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 20:03:27 UTC

Update Date

2022-03-07 02:54:22 UTC

HMDB ID

HMDB0035113

Secondary Accession Numbers

HMDB35113

Metabolite Identification

Common Name

17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione

Description

17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. 17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione 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 05061308142D          

 34 38  0  0  0  0            999 V2000
   -1.4952   -1.6087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7802   -2.0211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0667   -1.6087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0667   -0.7837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7802   -0.3713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7802    0.4537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0667    0.8661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6483    0.4537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4403    1.2746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9173    0.0412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4333    0.7080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2170    0.9638    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2170    1.7887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4333    2.0431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9480    1.3763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3651    1.9592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4952    0.0412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4952   -0.7837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2087   -0.3713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9237   -0.7837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9237   -1.6087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6386   -2.0211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7394   -2.6535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2087   -2.0211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6794   -2.6535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9612   -3.4290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7349   -1.1919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6483   -0.3713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4333   -0.6270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6877   -1.4107    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0452    3.4290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7987    3.0935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8853    2.2728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6386    1.9372    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1 18  1  0  0  0  0
  1 24  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4 28  1  0  0  0  0
  5  6  1  0  0  0  0
  5 18  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 11  1  0  0  0  0
  8 28  1  0  0  0  0
 10 11  1  0  0  0  0
 10 29  1  0  0  0  0
 11 12  1  0  0  0  0
 11 15  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 33  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 24  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
M  END

HMDB0035113
     RDKit          3D
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione
 76 80  0  0  0  0  0  0  0  0999 V2000
    7.4126   -0.2238   -0.7793 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1702    0.0522    0.6858 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7795    0.4795    0.9817 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4746    0.9301    2.0818 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6585    0.3963   -0.0210 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4449   -1.0764   -0.2589 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0298   -1.3329    0.2052 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1491   -2.1335    1.5115 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4760    0.0075    0.4075 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8247    0.0458    1.8010 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9357    1.2182    1.7091 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6878    1.9940    2.6052 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4206    1.2326    0.2907 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3348    2.7077   -0.0913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9426    0.6962    0.3303 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3460   -0.4161   -0.2472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3013   -1.3639   -0.6950 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7673   -0.5384   -1.3688 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4144    0.4898   -0.5192 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1251    1.4161   -1.5319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7767   -0.6956   -0.4571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8607   -2.2178   -0.7235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1310   -0.0083   -1.7422 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5460    0.3046   -1.9894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1299    0.9034   -0.7779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6654    1.9802   -0.8030 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0062    0.0833    0.4568 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5587    0.9190    1.5913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0016   -1.0657    0.2827 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2802   -0.4690    0.1515 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6047   -0.3916    0.7251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9239    0.4909    1.7721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9719    1.4688    1.0970 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5036    0.9258    0.4628 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0813    0.6560   -1.3979 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5052   -0.3024   -0.9667 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9269   -1.1066   -1.1793 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3839   -0.8269    1.3178 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8332    0.9215    0.9526 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0426    0.9078   -0.9267 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1756   -1.7254    0.2803 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5379   -1.2984   -1.3370 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5637   -2.0035   -0.5037 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2449   -2.7006    1.7335 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9610   -2.8905    1.2976 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5424   -1.5203    2.3333 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3128   -0.8792    2.0471 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6256    0.2804    2.5611 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0510    2.8583   -1.1387 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2660    3.2227    0.2125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4755    3.1769    0.5204 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0393   -1.9770    0.1286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6706   -2.0645   -1.4985 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4698   -1.1486   -1.9733 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2008    0.0405   -2.1683 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3869    1.6988   -2.3407 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5724    2.2737   -1.0358 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8536    0.7546   -2.0462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0283   -2.7197   -0.1439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8183   -2.4099   -1.7920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7742   -2.6586   -0.2996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5322    0.9388   -1.8418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7608   -0.6631   -2.5724 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1558   -0.5451   -2.3620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5888    1.0703   -2.8025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5245    0.4280    2.5684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6665    1.0058    1.3619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2099    1.9714    1.5743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8654   -1.6065   -0.6695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0638   -1.7093    1.1797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2948   -0.0586   -0.7550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7587   -1.3592    1.3023 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6080    1.0533    2.3940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2828   -0.1151    2.4597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5243    2.1492    0.4090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5366    2.0719    1.9190 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  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  2  0
 11 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 16 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  2  0
 25 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 27 31  1  0
 31 32  1  0
 32 33  1  0
  9 34  1  0
 34  5  1  0
 19  9  1  0
 31 21  1  0
 19 13  1  0
 33 15  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  2 38  1  0
  2 39  1  0
  5 40  1  0
  6 41  1  0
  6 42  1  0
  7 43  1  0
  8 44  1  0
  8 45  1  0
  8 46  1  0
 10 47  1  0
 10 48  1  0
 14 49  1  0
 14 50  1  0
 14 51  1  0
 17 52  1  0
 17 53  1  0
 18 54  1  0
 18 55  1  0
 20 56  1  0
 20 57  1  0
 20 58  1  0
 22 59  1  0
 22 60  1  0
 22 61  1  0
 23 62  1  0
 23 63  1  0
 24 64  1  0
 24 65  1  0
 28 66  1  0
 28 67  1  0
 28 68  1  0
 29 69  1  0
 29 70  1  0
 30 71  1  0
 31 72  1  0
 32 73  1  0
 32 74  1  0
 33 75  1  0
 33 76  1  0
M  END


  Mrv0541 05061308142D          

 34 38  0  0  0  0            999 V2000
   -1.4952   -1.6087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7802   -2.0211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0667   -1.6087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0667   -0.7837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7802   -0.3713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7802    0.4537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0667    0.8661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6483    0.4537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4403    1.2746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9173    0.0412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4333    0.7080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2170    0.9638    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2170    1.7887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4333    2.0431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9480    1.3763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3651    1.9592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4952    0.0412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4952   -0.7837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2087   -0.3713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9237   -0.7837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9237   -1.6087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6386   -2.0211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7394   -2.6535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2087   -2.0211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6794   -2.6535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9612   -3.4290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7349   -1.1919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6483   -0.3713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4333   -0.6270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6877   -1.4107    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0452    3.4290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7987    3.0935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8853    2.2728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6386    1.9372    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1 18  1  0  0  0  0
  1 24  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4 28  1  0  0  0  0
  5  6  1  0  0  0  0
  5 18  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 11  1  0  0  0  0
  8 28  1  0  0  0  0
 10 11  1  0  0  0  0
 10 29  1  0  0  0  0
 11 12  1  0  0  0  0
 11 15  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 33  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 24  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0035113

> <DATABASE_NAME>
hmdb

> <SMILES>
CCC(=O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC23C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1

> <INCHI_IDENTIFIER>
InChI=1S/C29H42O5/c1-7-20(31)21-14-17(2)29(34-21)15-24(33)28(6)19-8-9-22-25(3,18(19)10-13-27(28,29)5)12-11-23(32)26(22,4)16-30/h17,21-22,30H,7-16H2,1-6H3

> <INCHI_KEY>
DVXXYXKKUSGEIB-UHFFFAOYSA-N

> <FORMULA>
C29H42O5

> <MOLECULAR_WEIGHT>
470.6408

> <EXACT_MASS>
470.303224454

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
54.190133303548066

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6'-(hydroxymethyl)-2',3,6',11',15'-pentamethyl-5-propanoylspiro[oxolane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan]-1'(10')-ene-5',12'-dione

> <ALOGPS_LOGP>
4.22

> <JCHEM_LOGP>
4.626687445

> <ALOGPS_LOGS>
-4.91

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.618929639012425

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.95346382375174

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8187196683087237

> <JCHEM_POLAR_SURFACE_AREA>
80.67

> <JCHEM_REFRACTIVITY>
130.71229999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.79e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6'-(hydroxymethyl)-2',3,6',11',15'-pentamethyl-5-propanoylspiro[oxolane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan]-1'(10')-ene-5',12'-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0035113
     RDKit          3D
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione
 76 80  0  0  0  0  0  0  0  0999 V2000
    7.4126   -0.2238   -0.7793 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1702    0.0522    0.6858 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7795    0.4795    0.9817 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4746    0.9301    2.0818 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6585    0.3963   -0.0210 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4449   -1.0764   -0.2589 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0298   -1.3329    0.2052 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1491   -2.1335    1.5115 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4760    0.0075    0.4075 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8247    0.0458    1.8010 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9357    1.2182    1.7091 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6878    1.9940    2.6052 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4206    1.2326    0.2907 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3348    2.7077   -0.0913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9426    0.6962    0.3303 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3460   -0.4161   -0.2472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3013   -1.3639   -0.6950 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7673   -0.5384   -1.3688 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4144    0.4898   -0.5192 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1251    1.4161   -1.5319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7767   -0.6956   -0.4571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8607   -2.2178   -0.7235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1310   -0.0083   -1.7422 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5460    0.3046   -1.9894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1299    0.9034   -0.7779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6654    1.9802   -0.8030 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0062    0.0833    0.4568 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5587    0.9190    1.5913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0016   -1.0657    0.2827 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2802   -0.4690    0.1515 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6047   -0.3916    0.7251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9239    0.4909    1.7721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9719    1.4688    1.0970 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5036    0.9258    0.4628 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0813    0.6560   -1.3979 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5052   -0.3024   -0.9667 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9269   -1.1066   -1.1793 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3839   -0.8269    1.3178 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8332    0.9215    0.9526 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0426    0.9078   -0.9267 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1756   -1.7254    0.2803 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5379   -1.2984   -1.3370 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5637   -2.0035   -0.5037 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2449   -2.7006    1.7335 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9610   -2.8905    1.2976 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5424   -1.5203    2.3333 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3128   -0.8792    2.0471 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6256    0.2804    2.5611 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0510    2.8583   -1.1387 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2660    3.2227    0.2125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4755    3.1769    0.5204 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0393   -1.9770    0.1286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6706   -2.0645   -1.4985 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4698   -1.1486   -1.9733 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2008    0.0405   -2.1683 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3869    1.6988   -2.3407 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5724    2.2737   -1.0358 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8536    0.7546   -2.0462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0283   -2.7197   -0.1439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8183   -2.4099   -1.7920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7742   -2.6586   -0.2996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5322    0.9388   -1.8418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7608   -0.6631   -2.5724 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1558   -0.5451   -2.3620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5888    1.0703   -2.8025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5245    0.4280    2.5684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6665    1.0058    1.3619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2099    1.9714    1.5743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8654   -1.6065   -0.6695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0638   -1.7093    1.1797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2948   -0.0586   -0.7550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7587   -1.3592    1.3023 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6080    1.0533    2.3940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2828   -0.1151    2.4597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5243    2.1492    0.4090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5366    2.0719    1.9190 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  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  2  0
 11 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 16 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  2  0
 25 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 27 31  1  0
 31 32  1  0
 32 33  1  0
  9 34  1  0
 34  5  1  0
 19  9  1  0
 31 21  1  0
 19 13  1  0
 33 15  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  2 38  1  0
  2 39  1  0
  5 40  1  0
  6 41  1  0
  6 42  1  0
  7 43  1  0
  8 44  1  0
  8 45  1  0
  8 46  1  0
 10 47  1  0
 10 48  1  0
 14 49  1  0
 14 50  1  0
 14 51  1  0
 17 52  1  0
 17 53  1  0
 18 54  1  0
 18 55  1  0
 20 56  1  0
 20 57  1  0
 20 58  1  0
 22 59  1  0
 22 60  1  0
 22 61  1  0
 23 62  1  0
 23 63  1  0
 24 64  1  0
 24 65  1  0
 28 66  1  0
 28 67  1  0
 28 68  1  0
 29 69  1  0
 29 70  1  0
 30 71  1  0
 31 72  1  0
 32 73  1  0
 32 74  1  0
 33 75  1  0
 33 76  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      -2.791  -3.003   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.456  -3.773   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.125  -3.003   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.125  -1.463   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.456  -0.693   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.456   0.847   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.125   1.617   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.210   0.847   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.822   2.379   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.579   0.077   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.675   1.322   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.138   1.799   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.138   3.339   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.675   3.814   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.770   2.569   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.682   3.657   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.791   0.077   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.791  -1.463   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.123  -0.693   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -5.458  -1.463   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -5.458  -3.003   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -6.792  -3.773   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -5.114  -4.953   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -4.123  -3.773   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -3.135  -4.953   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -3.661  -6.401   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       1.372  -2.225   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.210  -0.693   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.675  -1.170   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       3.150  -2.633   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       3.818   6.401   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.224   5.775   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.386   4.243   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       6.792   3.616   0.000  0.00  0.00           O+0
CONECT    1    2   18   24                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   28                                                  
CONECT    5    4    6   18                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   11   28                                             
CONECT    9    8                                                            
CONECT   10   11   29                                                       
CONECT   11    8   10   12   15                                             
CONECT   12   11   13                                                       
CONECT   13   12   14   33                                                  
CONECT   14   13   15                                                       
CONECT   15   11   14   16                                                  
CONECT   16   15                                                            
CONECT   17   18                                                            
CONECT   18    1    5   17   19                                             
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   24                                                  
CONECT   22   21                                                            
CONECT   23   24                                                            
CONECT   24    1   21   23   25                                             
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   28                                                            
CONECT   28    4    8   27   29                                             
CONECT   29   10   28   30                                                  
CONECT   30   29                                                            
CONECT   31   32                                                            
CONECT   32   31   33                                                       
CONECT   33   13   32   34                                                  
CONECT   34   33                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   76    0
END

COMPND    HMDB0035113
HETATM    1  C1  UNL     1       7.413  -0.224  -0.779  1.00  0.00           C  
HETATM    2  C2  UNL     1       7.170   0.052   0.686  1.00  0.00           C  
HETATM    3  C3  UNL     1       5.780   0.479   0.982  1.00  0.00           C  
HETATM    4  O1  UNL     1       5.475   0.930   2.082  1.00  0.00           O  
HETATM    5  C4  UNL     1       4.658   0.396  -0.021  1.00  0.00           C  
HETATM    6  C5  UNL     1       4.445  -1.076  -0.259  1.00  0.00           C  
HETATM    7  C6  UNL     1       3.030  -1.333   0.205  1.00  0.00           C  
HETATM    8  C7  UNL     1       3.149  -2.134   1.512  1.00  0.00           C  
HETATM    9  C8  UNL     1       2.476   0.008   0.407  1.00  0.00           C  
HETATM   10  C9  UNL     1       1.825   0.046   1.801  1.00  0.00           C  
HETATM   11  C10 UNL     1       0.936   1.218   1.709  1.00  0.00           C  
HETATM   12  O2  UNL     1       0.688   1.994   2.605  1.00  0.00           O  
HETATM   13  C11 UNL     1       0.421   1.233   0.291  1.00  0.00           C  
HETATM   14  C12 UNL     1       0.335   2.708  -0.091  1.00  0.00           C  
HETATM   15  C13 UNL     1      -0.943   0.696   0.330  1.00  0.00           C  
HETATM   16  C14 UNL     1      -1.346  -0.416  -0.247  1.00  0.00           C  
HETATM   17  C15 UNL     1      -0.301  -1.364  -0.695  1.00  0.00           C  
HETATM   18  C16 UNL     1       0.767  -0.538  -1.369  1.00  0.00           C  
HETATM   19  C17 UNL     1       1.414   0.490  -0.519  1.00  0.00           C  
HETATM   20  C18 UNL     1       2.125   1.416  -1.532  1.00  0.00           C  
HETATM   21  C19 UNL     1      -2.777  -0.696  -0.457  1.00  0.00           C  
HETATM   22  C20 UNL     1      -2.861  -2.218  -0.723  1.00  0.00           C  
HETATM   23  C21 UNL     1      -3.131  -0.008  -1.742  1.00  0.00           C  
HETATM   24  C22 UNL     1      -4.546   0.305  -1.989  1.00  0.00           C  
HETATM   25  C23 UNL     1      -5.130   0.903  -0.778  1.00  0.00           C  
HETATM   26  O3  UNL     1      -5.665   1.980  -0.803  1.00  0.00           O  
HETATM   27  C24 UNL     1      -5.006   0.083   0.457  1.00  0.00           C  
HETATM   28  C25 UNL     1      -5.559   0.919   1.591  1.00  0.00           C  
HETATM   29  C26 UNL     1      -6.002  -1.066   0.283  1.00  0.00           C  
HETATM   30  O4  UNL     1      -7.280  -0.469   0.151  1.00  0.00           O  
HETATM   31  C27 UNL     1      -3.605  -0.392   0.725  1.00  0.00           C  
HETATM   32  C28 UNL     1      -2.924   0.491   1.772  1.00  0.00           C  
HETATM   33  C29 UNL     1      -1.972   1.469   1.097  1.00  0.00           C  
HETATM   34  O5  UNL     1       3.504   0.926   0.463  1.00  0.00           O  
HETATM   35  H1  UNL     1       7.081   0.656  -1.398  1.00  0.00           H  
HETATM   36  H2  UNL     1       8.505  -0.302  -0.967  1.00  0.00           H  
HETATM   37  H3  UNL     1       6.927  -1.107  -1.179  1.00  0.00           H  
HETATM   38  H4  UNL     1       7.384  -0.827   1.318  1.00  0.00           H  
HETATM   39  H5  UNL     1       7.833   0.921   0.953  1.00  0.00           H  
HETATM   40  H6  UNL     1       5.043   0.908  -0.927  1.00  0.00           H  
HETATM   41  H7  UNL     1       5.176  -1.725   0.280  1.00  0.00           H  
HETATM   42  H8  UNL     1       4.538  -1.298  -1.337  1.00  0.00           H  
HETATM   43  H9  UNL     1       2.564  -2.003  -0.504  1.00  0.00           H  
HETATM   44  H10 UNL     1       2.245  -2.701   1.734  1.00  0.00           H  
HETATM   45  H11 UNL     1       3.961  -2.890   1.298  1.00  0.00           H  
HETATM   46  H12 UNL     1       3.542  -1.520   2.333  1.00  0.00           H  
HETATM   47  H13 UNL     1       1.313  -0.879   2.047  1.00  0.00           H  
HETATM   48  H14 UNL     1       2.626   0.280   2.561  1.00  0.00           H  
HETATM   49  H15 UNL     1       0.051   2.858  -1.139  1.00  0.00           H  
HETATM   50  H16 UNL     1       1.266   3.223   0.213  1.00  0.00           H  
HETATM   51  H17 UNL     1      -0.475   3.177   0.520  1.00  0.00           H  
HETATM   52  H18 UNL     1       0.039  -1.977   0.129  1.00  0.00           H  
HETATM   53  H19 UNL     1      -0.671  -2.065  -1.499  1.00  0.00           H  
HETATM   54  H20 UNL     1       1.470  -1.149  -1.973  1.00  0.00           H  
HETATM   55  H21 UNL     1       0.201   0.040  -2.168  1.00  0.00           H  
HETATM   56  H22 UNL     1       1.387   1.699  -2.341  1.00  0.00           H  
HETATM   57  H23 UNL     1       2.572   2.274  -1.036  1.00  0.00           H  
HETATM   58  H24 UNL     1       2.854   0.755  -2.046  1.00  0.00           H  
HETATM   59  H25 UNL     1      -2.028  -2.720  -0.144  1.00  0.00           H  
HETATM   60  H26 UNL     1      -2.818  -2.410  -1.792  1.00  0.00           H  
HETATM   61  H27 UNL     1      -3.774  -2.659  -0.300  1.00  0.00           H  
HETATM   62  H28 UNL     1      -2.532   0.939  -1.842  1.00  0.00           H  
HETATM   63  H29 UNL     1      -2.761  -0.663  -2.572  1.00  0.00           H  
HETATM   64  H30 UNL     1      -5.156  -0.545  -2.362  1.00  0.00           H  
HETATM   65  H31 UNL     1      -4.589   1.070  -2.802  1.00  0.00           H  
HETATM   66  H32 UNL     1      -5.525   0.428   2.568  1.00  0.00           H  
HETATM   67  H33 UNL     1      -6.667   1.006   1.362  1.00  0.00           H  
HETATM   68  H34 UNL     1      -5.210   1.971   1.574  1.00  0.00           H  
HETATM   69  H35 UNL     1      -5.865  -1.607  -0.669  1.00  0.00           H  
HETATM   70  H36 UNL     1      -6.064  -1.709   1.180  1.00  0.00           H  
HETATM   71  H37 UNL     1      -7.295  -0.059  -0.755  1.00  0.00           H  
HETATM   72  H38 UNL     1      -3.759  -1.359   1.302  1.00  0.00           H  
HETATM   73  H39 UNL     1      -3.608   1.053   2.394  1.00  0.00           H  
HETATM   74  H40 UNL     1      -2.283  -0.115   2.460  1.00  0.00           H  
HETATM   75  H41 UNL     1      -2.524   2.149   0.409  1.00  0.00           H  
HETATM   76  H42 UNL     1      -1.537   2.072   1.919  1.00  0.00           H  
CONECT    1    2   35   36   37
CONECT    2    3   38   39
CONECT    3    4    4    5
CONECT    5    6   34   40
CONECT    6    7   41   42
CONECT    7    8    9   43
CONECT    8   44   45   46
CONECT    9   10   19   34
CONECT   10   11   47   48
CONECT   11   12   12   13
CONECT   13   14   15   19
CONECT   14   49   50   51
CONECT   15   16   16   33
CONECT   16   17   21
CONECT   17   18   52   53
CONECT   18   19   54   55
CONECT   19   20
CONECT   20   56   57   58
CONECT   21   22   23   31
CONECT   22   59   60   61
CONECT   23   24   62   63
CONECT   24   25   64   65
CONECT   25   26   26   27
CONECT   27   28   29   31
CONECT   28   66   67   68
CONECT   29   30   69   70
CONECT   30   71
CONECT   31   32   72
CONECT   32   33   73   74
CONECT   33   75   76
END

