0.5415    0.5346 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3312    1.6210   -0.2536 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2313    0.3896    0.5113 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6038    1.7714    0.7033 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1392    2.0739   -0.6888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6155    0.8000   -0.9924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8261    0.7393   -0.1881 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4613    1.8055    0.2312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6884    1.6558    1.0482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5057    0.4545    0.7649 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.8858    0.7339    0.2139 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.5340    1.7254    1.1911 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7001   -0.5141    0.2582 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.8392   -0.2976   -0.5512 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0412   -1.7515   -0.2184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5728   -1.8559    0.0400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8631   -0.5452   -0.1782 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0954   -0.1451   -1.6160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4178   -0.6025    0.1869 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6363   -1.6125   -0.6256 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2181   -1.4942   -0.1111 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4697   -0.2155   -0.5608 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1608   -0.6177   -1.8365 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3279   -0.3970    0.5237 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1599   -1.6517    0.2483 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9650    0.7312   -0.2882 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6734   -1.1027   -1.9073 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2117   -1.9883   -1.3339 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1327   -0.2294   -1.8909 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0721   -0.2124    1.8999 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5871   -0.8974   -0.7365 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0869   -1.5731    0.9133 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9361    0.8224    1.6154 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3781    1.7355    0.1742 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8896    2.6357   -0.0887 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5105    1.4396   -1.3092 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9430   -0.1455    1.4770 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2796    2.4938    1.1436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2907    1.7194    1.3549 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9741    2.1031   -1.4251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3991    2.9971   -0.7885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8150    0.7154   -2.0845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1598    2.8295    0.0244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3248    1.6256    2.1189 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3205    2.5905    1.0301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6787   -0.1238    1.7203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8643    1.2466   -0.7551 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1481    1.4919    2.2110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3511    2.7648    0.8934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6363    1.5787    1.2199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1165   -0.6205    1.2974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6454   -0.5672   -1.4938 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2961   -1.9409   -1.3024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5254   -2.6212    0.3176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4383   -2.1357    1.1251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1667   -2.6716   -0.6037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5156   -0.7902   -2.2740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1670   -0.3302   -1.8417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8808    0.9012   -1.8295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3080   -0.8369    1.2422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6653   -1.4225   -1.7080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9562   -2.6542   -0.4194 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3676   -2.4047   -0.4125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2238   -1.5173    1.0039 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8015    0.1219   -2.2936 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3149   -0.7600   -2.5844 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5882   -1.6591   -1.7857 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4358   -0.1630    1.5822 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0955   -1.4081   -0.2963 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3919   -2.2016    1.1774 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5987   -2.3634   -0.4028 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2087    1.4512   -0.6409 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4656    0.3240   -1.2098 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7441    1.2517    0.2821 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  3
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  6
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  6
  2 28  1  0
 28 29  1  0
 28 30  1  0
 26  7  1  0
 26 10  1  0
 23 11  1  0
 21 14  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  1
  6 38  1  0
  6 39  1  0
  6 40  1  0
  7 41  1  1
  8 42  1  0
  8 43  1  0
  9 44  1  0
  9 45  1  0
 10 46  1  0
 12 47  1  0
 13 48  1  0
 13 49  1  0
 14 50  1  1
 15 51  1  6
 16 52  1  0
 16 53  1  0
 16 54  1  0
 17 55  1  1
 18 56  1  0
 19 57  1  0
 19 58  1  0
 20 59  1  0
 20 60  1  0
 22 61  1  0
 22 62  1  0
 22 63  1  0
 23 64  1  0
 24 65  1  0
 24 66  1  0
 25 67  1  0
 25 68  1  0
 27 69  1  0
 27 70  1  0
 27 71  1  0
 28 72  1  0
 29 73  1  0
 29 74  1  0
 29 75  1  0
 30 76  1  0
 30 77  1  0
 30 78  1  0
M  END


  Mrv0541 02241212332D          

 31 34  0  0  0  0            999 V2000
   -2.3977   -1.5105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1122   -1.9230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1122   -2.7480    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3977   -3.1605    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6833   -2.7480    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6833   -1.9230    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9688   -1.5105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9688   -3.1605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2543   -2.7480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2543   -1.9230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2543   -0.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9688   -0.6855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1746   -0.2730    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4601   -0.6855    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4601   -1.5105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8890   -1.5105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8890   -0.6855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8267   -3.1605    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6833   -1.0980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4601    0.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8891    0.9645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1746    0.5520    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6035    0.5520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3180    0.9645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0325    0.5520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7469    0.9645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0325   -0.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4601    0.9645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3977   -3.9855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6833   -3.5730    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3180    1.7895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3 18  1  1  0  0  0
  4  5  1  0  0  0  0
  6  5  1  0  0  0  0
  5  8  1  0  0  0  0
  7  6  1  0  0  0  0
  6 19  1  1  0  0  0
 12  7  1  0  0  0  0
  7 10  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 15  1  0  0  0  0
 11 12  1  0  0  0  0
 11 14  1  0  0  0  0
 13 14  1  0  0  0  0
 13 17  1  0  0  0  0
 14 15  1  0  0  0  0
 14 20  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 22 28  1  6  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
  4 29  1  6  0  0  0
  5 30  1  6  0  0  0
 13 22  1  1  0  0  0
 24 31  1  4  0  0  0
M  END
> <DATABASE_ID>
HMDB0303083

> <DATABASE_NAME>
hmdb

> <SMILES>
[H][C@@]12CC=C3C4CC[C@H]([C@H](C)CC=C(C)C(C)C)[C@@]4(C)CCC3[C@@]1(C)CC[C@H](O)[C@H]2C

> <INCHI_IDENTIFIER>
InChI=1S/C29H48O/c1-18(2)19(3)8-9-20(4)23-12-13-25-22-10-11-24-21(5)27(30)15-17-29(24,7)26(22)14-16-28(23,25)6/h8,10,18,20-21,23-27,30H,9,11-17H2,1-7H3/t20-,21+,23-,24+,25?,26?,27+,28-,29+/m1/s1

> <INCHI_KEY>
CTWRZEHGRSDRPG-UGTAPSEZSA-N

> <FORMULA>
C29H48O

> <MOLECULAR_WEIGHT>
412.6908

> <EXACT_MASS>
412.370516158

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
52.88284419591206

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,5S,6S,7S,14R,15R)-14-[(2R)-5,6-dimethylhept-4-en-2-yl]-2,6,15-trimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-9-en-5-ol

> <ALOGPS_LOGP>
7.43

> <JCHEM_LOGP>
7.359301472000002

> <ALOGPS_LOGS>
-6.60

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.957638198850066

> <JCHEM_PKA_STRONGEST_BASIC>
-1.0677290518229814

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
130.48669999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.05e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,5S,6S,7S,14R,15R)-14-[(2R)-5,6-dimethylhept-4-en-2-yl]-2,6,15-trimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-9-en-5-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0303083
     RDKit          3D
trans-24-Methyl-23-dehydrolophenol
 78 81  0  0  0  0  0  0  0  0999 V2000
    5.7209   -0.9996   -1.3473 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9477   -0.6158    0.0767 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8799   -0.4967    0.8521 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4922   -0.7291    0.3556 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6769    0.5415    0.5346 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3312    1.6210   -0.2536 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2313    0.3896    0.5113 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6038    1.7714    0.7033 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1392    2.0739   -0.6888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6155    0.8000   -0.9924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8261    0.7393   -0.1881 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4613    1.8055    0.2312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6884    1.6558    1.0482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5057    0.4545    0.7649 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.8858    0.7339    0.2139 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.5340    1.7254    1.1911 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7001   -0.5141    0.2582 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.8392   -0.2976   -0.5512 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0412   -1.7515   -0.2184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5728   -1.8559    0.0400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8631   -0.5452   -0.1782 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0954   -0.1451   -1.6160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4178   -0.6025    0.1869 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6363   -1.6125   -0.6256 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2181   -1.4942   -0.1111 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4697   -0.2155   -0.5608 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1608   -0.6177   -1.8365 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3279   -0.3970    0.5237 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1599   -1.6517    0.2483 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9650    0.7312   -0.2882 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6734   -1.1027   -1.9073 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2117   -1.9883   -1.3339 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1327   -0.2294   -1.8909 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0721   -0.2124    1.8999 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5871   -0.8974   -0.7365 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0869   -1.5731    0.9133 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9361    0.8224    1.6154 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3781    1.7355    0.1742 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8896    2.6357   -0.0887 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5105    1.4396   -1.3092 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9430   -0.1455    1.4770 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2796    2.4938    1.1436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2907    1.7194    1.3549 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9741    2.1031   -1.4251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3991    2.9971   -0.7885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8150    0.7154   -2.0845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1598    2.8295    0.0244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3248    1.6256    2.1189 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3205    2.5905    1.0301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6787   -0.1238    1.7203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8643    1.2466   -0.7551 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1481    1.4919    2.2110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3511    2.7648    0.8934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6363    1.5787    1.2199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1165   -0.6205    1.2974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6454   -0.5672   -1.4938 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2961   -1.9409   -1.3024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5254   -2.6212    0.3176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4383   -2.1357    1.1251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1667   -2.6716   -0.6037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5156   -0.7902   -2.2740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1670   -0.3302   -1.8417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8808    0.9012   -1.8295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3080   -0.8369    1.2422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6653   -1.4225   -1.7080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9562   -2.6542   -0.4194 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3676   -2.4047   -0.4125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2238   -1.5173    1.0039 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8015    0.1219   -2.2936 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3149   -0.7600   -2.5844 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5882   -1.6591   -1.7857 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4358   -0.1630    1.5822 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0955   -1.4081   -0.2963 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3919   -2.2016    1.1774 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5987   -2.3634   -0.4028 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2087    1.4512   -0.6409 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4656    0.3240   -1.2098 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7441    1.2517    0.2821 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  3
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  6
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  6
  2 28  1  0
 28 29  1  0
 28 30  1  0
 26  7  1  0
 26 10  1  0
 23 11  1  0
 21 14  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  1
  6 38  1  0
  6 39  1  0
  6 40  1  0
  7 41  1  1
  8 42  1  0
  8 43  1  0
  9 44  1  0
  9 45  1  0
 10 46  1  0
 12 47  1  0
 13 48  1  0
 13 49  1  0
 14 50  1  1
 15 51  1  6
 16 52  1  0
 16 53  1  0
 16 54  1  0
 17 55  1  1
 18 56  1  0
 19 57  1  0
 19 58  1  0
 20 59  1  0
 20 60  1  0
 22 61  1  0
 22 62  1  0
 22 63  1  0
 23 64  1  0
 24 65  1  0
 24 66  1  0
 25 67  1  0
 25 68  1  0
 27 69  1  0
 27 70  1  0
 27 71  1  0
 28 72  1  0
 29 73  1  0
 29 74  1  0
 29 75  1  0
 30 76  1  0
 30 77  1  0
 30 78  1  0
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -4.476  -2.820   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.809  -3.590   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.809  -5.130   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.476  -5.900   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.142  -5.130   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.142  -3.590   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.808  -2.820   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.808  -5.900   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.475  -5.130   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.475  -3.590   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.475  -0.510   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.808  -1.280   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.193  -0.510   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.859  -1.280   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.859  -2.820   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.526  -2.820   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.526  -1.280   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -7.143  -5.900   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -3.142  -2.050   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.859   0.260   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.526   1.800   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.193   1.030   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.860   1.030   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.194   1.800   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.527   1.030   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.861   1.800   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.527  -0.510   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.859   1.800   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -4.476  -7.440   0.000  0.00  0.00           C+0
HETATM   30  H   UNK     0      -3.142  -6.670   0.000  0.00  0.00           H+0
HETATM   31  C   UNK     0       6.194   3.340   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   18                                                  
CONECT    4    3    5   29                                                  
CONECT    5    4    6    8   30                                             
CONECT    6    1    5    7   19                                             
CONECT    7    6   12   10                                                  
CONECT    8    5    9                                                       
CONECT    9    8   10                                                       
CONECT   10    7    9   15                                                  
CONECT   11   12   14                                                       
CONECT   12    7   11                                                       
CONECT   13   14   17   22                                                  
CONECT   14   11   13   15   20                                             
CONECT   15   10   14   16                                                  
CONECT   16   15   17                                                       
CONECT   17   13   16                                                       
CONECT   18    3                                                            
CONECT   19    6                                                            
CONECT   20   14                                                            
CONECT   21   22   23                                                       
CONECT   22   21   28   13                                                  
CONECT   23   21   24                                                       
CONECT   24   23   25   31                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   22                                                            
CONECT   29    4                                                            
CONECT   30    5                                                            
CONECT   31   24                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

COMPND    HMDB0303083
HETATM    1  C1  UNL     1       5.721  -1.000  -1.347  1.00  0.00           C  
HETATM    2  C2  UNL     1       5.948  -0.616   0.077  1.00  0.00           C  
HETATM    3  C3  UNL     1       4.880  -0.497   0.852  1.00  0.00           C  
HETATM    4  C4  UNL     1       3.492  -0.729   0.356  1.00  0.00           C  
HETATM    5  C5  UNL     1       2.677   0.541   0.535  1.00  0.00           C  
HETATM    6  C6  UNL     1       3.331   1.621  -0.254  1.00  0.00           C  
HETATM    7  C7  UNL     1       1.231   0.390   0.511  1.00  0.00           C  
HETATM    8  C8  UNL     1       0.604   1.771   0.703  1.00  0.00           C  
HETATM    9  C9  UNL     1       0.139   2.074  -0.689  1.00  0.00           C  
HETATM   10  C10 UNL     1      -0.616   0.800  -0.992  1.00  0.00           C  
HETATM   11  C11 UNL     1      -1.826   0.739  -0.188  1.00  0.00           C  
HETATM   12  C12 UNL     1      -2.461   1.806   0.231  1.00  0.00           C  
HETATM   13  C13 UNL     1      -3.688   1.656   1.048  1.00  0.00           C  
HETATM   14  C14 UNL     1      -4.506   0.455   0.765  1.00  0.00           C  
HETATM   15  C15 UNL     1      -5.886   0.734   0.214  1.00  0.00           C  
HETATM   16  C16 UNL     1      -6.534   1.725   1.191  1.00  0.00           C  
HETATM   17  C17 UNL     1      -6.700  -0.514   0.258  1.00  0.00           C  
HETATM   18  O1  UNL     1      -7.839  -0.298  -0.551  1.00  0.00           O  
HETATM   19  C18 UNL     1      -6.041  -1.752  -0.218  1.00  0.00           C  
HETATM   20  C19 UNL     1      -4.573  -1.856   0.040  1.00  0.00           C  
HETATM   21  C20 UNL     1      -3.863  -0.545  -0.178  1.00  0.00           C  
HETATM   22  C21 UNL     1      -4.095  -0.145  -1.616  1.00  0.00           C  
HETATM   23  C22 UNL     1      -2.418  -0.603   0.187  1.00  0.00           C  
HETATM   24  C23 UNL     1      -1.636  -1.613  -0.626  1.00  0.00           C  
HETATM   25  C24 UNL     1      -0.218  -1.494  -0.111  1.00  0.00           C  
HETATM   26  C25 UNL     1       0.470  -0.215  -0.561  1.00  0.00           C  
HETATM   27  C26 UNL     1       1.161  -0.618  -1.837  1.00  0.00           C  
HETATM   28  C27 UNL     1       7.328  -0.397   0.524  1.00  0.00           C  
HETATM   29  C28 UNL     1       8.160  -1.652   0.248  1.00  0.00           C  
HETATM   30  C29 UNL     1       7.965   0.731  -0.288  1.00  0.00           C  
HETATM   31  H1  UNL     1       6.673  -1.103  -1.907  1.00  0.00           H  
HETATM   32  H2  UNL     1       5.212  -1.988  -1.334  1.00  0.00           H  
HETATM   33  H3  UNL     1       5.133  -0.229  -1.891  1.00  0.00           H  
HETATM   34  H4  UNL     1       5.072  -0.212   1.900  1.00  0.00           H  
HETATM   35  H5  UNL     1       3.587  -0.897  -0.736  1.00  0.00           H  
HETATM   36  H6  UNL     1       3.087  -1.573   0.913  1.00  0.00           H  
HETATM   37  H7  UNL     1       2.936   0.822   1.615  1.00  0.00           H  
HETATM   38  H8  UNL     1       4.378   1.736   0.174  1.00  0.00           H  
HETATM   39  H9  UNL     1       2.890   2.636  -0.089  1.00  0.00           H  
HETATM   40  H10 UNL     1       3.510   1.440  -1.309  1.00  0.00           H  
HETATM   41  H11 UNL     1       0.943  -0.146   1.477  1.00  0.00           H  
HETATM   42  H12 UNL     1       1.280   2.494   1.144  1.00  0.00           H  
HETATM   43  H13 UNL     1      -0.291   1.719   1.355  1.00  0.00           H  
HETATM   44  H14 UNL     1       0.974   2.103  -1.425  1.00  0.00           H  
HETATM   45  H15 UNL     1      -0.399   2.997  -0.789  1.00  0.00           H  
HETATM   46  H16 UNL     1      -0.815   0.715  -2.085  1.00  0.00           H  
HETATM   47  H17 UNL     1      -2.160   2.829   0.024  1.00  0.00           H  
HETATM   48  H18 UNL     1      -3.325   1.626   2.119  1.00  0.00           H  
HETATM   49  H19 UNL     1      -4.320   2.591   1.030  1.00  0.00           H  
HETATM   50  H20 UNL     1      -4.679  -0.124   1.720  1.00  0.00           H  
HETATM   51  H21 UNL     1      -5.864   1.247  -0.755  1.00  0.00           H  
HETATM   52  H22 UNL     1      -6.148   1.492   2.211  1.00  0.00           H  
HETATM   53  H23 UNL     1      -6.351   2.765   0.893  1.00  0.00           H  
HETATM   54  H24 UNL     1      -7.636   1.579   1.220  1.00  0.00           H  
HETATM   55  H25 UNL     1      -7.116  -0.620   1.297  1.00  0.00           H  
HETATM   56  H26 UNL     1      -7.645  -0.567  -1.494  1.00  0.00           H  
HETATM   57  H27 UNL     1      -6.296  -1.941  -1.302  1.00  0.00           H  
HETATM   58  H28 UNL     1      -6.525  -2.621   0.318  1.00  0.00           H  
HETATM   59  H29 UNL     1      -4.438  -2.136   1.125  1.00  0.00           H  
HETATM   60  H30 UNL     1      -4.167  -2.672  -0.604  1.00  0.00           H  
HETATM   61  H31 UNL     1      -3.516  -0.790  -2.274  1.00  0.00           H  
HETATM   62  H32 UNL     1      -5.167  -0.330  -1.842  1.00  0.00           H  
HETATM   63  H33 UNL     1      -3.881   0.901  -1.829  1.00  0.00           H  
HETATM   64  H34 UNL     1      -2.308  -0.837   1.242  1.00  0.00           H  
HETATM   65  H35 UNL     1      -1.665  -1.423  -1.708  1.00  0.00           H  
HETATM   66  H36 UNL     1      -1.956  -2.654  -0.419  1.00  0.00           H  
HETATM   67  H37 UNL     1       0.368  -2.405  -0.413  1.00  0.00           H  
HETATM   68  H38 UNL     1      -0.224  -1.517   1.004  1.00  0.00           H  
HETATM   69  H39 UNL     1       1.802   0.122  -2.294  1.00  0.00           H  
HETATM   70  H40 UNL     1       0.315  -0.760  -2.584  1.00  0.00           H  
HETATM   71  H41 UNL     1       1.588  -1.659  -1.786  1.00  0.00           H  
HETATM   72  H42 UNL     1       7.436  -0.163   1.582  1.00  0.00           H  
HETATM   73  H43 UNL     1       9.096  -1.408  -0.296  1.00  0.00           H  
HETATM   74  H44 UNL     1       8.392  -2.202   1.177  1.00  0.00           H  
HETATM   75  H45 UNL     1       7.599  -2.363  -0.403  1.00  0.00           H  
HETATM   76  H46 UNL     1       7.209   1.451  -0.641  1.00  0.00           H  
HETATM   77  H47 UNL     1       8.466   0.324  -1.210  1.00  0.00           H  
HETATM   78  H48 UNL     1       8.744   1.252   0.282  1.00  0.00           H  
CONECT    1    2   31   32   33
CONECT    2    3    3   28
CONECT    3    4   34
CONECT    4    5   35   36
CONECT    5    6    7   37
CONECT    6   38   39   40
CONECT    7    8   26   41
CONECT    8    9   42   43
CONECT    9   10   44   45
CONECT   10   11   26   46
CONECT   11   12   12   23
CONECT   12   13   47
CONECT   13   14   48   49
CONECT   14   15   21   50
CONECT   15   16   17   51
CONECT   16   52   53   54
CONECT   17   18   19   55
CONECT   18   56
CONECT   19   20   57   58
CONECT   20   21   59   60
CONECT   21   22   23
CONECT   22   61   62   63
CONECT   23   24   64
CONECT   24   25   65   66
CONECT   25   26   67   68
CONECT   26   27
CONECT   27   69   70   71
CONECT   28   29   30   72
CONECT   29   73   74   75
CONECT   30   76   77   78
END

HMDB0303083
     RDKit          3D
trans-24-Methyl-23-dehydrolophenol
 78 81  0  0  0  0  0  0  0  0999 V2000
    5.7209   -0.9996   -1.3473 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9477   -0.6158    0.0767 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8799   -0.4967    0.8521 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4922   -0.7291    0.3556 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6769    0.5415    0.5346 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3312    1.6210   -0.2536 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2313    0.3896    0.5113 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6038    1.7714    0.7033 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1392    2.0739   -0.6888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6155    0.8000   -0.9924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8261    0.7393   -0.1881 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4613    1.8055    0.2312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6884    1.6558    1.0482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5057    0.4545    0.7649 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.8858    0.7339    0.2139 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.5340    1.7254    1.1911 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7001   -0.5141    0.2582 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.8392   -0.2976   -0.5512 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0412   -1.7515   -0.2184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5728   -1.8559    0.0400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8631   -0.5452   -0.1782 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0954   -0.1451   -1.6160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4178   -0.6025    0.1869 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6363   -1.6125   -0.6256 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2181   -1.4942   -0.1111 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4697   -0.2155   -0.5608 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1608   -0.6177   -1.8365 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3279   -0.3970    0.5237 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1599   -1.6517    0.2483 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9650    0.7312   -0.2882 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6734   -1.1027   -1.9073 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2117   -1.9883   -1.3339 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1327   -0.2294   -1.8909 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0721   -0.2124    1.8999 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5871   -0.8974   -0.7365 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0869   -1.5731    0.9133 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9361    0.8224    1.6154 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3781    1.7355    0.1742 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8896    2.6357   -0.0887 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5105    1.4396   -1.3092 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9430   -0.1455    1.4770 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2796    2.4938    1.1436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2907    1.7194    1.3549 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9741    2.1031   -1.4251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3991    2.9971   -0.7885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8150    0.7154   -2.0845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1598    2.8295    0.0244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3248    1.6256    2.1189 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3205    2.5905    1.0301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6787   -0.1238    1.7203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8643    1.2466   -0.7551 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1481    1.4919    2.2110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3511    2.7648    0.8934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6363    1.5787    1.2199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1165   -0.6205    1.2974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6454   -0.5672   -1.4938 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2961   -1.9409   -1.3024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5254   -2.6212    0.3176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4383   -2.1357    1.1251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1667   -2.6716   -0.6037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5156   -0.7902   -2.2740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1670   -0.3302   -1.8417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8808    0.9012   -1.8295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3080   -0.8369    1.2422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6653   -1.4225   -1.7080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9562   -2.6542   -0.4194 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3676   -2.4047   -0.4125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2238   -1.5173    1.0039 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8015    0.1219   -2.2936 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3149   -0.7600   -2.5844 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5882   -1.6591   -1.7857 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4358   -0.1630    1.5822 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0955   -1.4081   -0.2963 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3919   -2.2016    1.1774 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5987   -2.3634   -0.4028 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2087    1.4512   -0.6409 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4656    0.3240   -1.2098 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7441    1.2517    0.2821 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  3
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  6
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  6
  2 28  1  0
 28 29  1  0
 28 30  1  0
 26  7  1  0
 26 10  1  0
 23 11  1  0
 21 14  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  1
  6 38  1  0
  6 39  1  0
  6 40  1  0
  7 41  1  1
  8 42  1  0
  8 43  1  0
  9 44  1  0
  9 45  1  0
 10 46  1  0
 12 47  1  0
 13 48  1  0
 13 49  1  0
 14 50  1  1
 15 51  1  6
 16 52  1  0
 16 53  1  0
 16 54  1  0
 17 55  1  1
 18 56  1  0
 19 57  1  0
 19 58  1  0
 20 59  1  0
 20 60  1  0
 22 61  1  0
 22 62  1  0
 22 63  1  0
 23 64  1  0
 24 65  1  0
 24 66  1  0
 25 67  1  0
 25 68  1  0
 27 69  1  0
 27 70  1  0
 27 71  1  0
 28 72  1  0
 29 73  1  0
 29 74  1  0
 29 75  1  0
 30 76  1  0
 30 77  1  0
 30 78  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₉H₄₈O

Average Molecular Weight

412.6908

Monoisotopic Molecular Weight

412.370516158

IUPAC Name

(2S,5S,6S,7S,14R,15R)-14-[(2R)-5,6-dimethylhept-4-en-2-yl]-2,6,15-trimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-9-en-5-ol

Traditional Name

(2S,5S,6S,7S,14R,15R)-14-[(2R)-5,6-dimethylhept-4-en-2-yl]-2,6,15-trimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-9-en-5-ol

CAS Registry Number

Not Available

SMILES

[H][C@@]12CC=C3C4CC[C@H]([C@H](C)CC=C(C)C(C)C)[C@@]4(C)CCC3[C@@]1(C)CC[C@H](O)[C@H]2C

InChI Identifier

InChI=1S/C29H48O/c1-18(2)19(3)8-9-20(4)23-12-13-25-22-10-11-24-21(5)27(30)15-17-29(24,7)26(22)14-16-28(23,25)6/h8,10,18,20-21,23-27,30H,9,11-17H2,1-7H3/t20-,21+,23-,24+,25?,26?,27+,28-,29+/m1/s1

InChI Key

CTWRZEHGRSDRPG-UGTAPSEZSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as ergosterols and derivatives. These are steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Ergostane steroids

Direct Parent

Ergosterols and derivatives

Alternative Parents

Substituents

Ergosterol-skeleton
3-beta-hydroxysteroid
Hydroxysteroid
3-hydroxysteroid
3-hydroxy-delta-7-steroid
Delta-7-steroid
Cyclic alcohol
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Cereal and cereal product

Cereal

Corn (FooDB: FOOD00205)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular 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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	7.43	ALOGPS
logP	7.36	ChemAxon
logS	-6.6	ALOGPS
pKa (Strongest Acidic)	18.96	ChemAxon
pKa (Strongest Basic)	-1.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	20.23 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	130.49 m³·mol⁻¹	ChemAxon
Polarizability	52.88 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
AllCCS	[M+H]+	208.844	32859911
AllCCS	[M+H-H2O]+	206.801	32859911
AllCCS	[M+Na]+	211.26	32859911
AllCCS	[M+NH4]+	210.723	32859911
AllCCS	[M-H]-	208.248	32859911
AllCCS	[M+Na-2H]-	210.314	32859911
AllCCS	[M+HCOO]-	212.743	32859911
DeepCCS	[M-2H]-	253.168	30932474
DeepCCS	[M+Na]+	228.232	30932474

Predicted Kovats Retention Indices

Not Available

Spectra

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - trans-24-Methyl-23-dehydrolophenol 10V, Positive-QTOF	splash10-01ot-2009400000-c39096fcf5ce574be651	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - trans-24-Methyl-23-dehydrolophenol 20V, Positive-QTOF	splash10-040s-6129100000-d62df578e8388cbb29a2	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - trans-24-Methyl-23-dehydrolophenol 40V, Positive-QTOF	splash10-00lr-7069000000-0ed3888691b3f259b645	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - trans-24-Methyl-23-dehydrolophenol 10V, Negative-QTOF	splash10-03di-0002900000-45f4160e3b7bad7e5433	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - trans-24-Methyl-23-dehydrolophenol 20V, Negative-QTOF	splash10-03di-0004900000-2d037c34b3518b7500b6	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - trans-24-Methyl-23-dehydrolophenol 40V, Negative-QTOF	splash10-0002-2009000000-b229e18d582dde98a23a	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - trans-24-Methyl-23-dehydrolophenol 10V, Positive-QTOF	splash10-03xs-0059300000-24ae2b9a95031d1a3e07	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - trans-24-Methyl-23-dehydrolophenol 20V, Positive-QTOF	splash10-0159-9432000000-7ee704d90b9b149ee61a	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - trans-24-Methyl-23-dehydrolophenol 40V, Positive-QTOF	splash10-053u-9330000000-f32999d83f67d829f5bb	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - trans-24-Methyl-23-dehydrolophenol 10V, Negative-QTOF	splash10-03di-0000900000-363450e12a0ea926276e	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - trans-24-Methyl-23-dehydrolophenol 20V, Negative-QTOF	splash10-03di-0000900000-363450e12a0ea926276e	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - trans-24-Methyl-23-dehydrolophenol 40V, Negative-QTOF	splash10-08fr-1005900000-30b343a5fd7b6466eb39	2021-10-21	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB007701

KNApSAcK ID

Not Available

Chemspider ID

Not Available

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

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Not Available

Showing metabocard for trans-24-Methyl-23-dehydrolophenol (HMDB0303083)

MOL for HMDB0303083 (trans-24-Methyl-23-dehydrolophenol)

3D MOL for HMDB0303083 (trans-24-Methyl-23-dehydrolophenol)

3D SDF for HMDB0303083 (trans-24-Methyl-23-dehydrolophenol)

3D-SDF for HMDB0303083 (trans-24-Methyl-23-dehydrolophenol)

PDB for HMDB0303083 (trans-24-Methyl-23-dehydrolophenol)

3D PDB for HMDB0303083 (trans-24-Methyl-23-dehydrolophenol)

SMILES for HMDB0303083 (trans-24-Methyl-23-dehydrolophenol)

INCHI for HMDB0303083 (trans-24-Methyl-23-dehydrolophenol)

Structure for HMDB0303083 (trans-24-Methyl-23-dehydrolophenol)

3D Structure for HMDB0303083 (trans-24-Methyl-23-dehydrolophenol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

MS/MS Spectra