NP-MRD: Showing NP-Card for godavarin J (NP0039873)

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Record Information

Version

2.0

Created at

2021-06-20 22:11:09 UTC

Updated at

2021-06-30 00:13:26 UTC

NP-MRD ID

NP0039873

Secondary Accession Numbers

None

Natural Product Identification

Common Name

godavarin J

Provided By

JEOL Database JEOL Logo

Description

Methyl 2-[(1R,2S,5R,6R,9R,13S,14R,16S)-14-(acetyloxy)-6-(furan-3-yl)-9-hydroxy-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]Heptadec-10-en-16-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. godavarin J is found in Xylocarpus moluccensis. godavarin J was first documented in 2010 (Li, J., et al.). Based on a literature review very few articles have been published on methyl 2-[(1R,2S,5R,6R,9R,13S,14R,16S)-14-(acetyloxy)-6-(furan-3-yl)-9-hydroxy-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]Heptadec-10-en-16-yl]acetate.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306212100113D          

 74 78  0  0  0  0            999 V2000
   -0.0635    2.4688   -5.2492 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4530    2.6806   -3.9342 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2262    2.0215   -2.9571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2090    1.3136   -3.1341 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3807    2.3289   -1.6028 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3466    1.1390   -0.6057 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4365    0.0222   -0.8704 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8820    0.5595   -0.7030 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3693   -0.5152   -2.3241 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1888   -1.1913    0.1154 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1812   -2.0645   -0.4500 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3863   -3.4019   -0.2767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6666   -4.1936   -0.9900 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2805   -3.8993    0.3916 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8038   -0.8130    1.5605 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6621   -0.9931    2.0039 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6369    0.0317    1.4208 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8336   -0.2926    0.8629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3314   -1.7214    0.7536 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4170   -2.2692    2.0709 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6781   -1.9517    0.0432 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.0807   -1.0498   -0.8726 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3063    0.1473   -1.0970 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1304    1.0946   -1.9267 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.7809    0.7500    0.2509 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -3.0364    2.0787   -0.0292 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1604    2.5283    1.1279 C   0  0  2  0  0  0  0  0  0  0  0  0
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    0.9088    3.0128    1.1599 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2299    3.1600   -1.2359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5996    0.6258   -0.8083 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1069    1.3427   -1.4342 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6120   -0.2423   -0.8685 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0902    0.9731    0.2835 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3531   -0.8093   -2.6054 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7217    0.2246   -3.0498 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0112   -1.3967   -2.4420 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.0349   -3.6432   -1.8605 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.9645   -2.0254    1.8148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7046   -0.8731    3.0962 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6038   -2.3077    0.1836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9982   -3.0532    2.0033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4491   -0.1584   -1.7158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2150    0.9906   -1.0759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7212    2.8194   -3.0812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7498    1.9423   -3.5136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5782    0.1498    1.4009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5588    1.8487    0.9329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5364    1.2788    2.2502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4185    1.9825   -0.9248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7547    2.8796   -0.2467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8051    2.7530    1.9876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6924    3.4828    0.8754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0012    1.6411    2.6409 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3752    3.8171    0.6503 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9010    3.2666    2.2272 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9526    3.0543    0.8289 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 37  1  0  0  0  0
 37 35  1  0  0  0  0
 30 24  1  0  0  0  0
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  3  2  1  0  0  0  0
 35 34  1  0  0  0  0
 21 22  2  0  0  0  0
  3  4  2  0  0  0  0
 35 36  1  6  0  0  0
 15 16  1  0  0  0  0
 30 31  1  1  0  0  0
  3  5  1  0  0  0  0
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 16 17  1  0  0  0  0
 33 34  1  0  0  0  0
  7  8  1  1  0  0  0
  6  5  1  0  0  0  0
 29 28  1  0  0  0  0
 28 27  1  0  0  0  0
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 26 25  1  0  0  0  0
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 34 17  1  0  0  0  0
 10 11  1  0  0  0  0
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 11 12  1  0  0  0  0
 30 32  1  0  0  0  0
 12 14  2  0  0  0  0
 30 18  1  0  0  0  0
 12 13  1  0  0  0  0
  2  1  1  0  0  0  0
  6  7  1  0  0  0  0
 37 38  2  0  0  0  0
  6 35  1  0  0  0  0
  7 10  1  0  0  0  0
  7  9  1  0  0  0  0
 10 15  1  0  0  0  0
 19 20  1  0  0  0  0
  8 45  1  0  0  0  0
  8 46  1  0  0  0  0
  8 47  1  0  0  0  0
  5 42  1  0  0  0  0
  5 43  1  0  0  0  0
  6 44  1  6  0  0  0
 10 51  1  1  0  0  0
 15 55  1  1  0  0  0
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 16 57  1  0  0  0  0
 33 69  1  0  0  0  0
 33 70  1  0  0  0  0
 32 67  1  0  0  0  0
 32 68  1  0  0  0  0
 19 58  1  6  0  0  0
 24 60  1  6  0  0  0
 36 72  1  0  0  0  0
 36 73  1  0  0  0  0
 36 74  1  0  0  0  0
 31 64  1  0  0  0  0
 31 65  1  0  0  0  0
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 29 63  1  0  0  0  0
 27 62  1  0  0  0  0
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 13 52  1  0  0  0  0
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 13 54  1  0  0  0  0
  1 39  1  0  0  0  0
  1 40  1  0  0  0  0
  1 41  1  0  0  0  0
  9 48  1  0  0  0  0
  9 49  1  0  0  0  0
  9 50  1  0  0  0  0
 20 59  1  0  0  0  0
M  END

     RDKit          3D

 74 78  0  0  0  0  0  0  0  0999 V2000
   -0.0635    2.4688   -5.2492 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4530    2.6806   -3.9342 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2262    2.0215   -2.9571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2090    1.3136   -3.1341 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3807    2.3289   -1.6028 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3466    1.1390   -0.6057 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4365    0.0222   -0.8704 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8820    0.5595   -0.7030 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3693   -0.5152   -2.3241 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1888   -1.1913    0.1154 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1812   -2.0645   -0.4500 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3863   -3.4019   -0.2767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6666   -4.1936   -0.9900 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.3314   -1.7214    0.7536 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4170   -2.2692    2.0709 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6781   -1.9517    0.0432 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3559   -2.9482    0.2965 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.0012    1.6411    2.6409 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.9010    3.2666    2.2272 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9526    3.0543    0.8289 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 37  1  0
 37 35  1  0
 30 24  1  0
 18 19  1  0
 19 21  1  0
 21 23  1  0
 23 24  1  0
  3  2  1  0
 35 34  1  0
 21 22  2  0
  3  4  2  0
 35 36  1  6
 15 16  1  0
 30 31  1  1
  3  5  1  0
 24 25  1  0
 25 29  2  0
 16 17  1  0
 33 34  1  0
  7  8  1  1
  6  5  1  0
 29 28  1  0
 28 27  1  0
 27 26  2  0
 26 25  1  0
 33 32  1  0
 34 71  1  1
 34 17  1  0
 10 11  1  0
 17 18  2  0
 11 12  1  0
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 12 14  2  0
 30 18  1  0
 12 13  1  0
  2  1  1  0
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 37 38  2  0
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  7 10  1  0
  7  9  1  0
 10 15  1  0
 19 20  1  0
  8 45  1  0
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  5 42  1  0
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 10 51  1  1
 15 55  1  1
 16 56  1  0
 16 57  1  0
 33 69  1  0
 33 70  1  0
 32 67  1  0
 32 68  1  0
 19 58  1  6
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 31 64  1  0
 31 65  1  0
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 27 62  1  0
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 13 52  1  0
 13 53  1  0
 13 54  1  0
  1 39  1  0
  1 40  1  0
  1 41  1  0
  9 48  1  0
  9 49  1  0
  9 50  1  0
 20 59  1  0
M  END


  Mrv1652306212100113D          

 74 78  0  0  0  0            999 V2000
   -0.0635    2.4688   -5.2492 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4530    2.6806   -3.9342 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2262    2.0215   -2.9571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2090    1.3136   -3.1341 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3807    2.3289   -1.6028 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3466    1.1390   -0.6057 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4365    0.0222   -0.8704 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8820    0.5595   -0.7030 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3693   -0.5152   -2.3241 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1888   -1.1913    0.1154 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1812   -2.0645   -0.4500 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3863   -3.4019   -0.2767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6666   -4.1936   -0.9900 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2805   -3.8993    0.3916 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8038   -0.8130    1.5605 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6621   -0.9931    2.0039 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6369    0.0317    1.4208 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8336   -0.2926    0.8629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3314   -1.7214    0.7536 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4170   -2.2692    2.0709 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6781   -1.9517    0.0432 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3559   -2.9482    0.2965 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0807   -1.0498   -0.8726 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3063    0.1473   -1.0970 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1304    1.0946   -1.9267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5188    1.3958   -1.7978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8178    2.3056   -2.7835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7143    2.5814   -3.5219 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7018    1.8379   -3.0103 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7809    0.7500    0.2509 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.9257    1.0170    1.2596 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0364    2.0787   -0.0292 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1604    2.5283    1.1279 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1293    1.4744    1.5584 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3049    1.6107    0.9184 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9088    3.0128    1.1599 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1293    0.6329    1.7723 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9735    0.9830    2.5946 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0928    2.8343   -5.3195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0087    1.4085   -5.5154 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5545    3.0350   -5.9514 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4010    2.7023   -1.7282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2299    3.1600   -1.2359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5996    0.6258   -0.8083 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1069    1.3427   -1.4342 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6120   -0.2423   -0.8685 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0902    0.9731    0.2835 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3531   -0.8093   -2.6054 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7217    0.2246   -3.0498 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0112   -1.3967   -2.4420 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1412   -1.7385    0.1565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0349   -3.6432   -1.8605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2299   -5.1294   -1.3496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4918   -4.4062   -0.3073 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4264   -1.4095    2.2402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9645   -2.0254    1.8148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7046   -0.8731    3.0962 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6038   -2.3077    0.1836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9982   -3.0532    2.0033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4491   -0.1584   -1.7158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2150    0.9906   -1.0759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7212    2.8194   -3.0812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7498    1.9423   -3.5136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5782    0.1498    1.4009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5588    1.8487    0.9329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5364    1.2788    2.2502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4185    1.9825   -0.9248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7547    2.8796   -0.2467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8051    2.7530    1.9876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6924    3.4828    0.8754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0012    1.6411    2.6409 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3752    3.8171    0.6503 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9010    3.2666    2.2272 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9526    3.0543    0.8289 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 37  1  0  0  0  0
 37 35  1  0  0  0  0
 30 24  1  0  0  0  0
 18 19  1  0  0  0  0
 19 21  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
  3  2  1  0  0  0  0
 35 34  1  0  0  0  0
 21 22  2  0  0  0  0
  3  4  2  0  0  0  0
 35 36  1  6  0  0  0
 15 16  1  0  0  0  0
 30 31  1  1  0  0  0
  3  5  1  0  0  0  0
 24 25  1  0  0  0  0
 25 29  2  0  0  0  0
 16 17  1  0  0  0  0
 33 34  1  0  0  0  0
  7  8  1  1  0  0  0
  6  5  1  0  0  0  0
 29 28  1  0  0  0  0
 28 27  1  0  0  0  0
 27 26  2  0  0  0  0
 26 25  1  0  0  0  0
 33 32  1  0  0  0  0
 34 71  1  1  0  0  0
 34 17  1  0  0  0  0
 10 11  1  0  0  0  0
 17 18  2  0  0  0  0
 11 12  1  0  0  0  0
 30 32  1  0  0  0  0
 12 14  2  0  0  0  0
 30 18  1  0  0  0  0
 12 13  1  0  0  0  0
  2  1  1  0  0  0  0
  6  7  1  0  0  0  0
 37 38  2  0  0  0  0
  6 35  1  0  0  0  0
  7 10  1  0  0  0  0
  7  9  1  0  0  0  0
 10 15  1  0  0  0  0
 19 20  1  0  0  0  0
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 10 51  1  1  0  0  0
 15 55  1  1  0  0  0
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 33 69  1  0  0  0  0
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 32 67  1  0  0  0  0
 32 68  1  0  0  0  0
 19 58  1  6  0  0  0
 24 60  1  6  0  0  0
 36 72  1  0  0  0  0
 36 73  1  0  0  0  0
 36 74  1  0  0  0  0
 31 64  1  0  0  0  0
 31 65  1  0  0  0  0
 31 66  1  0  0  0  0
 29 63  1  0  0  0  0
 27 62  1  0  0  0  0
 26 61  1  0  0  0  0
 13 52  1  0  0  0  0
 13 53  1  0  0  0  0
 13 54  1  0  0  0  0
  1 39  1  0  0  0  0
  1 40  1  0  0  0  0
  1 41  1  0  0  0  0
  9 48  1  0  0  0  0
  9 49  1  0  0  0  0
  9 50  1  0  0  0  0
 20 59  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0039873

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@@]1([H])C(=O)O[C@@]([H])(C2=C([H])OC([H])=C2[H])[C@]2(C1=C1C([H])([H])[C@]3([H])C(=O)[C@](C([H])([H])[H])([C@@]1([H])C([H])([H])C2([H])[H])[C@@]([H])(C([H])([H])C(=O)OC([H])([H])[H])C(C([H])([H])[H])(C([H])([H])[H])[C@]3([H])OC(=O)C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C29H36O9/c1-14(30)37-25-17-11-16-18(29(5,23(17)33)19(27(25,2)3)12-20(31)35-6)7-9-28(4)21(16)22(32)26(34)38-24(28)15-8-10-36-13-15/h8,10,13,17-19,22,24-25,32H,7,9,11-12H2,1-6H3/t17-,18+,19+,22-,24+,25-,28-,29-/m1/s1

> <INCHI_KEY>
KVEVULZYQPAVGE-IMPNESGQSA-N

> <FORMULA>
C29H36O9

> <MOLECULAR_WEIGHT>
528.598

> <EXACT_MASS>
528.235932739

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
74

> <JCHEM_AVERAGE_POLARIZABILITY>
53.955966113246525

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 2-[(1R,2S,5R,6R,9R,13S,14R,16S)-14-(acetyloxy)-6-(furan-3-yl)-9-hydroxy-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0^{2,11}.0^{5,10}]heptadec-10-en-16-yl]acetate

> <ALOGPS_LOGP>
3.26

> <JCHEM_LOGP>
2.7632036993333315

> <ALOGPS_LOGS>
-3.99

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.167087561670584

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.100636790748451

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8888525709943202

> <JCHEM_POLAR_SURFACE_AREA>
129.34

> <JCHEM_REFRACTIVITY>
133.153

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.39e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl [(1R,2S,5R,6R,9R,13S,14R,16S)-14-(acetyloxy)-6-(furan-3-yl)-9-hydroxy-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0^{2,11}.0^{5,10}]heptadec-10-en-16-yl]acetate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 74 78  0  0  0  0  0  0  0  0999 V2000
   -0.0635    2.4688   -5.2492 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4530    2.6806   -3.9342 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2262    2.0215   -2.9571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2090    1.3136   -3.1341 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3807    2.3289   -1.6028 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3466    1.1390   -0.6057 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4365    0.0222   -0.8704 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8820    0.5595   -0.7030 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3693   -0.5152   -2.3241 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1888   -1.1913    0.1154 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1812   -2.0645   -0.4500 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3863   -3.4019   -0.2767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6666   -4.1936   -0.9900 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.8038   -0.8130    1.5605 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6621   -0.9931    2.0039 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6369    0.0317    1.4208 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.3314   -1.7214    0.7536 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -5.3559   -2.9482    0.2965 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0807   -1.0498   -0.8726 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3063    0.1473   -1.0970 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1304    1.0946   -1.9267 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.0364    2.0787   -0.0292 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1604    2.5283    1.1279 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.9088    3.0128    1.1599 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1293    0.6329    1.7723 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9735    0.9830    2.5946 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0928    2.8343   -5.3195 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.4010    2.7023   -1.7282 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.5996    0.6258   -0.8083 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.3531   -0.8093   -2.6054 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.0112   -1.3967   -2.4420 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1412   -1.7385    0.1565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0349   -3.6432   -1.8605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2299   -5.1294   -1.3496 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.9645   -2.0254    1.8148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7046   -0.8731    3.0962 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6038   -2.3077    0.1836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9982   -3.0532    2.0033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4491   -0.1584   -1.7158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2150    0.9906   -1.0759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7212    2.8194   -3.0812 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.5782    0.1498    1.4009 H   0  0  0  0  0  0  0  0  0  0  0  0
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 20 59  1  0
M  END

HEADER    PROTEIN                                 21-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   21-JUN-21         0                                  
HETATM    1  C   UNK     0      -0.064   2.469  -5.249  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.453   2.681  -3.934  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.226   2.022  -2.957  0.00  0.00           C+0
HETATM    4  O   UNK     0      -1.209   1.314  -3.134  0.00  0.00           O+0
HETATM    5  C   UNK     0       0.381   2.329  -1.603  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.347   1.139  -0.606  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.437   0.022  -0.870  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.882   0.560  -0.703  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.369  -0.515  -2.324  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.189  -1.191   0.115  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.181  -2.064  -0.450  0.00  0.00           O+0
HETATM   12  C   UNK     0       0.386  -3.402  -0.277  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.667  -4.194  -0.990  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.281  -3.899   0.392  0.00  0.00           O+0
HETATM   15  C   UNK     0       0.804  -0.813   1.561  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.662  -0.993   2.004  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.637   0.032   1.421  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.834  -0.293   0.863  0.00  0.00           C+0
HETATM   19  C   UNK     0      -3.331  -1.721   0.754  0.00  0.00           C+0
HETATM   20  O   UNK     0      -3.417  -2.269   2.071  0.00  0.00           O+0
HETATM   21  C   UNK     0      -4.678  -1.952   0.043  0.00  0.00           C+0
HETATM   22  O   UNK     0      -5.356  -2.948   0.297  0.00  0.00           O+0
HETATM   23  O   UNK     0      -5.081  -1.050  -0.873  0.00  0.00           O+0
HETATM   24  C   UNK     0      -4.306   0.147  -1.097  0.00  0.00           C+0
HETATM   25  C   UNK     0      -5.130   1.095  -1.927  0.00  0.00           C+0
HETATM   26  C   UNK     0      -6.519   1.396  -1.798  0.00  0.00           C+0
HETATM   27  C   UNK     0      -6.818   2.306  -2.784  0.00  0.00           C+0
HETATM   28  O   UNK     0      -5.714   2.581  -3.522  0.00  0.00           O+0
HETATM   29  C   UNK     0      -4.702   1.838  -3.010  0.00  0.00           C+0
HETATM   30  C   UNK     0      -3.781   0.750   0.251  0.00  0.00           C+0
HETATM   31  C   UNK     0      -4.926   1.017   1.260  0.00  0.00           C+0
HETATM   32  C   UNK     0      -3.036   2.079  -0.029  0.00  0.00           C+0
HETATM   33  C   UNK     0      -2.160   2.528   1.128  0.00  0.00           C+0
HETATM   34  C   UNK     0      -1.129   1.474   1.558  0.00  0.00           C+0
HETATM   35  C   UNK     0       0.305   1.611   0.918  0.00  0.00           C+0
HETATM   36  C   UNK     0       0.909   3.013   1.160  0.00  0.00           C+0
HETATM   37  C   UNK     0       1.129   0.633   1.772  0.00  0.00           C+0
HETATM   38  O   UNK     0       1.974   0.983   2.595  0.00  0.00           O+0
HETATM   39  H   UNK     0      -1.093   2.834  -5.319  0.00  0.00           H+0
HETATM   40  H   UNK     0      -0.009   1.409  -5.515  0.00  0.00           H+0
HETATM   41  H   UNK     0       0.555   3.035  -5.951  0.00  0.00           H+0
HETATM   42  H   UNK     0       1.401   2.702  -1.728  0.00  0.00           H+0
HETATM   43  H   UNK     0      -0.230   3.160  -1.236  0.00  0.00           H+0
HETATM   44  H   UNK     0      -0.600   0.626  -0.808  0.00  0.00           H+0
HETATM   45  H   UNK     0       3.107   1.343  -1.434  0.00  0.00           H+0
HETATM   46  H   UNK     0       3.612  -0.242  -0.869  0.00  0.00           H+0
HETATM   47  H   UNK     0       3.090   0.973   0.284  0.00  0.00           H+0
HETATM   48  H   UNK     0       0.353  -0.809  -2.605  0.00  0.00           H+0
HETATM   49  H   UNK     0       1.722   0.225  -3.050  0.00  0.00           H+0
HETATM   50  H   UNK     0       2.011  -1.397  -2.442  0.00  0.00           H+0
HETATM   51  H   UNK     0       2.141  -1.738   0.157  0.00  0.00           H+0
HETATM   52  H   UNK     0      -1.035  -3.643  -1.861  0.00  0.00           H+0
HETATM   53  H   UNK     0      -0.230  -5.129  -1.350  0.00  0.00           H+0
HETATM   54  H   UNK     0      -1.492  -4.406  -0.307  0.00  0.00           H+0
HETATM   55  H   UNK     0       1.426  -1.410   2.240  0.00  0.00           H+0
HETATM   56  H   UNK     0      -0.965  -2.025   1.815  0.00  0.00           H+0
HETATM   57  H   UNK     0      -0.705  -0.873   3.096  0.00  0.00           H+0
HETATM   58  H   UNK     0      -2.604  -2.308   0.184  0.00  0.00           H+0
HETATM   59  H   UNK     0      -3.998  -3.053   2.003  0.00  0.00           H+0
HETATM   60  H   UNK     0      -3.449  -0.158  -1.716  0.00  0.00           H+0
HETATM   61  H   UNK     0      -7.215   0.991  -1.076  0.00  0.00           H+0
HETATM   62  H   UNK     0      -7.721   2.819  -3.081  0.00  0.00           H+0
HETATM   63  H   UNK     0      -3.750   1.942  -3.514  0.00  0.00           H+0
HETATM   64  H   UNK     0      -5.578   0.150   1.401  0.00  0.00           H+0
HETATM   65  H   UNK     0      -5.559   1.849   0.933  0.00  0.00           H+0
HETATM   66  H   UNK     0      -4.536   1.279   2.250  0.00  0.00           H+0
HETATM   67  H   UNK     0      -2.418   1.982  -0.925  0.00  0.00           H+0
HETATM   68  H   UNK     0      -3.755   2.880  -0.247  0.00  0.00           H+0
HETATM   69  H   UNK     0      -2.805   2.753   1.988  0.00  0.00           H+0
HETATM   70  H   UNK     0      -1.692   3.483   0.875  0.00  0.00           H+0
HETATM   71  H   UNK     0      -1.001   1.641   2.641  0.00  0.00           H+0
HETATM   72  H   UNK     0       0.375   3.817   0.650  0.00  0.00           H+0
HETATM   73  H   UNK     0       0.901   3.267   2.227  0.00  0.00           H+0
HETATM   74  H   UNK     0       1.953   3.054   0.829  0.00  0.00           H+0
CONECT    1    2   39   40   41                                             
CONECT    2    3    1                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   42   43                                             
CONECT    6    5    7   35   44                                             
CONECT    7    8    6   10    9                                             
CONECT    8    7   45   46   47                                             
CONECT    9    7   48   49   50                                             
CONECT   10   11    7   15   51                                             
CONECT   11   10   12                                                       
CONECT   12   11   14   13                                                  
CONECT   13   12   52   53   54                                             
CONECT   14   12                                                            
CONECT   15   37   16   10   55                                             
CONECT   16   15   17   56   57                                             
CONECT   17   16   34   18                                                  
CONECT   18   19   17   30                                                  
CONECT   19   18   21   20   58                                             
CONECT   20   19   59                                                       
CONECT   21   19   23   22                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   30   23   25   60                                             
CONECT   25   24   29   26                                                  
CONECT   26   27   25   61                                                  
CONECT   27   28   26   62                                                  
CONECT   28   29   27                                                       
CONECT   29   25   28   63                                                  
CONECT   30   24   31   32   18                                             
CONECT   31   30   64   65   66                                             
CONECT   32   33   30   67   68                                             
CONECT   33   34   32   69   70                                             
CONECT   34   35   33   71   17                                             
CONECT   35   37   34   36    6                                             
CONECT   36   35   72   73   74                                             
CONECT   37   15   35   38                                                  
CONECT   38   37                                                            
CONECT   39    1                                                            
CONECT   40    1                                                            
CONECT   41    1                                                            
CONECT   42    5                                                            
CONECT   43    5                                                            
CONECT   44    6                                                            
CONECT   45    8                                                            
CONECT   46    8                                                            
CONECT   47    8                                                            
CONECT   48    9                                                            
CONECT   49    9                                                            
CONECT   50    9                                                            
CONECT   51   10                                                            
CONECT   52   13                                                            
CONECT   53   13                                                            
CONECT   54   13                                                            
CONECT   55   15                                                            
CONECT   56   16                                                            
CONECT   57   16                                                            
CONECT   58   19                                                            
CONECT   59   20                                                            
CONECT   60   24                                                            
CONECT   61   26                                                            
CONECT   62   27                                                            
CONECT   63   29                                                            
CONECT   64   31                                                            
CONECT   65   31                                                            
CONECT   66   31                                                            
CONECT   67   32                                                            
CONECT   68   32                                                            
CONECT   69   33                                                            
CONECT   70   33                                                            
CONECT   71   34                                                            
CONECT   72   36                                                            
CONECT   73   36                                                            
CONECT   74   36                                                            
MASTER        0    0    0    0    0    0    0    0   74    0  156    0
END

RDKit          3D

74 78  0  0  0  0  0  0  0  0999 V2000
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    1.4365    0.0222   -0.8704 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8820    0.5595   -0.7030 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3693   -0.5152   -2.3241 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1888   -1.1913    0.1154 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1812   -2.0645   -0.4500 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.1293    1.4744    1.5584 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3049    1.6107    0.9184 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9088    3.0128    1.1599 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.9735    0.9830    2.5946 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.1069    1.3427   -1.4342 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6120   -0.2423   -0.8685 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0902    0.9731    0.2835 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3531   -0.8093   -2.6054 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7217    0.2246   -3.0498 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0112   -1.3967   -2.4420 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1412   -1.7385    0.1565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0349   -3.6432   -1.8605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2299   -5.1294   -1.3496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4918   -4.4062   -0.3073 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4264   -1.4095    2.2402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9645   -2.0254    1.8148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7046   -0.8731    3.0962 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6038   -2.3077    0.1836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9982   -3.0532    2.0033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4491   -0.1584   -1.7158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2150    0.9906   -1.0759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7212    2.8194   -3.0812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7498    1.9423   -3.5136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5782    0.1498    1.4009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5588    1.8487    0.9329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5364    1.2788    2.2502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4185    1.9825   -0.9248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7547    2.8796   -0.2467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8051    2.7530    1.9876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6924    3.4828    0.8754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0012    1.6411    2.6409 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3752    3.8171    0.6503 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9010    3.2666    2.2272 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9526    3.0543    0.8289 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 37  1  0
 37 35  1  0
 30 24  1  0
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 20 59  1  0
M  END

View in JSmol

Synonyms

Value	Source
Methyl 2-[(1R,2S,5R,6R,9R,13S,14R,16S)-14-(acetyloxy)-6-(furan-3-yl)-9-hydroxy-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0,.0,]heptadec-10-en-16-yl]acetic acid	Generator

Chemical Formula

C₂₉H₃₆O₉

Average Mass

528.5980 Da

Monoisotopic Mass

528.23593 Da

IUPAC Name

methyl 2-[(1R,2S,5R,6R,9R,13S,14R,16S)-14-(acetyloxy)-6-(furan-3-yl)-9-hydroxy-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0^{2,11}.0^{5,10}]heptadec-10-en-16-yl]acetate

Traditional Name

methyl [(1R,2S,5R,6R,9R,13S,14R,16S)-14-(acetyloxy)-6-(furan-3-yl)-9-hydroxy-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0^{2,11}.0^{5,10}]heptadec-10-en-16-yl]acetate

CAS Registry Number

Not Available

SMILES

[H]O[C@@]1([H])C(=O)O[C@@]([H])(C2=C([H])OC([H])=C2[H])[C@]2(C1=C1C([H])([H])[C@]3([H])C(=O)[C@](C([H])([H])[H])([C@@]1([H])C([H])([H])C2([H])[H])[C@@]([H])(C([H])([H])C(=O)OC([H])([H])[H])C(C([H])([H])[H])(C([H])([H])[H])[C@]3([H])OC(=O)C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C29H36O9/c1-14(30)37-25-17-11-16-18(29(5,23(17)33)19(27(25,2)3)12-20(31)35-6)7-9-28(4)21(16)22(32)26(34)38-24(28)15-8-10-36-13-15/h8,10,13,17-19,22,24-25,32H,7,9,11-12H2,1-6H3/t17-,18+,19+,22-,24+,25-,28-,29-/m1/s1

InChI Key

KVEVULZYQPAVGE-IMPNESGQSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Xylocarpus moluccensis	JEOL database	Li, J., et al, Phytochem. 71, 1917 (2010)

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
Mexicanolide
Naphthopyran
Naphthalene
Tricarboxylic acid or derivatives
Delta valerolactone
Delta_valerolactone
Oxane
Pyran
Furan
Heteroaromatic compound
Methyl ester
Lactone
Ketone
Carboxylic acid ester
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Alcohol
Organic oxygen compound
Organooxygen 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	3.26	ALOGPS
logP	2.76	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	12.1	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	129.34 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	133.15 m³·mol⁻¹	ChemAxon
Polarizability	53.96 Å³	ChemAxon
Number of Rings	5	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

29214377

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

49818113

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Li, J., et al. (2010). Li, J., et al, Phytochem. 71, 1917 (2010). Phytochem..

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