NP-MRD: Showing NP-Card for 1,8,10,12,14,15-hexakis(acetyloxy)-3,7,7,15-tetramethyl-11-methylidene-2-oxo-5-oxatricyclo[11.3.0.0⁴,⁶]hexadecan-9-yl 2-methylpropanoate (NP0253997)

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Record Information

Version

2.0

Created at

2022-09-07 18:01:52 UTC

Updated at

2022-09-07 18:01:52 UTC

NP-MRD ID

NP0253997

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1,8,10,12,14,15-hexakis(acetyloxy)-3,7,7,15-tetramethyl-11-methylidene-2-oxo-5-oxatricyclo[11.3.0.0⁴,⁶]hexadecan-9-yl 2-methylpropanoate

Description

1,8,10,12,14,15-Hexakis(acetyloxy)-3,7,7,15-tetramethyl-11-methylidene-2-oxo-5-oxatricyclo[11.3.0.0⁴,⁶]Hexadecan-9-yl 2-methylpropanoate belongs to the class of organic compounds known as alpha-acyloxy ketones. These are ketones that have an acyloxy substituent alpha to the carbonyl group. They have the general structure R4C(=O)OC(R2)(R3)C(R1)=O (R1=organyl, R4=H or organyl; R2,R3 = any atom). 1,8,10,12,14,15-hexakis(acetyloxy)-3,7,7,15-tetramethyl-11-methylidene-2-oxo-5-oxatricyclo[11.3.0.0⁴,⁶]hexadecan-9-yl 2-methylpropanoate is found in Euphorbia salicifolia. Based on a literature review very few articles have been published on 1,8,10,12,14,15-hexakis(acetyloxy)-3,7,7,15-tetramethyl-11-methylidene-2-oxo-5-oxatricyclo[11.3.0.0⁴,⁶]Hexadecan-9-yl 2-methylpropanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072220012D          

 52 54  0  0  0  0            999 V2000
    3.8677   -0.9734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3393   -0.3398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6237    0.4346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0953    1.0682    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5815    2.1287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4788    1.7818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8514    2.4761    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4366    0.5754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7211    1.3498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1927    1.9834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3798    1.8426    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4772    2.7578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2901    2.8986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9488    3.3914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9650   -0.0581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7779    0.0827    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0624    0.8571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5340    1.4906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8753    0.9979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6806   -0.8325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4926   -0.9782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3963   -0.4222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2090   -1.4661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7374   -2.0997    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9245   -2.2405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1116   -2.3813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8271   -3.1557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5832   -1.7478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2685   -1.2885    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7703   -1.8886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2296   -2.5739    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8657   -3.3143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3250   -3.9997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0425   -3.3694    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3310   -2.5869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5311   -2.3849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7067   -2.3537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4138   -3.2016    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6480   -3.5083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5307   -4.3249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0006   -2.9984    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4760   -1.5618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7777   -1.1225    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0481   -1.5076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0168   -2.3320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6502   -1.0683    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2419   -1.2550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5264   -0.4806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9980    0.1530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1851    0.0121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9006   -0.7623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6567    0.6457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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
  5  7  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
  8 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
 30 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  2  0  0  0  0
 36 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  2  0  0  0  0
 42 47  1  0  0  0  0
 30 47  1  0  0  0  0
 47 48  1  0  0  0  0
  2 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 50 52  2  0  0  0  0
M  END

