NP-MRD: Showing NP-Card for (1r,3ar,5r,7s,9as,9br,11ar)-1-[(2r,3e,5r)-5,6-dimethylhept-3-en-2-yl]-5,9b-dihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl hexadecanoate (NP0164156)

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Record Information

Version

2.0

Created at

2022-09-02 22:58:56 UTC

Updated at

2022-09-02 22:58:56 UTC

NP-MRD ID

NP0164156

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3ar,5r,7s,9as,9br,11ar)-1-[(2r,3e,5r)-5,6-dimethylhept-3-en-2-yl]-5,9b-dihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl hexadecanoate

Description

Fusaristerol B belongs to the class of organic compounds known as steroid esters. Steroid esters are compounds containing a steroid moiety which bears a carboxylic acid ester group. Based on a literature review very few articles have been published on Fusaristerol B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032200582D          

 48 51  0  0  1  0            999 V2000
   12.8605   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.2920   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065   -2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   25.0065   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   26.4354   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   27.1499   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788   -3.3000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   29.3635   -3.0451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.8484   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.3635   -4.3799    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   29.6184   -5.1646    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   29.0664   -5.7777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.4254   -5.3361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.6803   -6.1207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.4873   -6.2922    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   32.0393   -5.6791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.7422   -7.0769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.5492   -7.2484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.1902   -7.6900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788   -4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   28.6651   -4.9455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499   -3.3000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   26.8143   -4.0537    0.0000 O   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  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 19 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  6  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  6  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 33 43  1  0  0  0  0
 30 43  1  0  0  0  0
 43 44  1  6  0  0  0
 43 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 29 47  1  0  0  0  0
 22 47  1  0  0  0  0
 47 48  1  6  0  0  0
M  END

     RDKit          3D

124127  0  0  0  0  0  0  0  0999 V2000
   12.6478    2.8119    1.0736 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8137    2.6771    0.0976 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2810    2.5904   -1.3138 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3533    1.3847   -1.5021 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0704    0.1147   -1.2227 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2838   -1.1186   -1.3776 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1819   -1.4691   -0.4907 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0180   -0.5617   -0.3249 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9411   -1.2345    0.5660 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7727   -0.3235    0.7471 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0638    0.0699   -0.5064 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4908   -1.1105   -1.2640 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4926   -1.8686   -0.4107 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3477   -1.0042    0.0220 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5435   -0.4292   -1.1214 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4774    0.3984   -0.5029 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7244    1.6041   -0.1868 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1925   -0.0424   -0.2294 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2205    0.8111    0.3679 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8992    0.9926   -0.6037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5512   -0.3673   -0.8392 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0956   -0.9486    0.4363 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3417   -2.2799    0.6372 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7188   -0.1131    1.6377 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2883    0.2290    1.6755 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1636   -0.8795    2.8515 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5278   -2.0423    3.1126 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6710   -0.9872    2.7716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3079   -1.1502    1.6345 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7531   -1.2346    1.6611 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4635   -2.2799    2.3945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8987   -2.1387    1.8369 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7883   -1.0284    0.7734 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.9550   -0.7857   -0.0290 C   0  0  2  0  0  0  0  0  0  0  0  0
   -9.5327   -1.8926   -0.8773 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9889    0.4922   -0.7929 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6256    1.5907   -0.4234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6349    2.8421   -1.2120 C   0  0  2  0  0  0  0  0  0  0  0  0
   -9.0584    4.0153   -0.4895 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0870    3.1522   -1.5599 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.7037    2.0334   -2.3705 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.8395    3.2910   -0.2440 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -1.3035    0.2748 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.3899   -2.6937   -0.2843 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7476   -0.2764   -0.5245 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2967   -0.5019   -0.7455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5693   -1.2306    0.3517 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5794   -2.5982   -0.0476 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.9494    3.4429    1.9357 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.3614    1.7977    1.4070 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.7808    3.3123    0.5795 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.4855    1.8599    0.3593 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.3840    3.6329    0.1504 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.1094    2.5290   -2.0264 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.6994    3.4875   -1.5429 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.1148    1.4117   -2.6194 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4364    1.5571   -0.9892 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.4990    0.1742   -0.1774 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.9916    0.0318   -1.8977 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.0507   -1.9838   -1.3957 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.9054   -1.1540   -2.4664 H   0  0  0  0  0  0  0  0  0  0  0  0
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   10.7558   -2.4660   -0.8471 H   0  0  0  0  0  0  0  0  0  0  0  0
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   10.3936    0.3127    0.3069 H   0  0  0  0  0  0  0  0  0  0  0  0
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    8.1661    0.6114    1.2300 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.7710    0.5820   -1.1771 H   0  0  0  0  0  0  0  0  0  0  0  0
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    6.0580   -0.7435   -2.1938 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0765   -2.6797   -1.0562 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9863   -2.3450    0.4325 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6537   -1.6543    0.6096 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6425   -0.1725    0.6788 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2198    0.2588   -1.7093 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1008   -1.2015   -1.7699 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6820    1.8278    0.5417 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.5446    1.3784   -1.5592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6896   -0.9882   -1.2473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2605   -0.3487   -1.6838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1378   -2.6678   -0.4075 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.4103   -0.5580    2.0103 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -9.7371   -2.8134   -0.2879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0320   -2.0504   -1.8397 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5937   -1.5966   -1.2070 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -9.8226    4.7763   -0.2243 H   0  0  0  0  0  0  0  0  0  0  0  0
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  -11.1075    4.1144   -2.0906 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.7399    2.3130   -2.5998 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1088    1.8114   -3.2645 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.7564    1.1437   -1.6887 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.3846    2.3372   -0.0647 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1520    3.4725    0.6080 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.5581    4.1406   -0.3652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9467   -2.6783   -1.3009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0051   -3.4713    0.3906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4398   -3.0640   -0.4837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1920   -0.0846   -1.5244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8819    0.7041    0.0203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1669   -1.0180   -1.7194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8607    0.5312   -0.9023 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5074   -2.6943   -1.0095 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  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  1
 22 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  2  0
 37 38  1  0
 38 39  1  0
 38 40  1  0
 40 41  1  0
 40 42  1  0
 33 43  1  0
 43 44  1  6
 43 45  1  0
 45 46  1  0
 46 47  1  0
 47 48  1  6
 25 19  1  0
 47 29  1  0
 47 22  1  0
 43 30  1  0
  1 49  1  0
  1 50  1  0
  1 51  1  0
  2 52  1  0
  2 53  1  0
  3 54  1  0
  3 55  1  0
  4 56  1  0
  4 57  1  0
  5 58  1  0
  5 59  1  0
  6 60  1  0
  6 61  1  0
  7 62  1  0
  7 63  1  0
  8 64  1  0
  8 65  1  0
  9 66  1  0
  9 67  1  0
 10 68  1  0
 10 69  1  0
 11 70  1  0
 11 71  1  0
 12 72  1  0
 12 73  1  0
 13 74  1  0
 13 75  1  0
 14 76  1  0
 14 77  1  0
 15 78  1  0
 15 79  1  0
 19 80  1  1
 20 81  1  0
 20 82  1  0
 21 83  1  0
 21 84  1  0
 23 85  1  0
 23 86  1  0
 23 87  1  0
 24 88  1  6
 25 89  1  0
 25 90  1  0
 26 91  1  1
 27 92  1  0
 28 93  1  0
 30 94  1  1
 31 95  1  0
 31 96  1  0
 32 97  1  0
 32 98  1  0
 33 99  1  1
 34100  1  1
 35101  1  0
 35102  1  0
 35103  1  0
 36104  1  0
 37105  1  0
 38106  1  6
 39107  1  0
 39108  1  0
 39109  1  0
 40110  1  0
 41111  1  0
 41112  1  0
 41113  1  0
 42114  1  0
 42115  1  0
 42116  1  0
 44117  1  0
 44118  1  0
 44119  1  0
 45120  1  0
 45121  1  0
 46122  1  0
 46123  1  0
 48124  1  0
M  END


  Mrv1652309032200582D          

 48 51  0  0  1  0            999 V2000
   12.8605   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.2920   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065   -2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   25.0065   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   26.4354   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   27.1499   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788   -3.3000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   29.3635   -3.0451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.8484   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.3635   -4.3799    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   29.6184   -5.1646    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   29.0664   -5.7777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.4254   -5.3361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.6803   -6.1207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.4873   -6.2922    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   32.0393   -5.6791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.7422   -7.0769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.5492   -7.2484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.1902   -7.6900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788   -4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   28.6651   -4.9455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499   -3.3000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   26.8143   -4.0537    0.0000 O   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  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 19 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  6  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  6  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 33 43  1  0  0  0  0
 30 43  1  0  0  0  0
 43 44  1  6  0  0  0
 43 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 29 47  1  0  0  0  0
 22 47  1  0  0  0  0
 47 48  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0164156

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCC(=O)O[C@H]1CC[C@@]2(C)C(C1)[C@H](O)C=C1[C@@H]3CC[C@H]([C@H](C)\C=C\[C@H](C)C(C)C)[C@@]3(C)CC[C@@]21O

> <INCHI_IDENTIFIER>
InChI=1S/C44H76O4/c1-8-9-10-11-12-13-14-15-16-17-18-19-20-21-41(46)48-35-26-27-43(7)39(30-35)40(45)31-38-37-25-24-36(34(5)23-22-33(4)32(2)3)42(37,6)28-29-44(38,43)47/h22-23,31-37,39-40,45,47H,8-21,24-30H2,1-7H3/b23-22+/t33-,34+,35-,36+,37-,39?,40+,42+,43-,44-/m0/s1

> <INCHI_KEY>
NSDKADJZZHEMKH-CFEGGGGCSA-N

> <FORMULA>
C44H76O4

> <MOLECULAR_WEIGHT>
669.088

> <EXACT_MASS>
668.574360927

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
124

> <JCHEM_AVERAGE_POLARIZABILITY>
85.34307882257195

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S,5S,8R,11R,14R,15R)-14-[(2R,3E,5R)-5,6-dimethylhept-3-en-2-yl]-1,8-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-5-yl hexadecanoate

> <ALOGPS_LOGP>
9.41

> <JCHEM_LOGP>
11.802790730666672

> <ALOGPS_LOGS>
-7.32

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.627229803752982

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.73607371772976

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0047222868279686

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
202.68570000000008

> <JCHEM_ROTATABLE_BOND_COUNT>
20

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.18e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,5S,8R,11R,14R,15R)-14-[(2R,3E,5R)-5,6-dimethylhept-3-en-2-yl]-1,8-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-5-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      24.006  -3.080   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      25.340  -3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      26.674  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      28.007  -3.850   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      29.341  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      30.675  -3.850   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      32.008  -3.080   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      33.342  -3.850   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      34.676  -3.080   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      36.009  -3.850   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      37.343  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      38.677  -3.850   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      40.010  -3.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      41.344  -3.850   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      42.678  -3.080   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      44.011  -3.850   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      44.011  -5.390   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      45.345  -3.080   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      46.679  -3.850   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      46.679  -5.390   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      48.012  -6.160   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      49.346  -5.390   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      49.346  -6.930   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      49.346  -3.850   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      48.012  -3.080   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      50.680  -3.080   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      50.680  -1.540   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      52.013  -3.850   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      52.013  -5.390   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      53.347  -6.160   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      54.812  -5.684   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      55.717  -6.930   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      54.812  -8.176   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      55.288  -9.641   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      54.257 -10.785   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      56.794  -9.961   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      57.270 -11.425   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      58.776 -11.746   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      59.807 -10.601   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      59.252 -13.210   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      60.758 -13.530   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      58.222 -14.355   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      53.347  -7.700   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      53.508  -9.232   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      52.013  -8.470   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      50.680  -7.700   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      50.680  -6.160   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      50.053  -7.567   0.000  0.00  0.00           O+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   25                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24   47                                             
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24   19                                                       
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30   47                                                  
CONECT   30   29   31   43                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   43                                                  
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40                                                            
CONECT   43   33   30   44   45                                             
CONECT   44   43                                                            
CONECT   45   43   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   29   22   48                                             
CONECT   48   47                                                            
MASTER        0    0    0    0    0    0    0    0   48    0  102    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₄H₇₆O₄

Average Mass

669.0880 Da

Monoisotopic Mass

668.57436 Da

IUPAC Name

(1R,2S,5S,8R,11R,14R,15R)-14-[(2R,3E,5R)-5,6-dimethylhept-3-en-2-yl]-1,8-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-5-yl hexadecanoate

Traditional Name

(1R,2S,5S,8R,11R,14R,15R)-14-[(2R,3E,5R)-5,6-dimethylhept-3-en-2-yl]-1,8-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-5-yl hexadecanoate

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCC(=O)O[C@H]1CC[C@@]2(C)C(C1)[C@H](O)C=C1[C@@H]3CC[C@H]([C@H](C)\C=C\[C@H](C)C(C)C)[C@@]3(C)CC[C@@]21O

InChI Identifier

InChI=1S/C44H76O4/c1-8-9-10-11-12-13-14-15-16-17-18-19-20-21-41(46)48-35-26-27-43(7)39(30-35)40(45)31-38-37-25-24-36(34(5)23-22-33(4)32(2)3)42(37,6)28-29-44(38,43)47/h22-23,31-37,39-40,45,47H,8-21,24-30H2,1-7H3/b23-22+/t33-,34+,35-,36+,37-,39?,40+,42+,43-,44-/m0/s1

InChI Key

NSDKADJZZHEMKH-CFEGGGGCSA-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 steroid esters. Steroid esters are compounds containing a steroid moiety which bears a carboxylic acid ester group.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid esters

Direct Parent

Steroid esters

Alternative Parents

Substituents

Steroid ester
Hydroxysteroid
6-hydroxysteroid
Delta-7-steroid
Tertiary alcohol
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	9.41	ALOGPS
logP	11.8	ChemAxon
logS	-7.3	ALOGPS
pKa (Strongest Acidic)	13.74	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	20	ChemAxon
Refractivity	202.69 m³·mol⁻¹	ChemAxon
Polarizability	85.34 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

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

146682467

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,3ar,5r,7s,9as,9br,11ar)-1-[(2r,3e,5r)-5,6-dimethylhept-3-en-2-yl]-5,9b-dihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl hexadecanoate (NP0164156)

MOL for NP0164156 ((1r,3ar,5r,7s,9as,9br,11ar)-1-[(2r,3e,5r)-5,6-dimethylhept-3-en-2-yl]-5,9b-dihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl hexadecanoate)

3D MOL for NP0164156 ((1r,3ar,5r,7s,9as,9br,11ar)-1-[(2r,3e,5r)-5,6-dimethylhept-3-en-2-yl]-5,9b-dihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl hexadecanoate)

3D SDF for NP0164156 ((1r,3ar,5r,7s,9as,9br,11ar)-1-[(2r,3e,5r)-5,6-dimethylhept-3-en-2-yl]-5,9b-dihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl hexadecanoate)

3D-SDF for NP0164156 ((1r,3ar,5r,7s,9as,9br,11ar)-1-[(2r,3e,5r)-5,6-dimethylhept-3-en-2-yl]-5,9b-dihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl hexadecanoate)

PDB for NP0164156 ((1r,3ar,5r,7s,9as,9br,11ar)-1-[(2r,3e,5r)-5,6-dimethylhept-3-en-2-yl]-5,9b-dihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl hexadecanoate)

3D PDB for NP0164156 ((1r,3ar,5r,7s,9as,9br,11ar)-1-[(2r,3e,5r)-5,6-dimethylhept-3-en-2-yl]-5,9b-dihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl hexadecanoate)

SMILES for NP0164156 ((1r,3ar,5r,7s,9as,9br,11ar)-1-[(2r,3e,5r)-5,6-dimethylhept-3-en-2-yl]-5,9b-dihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl hexadecanoate)

INCHI for NP0164156 ((1r,3ar,5r,7s,9as,9br,11ar)-1-[(2r,3e,5r)-5,6-dimethylhept-3-en-2-yl]-5,9b-dihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl hexadecanoate)

Structure for NP0164156 ((1r,3ar,5r,7s,9as,9br,11ar)-1-[(2r,3e,5r)-5,6-dimethylhept-3-en-2-yl]-5,9b-dihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl hexadecanoate)

3D Structure for NP0164156 ((1r,3ar,5r,7s,9as,9br,11ar)-1-[(2r,3e,5r)-5,6-dimethylhept-3-en-2-yl]-5,9b-dihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl hexadecanoate)