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

2012-09-11 17:48:06 UTC

Update Date

2022-03-07 02:53:15 UTC

HMDB ID

HMDB0032144

Secondary Accession Numbers

HMDB32144

Metabolite Identification

Common Name

24-Methyl-28-norcycloart-25-en-3-ol

Description

24-Methyl-28-norcycloart-25-en-3-ol belongs to the class of organic compounds known as cycloartanols and derivatives. These are steroids containing a cycloartanol moiety. 24-Methyl-28-norcycloart-25-en-3-ol 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 02241209252D          

 31 35  0  0  0  0            999 V2000
   -3.7061   -0.4093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7061   -1.2349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9920   -1.6477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2793   -1.2349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2793   -0.4093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9920    0.0020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5651   -1.6477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8524   -1.2349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8524   -0.4093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5651    0.0020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1411    0.0020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1411    0.8235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8524    1.2335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5651    0.8235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6391   -0.2510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1192    0.4134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6391    1.0753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2793    0.4162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4216   -1.6477    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9920   -2.4733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1411   -0.8235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1411    1.6491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8950    1.8596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3432    2.4733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7027    2.0302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2545    1.4166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0622    1.5872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6140    0.9735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3181    2.3715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3580    0.1892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4216    1.1441    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
  2 19  1  0  0  0  0
  3  4  1  0  0  0  0
  3 20  1  0  0  0  0
  4  5  1  0  0  0  0
  4  7  1  0  0  0  0
  5  6  1  0  0  0  0
  5 10  1  0  0  0  0
  5 18  1  0  0  0  0
  7  8  1  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
 10 14  1  0  0  0  0
 10 18  1  0  0  0  0
 11 12  1  0  0  0  0
 11 15  1  0  0  0  0
 11 21  1  0  0  0  0
 12 13  1  0  0  0  0
 12 17  1  0  0  0  0
 12 22  1  0  0  0  0
 13 14  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 28 30  2  0  0  0  0
 28 31  1  0  0  0  0
M  END

HMDB0032144
     RDKit          3D
24-Methyl-28-norcycloart-25-en-3-ol
 81 85  0  0  0  0  0  0  0  0999 V2000
   -6.8664    1.9722   -0.8141 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6699    0.6765   -0.9745 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3579   -0.0427   -2.0472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7151    0.0083   -0.0043 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5826   -1.0716    0.6518 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5679   -0.5992   -0.7580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5268   -1.2969    0.0210 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7043   -0.6470    1.0244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4396   -0.0485    2.1905 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6251    0.2674    0.6402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9443    0.8148    1.8851 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0106    1.7930    1.2078 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5106    0.9715    0.0479 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4964    1.8652   -1.1424 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8229    0.4114    0.4354 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9438    1.3082    0.8395 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0698    0.3521    1.2478 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2632   -0.7945    0.2431 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7761   -1.0049    0.0780 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4280   -0.9999    1.4478 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4212    0.0149   -0.7770 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5466    0.5621   -0.1464 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5269    1.1256   -1.2022 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2105    0.6050   -1.6929 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5314   -0.4411   -0.9381 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4847   -0.9886   -1.7719 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1454   -0.6428   -0.4953 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5756   -1.8430    0.2068 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1196   -1.5077    0.4343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4254   -0.2431   -0.0900 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8272   -0.4162   -1.5472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5384    2.5261   -1.4712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3774    2.5613   -0.0278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7881    0.6284   -2.7923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6195   -0.6957   -2.5889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1657   -0.7049   -1.6660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4522    0.6999    0.8020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1642   -1.6235   -0.1127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2266   -0.5957    1.4251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9689   -1.8172    1.1853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0988   -1.3725   -1.4208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1743    0.0831   -1.5500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0982   -2.1496    0.5350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9507   -1.9015   -0.7363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1196   -1.5063    1.5328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5955    1.0220    2.1742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3917   -0.5546    2.4454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8331   -0.1712    3.1587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0295    1.1357    0.0843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6239    1.3115    2.5913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3438    0.0918    2.4256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6493    2.6382    0.8550 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7391    2.1499    1.9022 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8070    2.8938   -0.7788 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1924    1.6340   -1.9445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5586    2.0146   -1.4708 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5701    0.0084    1.4873 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7433    1.8624    1.8148 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2040    2.1029    0.1765 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6749   -0.1475    2.1850 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9823    0.8418    1.5469 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9462   -1.7733    0.6635 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9432   -2.0304   -0.3409 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6775   -1.1239    2.2475 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2434   -1.7457    1.4905 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9199   -0.0062    1.6115 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8251   -0.4721   -1.7130 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7230    1.4893   -0.4362 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0408    1.6063   -2.0921 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4728    1.9675   -0.4945 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5097    0.1381   -2.7011 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5699    1.4524   -2.0742 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0523   -0.4876   -2.6459 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7557   -2.0410   -2.1020 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0423   -1.8570    1.2405 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7741   -2.8204   -0.2012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4194   -2.3439   -0.1079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1391   -1.7186    1.5150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1785    0.1721   -2.2435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8355   -0.0458   -1.7508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6781   -1.4854   -1.8776 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 30 10  1  0
 30 13  1  0
 27 15  1  0
 25 18  1  0
 27 25  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  0
  3 35  1  0
  3 36  1  0
  4 37  1  0
  5 38  1  0
  5 39  1  0
  5 40  1  0
  6 41  1  0
  6 42  1  0
  7 43  1  0
  7 44  1  0
  8 45  1  0
  9 46  1  0
  9 47  1  0
  9 48  1  0
 10 49  1  0
 11 50  1  0
 11 51  1  0
 12 52  1  0
 12 53  1  0
 14 54  1  0
 14 55  1  0
 14 56  1  0
 15 57  1  0
 16 58  1  0
 16 59  1  0
 17 60  1  0
 17 61  1  0
 18 62  1  0
 19 63  1  0
 20 64  1  0
 20 65  1  0
 20 66  1  0
 21 67  1  0
 22 68  1  0
 23 69  1  0
 23 70  1  0
 24 71  1  0
 24 72  1  0
 26 73  1  0
 26 74  1  0
 28 75  1  0
 28 76  1  0
 29 77  1  0
 29 78  1  0
 31 79  1  0
 31 80  1  0
 31 81  1  0
M  END


  Mrv0541 02241209252D          

 31 35  0  0  0  0            999 V2000
   -3.7061   -0.4093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7061   -1.2349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9920   -1.6477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2793   -1.2349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2793   -0.4093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9920    0.0020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5651   -1.6477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8524   -1.2349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8524   -0.4093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5651    0.0020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1411    0.0020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1411    0.8235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8524    1.2335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5651    0.8235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6391   -0.2510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1192    0.4134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6391    1.0753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2793    0.4162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4216   -1.6477    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9920   -2.4733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1411   -0.8235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1411    1.6491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8950    1.8596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3432    2.4733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7027    2.0302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2545    1.4166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0622    1.5872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6140    0.9735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3181    2.3715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3580    0.1892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4216    1.1441    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
  2 19  1  0  0  0  0
  3  4  1  0  0  0  0
  3 20  1  0  0  0  0
  4  5  1  0  0  0  0
  4  7  1  0  0  0  0
  5  6  1  0  0  0  0
  5 10  1  0  0  0  0
  5 18  1  0  0  0  0
  7  8  1  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
 10 14  1  0  0  0  0
 10 18  1  0  0  0  0
 11 12  1  0  0  0  0
 11 15  1  0  0  0  0
 11 21  1  0  0  0  0
 12 13  1  0  0  0  0
 12 17  1  0  0  0  0
 12 22  1  0  0  0  0
 13 14  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 28 30  2  0  0  0  0
 28 31  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0032144

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(CCC(C)C(C)=C)C1CCC2(C)C3CCC4C(C)C(O)CCC44CC34CCC12C

> <INCHI_IDENTIFIER>
InChI=1S/C30H50O/c1-19(2)20(3)8-9-21(4)23-12-14-28(7)26-11-10-24-22(5)25(31)13-15-29(24)18-30(26,29)17-16-27(23,28)6/h20-26,31H,1,8-18H2,2-7H3

> <INCHI_KEY>
QCGMIFBWAQSUQY-UHFFFAOYSA-N

> <FORMULA>
C30H50O

> <MOLECULAR_WEIGHT>
426.7174

> <EXACT_MASS>
426.386166222

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
55.14781501545015

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
15-(5,6-dimethylhept-6-en-2-yl)-7,12,16-trimethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-ol

> <ALOGPS_LOGP>
5.93

> <JCHEM_LOGP>
7.514614296000002

> <ALOGPS_LOGS>
-6.64

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.892582276698388

> <JCHEM_PKA_STRONGEST_BASIC>
-1.0961845121721243

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
131.11119999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.81e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
15-(5,6-dimethylhept-6-en-2-yl)-7,12,16-trimethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0032144
     RDKit          3D
24-Methyl-28-norcycloart-25-en-3-ol
 81 85  0  0  0  0  0  0  0  0999 V2000
   -6.8664    1.9722   -0.8141 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6699    0.6765   -0.9745 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3579   -0.0427   -2.0472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7151    0.0083   -0.0043 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5826   -1.0716    0.6518 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5679   -0.5992   -0.7580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5268   -1.2969    0.0210 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7043   -0.6470    1.0244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4396   -0.0485    2.1905 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6251    0.2674    0.6402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9443    0.8148    1.8851 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0106    1.7930    1.2078 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5106    0.9715    0.0479 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4964    1.8652   -1.1424 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8229    0.4114    0.4354 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9438    1.3082    0.8395 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0698    0.3521    1.2478 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2632   -0.7945    0.2431 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7761   -1.0049    0.0780 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4280   -0.9999    1.4478 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4212    0.0149   -0.7770 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5466    0.5621   -0.1464 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5269    1.1256   -1.2022 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2105    0.6050   -1.6929 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5314   -0.4411   -0.9381 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4847   -0.9886   -1.7719 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1454   -0.6428   -0.4953 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5756   -1.8430    0.2068 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1196   -1.5077    0.4343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4254   -0.2431   -0.0900 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8272   -0.4162   -1.5472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5384    2.5261   -1.4712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3774    2.5613   -0.0278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7881    0.6284   -2.7923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6195   -0.6957   -2.5889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1657   -0.7049   -1.6660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4522    0.6999    0.8020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1642   -1.6235   -0.1127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2266   -0.5957    1.4251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9689   -1.8172    1.1853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0988   -1.3725   -1.4208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1743    0.0831   -1.5500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0982   -2.1496    0.5350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9507   -1.9015   -0.7363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1196   -1.5063    1.5328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5955    1.0220    2.1742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3917   -0.5546    2.4454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8331   -0.1712    3.1587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0295    1.1357    0.0843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6239    1.3115    2.5913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3438    0.0918    2.4256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6493    2.6382    0.8550 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7391    2.1499    1.9022 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8070    2.8938   -0.7788 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1924    1.6340   -1.9445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5586    2.0146   -1.4708 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5701    0.0084    1.4873 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7433    1.8624    1.8148 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2040    2.1029    0.1765 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6749   -0.1475    2.1850 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9823    0.8418    1.5469 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9462   -1.7733    0.6635 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9432   -2.0304   -0.3409 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6775   -1.1239    2.2475 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2434   -1.7457    1.4905 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9199   -0.0062    1.6115 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8251   -0.4721   -1.7130 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7230    1.4893   -0.4362 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0408    1.6063   -2.0921 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4728    1.9675   -0.4945 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5097    0.1381   -2.7011 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5699    1.4524   -2.0742 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0523   -0.4876   -2.6459 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7557   -2.0410   -2.1020 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0423   -1.8570    1.2405 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7741   -2.8204   -0.2012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4194   -2.3439   -0.1079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1391   -1.7186    1.5150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1785    0.1721   -2.2435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8355   -0.0458   -1.7508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6781   -1.4854   -1.8776 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 30 10  1  0
 30 13  1  0
 27 15  1  0
 25 18  1  0
 27 25  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  0
  3 35  1  0
  3 36  1  0
  4 37  1  0
  5 38  1  0
  5 39  1  0
  5 40  1  0
  6 41  1  0
  6 42  1  0
  7 43  1  0
  7 44  1  0
  8 45  1  0
  9 46  1  0
  9 47  1  0
  9 48  1  0
 10 49  1  0
 11 50  1  0
 11 51  1  0
 12 52  1  0
 12 53  1  0
 14 54  1  0
 14 55  1  0
 14 56  1  0
 15 57  1  0
 16 58  1  0
 16 59  1  0
 17 60  1  0
 17 61  1  0
 18 62  1  0
 19 63  1  0
 20 64  1  0
 20 65  1  0
 20 66  1  0
 21 67  1  0
 22 68  1  0
 23 69  1  0
 23 70  1  0
 24 71  1  0
 24 72  1  0
 26 73  1  0
 26 74  1  0
 28 75  1  0
 28 76  1  0
 29 77  1  0
 29 78  1  0
 31 79  1  0
 31 80  1  0
 31 81  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      -6.918  -0.764   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.918  -2.305   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.585  -3.076   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.255  -2.305   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.255  -0.764   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.585   0.004   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.922  -3.076   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.591  -2.305   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.591  -0.764   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.922   0.004   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.263   0.004   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.263   1.537   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.591   2.303   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.922   1.537   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.193  -0.469   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.089   0.772   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.193   2.007   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -4.255   0.777   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -8.254  -3.076   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -5.585  -4.617   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.263  -1.537   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.263   3.078   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.671   3.471   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.641   4.617   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.178   3.790   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.208   2.644   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.716   2.963   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.746   1.817   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.194   4.427   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.268   0.353   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       8.254   2.136   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3   19                                                  
CONECT    3    2    4   20                                                  
CONECT    4    3    5    7                                                  
CONECT    5    4    6   10   18                                             
CONECT    6    1    5                                                       
CONECT    7    4    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    5    9   14   18                                             
CONECT   11    9   12   15   21                                             
CONECT   12   11   13   17   22                                             
CONECT   13   12   14                                                       
CONECT   14   10   13                                                       
CONECT   15   11   16                                                       
CONECT   16   15   17                                                       
CONECT   17   12   16   23                                                  
CONECT   18    5   10                                                       
CONECT   19    2                                                            
CONECT   20    3                                                            
CONECT   21   11                                                            
CONECT   22   12                                                            
CONECT   23   17   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27   30   31                                                  
CONECT   29   27                                                            
CONECT   30   28                                                            
CONECT   31   28                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   70    0
END

COMPND    HMDB0032144
HETATM    1  C1  UNL     1      -6.866   1.972  -0.814  1.00  0.00           C  
HETATM    2  C2  UNL     1      -6.670   0.677  -0.975  1.00  0.00           C  
HETATM    3  C3  UNL     1      -7.358  -0.043  -2.047  1.00  0.00           C  
HETATM    4  C4  UNL     1      -5.715   0.008  -0.004  1.00  0.00           C  
HETATM    5  C5  UNL     1      -6.583  -1.072   0.652  1.00  0.00           C  
HETATM    6  C6  UNL     1      -4.568  -0.599  -0.758  1.00  0.00           C  
HETATM    7  C7  UNL     1      -3.527  -1.297   0.021  1.00  0.00           C  
HETATM    8  C8  UNL     1      -2.704  -0.647   1.024  1.00  0.00           C  
HETATM    9  C9  UNL     1      -3.440  -0.049   2.190  1.00  0.00           C  
HETATM   10  C10 UNL     1      -1.625   0.267   0.640  1.00  0.00           C  
HETATM   11  C11 UNL     1      -0.944   0.815   1.885  1.00  0.00           C  
HETATM   12  C12 UNL     1      -0.011   1.793   1.208  1.00  0.00           C  
HETATM   13  C13 UNL     1       0.511   0.972   0.048  1.00  0.00           C  
HETATM   14  C14 UNL     1       0.496   1.865  -1.142  1.00  0.00           C  
HETATM   15  C15 UNL     1       1.823   0.411   0.435  1.00  0.00           C  
HETATM   16  C16 UNL     1       2.944   1.308   0.840  1.00  0.00           C  
HETATM   17  C17 UNL     1       4.070   0.352   1.248  1.00  0.00           C  
HETATM   18  C18 UNL     1       4.263  -0.794   0.243  1.00  0.00           C  
HETATM   19  C19 UNL     1       5.776  -1.005   0.078  1.00  0.00           C  
HETATM   20  C20 UNL     1       6.428  -1.000   1.448  1.00  0.00           C  
HETATM   21  C21 UNL     1       6.421   0.015  -0.777  1.00  0.00           C  
HETATM   22  O1  UNL     1       7.547   0.562  -0.146  1.00  0.00           O  
HETATM   23  C22 UNL     1       5.527   1.126  -1.202  1.00  0.00           C  
HETATM   24  C23 UNL     1       4.210   0.605  -1.693  1.00  0.00           C  
HETATM   25  C24 UNL     1       3.531  -0.441  -0.938  1.00  0.00           C  
HETATM   26  C25 UNL     1       2.485  -0.989  -1.772  1.00  0.00           C  
HETATM   27  C26 UNL     1       2.145  -0.643  -0.495  1.00  0.00           C  
HETATM   28  C27 UNL     1       1.576  -1.843   0.207  1.00  0.00           C  
HETATM   29  C28 UNL     1       0.120  -1.508   0.434  1.00  0.00           C  
HETATM   30  C29 UNL     1      -0.425  -0.243  -0.090  1.00  0.00           C  
HETATM   31  C30 UNL     1      -0.827  -0.416  -1.547  1.00  0.00           C  
HETATM   32  H1  UNL     1      -7.538   2.526  -1.471  1.00  0.00           H  
HETATM   33  H2  UNL     1      -6.377   2.561  -0.028  1.00  0.00           H  
HETATM   34  H3  UNL     1      -7.788   0.628  -2.792  1.00  0.00           H  
HETATM   35  H4  UNL     1      -6.619  -0.696  -2.589  1.00  0.00           H  
HETATM   36  H5  UNL     1      -8.166  -0.705  -1.666  1.00  0.00           H  
HETATM   37  H6  UNL     1      -5.452   0.700   0.802  1.00  0.00           H  
HETATM   38  H7  UNL     1      -7.164  -1.624  -0.113  1.00  0.00           H  
HETATM   39  H8  UNL     1      -7.227  -0.596   1.425  1.00  0.00           H  
HETATM   40  H9  UNL     1      -5.969  -1.817   1.185  1.00  0.00           H  
HETATM   41  H10 UNL     1      -5.099  -1.373  -1.421  1.00  0.00           H  
HETATM   42  H11 UNL     1      -4.174   0.083  -1.550  1.00  0.00           H  
HETATM   43  H12 UNL     1      -4.098  -2.150   0.535  1.00  0.00           H  
HETATM   44  H13 UNL     1      -2.951  -1.901  -0.736  1.00  0.00           H  
HETATM   45  H14 UNL     1      -2.120  -1.506   1.533  1.00  0.00           H  
HETATM   46  H15 UNL     1      -3.596   1.022   2.174  1.00  0.00           H  
HETATM   47  H16 UNL     1      -4.392  -0.555   2.445  1.00  0.00           H  
HETATM   48  H17 UNL     1      -2.833  -0.171   3.159  1.00  0.00           H  
HETATM   49  H18 UNL     1      -2.030   1.136   0.084  1.00  0.00           H  
HETATM   50  H19 UNL     1      -1.624   1.312   2.591  1.00  0.00           H  
HETATM   51  H20 UNL     1      -0.344   0.092   2.426  1.00  0.00           H  
HETATM   52  H21 UNL     1      -0.649   2.638   0.855  1.00  0.00           H  
HETATM   53  H22 UNL     1       0.739   2.150   1.902  1.00  0.00           H  
HETATM   54  H23 UNL     1       0.807   2.894  -0.779  1.00  0.00           H  
HETATM   55  H24 UNL     1       1.192   1.634  -1.945  1.00  0.00           H  
HETATM   56  H25 UNL     1      -0.559   2.015  -1.471  1.00  0.00           H  
HETATM   57  H26 UNL     1       1.570   0.008   1.487  1.00  0.00           H  
HETATM   58  H27 UNL     1       2.743   1.862   1.815  1.00  0.00           H  
HETATM   59  H28 UNL     1       3.204   2.103   0.177  1.00  0.00           H  
HETATM   60  H29 UNL     1       3.675  -0.147   2.185  1.00  0.00           H  
HETATM   61  H30 UNL     1       4.982   0.842   1.547  1.00  0.00           H  
HETATM   62  H31 UNL     1       3.946  -1.773   0.663  1.00  0.00           H  
HETATM   63  H32 UNL     1       5.943  -2.030  -0.341  1.00  0.00           H  
HETATM   64  H33 UNL     1       5.677  -1.124   2.248  1.00  0.00           H  
HETATM   65  H34 UNL     1       7.243  -1.746   1.490  1.00  0.00           H  
HETATM   66  H35 UNL     1       6.920  -0.006   1.612  1.00  0.00           H  
HETATM   67  H36 UNL     1       6.825  -0.472  -1.713  1.00  0.00           H  
HETATM   68  H37 UNL     1       7.723   1.489  -0.436  1.00  0.00           H  
HETATM   69  H38 UNL     1       6.041   1.606  -2.092  1.00  0.00           H  
HETATM   70  H39 UNL     1       5.473   1.967  -0.494  1.00  0.00           H  
HETATM   71  H40 UNL     1       4.510   0.138  -2.701  1.00  0.00           H  
HETATM   72  H41 UNL     1       3.570   1.452  -2.074  1.00  0.00           H  
HETATM   73  H42 UNL     1       2.052  -0.488  -2.646  1.00  0.00           H  
HETATM   74  H43 UNL     1       2.756  -2.041  -2.102  1.00  0.00           H  
HETATM   75  H44 UNL     1       2.042  -1.857   1.241  1.00  0.00           H  
HETATM   76  H45 UNL     1       1.774  -2.820  -0.201  1.00  0.00           H  
HETATM   77  H46 UNL     1      -0.419  -2.344  -0.108  1.00  0.00           H  
HETATM   78  H47 UNL     1      -0.139  -1.719   1.515  1.00  0.00           H  
HETATM   79  H48 UNL     1      -0.179   0.172  -2.243  1.00  0.00           H  
HETATM   80  H49 UNL     1      -1.835  -0.046  -1.751  1.00  0.00           H  
HETATM   81  H50 UNL     1      -0.678  -1.485  -1.878  1.00  0.00           H  
CONECT    1    2    2   32   33
CONECT    2    3    4
CONECT    3   34   35   36
CONECT    4    5    6   37
CONECT    5   38   39   40
CONECT    6    7   41   42
CONECT    7    8   43   44
CONECT    8    9   10   45
CONECT    9   46   47   48
CONECT   10   11   30   49
CONECT   11   12   50   51
CONECT   12   13   52   53
CONECT   13   14   15   30
CONECT   14   54   55   56
CONECT   15   16   27   57
CONECT   16   17   58   59
CONECT   17   18   60   61
CONECT   18   19   25   62
CONECT   19   20   21   63
CONECT   20   64   65   66
CONECT   21   22   23   67
CONECT   22   68
CONECT   23   24   69   70
CONECT   24   25   71   72
CONECT   25   26   27
CONECT   26   27   73   74
CONECT   27   28
CONECT   28   29   75   76
CONECT   29   30   77   78
CONECT   30   31
CONECT   31   79   80   81
END

HMDB0032144
     RDKit          3D
24-Methyl-28-norcycloart-25-en-3-ol
 81 85  0  0  0  0  0  0  0  0999 V2000
   -6.8664    1.9722   -0.8141 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6699    0.6765   -0.9745 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3579   -0.0427   -2.0472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7151    0.0083   -0.0043 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5826   -1.0716    0.6518 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5679   -0.5992   -0.7580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5268   -1.2969    0.0210 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7043   -0.6470    1.0244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4396   -0.0485    2.1905 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6251    0.2674    0.6402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9443    0.8148    1.8851 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0106    1.7930    1.2078 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5106    0.9715    0.0479 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4964    1.8652   -1.1424 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8229    0.4114    0.4354 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9438    1.3082    0.8395 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0698    0.3521    1.2478 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2632   -0.7945    0.2431 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7761   -1.0049    0.0780 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4280   -0.9999    1.4478 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4212    0.0149   -0.7770 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5466    0.5621   -0.1464 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5269    1.1256   -1.2022 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2105    0.6050   -1.6929 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5314   -0.4411   -0.9381 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4847   -0.9886   -1.7719 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1454   -0.6428   -0.4953 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5756   -1.8430    0.2068 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1196   -1.5077    0.4343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4254   -0.2431   -0.0900 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8272   -0.4162   -1.5472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5384    2.5261   -1.4712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3774    2.5613   -0.0278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7881    0.6284   -2.7923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6195   -0.6957   -2.5889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1657   -0.7049   -1.6660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4522    0.6999    0.8020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1642   -1.6235   -0.1127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2266   -0.5957    1.4251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9689   -1.8172    1.1853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0988   -1.3725   -1.4208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1743    0.0831   -1.5500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0982   -2.1496    0.5350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9507   -1.9015   -0.7363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1196   -1.5063    1.5328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5955    1.0220    2.1742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3917   -0.5546    2.4454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8331   -0.1712    3.1587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0295    1.1357    0.0843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6239    1.3115    2.5913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3438    0.0918    2.4256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6493    2.6382    0.8550 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7391    2.1499    1.9022 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8070    2.8938   -0.7788 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1924    1.6340   -1.9445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5586    2.0146   -1.4708 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5701    0.0084    1.4873 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7433    1.8624    1.8148 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2040    2.1029    0.1765 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6749   -0.1475    2.1850 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9823    0.8418    1.5469 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9462   -1.7733    0.6635 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9432   -2.0304   -0.3409 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6775   -1.1239    2.2475 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2434   -1.7457    1.4905 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9199   -0.0062    1.6115 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8251   -0.4721   -1.7130 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7230    1.4893   -0.4362 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0408    1.6063   -2.0921 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4728    1.9675   -0.4945 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5097    0.1381   -2.7011 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5699    1.4524   -2.0742 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0523   -0.4876   -2.6459 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7557   -2.0410   -2.1020 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0423   -1.8570    1.2405 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7741   -2.8204   -0.2012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4194   -2.3439   -0.1079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1391   -1.7186    1.5150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1785    0.1721   -2.2435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8355   -0.0458   -1.7508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6781   -1.4854   -1.8776 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 30 10  1  0
 30 13  1  0
 27 15  1  0
 25 18  1  0
 27 25  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  0
  3 35  1  0
  3 36  1  0
  4 37  1  0
  5 38  1  0
  5 39  1  0
  5 40  1  0
  6 41  1  0
  6 42  1  0
  7 43  1  0
  7 44  1  0
  8 45  1  0
  9 46  1  0
  9 47  1  0
  9 48  1  0
 10 49  1  0
 11 50  1  0
 11 51  1  0
 12 52  1  0
 12 53  1  0
 14 54  1  0
 14 55  1  0
 14 56  1  0
 15 57  1  0
 16 58  1  0
 16 59  1  0
 17 60  1  0
 17 61  1  0
 18 62  1  0
 19 63  1  0
 20 64  1  0
 20 65  1  0
 20 66  1  0
 21 67  1  0
 22 68  1  0
 23 69  1  0
 23 70  1  0
 24 71  1  0
 24 72  1  0
 26 73  1  0
 26 74  1  0
 28 75  1  0
 28 76  1  0
 29 77  1  0
 29 78  1  0
 31 79  1  0
 31 80  1  0
 31 81  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₃₀H₅₀O

Average Molecular Weight

426.7174

Monoisotopic Molecular Weight

426.386166222

IUPAC Name

15-(5,6-dimethylhept-6-en-2-yl)-7,12,16-trimethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-ol

Traditional Name

15-(5,6-dimethylhept-6-en-2-yl)-7,12,16-trimethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-ol

CAS Registry Number

92694-03-6

SMILES

CC(CCC(C)C(C)=C)C1CCC2(C)C3CCC4C(C)C(O)CCC44CC34CCC12C

InChI Identifier

InChI=1S/C30H50O/c1-19(2)20(3)8-9-21(4)23-12-14-28(7)26-11-10-24-22(5)25(31)13-15-29(24)18-30(26,29)17-16-27(23,28)6/h20-26,31H,1,8-18H2,2-7H3

InChI Key

QCGMIFBWAQSUQY-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cycloartanols and derivatives. These are steroids containing a cycloartanol moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Cycloartanols and derivatives

Direct Parent

Cycloartanols and derivatives

Alternative Parents

Substituents

Cycloartanol-skeleton
Triterpenoid
Cycloartane-skeleton
9b,19-cyclo-lanostane-skeleton
Hydroxysteroid
3-hydroxysteroid
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

French plantain (FooDB: FOOD00436)

Fruits (FooDB: FOOD00871)

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
Water Solubility	9.8e-05 g/L	ALOGPS
logP	5.93	ALOGPS
logP	7.51	ChemAxon
logS	-6.6	ALOGPS
pKa (Strongest Acidic)	18.89	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	5	ChemAxon
Refractivity	131.11 m³·mol⁻¹	ChemAxon
Polarizability	55.15 Å³	ChemAxon
Number of Rings	5	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
DarkChem	[M+H]+	201.165	31661259
DarkChem	[M-H]-	193.127	31661259
DeepCCS	[M-2H]-	243.996	30932474
DeepCCS	[M+Na]+	219.223	30932474
AllCCS	[M+H]+	212.6	32859911
AllCCS	[M+H-H2O]+	210.8	32859911
AllCCS	[M+NH4]+	214.3	32859911
AllCCS	[M+Na]+	214.8	32859911
AllCCS	[M-H]-	208.9	32859911
AllCCS	[M+Na-2H]-	211.0	32859911
AllCCS	[M+HCOO]-	213.5	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
24-Methyl-28-norcycloart-25-en-3-ol	CC(CCC(C)C(C)=C)C1CCC2(C)C3CCC4C(C)C(O)CCC44CC34CCC12C	2502.2	Standard polar	33892256
24-Methyl-28-norcycloart-25-en-3-ol	CC(CCC(C)C(C)=C)C1CCC2(C)C3CCC4C(C)C(O)CCC44CC34CCC12C	3257.5	Standard non polar	33892256
24-Methyl-28-norcycloart-25-en-3-ol	CC(CCC(C)C(C)=C)C1CCC2(C)C3CCC4C(C)C(O)CCC44CC34CCC12C	3412.7	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
24-Methyl-28-norcycloart-25-en-3-ol,1TMS,isomer #1	C=C(C)C(C)CCC(C)C1CCC2(C)C3CCC4C(C)C(O[Si](C)(C)C)CCC45CC35CCC12C	3493.6	Semi standard non polar	33892256
24-Methyl-28-norcycloart-25-en-3-ol,1TBDMS,isomer #1	C=C(C)C(C)CCC(C)C1CCC2(C)C3CCC4C(C)C(O[Si](C)(C)C(C)(C)C)CCC45CC35CCC12C	3713.6	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 24-Methyl-28-norcycloart-25-en-3-ol GC-MS (Non-derivatized) - 70eV, Positive	splash10-03di-4029600000-5f2497d6b312c673ccae	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 24-Methyl-28-norcycloart-25-en-3-ol GC-MS (1 TMS) - 70eV, Positive	splash10-0089-5011900000-b4cb45f050ab45b0f9a6	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 24-Methyl-28-norcycloart-25-en-3-ol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 24-Methyl-28-norcycloart-25-en-3-ol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 24-Methyl-28-norcycloart-25-en-3-ol 10V, Positive-QTOF	splash10-056r-1003900000-9b1a712107bb829572bd	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 24-Methyl-28-norcycloart-25-en-3-ol 20V, Positive-QTOF	splash10-003r-5029300000-85252b6052cb8af87696	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 24-Methyl-28-norcycloart-25-en-3-ol 40V, Positive-QTOF	splash10-001i-8069000000-dc4f4234e033f403d71b	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 24-Methyl-28-norcycloart-25-en-3-ol 10V, Negative-QTOF	splash10-004i-0000900000-401e5dc29a4d92a5f0c5	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 24-Methyl-28-norcycloart-25-en-3-ol 20V, Negative-QTOF	splash10-004i-0000900000-23bab4a3578095a9fddc	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 24-Methyl-28-norcycloart-25-en-3-ol 40V, Negative-QTOF	splash10-0a4l-2009300000-8992f826ecf9b4e32275	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 24-Methyl-28-norcycloart-25-en-3-ol 10V, Positive-QTOF	splash10-0040-9125300000-6b8ba901a1aade7cd5c9	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 24-Methyl-28-norcycloart-25-en-3-ol 20V, Positive-QTOF	splash10-053r-9121000000-ea5346a1e9f0f77519bd	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 24-Methyl-28-norcycloart-25-en-3-ol 40V, Positive-QTOF	splash10-001i-9320100000-edd485a7cb97ee270e82	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 24-Methyl-28-norcycloart-25-en-3-ol 10V, Negative-QTOF	splash10-004i-0000900000-590c9e4adfdd12b64d93	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 24-Methyl-28-norcycloart-25-en-3-ol 20V, Negative-QTOF	splash10-004i-0000900000-590c9e4adfdd12b64d93	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 24-Methyl-28-norcycloart-25-en-3-ol 40V, Negative-QTOF	splash10-00fr-0000900000-290cee774a4bbe54158a	2021-09-22	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Membrane

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

FDB008871

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

131751264

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

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for 24-Methyl-28-norcycloart-25-en-3-ol (HMDB0032144)

MOL for HMDB0032144 (24-Methyl-28-norcycloart-25-en-3-ol)

3D MOL for HMDB0032144 (24-Methyl-28-norcycloart-25-en-3-ol)

3D SDF for HMDB0032144 (24-Methyl-28-norcycloart-25-en-3-ol)

3D-SDF for HMDB0032144 (24-Methyl-28-norcycloart-25-en-3-ol)

PDB for HMDB0032144 (24-Methyl-28-norcycloart-25-en-3-ol)

3D PDB for HMDB0032144 (24-Methyl-28-norcycloart-25-en-3-ol)

SMILES for HMDB0032144 (24-Methyl-28-norcycloart-25-en-3-ol)

INCHI for HMDB0032144 (24-Methyl-28-norcycloart-25-en-3-ol)

Structure for HMDB0032144 (24-Methyl-28-norcycloart-25-en-3-ol)

3D Structure for HMDB0032144 (24-Methyl-28-norcycloart-25-en-3-ol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra