NP-MRD: Showing NP-Card for 7,7,12,16-tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl deca-2,4-dienoate (NP0177583)

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Record Information

Version

2.0

Created at

2022-09-03 15:26:30 UTC

Updated at

2022-09-03 15:26:30 UTC

NP-MRD ID

NP0177583

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7,7,12,16-tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl deca-2,4-dienoate

Description

7,7,12,16-Tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]Octadecan-6-yl deca-2,4-dienoate belongs to the class of organic compounds known as cycloartanols and derivatives. These are steroids containing a cycloartanol moiety. 7,7,12,16-tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl deca-2,4-dienoate is found in Euphorbia retusa. 7,7,12,16-Tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]Octadecan-6-yl deca-2,4-dienoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251508262D          

 43 47  0  0  0  0            999 V2000
    1.0623   -8.1486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5305   -7.5179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8108   -6.7420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2790   -6.1112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5593   -5.3353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0274   -4.7046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3077   -3.9287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2241   -3.2980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0562   -2.5221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4756   -1.8914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2877   -2.0366    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1953   -1.1154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6168   -0.9702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8971   -0.1943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7092   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2411   -0.6798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5214    0.0961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0532   -0.5346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3335    0.2414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1456    0.3866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6774   -0.2441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0373    0.4982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5020   -0.2709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7313   -1.0634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0484   -1.5264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3971   -1.0201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1995   -1.8210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5850   -1.1653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3047   -1.9412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4926   -2.0864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9608   -1.4557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1486   -1.6009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2654   -2.4176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5369   -2.1544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0083    0.3804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8256    0.2675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6974    1.1446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2038    1.7959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8929    2.5601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0757    2.6729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3993    3.2114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0884    3.9756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2165    3.0986    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
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  8  7  1  4  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 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
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 21 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 18 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
 16 31  1  0  0  0  0
 31 32  1  0  0  0  0
 13 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 23 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
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
M  END

     RDKit          3D

109113  0  0  0  0  0  0  0  0999 V2000
   -8.4422    1.3946   -0.2386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9907    0.3604   -0.8257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3584   -0.3227   -1.9888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9151    0.0303   -2.2085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0630   -0.4390   -1.0565 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.2486   -1.9706   -1.0390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6186   -0.0646   -1.2052 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.4281    1.4237   -1.4024 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0553    1.8377    0.0045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0438    0.7608    0.4348 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1337    0.8305    1.9475 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7323    1.1763   -0.1110 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0090    2.2055    0.7054 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0802    1.7191    1.7459 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6870    0.4835    1.4213 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1940    0.6754    1.5868 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5883    0.4055    3.0471 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.9752   -0.3280    0.7660 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2843   -0.3876    1.2819 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4248   -0.1119    0.4854 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1621    0.1857   -0.7012 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7498   -0.1835    1.0448 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8732    0.0394    0.4338 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0555    0.4086   -0.9391 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1976    0.6309   -1.5436 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5039    0.5235   -0.8484 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3061   -0.5480   -1.5547 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6479   -0.7002   -0.9099 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4898   -1.1080    0.5245 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8737   -1.2793    1.1630 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2619   -1.6598    0.8781 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9885   -1.5453    0.1065 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4376   -0.1118    0.0954 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4922    0.6144   -1.1718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8065    0.1026   -0.5602 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5345   -0.8550   -1.4680 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6125   -1.4675   -0.6293 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6650   -0.4842   -0.1503 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3203   -1.2731    1.0006 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2738   -0.1859   -0.3615 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3542   -0.0872   -1.4355 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7778    0.6113    0.8131 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4957    1.8534   -0.5308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9802    1.8386    0.6215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6229   -1.3745   -2.0560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9042    0.1472   -2.8889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6268   -0.4719   -3.1645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9148    1.1473   -2.3407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5213   -0.1163   -0.1291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3124   -2.4466   -1.3318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9827   -2.3029   -1.8145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5368   -2.3409   -0.0391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2699   -0.5354   -2.1726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6421    1.6720   -2.1379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3065    1.9894   -1.6769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5310    2.8159   -0.0057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9070    1.9041    0.6742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0770    1.9304    2.2302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1863    0.5940    2.2192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4087    0.2335    2.4846 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9527    1.7204   -1.0891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7163    2.9370    1.1618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4062    2.8679    0.0047 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6902    2.5355    1.9150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5254    1.6462    2.7838 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6228    0.0109    3.0841 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8838   -0.3381    3.4616 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4775    1.3351    3.6609 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7307    1.9560    0.8793 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7977    2.6849    2.1882 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1285    2.5762    0.4749 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0622   -0.0330   -0.3100 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8176   -0.4608    2.1210 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8022   -0.0674    1.0305 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1470    0.5216   -1.5673 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2040    0.9139   -2.6261 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4446    0.4203    0.2290 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0120    1.5357   -1.0133 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7500   -1.5047   -1.3790 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.3745   -0.3198   -2.6373 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.2406   -1.4431   -1.4941 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.2243    0.2714   -0.9105 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.9946   -0.3475    1.1578 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.9080   -2.0543    0.6127 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.4897   -1.8544    0.4654 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.2730   -0.2515    1.3587 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.7272   -1.7623    2.1487 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1515   -1.8832    1.9394 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.6926    1.6792   -1.2128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9337   -0.3027   -2.3307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8880   -1.6540   -1.8269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0930   -1.8772    0.2856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0621   -2.3198   -1.1123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2695   -0.8615    1.3186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3201   -2.3633    0.7534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5378   -1.2452    1.8250 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2062   -1.2728   -0.1284 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.2453   -0.5849   -1.0233 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5794    0.9882   -1.5693 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0206   -0.5112   -2.3999 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0940    0.5685    1.6946 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9669    1.6468    0.4639 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.7738    0.1673    1.0697 H   0  0  0  0  0  0  0  0  0  0  0  0
 31 30  1  0
 30 29  1  0
 29 28  1  0
 28 27  1  0
 27 26  1  0
 26 25  2  0
 25 24  1  0
 24 23  2  0
 23 21  1  0
 21 22  2  0
 21 20  1  0
 20 19  1  0
 19 32  1  0
 32 33  1  0
 34 33  1  6
 34 35  1  0
 36 35  1  6
 36 37  1  0
 37 38  1  0
 38 39  1  0
 39 40  1  1
 39  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  1
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 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
  7  5  1  0
  5  6  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
  2 41  1  0
 41 42  1  0
 41 43  1  0
 16 19  1  0
 36 34  1  0
 12 36  1  0
 15 34  1  0
 10 39  1  0
 31 87  1  0
 31 88  1  0
 31 89  1  0
 30 85  1  0
 30 86  1  0
 29 83  1  0
 29 84  1  0
 28 81  1  0
 28 82  1  0
 27 79  1  0
 27 80  1  0
 26 78  1  0
 25 77  1  0
 24 76  1  0
 23 75  1  0
 19 74  1  6
 32 90  1  0
 32 91  1  0
 33 92  1  0
 33 93  1  0
 35 94  1  0
 35 95  1  0
 37 96  1  0
 37 97  1  0
 38 98  1  0
 38 99  1  0
 40100  1  0
 40101  1  0
 40102  1  0
  7 54  1  6
  8 55  1  0
  8 56  1  0
  9 57  1  0
  9 58  1  0
 11 59  1  0
 11 60  1  0
 11 61  1  0
 12 62  1  6
 13 63  1  0
 13 64  1  0
 14 65  1  0
 14 66  1  0
 15 67  1  1
 17 68  1  0
 17 69  1  0
 17 70  1  0
 18 71  1  0
 18 72  1  0
 18 73  1  0
  5 50  1  1
  6 51  1  0
  6 52  1  0
  6 53  1  0
  4 48  1  0
  4 49  1  0
  3 46  1  0
  3 47  1  0
  1 44  1  0
  1 45  1  0
 41103  1  0
 42104  1  0
 42105  1  0
 42106  1  0
 43107  1  0
 43108  1  0
 43109  1  0
M  END


  Mrv1533004251508262D          

 43 47  0  0  0  0            999 V2000
    1.0623   -8.1486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5305   -7.5179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8108   -6.7420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2790   -6.1112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5593   -5.3353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0274   -4.7046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3077   -3.9287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2241   -3.2980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0562   -2.5221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4756   -1.8914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2877   -2.0366    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1953   -1.1154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6168   -0.9702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8971   -0.1943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7092   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2411   -0.6798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5214    0.0961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0532   -0.5346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3335    0.2414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1456    0.3866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6774   -0.2441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0373    0.4982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5020   -0.2709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7313   -1.0634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0484   -1.5264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3971   -1.0201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1995   -1.8210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5850   -1.1653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3047   -1.9412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4926   -2.0864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9608   -1.4557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1486   -1.6009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2654   -2.4176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5369   -2.1544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0083    0.3804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8256    0.2675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6974    1.1446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2038    1.7959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8929    2.5601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0757    2.6729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3993    3.2114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0884    3.9756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2165    3.0986    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
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  8  7  1  4  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 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
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 21 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 18 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
 16 31  1  0  0  0  0
 31 32  1  0  0  0  0
 13 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 23 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
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0177583

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCC=CC=CC(=O)OC1CCC23CC22CCC4(C)C(CCC4(C)C2CCC3C1(C)C)C(C)CCC(=C)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C41H66O2/c1-10-11-12-13-14-15-16-17-36(42)43-35-23-25-40-28-41(40)27-26-38(8)32(31(5)19-18-30(4)29(2)3)22-24-39(38,9)34(41)21-20-33(40)37(35,6)7/h14-17,29,31-35H,4,10-13,18-28H2,1-3,5-9H3

> <INCHI_KEY>
KJCDIXARAHBDPC-UHFFFAOYSA-N

> <FORMULA>
C41H66O2

> <MOLECULAR_WEIGHT>
590.977

> <EXACT_MASS>
590.506281365

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
109

> <JCHEM_AVERAGE_POLARIZABILITY>
76.07603577354105

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
7,7,12,16-tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl deca-2,4-dienoate

> <ALOGPS_LOGP>
9.88

> <JCHEM_LOGP>
12.01549222466667

> <ALOGPS_LOGS>
-7.59

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.81468049296766

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
183.70460000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.53e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7,7,12,16-tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl deca-2,4-dienoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0       1.983 -15.211   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.990 -14.033   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.513 -12.585   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.521 -11.408   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.044  -9.959   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.051  -8.782   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.574  -7.334   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.418  -6.156   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.105  -4.708   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.888  -3.531   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -2.404  -3.802   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0      -0.365  -2.082   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       1.151  -1.811   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.675  -0.363   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.191  -0.092   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.183  -1.269   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.707   0.179   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.699  -0.998   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.222   0.451   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.738   0.722   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.731  -0.456   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.403   0.930   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.270  -0.506   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.698  -1.985   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.424  -2.849   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.208  -1.904   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.839  -3.399   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.692  -2.175   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.169  -3.624   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.653  -3.895   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.660  -2.717   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.144  -2.988   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.362  -4.513   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       1.002  -4.022   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      11.216   0.710   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      12.741   0.499   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      10.635   2.137   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      11.580   3.352   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      11.000   4.779   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       9.475   4.989   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      11.945   5.995   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      11.365   7.421   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      13.471   5.784   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   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   32                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18   31                                             
CONECT   17   16   18                                                       
CONECT   18   17   16   19   28                                             
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23   26                                             
CONECT   22   21                                                            
CONECT   23   21   24   35                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   21   27   28                                             
CONECT   27   26                                                            
CONECT   28   26   18   29                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   16   32                                                  
CONECT   32   31   13   33   34                                             
CONECT   33   32                                                            
CONECT   34   32                                                            
CONECT   35   23   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   94    0
END

View in JSmol

Synonyms

Value	Source
7,7,12,16-Tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.0,.0,.0,]octadecan-6-yl deca-2,4-dienoic acid	Generator
7,7,12,16-Tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl deca-2,4-dienoic acid	Generator

Chemical Formula

C₄₁H₆₆O₂

Average Mass

590.9770 Da

Monoisotopic Mass

590.50628 Da

IUPAC Name

7,7,12,16-tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl deca-2,4-dienoate

Traditional Name

7,7,12,16-tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl deca-2,4-dienoate

CAS Registry Number

Not Available

SMILES

CCCCCC=CC=CC(=O)OC1CCC23CC22CCC4(C)C(CCC4(C)C2CCC3C1(C)C)C(C)CCC(=C)C(C)C

InChI Identifier

InChI=1S/C41H66O2/c1-10-11-12-13-14-15-16-17-36(42)43-35-23-25-40-28-41(40)27-26-38(8)32(31(5)19-18-30(4)29(2)3)22-24-39(38,9)34(41)21-20-33(40)37(35,6)7/h14-17,29,31-35H,4,10-13,18-28H2,1-3,5-9H3

InChI Key

KJCDIXARAHBDPC-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
Euphorbia retusa	LOTUS Database	35616633

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Cycloartanols and derivatives

Direct Parent

Cycloartanols and derivatives

Alternative Parents

Substituents

Cycloartanol-skeleton
9b,19-cyclo-lanostane-skeleton
Cycloartane-skeleton
Triterpenoid
Steroid ester
Fatty acid ester
Fatty acyl
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organooxygen compound
Carbonyl group
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	9.88	ALOGPS
logP	12.02	ChemAxon
logS	-7.6	ALOGPS
pKa (Strongest Basic)	-6.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	26.3 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	183.7 m³·mol⁻¹	ChemAxon
Polarizability	76.08 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

74959366

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7,7,12,16-tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl deca-2,4-dienoate (NP0177583)

MOL for NP0177583 (7,7,12,16-tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl deca-2,4-dienoate)

3D MOL for NP0177583 (7,7,12,16-tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl deca-2,4-dienoate)

3D SDF for NP0177583 (7,7,12,16-tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl deca-2,4-dienoate)

3D-SDF for NP0177583 (7,7,12,16-tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl deca-2,4-dienoate)

PDB for NP0177583 (7,7,12,16-tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl deca-2,4-dienoate)

3D PDB for NP0177583 (7,7,12,16-tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl deca-2,4-dienoate)

SMILES for NP0177583 (7,7,12,16-tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl deca-2,4-dienoate)

INCHI for NP0177583 (7,7,12,16-tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl deca-2,4-dienoate)

Structure for NP0177583 (7,7,12,16-tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl deca-2,4-dienoate)

3D Structure for NP0177583 (7,7,12,16-tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl deca-2,4-dienoate)