NP-MRD: Showing NP-Card for 4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl dodecanoate (NP0184885)

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Record Information

Version

1.0

Created at

2022-09-04 00:07:44 UTC

Updated at

2022-09-04 00:07:45 UTC

NP-MRD ID

NP0184885

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl dodecanoate

Description

4-Hydroxy-1,2,5,14,18,18-hexamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]Henicosan-17-yl dodecanoate belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. 4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl dodecanoate is found in Arnica lonchophylla. 4-Hydroxy-1,2,5,14,18,18-hexamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]Henicosan-17-yl dodecanoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191517502D          

 45 49  0  0  0  0            999 V2000
   10.7171   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.2920   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0766   -5.5201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.5616   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0766   -6.8549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.2920   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.3782   -7.4205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.5275   -6.5287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.3316   -4.7354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.7795   -4.1223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.1385   -4.5639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.5680   -4.8246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1807   -4.1538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  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
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 18 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 29 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 23 38  1  0  0  0  0
 28 38  1  0  0  0  0
 38 39  1  0  0  0  0
 30 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
 20 43  1  0  0  0  0
 15 43  1  0  0  0  0
 43 44  1  0  0  0  0
 43 45  1  0  0  0  0
M  END

     RDKit          3D

117121  0  0  0  0  0  0  0  0999 V2000
   -8.4593    1.5164    3.2611 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2251    0.2578    3.0163 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7597   -0.7439    4.0374 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4997   -0.2366    1.8516 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.4529   -1.1241    1.0736 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6089   -0.5494   -0.2885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8171    0.7521   -0.3053 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.8902    1.8460   -0.1245 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9136    0.7405    0.8857 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.4637    0.5114    0.6398 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7845   -0.3657    1.6663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2815   -0.0759    1.4875 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7769   -0.5418    0.1451 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -1.6655    1.8093   -0.6703 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8244    0.5998   -0.8466 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6460    0.8544   -0.9171 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8136    1.7275   -2.1881 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2479    1.6446    0.1835 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3375   -0.4432   -1.2372 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2796   -0.8486   -0.2811 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6136   -1.1162   -0.5696 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9708   -0.9823   -1.7465 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5734   -1.5427    0.4739 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9732   -1.7395   -0.0109 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6320   -0.5281   -0.5775 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0467   -0.8183   -1.0407 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9442   -1.3037    0.0465 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1213   -0.3602    1.1882 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7112    0.9624    0.7795 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0654    0.8243    0.1522 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0895    0.1940    1.0435 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3947    0.1356    0.2447 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2051   -0.6932   -1.0142 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3203   -1.5602   -1.5150 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6362   -1.7672   -0.3920 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3003   -0.4696    0.0686 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7783   -0.2792    1.5039 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0590    0.0337   -0.7008 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.4115   -1.4035   -0.9707 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7360    0.9376   -1.7108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2248    0.9245   -1.6362 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.7041   -0.0554   -2.5449 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1478    2.3255    2.6378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0306    1.7543    4.1977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8415   -0.8650    3.9277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1803   -1.6830    3.9987 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -9.4438   -1.2308    1.5802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7029   -0.3858   -0.4901 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -8.3614    2.7252    0.2823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6414    1.5001    0.6140 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.9997    1.7484    1.3342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9295    1.5071    0.7732 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.7622    2.5972   -0.1609 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.5853   -0.7434    1.2504 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2489   -2.5208    0.9163 H   0  0  0  0  0  0  0  0  0  0  0  0
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    6.6404    0.3344    0.1235 H   0  0  0  0  0  0  0  0  0  0  0  0
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   14.0912   -1.3535   -1.2102 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.9899   -1.2788    1.9946 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.9717   -1.8895   -0.1447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0450   -1.5435   -1.8752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4408    0.7624   -2.7544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4235    2.0039   -1.5047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5715    1.8845   -2.1339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1072    0.0211   -3.3518 H   0  0  0  0  0  0  0  0  0  0  0  0
 36 35  1  0
 35 34  1  0
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 39 18  1  0
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 12 11  1  0
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 10  9  1  0
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  6  7  1  0
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  7 44  1  0
 44 45  1  0
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  4  2  1  0
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  2  1  2  3
 18 19  1  0
 19 20  1  0
 19 21  1  0
 19 22  1  0
 13 39  1  0
 41 10  1  0
 41 14  1  0
  7  9  1  0
 36101  1  0
 36102  1  0
 36103  1  0
 35 99  1  0
 35100  1  0
 34 97  1  0
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 32 93  1  0
 32 94  1  0
 31 91  1  0
 31 92  1  0
 30 89  1  0
 30 90  1  0
 29 87  1  0
 29 88  1  0
 28 85  1  0
 28 86  1  0
 27 83  1  0
 27 84  1  0
 26 81  1  0
 26 82  1  0
 22 80  1  6
 37104  1  0
 37105  1  0
 38106  1  0
 38107  1  0
 40108  1  0
 40109  1  0
 40110  1  0
 18 73  1  6
 17 71  1  0
 17 72  1  0
 16 69  1  0
 16 70  1  0
 15 66  1  0
 15 67  1  0
 15 68  1  0
 13 65  1  1
 12 63  1  0
 12 64  1  0
 11 61  1  0
 11 62  1  0
 10 60  1  1
  9 59  1  1
  4 51  1  1
  5 52  1  0
  5 53  1  0
  6 54  1  0
  6 55  1  0
  8 56  1  0
  8 57  1  0
  8 58  1  0
 44116  1  6
 45117  1  0
 43114  1  0
 43115  1  0
 42111  1  0
 42112  1  0
 42113  1  0
  3 48  1  0
  3 49  1  0
  3 50  1  0
  1 46  1  0
  1 47  1  0
 20 74  1  0
 20 75  1  0
 20 76  1  0
 21 77  1  0
 21 78  1  0
 21 79  1  0
M  END


  Mrv1533004191517502D          

 45 49  0  0  0  0            999 V2000
   10.7171   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.2920   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0766   -5.5201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.5616   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0766   -6.8549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.2920   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.3782   -7.4205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.5275   -6.5287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.3316   -4.7354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.7795   -4.1223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.1385   -4.5639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.5680   -4.8246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1807   -4.1538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  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
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 18 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 29 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 23 38  1  0  0  0  0
 28 38  1  0  0  0  0
 38 39  1  0  0  0  0
 30 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
 20 43  1  0  0  0  0
 15 43  1  0  0  0  0
 43 44  1  0  0  0  0
 43 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0184885

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCC(=O)OC1CCC2(C)C(CCC3(C)C2CCC2C4C(CCC4(C)C(O)CC32C)C(C)=C)C1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C42H72O3/c1-10-11-12-13-14-15-16-17-18-19-36(44)45-35-24-26-39(6)32(38(35,4)5)23-27-41(8)33(39)21-20-31-37-30(29(2)3)22-25-40(37,7)34(43)28-42(31,41)9/h30-35,37,43H,2,10-28H2,1,3-9H3

> <INCHI_KEY>
LIWKTAWWXCGRNF-UHFFFAOYSA-N

> <FORMULA>
C42H72O3

> <MOLECULAR_WEIGHT>
625.035

> <EXACT_MASS>
624.548146178

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
117

> <JCHEM_AVERAGE_POLARIZABILITY>
79.70202001586047

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-hydroxy-1,2,5,14,18,18-hexamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicosan-17-yl dodecanoate

> <ALOGPS_LOGP>
8.86

> <JCHEM_LOGP>
11.36001465633333

> <ALOGPS_LOGS>
-7.50

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-0.3903221726765621

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
187.6112

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.98e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-hydroxy-1,2,5,14,18,18-hexamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicosan-17-yl dodecanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0      20.005  -5.390   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      21.339  -6.160   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      22.673  -5.390   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      24.006  -6.160   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      25.340  -5.390   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      26.674  -6.160   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      28.007  -5.390   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      29.341  -6.160   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      30.675  -5.390   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      32.008  -6.160   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      33.342  -5.390   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      34.676  -6.160   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      34.676  -7.700   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      36.009  -5.390   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      37.343  -6.160   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      38.677  -5.390   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      40.010  -6.160   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      40.010  -7.700   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      41.344  -6.930   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      38.677  -8.470   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      38.677 -10.010   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      40.010 -10.780   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      41.344 -10.010   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      41.344 -11.550   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      41.344  -8.470   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      42.678  -7.700   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      44.011  -8.470   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      44.011 -10.010   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      45.345 -10.780   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      46.810 -10.304   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      47.715 -11.550   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      46.810 -12.796   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      45.345 -12.320   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      45.506 -13.852   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      44.011 -13.090   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      44.011 -14.630   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      42.678 -12.320   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      42.678 -10.780   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      42.051 -12.187   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      47.286  -8.839   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      46.255  -7.695   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      48.792  -8.519   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      37.343  -7.700   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      36.527  -9.006   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      35.804  -7.754   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   43                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20   25                                             
CONECT   19   18                                                            
CONECT   20   18   21   43                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25   38                                             
CONECT   24   23                                                            
CONECT   25   23   18   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   38                                                  
CONECT   29   28   30   33                                                  
CONECT   30   29   31   40                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   29   34   35                                             
CONECT   34   33                                                            
CONECT   35   33   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   23   28   39                                             
CONECT   39   38                                                            
CONECT   40   30   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40                                                            
CONECT   43   20   15   44   45                                             
CONECT   44   43                                                            
CONECT   45   43                                                            
MASTER        0    0    0    0    0    0    0    0   45    0   98    0
END

View in JSmol

Synonyms

Value	Source
4-Hydroxy-1,2,5,14,18,18-hexamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0,.0,.0,]henicosan-17-yl dodecanoic acid	Generator
4-Hydroxy-1,2,5,14,18,18-hexamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicosan-17-yl dodecanoic acid	Generator

Chemical Formula

C₄₂H₇₂O₃

Average Mass

625.0350 Da

Monoisotopic Mass

624.54815 Da

IUPAC Name

4-hydroxy-1,2,5,14,18,18-hexamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicosan-17-yl dodecanoate

Traditional Name

4-hydroxy-1,2,5,14,18,18-hexamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicosan-17-yl dodecanoate

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCC(=O)OC1CCC2(C)C(CCC3(C)C2CCC2C4C(CCC4(C)C(O)CC32C)C(C)=C)C1(C)C

InChI Identifier

InChI=1S/C42H72O3/c1-10-11-12-13-14-15-16-17-18-19-36(44)45-35-24-26-39(6)32(38(35,4)5)23-27-41(8)33(39)21-20-31-37-30(29(2)3)22-25-40(37,7)34(43)28-42(31,41)9/h30-35,37,43H,2,10-28H2,1,3-9H3

InChI Key

LIWKTAWWXCGRNF-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Arnica lonchophylla	LOTUS Database	35616633

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
12-hydroxysteroid
Hydroxysteroid
Steroid
Fatty acid ester
Fatty acyl
Cyclic alcohol
Carboxylic acid ester
Secondary alcohol
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
Organooxygen compound
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	8.86	ALOGPS
logP	11.36	ChemAxon
logS	-7.5	ALOGPS
pKa (Strongest Basic)	-0.39	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	46.53 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	187.61 m³·mol⁻¹	ChemAxon
Polarizability	79.7 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl dodecanoate (NP0184885)

MOL for NP0184885 (4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl dodecanoate)

3D MOL for NP0184885 (4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl dodecanoate)

3D SDF for NP0184885 (4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl dodecanoate)

3D-SDF for NP0184885 (4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl dodecanoate)

PDB for NP0184885 (4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl dodecanoate)

3D PDB for NP0184885 (4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl dodecanoate)

SMILES for NP0184885 (4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl dodecanoate)

INCHI for NP0184885 (4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl dodecanoate)

Structure for NP0184885 (4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl dodecanoate)

3D Structure for NP0184885 (4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl dodecanoate)