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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 20:46:22 UTC

Update Date

2022-03-07 02:54:37 UTC

HMDB ID

HMDB0035751

Secondary Accession Numbers

HMDB35751

Metabolite Identification

Common Name

Ganolucidic acid B

Description

Ganolucidic acid B, also known as ganolucidate b, belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Based on a literature review a significant number of articles have been published on Ganolucidic acid B.

Structure

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


  Mrv0541 05061308422D          

 36 39  0  0  0  0            999 V2000
   -2.6866    3.0561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1713    3.0561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9634    1.4027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7516    2.1124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0236    3.2818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5416    2.7062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1917    0.8736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0658    1.0995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8727    1.2710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6375    3.6249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8306    3.4534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9721    1.8186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5432    1.8186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4873    0.9981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4097    2.9388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6866    2.2311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1713    2.2311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2576    2.2311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5137    1.7126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4010    1.8186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2166    3.1103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1277    2.0556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1896    3.0118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2942    0.8266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7687    2.4972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8858    1.8186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9346    2.2272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5756    2.6687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1547    2.1542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7067    1.5411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2576    3.0561    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4716    3.8949    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9965    3.1833    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6298    0.0729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6003    2.2311    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8858    0.9936    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0  0  0  0
 11 10  1  0  0  0  0
 16  1  1  0  0  0  0
 16 12  1  0  0  0  0
 17  2  1  0  0  0  0
 17 13  1  0  0  0  0
 18 12  1  0  0  0  0
 18 13  1  0  0  0  0
 19  8  1  0  0  0  0
 20 14  1  0  0  0  0
 20 16  1  0  0  0  0
 21 15  1  0  0  0  0
 22  9  1  0  0  0  0
 23 10  1  0  0  0  0
 24 14  1  0  0  0  0
 25 19  2  0  0  0  0
 25 21  1  0  0  0  0
 26 17  1  0  0  0  0
 27  3  1  0  0  0  0
 27  4  1  0  0  0  0
 27 22  1  0  0  0  0
 27 23  1  0  0  0  0
 28  5  1  0  0  0  0
 28 11  1  0  0  0  0
 28 22  1  0  0  0  0
 28 25  1  0  0  0  0
 29  6  1  0  0  0  0
 29 15  1  0  0  0  0
 29 20  1  0  0  0  0
 30  7  1  0  0  0  0
 30 19  1  0  0  0  0
 30 24  1  0  0  0  0
 30 29  1  0  0  0  0
 31 18  2  0  0  0  0
 32 21  2  0  0  0  0
 33 23  1  0  0  0  0
 34 24  1  0  0  0  0
 35 26  2  0  0  0  0
 36 26  1  0  0  0  0
M  END

HMDB0035751
     RDKit          3D
Ganolucidic acid B
 82 85  0  0  0  0  0  0  0  0999 V2000
    7.7283    0.3107    2.1532 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5472    0.1761    1.1735 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5971    1.2807    1.4695 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4010    1.3583    0.6024 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5480    2.1560    0.9513 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1813    0.5542   -0.6320 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9209    0.8981   -1.3671 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0662    2.3891   -1.7599 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6540    0.6578   -0.6726 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4970    1.1500   -1.6169 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2309   -0.1510   -2.3385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7655   -0.0808   -3.2511 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0446   -1.0363   -1.1295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0581   -2.4665   -1.6132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3073   -0.7457   -0.4826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5026   -0.2194    0.7175 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3081   -0.0902    1.5436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2725    0.5653    2.6152 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9643   -0.7452    1.1514 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2118   -0.7311   -0.3472 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2332   -1.8231   -0.5483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8168    0.2175    1.2462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5424    1.4134    2.1620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2760   -0.8786    2.1831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6617   -0.5694    2.7174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5445   -0.7233    1.4938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4523   -2.0201    1.0703 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2519    0.3154    0.4774 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9691   -0.1295   -0.8108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0216    1.5616    0.9086 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8092    0.6246    0.2146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3729    0.2480   -1.1903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5753   -1.0596   -1.2057 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9796   -1.1780    1.4497 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9118   -1.3025    2.0376 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6889   -2.2834    1.0300 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6227   -0.1791    1.7138 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4193   -0.1951    3.0807 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9168    1.4024    2.3138 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9498    0.1990    0.1442 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1404    2.2535    1.3355 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3053    1.1951    2.5527 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3807   -0.4824   -0.4356 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0774    0.8648   -1.3082 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9778    0.3979   -2.3803 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6793    2.5696   -2.7859 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6469    3.0463   -1.0050 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1545    2.5721   -1.8292 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5583    1.3613    0.1829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3764    1.3939   -1.0015 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8338    1.9595   -2.2559 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1969   -0.5070   -2.7549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8570    0.8681   -3.5485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2759   -3.2083   -0.8201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9346   -2.6270   -2.3268 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8111   -2.7282   -2.2592 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9836   -1.8016    1.5302 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7989   -0.2118    1.6042 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6375   -2.8018   -0.4772 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7725   -1.8034   -1.4863 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8741   -1.9399    0.3756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4839    2.0489    2.1311 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7743    2.0924    1.7385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4271    1.1500    3.2080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5919   -0.8508    3.0627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2908   -1.8696    1.7305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9302   -1.3639    3.4491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7336    0.4601    3.1363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5881   -0.5777    1.8636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1652   -2.3186    0.4656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1161    0.7053   -1.5063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5888   -1.0588   -1.2194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0111   -0.3768   -0.4417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0825    1.4162    0.6200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6473    2.4616    0.4068 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.6506    1.0131   -1.6102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1912    0.2330   -1.9151 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.4631   -1.3192   -2.2496 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5493   -2.6357    0.0818 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
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 13 14  1  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
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 17 19  1  0
 19 20  1  0
 20 21  1  0
 16 22  1  0
 22 23  1  0
 22 24  1  0
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 26 28  1  0
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 28 31  1  0
 31 32  1  0
 32 33  1  0
  2 34  1  0
 34 35  2  0
 34 36  1  0
 20  9  1  0
 31 22  1  0
 20 13  1  0
 33 15  1  0
  1 37  1  0
  1 38  1  0
  1 39  1  0
  2 40  1  0
  3 41  1  0
  3 42  1  0
  6 43  1  0
  6 44  1  0
  7 45  1  0
  8 46  1  0
  8 47  1  0
  8 48  1  0
  9 49  1  0
 10 50  1  0
 10 51  1  0
 11 52  1  0
 12 53  1  0
 14 54  1  0
 14 55  1  0
 14 56  1  0
 19 57  1  0
 19 58  1  0
 21 59  1  0
 21 60  1  0
 21 61  1  0
 23 62  1  0
 23 63  1  0
 23 64  1  0
 24 65  1  0
 24 66  1  0
 25 67  1  0
 25 68  1  0
 26 69  1  0
 27 70  1  0
 29 71  1  0
 29 72  1  0
 29 73  1  0
 30 74  1  0
 30 75  1  0
 30 76  1  0
 31 77  1  0
 32 78  1  0
 32 79  1  0
 33 80  1  0
 33 81  1  0
 36 82  1  0
M  END


  Mrv0541 05061308422D          

 36 39  0  0  0  0            999 V2000
   -2.6866    3.0561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1713    3.0561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9634    1.4027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7516    2.1124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0236    3.2818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5416    2.7062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1917    0.8736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0658    1.0995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8727    1.2710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6375    3.6249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8306    3.4534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.4010    1.8186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2166    3.1103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1277    2.0556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1896    3.0118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2942    0.8266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.8858    1.8186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9346    2.2272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.7067    1.5411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2576    3.0561    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    1.6003    2.2311    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8858    0.9936    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0  0  0  0
 11 10  1  0  0  0  0
 16  1  1  0  0  0  0
 16 12  1  0  0  0  0
 17  2  1  0  0  0  0
 17 13  1  0  0  0  0
 18 12  1  0  0  0  0
 18 13  1  0  0  0  0
 19  8  1  0  0  0  0
 20 14  1  0  0  0  0
 20 16  1  0  0  0  0
 21 15  1  0  0  0  0
 22  9  1  0  0  0  0
 23 10  1  0  0  0  0
 24 14  1  0  0  0  0
 25 19  2  0  0  0  0
 25 21  1  0  0  0  0
 26 17  1  0  0  0  0
 27  3  1  0  0  0  0
 27  4  1  0  0  0  0
 27 22  1  0  0  0  0
 27 23  1  0  0  0  0
 28  5  1  0  0  0  0
 28 11  1  0  0  0  0
 28 22  1  0  0  0  0
 28 25  1  0  0  0  0
 29  6  1  0  0  0  0
 29 15  1  0  0  0  0
 29 20  1  0  0  0  0
 30  7  1  0  0  0  0
 30 19  1  0  0  0  0
 30 24  1  0  0  0  0
 30 29  1  0  0  0  0
 31 18  2  0  0  0  0
 32 21  2  0  0  0  0
 33 23  1  0  0  0  0
 34 24  1  0  0  0  0
 35 26  2  0  0  0  0
 36 26  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0035751

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(CC(=O)CC(C)C(O)=O)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3

> <INCHI_IDENTIFIER>
InChI=1S/C30H46O6/c1-16(12-18(31)13-17(2)26(35)36)20-14-24(34)30(7)19-8-9-22-27(3,4)23(33)10-11-28(22,5)25(19)21(32)15-29(20,30)6/h16-17,20,22-24,33-34H,8-15H2,1-7H3,(H,35,36)

> <INCHI_KEY>
YPYHGMCHNBTMDB-UHFFFAOYSA-N

> <FORMULA>
C30H46O6

> <MOLECULAR_WEIGHT>
502.6826

> <EXACT_MASS>
502.329439204

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_AVERAGE_POLARIZABILITY>
57.12605703296067

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-{5,12-dihydroxy-2,6,6,11,15-pentamethyl-17-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl}-2-methyl-4-oxoheptanoic acid

> <ALOGPS_LOGP>
4.14

> <JCHEM_LOGP>
3.9706652656666668

> <ALOGPS_LOGS>
-4.95

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
19.55377231056278

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.3517701034894785

> <JCHEM_PKA_STRONGEST_BASIC>
-0.284133362984642

> <JCHEM_POLAR_SURFACE_AREA>
111.90000000000002

> <JCHEM_REFRACTIVITY>
138.23609999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.59e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-{5,12-dihydroxy-2,6,6,11,15-pentamethyl-17-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl}-2-methyl-4-oxoheptanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0035751
     RDKit          3D
Ganolucidic acid B
 82 85  0  0  0  0  0  0  0  0999 V2000
    7.7283    0.3107    2.1532 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5472    0.1761    1.1735 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5971    1.2807    1.4695 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4010    1.3583    0.6024 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5480    2.1560    0.9513 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1813    0.5542   -0.6320 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9209    0.8981   -1.3671 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0662    2.3891   -1.7599 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6540    0.6578   -0.6726 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4970    1.1500   -1.6169 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2309   -0.1510   -2.3385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7655   -0.0808   -3.2511 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0446   -1.0363   -1.1295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0581   -2.4665   -1.6132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3073   -0.7457   -0.4826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5026   -0.2194    0.7175 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3081   -0.0902    1.5436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2725    0.5653    2.6152 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9643   -0.7452    1.1514 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2118   -0.7311   -0.3472 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2332   -1.8231   -0.5483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8168    0.2175    1.2462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5424    1.4134    2.1620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2760   -0.8786    2.1831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6617   -0.5694    2.7174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5445   -0.7233    1.4938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4523   -2.0201    1.0703 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2519    0.3154    0.4774 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9691   -0.1295   -0.8108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0216    1.5616    0.9086 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8092    0.6246    0.2146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3729    0.2480   -1.1903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5753   -1.0596   -1.2057 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9796   -1.1780    1.4497 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9118   -1.3025    2.0376 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6889   -2.2834    1.0300 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6227   -0.1791    1.7138 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4193   -0.1951    3.0807 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9168    1.4024    2.3138 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9498    0.1990    0.1442 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1404    2.2535    1.3355 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3053    1.1951    2.5527 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3807   -0.4824   -0.4356 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0774    0.8648   -1.3082 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9778    0.3979   -2.3803 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6793    2.5696   -2.7859 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6469    3.0463   -1.0050 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1545    2.5721   -1.8292 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5583    1.3613    0.1829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3764    1.3939   -1.0015 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8338    1.9595   -2.2559 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1969   -0.5070   -2.7549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8570    0.8681   -3.5485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2759   -3.2083   -0.8201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9346   -2.6270   -2.3268 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8111   -2.7282   -2.2592 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9836   -1.8016    1.5302 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7989   -0.2118    1.6042 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6375   -2.8018   -0.4772 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7725   -1.8034   -1.4863 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8741   -1.9399    0.3756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4839    2.0489    2.1311 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7743    2.0924    1.7385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4271    1.1500    3.2080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5919   -0.8508    3.0627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2908   -1.8696    1.7305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9302   -1.3639    3.4491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7336    0.4601    3.1363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5881   -0.5777    1.8636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1652   -2.3186    0.4656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1161    0.7053   -1.5063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5888   -1.0588   -1.2194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0111   -0.3768   -0.4417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0825    1.4162    0.6200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6473    2.4616    0.4068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0318    1.6495    2.0155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7684    1.7635    0.1602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6506    1.0131   -1.6102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1912    0.2330   -1.9151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1167   -1.8633   -0.6647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4631   -1.3192   -2.2496 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5493   -2.6357    0.0818 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  4  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
 11 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 16 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 28 30  1  0
 28 31  1  0
 31 32  1  0
 32 33  1  0
  2 34  1  0
 34 35  2  0
 34 36  1  0
 20  9  1  0
 31 22  1  0
 20 13  1  0
 33 15  1  0
  1 37  1  0
  1 38  1  0
  1 39  1  0
  2 40  1  0
  3 41  1  0
  3 42  1  0
  6 43  1  0
  6 44  1  0
  7 45  1  0
  8 46  1  0
  8 47  1  0
  8 48  1  0
  9 49  1  0
 10 50  1  0
 10 51  1  0
 11 52  1  0
 12 53  1  0
 14 54  1  0
 14 55  1  0
 14 56  1  0
 19 57  1  0
 19 58  1  0
 21 59  1  0
 21 60  1  0
 21 61  1  0
 23 62  1  0
 23 63  1  0
 23 64  1  0
 24 65  1  0
 24 66  1  0
 25 67  1  0
 25 68  1  0
 26 69  1  0
 27 70  1  0
 29 71  1  0
 29 72  1  0
 29 73  1  0
 30 74  1  0
 30 75  1  0
 30 76  1  0
 31 77  1  0
 32 78  1  0
 32 79  1  0
 33 80  1  0
 33 81  1  0
 36 82  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      -5.015   5.705   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.320   5.705   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -14.865   2.618   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -16.336   3.943   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -11.244   6.126   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -6.611   5.052   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -9.691   1.631   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -11.323   2.052   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -12.829   2.373   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -14.257   6.766   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -12.750   6.446   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.681   3.395   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.014   3.395   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -6.510   1.863   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -8.231   5.486   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -5.015   4.165   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.320   4.165   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.348   4.165   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0     -10.292   3.197   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -6.349   3.395   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -9.738   5.806   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0     -13.305   3.837   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0     -15.287   5.622   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -8.016   1.543   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0     -10.768   4.661   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.653   3.395   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0     -14.811   4.157   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0     -12.274   4.982   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -7.755   4.021   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -8.786   2.877   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -2.348   5.705   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0     -10.214   7.270   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0     -16.793   5.942   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      -8.642   0.136   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0       2.987   4.165   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0       1.653   1.855   0.000  0.00  0.00           O+0
CONECT    1   16                                                            
CONECT    2   17                                                            
CONECT    3   27                                                            
CONECT    4   27                                                            
CONECT    5   28                                                            
CONECT    6   29                                                            
CONECT    7   30                                                            
CONECT    8    9   19                                                       
CONECT    9    8   22                                                       
CONECT   10   11   23                                                       
CONECT   11   10   28                                                       
CONECT   12   16   18                                                       
CONECT   13   17   18                                                       
CONECT   14   20   24                                                       
CONECT   15   21   29                                                       
CONECT   16    1   12   20                                                  
CONECT   17    2   13   26                                                  
CONECT   18   12   13   31                                                  
CONECT   19    8   25   30                                                  
CONECT   20   14   16   29                                                  
CONECT   21   15   25   32                                                  
CONECT   22    9   27   28                                                  
CONECT   23   10   27   33                                                  
CONECT   24   14   30   34                                                  
CONECT   25   19   21   28                                                  
CONECT   26   17   35   36                                                  
CONECT   27    3    4   22   23                                             
CONECT   28    5   11   22   25                                             
CONECT   29    6   15   20   30                                             
CONECT   30    7   19   24   29                                             
CONECT   31   18                                                            
CONECT   32   21                                                            
CONECT   33   23                                                            
CONECT   34   24                                                            
CONECT   35   26                                                            
CONECT   36   26                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   78    0
END

COMPND    HMDB0035751
HETATM    1  C1  UNL     1       7.728   0.311   2.153  1.00  0.00           C  
HETATM    2  C2  UNL     1       6.547   0.176   1.173  1.00  0.00           C  
HETATM    3  C3  UNL     1       5.597   1.281   1.470  1.00  0.00           C  
HETATM    4  C4  UNL     1       4.401   1.358   0.602  1.00  0.00           C  
HETATM    5  O1  UNL     1       3.548   2.156   0.951  1.00  0.00           O  
HETATM    6  C5  UNL     1       4.181   0.554  -0.632  1.00  0.00           C  
HETATM    7  C6  UNL     1       2.921   0.898  -1.367  1.00  0.00           C  
HETATM    8  C7  UNL     1       3.066   2.389  -1.760  1.00  0.00           C  
HETATM    9  C8  UNL     1       1.654   0.658  -0.673  1.00  0.00           C  
HETATM   10  C9  UNL     1       0.497   1.150  -1.617  1.00  0.00           C  
HETATM   11  C10 UNL     1       0.231  -0.151  -2.338  1.00  0.00           C  
HETATM   12  O2  UNL     1      -0.765  -0.081  -3.251  1.00  0.00           O  
HETATM   13  C11 UNL     1      -0.045  -1.036  -1.130  1.00  0.00           C  
HETATM   14  C12 UNL     1      -0.058  -2.466  -1.613  1.00  0.00           C  
HETATM   15  C13 UNL     1      -1.307  -0.746  -0.483  1.00  0.00           C  
HETATM   16  C14 UNL     1      -1.503  -0.219   0.717  1.00  0.00           C  
HETATM   17  C15 UNL     1      -0.308  -0.090   1.544  1.00  0.00           C  
HETATM   18  O3  UNL     1      -0.273   0.565   2.615  1.00  0.00           O  
HETATM   19  C16 UNL     1       0.964  -0.745   1.151  1.00  0.00           C  
HETATM   20  C17 UNL     1       1.212  -0.731  -0.347  1.00  0.00           C  
HETATM   21  C18 UNL     1       2.233  -1.823  -0.548  1.00  0.00           C  
HETATM   22  C19 UNL     1      -2.817   0.217   1.246  1.00  0.00           C  
HETATM   23  C20 UNL     1      -2.542   1.413   2.162  1.00  0.00           C  
HETATM   24  C21 UNL     1      -3.276  -0.879   2.183  1.00  0.00           C  
HETATM   25  C22 UNL     1      -4.662  -0.569   2.717  1.00  0.00           C  
HETATM   26  C23 UNL     1      -5.545  -0.723   1.494  1.00  0.00           C  
HETATM   27  O4  UNL     1      -5.452  -2.020   1.070  1.00  0.00           O  
HETATM   28  C24 UNL     1      -5.252   0.315   0.477  1.00  0.00           C  
HETATM   29  C25 UNL     1      -5.969  -0.130  -0.811  1.00  0.00           C  
HETATM   30  C26 UNL     1      -6.022   1.562   0.909  1.00  0.00           C  
HETATM   31  C27 UNL     1      -3.809   0.625   0.215  1.00  0.00           C  
HETATM   32  C28 UNL     1      -3.373   0.248  -1.190  1.00  0.00           C  
HETATM   33  C29 UNL     1      -2.575  -1.060  -1.206  1.00  0.00           C  
HETATM   34  C30 UNL     1       5.980  -1.178   1.450  1.00  0.00           C  
HETATM   35  O5  UNL     1       4.912  -1.303   2.038  1.00  0.00           O  
HETATM   36  O6  UNL     1       6.689  -2.283   1.030  1.00  0.00           O  
HETATM   37  H1  UNL     1       8.623  -0.179   1.714  1.00  0.00           H  
HETATM   38  H2  UNL     1       7.419  -0.195   3.081  1.00  0.00           H  
HETATM   39  H3  UNL     1       7.917   1.402   2.314  1.00  0.00           H  
HETATM   40  H4  UNL     1       6.950   0.199   0.144  1.00  0.00           H  
HETATM   41  H5  UNL     1       6.140   2.253   1.335  1.00  0.00           H  
HETATM   42  H6  UNL     1       5.305   1.195   2.553  1.00  0.00           H  
HETATM   43  H7  UNL     1       4.381  -0.482  -0.436  1.00  0.00           H  
HETATM   44  H8  UNL     1       5.077   0.865  -1.308  1.00  0.00           H  
HETATM   45  H9  UNL     1       2.978   0.398  -2.380  1.00  0.00           H  
HETATM   46  H10 UNL     1       2.679   2.570  -2.786  1.00  0.00           H  
HETATM   47  H11 UNL     1       2.647   3.046  -1.005  1.00  0.00           H  
HETATM   48  H12 UNL     1       4.155   2.572  -1.829  1.00  0.00           H  
HETATM   49  H13 UNL     1       1.558   1.361   0.183  1.00  0.00           H  
HETATM   50  H14 UNL     1      -0.376   1.394  -1.001  1.00  0.00           H  
HETATM   51  H15 UNL     1       0.834   1.959  -2.256  1.00  0.00           H  
HETATM   52  H16 UNL     1       1.197  -0.507  -2.755  1.00  0.00           H  
HETATM   53  H17 UNL     1      -0.857   0.868  -3.549  1.00  0.00           H  
HETATM   54  H18 UNL     1      -0.276  -3.208  -0.820  1.00  0.00           H  
HETATM   55  H19 UNL     1      -0.935  -2.627  -2.327  1.00  0.00           H  
HETATM   56  H20 UNL     1       0.811  -2.728  -2.259  1.00  0.00           H  
HETATM   57  H21 UNL     1       0.984  -1.802   1.530  1.00  0.00           H  
HETATM   58  H22 UNL     1       1.799  -0.212   1.604  1.00  0.00           H  
HETATM   59  H23 UNL     1       1.637  -2.802  -0.477  1.00  0.00           H  
HETATM   60  H24 UNL     1       2.773  -1.803  -1.486  1.00  0.00           H  
HETATM   61  H25 UNL     1       2.874  -1.940   0.376  1.00  0.00           H  
HETATM   62  H26 UNL     1      -3.484   2.049   2.131  1.00  0.00           H  
HETATM   63  H27 UNL     1      -1.774   2.092   1.738  1.00  0.00           H  
HETATM   64  H28 UNL     1      -2.427   1.150   3.208  1.00  0.00           H  
HETATM   65  H29 UNL     1      -2.592  -0.851   3.063  1.00  0.00           H  
HETATM   66  H30 UNL     1      -3.291  -1.870   1.730  1.00  0.00           H  
HETATM   67  H31 UNL     1      -4.930  -1.364   3.449  1.00  0.00           H  
HETATM   68  H32 UNL     1      -4.734   0.460   3.136  1.00  0.00           H  
HETATM   69  H33 UNL     1      -6.588  -0.578   1.864  1.00  0.00           H  
HETATM   70  H34 UNL     1      -6.165  -2.319   0.466  1.00  0.00           H  
HETATM   71  H35 UNL     1      -6.116   0.705  -1.506  1.00  0.00           H  
HETATM   72  H36 UNL     1      -5.589  -1.059  -1.219  1.00  0.00           H  
HETATM   73  H37 UNL     1      -7.011  -0.377  -0.442  1.00  0.00           H  
HETATM   74  H38 UNL     1      -7.082   1.416   0.620  1.00  0.00           H  
HETATM   75  H39 UNL     1      -5.647   2.462   0.407  1.00  0.00           H  
HETATM   76  H40 UNL     1      -6.032   1.649   2.016  1.00  0.00           H  
HETATM   77  H41 UNL     1      -3.768   1.763   0.160  1.00  0.00           H  
HETATM   78  H42 UNL     1      -2.651   1.013  -1.610  1.00  0.00           H  
HETATM   79  H43 UNL     1      -4.191   0.233  -1.915  1.00  0.00           H  
HETATM   80  H44 UNL     1      -3.117  -1.863  -0.665  1.00  0.00           H  
HETATM   81  H45 UNL     1      -2.463  -1.319  -2.250  1.00  0.00           H  
HETATM   82  H46 UNL     1       6.549  -2.636   0.082  1.00  0.00           H  
CONECT    1    2   37   38   39
CONECT    2    3   34   40
CONECT    3    4   41   42
CONECT    4    5    5    6
CONECT    6    7   43   44
CONECT    7    8    9   45
CONECT    8   46   47   48
CONECT    9   10   20   49
CONECT   10   11   50   51
CONECT   11   12   13   52
CONECT   12   53
CONECT   13   14   15   20
CONECT   14   54   55   56
CONECT   15   16   16   33
CONECT   16   17   22
CONECT   17   18   18   19
CONECT   19   20   57   58
CONECT   20   21
CONECT   21   59   60   61
CONECT   22   23   24   31
CONECT   23   62   63   64
CONECT   24   25   65   66
CONECT   25   26   67   68
CONECT   26   27   28   69
CONECT   27   70
CONECT   28   29   30   31
CONECT   29   71   72   73
CONECT   30   74   75   76
CONECT   31   32   77
CONECT   32   33   78   79
CONECT   33   80   81
CONECT   34   35   35   36
CONECT   36   82
END

HMDB0035751
     RDKit          3D
Ganolucidic acid B
 82 85  0  0  0  0  0  0  0  0999 V2000
    7.7283    0.3107    2.1532 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5472    0.1761    1.1735 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5971    1.2807    1.4695 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4010    1.3583    0.6024 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5480    2.1560    0.9513 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1813    0.5542   -0.6320 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9209    0.8981   -1.3671 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0662    2.3891   -1.7599 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6540    0.6578   -0.6726 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4970    1.1500   -1.6169 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2309   -0.1510   -2.3385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7655   -0.0808   -3.2511 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0446   -1.0363   -1.1295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0581   -2.4665   -1.6132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3073   -0.7457   -0.4826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5026   -0.2194    0.7175 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3081   -0.0902    1.5436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2725    0.5653    2.6152 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9643   -0.7452    1.1514 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2118   -0.7311   -0.3472 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2332   -1.8231   -0.5483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8168    0.2175    1.2462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5424    1.4134    2.1620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2760   -0.8786    2.1831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6617   -0.5694    2.7174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5445   -0.7233    1.4938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4523   -2.0201    1.0703 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2519    0.3154    0.4774 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9691   -0.1295   -0.8108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0216    1.5616    0.9086 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8092    0.6246    0.2146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3729    0.2480   -1.1903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5753   -1.0596   -1.2057 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9796   -1.1780    1.4497 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9118   -1.3025    2.0376 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6889   -2.2834    1.0300 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6227   -0.1791    1.7138 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4193   -0.1951    3.0807 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9168    1.4024    2.3138 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9498    0.1990    0.1442 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1404    2.2535    1.3355 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3053    1.1951    2.5527 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3807   -0.4824   -0.4356 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0774    0.8648   -1.3082 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9778    0.3979   -2.3803 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6793    2.5696   -2.7859 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6469    3.0463   -1.0050 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1545    2.5721   -1.8292 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5583    1.3613    0.1829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3764    1.3939   -1.0015 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8338    1.9595   -2.2559 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1969   -0.5070   -2.7549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8570    0.8681   -3.5485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2759   -3.2083   -0.8201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9346   -2.6270   -2.3268 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8111   -2.7282   -2.2592 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9836   -1.8016    1.5302 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7989   -0.2118    1.6042 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6375   -2.8018   -0.4772 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7725   -1.8034   -1.4863 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8741   -1.9399    0.3756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4839    2.0489    2.1311 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7743    2.0924    1.7385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4271    1.1500    3.2080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5919   -0.8508    3.0627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2908   -1.8696    1.7305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9302   -1.3639    3.4491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7336    0.4601    3.1363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5881   -0.5777    1.8636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1652   -2.3186    0.4656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1161    0.7053   -1.5063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5888   -1.0588   -1.2194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0111   -0.3768   -0.4417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0825    1.4162    0.6200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6473    2.4616    0.4068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0318    1.6495    2.0155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7684    1.7635    0.1602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6506    1.0131   -1.6102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1912    0.2330   -1.9151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1167   -1.8633   -0.6647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4631   -1.3192   -2.2496 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5493   -2.6357    0.0818 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  4  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
 11 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 16 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 28 30  1  0
 28 31  1  0
 31 32  1  0
 32 33  1  0
  2 34  1  0
 34 35  2  0
 34 36  1  0
 20  9  1  0
 31 22  1  0
 20 13  1  0
 33 15  1  0
  1 37  1  0
  1 38  1  0
  1 39  1  0
  2 40  1  0
  3 41  1  0
  3 42  1  0
  6 43  1  0
  6 44  1  0
  7 45  1  0
  8 46  1  0
  8 47  1  0
  8 48  1  0
  9 49  1  0
 10 50  1  0
 10 51  1  0
 11 52  1  0
 12 53  1  0
 14 54  1  0
 14 55  1  0
 14 56  1  0
 19 57  1  0
 19 58  1  0
 21 59  1  0
 21 60  1  0
 21 61  1  0
 23 62  1  0
 23 63  1  0
 23 64  1  0
 24 65  1  0
 24 66  1  0
 25 67  1  0
 25 68  1  0
 26 69  1  0
 27 70  1  0
 29 71  1  0
 29 72  1  0
 29 73  1  0
 30 74  1  0
 30 75  1  0
 30 76  1  0
 31 77  1  0
 32 78  1  0
 32 79  1  0
 33 80  1  0
 33 81  1  0
 36 82  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
Ganolucidate b	Generator
3,15-Dihydroxy-11,23-dioxolanost-8-en-26-Oic acid	HMDB
6-{5,12-dihydroxy-2,6,6,11,15-pentamethyl-17-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl}-2-methyl-4-oxoheptanoate	Generator

Chemical Formula

C₃₀H₄₆O₆

Average Molecular Weight

502.6826

Monoisotopic Molecular Weight

502.329439204

IUPAC Name

6-{5,12-dihydroxy-2,6,6,11,15-pentamethyl-17-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl}-2-methyl-4-oxoheptanoic acid

Traditional Name

6-{5,12-dihydroxy-2,6,6,11,15-pentamethyl-17-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl}-2-methyl-4-oxoheptanoic acid

CAS Registry Number

98683-75-1

SMILES

CC(CC(=O)CC(C)C(O)=O)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3

InChI Identifier

InChI=1S/C30H46O6/c1-16(12-18(31)13-17(2)26(35)36)20-14-24(34)30(7)19-8-9-22-27(3,4)23(33)10-11-28(22,5)25(19)21(32)15-29(20,30)6/h16-17,20,22-24,33-34H,8-15H2,1-7H3,(H,35,36)

InChI Key

YPYHGMCHNBTMDB-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

Substituents

Triterpenoid
Dihydroxy bile acid, alcohol, or derivatives
Hydroxy bile acid, alcohol, or derivatives
23-oxosteroid
Bile acid, alcohol, or derivatives
Steroid acid
Oxosteroid
11-oxosteroid
3-hydroxysteroid
15-hydroxysteroid
Hydroxysteroid
Steroid
Medium-chain keto acid
Gamma-keto acid
Cyclohexenone
Keto acid
Cyclic alcohol
Secondary alcohol
Ketone
Carboxylic acid
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Route of exposure

Enteral

Ingestion (HMDB: HMDB0035751)

Source

Endogenous

Endogenous (HMDB: HMDB0035751)

Plant

Plant (HMDB: HMDB0035751)

Animal

Animal (HMDB: HMDB0035751)

Exogenous

Food

Food (HMDB: HMDB0035751)

Vegetable

Mushroom

Exogenous (HMDB: HMDB0035751)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0035751)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0035751)

Lipid metabolism pathway (HMDB: HMDB0035751)

Cellular process

Cell signaling (HMDB: HMDB0035751)

Biochemical process

Lipid transport (HMDB: HMDB0035751)

Role

Biological role

Energy source (HMDB: HMDB0035751)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0035751)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	167 - 169 °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	0.0056 g/L	ALOGPS
logP	4.14	ALOGPS
logP	3.97	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	4.35	ChemAxon
pKa (Strongest Basic)	-0.28	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	111.9 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	138.24 m³·mol⁻¹	ChemAxon
Polarizability	57.13 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	218.633	31661259
DarkChem	[M-H]-	211.157	31661259
DeepCCS	[M-2H]-	252.252	30932474
DeepCCS	[M+Na]+	227.676	30932474
AllCCS	[M+H]+	219.8	32859911
AllCCS	[M+H-H2O]+	218.3	32859911
AllCCS	[M+NH4]+	221.2	32859911
AllCCS	[M+Na]+	221.6	32859911
AllCCS	[M-H]-	219.2	32859911
AllCCS	[M+Na-2H]-	222.0	32859911
AllCCS	[M+HCOO]-	225.2	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.	7.75 minutes	32390414
Predicted by Siyang on May 30, 2022	14.7578 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	2.01 minutes	32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid	64.5 seconds	40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	3083.7 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	173.7 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	228.1 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	163.6 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	195.2 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	699.0 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	722.9 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	89.7 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	1159.5 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	595.0 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	1711.9 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	372.1 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	495.1 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	209.8 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	284.7 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	9.6 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Ganolucidic acid B	CC(CC(=O)CC(C)C(O)=O)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3	4789.3	Standard polar	33892256
Ganolucidic acid B	CC(CC(=O)CC(C)C(O)=O)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3	3235.1	Standard non polar	33892256
Ganolucidic acid B	CC(CC(=O)CC(C)C(O)=O)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3	4137.5	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Ganolucidic acid B,1TMS,isomer #1	CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3)C(=O)O[Si](C)(C)C	4106.9	Semi standard non polar	33892256
Ganolucidic acid B,1TMS,isomer #2	CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3)C(=O)O	4088.4	Semi standard non polar	33892256
Ganolucidic acid B,1TMS,isomer #3	CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)C(=O)O	4149.4	Semi standard non polar	33892256
Ganolucidic acid B,1TMS,isomer #4	CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O	4137.0	Semi standard non polar	33892256
Ganolucidic acid B,1TMS,isomer #5	CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O	4147.8	Semi standard non polar	33892256
Ganolucidic acid B,1TMS,isomer #6	CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3)C(=O)O	3980.5	Semi standard non polar	33892256
Ganolucidic acid B,2TMS,isomer #1	CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3)C(=O)O[Si](C)(C)C	4014.1	Semi standard non polar	33892256
Ganolucidic acid B,2TMS,isomer #10	CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O	4107.9	Semi standard non polar	33892256
Ganolucidic acid B,2TMS,isomer #11	CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O	4105.9	Semi standard non polar	33892256
Ganolucidic acid B,2TMS,isomer #12	CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)C(=O)O	3891.3	Semi standard non polar	33892256
Ganolucidic acid B,2TMS,isomer #13	CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O	3913.7	Semi standard non polar	33892256
Ganolucidic acid B,2TMS,isomer #14	CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O	3919.9	Semi standard non polar	33892256
Ganolucidic acid B,2TMS,isomer #2	CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)C(=O)O[Si](C)(C)C	4090.4	Semi standard non polar	33892256
Ganolucidic acid B,2TMS,isomer #3	CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4084.2	Semi standard non polar	33892256
Ganolucidic acid B,2TMS,isomer #4	CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4078.5	Semi standard non polar	33892256
Ganolucidic acid B,2TMS,isomer #5	CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3)C(=O)O[Si](C)(C)C	3900.2	Semi standard non polar	33892256
Ganolucidic acid B,2TMS,isomer #6	CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)C(=O)O	3999.9	Semi standard non polar	33892256
Ganolucidic acid B,2TMS,isomer #7	CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O	4028.7	Semi standard non polar	33892256
Ganolucidic acid B,2TMS,isomer #8	CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O	4023.5	Semi standard non polar	33892256
Ganolucidic acid B,2TMS,isomer #9	CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3)C(=O)O	3841.4	Semi standard non polar	33892256
Ganolucidic acid B,3TMS,isomer #1	CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)C(=O)O[Si](C)(C)C	3904.7	Semi standard non polar	33892256
Ganolucidic acid B,3TMS,isomer #10	CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O	3862.2	Semi standard non polar	33892256
Ganolucidic acid B,3TMS,isomer #11	CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O	3859.9	Semi standard non polar	33892256
Ganolucidic acid B,3TMS,isomer #12	CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)C(=O)O	3730.9	Semi standard non polar	33892256
Ganolucidic acid B,3TMS,isomer #13	CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O	3736.8	Semi standard non polar	33892256
Ganolucidic acid B,3TMS,isomer #14	CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O	3743.5	Semi standard non polar	33892256
Ganolucidic acid B,3TMS,isomer #15	CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O	3783.0	Semi standard non polar	33892256
Ganolucidic acid B,3TMS,isomer #16	CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O	3785.4	Semi standard non polar	33892256
Ganolucidic acid B,3TMS,isomer #2	CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3894.2	Semi standard non polar	33892256
Ganolucidic acid B,3TMS,isomer #3	CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3884.3	Semi standard non polar	33892256
Ganolucidic acid B,3TMS,isomer #4	CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3)C(=O)O[Si](C)(C)C	3752.7	Semi standard non polar	33892256
Ganolucidic acid B,3TMS,isomer #5	CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3995.9	Semi standard non polar	33892256
Ganolucidic acid B,3TMS,isomer #6	CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3997.5	Semi standard non polar	33892256
Ganolucidic acid B,3TMS,isomer #7	CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)C(=O)O[Si](C)(C)C	3812.9	Semi standard non polar	33892256
Ganolucidic acid B,3TMS,isomer #8	CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3799.6	Semi standard non polar	33892256
Ganolucidic acid B,3TMS,isomer #9	CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3802.1	Semi standard non polar	33892256
Ganolucidic acid B,4TMS,isomer #1	CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3773.5	Semi standard non polar	33892256
Ganolucidic acid B,4TMS,isomer #1	CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3837.6	Standard non polar	33892256
Ganolucidic acid B,4TMS,isomer #2	CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3762.7	Semi standard non polar	33892256
Ganolucidic acid B,4TMS,isomer #2	CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3843.1	Standard non polar	33892256
Ganolucidic acid B,4TMS,isomer #3	CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)C(=O)O[Si](C)(C)C	3674.5	Semi standard non polar	33892256
Ganolucidic acid B,4TMS,isomer #3	CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)C(=O)O[Si](C)(C)C	3736.5	Standard non polar	33892256
Ganolucidic acid B,4TMS,isomer #4	CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3672.5	Semi standard non polar	33892256
Ganolucidic acid B,4TMS,isomer #4	CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3810.8	Standard non polar	33892256
Ganolucidic acid B,4TMS,isomer #5	CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3676.8	Semi standard non polar	33892256
Ganolucidic acid B,4TMS,isomer #5	CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3812.3	Standard non polar	33892256
Ganolucidic acid B,4TMS,isomer #6	CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3717.3	Semi standard non polar	33892256
Ganolucidic acid B,4TMS,isomer #6	CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3835.3	Standard non polar	33892256
Ganolucidic acid B,4TMS,isomer #7	CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3729.7	Semi standard non polar	33892256
Ganolucidic acid B,4TMS,isomer #7	CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3840.9	Standard non polar	33892256
Ganolucidic acid B,4TMS,isomer #8	CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O	3641.5	Semi standard non polar	33892256
Ganolucidic acid B,4TMS,isomer #8	CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O	3725.1	Standard non polar	33892256
Ganolucidic acid B,4TMS,isomer #9	CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O	3645.9	Semi standard non polar	33892256
Ganolucidic acid B,4TMS,isomer #9	CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O	3768.9	Standard non polar	33892256
Ganolucidic acid B,5TMS,isomer #1	CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3591.4	Semi standard non polar	33892256
Ganolucidic acid B,5TMS,isomer #1	CC(CC(=CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3775.3	Standard non polar	33892256
Ganolucidic acid B,5TMS,isomer #2	CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3598.0	Semi standard non polar	33892256
Ganolucidic acid B,5TMS,isomer #2	CC(C=C(CC(C)C1CC(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3782.4	Standard non polar	33892256
Ganolucidic acid B,1TBDMS,isomer #1	CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3)C(=O)O[Si](C)(C)C(C)(C)C	4360.6	Semi standard non polar	33892256
Ganolucidic acid B,1TBDMS,isomer #2	CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3)C(=O)O	4318.2	Semi standard non polar	33892256
Ganolucidic acid B,1TBDMS,isomer #3	CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3)C(=O)O	4371.6	Semi standard non polar	33892256
Ganolucidic acid B,1TBDMS,isomer #4	CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C(C)(C)C)C(=O)O	4365.8	Semi standard non polar	33892256
Ganolucidic acid B,1TBDMS,isomer #5	CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C(C)(C)C)C(=O)O	4377.2	Semi standard non polar	33892256
Ganolucidic acid B,1TBDMS,isomer #6	CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3)C(=O)O	4233.0	Semi standard non polar	33892256
Ganolucidic acid B,2TBDMS,isomer #1	CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3)C(=O)O[Si](C)(C)C(C)(C)C	4511.5	Semi standard non polar	33892256
Ganolucidic acid B,2TBDMS,isomer #10	CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C(C)(C)C)C(=O)O	4579.8	Semi standard non polar	33892256
Ganolucidic acid B,2TBDMS,isomer #11	CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C(C)(C)C)C(=O)O	4580.4	Semi standard non polar	33892256
Ganolucidic acid B,2TBDMS,isomer #12	CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3)C(=O)O	4355.2	Semi standard non polar	33892256
Ganolucidic acid B,2TBDMS,isomer #13	CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C(C)(C)C)C(=O)O	4385.9	Semi standard non polar	33892256
Ganolucidic acid B,2TBDMS,isomer #14	CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C(C)(C)C)C(=O)O	4399.8	Semi standard non polar	33892256
Ganolucidic acid B,2TBDMS,isomer #2	CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3)C(=O)O[Si](C)(C)C(C)(C)C	4588.2	Semi standard non polar	33892256
Ganolucidic acid B,2TBDMS,isomer #3	CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4567.7	Semi standard non polar	33892256
Ganolucidic acid B,2TBDMS,isomer #4	CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4561.9	Semi standard non polar	33892256
Ganolucidic acid B,2TBDMS,isomer #5	CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3)C(=O)O[Si](C)(C)C(C)(C)C	4376.5	Semi standard non polar	33892256
Ganolucidic acid B,2TBDMS,isomer #6	CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3)C(=O)O	4473.1	Semi standard non polar	33892256
Ganolucidic acid B,2TBDMS,isomer #7	CC(CC(=CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C(C)(C)C)C(=O)O	4498.8	Semi standard non polar	33892256
Ganolucidic acid B,2TBDMS,isomer #8	CC(C=C(CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C(C)(C)C)C(=O)O	4490.9	Semi standard non polar	33892256
Ganolucidic acid B,2TBDMS,isomer #9	CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3)C(=O)O	4311.1	Semi standard non polar	33892256
Ganolucidic acid B,3TBDMS,isomer #1	CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3)C(=O)O[Si](C)(C)C(C)(C)C	4640.6	Semi standard non polar	33892256
Ganolucidic acid B,3TBDMS,isomer #10	CC(CC(=CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C(C)(C)C)C(=O)O	4582.3	Semi standard non polar	33892256
Ganolucidic acid B,3TBDMS,isomer #11	CC(C=C(CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C(C)(C)C)C(=O)O	4577.4	Semi standard non polar	33892256
Ganolucidic acid B,3TBDMS,isomer #12	CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3)C(=O)O	4412.5	Semi standard non polar	33892256
Ganolucidic acid B,3TBDMS,isomer #13	CC(CC(=CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C(C)(C)C)C(=O)O	4414.9	Semi standard non polar	33892256
Ganolucidic acid B,3TBDMS,isomer #14	CC(C=C(CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C(C)(C)C)C(=O)O	4413.9	Semi standard non polar	33892256
Ganolucidic acid B,3TBDMS,isomer #15	CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C(C)(C)C)C(=O)O	4457.3	Semi standard non polar	33892256
Ganolucidic acid B,3TBDMS,isomer #16	CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C(C)(C)C)C(=O)O	4457.1	Semi standard non polar	33892256
Ganolucidic acid B,3TBDMS,isomer #2	CC(CC(=CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4587.7	Semi standard non polar	33892256
Ganolucidic acid B,3TBDMS,isomer #3	CC(C=C(CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4576.3	Semi standard non polar	33892256
Ganolucidic acid B,3TBDMS,isomer #4	CC(CC(=O)CC(C)C1CC(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3)C(=O)O[Si](C)(C)C(C)(C)C	4427.6	Semi standard non polar	33892256
Ganolucidic acid B,3TBDMS,isomer #5	CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4689.5	Semi standard non polar	33892256
Ganolucidic acid B,3TBDMS,isomer #6	CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4685.9	Semi standard non polar	33892256
Ganolucidic acid B,3TBDMS,isomer #7	CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3)C(=O)O[Si](C)(C)C(C)(C)C	4492.0	Semi standard non polar	33892256
Ganolucidic acid B,3TBDMS,isomer #8	CC(CC(=CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4464.2	Semi standard non polar	33892256
Ganolucidic acid B,3TBDMS,isomer #9	CC(C=C(CC(C)C1CC(O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(O)C(C)(C)C1CC3)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4461.9	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Ganolucidic acid B GC-MS (Non-derivatized) - 70eV, Positive	splash10-059i-2013900000-425f64b602f5602dcc7a	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Ganolucidic acid B GC-MS (2 TMS) - 70eV, Positive	splash10-001i-6120539000-32ba9c12e6224c1c7842	2017-10-06	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 - Ganolucidic acid B 10V, Positive-QTOF	splash10-00kr-0001910000-e6d54ea50911007c3636	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ganolucidic acid B 20V, Positive-QTOF	splash10-00kr-2002900000-abd111e92e7941ba4e28	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ganolucidic acid B 40V, Positive-QTOF	splash10-00ku-9207700000-65a2cf8374f586c414cb	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ganolucidic acid B 10V, Negative-QTOF	splash10-0udi-0000790000-8bd3e991a754a3a62185	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ganolucidic acid B 20V, Negative-QTOF	splash10-0kh0-6101920000-1a955b384c3c4ae67e0b	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ganolucidic acid B 40V, Negative-QTOF	splash10-0a5c-9002600000-b501e90493554300795a	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ganolucidic acid B 10V, Negative-QTOF	splash10-0udi-0000190000-201824a7cc674c84385a	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ganolucidic acid B 20V, Negative-QTOF	splash10-05g0-2008920000-e57972a3ad2a78bb7c81	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ganolucidic acid B 40V, Negative-QTOF	splash10-0600-6009500000-ef8f4dcc809e5197dc62	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ganolucidic acid B 10V, Positive-QTOF	splash10-0l4r-0209310000-497443bf05927dfc635d	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ganolucidic acid B 20V, Positive-QTOF	splash10-06ui-4609300000-d192fdbfa06da416ed67	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ganolucidic acid B 40V, Positive-QTOF	splash10-00xu-9626000000-85acf639cb45552481fb	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular

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

FDB014483

KNApSAcK ID

C00024063

Chemspider ID

74886431

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

73657197

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1851411

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.. .
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Showing metabocard for Ganolucidic acid B (HMDB0035751)

MOL for HMDB0035751 (Ganolucidic acid B)

3D MOL for HMDB0035751 (Ganolucidic acid B)

3D SDF for HMDB0035751 (Ganolucidic acid B)

3D-SDF for HMDB0035751 (Ganolucidic acid B)

PDB for HMDB0035751 (Ganolucidic acid B)

3D PDB for HMDB0035751 (Ganolucidic acid B)

SMILES for HMDB0035751 (Ganolucidic acid B)

INCHI for HMDB0035751 (Ganolucidic acid B)

Structure for HMDB0035751 (Ganolucidic acid B)

3D Structure for HMDB0035751 (Ganolucidic acid B)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra