NP-MRD: Showing NP-Card for (1r,3as,3bs,7s,9ar,9bs,11ar)-1-[(2r,5r)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl dodecanoate (NP0270917)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-08 17:01:49 UTC

Updated at

2022-09-08 17:01:49 UTC

NP-MRD ID

NP0270917

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3as,3bs,7s,9ar,9bs,11ar)-1-[(2r,5r)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl dodecanoate

Description

SCHEMBL4782193 belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. (1r,3as,3bs,7s,9ar,9bs,11ar)-1-[(2r,5r)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl dodecanoate is found in Serenoa repens. Based on a literature review very few articles have been published on SCHEMBL4782193.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082219012D          

 43 46  0  0  1  0            999 V2000
   -7.8592   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -8.2500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -9.0750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5724   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -9.4875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579  -10.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724  -10.3125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5724   -9.4875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2868   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -9.4875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013  -10.3125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7550   -9.9769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868  -10.7250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4584  -11.5320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2788  -11.6182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6144  -10.8645    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4214  -10.6930    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.9734  -11.3061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6763   -9.9084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4833   -9.7369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7382   -8.9522    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.5452   -8.7807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8001   -7.9961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1862   -8.3391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3792   -8.5107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4411   -7.5545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -9.0750    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
 15 14  1  1  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  1  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 23 22  1  6  0  0  0
 23 24  1  0  0  0  0
 18 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 23 29  1  0  0  0  0
 29 30  1  1  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 27 32  1  0  0  0  0
 32 33  1  1  0  0  0
 33 34  1  1  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 37 36  1  6  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 37 40  1  0  0  0  0
 40 41  1  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
M  END

     RDKit          3D

115118  0  0  0  0  0  0  0  0999 V2000
   13.0225    1.7123   -0.8605 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4873    0.3504   -0.4279 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1984    0.1058    1.0416 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6937    0.2024    1.3113 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9337   -0.8114    0.5132 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4683   -0.7013    0.8121 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9439    0.6481    0.4606 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4578    0.7800    0.7409 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6423   -0.2055   -0.0266 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8048   -0.0591   -1.5275 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9301   -1.1132   -2.2199 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5090   -0.9097   -1.8517 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8530   -0.0602   -2.5257 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8619   -1.5857   -0.8259 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5205   -1.3004   -0.5828 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5963   -2.4833   -0.6243 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1658   -2.0298   -0.6726 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1908   -1.0602    0.4467 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5146   -1.9264    1.6623 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9060   -0.1347    0.7500 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6982    1.1397    0.9790 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6159    1.8127    0.9672 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7764    0.8178    0.9712 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3663   -0.2732   -0.0164 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5059   -1.1960   -0.3435 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6823   -0.4323   -0.9434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1204    0.5780    0.0581 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.6329   -0.0262    1.3135 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9412    1.5071    0.3966 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6538    2.5094    1.2343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0530    2.6227    0.5963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0035    1.6609   -0.5348 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.2309    1.2379   -1.1852 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.9404    2.4991   -1.7111 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2004    0.4245   -0.3466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3642    0.1025   -1.2106 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4777   -0.6838   -0.6339 C   0  0  1  0  0  0  0  0  0  0  0  0
   -9.1847   -2.0304   -0.1127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2359   -2.2502    0.9688 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5075    0.1244    0.1194 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0200    0.9009    1.2824 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6771   -0.7574    0.5033 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3132   -0.6519    0.7973 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6622    2.0292   -1.7176 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.0879    2.4467   -0.0294 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.9845    1.6619   -1.2764 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.5928    0.3190   -0.5528 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.0695   -0.4125   -1.0847 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.6955    0.8623    1.6527 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.5461   -0.8896    1.3336 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4066    1.2444    1.0601 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.5581    0.0583    2.3956 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.3029   -1.8326    0.7540 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1138   -0.6557   -0.5741 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9537   -1.5279    0.2743 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3370   -0.9435    1.8959 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4307    1.3981    1.1508 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1979    0.9701   -0.5650 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1532    1.7917    0.4645 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3115    0.5649    1.8207 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7765   -1.2567    0.2941 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5641    0.0311    0.1923 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8271   -0.1976   -1.8770 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4499    0.9326   -1.8716 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2519   -2.1233   -1.9048 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0536   -0.9986   -3.3166 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1224   -0.5233   -1.2989 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7588   -3.1921    0.1974 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7901   -3.0062   -1.5957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0576   -1.5351   -1.6427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4776   -2.9271   -0.5851 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3144   -1.5040    2.2740 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4503   -2.0060    2.2309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7519   -2.9787    1.3534 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5576    1.7937    1.2031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6551    2.4241    0.0252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6856    2.5099    1.8251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8462    0.4442    1.9906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0842    0.2480   -0.9469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8151   -1.8273    0.4899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1455   -1.8710   -1.1526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4982   -1.1408   -1.1208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3419    0.0815   -1.8563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8108    0.0334    2.0906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7895   -1.1191    1.1935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4626    0.5217    1.7504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6181    2.0078   -0.5510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7371    2.2325    2.3019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1490    3.4895    1.1320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8351    2.4781    1.3345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1967    3.6494    0.1653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3310    2.1464   -1.3118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9868    0.6422   -2.0856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4862    2.2118   -2.6101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0997    3.1633   -2.0719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5266    2.9923   -0.9288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4301    1.0229    0.5387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6845   -0.5039   -0.1067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9621   -0.4136   -2.1297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8224    1.0493   -1.6193 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0848   -0.9439   -1.5906 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1839   -2.5074    0.1289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8398   -2.6642   -0.9913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9748   -1.4540    1.6511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6419   -3.0711    1.6406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2504   -2.7054    0.6425 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9520    0.8806   -0.5955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6149    1.8879    0.9416 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9409    1.2145    1.8686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4037    0.3932    2.0172 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.4925   -1.3234    1.4349 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.9727   -1.3843   -0.3530 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.5294   -0.0786    0.7181 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0450    0.1285    0.9973 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3215   -1.4922    1.5232 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
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  1
 18 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  1
 27 32  1  0
 32 31  1  0
 31 30  1  0
 30 29  1  0
 29 23  1  0
 23 22  1  0
 22 21  1  0
 21 20  2  0
 20 43  1  0
 32 33  1  0
 33 34  1  0
 33 35  1  0
 35 36  1  0
 36 37  1  0
 37 38  1  0
 38 39  1  0
 37 40  1  0
 40 41  1  0
 40 42  1  0
 43 15  1  0
 20 18  1  0
 23 24  1  0
 29 27  1  0
  1 44  1  0
  1 45  1  0
  1 46  1  0
  2 47  1  0
  2 48  1  0
  3 49  1  0
  3 50  1  0
  4 51  1  0
  4 52  1  0
  5 53  1  0
  5 54  1  0
  6 55  1  0
  6 56  1  0
  7 57  1  0
  7 58  1  0
  8 59  1  0
  8 60  1  0
  9 61  1  0
  9 62  1  0
 10 63  1  0
 10 64  1  0
 11 65  1  0
 11 66  1  0
 15 67  1  6
 16 68  1  0
 16 69  1  0
 17 70  1  0
 17 71  1  0
 19 72  1  0
 19 73  1  0
 19 74  1  0
 24 79  1  6
 25 80  1  0
 25 81  1  0
 26 82  1  0
 26 83  1  0
 28 84  1  0
 28 85  1  0
 28 86  1  0
 32 92  1  6
 31 90  1  0
 31 91  1  0
 30 88  1  0
 30 89  1  0
 29 87  1  6
 23 78  1  1
 22 76  1  0
 22 77  1  0
 21 75  1  0
 43114  1  0
 43115  1  0
 33 93  1  6
 34 94  1  0
 34 95  1  0
 34 96  1  0
 35 97  1  0
 35 98  1  0
 36 99  1  0
 36100  1  0
 37101  1  6
 38102  1  0
 38103  1  0
 39104  1  0
 39105  1  0
 39106  1  0
 40107  1  0
 41108  1  0
 41109  1  0
 41110  1  0
 42111  1  0
 42112  1  0
 42113  1  0
M  END


  Mrv1652309082219012D          

 43 46  0  0  1  0            999 V2000
   -7.8592   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -8.2500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -9.0750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5724   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -9.4875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579  -10.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724  -10.3125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5724   -9.4875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2868   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -9.4875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013  -10.3125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7550   -9.9769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868  -10.7250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4584  -11.5320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2788  -11.6182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6144  -10.8645    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4214  -10.6930    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.9734  -11.3061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6763   -9.9084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4833   -9.7369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7382   -8.9522    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.5452   -8.7807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8001   -7.9961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1862   -8.3391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3792   -8.5107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4411   -7.5545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -9.0750    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
 15 14  1  1  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  1  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 23 22  1  6  0  0  0
 23 24  1  0  0  0  0
 18 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 23 29  1  0  0  0  0
 29 30  1  1  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 27 32  1  0  0  0  0
 32 33  1  1  0  0  0
 33 34  1  1  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 37 36  1  6  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 37 40  1  0  0  0  0
 40 41  1  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
M  END
> <DATABASE_ID>
NP0270917

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCC(=O)O[C@H]1CC[C@]2(C)[C@H]3CC[C@]4(C)[C@H](CC[C@H]4[C@@H]3CC=C2C1)[C@H](C)CC[C@@H](CC)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C41H72O2/c1-8-10-11-12-13-14-15-16-17-18-39(42)43-34-25-27-40(6)33(29-34)21-22-35-37-24-23-36(41(37,7)28-26-38(35)40)31(5)19-20-32(9-2)30(3)4/h21,30-32,34-38H,8-20,22-29H2,1-7H3/t31-,32-,34+,35+,36-,37+,38+,40+,41-/m1/s1

> <INCHI_KEY>
ZKAAVBQKARRBFN-CIKJAVNGSA-N

> <FORMULA>
C41H72O2

> <MOLECULAR_WEIGHT>
597.025

> <EXACT_MASS>
596.553231558

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
115

> <JCHEM_AVERAGE_POLARIZABILITY>
80.15776244069126

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,5S,10S,11S,14R,15R)-14-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-5-yl dodecanoate

> <JCHEM_LOGP>
12.987256034333337

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-7.0421985486871135

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
184.95350000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
18

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,5S,10S,11S,14R,15R)-14-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-5-yl dodecanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0     -14.670 -14.630   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -13.337 -15.400   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -12.003 -14.630   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -10.669 -15.400   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -9.336 -14.630   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -8.002 -15.400   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -6.668 -14.630   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.335 -15.400   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.001 -14.630   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.667 -15.400   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.334 -14.630   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000 -15.400   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       0.000 -16.940   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       1.334 -14.630   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.667 -15.400   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.001 -14.630   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.335 -15.400   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.335 -16.940   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.668 -16.170   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.001 -17.710   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.001 -19.250   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.335 -20.020   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.668 -19.250   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.668 -17.710   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.002 -16.940   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.336 -17.710   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.336 -19.250   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.743 -18.624   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.002 -20.020   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.322 -21.526   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.854 -21.687   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      10.480 -20.280   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      11.987 -19.960   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      13.017 -21.105   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      12.462 -18.496   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      13.969 -18.175   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      14.445 -16.711   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      15.951 -16.391   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      16.427 -14.926   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      13.414 -15.566   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      11.908 -15.887   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      13.890 -14.102   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       2.667 -16.940   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   24                                             
CONECT   19   18                                                            
CONECT   20   18   21   43                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   29                                                  
CONECT   24   23   18   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29   32                                             
CONECT   28   27                                                            
CONECT   29   27   23   30                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   27   33                                                  
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38   40                                                  
CONECT   38   37   39                                                       
CONECT   39   38                                                            
CONECT   40   37   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40                                                            
CONECT   43   20   15                                                       
MASTER        0    0    0    0    0    0    0    0   43    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₁H₇₂O₂

Average Mass

597.0250 Da

Monoisotopic Mass

596.55323 Da

IUPAC Name

(1S,2R,5S,10S,11S,14R,15R)-14-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-5-yl dodecanoate

Traditional Name

(1S,2R,5S,10S,11S,14R,15R)-14-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-5-yl dodecanoate

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCC(=O)O[C@H]1CC[C@]2(C)[C@H]3CC[C@]4(C)[C@H](CC[C@H]4[C@@H]3CC=C2C1)[C@H](C)CC[C@@H](CC)C(C)C

InChI Identifier

InChI=1S/C41H72O2/c1-8-10-11-12-13-14-15-16-17-18-39(42)43-34-25-27-40(6)33(29-34)21-22-35-37-24-23-36(41(37,7)28-26-38(35)40)31(5)19-20-32(9-2)30(3)4/h21,30-32,34-38H,8-20,22-29H2,1-7H3/t31-,32-,34+,35+,36-,37+,38+,40+,41-/m1/s1

InChI Key

ZKAAVBQKARRBFN-CIKJAVNGSA-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
Serenoa repens	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
C24-propyl-sterol-skeleton
Steroid ester
Steroid
Delta-5-steroid
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
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	12.99	ChemAxon
pKa (Strongest Basic)	-7	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	18	ChemAxon
Refractivity	184.95 m³·mol⁻¹	ChemAxon
Polarizability	80.16 Å³	ChemAxon
Number of Rings	4	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

58805429

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

15086444

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,3as,3bs,7s,9ar,9bs,11ar)-1-[(2r,5r)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl dodecanoate (NP0270917)

MOL for NP0270917 ((1r,3as,3bs,7s,9ar,9bs,11ar)-1-[(2r,5r)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl dodecanoate)

3D MOL for NP0270917 ((1r,3as,3bs,7s,9ar,9bs,11ar)-1-[(2r,5r)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl dodecanoate)

3D SDF for NP0270917 ((1r,3as,3bs,7s,9ar,9bs,11ar)-1-[(2r,5r)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl dodecanoate)

3D-SDF for NP0270917 ((1r,3as,3bs,7s,9ar,9bs,11ar)-1-[(2r,5r)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl dodecanoate)

PDB for NP0270917 ((1r,3as,3bs,7s,9ar,9bs,11ar)-1-[(2r,5r)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl dodecanoate)

3D PDB for NP0270917 ((1r,3as,3bs,7s,9ar,9bs,11ar)-1-[(2r,5r)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl dodecanoate)

SMILES for NP0270917 ((1r,3as,3bs,7s,9ar,9bs,11ar)-1-[(2r,5r)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl dodecanoate)

INCHI for NP0270917 ((1r,3as,3bs,7s,9ar,9bs,11ar)-1-[(2r,5r)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl dodecanoate)

Structure for NP0270917 ((1r,3as,3bs,7s,9ar,9bs,11ar)-1-[(2r,5r)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl dodecanoate)

3D Structure for NP0270917 ((1r,3as,3bs,7s,9ar,9bs,11ar)-1-[(2r,5r)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl dodecanoate)