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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2021-09-23 22:34:30 UTC

Update Date

2021-09-23 22:34:30 UTC

HMDB ID

HMDB0303010

Secondary Accession Numbers

None

Metabolite Identification

Common Name

31-Norcycloartenol

Description

31-norcycloartenol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). 31-norcycloartenol can be found in dandelion and garden onion, which makes 31-norcycloartenol a potential biomarker for the consumption of these food products.

Structure

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


  Mrv0541 02241212542D          

 32 36  0  0  0  0            999 V2000
   -3.2227   -0.0668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9372   -0.4793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9372   -1.3043    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2227   -1.7168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5083   -1.3043    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5083   -0.4793    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7938   -0.0668    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7938   -1.7168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0793   -1.3043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0793   -0.4793    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0793    1.1707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7938    0.7582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3496    1.1707    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3649    0.7582    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3649   -0.0668    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0640   -0.0668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0640    0.7582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6517   -1.7168    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5083    0.3457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3649    1.5832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0641    2.4082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3496    1.9957    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7785    1.9957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4930    2.4082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2075    1.9957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9219    2.4082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2075    1.1707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3649    2.4082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3649   -0.8918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2227   -2.5418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0793    0.3457    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5083   -2.1293    0.0000 H   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
 10  9  1  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  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 15 29  1  6  0  0  0
  7 19  1  1  0  0  0
 13 22  1  1  0  0  0
  4 30  1  0  0  0  0
 10 31  1  1  0  0  0
  5 32  1  6  0  0  0
M  END

HMDB0303010
     RDKit          3D
31-Norcycloartenol
 78 82  0  0  0  0  0  0  0  0999 V2000
    5.1474   -1.8604   -0.7170 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7940   -0.6319   -1.2427 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3300   -0.6069   -2.6443 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8851    0.4286   -0.4570 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3956    0.5257    0.9314 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4422    1.6126    1.2385 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1312    1.6513    0.5698 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3396    1.7576   -0.9174 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1705    0.5601    0.9839 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8925    0.6201    2.4809 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4000    0.4478    2.6918 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0068   -0.2225    1.4038 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5375   -1.6200    1.5498 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4406   -0.3024    1.1159 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9316   -1.7611    1.0301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4639   -1.6494    1.1348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8849   -1.2765   -0.2643 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3801   -1.2317   -0.4242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9119   -2.3821   -1.2567 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8461    0.0452   -1.0846 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.9835    1.0968   -0.1964 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0311    0.3976   -2.2937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5517    0.2449   -2.1030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2504   -0.0003   -0.6289 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2351    1.2133    0.1769 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9661    0.3829   -0.0702 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9826    0.8578   -1.0867 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4170    0.3048   -0.8707 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7984    0.6834    0.4809 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3681    2.1250    0.7502 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4461   -2.6969   -1.3945 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0686   -1.7702   -0.6074 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5809   -2.1442    0.2832 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0778    0.3594   -3.1323 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4155   -0.8168   -2.6761 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8029   -1.3988   -3.2063 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3902    1.3168   -0.8908 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3461    0.6093    1.5512 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0022   -0.4868    1.2601 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9612    2.5714    0.8976 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4013    1.7783    2.3445 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6780    2.6575    0.8457 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5411    2.3692   -1.4057 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3332    0.7733   -1.4171 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2869    2.3156   -1.0952 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6539   -0.3604    0.6484 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4453   -0.1617    3.0278 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1575    1.5845    2.9263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1381    1.3670    2.9193 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1994   -0.2418    3.5476 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1820   -1.9569    2.5787 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2425   -2.3100    0.7611 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6335   -1.7014    1.6966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9549    0.0656    2.0598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6492   -2.1456    0.0291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6482   -2.3779    1.8679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9076   -2.5893    1.4911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7277   -0.8450    1.8481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5045   -2.0751   -0.9359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9012   -1.2841    0.5608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9327   -2.0795   -2.3198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1556   -3.2000   -1.1655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9007   -2.7270   -0.8933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8885   -0.1752   -1.4623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8623    1.1200    0.2534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3436    1.4230   -2.6052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3096   -0.2559   -3.1639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0988   -0.5225   -2.7486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1140    1.2502   -2.3779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6287    1.2553    1.2134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2248    2.2188   -0.3065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2390    0.5388   -2.1308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0001    1.9662   -1.1006 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164    0.6118   -1.7126 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2804   -0.8177   -0.9439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6903    2.2299    0.9754 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8793    2.5479    1.6625 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6014    2.8010   -0.0788 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  1
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 24 23  1  6
 24 25  1  0
 26 25  1  1
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  1
 29  9  1  0
 29 12  1  0
 26 14  1  0
 24 17  1  0
 26 24  1  0
  1 31  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
  6 40  1  0
  6 41  1  0
  7 42  1  1
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  8 44  1  0
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 11 49  1  0
 11 50  1  0
 13 51  1  0
 13 52  1  0
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 15 56  1  0
 16 57  1  0
 16 58  1  0
 17 59  1  6
 18 60  1  0
 19 61  1  0
 19 62  1  0
 19 63  1  0
 20 64  1  6
 21 65  1  0
 22 66  1  0
 22 67  1  0
 23 68  1  0
 23 69  1  0
 25 70  1  0
 25 71  1  0
 27 72  1  0
 27 73  1  0
 28 74  1  0
 28 75  1  0
 30 76  1  0
 30 77  1  0
 30 78  1  0
M  END


