NP-MRD: Showing NP-Card for methyl 2-[4,5,11,16-tetrakis(acetyloxy)-13-(furan-3-yl)-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.0¹,¹².0³,⁸]heptadecan-7-yl]acetate (NP0222105)

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Record Information

Version

2.0

Created at

2022-09-05 23:51:22 UTC

Updated at

2022-09-05 23:51:22 UTC

NP-MRD ID

NP0222105

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 2-[4,5,11,16-tetrakis(acetyloxy)-13-(furan-3-yl)-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.0¹,¹².0³,⁸]heptadecan-7-yl]acetate

Description

Methyl 2-[4,5,11,16-tetrakis(acetyloxy)-13-(furan-3-yl)-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.0¹,¹².0³,⁸]Heptadecan-7-yl]acetate belongs to the class of organic compounds known as hexacarboxylic acids and derivatives. These are carboxylic acids containing exactly six carboxyl groups. methyl 2-[4,5,11,16-tetrakis(acetyloxy)-13-(furan-3-yl)-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.0¹,¹².0³,⁸]heptadecan-7-yl]acetate is found in Cipadessa cinerascens. Methyl 2-[4,5,11,16-tetrakis(acetyloxy)-13-(furan-3-yl)-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.0¹,¹².0³,⁸]Heptadecan-7-yl]acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241509272D          

 50 54  0  0  0  0            999 V2000
    6.0801    1.6817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2619    1.5766    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9437    0.8154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4439    0.1593    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1255    0.7103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8074   -0.0509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3075   -0.7070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0019   -1.1525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8668   -0.1005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9894   -1.4682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4896   -2.1243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3079   -2.0192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6260   -1.2580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8080   -2.6753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1711   -1.5734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8530   -2.3346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3532   -2.9907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1715   -2.8855    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0351   -3.7519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6710   -0.9173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8341   -1.1046    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0900   -0.6174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7953   -1.4190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3456   -2.0335    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0886   -2.8175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6390   -3.4321    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2812   -2.9868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0082   -1.6175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2436   -2.4082    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5738   -1.0100    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3412   -0.2127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9179    0.3772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7796    1.1906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5104    1.5734    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1004    0.9967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7342    0.2574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4684    0.0036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0641    0.6338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8340    0.8036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4195    1.5169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8300    2.2325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4155    2.9458    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6550    2.2348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6936    0.7266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4657    0.0137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2179   -0.3251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5526    0.5891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0183    1.2701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9891   -0.1561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3528    0.5844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 10 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 23 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  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 32 36  1  0  0  0  0
 31 37  1  0  0  0  0
 22 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 41 43  1  0  0  0  0
 39 44  1  0  0  0  0
 44 45  1  0  0  0  0
 22 45  1  0  0  0  0
 45 46  2  0  0  0  0
 44 47  1  0  0  0  0
 47 48  2  0  0  0  0
 47 49  1  0  0  0  0
  6 49  1  0  0  0  0
 20 49  1  0  0  0  0
 49 50  1  0  0  0  0
M  END

     RDKit          3D

 92 96  0  0  0  0  0  0  0  0999 V2000
   -0.0706    1.2370    2.7213 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6553    1.1455    1.6195 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8389    2.1580    0.5372 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0268    1.7944   -0.5793 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0980    2.5289   -1.5465 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0304    0.7250   -0.8125 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1263    0.4840   -2.2994 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4136   -0.5099   -0.0981 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9366   -0.4369   -0.0281 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5188   -0.0031    1.1364 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7513   -1.0300    2.1593 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8958   -2.1554    2.1419 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1673   -2.6338    3.2010 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6934   -3.8304    3.0383 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2239   -2.0698    4.3037 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1766   -1.5302    2.0334 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6797   -2.1557    3.0274 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8336   -1.2789    0.8590 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9155    0.0659    0.3242 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1210   -0.0071   -1.1077 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0345    0.7008   -1.8764 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8745    0.2900   -3.1762 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9361   -0.5990   -3.1923 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4533   -0.8164   -2.0017 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8092    0.8002    0.9196 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2784    1.1168    2.3680 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3206    2.0547    0.2851 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8018    2.4632   -0.9041 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5063    3.5798   -1.2112 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0070    3.9786   -2.5300 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7053    4.2849   -0.2141 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0439   -1.7286   -0.6023 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6322   -2.2929   -1.7899 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0742   -3.4954   -2.0535 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3301   -4.0065   -3.3613 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0696   -4.1603   -1.0248 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5474   -1.6627   -0.5559 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0803   -2.4501    0.5291 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8222   -3.5677    0.4263 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2973   -4.2599    1.6367 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1069   -4.0158   -0.6851 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2011   -0.3493   -0.6126 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3134   -0.3397    0.4692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9590   -0.1434   -1.9050 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3645    0.8649   -0.2396 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1605    2.0880   -0.3249 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5264    3.3671    0.0103 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3025    4.1818   -0.9562 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1566    3.7640    1.2753 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5553    5.0511    1.4370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1280    0.4590    3.4331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6169    2.1548    2.8760 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5024    3.1287    0.9481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4145    1.4193   -2.7841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0428    0.3443   -2.6205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6219   -0.4228   -2.6101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7393   -0.3678    0.9597 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6468   -0.6176    3.1813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0684   -4.7657    3.0075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3960   -3.9838    3.8658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2619   -3.8097    2.1033 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9213    0.4004    0.7466 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7236    1.4251   -1.5104 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4279    0.6344   -4.0649 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6457   -1.5411   -1.8075 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6582    2.1887    2.2616 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4582    1.2038    3.0670 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1620    0.5614    2.6541 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6929    2.8784    0.9736 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0728    3.7079   -2.6058 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9214    5.0688   -2.7207 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3948    3.4867   -3.3181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7854   -2.5540    0.1270 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4078   -4.6643   -3.8557 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2867   -4.5815   -3.3149 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5325   -3.1596   -4.0655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9338   -2.2579   -1.4174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5796   -4.2415    2.4827 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4983   -5.3200    1.3702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2713   -3.8154    1.9959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1387    0.3614    0.1491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9338    0.0837    1.4208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7871   -1.3129    0.5779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9269   -1.0897   -2.5345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6699    0.6943   -2.5179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0734   -0.0240   -1.7423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2152    0.7041    0.8897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7163    2.2148   -1.2897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9713    1.9957    0.4828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6561    5.0242    2.0746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3155    5.5015    0.4393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3110    5.6923    1.9218 H   0  0  0  0  0  0  0  0  0  0  0  0
 50 49  1  0
 49 47  1  0
 47 48  2  0
 47 46  1  0
 46 45  1  0
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 42 43  1  0
 42 44  1  0
 42 37  1  0
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 39 40  1  0
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 37 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 34 36  2  0
 32  8  1  0
  8  9  1  0
 10  9  1  6
 10 11  1  0
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 12 13  1  0
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 20 24  2  0
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 19 25  1  0
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 27  3  1  0
  3  2  1  0
  2  1  2  3
  3  4  1  0
  4  5  2  0
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 32 73  1  1
 35 74  1  0
 35 75  1  0
 35 76  1  0
  8 57  1  1
 11 58  1  1
 14 59  1  0
 14 60  1  0
 14 61  1  0
 19 62  1  1
 24 65  1  0
 22 64  1  0
 21 63  1  0
 26 66  1  0
 26 67  1  0
 26 68  1  0
 27 69  1  1
 30 70  1  0
 30 71  1  0
 30 72  1  0
  3 53  1  1
  1 51  1  0
  1 52  1  0
  7 54  1  0
  7 55  1  0
  7 56  1  0
M  END


  Mrv1533004241509272D          

 50 54  0  0  0  0            999 V2000
    6.0801    1.6817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2619    1.5766    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9437    0.8154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4439    0.1593    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1255    0.7103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8074   -0.0509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3075   -0.7070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0019   -1.1525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8668   -0.1005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9894   -1.4682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4896   -2.1243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3079   -2.0192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6260   -1.2580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8080   -2.6753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1711   -1.5734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8530   -2.3346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3532   -2.9907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1715   -2.8855    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0351   -3.7519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6710   -0.9173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8341   -1.1046    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0900   -0.6174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7953   -1.4190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3456   -2.0335    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0886   -2.8175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6390   -3.4321    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2812   -2.9868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0082   -1.6175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2436   -2.4082    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5738   -1.0100    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3412   -0.2127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9179    0.3772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7796    1.1906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5104    1.5734    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1004    0.9967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7342    0.2574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4684    0.0036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0641    0.6338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8340    0.8036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4195    1.5169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8300    2.2325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4155    2.9458    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6550    2.2348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6936    0.7266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4657    0.0137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2179   -0.3251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5526    0.5891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0183    1.2701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9891   -0.1561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3528    0.5844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 10 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 23 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  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 32 36  1  0  0  0  0
 31 37  1  0  0  0  0
 22 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 41 43  1  0  0  0  0
 39 44  1  0  0  0  0
 44 45  1  0  0  0  0
 22 45  1  0  0  0  0
 45 46  2  0  0  0  0
 44 47  1  0  0  0  0
 47 48  2  0  0  0  0
 47 49  1  0  0  0  0
  6 49  1  0  0  0  0
 20 49  1  0  0  0  0
 49 50  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0222105

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)CC1C(C)(C)C(OC(C)=O)C(OC(C)=O)C2OC34C(OC(C)=O)C(=O)OC(C5=COC=C5)C3(C)C(OC(C)=O)C(C4=C)C(=O)C12C

> <INCHI_IDENTIFIER>
InChI=1S/C35H42O15/c1-15-23-25(41)33(8)21(13-22(40)43-10)32(6,7)28(47-18(4)38)24(45-16(2)36)29(33)50-35(15)30(48-19(5)39)31(42)49-26(20-11-12-44-14-20)34(35,9)27(23)46-17(3)37/h11-12,14,21,23-24,26-30H,1,13H2,2-10H3

> <INCHI_KEY>
ZNZNNEJUEZHONU-UHFFFAOYSA-N

> <FORMULA>
C35H42O15

> <MOLECULAR_WEIGHT>
702.706

> <EXACT_MASS>
702.252370652

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
92

> <JCHEM_AVERAGE_POLARIZABILITY>
68.92706250157912

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 2-[4,5,11,16-tetrakis(acetyloxy)-13-(furan-3-yl)-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.0¹,¹².0³,⁸]heptadecan-7-yl]acetate

> <ALOGPS_LOGP>
2.29

> <JCHEM_LOGP>
1.8989548029999987

> <ALOGPS_LOGS>
-3.90

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.50538091627675

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8711382724191994

> <JCHEM_POLAR_SURFACE_AREA>
197.23999999999998

> <JCHEM_REFRACTIVITY>
163.45070000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.92e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 2-[4,5,11,16-tetrakis(acetyloxy)-13-(furan-3-yl)-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.0¹,¹².0³,⁸]heptadecan-7-yl]acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      11.350   3.139   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       9.822   2.943   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       9.228   1.522   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      10.162   0.297   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       7.701   1.326   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.107  -0.095   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.041  -1.320   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.337  -2.151   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.085  -0.188   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.447  -2.741   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       8.381  -3.965   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       9.908  -3.769   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      10.502  -2.348   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      10.842  -4.994   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.919  -2.937   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       5.326  -4.358   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       6.259  -5.583   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.787  -5.386   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.665  -7.003   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.986  -1.712   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       3.424  -2.062   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.035  -1.152   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.484  -2.649   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.512  -3.796   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       2.032  -5.259   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       3.059  -6.407   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       0.525  -5.575   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.015  -3.019   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -0.455  -4.495   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -1.071  -1.885   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -0.637  -0.397   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -1.713   0.704   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -1.455   2.222   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -2.819   2.937   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -3.921   1.860   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -3.237   0.481   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       0.874   0.007   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -0.120   1.183   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       1.557   1.500   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       0.783   2.832   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       1.549   4.167   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       0.776   5.499   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       3.089   4.172   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       3.161   1.356   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       2.736   0.026   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       4.140  -0.607   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       4.765   1.100   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0       5.634   2.371   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0       5.580  -0.291   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       6.259   1.091   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                                                       
CONECT    6    5    7   49                                                  
CONECT    7    6    8    9   10                                             
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    7   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   10   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   15   21   49                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   37   45                                             
CONECT   23   22   24   28                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   23   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32   37                                                  
CONECT   32   31   33   36                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   32                                                       
CONECT   37   31   22   38   39                                             
CONECT   38   37                                                            
CONECT   39   37   40   44                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41                                                            
CONECT   44   39   45   47                                                  
CONECT   45   44   22   46                                                  
CONECT   46   45                                                            
CONECT   47   44   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47    6   20   50                                             
CONECT   50   49                                                            
MASTER        0    0    0    0    0    0    0    0   50    0  108    0
END

View in JSmol

Synonyms

Value	Source
Methyl 2-[4,5,11,16-tetrakis(acetyloxy)-13-(furan-3-yl)-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.0,.0,]heptadecan-7-yl]acetic acid	Generator
Methyl 2-[4,5,11,16-tetrakis(acetyloxy)-13-(furan-3-yl)-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.0¹,¹².0³,⁸]heptadecan-7-yl]acetic acid	Generator

Chemical Formula

C₃₅H₄₂O₁₅

Average Mass

702.7060 Da

Monoisotopic Mass

702.25237 Da

IUPAC Name

methyl 2-[4,5,11,16-tetrakis(acetyloxy)-13-(furan-3-yl)-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.0¹,¹².0³,⁸]heptadecan-7-yl]acetate

Traditional Name

methyl 2-[4,5,11,16-tetrakis(acetyloxy)-13-(furan-3-yl)-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.0¹,¹².0³,⁸]heptadecan-7-yl]acetate

CAS Registry Number

Not Available

SMILES

COC(=O)CC1C(C)(C)C(OC(C)=O)C(OC(C)=O)C2OC34C(OC(C)=O)C(=O)OC(C5=COC=C5)C3(C)C(OC(C)=O)C(C4=C)C(=O)C12C

InChI Identifier

InChI=1S/C35H42O15/c1-15-23-25(41)33(8)21(13-22(40)43-10)32(6,7)28(47-18(4)38)24(45-16(2)36)29(33)50-35(15)30(48-19(5)39)31(42)49-26(20-11-12-44-14-20)34(35,9)27(23)46-17(3)37/h11-12,14,21,23-24,26-30H,1,13H2,2-10H3

InChI Key

ZNZNNEJUEZHONU-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
Cipadessa cinerascens	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
Delta valerolactone
Oxepane
Delta_valerolactone
Oxane
Furan
Heteroaromatic compound
Methyl ester
Carboxylic acid ester
Ketone
Lactone
Dialkyl ether
Ether
Oxacycle
Organoheterocyclic compound
Carbonyl group
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	2.29	ALOGPS
logP	1.9	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	11.51	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	197.24 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	163.45 m³·mol⁻¹	ChemAxon
Polarizability	68.93 Å³	ChemAxon
Number of Rings	5	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 2-[4,5,11,16-tetrakis(acetyloxy)-13-(furan-3-yl)-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.0¹,¹².0³,⁸]heptadecan-7-yl]acetate (NP0222105)

MOL for NP0222105 (methyl 2-[4,5,11,16-tetrakis(acetyloxy)-13-(furan-3-yl)-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.0¹,¹².0³,⁸]heptadecan-7-yl]acetate)

3D MOL for NP0222105 (methyl 2-[4,5,11,16-tetrakis(acetyloxy)-13-(furan-3-yl)-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.0¹,¹².0³,⁸]heptadecan-7-yl]acetate)

3D SDF for NP0222105 (methyl 2-[4,5,11,16-tetrakis(acetyloxy)-13-(furan-3-yl)-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.0¹,¹².0³,⁸]heptadecan-7-yl]acetate)

3D-SDF for NP0222105 (methyl 2-[4,5,11,16-tetrakis(acetyloxy)-13-(furan-3-yl)-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.0¹,¹².0³,⁸]heptadecan-7-yl]acetate)

PDB for NP0222105 (methyl 2-[4,5,11,16-tetrakis(acetyloxy)-13-(furan-3-yl)-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.0¹,¹².0³,⁸]heptadecan-7-yl]acetate)

3D PDB for NP0222105 (methyl 2-[4,5,11,16-tetrakis(acetyloxy)-13-(furan-3-yl)-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.0¹,¹².0³,⁸]heptadecan-7-yl]acetate)

SMILES for NP0222105 (methyl 2-[4,5,11,16-tetrakis(acetyloxy)-13-(furan-3-yl)-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.0¹,¹².0³,⁸]heptadecan-7-yl]acetate)

INCHI for NP0222105 (methyl 2-[4,5,11,16-tetrakis(acetyloxy)-13-(furan-3-yl)-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.0¹,¹².0³,⁸]heptadecan-7-yl]acetate)

Structure for NP0222105 (methyl 2-[4,5,11,16-tetrakis(acetyloxy)-13-(furan-3-yl)-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.0¹,¹².0³,⁸]heptadecan-7-yl]acetate)

3D Structure for NP0222105 (methyl 2-[4,5,11,16-tetrakis(acetyloxy)-13-(furan-3-yl)-6,6,8,12-tetramethyl-17-methylidene-9,15-dioxo-2,14-dioxatetracyclo[8.6.1.0¹,¹².0³,⁸]heptadecan-7-yl]acetate)