NP-MRD: Showing NP-Card for methyl 2-[(1s,5ar,7ar,8r,9r,11ar,11br)-1-(acetyloxy)-9-(furan-3-carbonyl)-8-hydroxy-5,5,7a,9,11b-pentamethyl-3,7-dioxo-hexahydro-1h-naphtho[2,1-c]oxepin-8-yl]acetate (NP0322985)

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Record Information

Version

2.0

Created at

2022-09-12 02:06:50 UTC

Updated at

2022-09-12 02:06:50 UTC

NP-MRD ID

NP0322985

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 2-[(1s,5ar,7ar,8r,9r,11ar,11br)-1-(acetyloxy)-9-(furan-3-carbonyl)-8-hydroxy-5,5,7a,9,11b-pentamethyl-3,7-dioxo-hexahydro-1h-naphtho[2,1-c]oxepin-8-yl]acetate

Description

Methyl 2-[(1S,5aR,7aR,8R,9R,11aR,11bR)-1-(acetyloxy)-9-(furan-3-carbonyl)-8-hydroxy-5,5,7a,9,11b-pentamethyl-3,7-dioxo-tetradecahydronaphtho[2,1-c]oxepin-8-yl]acetate belongs to the class of organic compounds known as limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17. methyl 2-[(1s,5ar,7ar,8r,9r,11ar,11br)-1-(acetyloxy)-9-(furan-3-carbonyl)-8-hydroxy-5,5,7a,9,11b-pentamethyl-3,7-dioxo-hexahydro-1h-naphtho[2,1-c]oxepin-8-yl]acetate is found in Odontadenia macrantha. Based on a literature review very few articles have been published on methyl 2-[(1S,5aR,7aR,8R,9R,11aR,11bR)-1-(acetyloxy)-9-(furan-3-carbonyl)-8-hydroxy-5,5,7a,9,11b-pentamethyl-3,7-dioxo-tetradecahydronaphtho[2,1-c]oxepin-8-yl]acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122204062D          

 39 42  0  0  1  0            999 V2000
   -2.6212   -3.5766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0040   -4.1240    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2213   -3.8631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6040   -4.4105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0559   -3.0549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2732   -2.7940    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1522   -3.6101    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6660   -2.0685    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3123   -2.5813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2833   -1.5211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1179   -0.7129    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0660   -1.7820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3149   -2.5685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1399   -2.5748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4008   -1.7921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7370   -1.3022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2342   -1.3656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5905   -1.3881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9834   -2.1136    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8080   -2.1362    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3621   -1.4421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1303   -1.3767    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5859   -0.7569    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8506    0.0246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3062    0.6444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6596    0.1861    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9250   -1.1552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5937   -1.6384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3192   -1.2456    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6329   -2.4625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0130   -3.0069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6817   -3.4901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6907   -3.7663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2009   -2.8617    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7690   -3.5646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9443   -3.5420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5124   -4.2450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5515   -2.8166    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1196   -3.5195    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
  6  5  1  1  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  6  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 12 16  2  0  0  0  0
  8 17  1  0  0  0  0
 17 18  1  0  0  0  0
 19 18  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 22 27  1  0  0  0  0
 27 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
 31 33  1  0  0  0  0
 31 34  1  0  0  0  0
 20 34  1  0  0  0  0
 34 35  1  6  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
 19 38  1  0  0  0  0
  6 38  1  0  0  0  0
 38 39  1  6  0  0  0
M  END

     RDKit          3D

 77 80  0  0  0  0  0  0  0  0999 V2000
    1.5004    1.5907    4.1660 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6401    1.2641    2.7759 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2632    2.0886    1.8735 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7036    3.1735    2.4022 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5052    1.9575    0.4814 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9660    0.8544   -0.3608 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5864    1.2634   -1.6058 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6271   -0.4854   -0.1392 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6952   -0.4443    0.9492 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2905   -1.0583   -1.3321 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2494   -0.5089   -2.4729 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0573   -2.3069   -1.3375 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4035   -3.1521   -0.3129 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1537   -4.1811   -0.8659 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2436   -3.9545   -2.1377 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6316   -2.8830   -2.4878 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6529   -1.5512    0.2935 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4591   -1.4983   -0.6759 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2876   -0.2958   -0.2352 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7309   -0.3080   -0.5404 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9433   -1.1836   -1.7654 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.3725   -0.4879    1.7248 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7221   -0.7364    2.9003 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8490    0.1738    4.0949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0118   -1.7601    2.9416 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6492   -1.8151    0.1417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7165   -0.9353   -0.2738 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8414   -1.1814    0.2361 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6999    0.1235   -1.1341 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7144    1.0962   -1.3343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5225    1.4460   -2.7847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3829    2.3817   -0.7512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4756    0.9511   -0.5182 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6617    2.2238   -0.6658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2787    2.0189   -0.1675 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0885    2.7904    0.6425 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5208    0.9046   -0.6959 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3520    1.0688   -2.2287 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9171    0.8376    4.6935 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9221    2.5614    4.1675 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4785    1.8290    4.6106 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1410    2.9125   -0.0340 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6267    2.1128    0.3153 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5029    1.5486   -1.4650 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6879   -0.8496    0.5852 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4549   -1.1456    1.8032 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9716    0.5407    1.3037 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1668   -3.0722    0.7571 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5664   -4.9952   -0.3157 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5760   -2.5048   -3.4855 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1034   -2.5275    0.2955 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2315   -1.3759    1.2978 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.0046   -1.1990   -2.0848 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.6510   -2.0619    0.6724 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.3331    1.1218    3.7733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8996    0.3550    4.3326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4666   -2.5586   -0.6580 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.7811    0.8178   -3.3014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2384    2.5019   -2.9644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2659    2.3529    0.3386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4485    2.3777   -0.9953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8496    3.2766   -1.1541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8808    1.0710    0.5504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1472    3.0579   -0.0530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7276    2.6939   -1.6667 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7117    0.2446   -2.8075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6268    1.3363   -2.5436 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0196    1.9522   -2.4627 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  6  7  1  6
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  8  9  1  0
  8 17  1  0
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 38  6  1  0
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  5 43  1  0
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 22 60  1  1
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 25 62  1  0
 25 63  1  0
 16 51  1  0
 14 50  1  0
 13 49  1  0
M  END


  Mrv1652309122204062D          

 39 42  0  0  1  0            999 V2000
   -2.6212   -3.5766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0040   -4.1240    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2213   -3.8631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6040   -4.4105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0559   -3.0549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2732   -2.7940    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1522   -3.6101    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6660   -2.0685    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3123   -2.5813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2833   -1.5211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1179   -0.7129    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0660   -1.7820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3149   -2.5685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1399   -2.5748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4008   -1.7921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7370   -1.3022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2342   -1.3656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5905   -1.3881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.8080   -2.1362    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    2.1303   -1.3767    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5859   -0.7569    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8506    0.0246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3062    0.6444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6596    0.1861    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9250   -1.1552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5937   -1.6384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3192   -1.2456    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6329   -2.4625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0130   -3.0069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6817   -3.4901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6907   -3.7663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2009   -2.8617    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7690   -3.5646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9443   -3.5420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5124   -4.2450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5515   -2.8166    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1196   -3.5195    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
  6  5  1  1  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  6  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 12 16  2  0  0  0  0
  8 17  1  0  0  0  0
 17 18  1  0  0  0  0
 19 18  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 22 27  1  0  0  0  0
 27 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
 31 33  1  0  0  0  0
 31 34  1  0  0  0  0
 20 34  1  0  0  0  0
 34 35  1  6  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
 19 38  1  0  0  0  0
  6 38  1  0  0  0  0
 38 39  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0322985

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C[C@@]1(O)[C@@](C)(CC[C@@H]2[C@]3(C)[C@@H](CC(=O)[C@@]12C)C(C)(C)OC(=O)C[C@@H]3OC(C)=O)C(=O)C1=COC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C29H38O10/c1-16(30)38-21-13-22(32)39-25(2,3)19-12-20(31)28(6)18(27(19,21)5)8-10-26(4,24(34)17-9-11-37-15-17)29(28,35)14-23(33)36-7/h9,11,15,18-19,21,35H,8,10,12-14H2,1-7H3/t18-,19+,21+,26+,27-,28+,29-/m1/s1

> <INCHI_KEY>
OXGWTRSVBLAIAN-CSWCXXNHSA-N

> <FORMULA>
C29H38O10

> <MOLECULAR_WEIGHT>
546.613

> <EXACT_MASS>
546.246497424

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
77

> <JCHEM_AVERAGE_POLARIZABILITY>
56.075433243491474

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 2-[(1S,5aR,7aR,8R,9R,11aR,11bR)-1-(acetyloxy)-9-(furan-3-carbonyl)-8-hydroxy-5,5,7a,9,11b-pentamethyl-3,7-dioxo-tetradecahydronaphtho[2,1-c]oxepin-8-yl]acetate

> <JCHEM_LOGP>
2.4947245726666667

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.45192579513012

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.38850538727922

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0272835913156526

> <JCHEM_POLAR_SURFACE_AREA>
146.41

> <JCHEM_REFRACTIVITY>
135.5161

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl [(1S,5aR,7aR,8R,9R,11aR,11bR)-1-(acetyloxy)-9-(furan-3-carbonyl)-8-hydroxy-5,5,7a,9,11b-pentamethyl-3,7-dioxo-hexahydro-1H-naphtho[2,1-c]oxepin-8-yl]acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0      -4.893  -6.676   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -3.741  -7.698   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -2.280  -7.211   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -1.128  -8.233   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -1.971  -5.702   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.510  -5.215   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -0.284  -6.739   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -1.243  -3.861   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.450  -4.819   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.395  -2.839   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -2.087  -1.331   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -3.856  -3.326   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.321  -4.795   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -5.861  -4.806   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -6.348  -3.345   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -5.109  -2.431   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.437  -2.549   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.102  -2.591   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.836  -3.945   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.375  -3.988   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.543  -2.692   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.977  -2.570   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.960  -1.413   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       3.454   0.046   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.438   1.203   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       4.965   0.347   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       5.460  -2.156   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.708  -3.058   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       8.063  -2.325   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       6.781  -4.597   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       5.624  -5.613   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.872  -6.515   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.023  -7.030   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.108  -5.342   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       3.302  -6.654   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       1.763  -6.612   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       0.957  -7.924   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       1.029  -5.258   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       0.223  -6.570   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    8   38                                             
CONECT    7    6                                                            
CONECT    8    6    9   10   17                                             
CONECT    9    8                                                            
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   16                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   12                                                       
CONECT   17    8   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   38                                                  
CONECT   20   19   21   22   34                                             
CONECT   21   20                                                            
CONECT   22   20   23   27                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   22   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32   33   34                                             
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   31   20   35                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   19    6   39                                             
CONECT   39   38                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   84    0
END

View in JSmol

Synonyms

Value	Source
Methyl 2-[(1S,5ar,7ar,8R,9R,11ar,11BR)-1-(acetyloxy)-9-(furan-3-carbonyl)-8-hydroxy-5,5,7a,9,11b-pentamethyl-3,7-dioxo-tetradecahydronaphtho[2,1-c]oxepin-8-yl]acetic acid	Generator

Chemical Formula

C₂₉H₃₈O₁₀

Average Mass

546.6130 Da

Monoisotopic Mass

546.24650 Da

IUPAC Name

methyl 2-[(1S,5aR,7aR,8R,9R,11aR,11bR)-1-(acetyloxy)-9-(furan-3-carbonyl)-8-hydroxy-5,5,7a,9,11b-pentamethyl-3,7-dioxo-tetradecahydronaphtho[2,1-c]oxepin-8-yl]acetate

Traditional Name

methyl [(1S,5aR,7aR,8R,9R,11aR,11bR)-1-(acetyloxy)-9-(furan-3-carbonyl)-8-hydroxy-5,5,7a,9,11b-pentamethyl-3,7-dioxo-hexahydro-1H-naphtho[2,1-c]oxepin-8-yl]acetate

CAS Registry Number

Not Available

SMILES

COC(=O)C[C@@]1(O)[C@@](C)(CC[C@@H]2[C@]3(C)[C@@H](CC(=O)[C@@]12C)C(C)(C)OC(=O)C[C@@H]3OC(C)=O)C(=O)C1=COC=C1

InChI Identifier

InChI=1S/C29H38O10/c1-16(30)38-21-13-22(32)39-25(2,3)19-12-20(31)28(6)18(27(19,21)5)8-10-26(4,24(34)17-9-11-37-15-17)29(28,35)14-23(33)36-7/h9,11,15,18-19,21,35H,8,10,12-14H2,1-7H3/t18-,19+,21+,26+,27-,28+,29-/m1/s1

InChI Key

OXGWTRSVBLAIAN-CSWCXXNHSA-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
Odontadenia macrantha	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Limonoids

Alternative Parents

Substituents

Limonoid skeleton
Tricarboxylic acid or derivatives
Caprolactone
Aryl ketone
Aryl alkyl ketone
Oxepane
Cyclic alcohol
Furan
Tertiary alcohol
Heteroaromatic compound
Methyl ester
Lactone
Ketone
Carboxylic acid ester
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Alcohol
Organic oxygen compound
Carbonyl group
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	2.49	ChemAxon
pKa (Strongest Acidic)	13.39	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	146.41 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	135.52 m³·mol⁻¹	ChemAxon
Polarizability	56.08 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	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

553024

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

637408

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-[(1s,5ar,7ar,8r,9r,11ar,11br)-1-(acetyloxy)-9-(furan-3-carbonyl)-8-hydroxy-5,5,7a,9,11b-pentamethyl-3,7-dioxo-hexahydro-1h-naphtho[2,1-c]oxepin-8-yl]acetate (NP0322985)

MOL for NP0322985 (methyl 2-[(1s,5ar,7ar,8r,9r,11ar,11br)-1-(acetyloxy)-9-(furan-3-carbonyl)-8-hydroxy-5,5,7a,9,11b-pentamethyl-3,7-dioxo-hexahydro-1h-naphtho[2,1-c]oxepin-8-yl]acetate)

3D MOL for NP0322985 (methyl 2-[(1s,5ar,7ar,8r,9r,11ar,11br)-1-(acetyloxy)-9-(furan-3-carbonyl)-8-hydroxy-5,5,7a,9,11b-pentamethyl-3,7-dioxo-hexahydro-1h-naphtho[2,1-c]oxepin-8-yl]acetate)

3D SDF for NP0322985 (methyl 2-[(1s,5ar,7ar,8r,9r,11ar,11br)-1-(acetyloxy)-9-(furan-3-carbonyl)-8-hydroxy-5,5,7a,9,11b-pentamethyl-3,7-dioxo-hexahydro-1h-naphtho[2,1-c]oxepin-8-yl]acetate)

3D-SDF for NP0322985 (methyl 2-[(1s,5ar,7ar,8r,9r,11ar,11br)-1-(acetyloxy)-9-(furan-3-carbonyl)-8-hydroxy-5,5,7a,9,11b-pentamethyl-3,7-dioxo-hexahydro-1h-naphtho[2,1-c]oxepin-8-yl]acetate)

PDB for NP0322985 (methyl 2-[(1s,5ar,7ar,8r,9r,11ar,11br)-1-(acetyloxy)-9-(furan-3-carbonyl)-8-hydroxy-5,5,7a,9,11b-pentamethyl-3,7-dioxo-hexahydro-1h-naphtho[2,1-c]oxepin-8-yl]acetate)

3D PDB for NP0322985 (methyl 2-[(1s,5ar,7ar,8r,9r,11ar,11br)-1-(acetyloxy)-9-(furan-3-carbonyl)-8-hydroxy-5,5,7a,9,11b-pentamethyl-3,7-dioxo-hexahydro-1h-naphtho[2,1-c]oxepin-8-yl]acetate)

SMILES for NP0322985 (methyl 2-[(1s,5ar,7ar,8r,9r,11ar,11br)-1-(acetyloxy)-9-(furan-3-carbonyl)-8-hydroxy-5,5,7a,9,11b-pentamethyl-3,7-dioxo-hexahydro-1h-naphtho[2,1-c]oxepin-8-yl]acetate)

INCHI for NP0322985 (methyl 2-[(1s,5ar,7ar,8r,9r,11ar,11br)-1-(acetyloxy)-9-(furan-3-carbonyl)-8-hydroxy-5,5,7a,9,11b-pentamethyl-3,7-dioxo-hexahydro-1h-naphtho[2,1-c]oxepin-8-yl]acetate)

Structure for NP0322985 (methyl 2-[(1s,5ar,7ar,8r,9r,11ar,11br)-1-(acetyloxy)-9-(furan-3-carbonyl)-8-hydroxy-5,5,7a,9,11b-pentamethyl-3,7-dioxo-hexahydro-1h-naphtho[2,1-c]oxepin-8-yl]acetate)

3D Structure for NP0322985 (methyl 2-[(1s,5ar,7ar,8r,9r,11ar,11br)-1-(acetyloxy)-9-(furan-3-carbonyl)-8-hydroxy-5,5,7a,9,11b-pentamethyl-3,7-dioxo-hexahydro-1h-naphtho[2,1-c]oxepin-8-yl]acetate)