HMDB0035113
     RDKit          3D
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione
 76 80  0  0  0  0  0  0  0  0999 V2000
    7.4126   -0.2238   -0.7793 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1702    0.0522    0.6858 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7795    0.4795    0.9817 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4746    0.9301    2.0818 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6585    0.3963   -0.0210 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4449   -1.0764   -0.2589 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0298   -1.3329    0.2052 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1491   -2.1335    1.5115 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4760    0.0075    0.4075 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8247    0.0458    1.8010 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9357    1.2182    1.7091 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6878    1.9940    2.6052 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4206    1.2326    0.2907 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3348    2.7077   -0.0913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9426    0.6962    0.3303 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3460   -0.4161   -0.2472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3013   -1.3639   -0.6950 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7673   -0.5384   -1.3688 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4144    0.4898   -0.5192 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1251    1.4161   -1.5319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7767   -0.6956   -0.4571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8607   -2.2178   -0.7235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1310   -0.0083   -1.7422 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5460    0.3046   -1.9894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1299    0.9034   -0.7779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6654    1.9802   -0.8030 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0062    0.0833    0.4568 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5587    0.9190    1.5913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0016   -1.0657    0.2827 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2802   -0.4690    0.1515 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6047   -0.3916    0.7251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9239    0.4909    1.7721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9719    1.4688    1.0970 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5036    0.9258    0.4628 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0813    0.6560   -1.3979 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5052   -0.3024   -0.9667 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9269   -1.1066   -1.1793 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3839   -0.8269    1.3178 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8332    0.9215    0.9526 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0426    0.9078   -0.9267 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1756   -1.7254    0.2803 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5379   -1.2984   -1.3370 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5637   -2.0035   -0.5037 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2449   -2.7006    1.7335 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9610   -2.8905    1.2976 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5424   -1.5203    2.3333 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3128   -0.8792    2.0471 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6256    0.2804    2.5611 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0510    2.8583   -1.1387 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2660    3.2227    0.2125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4755    3.1769    0.5204 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0393   -1.9770    0.1286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6706   -2.0645   -1.4985 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4698   -1.1486   -1.9733 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2008    0.0405   -2.1683 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3869    1.6988   -2.3407 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5724    2.2737   -1.0358 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8536    0.7546   -2.0462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0283   -2.7197   -0.1439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8183   -2.4099   -1.7920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7742   -2.6586   -0.2996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5322    0.9388   -1.8418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7608   -0.6631   -2.5724 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1558   -0.5451   -2.3620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5888    1.0703   -2.8025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5245    0.4280    2.5684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6665    1.0058    1.3619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2099    1.9714    1.5743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8654   -1.6065   -0.6695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0638   -1.7093    1.1797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2948   -0.0586   -0.7550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7587   -1.3592    1.3023 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6080    1.0533    2.3940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2828   -0.1151    2.4597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5243    2.1492    0.4090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5366    2.0719    1.9190 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  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  2  0
 11 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 16 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  2  0
 25 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 27 31  1  0
 31 32  1  0
 32 33  1  0
  9 34  1  0
 34  5  1  0
 19  9  1  0
 31 21  1  0
 19 13  1  0
 33 15  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  2 38  1  0
  2 39  1  0
  5 40  1  0
  6 41  1  0
  6 42  1  0
  7 43  1  0
  8 44  1  0
  8 45  1  0
  8 46  1  0
 10 47  1  0
 10 48  1  0
 14 49  1  0
 14 50  1  0
 14 51  1  0
 17 52  1  0
 17 53  1  0
 18 54  1  0
 18 55  1  0
 20 56  1  0
 20 57  1  0
 20 58  1  0
 22 59  1  0
 22 60  1  0
 22 61  1  0
 23 62  1  0
 23 63  1  0
 24 64  1  0
 24 65  1  0
 28 66  1  0
 28 67  1  0
 28 68  1  0
 29 69  1  0
 29 70  1  0
 30 71  1  0
 31 72  1  0
 32 73  1  0
 32 74  1  0
 33 75  1  0
 33 76  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₉H₄₂O₅

Average Molecular Weight

470.6408

Monoisotopic Molecular Weight

470.303224454

IUPAC Name

6'-(hydroxymethyl)-2',3,6',11',15'-pentamethyl-5-propanoylspiro[oxolane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan]-1'(10')-ene-5',12'-dione

Traditional Name

6'-(hydroxymethyl)-2',3,6',11',15'-pentamethyl-5-propanoylspiro[oxolane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan]-1'(10')-ene-5',12'-dione

CAS Registry Number

Not Available

SMILES

CCC(=O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC23C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1

InChI Identifier

InChI=1S/C29H42O5/c1-7-20(31)21-14-17(2)29(34-21)15-24(33)28(6)19-8-9-22-25(3,18(19)10-13-27(28,29)5)12-11-23(32)26(22,4)16-30/h17,21-22,30H,7-16H2,1-6H3

InChI Key

DVXXYXKKUSGEIB-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Not Available

Substituents

Not Available

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cytoplasm (HMDB: HMDB0035113)
Cell membrane (HMDB: HMDB0035113)

Cellular substructure

Extracellular (HMDB: HMDB0035113)
Membrane (HMDB: HMDB0035113)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0035113)

Source

Endogenous

Endogenous (HMDB: HMDB0035113)

Plant

Plant (HMDB: HMDB0035113)

Animal

Animal (HMDB: HMDB0035113)

Exogenous

Food

Food (HMDB: HMDB0035113)

Herb and spice

Herbs and Spices (FooDB: FOOD00866)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0035113)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0035113)

Cellular process

Cell signaling (HMDB: HMDB0035113)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0035113)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0035113)

Nutrient

Nutrient (HMDB: HMDB0035113)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0035113)

Emulsifier (HMDB: HMDB0035113)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	184 - 186 °C	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	0.0058 g/L	ALOGPS
logP	4.22	ALOGPS
logP	4.63	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Acidic)	14.95	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	80.67 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	130.71 m³·mol⁻¹	ChemAxon
Polarizability	54.19 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	209.294	31661259
DarkChem	[M-H]-	206.147	31661259
DeepCCS	[M-2H]-	243.521	30932474
DeepCCS	[M+Na]+	218.775	30932474
AllCCS	[M+H]+	212.5	32859911
AllCCS	[M+H-H2O]+	210.7	32859911
AllCCS	[M+NH4]+	214.2	32859911
AllCCS	[M+Na]+	214.6	32859911
AllCCS	[M-H]-	216.3	32859911
AllCCS	[M+Na-2H]-	218.4	32859911
AllCCS	[M+HCOO]-	220.9	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione	CCC(=O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC23C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1	3384.9	Standard polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione	CCC(=O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC23C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1	3612.6	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione	CCC(=O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC23C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1	3970.3	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,1TMS,isomer #1	CCC(=O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C)C2CC4)O1	3690.5	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,1TMS,isomer #2	CCC(O[Si](C)(C)C)=C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1	3794.9	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,1TMS,isomer #3	CC=C(O[Si](C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1	3734.8	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,1TMS,isomer #4	CCC(=O)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1	3654.0	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,1TMS,isomer #5	CCC(=O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO)C2CC4)O1	3711.0	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TMS,isomer #1	CCC(O[Si](C)(C)C)=C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C)C2CC4)O1	3728.8	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TMS,isomer #1	CCC(O[Si](C)(C)C)=C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C)C2CC4)O1	3752.8	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TMS,isomer #2	CC=C(O[Si](C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C)C2CC4)O1	3654.5	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TMS,isomer #2	CC=C(O[Si](C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C)C2CC4)O1	3745.4	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TMS,isomer #3	CCC(=O)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C)C2CC4)O1	3562.6	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TMS,isomer #3	CCC(=O)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C)C2CC4)O1	3555.9	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TMS,isomer #4	CCC(=O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C2CC4)O1	3627.6	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TMS,isomer #4	CCC(=O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C2CC4)O1	3517.2	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TMS,isomer #5	CCC(O[Si](C)(C)C)=C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1	3674.6	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TMS,isomer #5	CCC(O[Si](C)(C)C)=C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1	3607.0	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TMS,isomer #6	CCC(O[Si](C)(C)C)=C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO)C2CC4)O1	3722.6	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TMS,isomer #6	CCC(O[Si](C)(C)C)=C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO)C2CC4)O1	3560.4	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TMS,isomer #7	CC=C(O[Si](C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1	3607.0	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TMS,isomer #7	CC=C(O[Si](C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1	3576.8	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TMS,isomer #8	CC=C(O[Si](C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO)C2CC4)O1	3648.6	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TMS,isomer #8	CC=C(O[Si](C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO)C2CC4)O1	3541.0	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TMS,isomer #9	CCC(=O)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO)C2CC4)O1	3557.2	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TMS,isomer #9	CCC(=O)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO)C2CC4)O1	3432.1	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TMS,isomer #1	CCC(O[Si](C)(C)C)=C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C)C2CC4)O1	3595.6	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TMS,isomer #1	CCC(O[Si](C)(C)C)=C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C)C2CC4)O1	3643.6	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TMS,isomer #2	CCC(O[Si](C)(C)C)=C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C2CC4)O1	3658.9	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TMS,isomer #2	CCC(O[Si](C)(C)C)=C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C2CC4)O1	3591.0	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TMS,isomer #3	CC=C(O[Si](C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C)C2CC4)O1	3532.4	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TMS,isomer #3	CC=C(O[Si](C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C)C2CC4)O1	3609.7	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TMS,isomer #4	CC=C(O[Si](C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C2CC4)O1	3594.9	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TMS,isomer #4	CC=C(O[Si](C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C2CC4)O1	3561.4	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TMS,isomer #5	CCC(=O)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C2CC4)O1	3512.1	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TMS,isomer #5	CCC(=O)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C2CC4)O1	3459.6	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TMS,isomer #6	CCC(O[Si](C)(C)C)=C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO)C2CC4)O1	3592.6	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TMS,isomer #6	CCC(O[Si](C)(C)C)=C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO)C2CC4)O1	3515.2	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TMS,isomer #7	CC=C(O[Si](C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO)C2CC4)O1	3520.3	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TMS,isomer #7	CC=C(O[Si](C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO)C2CC4)O1	3493.1	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,4TMS,isomer #1	CCC(O[Si](C)(C)C)=C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C2CC4)O1	3531.2	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,4TMS,isomer #1	CCC(O[Si](C)(C)C)=C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C2CC4)O1	3530.4	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,4TMS,isomer #2	CC=C(O[Si](C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C2CC4)O1	3474.5	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,4TMS,isomer #2	CC=C(O[Si](C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C2CC4)O1	3511.9	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,1TBDMS,isomer #1	CCC(=O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	3952.0	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,1TBDMS,isomer #2	CCC(O[Si](C)(C)C(C)(C)C)=C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1	4038.8	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,1TBDMS,isomer #3	CC=C(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1	3965.3	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,1TBDMS,isomer #4	CCC(=O)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1	3912.3	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,1TBDMS,isomer #5	CCC(=O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO)C2CC4)O1	3955.6	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TBDMS,isomer #1	CCC(O[Si](C)(C)C(C)(C)C)=C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	4189.5	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TBDMS,isomer #1	CCC(O[Si](C)(C)C(C)(C)C)=C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	4236.2	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TBDMS,isomer #2	CC=C(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	4111.2	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TBDMS,isomer #2	CC=C(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	4239.6	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TBDMS,isomer #3	CCC(=O)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	4046.2	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TBDMS,isomer #3	CCC(=O)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	3950.6	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TBDMS,isomer #4	CCC(=O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	4102.8	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TBDMS,isomer #4	CCC(=O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	3877.5	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TBDMS,isomer #5	CCC(O[Si](C)(C)C(C)(C)C)=C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1	4122.1	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TBDMS,isomer #5	CCC(O[Si](C)(C)C(C)(C)C)=C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1	3964.3	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TBDMS,isomer #6	CCC(O[Si](C)(C)C(C)(C)C)=C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO)C2CC4)O1	4164.2	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TBDMS,isomer #6	CCC(O[Si](C)(C)C(C)(C)C)=C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO)C2CC4)O1	3893.5	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TBDMS,isomer #7	CC=C(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1	4061.9	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TBDMS,isomer #7	CC=C(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1	3958.3	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TBDMS,isomer #8	CC=C(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO)C2CC4)O1	4098.5	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TBDMS,isomer #8	CC=C(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO)C2CC4)O1	3882.9	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TBDMS,isomer #9	CCC(=O)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO)C2CC4)O1	4022.3	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,2TBDMS,isomer #9	CCC(=O)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO)C2CC4)O1	3706.5	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TBDMS,isomer #1	CCC(O[Si](C)(C)C(C)(C)C)=C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	4237.9	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TBDMS,isomer #1	CCC(O[Si](C)(C)C(C)(C)C)=C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	4155.1	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TBDMS,isomer #2	CCC(O[Si](C)(C)C(C)(C)C)=C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	4316.5	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TBDMS,isomer #2	CCC(O[Si](C)(C)C(C)(C)C)=C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	4061.1	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TBDMS,isomer #3	CC=C(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	4187.5	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TBDMS,isomer #3	CC=C(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	4164.7	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TBDMS,isomer #4	CC=C(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	4242.2	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TBDMS,isomer #4	CC=C(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	4065.1	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TBDMS,isomer #5	CCC(=O)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	4163.5	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TBDMS,isomer #5	CCC(=O)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	3873.0	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TBDMS,isomer #6	CCC(O[Si](C)(C)C(C)(C)C)=C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO)C2CC4)O1	4209.3	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TBDMS,isomer #6	CCC(O[Si](C)(C)C(C)(C)C)=C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO)C2CC4)O1	3913.2	Standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TBDMS,isomer #7	CC=C(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO)C2CC4)O1	4144.6	Semi standard non polar	33892256
17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione,3TBDMS,isomer #7	CC=C(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO)C2CC4)O1	3914.6	Standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a6u-3116900000-f54be43517721e197412	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione GC-MS (1 TMS) - 70eV, Positive	splash10-06vi-5303590000-37c88767553e408106b7	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione 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 - 17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione 10V, Positive-QTOF	splash10-0uk9-0002900000-bb413f83002a8462e8a0	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione 20V, Positive-QTOF	splash10-0udr-1143900000-54344832b0d4b61094fb	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione 40V, Positive-QTOF	splash10-0019-0179000000-2617998ceb011982452d	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione 10V, Negative-QTOF	splash10-014i-0000900000-9bfe6233afed70ae1274	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione 20V, Negative-QTOF	splash10-0fri-1001900000-fe1ac6760635496369f1	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione 40V, Negative-QTOF	splash10-0pw9-2019300000-465072a5d317097c1f1c	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione 10V, Negative-QTOF	splash10-014i-0000900000-80daa39ed61599c50028	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione 20V, Negative-QTOF	splash10-03di-2004900000-cd3ed93e771659887a74	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione 40V, Negative-QTOF	splash10-0a4l-9001500000-e1feb2e0a5fcc90b985d	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione 10V, Positive-QTOF	splash10-0uk9-0001900000-7c47aa16d9b502f1ca67	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione 20V, Positive-QTOF	splash10-0udi-0023900000-ccf300c7db8761aaaf82	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione 40V, Positive-QTOF	splash10-01p9-9234800000-ddcf09be1fe63215ba86	2021-09-23	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

FDB013744

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

131751668

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 17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione (HMDB0035113)

MOL for HMDB0035113 (17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione)

3D MOL for HMDB0035113 (17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione)

3D SDF for HMDB0035113 (17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione)

3D-SDF for HMDB0035113 (17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione)

PDB for HMDB0035113 (17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione)

3D PDB for HMDB0035113 (17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione)

SMILES for HMDB0035113 (17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione)

INCHI for HMDB0035113 (17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione)

Structure for HMDB0035113 (17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione)

3D Structure for HMDB0035113 (17,23-Epoxy-29-hydroxy-27-norlanost-8-ene-3,15,24-trione)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra