NP-MRD: Showing NP-Card for (1's,2r,4's,5s,6'r,9's,10'r,13'r)-5',5',9'-trimethyl-5-[(1s,4r,9r,10r,13r,14r)-5,5,9-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-14-yl]spiro[1,4-dioxolane-2,14'-tetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan]-6'-yl acetate (NP0213229)

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Record Information

Version

2.0

Created at

2022-09-05 12:09:02 UTC

Updated at

2022-09-05 12:09:02 UTC

NP-MRD ID

NP0213229

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1's,2r,4's,5s,6'r,9's,10'r,13'r)-5',5',9'-trimethyl-5-[(1s,4r,9r,10r,13r,14r)-5,5,9-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-14-yl]spiro[1,4-dioxolane-2,14'-tetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan]-6'-yl acetate

Description

Fritillebinide C belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D. (1's,2r,4's,5s,6'r,9's,10'r,13'r)-5',5',9'-trimethyl-5-[(1s,4r,9r,10r,13r,14r)-5,5,9-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-14-yl]spiro[1,4-dioxolane-2,14'-tetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan]-6'-yl acetate is found in Fritillaria ebeiensis. Based on a literature review very few articles have been published on Fritillebinide C.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052214092D          

 46 54  0  0  1  0            999 V2000
  -12.5616    0.4463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.7389    0.5079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3809    1.2512    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2742   -0.1738    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4515   -0.1122    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -9.9868   -0.7939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1641   -0.7323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8061    0.0110    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.3472   -0.6746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2708    0.6926    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.9220    1.4506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0989    1.5238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5800    0.8584    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.9712    0.4851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2853    0.2051    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.6318   -0.5873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4872   -0.6788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9654    0.0596    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.1434    1.0566    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.0034    1.8696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1869    1.9877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8223    1.2476    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0093    1.1076    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3865    1.7144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5765    1.3315    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2713    2.1182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4619    2.2850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9076    1.6658    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1021    1.8437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4172    2.6062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5941    2.2864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4548    1.2350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2061    0.4484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5995    0.2705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1564    0.8792    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3958    0.0897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9775    0.6775    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2227   -0.1673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0682   -0.3260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6281    0.3331    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0518    0.7989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4135    0.6722    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9147    1.4582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0935    0.6311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1837    1.4511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8238    1.0148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  1  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  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 15 14  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 18 17  1  1  0  0  0
 13 18  1  0  0  0  0
  8 18  1  0  0  0  0
 15 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 28 27  1  6  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 29 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 28 35  1  0  0  0  0
 35 36  1  6  0  0  0
 35 37  1  0  0  0  0
 25 37  1  0  0  0  0
 37 38  1  6  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 23 40  1  0  0  0  0
 40 41  1  6  0  0  0
 25 41  1  6  0  0  0
 22 42  1  0  0  0  0
 19 42  1  1  0  0  0
 19 43  1  0  0  0  0
 13 43  1  0  0  0  0
 10 44  1  0  0  0  0
  5 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
M  END

     RDKit          3D

112120  0  0  0  0  0  0  0  0999 V2000
   11.6509    1.0563    0.3895 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2301    1.3652    0.7345 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9596    2.4638    1.2988 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1938    0.5029    0.4645 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8379    0.7677    0.7793 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.3761   -0.2395    1.7620 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8847   -0.3800    1.8587 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2676   -0.6740    0.4852 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8795   -1.9764    0.0370 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6342    0.4797   -0.3791 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9975    0.2790   -1.7283 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5141    0.4796   -1.4964 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9311   -0.3863   -0.4464 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1961   -1.5306   -1.1588 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2256   -1.9583   -0.1056 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0136   -2.5677    1.0378 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5000   -2.3290    0.8995 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8032   -0.8468    0.6356 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6647   -0.6552    0.3826 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2333   -0.6952    1.8305 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7572    0.2952    1.8725 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9682    0.7292    0.5857 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4164    1.0803    0.3198 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3237   -0.1284    0.5389 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3301    0.0271   -0.6146 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8969   -1.3042   -0.9038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1116   -1.6738   -0.1375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8513   -0.5130    0.4625 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.2370   -0.9473    0.7907 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1280   -1.8369    2.0418 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9177   -1.7609   -0.2513 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1459    0.2035    1.2036 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2320    1.3333    1.6245 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4344    1.8554    0.4658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7318    0.7554   -0.3125 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.3768    0.7071   -1.6686 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2686    1.1312   -0.3650 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0041    2.2814   -1.3162 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5566    2.7078   -1.1091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6130    1.5201   -1.1117 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3217    0.3515   -1.7301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5267   -0.2972   -0.2475 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7155    0.3674    0.1190 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0683    0.7915   -0.5143 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8016   -0.0216   -1.5574 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1300    2.2557   -0.9964 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1448    2.0254    0.1192 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6916    0.3442   -0.4509 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.1721    0.6978    1.2995 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8407    1.7868    1.2676 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8814   -1.2439    1.6572 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7137    0.1112    2.7830 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4735    0.5965    2.1801 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6586   -1.1944    2.5725 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7253   -2.6993    0.8919 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9983   -1.9155   -0.0523 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5118   -2.3492   -0.9151 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1270    1.3864    0.0658 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3078    1.0538   -2.4581 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1095   -0.7544   -2.1198 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4065    1.5500   -1.1566 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9431    0.3926   -2.4432 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6142   -1.0746   -1.9905 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8656   -2.2981   -1.5305 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4707   -2.6454   -0.5091 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8691   -3.6738    0.9509 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6733   -2.2546    2.0230 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8657   -2.9808    0.1076 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9473   -2.6316    1.8886 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4884   -0.3373    1.5949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2728   -1.6454    2.0756 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0129   -0.3935    2.5341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3875    1.6617    0.4413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7186    1.8839    1.0205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8507   -0.0494    1.5119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7962   -1.0738    0.3850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0884   -2.0694   -0.7012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0427   -1.3811   -2.0217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8198   -2.3649    0.7089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7522   -2.3114   -0.7951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3466   -0.3053    1.4557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0222   -1.7324    2.6836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9773   -2.8953    1.7485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2466   -1.5485    2.6479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8264   -2.8692   -0.0523 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0221   -1.5705   -0.2030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6035   -1.6082   -1.2762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8551    0.4895    0.4174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7573   -0.0517    2.1001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6431    1.0242    2.4860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8963    2.1623    1.9614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7163    2.6045    0.8833 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1299    2.4459   -0.1694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4859    0.7719   -1.5320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1131    1.6711   -2.1832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0498   -0.1012   -2.3121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0436    1.5574    0.6603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6358    3.1486   -1.0281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1196    2.0353   -2.3674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5177    3.2322   -0.1325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2698    3.4298   -1.8850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6493    1.7540   -1.6171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6149   -0.5104   -1.7438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7889    0.5300   -2.6895 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0331    0.7791    1.1211 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4131    1.1982   -0.5165 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2847    0.6247   -2.3458 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1456   -0.7095   -2.1195 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6805   -0.5642   -1.0986 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1353    2.6675   -0.7901 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3247    2.8514   -0.5045 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9710    2.2749   -2.0978 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
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  8  9  1  6
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 18 17  1  0
 17 16  1  0
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 43 19  1  0
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 18 70  1  1
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 43105  1  0
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 20 71  1  0
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 41103  1  0
 41104  1  0
 40102  1  6
 39100  1  0
 39101  1  0
 38 98  1  0
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 36 94  1  0
 36 95  1  0
 36 96  1  0
 34 92  1  0
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 33 90  1  0
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 32 89  1  0
 30 82  1  0
 30 83  1  0
 30 84  1  0
 31 85  1  0
 31 86  1  0
 31 87  1  0
 28 81  1  1
 27 79  1  0
 27 80  1  0
 26 77  1  0
 26 78  1  0
 12 61  1  0
 12 62  1  0
 11 59  1  0
 11 60  1  0
 10 58  1  1
 45107  1  0
 45108  1  0
 45109  1  0
 46110  1  0
 46111  1  0
 46112  1  0
M  END


  Mrv1652309052214092D          

 46 54  0  0  1  0            999 V2000
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  -11.7389    0.5079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3809    1.2512    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2742   -0.1738    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4515   -0.1122    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -9.9868   -0.7939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1641   -0.7323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8061    0.0110    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.3472   -0.6746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2708    0.6926    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.9220    1.4506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0989    1.5238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5800    0.8584    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.9712    0.4851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2853    0.2051    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.6318   -0.5873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4872   -0.6788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9654    0.0596    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.1434    1.0566    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.0034    1.8696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1869    1.9877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8223    1.2476    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0093    1.1076    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3865    1.7144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5765    1.3315    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2713    2.1182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4619    2.2850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9076    1.6658    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1021    1.8437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4172    2.6062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5941    2.2864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4548    1.2350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2061    0.4484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5995    0.2705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1564    0.8792    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3958    0.0897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9775    0.6775    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2227   -0.1673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0682   -0.3260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6281    0.3331    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0518    0.7989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4135    0.6722    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9147    1.4582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0935    0.6311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1837    1.4511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8238    1.0148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  1  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  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 15 14  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 18 17  1  1  0  0  0
 13 18  1  0  0  0  0
  8 18  1  0  0  0  0
 15 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 28 27  1  6  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 29 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 28 35  1  0  0  0  0
 35 36  1  6  0  0  0
 35 37  1  0  0  0  0
 25 37  1  0  0  0  0
 37 38  1  6  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 23 40  1  0  0  0  0
 40 41  1  6  0  0  0
 25 41  1  6  0  0  0
 22 42  1  0  0  0  0
 19 42  1  1  0  0  0
 19 43  1  0  0  0  0
 13 43  1  0  0  0  0
 10 44  1  0  0  0  0
  5 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0213229

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@@H]1CC[C@@]2(C)[C@@H]3CC[C@@H]4C[C@]3(C[C@]43CO[C@@H](O3)[C@@H]3C[C@]45C[C@H]3CC[C@H]4[C@]3(C)CCCC(C)(C)[C@H]3CC5)CC[C@@H]2C1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C42H66O4/c1-26(43)45-34-15-18-39(7)31(37(34,4)5)14-20-41-22-28(10-12-33(39)41)42(24-41)25-44-35(46-42)29-23-40-19-13-30-36(2,3)16-8-17-38(30,6)32(40)11-9-27(29)21-40/h27-35H,8-25H2,1-7H3/t27-,28-,29-,30-,31-,32+,33+,34-,35+,38-,39-,40+,41+,42+/m1/s1

> <INCHI_KEY>
SYDUXPBOZNFOTN-MZOYDABFSA-N

> <FORMULA>
C42H66O4

> <MOLECULAR_WEIGHT>
634.986

> <EXACT_MASS>
634.496110605

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
112

> <JCHEM_AVERAGE_POLARIZABILITY>
78.51701293306621

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1'S,2R,4'S,5S,6'R,9'S,10'R,13'R)-5',5',9'-trimethyl-5-[(1S,4R,9R,10R,13R,14R)-5,5,9-trimethyltetracyclo[11.2.1.0^{1,10}.0^{4,9}]hexadecan-14-yl]spiro[1,4-dioxolane-2,14'-tetracyclo[11.2.1.0^{1,10}.0^{4,9}]hexadecane]-6'-yl acetate

> <JCHEM_LOGP>
9.261872687666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
9

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.058140452761743

> <JCHEM_POLAR_SURFACE_AREA>
44.760000000000005

> <JCHEM_REFRACTIVITY>
181.5472

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1'S,2R,4'S,5S,6'R,9'S,10'R,13'R)-5',5',9'-trimethyl-5-[(1S,4R,9R,10R,13R,14R)-5,5,9-trimethyltetracyclo[11.2.1.0^{1,10}.0^{4,9}]hexadecan-14-yl]spiro[1,4-dioxolane-2,14'-tetracyclo[11.2.1.0^{1,10}.0^{4,9}]hexadecane]-6'-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0     -23.448   0.833   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -21.913   0.948   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0     -21.244   2.336   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0     -21.045  -0.324   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0     -19.509  -0.209   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -18.642  -1.482   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -17.106  -1.367   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -16.438   0.020   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -15.581  -1.259   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -17.305   1.293   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -16.654   2.708   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -15.118   2.844   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -14.149   1.602   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -13.013   0.906   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -11.733   0.383   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -12.379  -1.096   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0     -13.976  -1.267   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0     -14.869   0.111   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0     -11.468   1.972   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0     -11.206   3.490   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -9.682   3.710   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -9.002   2.329   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -7.484   2.068   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -6.321   3.200   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -4.809   2.486   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -4.240   3.954   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -2.729   4.265   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.694   3.110   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -0.191   3.442   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -0.779   4.865   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.109   4.268   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       0.849   2.305   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       0.385   0.837   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -1.119   0.505   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -2.159   1.641   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -2.605   0.167   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -3.691   1.265   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -4.149  -0.312   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -5.727  -0.609   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -6.772   0.622   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -5.697   1.491   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0     -10.105   1.255   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0     -12.907   2.722   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0     -18.841   1.178   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0     -19.010   2.709   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0     -20.204   1.894   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   44                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10   18                                             
CONECT    9    8                                                            
CONECT   10    8   11   44                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   18   43                                             
CONECT   14   13   15                                                       
CONECT   15   14   16   19                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   13    8                                                  
CONECT   19   15   20   42   43                                             
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   42                                                  
CONECT   23   22   24   40                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   37   41                                             
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   35                                                  
CONECT   29   28   30   31   32                                             
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32   29   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   28   36   37                                             
CONECT   36   35                                                            
CONECT   37   35   25   38                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   23   41                                                  
CONECT   41   40   25                                                       
CONECT   42   22   19                                                       
CONECT   43   19   13                                                       
CONECT   44   10    5   45   46                                             
CONECT   45   44                                                            
CONECT   46   44                                                            
MASTER        0    0    0    0    0    0    0    0   46    0  108    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₂H₆₆O₄

Average Mass

634.9860 Da

Monoisotopic Mass

634.49611 Da

IUPAC Name

(1'S,2R,4'S,5S,6'R,9'S,10'R,13'R)-5',5',9'-trimethyl-5-[(1S,4R,9R,10R,13R,14R)-5,5,9-trimethyltetracyclo[11.2.1.0^{1,10}.0^{4,9}]hexadecan-14-yl]spiro[1,4-dioxolane-2,14'-tetracyclo[11.2.1.0^{1,10}.0^{4,9}]hexadecane]-6'-yl acetate

Traditional Name

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@@H]1CC[C@@]2(C)[C@@H]3CC[C@@H]4C[C@]3(C[C@]43CO[C@@H](O3)[C@@H]3C[C@]45C[C@H]3CC[C@H]4[C@]3(C)CCCC(C)(C)[C@H]3CC5)CC[C@@H]2C1(C)C

InChI Identifier

InChI=1S/C42H66O4/c1-26(43)45-34-15-18-39(7)31(37(34,4)5)14-20-41-22-28(10-12-33(39)41)42(24-41)25-44-35(46-42)29-23-40-19-13-30-36(2,3)16-8-17-38(30,6)32(40)11-9-27(29)21-40/h27-35H,8-25H2,1-7H3/t27-,28-,29-,30-,31-,32+,33+,34-,35+,38-,39-,40+,41+,42+/m1/s1

InChI Key

SYDUXPBOZNFOTN-MZOYDABFSA-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
Fritillaria ebeiensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Kaurane diterpenoids

Alternative Parents

Substituents

Kaurane diterpenoid
Meta-dioxolane
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	9.26	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	44.76 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	181.55 m³·mol⁻¹	ChemAxon
Polarizability	78.52 Å³	ChemAxon
Number of Rings	9	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

102157321

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1's,2r,4's,5s,6'r,9's,10'r,13'r)-5',5',9'-trimethyl-5-[(1s,4r,9r,10r,13r,14r)-5,5,9-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-14-yl]spiro[1,4-dioxolane-2,14'-tetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan]-6'-yl acetate (NP0213229)

MOL for NP0213229 ((1's,2r,4's,5s,6'r,9's,10'r,13'r)-5',5',9'-trimethyl-5-[(1s,4r,9r,10r,13r,14r)-5,5,9-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-14-yl]spiro[1,4-dioxolane-2,14'-tetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan]-6'-yl acetate)

3D MOL for NP0213229 ((1's,2r,4's,5s,6'r,9's,10'r,13'r)-5',5',9'-trimethyl-5-[(1s,4r,9r,10r,13r,14r)-5,5,9-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-14-yl]spiro[1,4-dioxolane-2,14'-tetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan]-6'-yl acetate)

3D SDF for NP0213229 ((1's,2r,4's,5s,6'r,9's,10'r,13'r)-5',5',9'-trimethyl-5-[(1s,4r,9r,10r,13r,14r)-5,5,9-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-14-yl]spiro[1,4-dioxolane-2,14'-tetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan]-6'-yl acetate)

3D-SDF for NP0213229 ((1's,2r,4's,5s,6'r,9's,10'r,13'r)-5',5',9'-trimethyl-5-[(1s,4r,9r,10r,13r,14r)-5,5,9-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-14-yl]spiro[1,4-dioxolane-2,14'-tetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan]-6'-yl acetate)

PDB for NP0213229 ((1's,2r,4's,5s,6'r,9's,10'r,13'r)-5',5',9'-trimethyl-5-[(1s,4r,9r,10r,13r,14r)-5,5,9-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-14-yl]spiro[1,4-dioxolane-2,14'-tetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan]-6'-yl acetate)

3D PDB for NP0213229 ((1's,2r,4's,5s,6'r,9's,10'r,13'r)-5',5',9'-trimethyl-5-[(1s,4r,9r,10r,13r,14r)-5,5,9-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-14-yl]spiro[1,4-dioxolane-2,14'-tetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan]-6'-yl acetate)

SMILES for NP0213229 ((1's,2r,4's,5s,6'r,9's,10'r,13'r)-5',5',9'-trimethyl-5-[(1s,4r,9r,10r,13r,14r)-5,5,9-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-14-yl]spiro[1,4-dioxolane-2,14'-tetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan]-6'-yl acetate)

INCHI for NP0213229 ((1's,2r,4's,5s,6'r,9's,10'r,13'r)-5',5',9'-trimethyl-5-[(1s,4r,9r,10r,13r,14r)-5,5,9-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-14-yl]spiro[1,4-dioxolane-2,14'-tetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan]-6'-yl acetate)

Structure for NP0213229 ((1's,2r,4's,5s,6'r,9's,10'r,13'r)-5',5',9'-trimethyl-5-[(1s,4r,9r,10r,13r,14r)-5,5,9-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-14-yl]spiro[1,4-dioxolane-2,14'-tetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan]-6'-yl acetate)

3D Structure for NP0213229 ((1's,2r,4's,5s,6'r,9's,10'r,13'r)-5',5',9'-trimethyl-5-[(1s,4r,9r,10r,13r,14r)-5,5,9-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-14-yl]spiro[1,4-dioxolane-2,14'-tetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan]-6'-yl acetate)