NP-MRD: Showing NP-Card for (1s,2r,5s,6s,13s,14r,17r,18s)-6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-17-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadec-10-en-14-yl (2s)-2-methylbutanoate (NP0300959)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-10 13:38:53 UTC

Updated at

2022-09-10 13:38:54 UTC

NP-MRD ID

NP0300959

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,5s,6s,13s,14r,17r,18s)-6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-17-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadec-10-en-14-yl (2s)-2-methylbutanoate

Description

Moluccensin B 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. (1s,2r,5s,6s,13s,14r,17r,18s)-6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-17-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadec-10-en-14-yl (2s)-2-methylbutanoate is found in Xylocarpus moluccensis. Based on a literature review very few articles have been published on Moluccensin B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102215382D          

 47 52  0  0  1  0            999 V2000
   -4.5476    1.3610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8561    0.8836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0803    1.2620    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0576    2.1076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3019    0.9100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6480    0.1543    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4483    0.9686    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7166    0.4223    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6106   -0.4076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3866   -0.6503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2187    0.4295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3822   -0.1837    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1220    0.1637    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7038    0.9430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4217    0.6311    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7673    1.8245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8489    2.0291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3616    2.4068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3604    0.5551    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2698    1.4995    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2335    0.5873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2147    1.4954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8049   -0.0701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6216    0.0465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9289    0.8121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7457    0.9287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2008    1.6764    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2550    0.2797    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9476   -0.4859    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4570   -1.1349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2814   -1.1043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5653   -1.8789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9163   -2.3882    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2313   -1.9284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1309   -0.6025    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3990   -1.4121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8236   -1.3681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0068   -1.4847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4975   -0.8357    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6438   -0.9469    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7250   -1.8303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1661   -1.1698    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6153   -1.9227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3527   -2.3606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1176   -2.0107    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5480   -3.1927    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3437   -3.4807    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  1  6  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 12 19  1  0  0  0  0
  8 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  6  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 30 34  2  0  0  0  0
 29 35  1  0  0  0  0
 24 35  1  0  0  0  0
 35 36  1  6  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 39 38  1  6  0  0  0
 23 39  1  0  0  0  0
 39 40  1  0  0  0  0
 12 40  1  0  0  0  0
 40 41  1  1  0  0  0
 40 42  1  0  0  0  0
  9 42  1  0  0  0  0
 42 43  1  1  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 44 46  1  0  0  0  0
 46 47  1  0  0  0  0
M  END

     RDKit          2D

 93 98  0  0  0  0  0  0  0  0999 V2000
   -8.5037    8.9089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7537    7.6099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0037    6.3109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7047    7.0609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2537    5.0118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7649    4.8290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0037    3.7128    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2537    2.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6240    1.8037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9231    2.5537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4672    0.3119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8817   -1.2135    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3735   -1.0567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9836    0.3136    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2551   -2.2703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1368   -3.4838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4687   -1.3886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2500    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6399    2.6694    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7500    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8472    2.4970    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7500    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7500    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5000    2.5981    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5000    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7500   -1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1595   -1.8121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5730   -3.2540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0721   -3.3063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5851   -1.8968    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4031   -0.9733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7500   -1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -2.5981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5000   -2.5981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0000   -2.5981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7500   -1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2500   -1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0000   -2.5981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6876   -0.8710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9630   -2.3455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2384   -3.8201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5817   -4.4875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0991   -4.7958    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3745   -6.2703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2537   10.2080    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2047    9.6589    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8027    8.1589    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5558    8.5127    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0527    6.8599    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3027    5.5609    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4056    7.8109    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2907    8.4416    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8019    5.8629    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2896    3.5629    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2221    3.3037    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6731    1.2546    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1731    3.8527    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5821   -0.6916    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9226    0.6748    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0416   -3.1519    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0185   -4.6973    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0398   -4.5068    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.4488   -2.7566    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6822   -0.5069    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.4917   -2.4856    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9068    0.0022    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1783    3.0068    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1595    1.8121    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4895    2.7762    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0363   -2.7715    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6495   -4.4360    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9109   -4.5499    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4554    0.5258    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7500   -3.8971    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9439   -3.7639    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4419   -2.1847    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3680   -3.5823    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9386   -4.0325    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7395   -4.0753    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2435   -3.4369    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5000   -2.5981    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4134   -4.0400    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4943   -2.7290    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9210   -3.6401    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1571   -0.5699    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5990   -2.9695    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4375   -2.0702    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6499   -7.7448    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9000   -6.5457    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8490   -5.9949    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  1
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 16 18  1  0
 12 40  1  0
 40 41  1  1
 40 42  1  0
 42 43  1  0
 43 44  1  0
 44 45  2  0
 44 46  1  0
 46 47  1  0
 40 39  1  0
 39 38  1  0
 38 37  1  0
 37 35  1  0
 35 36  1  6
 35 29  1  0
 29 28  1  0
 28 26  1  0
 26 27  2  0
 26 25  1  0
 25 24  1  0
 24 23  2  0
 23 21  1  0
 21 22  2  0
 21 19  1  0
 19 20  1  6
 29 30  1  0
 30 34  2  0
 34 33  1  0
 33 32  1  0
 32 31  2  0
 19  8  1  0
 31 30  1  0
 42  9  1  0
 23 39  1  0
 19 12  1  0
 24 35  1  0
  1 48  1  0
  1 49  1  0
  1 50  1  0
  2 51  1  0
  2 52  1  0
  3 53  1  1
  4 54  1  0
  4 55  1  0
  4 56  1  0
  8 57  1  6
 10 58  1  0
 10 59  1  0
 10 60  1  0
 11 61  1  0
 11 62  1  0
 16 63  1  0
 17 64  1  0
 17 65  1  0
 17 66  1  0
 18 67  1  0
 18 68  1  0
 18 69  1  0
 41 85  1  0
 41 86  1  0
 41 87  1  0
 42 88  1  6
 43 89  1  0
 43 90  1  0
 47 91  1  0
 47 92  1  0
 47 93  1  0
 39 84  1  1
 38 82  1  0
 38 83  1  0
 37 80  1  0
 37 81  1  0
 36 77  1  0
 36 78  1  0
 36 79  1  0
 29 73  1  1
 25 71  1  0
 25 72  1  0
 20 70  1  0
 34 76  1  0
 32 75  1  0
 31 74  1  0
M  END


  Mrv1652309102215382D          

 47 52  0  0  1  0            999 V2000
   -4.5476    1.3610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8561    0.8836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0803    1.2620    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0576    2.1076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3019    0.9100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6480    0.1543    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4483    0.9686    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7166    0.4223    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6106   -0.4076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3866   -0.6503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2187    0.4295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3822   -0.1837    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1220    0.1637    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7038    0.9430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4217    0.6311    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7673    1.8245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8489    2.0291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3616    2.4068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3604    0.5551    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2698    1.4995    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2335    0.5873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2147    1.4954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8049   -0.0701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6216    0.0465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9289    0.8121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7457    0.9287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2008    1.6764    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2550    0.2797    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9476   -0.4859    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4570   -1.1349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2814   -1.1043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5653   -1.8789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9163   -2.3882    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2313   -1.9284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1309   -0.6025    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3990   -1.4121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8236   -1.3681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0068   -1.4847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4975   -0.8357    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6438   -0.9469    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7250   -1.8303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1661   -1.1698    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6153   -1.9227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3527   -2.3606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1176   -2.0107    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5480   -3.1927    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3437   -3.4807    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  1  6  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 12 19  1  0  0  0  0
  8 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  6  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 30 34  2  0  0  0  0
 29 35  1  0  0  0  0
 24 35  1  0  0  0  0
 35 36  1  6  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 39 38  1  6  0  0  0
 23 39  1  0  0  0  0
 39 40  1  0  0  0  0
 12 40  1  0  0  0  0
 40 41  1  1  0  0  0
 40 42  1  0  0  0  0
  9 42  1  0  0  0  0
 42 43  1  1  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 44 46  1  0  0  0  0
 46 47  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0300959

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H](C)C(=O)O[C@@H]1C2(C)C[C@@]3(OC(=O)C(C)C)[C@@](C)([C@H]2CC(=O)OC)[C@H]2CC[C@]4(C)[C@H](OC(=O)CC4=C2C(=O)[C@]13O)C1=COC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C36H46O11/c1-9-19(4)30(41)46-31-33(6)17-35(47-29(40)18(2)3)34(7,23(33)15-24(37)43-8)21-10-12-32(5)22(26(21)27(39)36(31,35)42)14-25(38)45-28(32)20-11-13-44-16-20/h11,13,16,18-19,21,23,28,31,42H,9-10,12,14-15,17H2,1-8H3/t19-,21-,23-,28+,31+,32-,33?,34+,35+,36-/m0/s1

> <INCHI_KEY>
LLNKVAPYAWFFFK-WJHJQCJRSA-N

> <FORMULA>
C36H46O11

> <MOLECULAR_WEIGHT>
654.753

> <EXACT_MASS>
654.304012301

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
93

> <JCHEM_AVERAGE_POLARIZABILITY>
42.002193641609956

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,5S,6S,13S,14R,17R,18S)-6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-17-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0^{2,11}.0^{5,10}.0^{13,17}]octadec-10-en-14-yl (2S)-2-methylbutanoate

> <JCHEM_LOGP>
4.6349150466666655

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.0533087741466

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8887854553341987

> <JCHEM_POLAR_SURFACE_AREA>
155.64

> <JCHEM_REFRACTIVITY>
164.73560000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,5S,6S,13S,14R,17R,18S)-6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-17-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0^{2,11}.0^{5,10}.0^{13,17}]octadec-10-en-14-yl (2S)-2-methylbutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      -8.489   2.541   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -7.198   1.649   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.750   2.356   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.708   3.934   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.297   1.699   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -4.943   0.288   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      -2.703   1.808   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -1.338   0.788   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.140  -0.761   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.588  -1.214   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.408   0.802   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.713  -0.343   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       2.094   0.306   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       3.180   1.760   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.520   1.178   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       3.299   3.406   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.585   3.788   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.408   4.493   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.673   1.036   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.504   2.799   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.303   1.096   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       2.267   2.791   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       3.369  -0.131   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.894   0.087   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.467   1.516   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.992   1.734   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       7.841   3.129   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       7.943   0.522   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       7.369  -0.907   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.320  -2.118   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.859  -2.061   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      10.389  -3.507   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       9.177  -4.458   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       7.899  -3.600   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.844  -1.125   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       6.345  -2.636   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       5.271  -2.554   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       3.746  -2.771   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       2.795  -1.560   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       1.202  -1.768   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       1.353  -3.417   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -0.310  -2.184   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -1.149  -3.589   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -2.525  -4.406   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      -3.953  -3.753   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0      -2.890  -5.960   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0      -4.375  -6.497   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   19                                                  
CONECT    9    8   10   11   42                                             
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   19   40                                             
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   12    8   20   21                                             
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   39                                                  
CONECT   24   23   25   35                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30   35                                                  
CONECT   30   29   31   34                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   30                                                       
CONECT   35   29   24   36   37                                             
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   23   40                                                  
CONECT   40   39   12   41   42                                             
CONECT   41   40                                                            
CONECT   42   40    9   43                                                  
CONECT   43   42   44                                                       
CONECT   44   43   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   47                                                       
CONECT   47   46                                                            
MASTER        0    0    0    0    0    0    0    0   47    0  104    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₆H₄₆O₁₁

Average Mass

654.7530 Da

Monoisotopic Mass

654.30401 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC[C@H](C)C(=O)O[C@@H]1C2(C)C[C@@]3(OC(=O)C(C)C)[C@@](C)([C@H]2CC(=O)OC)[C@H]2CC[C@]4(C)[C@H](OC(=O)CC4=C2C(=O)[C@]13O)C1=COC=C1

InChI Identifier

InChI=1S/C36H46O11/c1-9-19(4)30(41)46-31-33(6)17-35(47-29(40)18(2)3)34(7,23(33)15-24(37)43-8)21-10-12-32(5)22(26(21)27(39)36(31,35)42)14-25(38)45-28(32)20-11-13-44-16-20/h11,13,16,18-19,21,23,28,31,42H,9-10,12,14-15,17H2,1-8H3/t19-,21-,23-,28+,31+,32-,33?,34+,35+,36-/m0/s1

InChI Key

LLNKVAPYAWFFFK-WJHJQCJRSA-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
Xylocarpus moluccensis	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

Mexicanolide
Limonoid skeleton
Prostaglandin skeleton
Steroid lactone
Eicosanoid
12-beta-hydroxysteroid
2-oxosteroid
Oxosteroid
11-oxosteroid
Hydroxysteroid
12-hydroxysteroid
Steroid
3-oxasteroid
Naphthopyran
Tetracarboxylic acid or derivatives
Naphthalene
Delta_valerolactone
Fatty acid ester
Delta valerolactone
Fatty acyl
Pyran
Oxane
Heteroaromatic compound
Methyl ester
Tertiary alcohol
Furan
Cyclic alcohol
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00048011

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

102418507

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2r,5s,6s,13s,14r,17r,18s)-6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-17-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadec-10-en-14-yl (2s)-2-methylbutanoate (NP0300959)

MOL for NP0300959 ((1s,2r,5s,6s,13s,14r,17r,18s)-6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-17-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadec-10-en-14-yl (2s)-2-methylbutanoate)

3D MOL for NP0300959 ((1s,2r,5s,6s,13s,14r,17r,18s)-6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-17-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadec-10-en-14-yl (2s)-2-methylbutanoate)

3D SDF for NP0300959 ((1s,2r,5s,6s,13s,14r,17r,18s)-6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-17-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadec-10-en-14-yl (2s)-2-methylbutanoate)

3D-SDF for NP0300959 ((1s,2r,5s,6s,13s,14r,17r,18s)-6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-17-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadec-10-en-14-yl (2s)-2-methylbutanoate)

PDB for NP0300959 ((1s,2r,5s,6s,13s,14r,17r,18s)-6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-17-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadec-10-en-14-yl (2s)-2-methylbutanoate)

3D PDB for NP0300959 ((1s,2r,5s,6s,13s,14r,17r,18s)-6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-17-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadec-10-en-14-yl (2s)-2-methylbutanoate)

SMILES for NP0300959 ((1s,2r,5s,6s,13s,14r,17r,18s)-6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-17-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadec-10-en-14-yl (2s)-2-methylbutanoate)

INCHI for NP0300959 ((1s,2r,5s,6s,13s,14r,17r,18s)-6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-17-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadec-10-en-14-yl (2s)-2-methylbutanoate)

Structure for NP0300959 ((1s,2r,5s,6s,13s,14r,17r,18s)-6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-17-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadec-10-en-14-yl (2s)-2-methylbutanoate)

3D Structure for NP0300959 ((1s,2r,5s,6s,13s,14r,17r,18s)-6-(furan-3-yl)-13-hydroxy-18-(2-methoxy-2-oxoethyl)-1,5,15-trimethyl-17-[(2-methylpropanoyl)oxy]-8,12-dioxo-7-oxapentacyclo[13.2.1.0²,¹¹.0⁵,¹⁰.0¹³,¹⁷]octadec-10-en-14-yl (2s)-2-methylbutanoate)