  Mrv0541 02241212542D          

 32 36  0  0  0  0            999 V2000
   -3.2227   -0.0668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9372   -0.4793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9372   -1.3043    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2227   -1.7168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5083   -1.3043    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5083   -0.4793    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7938   -0.0668    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7938   -1.7168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0793   -1.3043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0793   -0.4793    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0793    1.1707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7938    0.7582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3496    1.1707    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3649    0.7582    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3649   -0.0668    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0640   -0.0668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0640    0.7582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6517   -1.7168    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5083    0.3457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.3496    1.9957    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7785    1.9957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4930    2.4082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2075    1.9957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9219    2.4082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2075    1.1707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3649    2.4082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3649   -0.8918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2227   -2.5418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0793    0.3457    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5083   -2.1293    0.0000 H   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
 10  9  1  0  0  0  0
 10 15  1  0  0  0  0
 11 12  1  0  0  0  0
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 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  1  0  0  0  0
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 15 29  1  6  0  0  0
  7 19  1  1  0  0  0
 13 22  1  1  0  0  0
  4 30  1  0  0  0  0
 10 31  1  1  0  0  0
  5 32  1  6  0  0  0
M  END
> <DATABASE_ID>
HMDB0303010

> <DATABASE_NAME>
hmdb

> <SMILES>
[H][C@@]12CC[C@]3([H])[C@@]4(C[C@]14CC[C@H](O)C2C)CC[C@]1(C)[C@H](CC[C@@]31C)[C@H](C)CCC=C(C)C

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

> <INCHI_KEY>
XZEUYTKSAYNYPK-TUHQVYAESA-N

> <FORMULA>
C29H48O

> <MOLECULAR_WEIGHT>
412.6908

> <EXACT_MASS>
412.370516158

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
53.26433367718177

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,3R,6S,8S,11S,12S,15R,16R)-7,12,16-trimethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-ol