     RDKit          3D

102104  0  0  0  0  0  0  0  0999 V2000
    0.5607    1.4291    1.3091 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4815    1.0729    0.0481 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7952    1.2747   -0.6906 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0806    2.6687   -0.4768 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1929    3.5991   -1.4635 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4887    5.0441   -1.2102 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0471    3.2604   -2.6483 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9123    0.4003   -0.2715 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9196   -0.0461    1.0533 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8664    0.3140    2.0176 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7773    1.1146    1.6170 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8336   -0.1877    3.4146 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5117    0.2643    4.0226 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9348    0.5155    4.1775 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3183   -0.6753   -1.2535 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7917   -0.3956   -2.5335 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5908   -0.2276   -3.6566 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0630    0.0616   -4.9912 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8350   -0.3363   -3.4857 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9757   -2.0902   -0.8293 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2828   -2.9808   -2.0113 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9084   -2.5521    0.2975 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5467   -2.2384   -0.4481 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7677   -2.5285   -1.5644 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7857   -3.3556   -0.4815 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4936   -3.3287    0.3191 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1997   -4.3190    1.4777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9737   -2.0524    0.8526 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3234   -1.5868    1.8057 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1135   -1.2080    0.4616 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0210   -2.0687   -0.2644 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5309   -3.2352    0.2127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4540   -4.1014   -0.6223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2149   -3.5783    1.3712 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8602   -0.6923    1.7110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7910    0.3682    1.1247 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.9704   -0.2190    0.4205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2746    1.2434    2.1167 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1712    0.9309    3.0935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5759    1.9884    4.0677 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6305   -0.2239    3.1508 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8309    1.1004    0.2589 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4079    1.8997   -0.7207 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3375    3.2773   -0.7723 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9554    4.1145   -1.8183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6854    3.7785    0.1714 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8746    0.0577   -0.2722 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6023    0.5484   -0.7362 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8938    1.6818   -1.6470 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7144    1.6060   -2.9907 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0023    2.7540   -3.9105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2875    0.5370   -3.5194 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3073    1.3334    1.9449 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4354    1.8284    1.8057 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6894    1.1849   -1.7850 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0564    5.2944   -0.2123 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5982    5.0995   -1.0616 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1338    5.6934   -2.0130 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8249    1.0964   -0.3047 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9362   -1.2902    3.4591 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4328    1.3595    3.9634 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6505   -0.1690    3.4988 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5276    0.0004    5.1022 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7508    0.5881    5.2499 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9259    0.0762    3.9235 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9698    1.5658    3.7671 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4427   -0.7139   -1.3980 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4509   -0.6751   -5.7254 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3679    1.0960   -5.2771 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9750    0.0313   -4.9805 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9321   -4.0252   -1.8635 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3849   -2.9301   -2.1657 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8287   -2.5072   -2.9056 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8215   -1.9571    0.2667 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3823   -2.4995    1.2864 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2065   -3.6136    0.1748 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2804   -1.4863    0.3105 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1754   -4.4015   -0.5865 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2319   -3.8059   -0.3998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6875   -3.9172    2.3891 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8652   -4.3948    1.6932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6645   -5.2794    1.2077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2112   -3.4603   -1.1191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8716   -4.6833   -1.3421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9924   -4.7422    0.0828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4992   -1.4208    2.1789 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0945   -0.2054    2.3272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7766   -0.5820   -0.5943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8052    0.5108    0.4747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2983   -1.0958    1.0179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7734    2.1439    4.8069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5623    1.7461    4.5237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7128    2.9389    3.5157 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3277    1.8053    0.9471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3558    5.0534   -2.0021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9675    4.4896   -1.5422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0879    3.5550   -2.7688 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4221   -0.1709   -1.2922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2013   -0.1822   -1.4672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1202    2.7404   -4.0523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4982    2.6024   -4.8844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6539    3.6977   -3.4575 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 12  1  0
 12 14  1  0
 12 10  1  0
 10 11  2  0
 10  9  1  0
  9  8  1  0
  8  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  3  2  1  0
  2  1  2  3
  2 48  1  0
 48 49  1  0
 49 50  1  0
 50 51  1  0
 50 52  2  0
 48 47  1  0
 47 42  1  0
 42 43  1  0
 43 44  1  0
 44 45  1  0
 44 46  2  0
 42 36  1  0
 36 37  1  0
 36 35  1  0
 35 30  1  0
 30 31  1  6
 31 32  1  0
 32 33  1  0
 32 34  2  0
 30 28  1  0
 28 29  2  0
 28 26  1  0
 26 27  1  0
 26 25  1  0
 25 24  1  0
 24 23  1  0
 23 20  1  0
 20 21  1  0
 20 22  1  0
 20 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 36 38  1  1
 38 39  1  0
 39 40  1  0
 39 41  2  0
 15  8  1  0
 30 47  1  0
 23 25  1  0
 13 61  1  0
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 12 60  1  0
 14 64  1  0
 14 65  1  0
 14 66  1  0
  8 59  1  1
  3 55  1  6
  6 56  1  0
  6 57  1  0
  6 58  1  0
  1 53  1  0
  1 54  1  0
 48 99  1  6
 51100  1  0
 51101  1  0
 51102  1  0
 47 98  1  6
 42 94  1  1
 45 95  1  0
 45 96  1  0
 45 97  1  0
 37 88  1  0
 37 89  1  0
 37 90  1  0
 35 86  1  0
 35 87  1  0
 33 83  1  0
 33 84  1  0
 33 85  1  0
 26 79  1  6
 27 80  1  0
 27 81  1  0
 27 82  1  0
 25 78  1  6
 23 77  1  1
 21 71  1  0
 21 72  1  0
 21 73  1  0
 22 74  1  0
 22 75  1  0
 22 76  1  0
 15 67  1  6
 18 68  1  0
 18 69  1  0
 18 70  1  0
 40 91  1  0
 40 92  1  0
 40 93  1  0
M  END


  Mrv1652309072220012D          

 52 54  0  0  0  0            999 V2000
    3.8677   -0.9734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3393   -0.3398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6237    0.4346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0953    1.0682    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5815    2.1287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4788    1.7818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8514    2.4761    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4366    0.5754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7211    1.3498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1927    1.9834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3798    1.8426    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4772    2.7578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2901    2.8986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9488    3.3914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9650   -0.0581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7779    0.0827    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0624    0.8571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5340    1.4906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8753    0.9979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6806   -0.8325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4926   -0.9782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3963   -0.4222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2090   -1.4661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7374   -2.0997    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9245   -2.2405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1116   -2.3813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8271   -3.1557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5832   -1.7478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2685   -1.2885    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7703   -1.8886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2296   -2.5739    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8657   -3.3143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3250   -3.9997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0425   -3.3694    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3310   -2.5869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5311   -2.3849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7067   -2.3537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4138   -3.2016    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6480   -3.5083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5307   -4.3249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0006   -2.9984    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4760   -1.5618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7777   -1.1225    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0481   -1.5076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0168   -2.3320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6502   -1.0683    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2419   -1.2550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5264   -0.4806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9980    0.1530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1851    0.0121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9006   -0.7623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6567    0.6457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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
  5  7  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
  8 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
 30 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  2  0  0  0  0
 36 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  2  0  0  0  0
 42 47  1  0  0  0  0
 30 47  1  0  0  0  0
 47 48  1  0  0  0  0
  2 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 50 52  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0253997

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C(=O)OC1C(OC(C)=O)C(=C)C(OC(C)=O)C2C(OC(C)=O)C(C)(CC2(OC(C)=O)C(=O)C(C)C2OC2C(C)(C)C1OC(C)=O)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C36H50O16/c1-15(2)33(44)50-28-26(46-19(6)38)16(3)25(45-18(5)37)24-30(47-20(7)39)35(13,51-22(9)41)14-36(24,52-23(10)42)29(43)17(4)27-31(49-27)34(11,12)32(28)48-21(8)40/h15,17,24-28,30-32H,3,14H2,1-2,4-13H3

> <INCHI_KEY>
MBQJEJCDRDNKGX-UHFFFAOYSA-N

> <FORMULA>
C36H50O16

> <MOLECULAR_WEIGHT>
738.78

> <EXACT_MASS>
738.30988553

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
102

> <JCHEM_AVERAGE_POLARIZABILITY>
74.14836611726783

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1,8,10,12,14,15-hexakis(acetyloxy)-3,7,7,15-tetramethyl-11-methylidene-2-oxo-5-oxatricyclo[11.3.0.0^{4,6}]hexadecan-9-yl 2-methylpropanoate

> <JCHEM_LOGP>
2.1470721930000014

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.64755837653237

> <JCHEM_PKA_STRONGEST_BASIC>
-4.208322740883592

> <JCHEM_POLAR_SURFACE_AREA>
213.69999999999996

> <JCHEM_REFRACTIVITY>
172.4174

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
1,8,10,12,14,15-hexakis(acetyloxy)-3,7,7,15-tetramethyl-11-methylidene-2-oxo-5-oxatricyclo[11.3.0.0^{4,6}]hexadecan-9-yl 2-methylpropanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       7.220  -1.817   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.233  -0.634   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.764   0.811   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       5.778   1.994   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.685   3.974   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.361   3.326   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       5.323   4.622   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       8.282   1.074   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       8.813   2.520   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       7.826   3.702   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       6.309   3.439   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       8.357   5.148   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.875   5.411   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.371   6.331   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.268  -0.109   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      10.785   0.154   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      11.317   1.600   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.330   2.783   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      12.834   1.863   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       8.737  -1.554   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.253  -1.826   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.073  -0.788   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.723  -2.737   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      10.710  -3.919   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       9.192  -4.182   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.675  -4.445   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.144  -5.891   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.689  -3.262   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       7.968  -2.405   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       5.171  -3.525   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       6.029  -4.805   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       5.349  -6.187   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.207  -7.466   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       3.813  -6.290   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       4.351  -4.829   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       2.858  -4.452   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       1.319  -4.394   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       2.639  -5.976   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       1.210  -6.549   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       0.991  -8.073   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      -0.001  -5.597   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       2.755  -2.915   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       1.452  -2.095   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0       0.090  -2.814   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       0.031  -4.353   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0      -1.214  -1.994   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0       4.185  -2.343   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       4.716  -0.897   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0       3.730   0.286   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0       2.212   0.023   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       1.681  -1.423   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0       1.226   1.205   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   48                                                  
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5                                                            
CONECT    8    3    9   15                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15    8   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   15   21   22   23                                             
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   20   24   25                                                  
CONECT   24   23   25                                                       
CONECT   25   24   23   26                                                  
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   35   47                                             
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32                                                            
CONECT   35   30   36                                                       
CONECT   36   35   37   38   42                                             
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39                                                            
CONECT   42   36   43   47                                                  
CONECT   43   42   44                                                       
CONECT   44   43   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44                                                            
CONECT   47   42   30   48                                                  
CONECT   48   47    2   49                                                  
CONECT   49   48   50                                                       
CONECT   50   49   51   52                                                  
CONECT   51   50                                                            
CONECT   52   50                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  108    0
END

View in JSmol

Synonyms

Value	Source
1,8,10,12,14,15-Hexakis(acetyloxy)-3,7,7,15-tetramethyl-11-methylidene-2-oxo-5-oxatricyclo[11.3.0.0,]hexadecan-9-yl 2-methylpropanoic acid	Generator

Chemical Formula

C₃₆H₅₀O₁₆

Average Mass

738.7800 Da

Monoisotopic Mass

738.30989 Da

IUPAC Name

1,8,10,12,14,15-hexakis(acetyloxy)-3,7,7,15-tetramethyl-11-methylidene-2-oxo-5-oxatricyclo[11.3.0.0^{4,6}]hexadecan-9-yl 2-methylpropanoate

Traditional Name

1,8,10,12,14,15-hexakis(acetyloxy)-3,7,7,15-tetramethyl-11-methylidene-2-oxo-5-oxatricyclo[11.3.0.0^{4,6}]hexadecan-9-yl 2-methylpropanoate

CAS Registry Number

Not Available

SMILES

CC(C)C(=O)OC1C(OC(C)=O)C(=C)C(OC(C)=O)C2C(OC(C)=O)C(C)(CC2(OC(C)=O)C(=O)C(C)C2OC2C(C)(C)C1OC(C)=O)OC(C)=O

InChI Identifier

InChI=1S/C36H50O16/c1-15(2)33(44)50-28-26(46-19(6)38)16(3)25(45-18(5)37)24-30(47-20(7)39)35(13,51-22(9)41)14-36(24,52-23(10)42)29(43)17(4)27-31(49-27)34(11,12)32(28)48-21(8)40/h15,17,24-28,30-32H,3,14H2,1-2,4-13H3

InChI Key

MBQJEJCDRDNKGX-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Euphorbia salicifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alpha-acyloxy ketones. These are ketones that have an acyloxy substituent alpha to the carbonyl group. They have the general structure R4C(=O)OC(R2)(R3)C(R1)=O (R1=organyl, R4=H or organyl; R2,R3 = any atom).

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Alpha-acyloxy ketones

Alternative Parents

Substituents

Alpha-acyloxy ketone
Cyclitol or derivatives
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organic oxide
Hydrocarbon derivative
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	2.15	ChemAxon
pKa (Strongest Acidic)	15.65	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	213.7 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	172.42 m³·mol⁻¹	ChemAxon
Polarizability	74.15 Å³	ChemAxon
Number of Rings	3	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

163019029

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1,8,10,12,14,15-hexakis(acetyloxy)-3,7,7,15-tetramethyl-11-methylidene-2-oxo-5-oxatricyclo[11.3.0.0⁴,⁶]hexadecan-9-yl 2-methylpropanoate (NP0253997)

MOL for NP0253997 (1,8,10,12,14,15-hexakis(acetyloxy)-3,7,7,15-tetramethyl-11-methylidene-2-oxo-5-oxatricyclo[11.3.0.0⁴,⁶]hexadecan-9-yl 2-methylpropanoate)

3D MOL for NP0253997 (1,8,10,12,14,15-hexakis(acetyloxy)-3,7,7,15-tetramethyl-11-methylidene-2-oxo-5-oxatricyclo[11.3.0.0⁴,⁶]hexadecan-9-yl 2-methylpropanoate)

3D SDF for NP0253997 (1,8,10,12,14,15-hexakis(acetyloxy)-3,7,7,15-tetramethyl-11-methylidene-2-oxo-5-oxatricyclo[11.3.0.0⁴,⁶]hexadecan-9-yl 2-methylpropanoate)

3D-SDF for NP0253997 (1,8,10,12,14,15-hexakis(acetyloxy)-3,7,7,15-tetramethyl-11-methylidene-2-oxo-5-oxatricyclo[11.3.0.0⁴,⁶]hexadecan-9-yl 2-methylpropanoate)

PDB for NP0253997 (1,8,10,12,14,15-hexakis(acetyloxy)-3,7,7,15-tetramethyl-11-methylidene-2-oxo-5-oxatricyclo[11.3.0.0⁴,⁶]hexadecan-9-yl 2-methylpropanoate)

3D PDB for NP0253997 (1,8,10,12,14,15-hexakis(acetyloxy)-3,7,7,15-tetramethyl-11-methylidene-2-oxo-5-oxatricyclo[11.3.0.0⁴,⁶]hexadecan-9-yl 2-methylpropanoate)

SMILES for NP0253997 (1,8,10,12,14,15-hexakis(acetyloxy)-3,7,7,15-tetramethyl-11-methylidene-2-oxo-5-oxatricyclo[11.3.0.0⁴,⁶]hexadecan-9-yl 2-methylpropanoate)

INCHI for NP0253997 (1,8,10,12,14,15-hexakis(acetyloxy)-3,7,7,15-tetramethyl-11-methylidene-2-oxo-5-oxatricyclo[11.3.0.0⁴,⁶]hexadecan-9-yl 2-methylpropanoate)

Structure for NP0253997 (1,8,10,12,14,15-hexakis(acetyloxy)-3,7,7,15-tetramethyl-11-methylidene-2-oxo-5-oxatricyclo[11.3.0.0⁴,⁶]hexadecan-9-yl 2-methylpropanoate)

3D Structure for NP0253997 (1,8,10,12,14,15-hexakis(acetyloxy)-3,7,7,15-tetramethyl-11-methylidene-2-oxo-5-oxatricyclo[11.3.0.0⁴,⁶]hexadecan-9-yl 2-methylpropanoate)