NP-MRD: Showing NP-Card for (1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15s,16r)-4,7,8,15,16-pentakis(acetyloxy)-5,9,12,12-tetramethyl-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-2-yl (2e)-2-methylbut-2-enoate (NP0242191)

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Record Information

Version

2.0

Created at

2022-09-07 02:27:04 UTC

Updated at

2022-09-07 02:27:05 UTC

NP-MRD ID

NP0242191

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15s,16r)-4,7,8,15,16-pentakis(acetyloxy)-5,9,12,12-tetramethyl-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-2-yl (2e)-2-methylbut-2-enoate

Description

Aleppicatine A belongs to the class of organic compounds known as hexacarboxylic acids and derivatives. These are carboxylic acids containing exactly six carboxyl groups. (1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15s,16r)-4,7,8,15,16-pentakis(acetyloxy)-5,9,12,12-tetramethyl-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-2-yl (2e)-2-methylbut-2-enoate is found in Euphorbia aleppica. (1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15s,16r)-4,7,8,15,16-pentakis(acetyloxy)-5,9,12,12-tetramethyl-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-2-yl (2e)-2-methylbut-2-enoate was first documented in 1996 (PMID: 8688177). Based on a literature review very few articles have been published on Aleppicatine A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072204272D          

 48 52  0  0  1  0            999 V2000
    4.3218   -3.1341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7622   -2.5279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0074   -1.7402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8122   -1.5587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4478   -1.1340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6431   -1.3155    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6973   -0.3327    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4002    0.5014    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8748    1.1762    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6915    1.0598    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4311    0.5966    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2116    0.2505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8783    0.7364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2991   -0.5699    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0546    1.8006    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9045    1.9262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4623    2.3749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7331    1.9890    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9060    2.9111    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5863    3.4318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4796    4.2498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3481    3.1151    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0582    2.4635    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9567    3.3746    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6332    4.1557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8153    4.2634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1355    4.8102    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2455    2.3218    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9633    3.1552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6755    1.7141    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9126    0.8342    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2413    0.0318    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4730    0.5693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2746    0.2203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5446    1.3912    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5875    0.3597    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8451   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9222   -0.9154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4444   -1.6106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7995   -2.3552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6219   -1.5459    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1623    0.4631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2220    1.2859    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9644    1.6456    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6472    1.1825    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2817    2.1087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8142    2.8778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4823    2.5725    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
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 10 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 18 17  1  0  0  0  0
  9 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 28 23  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 31 30  1  0  0  0  0
 31 32  1  1  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  2  0  0  0  0
 36 31  1  1  0  0  0
 36  8  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  1  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  2  0  0  0  0
 37 42  1  0  0  0  0
 43 42  1  6  0  0  0
 44 43  1  0  0  0  0
 45 44  1  6  0  0  0
 45 28  1  0  0  0  0
 36 45  1  0  0  0  0
 44 46  1  6  0  0  0
 43 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
M  END

     RDKit          3D

 96100  0  0  0  0  0  0  0  0999 V2000
    1.0438    6.6139   -0.4979 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6853    5.2969    0.1121 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7782    4.1597   -0.5403 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2592    4.1841   -1.9427 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4365    2.8806    0.0473 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0355    2.8705    1.2358 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5380    1.6900   -0.6519 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2192    0.4017   -0.1232 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3694   -0.5081   -0.0757 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6545    0.1636    0.3982 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5837    0.8652    1.5771 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1452    2.1121    1.7633 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0672    2.8701    3.0333 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7559    2.6332    0.8013 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5587   -1.0843    0.5739 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5159   -0.8177    1.6936 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6519   -2.2018    0.9166 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2159   -1.6433    0.8999 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9239   -1.0234    2.1342 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7316   -1.5919    3.3427 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4217   -0.7149    4.5215 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8021   -2.8077    3.5129 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2484   -2.7115    0.5398 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9325   -3.6873   -0.2716 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2168   -4.9691    0.1476 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9162   -5.9586   -0.7067 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8720   -5.3191    1.2982 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0087   -2.3903   -0.1501 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9648   -3.5662    0.1295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9367   -2.3748   -1.5298 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8031   -1.0456   -1.9287 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2123   -0.8470   -2.8320 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2614   -0.6913   -4.1636 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4947   -0.4742   -4.9707 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8484   -0.7446   -4.6979 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0189   -0.1655   -0.8136 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8898    1.0335   -1.1014 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5921    0.7979   -2.3067 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.2043    1.4421   -4.6219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7062    2.6680   -3.1854 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.8173    0.1824    0.2227 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -1.6379   -1.0736    0.2228 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -3.0620   -0.1257    2.7157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2020   -1.1227    1.8554 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.3332    5.2723    1.1389 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.0939    0.6058    0.9178 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.0656    2.7263    3.4943 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.0823   -1.3162   -0.3776 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0
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  4 55  1  0
  8 56  1  1
  9 57  1  6
 10 58  1  6
 13 59  1  0
 13 60  1  0
 13 61  1  0
 15 62  1  6
 16 63  1  0
 16 64  1  0
 16 65  1  0
 17 66  1  0
 17 67  1  0
 21 68  1  0
 21 69  1  0
 21 70  1  0
 23 71  1  1
 26 72  1  0
 26 73  1  0
 26 74  1  0
 29 75  1  0
 29 76  1  0
 29 77  1  0
 31 78  1  6
 34 79  1  0
 34 80  1  0
 34 81  1  0
 45 90  1  1
 44 89  1  6
 43 88  1  6
 42 86  1  0
 42 87  1  0
 37 82  1  6
 40 83  1  0
 40 84  1  0
 40 85  1  0
 47 91  1  0
 47 92  1  0
 47 93  1  0
 48 94  1  0
 48 95  1  0
 48 96  1  0
M  END


  Mrv1652309072204272D          

 48 52  0  0  1  0            999 V2000
    4.3218   -3.1341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7622   -2.5279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0074   -1.7402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8122   -1.5587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4478   -1.1340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6431   -1.3155    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6973   -0.3327    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4002    0.5014    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8748    1.1762    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6915    1.0598    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4311    0.5966    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2116    0.2505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8783    0.7364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2991   -0.5699    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0546    1.8006    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9045    1.9262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4623    2.3749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7331    1.9890    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9060    2.9111    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5863    3.4318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4796    4.2498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3481    3.1151    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0582    2.4635    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9567    3.3746    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6332    4.1557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8153    4.2634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1355    4.8102    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2455    2.3218    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9633    3.1552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6755    1.7141    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9126    0.8342    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2413    0.0318    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4730    0.5693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2746    0.2203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5446    1.3912    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5875    0.3597    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8451   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9222   -0.9154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4444   -1.6106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7995   -2.3552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6219   -1.5459    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1623    0.4631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2220    1.2859    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9644    1.6456    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6472    1.1825    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2817    2.1087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8142    2.8778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4823    2.5725    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
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 10 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 18 17  1  0  0  0  0
  9 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 28 23  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 31 30  1  0  0  0  0
 31 32  1  1  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  2  0  0  0  0
 36 31  1  1  0  0  0
 36  8  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  1  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  2  0  0  0  0
 37 42  1  0  0  0  0
 43 42  1  6  0  0  0
 44 43  1  0  0  0  0
 45 44  1  6  0  0  0
 45 28  1  0  0  0  0
 36 45  1  0  0  0  0
 44 46  1  6  0  0  0
 43 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0242191

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C(/C)C(=O)O[C@@H]1[C@H]2[C@@H](OC(C)=O)[C@@H](C)C[C@]2(OC(C)=O)[C@H](OC(C)=O)[C@]2(C)O[C@H](OC(C)=O)[C@@]11[C@H]2[C@@H]2[C@H](C[C@@H]1OC(C)=O)C2(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C35H48O13/c1-12-15(2)29(41)46-28-25-26(43-18(5)37)16(3)14-34(25,47-21(8)40)30(44-19(6)38)33(11)27-24-22(32(24,9)10)13-23(42-17(4)36)35(27,28)31(48-33)45-20(7)39/h12,16,22-28,30-31H,13-14H2,1-11H3/b15-12+/t16-,22-,23-,24-,25+,26-,27-,28+,30+,31-,33+,34+,35-/m0/s1

> <INCHI_KEY>
JGNWCQQRLBPBFT-QCTPGYFZSA-N

> <FORMULA>
C35H48O13

> <MOLECULAR_WEIGHT>
676.756

> <EXACT_MASS>
676.309491606

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
96

> <JCHEM_AVERAGE_POLARIZABILITY>
69.09972247736073

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,3R,4S,5S,7R,8R,9R,10R,11S,13S,15S,16R)-4,7,8,15,16-pentakis(acetyloxy)-5,9,12,12-tetramethyl-17-oxapentacyclo[7.6.2.0^{1,10}.0^{3,7}.0^{11,13}]heptadecan-2-yl (2E)-2-methylbut-2-enoate

> <JCHEM_LOGP>
2.945178684333333

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.382835003082669

> <JCHEM_POLAR_SURFACE_AREA>
167.03

> <JCHEM_REFRACTIVITY>
163.27640000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,3R,4S,5S,7R,8R,9R,10R,11S,13S,15S,16R)-4,7,8,15,16-pentakis(acetyloxy)-5,9,12,12-tetramethyl-17-oxapentacyclo[7.6.2.0^{1,10}.0^{3,7}.0^{11,13}]heptadecan-2-yl (2E)-2-methylbut-2-enoate

> <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       8.067  -5.850   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.023  -4.719   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.481  -3.248   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.983  -2.910   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.436  -2.117   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       4.934  -2.456   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       6.902  -0.621   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.347   0.936   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.233   2.196   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.757   1.978   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      10.138   1.114   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      11.595   0.468   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.840   1.375   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      11.758  -1.064   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       9.435   3.361   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.022   3.596   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.330   4.433   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.968   3.713   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       7.291   5.434   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       8.561   6.406   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.362   7.933   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       9.983   5.815   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       5.709   4.599   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       5.519   6.299   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       4.915   7.757   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.389   7.958   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       5.853   8.979   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       4.192   4.334   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.665   5.890   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       3.128   3.200   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       3.570   1.557   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       2.317   0.059   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       0.883   1.063   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -0.513   0.411   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       1.017   2.597   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       4.830   0.671   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       3.444  -0.000   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       3.588  -1.709   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       2.696  -3.006   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       3.359  -4.396   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       1.161  -2.886   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       2.170   0.864   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       2.281   2.400   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       3.667   3.072   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       4.941   2.207   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       2.392   3.936   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       1.520   5.372   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       0.900   4.802   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   36                                                  
CONECT    9    8   10   18                                                  
CONECT   10    9   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   10   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17    9   19   23                                             
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   18   24   28                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   23   29   30   45                                             
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32   36                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33                                                            
CONECT   36   31    8   37   45                                             
CONECT   37   36   38   42                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39                                                            
CONECT   42   37   43                                                       
CONECT   43   42   44   46                                                  
CONECT   44   43   45   46                                                  
CONECT   45   44   28   36                                                  
CONECT   46   44   43   47   48                                             
CONECT   47   46                                                            
CONECT   48   46                                                            
MASTER        0    0    0    0    0    0    0    0   48    0  104    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₅H₄₈O₁₃

Average Mass

676.7560 Da

Monoisotopic Mass

676.30949 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C\C=C(/C)C(=O)O[C@@H]1[C@H]2[C@@H](OC(C)=O)[C@@H](C)C[C@]2(OC(C)=O)[C@H](OC(C)=O)[C@]2(C)O[C@H](OC(C)=O)[C@@]11[C@H]2[C@@H]2[C@H](C[C@@H]1OC(C)=O)C2(C)C

InChI Identifier

InChI=1S/C35H48O13/c1-12-15(2)29(41)46-28-25-26(43-18(5)37)16(3)14-34(25,47-21(8)40)30(44-19(6)38)33(11)27-24-22(32(24,9)10)13-23(42-17(4)36)35(27,28)31(48-33)45-20(7)39/h12,16,22-28,30-31H,13-14H2,1-11H3/b15-12+/t16-,22-,23-,24-,25+,26-,27-,28+,30+,31-,33+,34+,35-/m0/s1

InChI Key

JGNWCQQRLBPBFT-QCTPGYFZSA-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 aleppica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hexacarboxylic acids and derivatives. These are carboxylic acids containing exactly six carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Hexacarboxylic acids and derivatives

Direct Parent

Hexacarboxylic acids and derivatives

Alternative Parents

Substituents

Hexacarboxylic acid or derivatives
Carane monoterpenoid
Monoterpenoid
Fatty acid ester
Fatty acyl
Tetrahydrofuran
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Acetal
Oxacycle
Organoheterocyclic compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
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

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

101985971

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Oksuz S, Gurek F, Lin LZ, Gil RR, Pezzuto JM, Cordell GA: Aleppicatines A and B from Euphorbia aleppica. Phytochemistry. 1996 May;42(2):473-8. doi: 10.1016/0031-9422(95)00889-6. [PubMed:8688177 ]
LOTUS database [Link]

Showing NP-Card for (1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15s,16r)-4,7,8,15,16-pentakis(acetyloxy)-5,9,12,12-tetramethyl-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-2-yl (2e)-2-methylbut-2-enoate (NP0242191)

MOL for NP0242191 ((1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15s,16r)-4,7,8,15,16-pentakis(acetyloxy)-5,9,12,12-tetramethyl-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-2-yl (2e)-2-methylbut-2-enoate)

3D MOL for NP0242191 ((1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15s,16r)-4,7,8,15,16-pentakis(acetyloxy)-5,9,12,12-tetramethyl-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-2-yl (2e)-2-methylbut-2-enoate)

3D SDF for NP0242191 ((1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15s,16r)-4,7,8,15,16-pentakis(acetyloxy)-5,9,12,12-tetramethyl-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-2-yl (2e)-2-methylbut-2-enoate)

3D-SDF for NP0242191 ((1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15s,16r)-4,7,8,15,16-pentakis(acetyloxy)-5,9,12,12-tetramethyl-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-2-yl (2e)-2-methylbut-2-enoate)

PDB for NP0242191 ((1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15s,16r)-4,7,8,15,16-pentakis(acetyloxy)-5,9,12,12-tetramethyl-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-2-yl (2e)-2-methylbut-2-enoate)

3D PDB for NP0242191 ((1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15s,16r)-4,7,8,15,16-pentakis(acetyloxy)-5,9,12,12-tetramethyl-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-2-yl (2e)-2-methylbut-2-enoate)

SMILES for NP0242191 ((1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15s,16r)-4,7,8,15,16-pentakis(acetyloxy)-5,9,12,12-tetramethyl-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-2-yl (2e)-2-methylbut-2-enoate)

INCHI for NP0242191 ((1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15s,16r)-4,7,8,15,16-pentakis(acetyloxy)-5,9,12,12-tetramethyl-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-2-yl (2e)-2-methylbut-2-enoate)

Structure for NP0242191 ((1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15s,16r)-4,7,8,15,16-pentakis(acetyloxy)-5,9,12,12-tetramethyl-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-2-yl (2e)-2-methylbut-2-enoate)

3D Structure for NP0242191 ((1r,2r,3r,4s,5s,7r,8r,9r,10r,11s,13s,15s,16r)-4,7,8,15,16-pentakis(acetyloxy)-5,9,12,12-tetramethyl-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]heptadecan-2-yl (2e)-2-methylbut-2-enoate)