NP-MRD: Showing NP-Card for (1r,3s,4as,6as,6br,8ar,12ar,14bs)-1-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicen-3-yl hexadecanoate (NP0181768)

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Record Information

Version

2.0

Created at

2022-09-03 20:20:52 UTC

Updated at

2022-09-03 20:20:53 UTC

NP-MRD ID

NP0181768

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3s,4as,6as,6br,8ar,12ar,14bs)-1-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicen-3-yl hexadecanoate

Description

Ussuriensin B belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Based on a literature review very few articles have been published on Ussuriensin B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032222202D          

 49 53  0  0  1  0            999 V2000
    4.2868  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039  -16.0875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184  -14.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328  -15.2625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   17.1473  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -15.2625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.5762  -14.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -16.0875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   18.5762  -15.6750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -16.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907  -16.0875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -16.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -17.3250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197  -17.7375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   21.4341  -17.3250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486  -17.7375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.4308  -16.9623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.9611  -17.8808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197  -18.5625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   20.7197  -19.3875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907  -17.7375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   18.5762  -18.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -17.3250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.0913  -17.9924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -17.7375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473  -17.3250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473  -16.5000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   16.4328  -16.0875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.9956  -16.7871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6083  -16.1163    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  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  2  0  0  0  0
 16 18  1  0  0  0  0
 19 18  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 29 28  1  6  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 31 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 29 36  1  0  0  0  0
 36 37  1  1  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 28 40  1  0  0  0  0
 40 41  1  6  0  0  0
 40 42  1  0  0  0  0
 25 42  1  0  0  0  0
 42 43  1  1  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 46 45  1  1  0  0  0
 23 46  1  0  0  0  0
 46 47  1  0  0  0  0
 19 47  1  0  0  0  0
 47 48  1  0  0  0  0
 47 49  1  0  0  0  0
M  END

     RDKit          3D

127131  0  0  0  0  0  0  0  0999 V2000
   15.4627   -0.8523    0.5042 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4147   -0.1320    1.3021 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7018    0.9265    0.5317 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0013    0.3773   -0.6834 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9995   -0.6450   -0.2715 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2448   -1.2341   -1.4460 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4696   -0.2337   -2.2294 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4562    0.4649   -1.3820 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4938   -0.5392   -0.8117 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4357    0.1166    0.0500 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5835    1.1087   -0.6683 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8252    0.5183   -1.8213 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9242   -0.5984   -1.4053 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9262   -0.1231   -0.4019 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0251    0.9729   -0.9175 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0556    1.4048    0.1259 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4910    1.8571    1.1847 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7058    1.3614    0.0603 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2304    1.7406    0.9844 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2266    2.7930    0.6942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5108    2.3781    0.0596 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5698    3.0269   -1.2010 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7278    0.8953   -0.1241 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0581    0.4737   -1.4022 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1971    0.6096   -0.2395 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0105    1.5858   -0.5672 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4512    1.4508   -0.7025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0332    0.2937   -0.4705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5269    0.2379   -0.6605 C   0  0  2  0  0  0  0  0  0  0  0  0
   -9.3490    0.7939    0.4166 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5160    0.0672    0.9380 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6363    1.1030    1.2465 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3211   -0.6544    2.2524 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1195   -0.8209   -0.1144 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0242   -1.7752   -0.5491 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9591   -1.0490   -1.2992 C   0  0  1  0  0  0  0  0  0  0  0  0
   -9.5611   -0.8348   -2.7055 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7220   -1.8683   -1.5522 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9351   -2.0676   -0.3060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2376   -0.8144    0.0757 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4681   -0.7383    1.6270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7617   -0.7593   -0.1187 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3109   -1.6205   -1.2953 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0937   -1.3645    1.1078 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5862   -1.2373    1.0816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2415    0.2498    1.1141 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8622    0.4797    1.5612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0081   -0.7413    1.3411 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9042    0.5714    3.1061 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0676   -0.2050   -0.1510 H   0  0  0  0  0  0  0  0  0  0  0  0
   16.1870   -1.3042    1.2445 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.0424   -1.7469   -0.0277 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.9713    0.3984    2.1252 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.7054   -0.8479    1.7206 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.3905    1.7330    0.1926 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.9173    1.3869    1.1832 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.4873    1.2271   -1.1815 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.7964   -0.0553   -1.3327 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.3021   -0.2300    0.4657 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.5375   -1.4994    0.2229 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.9638   -1.7395   -2.1531 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.5796   -2.0353   -1.0965 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1061    0.5385   -2.7138 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0038   -0.7841   -3.0844 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8939    1.0244   -0.5432 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8312    1.1768   -1.9885 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0907   -1.1322   -1.6351 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0798   -1.1946   -0.1077 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.9873    0.6524    0.8564 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1641    1.9728   -1.0571 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8752    1.5393    0.0632 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2628    1.3271   -2.3227 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5064    0.1149   -2.6095 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4960   -1.4312   -0.9004 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3445   -1.0176   -2.2715 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2826   -1.0203   -0.1369 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4488    0.1825    0.5154 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6290    1.8347   -1.2707 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4387    0.5723   -1.7696 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3855    2.1319    1.8259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8348    3.6643    0.1237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5213    3.3269    1.6584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3373    2.7913    0.7164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6678    3.2778   -1.4320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8440    0.3682   -2.1752 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.6732    2.6067   -0.7685 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -8.6754    0.9812   -1.5255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6824    1.0428    1.3030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7255    1.8565    0.1727 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5107    1.4873    2.2873 H   0  0  0  0  0  0  0  0  0  0  0  0
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  -12.6219    0.6447    1.1810 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -9.8036   -1.6044    2.1691 H   0  0  0  0  0  0  0  0  0  0  0  0
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  -11.3913   -0.1962   -0.9900 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.9784   -1.4122    0.2630 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5422   -2.4985   -1.2501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7269   -2.3663    0.3065 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1489   -1.7241   -2.9642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7327   -0.6476   -3.4217 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2132    0.0673   -2.6324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1642   -1.2489   -2.3216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9483   -2.8161   -2.0888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7274   -2.2524    0.4963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3592   -3.0044   -0.2489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2092    0.2159    2.0333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5549   -0.9214    1.7332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0219   -1.6441    2.1134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7360   -2.6378   -1.2904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6672   -1.1739   -2.2669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2251   -1.8265   -1.2945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3501   -2.3977    1.3022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3652   -0.6453    1.9430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2681   -1.6248    2.0887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0555   -1.8122    0.3462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9471    0.6417    1.9150 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0359   -0.4182    1.6566 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0875   -1.0963    0.3281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2542   -1.5336    2.0838 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0964    0.3665    3.5331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7077   -0.0492    3.5094 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1038    1.6658    3.3052 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  1  0
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  6  7  1  0
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 11 12  1  0
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 16 18  1  0
 18 19  1  0
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 21 23  1  0
 23 24  1  6
 23 46  1  0
 46 45  1  0
 45 44  1  0
 44 42  1  0
 42 43  1  6
 42 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  2  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 31 33  1  0
 31 34  1  0
 34 35  1  0
 35 36  1  0
 36 37  1  6
 36 38  1  0
 38 39  1  0
 39 40  1  0
 40 41  1  1
 46 47  1  0
 47 48  1  0
 47 49  1  0
 47 19  1  0
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 40 28  1  0
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  1 50  1  0
  1 51  1  0
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  2 54  1  0
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  3 56  1  0
  4 57  1  0
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 19 81  1  1
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 21 84  1  1
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 24 86  1  0
 24 87  1  0
 24 88  1  0
 46121  1  1
 45119  1  0
 45120  1  0
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 44118  1  0
 43114  1  0
 43115  1  0
 43116  1  0
 26 89  1  0
 27 90  1  0
 29 91  1  6
 30 92  1  0
 30 93  1  0
 32 94  1  0
 32 95  1  0
 32 96  1  0
 33 97  1  0
 33 98  1  0
 33 99  1  0
 34100  1  0
 34101  1  0
 35102  1  0
 35103  1  0
 37104  1  0
 37105  1  0
 37106  1  0
 38107  1  0
 38108  1  0
 39109  1  0
 39110  1  0
 41111  1  0
 41112  1  0
 41113  1  0
 48122  1  0
 48123  1  0
 48124  1  0
 49125  1  0
 49126  1  0
 49127  1  0
M  END


  Mrv1652309032222202D          

 49 53  0  0  1  0            999 V2000
    4.2868  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039  -16.0875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184  -14.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328  -15.2625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   17.1473  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -15.2625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.5762  -14.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -16.0875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   18.5762  -15.6750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -16.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907  -16.0875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -16.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -17.3250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197  -17.7375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   21.4341  -17.3250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486  -17.7375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.4308  -16.9623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.9611  -17.8808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197  -18.5625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   20.7197  -19.3875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907  -17.7375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   18.5762  -18.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -17.3250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.0913  -17.9924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -17.7375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473  -17.3250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473  -16.5000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   16.4328  -16.0875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.9956  -16.7871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6083  -16.1163    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  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  2  0  0  0  0
 16 18  1  0  0  0  0
 19 18  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 29 28  1  6  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 31 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 29 36  1  0  0  0  0
 36 37  1  1  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 28 40  1  0  0  0  0
 40 41  1  6  0  0  0
 40 42  1  0  0  0  0
 25 42  1  0  0  0  0
 42 43  1  1  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 46 45  1  1  0  0  0
 23 46  1  0  0  0  0
 46 47  1  0  0  0  0
 19 47  1  0  0  0  0
 47 48  1  0  0  0  0
 47 49  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0181768

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCC(=O)O[C@H]1C[C@@H](O)[C@@]2(C)[C@@H](CC[C@]3(C)C2=CC=C2[C@@H]4CC(C)(C)CC[C@]4(C)CC[C@@]32C)C1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C46H78O3/c1-10-11-12-13-14-15-16-17-18-19-20-21-22-23-40(48)49-39-32-38(47)46(9)36(42(39,4)5)26-27-45(8)37(46)25-24-34-35-33-41(2,3)28-29-43(35,6)30-31-44(34,45)7/h24-25,35-36,38-39,47H,10-23,26-33H2,1-9H3/t35-,36-,38+,39-,43+,44+,45+,46-/m0/s1

> <INCHI_KEY>
XUYKACVIVNMPKZ-YXRUNKGDSA-N

> <FORMULA>
C46H78O3

> <MOLECULAR_WEIGHT>
679.127

> <EXACT_MASS>
678.595096372

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
127

> <JCHEM_AVERAGE_POLARIZABILITY>
88.37381813015315

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,3S,4aS,6aS,6bR,8aR,12aR,14bS)-1-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14b-octadecahydropicen-3-yl hexadecanoate

> <JCHEM_LOGP>
12.615010182333332

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.552110285003092

> <JCHEM_PKA_STRONGEST_BASIC>
-2.994706961339647

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
207.82060000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,3S,4aS,6aS,6bR,8aR,12aR,14bS)-1-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicen-3-yl hexadecanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       8.002 -27.720   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.336 -28.490   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.669 -27.720   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.003 -28.490   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.337 -27.720   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      14.670 -28.490   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      16.004 -27.720   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      17.338 -28.490   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      18.672 -27.720   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      20.005 -28.490   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      21.339 -27.720   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      22.673 -28.490   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      24.006 -27.720   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      25.340 -28.490   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      26.674 -27.720   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      28.007 -28.490   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      28.007 -30.030   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      29.341 -27.720   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      30.675 -28.490   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      32.008 -27.720   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      33.342 -28.490   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      34.676 -27.720   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      33.342 -30.030   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      34.676 -29.260   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      34.676 -30.800   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      36.009 -30.030   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      37.343 -30.800   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      37.343 -32.340   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      38.677 -33.110   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      40.010 -32.340   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      41.344 -33.110   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      41.871 -31.663   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      42.861 -33.377   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      41.344 -34.650   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      40.010 -35.420   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      38.677 -34.650   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      38.677 -36.190   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      37.343 -35.420   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      36.009 -34.650   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      36.009 -33.110   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      34.676 -33.880   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      34.676 -32.340   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      33.770 -33.586   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      33.342 -33.110   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      32.008 -32.340   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      32.008 -30.800   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      30.675 -30.030   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      29.859 -31.336   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      29.136 -30.084   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                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   47                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25   46                                             
CONECT   24   23                                                            
CONECT   25   23   26   42                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   40                                                  
CONECT   29   28   30   36                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33   34                                             
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   31   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   29   37   38                                             
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   28   41   42                                             
CONECT   41   40                                                            
CONECT   42   40   25   43   44                                             
CONECT   43   42                                                            
CONECT   44   42   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   23   47                                                  
CONECT   47   46   19   48   49                                             
CONECT   48   47                                                            
CONECT   49   47                                                            
MASTER        0    0    0    0    0    0    0    0   49    0  106    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₆H₇₈O₃

Average Mass

679.1270 Da

Monoisotopic Mass

678.59510 Da

IUPAC Name

(1R,3S,4aS,6aS,6bR,8aR,12aR,14bS)-1-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14b-octadecahydropicen-3-yl hexadecanoate

Traditional Name

(1R,3S,4aS,6aS,6bR,8aR,12aR,14bS)-1-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicen-3-yl hexadecanoate

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCC(=O)O[C@H]1C[C@@H](O)[C@@]2(C)[C@@H](CC[C@]3(C)C2=CC=C2[C@@H]4CC(C)(C)CC[C@]4(C)CC[C@@]32C)C1(C)C

InChI Identifier

InChI=1S/C46H78O3/c1-10-11-12-13-14-15-16-17-18-19-20-21-22-23-40(48)49-39-32-38(47)46(9)36(42(39,4)5)26-27-45(8)37(46)25-24-34-35-33-41(2,3)28-29-43(35,6)30-31-44(34,45)7/h24-25,35-36,38-39,47H,10-23,26-33H2,1-9H3/t35-,36-,38+,39-,43+,44+,45+,46-/m0/s1

InChI Key

XUYKACVIVNMPKZ-YXRUNKGDSA-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

Not Available

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
Fatty acid ester
Fatty acyl
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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	12.62	ChemAxon
pKa (Strongest Acidic)	14.55	ChemAxon
pKa (Strongest Basic)	-3	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	16	ChemAxon
Refractivity	207.82 m³·mol⁻¹	ChemAxon
Polarizability	88.37 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

101855164

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,3s,4as,6as,6br,8ar,12ar,14bs)-1-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicen-3-yl hexadecanoate (NP0181768)

MOL for NP0181768 ((1r,3s,4as,6as,6br,8ar,12ar,14bs)-1-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicen-3-yl hexadecanoate)

3D MOL for NP0181768 ((1r,3s,4as,6as,6br,8ar,12ar,14bs)-1-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicen-3-yl hexadecanoate)

3D SDF for NP0181768 ((1r,3s,4as,6as,6br,8ar,12ar,14bs)-1-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicen-3-yl hexadecanoate)

3D-SDF for NP0181768 ((1r,3s,4as,6as,6br,8ar,12ar,14bs)-1-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicen-3-yl hexadecanoate)

PDB for NP0181768 ((1r,3s,4as,6as,6br,8ar,12ar,14bs)-1-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicen-3-yl hexadecanoate)

3D PDB for NP0181768 ((1r,3s,4as,6as,6br,8ar,12ar,14bs)-1-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicen-3-yl hexadecanoate)

SMILES for NP0181768 ((1r,3s,4as,6as,6br,8ar,12ar,14bs)-1-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicen-3-yl hexadecanoate)

INCHI for NP0181768 ((1r,3s,4as,6as,6br,8ar,12ar,14bs)-1-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicen-3-yl hexadecanoate)

Structure for NP0181768 ((1r,3s,4as,6as,6br,8ar,12ar,14bs)-1-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicen-3-yl hexadecanoate)

3D Structure for NP0181768 ((1r,3s,4as,6as,6br,8ar,12ar,14bs)-1-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicen-3-yl hexadecanoate)