> <ALOGPS_LOGP>
6.01

> <JCHEM_LOGP>
7.169661529333334

> <ALOGPS_LOGS>
-7.03

> <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>
127.63509999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.85e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R,6S,8S,11S,12S,15R,16R)-7,12,16-trimethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0303010
     RDKit          3D
31-Norcycloartenol
 78 82  0  0  0  0  0  0  0  0999 V2000
    5.1474   -1.8604   -0.7170 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7940   -0.6319   -1.2427 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3300   -0.6069   -2.6443 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8851    0.4286   -0.4570 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3956    0.5257    0.9314 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4422    1.6126    1.2385 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1312    1.6513    0.5698 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3396    1.7576   -0.9174 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1705    0.5601    0.9839 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8925    0.6201    2.4809 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4000    0.4478    2.6918 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0068   -0.2225    1.4038 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5375   -1.6200    1.5498 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4406   -0.3024    1.1159 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9316   -1.7611    1.0301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4639   -1.6494    1.1348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8849   -1.2765   -0.2643 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3801   -1.2317   -0.4242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9119   -2.3821   -1.2567 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8461    0.0452   -1.0846 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.9835    1.0968   -0.1964 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0311    0.3976   -2.2937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5517    0.2449   -2.1030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2504   -0.0003   -0.6289 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2351    1.2133    0.1769 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9661    0.3829   -0.0702 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9826    0.8578   -1.0867 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4170    0.3048   -0.8707 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7984    0.6834    0.4809 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3681    2.1250    0.7502 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4461   -2.6969   -1.3945 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0686   -1.7702   -0.6074 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5809   -2.1442    0.2832 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0778    0.3594   -3.1323 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4155   -0.8168   -2.6761 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8029   -1.3988   -3.2063 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3902    1.3168   -0.8908 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3461    0.6093    1.5512 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0022   -0.4868    1.2601 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9612    2.5714    0.8976 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4013    1.7783    2.3445 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6780    2.6575    0.8457 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5411    2.3692   -1.4057 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3332    0.7733   -1.4171 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2869    2.3156   -1.0952 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6539   -0.3604    0.6484 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4453   -0.1617    3.0278 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1575    1.5845    2.9263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1381    1.3670    2.9193 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1994   -0.2418    3.5476 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1820   -1.9569    2.5787 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2425   -2.3100    0.7611 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6335   -1.7014    1.6966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9549    0.0656    2.0598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6492   -2.1456    0.0291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6482   -2.3779    1.8679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9076   -2.5893    1.4911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7277   -0.8450    1.8481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5045   -2.0751   -0.9359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9012   -1.2841    0.5608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9327   -2.0795   -2.3198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1556   -3.2000   -1.1655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9007   -2.7270   -0.8933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8885   -0.1752   -1.4623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8623    1.1200    0.2534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3436    1.4230   -2.6052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3096   -0.2559   -3.1639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0988   -0.5225   -2.7486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1140    1.2502   -2.3779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6287    1.2553    1.2134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2248    2.2188   -0.3065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2390    0.5388   -2.1308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0001    1.9662   -1.1006 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164    0.6118   -1.7126 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2804   -0.8177   -0.9439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6903    2.2299    0.9754 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8793    2.5479    1.6625 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6014    2.8010   -0.0788 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  1
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 24 23  1  6
 24 25  1  0
 26 25  1  1
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  1
 29  9  1  0
 29 12  1  0
 26 14  1  0
 24 17  1  0
 26 24  1  0
  1 31  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
  6 40  1  0
  6 41  1  0
  7 42  1  1
  8 43  1  0
  8 44  1  0
  8 45  1  0
  9 46  1  1
 10 47  1  0
 10 48  1  0
 11 49  1  0
 11 50  1  0
 13 51  1  0
 13 52  1  0
 13 53  1  0
 14 54  1  1
 15 55  1  0
 15 56  1  0
 16 57  1  0
 16 58  1  0
 17 59  1  6
 18 60  1  0
 19 61  1  0
 19 62  1  0
 19 63  1  0
 20 64  1  6
 21 65  1  0
 22 66  1  0
 22 67  1  0
 23 68  1  0
 23 69  1  0
 25 70  1  0
 25 71  1  0
 27 72  1  0
 27 73  1  0
 28 74  1  0
 28 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      -6.016  -0.125   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -7.349  -0.895   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -7.349  -2.435   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.016  -3.205   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.682  -2.435   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.682  -0.895   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.348  -0.125   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.348  -3.205   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.015  -2.435   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.015  -0.895   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.015   2.185   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.348   1.415   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.653   2.185   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.681   1.415   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.681  -0.125   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.986  -0.125   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.986   1.415   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -8.683  -3.205   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -4.682   0.645   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.681   2.955   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.986   4.495   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.653   3.725   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.320   3.725   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.654   4.495   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.987   3.725   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.321   4.495   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.987   2.185   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.681   4.495   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -0.681  -1.665   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -6.016  -4.745   0.000  0.00  0.00           C+0
HETATM   31  H   UNK     0      -2.015   0.645   0.000  0.00  0.00           H+0
HETATM   32  H   UNK     0      -4.682  -3.975   0.000  0.00  0.00           H+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   18                                                  
CONECT    4    3    5   30                                                  
CONECT    5    4    6    8   32                                             
CONECT    6    1    5    7   19                                             
CONECT    7    6   12   10   19                                             
CONECT    8    5    9                                                       
CONECT    9    8   10                                                       
CONECT   10    7    9   15   31                                             
CONECT   11   12   14                                                       
CONECT   12    7   11                                                       
CONECT   13   14   17   22                                                  
CONECT   14   11   13   15   20                                             
CONECT   15   10   14   16   29                                             
CONECT   16   15   17                                                       
CONECT   17   13   16                                                       
CONECT   18    3                                                            
CONECT   19    6    7                                                       
CONECT   20   14                                                            
CONECT   21   22   23                                                       
CONECT   22   21   28   13                                                  
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   22                                                            
CONECT   29   15                                                            
CONECT   30    4                                                            
CONECT   31   10                                                            
CONECT   32    5                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   72    0
END

COMPND    HMDB0303010
HETATM    1  C1  UNL     1       5.147  -1.860  -0.717  1.00  0.00           C  
HETATM    2  C2  UNL     1       5.794  -0.632  -1.243  1.00  0.00           C  
HETATM    3  C3  UNL     1       6.330  -0.607  -2.644  1.00  0.00           C  
HETATM    4  C4  UNL     1       5.885   0.429  -0.457  1.00  0.00           C  
HETATM    5  C5  UNL     1       5.396   0.526   0.931  1.00  0.00           C  
HETATM    6  C6  UNL     1       4.442   1.613   1.238  1.00  0.00           C  
HETATM    7  C7  UNL     1       3.131   1.651   0.570  1.00  0.00           C  
HETATM    8  C8  UNL     1       3.340   1.758  -0.917  1.00  0.00           C  
HETATM    9  C9  UNL     1       2.170   0.560   0.984  1.00  0.00           C  
HETATM   10  C10 UNL     1       1.893   0.620   2.481  1.00  0.00           C  
HETATM   11  C11 UNL     1       0.400   0.448   2.692  1.00  0.00           C  
HETATM   12  C12 UNL     1       0.007  -0.223   1.404  1.00  0.00           C  
HETATM   13  C13 UNL     1       0.538  -1.620   1.550  1.00  0.00           C  
HETATM   14  C14 UNL     1      -1.441  -0.302   1.116  1.00  0.00           C  
HETATM   15  C15 UNL     1      -1.932  -1.761   1.030  1.00  0.00           C  
HETATM   16  C16 UNL     1      -3.464  -1.649   1.135  1.00  0.00           C  
HETATM   17  C17 UNL     1      -3.885  -1.277  -0.264  1.00  0.00           C  
HETATM   18  C18 UNL     1      -5.380  -1.232  -0.424  1.00  0.00           C  
HETATM   19  C19 UNL     1      -5.912  -2.382  -1.257  1.00  0.00           C  
HETATM   20  C20 UNL     1      -5.846   0.045  -1.085  1.00  0.00           C  
HETATM   21  O1  UNL     1      -5.983   1.097  -0.196  1.00  0.00           O  
HETATM   22  C21 UNL     1      -5.031   0.398  -2.294  1.00  0.00           C  
HETATM   23  C22 UNL     1      -3.552   0.245  -2.103  1.00  0.00           C  
HETATM   24  C23 UNL     1      -3.250  -0.000  -0.629  1.00  0.00           C  
HETATM   25  C24 UNL     1      -3.235   1.213   0.177  1.00  0.00           C  
HETATM   26  C25 UNL     1      -1.966   0.383  -0.070  1.00  0.00           C  
HETATM   27  C26 UNL     1      -0.983   0.858  -1.087  1.00  0.00           C  
HETATM   28  C27 UNL     1       0.417   0.305  -0.871  1.00  0.00           C  
HETATM   29  C28 UNL     1       0.798   0.683   0.481  1.00  0.00           C  
HETATM   30  C29 UNL     1       0.368   2.125   0.750  1.00  0.00           C  
HETATM   31  H1  UNL     1       5.446  -2.697  -1.394  1.00  0.00           H  
HETATM   32  H2  UNL     1       4.069  -1.770  -0.607  1.00  0.00           H  
HETATM   33  H3  UNL     1       5.581  -2.144   0.283  1.00  0.00           H  
HETATM   34  H4  UNL     1       6.078   0.359  -3.132  1.00  0.00           H  
HETATM   35  H5  UNL     1       7.415  -0.817  -2.676  1.00  0.00           H  
HETATM   36  H6  UNL     1       5.803  -1.399  -3.206  1.00  0.00           H  
HETATM   37  H7  UNL     1       6.390   1.317  -0.891  1.00  0.00           H  
HETATM   38  H8  UNL     1       6.346   0.609   1.551  1.00  0.00           H  
HETATM   39  H9  UNL     1       5.002  -0.487   1.260  1.00  0.00           H  
HETATM   40  H10 UNL     1       4.961   2.571   0.898  1.00  0.00           H  
HETATM   41  H11 UNL     1       4.401   1.778   2.344  1.00  0.00           H  
HETATM   42  H12 UNL     1       2.678   2.657   0.846  1.00  0.00           H  
HETATM   43  H13 UNL     1       2.541   2.369  -1.406  1.00  0.00           H  
HETATM   44  H14 UNL     1       3.333   0.773  -1.417  1.00  0.00           H  
HETATM   45  H15 UNL     1       4.287   2.316  -1.095  1.00  0.00           H  
HETATM   46  H16 UNL     1       2.654  -0.360   0.648  1.00  0.00           H  
HETATM   47  H17 UNL     1       2.445  -0.162   3.028  1.00  0.00           H  
HETATM   48  H18 UNL     1       2.157   1.585   2.926  1.00  0.00           H  
HETATM   49  H19 UNL     1      -0.138   1.367   2.919  1.00  0.00           H  
HETATM   50  H20 UNL     1       0.199  -0.242   3.548  1.00  0.00           H  
HETATM   51  H21 UNL     1       0.182  -1.957   2.579  1.00  0.00           H  
HETATM   52  H22 UNL     1       0.243  -2.310   0.761  1.00  0.00           H  
HETATM   53  H23 UNL     1       1.634  -1.701   1.697  1.00  0.00           H  
HETATM   54  H24 UNL     1      -1.955   0.066   2.060  1.00  0.00           H  
HETATM   55  H25 UNL     1      -1.649  -2.146   0.029  1.00  0.00           H  
HETATM   56  H26 UNL     1      -1.648  -2.378   1.868  1.00  0.00           H  
HETATM   57  H27 UNL     1      -3.908  -2.589   1.491  1.00  0.00           H  
HETATM   58  H28 UNL     1      -3.728  -0.845   1.848  1.00  0.00           H  
HETATM   59  H29 UNL     1      -3.505  -2.075  -0.936  1.00  0.00           H  
HETATM   60  H30 UNL     1      -5.901  -1.284   0.561  1.00  0.00           H  
HETATM   61  H31 UNL     1      -5.933  -2.080  -2.320  1.00  0.00           H  
HETATM   62  H32 UNL     1      -5.156  -3.200  -1.166  1.00  0.00           H  
HETATM   63  H33 UNL     1      -6.901  -2.727  -0.893  1.00  0.00           H  
HETATM   64  H34 UNL     1      -6.888  -0.175  -1.462  1.00  0.00           H  
HETATM   65  H35 UNL     1      -6.862   1.120   0.253  1.00  0.00           H  
HETATM   66  H36 UNL     1      -5.344   1.423  -2.605  1.00  0.00           H  
HETATM   67  H37 UNL     1      -5.310  -0.256  -3.164  1.00  0.00           H  
HETATM   68  H38 UNL     1      -3.099  -0.522  -2.749  1.00  0.00           H  
HETATM   69  H39 UNL     1      -3.114   1.250  -2.378  1.00  0.00           H  
HETATM   70  H40 UNL     1      -3.629   1.255   1.213  1.00  0.00           H  
HETATM   71  H41 UNL     1      -3.225   2.219  -0.306  1.00  0.00           H  
HETATM   72  H42 UNL     1      -1.239   0.539  -2.131  1.00  0.00           H  
HETATM   73  H43 UNL     1      -1.000   1.966  -1.101  1.00  0.00           H  
HETATM   74  H44 UNL     1       1.016   0.612  -1.713  1.00  0.00           H  
HETATM   75  H45 UNL     1       0.280  -0.818  -0.944  1.00  0.00           H  
HETATM   76  H46 UNL     1      -0.690   2.230   0.975  1.00  0.00           H  
HETATM   77  H47 UNL     1       0.879   2.548   1.662  1.00  0.00           H  
HETATM   78  H48 UNL     1       0.601   2.801  -0.079  1.00  0.00           H  
CONECT    1    2   31   32   33
CONECT    2    3    4    4
CONECT    3   34   35   36
CONECT    4    5   37
CONECT    5    6   38   39
CONECT    6    7   40   41
CONECT    7    8    9   42
CONECT    8   43   44   45
CONECT    9   10   29   46
CONECT   10   11   47   48
CONECT   11   12   49   50
CONECT   12   13   14   29
CONECT   13   51   52   53
CONECT   14   15   26   54
CONECT   15   16   55   56
CONECT   16   17   57   58
CONECT   17   18   24   59
CONECT   18   19   20   60
CONECT   19   61   62   63
CONECT   20   21   22   64
CONECT   21   65
CONECT   22   23   66   67
CONECT   23   24   68   69
CONECT   24   25   26
CONECT   25   26   70   71
CONECT   26   27
CONECT   27   28   72   73
CONECT   28   29   74   75
CONECT   29   30
CONECT   30   76   77   78
END

HMDB0303010
     RDKit          3D
31-Norcycloartenol
 78 82  0  0  0  0  0  0  0  0999 V2000
    5.1474   -1.8604   -0.7170 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7940   -0.6319   -1.2427 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3300   -0.6069   -2.6443 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8851    0.4286   -0.4570 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3956    0.5257    0.9314 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4422    1.6126    1.2385 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1312    1.6513    0.5698 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3396    1.7576   -0.9174 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1705    0.5601    0.9839 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8925    0.6201    2.4809 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4000    0.4478    2.6918 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0068   -0.2225    1.4038 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5375   -1.6200    1.5498 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4406   -0.3024    1.1159 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9316   -1.7611    1.0301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4639   -1.6494    1.1348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8849   -1.2765   -0.2643 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3801   -1.2317   -0.4242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9119   -2.3821   -1.2567 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8461    0.0452   -1.0846 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.9835    1.0968   -0.1964 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0311    0.3976   -2.2937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5517    0.2449   -2.1030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2504   -0.0003   -0.6289 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2351    1.2133    0.1769 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9661    0.3829   -0.0702 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9826    0.8578   -1.0867 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4170    0.3048   -0.8707 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7984    0.6834    0.4809 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3681    2.1250    0.7502 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4461   -2.6969   -1.3945 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0686   -1.7702   -0.6074 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5809   -2.1442    0.2832 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0778    0.3594   -3.1323 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4155   -0.8168   -2.6761 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8029   -1.3988   -3.2063 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3902    1.3168   -0.8908 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3461    0.6093    1.5512 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0022   -0.4868    1.2601 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9612    2.5714    0.8976 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4013    1.7783    2.3445 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6780    2.6575    0.8457 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5411    2.3692   -1.4057 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3332    0.7733   -1.4171 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2869    2.3156   -1.0952 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6539   -0.3604    0.6484 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4453   -0.1617    3.0278 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1575    1.5845    2.9263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1381    1.3670    2.9193 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1994   -0.2418    3.5476 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1820   -1.9569    2.5787 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2425   -2.3100    0.7611 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6335   -1.7014    1.6966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9549    0.0656    2.0598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6492   -2.1456    0.0291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6482   -2.3779    1.8679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9076   -2.5893    1.4911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7277   -0.8450    1.8481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5045   -2.0751   -0.9359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9012   -1.2841    0.5608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9327   -2.0795   -2.3198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1556   -3.2000   -1.1655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9007   -2.7270   -0.8933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8885   -0.1752   -1.4623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8623    1.1200    0.2534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3436    1.4230   -2.6052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3096   -0.2559   -3.1639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0988   -0.5225   -2.7486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1140    1.2502   -2.3779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6287    1.2553    1.2134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2248    2.2188   -0.3065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2390    0.5388   -2.1308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0001    1.9662   -1.1006 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164    0.6118   -1.7126 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2804   -0.8177   -0.9439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6903    2.2299    0.9754 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8793    2.5479    1.6625 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6014    2.8010   -0.0788 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  1
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 24 23  1  6
 24 25  1  0
 26 25  1  1
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  1
 29  9  1  0
 29 12  1  0
 26 14  1  0
 24 17  1  0
 26 24  1  0
  1 31  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
  6 40  1  0
  6 41  1  0
  7 42  1  1
  8 43  1  0
  8 44  1  0
  8 45  1  0
  9 46  1  1
 10 47  1  0
 10 48  1  0
 11 49  1  0
 11 50  1  0
 13 51  1  0
 13 52  1  0
 13 53  1  0
 14 54  1  1
 15 55  1  0
 15 56  1  0
 16 57  1  0
 16 58  1  0
 17 59  1  6
 18 60  1  0
 19 61  1  0
 19 62  1  0
 19 63  1  0
 20 64  1  6
 21 65  1  0
 22 66  1  0
 22 67  1  0
 23 68  1  0
 23 69  1  0
 25 70  1  0
 25 71  1  0
 27 72  1  0
 27 73  1  0
 28 74  1  0
 28 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

(1S,3R,6S,8S,11S,12S,15R,16R)-7,12,16-trimethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-ol

Traditional Name

(1S,3R,6S,8S,11S,12S,15R,16R)-7,12,16-trimethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-ol

CAS Registry Number

Not Available

SMILES

[H][C@@]12CC[C@]3([H])[C@@]4(C[C@]14CC[C@H](O)C2C)CC[C@]1(C)[C@H](CC[C@@]31C)[C@H](C)CCC=C(C)C

InChI Identifier

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

InChI Key

XZEUYTKSAYNYPK-TUHQVYAESA-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
3-beta-hydroxysteroid
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

Dandelion (FooDB: FOOD00181)

Vegetable

Onion-family vegetable

Garden onion (FooDB: FOOD00006)

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	6.01	ALOGPS
logP	7.17	ChemAxon
logS	-7	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	4	ChemAxon
Refractivity	127.64 m³·mol⁻¹	ChemAxon
Polarizability	53.26 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
AllCCS	[M+H]+	210.337	32859911
AllCCS	[M+H-H2O]+	208.44	32859911
AllCCS	[M+Na]+	212.577	32859911
AllCCS	[M+NH4]+	212.079	32859911
AllCCS	[M-H]-	208.242	32859911
AllCCS	[M+Na-2H]-	210.136	32859911
AllCCS	[M+HCOO]-	212.377	32859911
DeepCCS	[M-2H]-	238.773	30932474
DeepCCS	[M+Na]+	213.236	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 - 31-Norcycloartenol 10V, Positive-QTOF	splash10-01ot-0009500000-5723952395e29cb02b94	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 31-Norcycloartenol 20V, Positive-QTOF	splash10-02bb-1029100000-f6a304cc0c71839e7b9b	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 31-Norcycloartenol 40V, Positive-QTOF	splash10-0fbi-2129000000-0c0bea1d5e231230c95e	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 31-Norcycloartenol 10V, Negative-QTOF	splash10-03di-0002900000-e30c287c47d4edd6ec9c	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 31-Norcycloartenol 20V, Negative-QTOF	splash10-03di-0005900000-53f02ec53982cb22ef62	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 31-Norcycloartenol 40V, Negative-QTOF	splash10-002b-1009000000-a0ef88e919d76d6ebbe2	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 31-Norcycloartenol 10V, Positive-QTOF	splash10-08fs-9113400000-27f3557b7c85d3f37398	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 31-Norcycloartenol 20V, Positive-QTOF	splash10-0a4i-9131100000-0f769622ad21bb74394f	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 31-Norcycloartenol 40V, Positive-QTOF	splash10-0a4l-9112100000-9958630bdd7bd31aa0c7	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 31-Norcycloartenol 10V, Negative-QTOF	splash10-03di-0000900000-363450e12a0ea926276e	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 31-Norcycloartenol 20V, Negative-QTOF	splash10-03di-0000900000-363450e12a0ea926276e	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 31-Norcycloartenol 40V, Negative-QTOF	splash10-03di-0002900000-f9ae6a57020dcb95d46f	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

FDB007256

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

102120876

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 31-Norcycloartenol (HMDB0303010)

MOL for HMDB0303010 (31-Norcycloartenol)

3D MOL for HMDB0303010 (31-Norcycloartenol)

3D SDF for HMDB0303010 (31-Norcycloartenol)

3D-SDF for HMDB0303010 (31-Norcycloartenol)

PDB for HMDB0303010 (31-Norcycloartenol)

3D PDB for HMDB0303010 (31-Norcycloartenol)

SMILES for HMDB0303010 (31-Norcycloartenol)

INCHI for HMDB0303010 (31-Norcycloartenol)

Structure for HMDB0303010 (31-Norcycloartenol)

3D Structure for HMDB0303010 (31-Norcycloartenol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

MS/MS Spectra