NP-MRD: Showing NP-Card for (1r,2s,3s,4s,6s,8s,9s,10r,11s,16r,17r,19s,20r)-2,8,9,10,17-pentakis(acetyloxy)-1,11-dihydroxy-3,7,7,17-tetramethyl-14-oxo-5,15-dioxatetracyclo[9.7.2.0⁴,⁶.0¹⁶,¹⁹]icosan-20-yl benzoate (NP0230767)

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Record Information

Version

2.0

Created at

2022-09-06 11:19:52 UTC

Updated at

2022-09-06 11:19:52 UTC

NP-MRD ID

NP0230767

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,3s,4s,6s,8s,9s,10r,11s,16r,17r,19s,20r)-2,8,9,10,17-pentakis(acetyloxy)-1,11-dihydroxy-3,7,7,17-tetramethyl-14-oxo-5,15-dioxatetracyclo[9.7.2.0⁴,⁶.0¹⁶,¹⁹]icosan-20-yl benzoate

Description

(1R,2S,3S,4S,6S,8S,9S,10R,11S,16R,17R,19S,20R)-2,8,9,10,17-pentakis(acetyloxy)-1,11-dihydroxy-3,7,7,17-tetramethyl-14-oxo-5,15-dioxatetracyclo[9.7.2.0⁴,⁶.0¹⁶,¹⁹]Icosan-20-yl benzoate belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members. (1r,2s,3s,4s,6s,8s,9s,10r,11s,16r,17r,19s,20r)-2,8,9,10,17-pentakis(acetyloxy)-1,11-dihydroxy-3,7,7,17-tetramethyl-14-oxo-5,15-dioxatetracyclo[9.7.2.0⁴,⁶.0¹⁶,¹⁹]icosan-20-yl benzoate is found in Euphorbia guyoniana. Based on a literature review very few articles have been published on (1R,2S,3S,4S,6S,8S,9S,10R,11S,16R,17R,19S,20R)-2,8,9,10,17-pentakis(acetyloxy)-1,11-dihydroxy-3,7,7,17-tetramethyl-14-oxo-5,15-dioxatetracyclo[9.7.2.0⁴,⁶.0¹⁶,¹⁹]Icosan-20-yl benzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062213192D          

 56 60  0  0  1  0            999 V2000
    4.8285    2.9130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5464    1.7810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7381    1.6158    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1147    1.5130    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8536    0.7304    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4008    0.1130    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6619    0.8956    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4702    1.0609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7312    1.8435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0174    0.4435    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2091    0.2782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9122    0.7100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9061    1.0456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7353   -0.6885    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.3036   -0.9565    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4743   -1.4711    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6660   -1.6364    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1187   -1.0190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4049   -2.4190    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9732   -2.6870    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7815   -2.5217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0215   -2.0885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3287   -3.1391    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6177   -2.2348    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1398   -2.8736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2948   -2.9940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4730   -2.9216    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6541   -3.0216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4869   -3.7465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7795   -4.1709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7933   -4.9958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0582   -3.7705    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2880   -2.1176    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4876   -1.9175    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0631   -1.2101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2471   -1.3315    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2632   -0.4097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9707    0.0147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7843   -0.2174    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3993    0.5123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0453    0.5652    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4981    1.1826    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7592    1.9652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5674    2.1304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2119    2.5826    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3315   -0.8348    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1398   -0.6696    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6870   -1.2870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4260   -2.0696    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4953   -1.1217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7564   -0.3391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5647   -0.1739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1119   -0.7913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8508   -1.5739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0425   -1.7391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0704   -1.6174    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  6  0  0  0
 16 15  1  1  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  6  0  0  0
 27 29  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
 27 33  1  0  0  0  0
 33 34  1  6  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  6  0  0  0
 39 41  1  0  0  0  0
  5 41  1  0  0  0  0
 41 42  1  6  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 43 45  2  0  0  0  0
 39 46  1  0  0  0  0
 46 47  1  6  0  0  0
 47 48  1  0  0  0  0
 48 49  2  0  0  0  0
 48 50  1  0  0  0  0
 50 51  2  0  0  0  0
 51 52  1  0  0  0  0
 52 53  2  0  0  0  0
 53 54  1  0  0  0  0
 54 55  2  0  0  0  0
 50 55  1  0  0  0  0
 46 56  1  0  0  0  0
 56 33  1  6  0  0  0
 24 56  1  0  0  0  0
M  END

     RDKit          3D

106110  0  0  0  0  0  0  0  0999 V2000
    4.8744    0.3527   -3.7017 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8235   -0.2163   -2.8200 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2318   -1.2929   -3.0668 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4927    0.4695   -1.6919 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4982    0.0808   -0.7282 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3179   -0.1851    0.4733 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2730    0.8497    0.5822 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5930    0.8174    0.2798 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5211    1.9634    0.4303 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9856   -0.2955   -0.1525 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8981   -0.8016    1.7107 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2089   -1.2278    2.4323 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1636   -0.0157    2.7419 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1535   -2.1212    1.5784 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8871   -2.5072    0.3142 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8681   -1.9347    1.0334 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2594   -2.8813    1.2907 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1190   -4.2138    0.6218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5944   -2.2432    0.8503 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5525   -3.2205    1.0786 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5284   -3.0299    2.0434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5648   -4.0545    2.3108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5073   -1.9637    2.6835 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5214   -1.7319   -0.5855 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2982   -2.1531   -1.0586 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5268   -2.5342   -1.3768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5660   -1.5918   -1.8757 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1293   -2.0705   -3.2110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6173   -1.3777   -0.9463 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5245   -2.3316   -0.5714 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5708   -1.9474    0.4177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4383   -3.4797   -1.0719 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8274   -0.3091   -2.0111 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0630   -0.3231   -3.1940 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3587    0.6710   -3.8830 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0747    0.3214   -5.0500 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8985    2.0062   -3.5228 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1904    2.0975   -2.5250 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2344    0.8861   -1.5532 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4553   -0.1598   -2.4586 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4730    1.1484   -0.7086 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1073    2.3601   -1.0990 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1652    3.4920   -0.3144 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8550    4.7013   -0.8289 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6208    3.4150    0.7963 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0422    0.8222   -0.8446 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8854    1.3759    0.4546 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4878    2.5546    0.8674 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2148    3.1475   -0.0003 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3628    3.1575    2.1777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0110    4.3414    2.4336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9431    4.9806    3.6617 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2039    4.4286    4.6814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5487    3.2447    4.4443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6298    2.6223    3.2097 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9042   -0.3552   -0.7765 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8534    0.0730   -3.2179 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8641    1.4653   -3.6878 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7685   -0.0622   -4.7019 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0624   -0.8095   -1.2043 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9979   -1.0224    0.0741 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5740    2.5752   -0.4940 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5456    1.6131    0.6316 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2336    2.5976    1.3172 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7448   -0.3338    2.8115 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9591   -1.8377    3.3255 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8309   -1.8484    1.7885 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5480   -0.1619    3.7759 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1264    1.0616    2.5800 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0910   -0.3341    2.8186 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2797   -2.8671    2.4046 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5141   -0.9149    0.9643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3782   -3.0237    2.3911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0435   -5.0523    1.3454 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8549   -4.1803    0.0503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8962   -4.3914   -0.1461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7673   -1.3602    1.5122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4258   -3.5361    2.7856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1263   -4.7890    3.0165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9257   -4.5551    1.4099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3040   -2.7429   -1.8257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9582   -3.3716   -0.7753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0348   -2.9608   -2.3065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6026   -1.4979   -4.0017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1977   -1.8364   -3.2309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8865   -3.1263   -3.3396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3308   -1.2719   -0.0206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0301   -2.8511    0.8969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0310   -1.4272    1.2584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4857    0.5880   -1.9503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7654    2.6138   -3.1227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5926    2.5915   -4.4395 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.1704    2.0202   -3.0797 H   0  0  0  0  0  0  0  0  0  0  0  0
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 22 80  1  0
M  END


  Mrv1652309062213192D          

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    2.4876   -1.9175    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    1.2471   -1.3315    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
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  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
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 27 33  1  0  0  0  0
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 35 36  2  0  0  0  0
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 39 40  1  6  0  0  0
 39 41  1  0  0  0  0
  5 41  1  0  0  0  0
 41 42  1  6  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 43 45  2  0  0  0  0
 39 46  1  0  0  0  0
 46 47  1  6  0  0  0
 47 48  1  0  0  0  0
 48 49  2  0  0  0  0
 48 50  1  0  0  0  0
 50 51  2  0  0  0  0
 51 52  1  0  0  0  0
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 53 54  1  0  0  0  0
 54 55  2  0  0  0  0
 50 55  1  0  0  0  0
 46 56  1  0  0  0  0
 56 33  1  6  0  0  0
 24 56  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0230767

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C39H50O17/c1-18-27-32(54-27)36(7,8)33(51-21(4)42)28(49-19(2)40)34(52-22(5)43)38(47)16-15-25(45)53-30-26(31(38)55-35(46)24-13-11-10-12-14-24)39(48,29(18)50-20(3)41)17-37(30,9)56-23(6)44/h10-14,18,26-34,47-48H,15-17H2,1-9H3/t18-,26+,27-,28-,29-,30+,31+,32+,33+,34+,37+,38-,39+/m0/s1

> <INCHI_KEY>
AYEWXCGYVJFQDW-WRKUMONDSA-N

> <FORMULA>
C39H50O17

> <MOLECULAR_WEIGHT>
790.812

> <EXACT_MASS>
790.30480015

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
106

> <JCHEM_AVERAGE_POLARIZABILITY>
77.77744880353863

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S,3S,4S,6S,8S,9S,10R,11S,16R,17R,19S,20R)-2,8,9,10,17-pentakis(acetyloxy)-1,11-dihydroxy-3,7,7,17-tetramethyl-14-oxo-5,15-dioxatetracyclo[9.7.2.0^{4,6}.0^{16,19}]icosan-20-yl benzoate

> <JCHEM_LOGP>
1.2383274006666682

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.428305719834906

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.637829762313938

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5332215839140098

> <JCHEM_POLAR_SURFACE_AREA>
237.08999999999995

> <JCHEM_REFRACTIVITY>
184.48139999999992

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,3S,4S,6S,8S,9S,10R,11S,16R,17R,19S,20R)-2,8,9,10,17-pentakis(acetyloxy)-1,11-dihydroxy-3,7,7,17-tetramethyl-14-oxo-5,15-dioxatetracyclo[9.7.2.0^{4,6}.0^{16,19}]icosan-20-yl benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       9.013   5.438   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.487   3.325   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       6.978   3.016   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       9.547   2.824   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       9.060   1.363   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.082   0.211   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      10.569   1.672   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      12.078   1.980   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.565   3.441   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      13.099   0.828   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      11.590   0.519   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.903   1.325   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.025   1.952   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.573  -1.285   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      13.633  -1.786   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      12.085  -2.746   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.576  -3.055   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.555  -1.902   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.089  -4.515   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      11.150  -5.016   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      12.659  -4.707   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      13.107  -3.899   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      13.680  -5.860   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       8.620  -4.172   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       9.594  -5.364   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       8.017  -5.589   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.483  -5.454   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.954  -5.640   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       6.509  -6.993   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       5.188  -7.786   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.214  -9.325   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       3.842  -7.038   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       6.138  -3.953   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       4.643  -3.579   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       3.851  -2.259   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       2.328  -2.485   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       4.225  -0.765   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       5.545   0.028   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       7.064  -0.406   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       6.345   0.956   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       7.551   1.055   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       6.530   2.207   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       7.017   3.668   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       8.526   3.977   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       5.996   4.821   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       8.085  -1.558   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0       9.594  -1.250   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0      10.616  -2.402   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      10.128  -3.863   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0      12.125  -2.094   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      12.612  -0.633   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      14.121  -0.325   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      15.142  -1.477   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      14.655  -2.938   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      13.146  -3.246   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0       7.598  -3.019   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   41                                                  
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    6   12   13   14                                             
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14   11   15   16                                                  
CONECT   15   14   16                                                       
CONECT   16   15   14   17                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   19   25   26   56                                             
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28   29   33                                             
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33   27   34   56                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40   41   46                                             
CONECT   40   39                                                            
CONECT   41   39    5   42                                                  
CONECT   42   41   43                                                       
CONECT   43   42   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43                                                            
CONECT   46   39   47   56                                                  
CONECT   47   46   48                                                       
CONECT   48   47   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48   51   55                                                  
CONECT   51   50   52                                                       
CONECT   52   51   53                                                       
CONECT   53   52   54                                                       
CONECT   54   53   55                                                       
CONECT   55   54   50                                                       
CONECT   56   46   33   24                                                  
MASTER        0    0    0    0    0    0    0    0   56    0  120    0
END

View in JSmol

Synonyms

Value	Source
(1R,2S,3S,4S,6S,8S,9S,10R,11S,16R,17R,19S,20R)-2,8,9,10,17-Pentakis(acetyloxy)-1,11-dihydroxy-3,7,7,17-tetramethyl-14-oxo-5,15-dioxatetracyclo[9.7.2.0,.0,]icosan-20-yl benzoic acid	Generator

Chemical Formula

C₃₉H₅₀O₁₇

Average Mass

790.8120 Da

Monoisotopic Mass

790.30480 Da

IUPAC Name

(1R,2S,3S,4S,6S,8S,9S,10R,11S,16R,17R,19S,20R)-2,8,9,10,17-pentakis(acetyloxy)-1,11-dihydroxy-3,7,7,17-tetramethyl-14-oxo-5,15-dioxatetracyclo[9.7.2.0^{4,6}.0^{16,19}]icosan-20-yl benzoate

Traditional Name

(1R,2S,3S,4S,6S,8S,9S,10R,11S,16R,17R,19S,20R)-2,8,9,10,17-pentakis(acetyloxy)-1,11-dihydroxy-3,7,7,17-tetramethyl-14-oxo-5,15-dioxatetracyclo[9.7.2.0^{4,6}.0^{16,19}]icosan-20-yl benzoate

CAS Registry Number

Not Available

SMILES

C[C@H]1[C@@H]2O[C@H]2C(C)(C)[C@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@]2(O)CCC(=O)O[C@@H]3[C@H]([C@H]2OC(=O)C2=CC=CC=C2)[C@](O)(C[C@@]3(C)OC(C)=O)[C@H]1OC(C)=O

InChI Identifier

InChI=1S/C39H50O17/c1-18-27-32(54-27)36(7,8)33(51-21(4)42)28(49-19(2)40)34(52-22(5)43)38(47)16-15-25(45)53-30-26(31(38)55-35(46)24-13-11-10-12-14-24)39(48,29(18)50-20(3)41)17-37(30,9)56-23(6)44/h10-14,18,26-34,47-48H,15-17H2,1-9H3/t18-,26+,27-,28-,29-,30+,31+,32+,33+,34+,37+,38-,39+/m0/s1

InChI Key

AYEWXCGYVJFQDW-WRKUMONDSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Euphorbia guyoniana	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Sub Class

Not Available

Direct Parent

Macrolides and analogues

Alternative Parents

Substituents

Macrolide
Benzoate ester
Benzoic acid or derivatives
Benzoyl
Cyclitol or derivatives
Monocyclic benzene moiety
Benzenoid
Tertiary alcohol
Cyclic alcohol
Carboxylic acid ester
Lactone
Organoheterocyclic compound
Carboxylic acid derivative
Oxacycle
Ether
Dialkyl ether
Oxirane
Hydrocarbon derivative
Carbonyl group
Organooxygen compound
Alcohol
Organic oxygen compound
Organic oxide
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	1.24	ChemAxon
pKa (Strongest Acidic)	12.64	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	237.09 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	184.48 m³·mol⁻¹	ChemAxon
Polarizability	77.78 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

45103728

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2s,3s,4s,6s,8s,9s,10r,11s,16r,17r,19s,20r)-2,8,9,10,17-pentakis(acetyloxy)-1,11-dihydroxy-3,7,7,17-tetramethyl-14-oxo-5,15-dioxatetracyclo[9.7.2.0⁴,⁶.0¹⁶,¹⁹]icosan-20-yl benzoate (NP0230767)

MOL for NP0230767 ((1r,2s,3s,4s,6s,8s,9s,10r,11s,16r,17r,19s,20r)-2,8,9,10,17-pentakis(acetyloxy)-1,11-dihydroxy-3,7,7,17-tetramethyl-14-oxo-5,15-dioxatetracyclo[9.7.2.0⁴,⁶.0¹⁶,¹⁹]icosan-20-yl benzoate)

3D MOL for NP0230767 ((1r,2s,3s,4s,6s,8s,9s,10r,11s,16r,17r,19s,20r)-2,8,9,10,17-pentakis(acetyloxy)-1,11-dihydroxy-3,7,7,17-tetramethyl-14-oxo-5,15-dioxatetracyclo[9.7.2.0⁴,⁶.0¹⁶,¹⁹]icosan-20-yl benzoate)

3D SDF for NP0230767 ((1r,2s,3s,4s,6s,8s,9s,10r,11s,16r,17r,19s,20r)-2,8,9,10,17-pentakis(acetyloxy)-1,11-dihydroxy-3,7,7,17-tetramethyl-14-oxo-5,15-dioxatetracyclo[9.7.2.0⁴,⁶.0¹⁶,¹⁹]icosan-20-yl benzoate)

3D-SDF for NP0230767 ((1r,2s,3s,4s,6s,8s,9s,10r,11s,16r,17r,19s,20r)-2,8,9,10,17-pentakis(acetyloxy)-1,11-dihydroxy-3,7,7,17-tetramethyl-14-oxo-5,15-dioxatetracyclo[9.7.2.0⁴,⁶.0¹⁶,¹⁹]icosan-20-yl benzoate)

PDB for NP0230767 ((1r,2s,3s,4s,6s,8s,9s,10r,11s,16r,17r,19s,20r)-2,8,9,10,17-pentakis(acetyloxy)-1,11-dihydroxy-3,7,7,17-tetramethyl-14-oxo-5,15-dioxatetracyclo[9.7.2.0⁴,⁶.0¹⁶,¹⁹]icosan-20-yl benzoate)

3D PDB for NP0230767 ((1r,2s,3s,4s,6s,8s,9s,10r,11s,16r,17r,19s,20r)-2,8,9,10,17-pentakis(acetyloxy)-1,11-dihydroxy-3,7,7,17-tetramethyl-14-oxo-5,15-dioxatetracyclo[9.7.2.0⁴,⁶.0¹⁶,¹⁹]icosan-20-yl benzoate)

SMILES for NP0230767 ((1r,2s,3s,4s,6s,8s,9s,10r,11s,16r,17r,19s,20r)-2,8,9,10,17-pentakis(acetyloxy)-1,11-dihydroxy-3,7,7,17-tetramethyl-14-oxo-5,15-dioxatetracyclo[9.7.2.0⁴,⁶.0¹⁶,¹⁹]icosan-20-yl benzoate)

INCHI for NP0230767 ((1r,2s,3s,4s,6s,8s,9s,10r,11s,16r,17r,19s,20r)-2,8,9,10,17-pentakis(acetyloxy)-1,11-dihydroxy-3,7,7,17-tetramethyl-14-oxo-5,15-dioxatetracyclo[9.7.2.0⁴,⁶.0¹⁶,¹⁹]icosan-20-yl benzoate)

Structure for NP0230767 ((1r,2s,3s,4s,6s,8s,9s,10r,11s,16r,17r,19s,20r)-2,8,9,10,17-pentakis(acetyloxy)-1,11-dihydroxy-3,7,7,17-tetramethyl-14-oxo-5,15-dioxatetracyclo[9.7.2.0⁴,⁶.0¹⁶,¹⁹]icosan-20-yl benzoate)

3D Structure for NP0230767 ((1r,2s,3s,4s,6s,8s,9s,10r,11s,16r,17r,19s,20r)-2,8,9,10,17-pentakis(acetyloxy)-1,11-dihydroxy-3,7,7,17-tetramethyl-14-oxo-5,15-dioxatetracyclo[9.7.2.0⁴,⁶.0¹⁶,¹⁹]icosan-20-yl benzoate)