NP-MRD: Showing NP-Card for (1r,2r,3r,4s,5s,7r,8r,9r,10s,11s,14r,16s)-2,8,11,16-tetrakis(acetyloxy)-1-{[2-(acetyloxy)acetyl]oxy}-7-hydroxy-5,9,12,12-tetramethyl-13-oxotetracyclo[7.6.1.0³,⁷.0¹⁰,¹⁴]hexadecan-4-yl benzoate (NP0267821)

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Record Information

Version

2.0

Created at

2022-09-08 12:43:16 UTC

Updated at

2022-09-08 12:43:16 UTC

NP-MRD ID

NP0267821

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,3r,4s,5s,7r,8r,9r,10s,11s,14r,16s)-2,8,11,16-tetrakis(acetyloxy)-1-{[2-(acetyloxy)acetyl]oxy}-7-hydroxy-5,9,12,12-tetramethyl-13-oxotetracyclo[7.6.1.0³,⁷.0¹⁰,¹⁴]hexadecan-4-yl benzoate

Description

(1R,2R,3R,4S,5S,7R,8R,9R,10S,11S,14R,16S)-2,8,11,16-tetrakis(acetyloxy)-1-{[2-(acetyloxy)acetyl]oxy}-7-hydroxy-5,9,12,12-tetramethyl-13-oxotetracyclo[7.6.1.0³,⁷.0¹⁰,¹⁴]Hexadecan-4-yl benzoate belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. (1r,2r,3r,4s,5s,7r,8r,9r,10s,11s,14r,16s)-2,8,11,16-tetrakis(acetyloxy)-1-{[2-(acetyloxy)acetyl]oxy}-7-hydroxy-5,9,12,12-tetramethyl-13-oxotetracyclo[7.6.1.0³,⁷.0¹⁰,¹⁴]hexadecan-4-yl benzoate is found in Euphorbia paralias. Based on a literature review very few articles have been published on (1R,2R,3R,4S,5S,7R,8R,9R,10S,11S,14R,16S)-2,8,11,16-tetrakis(acetyloxy)-1-{[2-(acetyloxy)acetyl]oxy}-7-hydroxy-5,9,12,12-tetramethyl-13-oxotetracyclo[7.6.1.0³,⁷.0¹⁰,¹⁴]Hexadecan-4-yl benzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082214432D          

 55 59  0  0  1  0            999 V2000
    6.5567   -2.1336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0120   -1.4856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6151   -0.8782    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1695   -1.6752    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4305   -1.2083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6070   -0.8962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5066   -1.7515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0184   -0.2096    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5132    0.5863    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2884    0.8685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7009    1.5829    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5179    1.4681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1116    0.8610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8796    2.2096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5962    2.6951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6540    1.8085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2861    2.7827    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8189    3.5106    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4222    4.1690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3694    5.0296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2692    4.2777    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5577    2.3954    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9257    2.9257    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3061    3.6567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4270    1.8076    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7107    1.9041    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1175    1.0973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4349    0.3611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2860    0.8587    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1007    2.9257    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0859    3.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2401    4.7878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7438    5.5013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8420    5.4075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4687    2.3954    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0267    3.2467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7403    2.7827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1468    2.2096    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6327    2.6176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5085    1.4681    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3666    0.9702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2400    0.9691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9028    1.5242    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4096    0.1205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9525   -0.5663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3187   -1.3056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1420   -1.3581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5992   -0.6713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2330    0.0680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3254    1.5829    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7379    0.8685    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3197   -0.1604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2422   -1.1048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7118   -1.8473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6771   -1.7772    0.0000 O   0  0  0  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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  9  8  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 22 17  1  1  0  0  0
 11 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
  9 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 23 30  1  0  0  0  0
 30 31  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
 30 35  1  0  0  0  0
 35 36  1  1  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  1  0  0  0
 38 40  1  0  0  0  0
 40 41  1  1  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 42 44  1  0  0  0  0
 44 45  2  0  0  0  0
 45 46  1  0  0  0  0
 46 47  2  0  0  0  0
 47 48  1  0  0  0  0
 48 49  2  0  0  0  0
 44 49  1  0  0  0  0
 50 40  1  1  0  0  0
 35 50  1  0  0  0  0
 50 51  1  0  0  0  0
  9 51  1  0  0  0  0
 51 52  1  6  0  0  0
 52 53  1  0  0  0  0
 53 54  1  0  0  0  0
 53 55  2  0  0  0  0
M  END

     RDKit          3D

103107  0  0  0  0  0  0  0  0999 V2000
   -0.0797    6.7125    3.7509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5263    5.8201    2.6345 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0882    5.7924    1.5428 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6185    5.0350    2.8285 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1580    4.1578    1.9083 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2125    3.0750    1.5112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0395    3.0702    1.9436 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6090    2.0697    0.6749 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8255    0.9766    0.2247 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4189    0.2775    1.4935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7073   -1.1303    1.6649 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5106   -1.5242    2.8869 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7848   -0.8222    3.8217 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8402   -2.9574    2.6017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2459   -3.3186    2.9512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8420   -3.7888    3.3679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6594   -3.1237    1.0761 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6544   -3.9462    0.5480 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3249   -5.1874   -0.0297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3430   -6.0935   -0.6014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1083   -5.4907   -0.0355 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6686   -1.7201    0.6524 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4743   -1.2929   -0.7159 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6903   -1.8281   -1.5098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7436    0.2167   -0.6795 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7525    0.7317   -1.9603 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8223    1.2531   -2.6445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6667    1.7707   -4.0271 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9369    1.2669   -2.0350 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2902   -1.6561   -1.4851 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6675   -1.5016   -2.8691 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7268   -2.5731   -3.7375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1290   -2.2831   -5.1394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4433   -3.7059   -3.3012 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9488   -0.8680   -1.3431 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7993   -1.2872   -0.3226 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7869   -1.2562   -2.5992 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8860   -0.1984   -2.5994 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1464   -0.8546   -2.1270 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4183    0.8850   -1.6227 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9822    0.6132   -0.3546 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7785    1.4597    0.3706 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0376    2.5886   -0.1368 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3346    1.1362    1.6741 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1277    2.0388    2.3463 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6653    1.7347    3.5999 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4100    0.5243    4.1848 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6202   -0.3900    3.5288 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0940   -0.0716    2.2835 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9165    0.5755   -1.5632 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3227    1.4936   -0.5594 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1320    2.5950   -1.3728 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4144    3.8427   -1.3586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1747    4.8963   -2.2611 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3737    4.0741   -0.6095 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.8384    7.5143    3.9250 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.5050    4.7236    1.0041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0361    3.6481    2.3954 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7083    0.4064    1.5543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7552    0.8140    2.4303 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1957   -1.7993    1.8010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6992   -4.0293    2.1980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9398   -2.4740    3.0374 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2404   -3.9196    3.9069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2809   -4.7750    3.5744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5357   -3.2881    4.2960 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0745   -3.8412    2.7274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6351   -3.5596    0.9756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2519   -5.5608   -0.9579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9168   -6.6173   -1.5039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5594   -6.8646    0.1428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6853   -1.3061    0.9642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5712   -1.7199   -0.8446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7983   -1.1988   -2.4346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5733   -2.8826   -1.7580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7795    0.2879   -0.2713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8559    0.9839   -4.7898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6538    2.2059   -4.1924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4136    2.5928   -4.2090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0600   -2.7240   -1.2849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2319   -2.1083   -5.1312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6966   -1.2991   -5.4845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7990   -3.0360   -5.8544 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6029   -2.2522   -0.1606 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1860   -2.2811   -2.4897 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2003   -1.1035   -3.5076 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0385    0.2159   -3.6054 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0290   -1.0811   -1.0384 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0607   -0.3099   -2.3644 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2132   -1.8478   -2.6283 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6424    1.8657   -2.0305 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3570    3.0079    1.9256 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2878    2.4281    4.1432 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8145    0.2600    5.1589 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4155   -1.3406    3.9791 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4794   -0.8125    1.7981 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5739    0.7512   -2.6258 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1198    1.8848    0.0951 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2122    4.6562   -3.2725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2563    4.7489   -2.2911 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0480    5.9088   -1.9178 H   0  0  0  0  0  0  0  0  0  0  0  0
 39 38  1  0
 38 37  1  0
 37 35  1  0
 35 36  1  1
 35 50  1  0
 50 40  1  0
 40 41  1  0
 41 42  1  0
 42 43  2  0
 42 44  1  0
 44 45  2  0
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 50 51  1  0
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 53 55  2  0
 51  9  1  0
  9 10  1  0
 10 11  1  0
 11 22  1  0
 22 17  1  0
 17 18  1  0
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 17 14  1  0
 14 15  1  0
 14 16  1  0
 14 12  1  0
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 22 23  1  0
 23 24  1  6
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 27 28  1  0
 27 29  2  0
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 32 34  2  0
  9  8  1  1
  8  6  1  0
  6  7  2  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
 40 38  1  0
 49 44  1  0
 25  9  1  0
 30 35  1  0
 12 11  1  0
 39 90  1  0
 39 91  1  0
 39 92  1  0
 38 89  1  6
 37 87  1  0
 37 88  1  0
 36 86  1  0
 50 99  1  6
 40 93  1  6
 45 94  1  0
 46 95  1  0
 47 96  1  0
 48 97  1  0
 49 98  1  0
 51100  1  1
 54101  1  0
 54102  1  0
 54103  1  0
 10 61  1  0
 10 62  1  0
 11 63  1  1
 22 74  1  1
 17 70  1  1
 20 71  1  0
 20 72  1  0
 20 73  1  0
 15 64  1  0
 15 65  1  0
 15 66  1  0
 16 67  1  0
 16 68  1  0
 16 69  1  0
 24 75  1  0
 24 76  1  0
 24 77  1  0
 25 78  1  1
 28 79  1  0
 28 80  1  0
 28 81  1  0
 30 82  1  6
 33 83  1  0
 33 84  1  0
 33 85  1  0
  5 59  1  0
  5 60  1  0
  1 56  1  0
  1 57  1  0
  1 58  1  0
M  END


  Mrv1652309082214432D          

 55 59  0  0  1  0            999 V2000
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    6.0120   -1.4856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6151   -0.8782    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1695   -1.6752    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4305   -1.2083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6070   -0.8962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5066   -1.7515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0184   -0.2096    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5132    0.5863    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2884    0.8685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7009    1.5829    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5179    1.4681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1116    0.8610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8796    2.2096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5962    2.6951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6540    1.8085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2861    2.7827    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8189    3.5106    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4222    4.1690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3694    5.0296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2692    4.2777    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5577    2.3954    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9257    2.9257    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3061    3.6567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4270    1.8076    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7107    1.9041    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1175    1.0973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4349    0.3611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2860    0.8587    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1007    2.9257    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0859    3.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2401    4.7878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7438    5.5013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8420    5.4075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4687    2.3954    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0267    3.2467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7403    2.7827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1468    2.2096    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6327    2.6176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5085    1.4681    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3666    0.9702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2400    0.9691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9028    1.5242    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4096    0.1205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9525   -0.5663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3187   -1.3056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1420   -1.3581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5992   -0.6713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2330    0.0680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3254    1.5829    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7379    0.8685    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3197   -0.1604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2422   -1.1048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7118   -1.8473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6771   -1.7772    0.0000 O   0  0  0  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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  9  8  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 22 17  1  1  0  0  0
 11 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
  9 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 23 30  1  0  0  0  0
 30 31  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
 30 35  1  0  0  0  0
 35 36  1  1  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  1  0  0  0
 38 40  1  0  0  0  0
 40 41  1  1  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 42 44  1  0  0  0  0
 44 45  2  0  0  0  0
 45 46  1  0  0  0  0
 46 47  2  0  0  0  0
 47 48  1  0  0  0  0
 48 49  2  0  0  0  0
 44 49  1  0  0  0  0
 50 40  1  1  0  0  0
 35 50  1  0  0  0  0
 50 51  1  0  0  0  0
  9 51  1  0  0  0  0
 51 52  1  6  0  0  0
 52 53  1  0  0  0  0
 53 54  1  0  0  0  0
 53 55  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0267821

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1C[C@@]2(O)[C@H]([C@H]1OC(=O)C1=CC=CC=C1)[C@@H](OC(C)=O)[C@@]1(C[C@@H]3[C@H]([C@H](OC(C)=O)C(C)(C)C3=O)[C@@](C)([C@@H]1OC(C)=O)[C@H]2OC(C)=O)OC(=O)COC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C39H48O16/c1-18-15-38(48)28(29(18)54-33(47)24-13-11-10-12-14-24)32(51-21(4)42)39(55-26(45)17-49-19(2)40)16-25-27(31(50-20(3)41)36(7,8)30(25)46)37(9,34(38)52-22(5)43)35(39)53-23(6)44/h10-14,18,25,27-29,31-32,34-35,48H,15-17H2,1-9H3/t18-,25+,27+,28+,29-,31-,32+,34+,35-,37+,38+,39+/m0/s1

> <INCHI_KEY>
UZNGNGIPDPIHBX-DFLPDNMSSA-N

> <FORMULA>
C39H48O16

> <MOLECULAR_WEIGHT>
772.797

> <EXACT_MASS>
772.294235466

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
103

> <JCHEM_AVERAGE_POLARIZABILITY>
77.25283885368717

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,3R,4S,5S,7R,8R,9R,10S,11S,14R,16S)-2,8,11,16-tetrakis(acetyloxy)-1-{[2-(acetyloxy)acetyl]oxy}-7-hydroxy-5,9,12,12-tetramethyl-13-oxotetracyclo[7.6.1.0^{3,7}.0^{10,14}]hexadecan-4-yl benzoate

> <JCHEM_LOGP>
2.239901160999998

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.322618942495595

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.396240363761173

> <JCHEM_PKA_STRONGEST_BASIC>
-3.497745831340411

> <JCHEM_POLAR_SURFACE_AREA>
221.39999999999998

> <JCHEM_REFRACTIVITY>
182.72979999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,3R,4S,5S,7R,8R,9R,10S,11S,14R,16S)-2,8,11,16-tetrakis(acetyloxy)-1-{[2-(acetyloxy)acetyl]oxy}-7-hydroxy-5,9,12,12-tetramethyl-13-oxotetracyclo[7.6.1.0^{3,7}.0^{10,14}]hexadecan-4-yl benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      12.239  -3.983   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.222  -2.773   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      12.348  -1.639   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       9.650  -3.127   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       8.270  -2.256   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.733  -1.673   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       6.546  -3.269   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0       5.634  -0.391   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.691   1.094   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.138   1.621   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.908   2.955   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.433   2.740   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       9.542   1.607   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       9.109   4.125   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.446   5.031   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.554   3.376   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.001   5.194   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       8.995   6.553   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      10.121   7.782   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.023   9.389   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      11.703   7.985   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       6.641   4.471   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.461   5.461   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.171   6.826   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.530   3.374   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       3.193   3.554   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.086   2.048   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.679   0.674   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       0.534   1.603   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       3.921   5.461   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       3.894   7.257   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       4.182   8.937   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       3.255  10.269   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       5.305  10.094   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       2.742   4.471   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       1.917   6.061   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       1.382   5.194   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       0.274   4.125   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -1.181   4.886   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       0.949   2.740   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      -0.684   1.811   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      -2.315   1.809   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      -3.552   2.845   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      -2.631   0.225   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -1.778  -1.057   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -2.462  -2.437   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      -3.998  -2.535   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      -4.852  -1.253   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      -4.168   0.127   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       2.474   2.955   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       3.244   1.621   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0       2.464  -0.299   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0       2.319  -2.062   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0       3.195  -3.448   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0       1.264  -3.317   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   25   51                                             
CONECT   10    9   11                                                       
CONECT   11   10   12   22                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16   17                                             
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   14   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   17   11   23                                                  
CONECT   23   22   24   25   30                                             
CONECT   24   23                                                            
CONECT   25   23    9   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   23   31   35                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32                                                            
CONECT   35   30   36   37   50                                             
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41   50                                                  
CONECT   41   40   42                                                       
CONECT   42   41   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   45   49                                                  
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   44                                                       
CONECT   50   40   35   51                                                  
CONECT   51   50    9   52                                                  
CONECT   52   51   53                                                       
CONECT   53   52   54   55                                                  
CONECT   54   53                                                            
CONECT   55   53                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  118    0
END

View in JSmol

Synonyms

Value	Source
(1R,2R,3R,4S,5S,7R,8R,9R,10S,11S,14R,16S)-2,8,11,16-Tetrakis(acetyloxy)-1-{[2-(acetyloxy)acetyl]oxy}-7-hydroxy-5,9,12,12-tetramethyl-13-oxotetracyclo[7.6.1.0,.0,]hexadecan-4-yl benzoic acid	Generator

Chemical Formula

C₃₉H₄₈O₁₆

Average Mass

772.7970 Da

Monoisotopic Mass

772.29424 Da

IUPAC Name

(1R,2R,3R,4S,5S,7R,8R,9R,10S,11S,14R,16S)-2,8,11,16-tetrakis(acetyloxy)-1-{[2-(acetyloxy)acetyl]oxy}-7-hydroxy-5,9,12,12-tetramethyl-13-oxotetracyclo[7.6.1.0^{3,7}.0^{10,14}]hexadecan-4-yl benzoate

Traditional Name

(1R,2R,3R,4S,5S,7R,8R,9R,10S,11S,14R,16S)-2,8,11,16-tetrakis(acetyloxy)-1-{[2-(acetyloxy)acetyl]oxy}-7-hydroxy-5,9,12,12-tetramethyl-13-oxotetracyclo[7.6.1.0^{3,7}.0^{10,14}]hexadecan-4-yl benzoate

CAS Registry Number

Not Available

SMILES

C[C@H]1C[C@@]2(O)[C@H]([C@H]1OC(=O)C1=CC=CC=C1)[C@@H](OC(C)=O)[C@@]1(C[C@@H]3[C@H]([C@H](OC(C)=O)C(C)(C)C3=O)[C@@](C)([C@@H]1OC(C)=O)[C@H]2OC(C)=O)OC(=O)COC(C)=O

InChI Identifier

InChI=1S/C39H48O16/c1-18-15-38(48)28(29(18)54-33(47)24-13-11-10-12-14-24)32(51-21(4)42)39(55-26(45)17-49-19(2)40)16-25-27(31(50-20(3)41)36(7,8)30(25)46)37(9,34(38)52-22(5)43)35(39)53-23(6)44/h10-14,18,25,27-29,31-32,34-35,48H,15-17H2,1-9H3/t18-,25+,27+,28+,29-,31-,32+,34+,35-,37+,38+,39+/m0/s1

InChI Key

UZNGNGIPDPIHBX-DFLPDNMSSA-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 paralias	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Benzoate ester
Benzoic acid or derivatives
Benzoyl
Monocyclic benzene moiety
Benzenoid
Tertiary alcohol
Cyclic alcohol
Carboxylic acid ester
Ketone
Carboxylic acid derivative
Carbonyl group
Alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organooxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	2.24	ChemAxon
pKa (Strongest Acidic)	13.4	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	221.4 Å²	ChemAxon
Rotatable Bond Count	16	ChemAxon
Refractivity	182.73 m³·mol⁻¹	ChemAxon
Polarizability	77.25 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

163044108

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2r,3r,4s,5s,7r,8r,9r,10s,11s,14r,16s)-2,8,11,16-tetrakis(acetyloxy)-1-{[2-(acetyloxy)acetyl]oxy}-7-hydroxy-5,9,12,12-tetramethyl-13-oxotetracyclo[7.6.1.0³,⁷.0¹⁰,¹⁴]hexadecan-4-yl benzoate (NP0267821)

MOL for NP0267821 ((1r,2r,3r,4s,5s,7r,8r,9r,10s,11s,14r,16s)-2,8,11,16-tetrakis(acetyloxy)-1-{[2-(acetyloxy)acetyl]oxy}-7-hydroxy-5,9,12,12-tetramethyl-13-oxotetracyclo[7.6.1.0³,⁷.0¹⁰,¹⁴]hexadecan-4-yl benzoate)

3D MOL for NP0267821 ((1r,2r,3r,4s,5s,7r,8r,9r,10s,11s,14r,16s)-2,8,11,16-tetrakis(acetyloxy)-1-{[2-(acetyloxy)acetyl]oxy}-7-hydroxy-5,9,12,12-tetramethyl-13-oxotetracyclo[7.6.1.0³,⁷.0¹⁰,¹⁴]hexadecan-4-yl benzoate)

3D SDF for NP0267821 ((1r,2r,3r,4s,5s,7r,8r,9r,10s,11s,14r,16s)-2,8,11,16-tetrakis(acetyloxy)-1-{[2-(acetyloxy)acetyl]oxy}-7-hydroxy-5,9,12,12-tetramethyl-13-oxotetracyclo[7.6.1.0³,⁷.0¹⁰,¹⁴]hexadecan-4-yl benzoate)

3D-SDF for NP0267821 ((1r,2r,3r,4s,5s,7r,8r,9r,10s,11s,14r,16s)-2,8,11,16-tetrakis(acetyloxy)-1-{[2-(acetyloxy)acetyl]oxy}-7-hydroxy-5,9,12,12-tetramethyl-13-oxotetracyclo[7.6.1.0³,⁷.0¹⁰,¹⁴]hexadecan-4-yl benzoate)

PDB for NP0267821 ((1r,2r,3r,4s,5s,7r,8r,9r,10s,11s,14r,16s)-2,8,11,16-tetrakis(acetyloxy)-1-{[2-(acetyloxy)acetyl]oxy}-7-hydroxy-5,9,12,12-tetramethyl-13-oxotetracyclo[7.6.1.0³,⁷.0¹⁰,¹⁴]hexadecan-4-yl benzoate)

3D PDB for NP0267821 ((1r,2r,3r,4s,5s,7r,8r,9r,10s,11s,14r,16s)-2,8,11,16-tetrakis(acetyloxy)-1-{[2-(acetyloxy)acetyl]oxy}-7-hydroxy-5,9,12,12-tetramethyl-13-oxotetracyclo[7.6.1.0³,⁷.0¹⁰,¹⁴]hexadecan-4-yl benzoate)

SMILES for NP0267821 ((1r,2r,3r,4s,5s,7r,8r,9r,10s,11s,14r,16s)-2,8,11,16-tetrakis(acetyloxy)-1-{[2-(acetyloxy)acetyl]oxy}-7-hydroxy-5,9,12,12-tetramethyl-13-oxotetracyclo[7.6.1.0³,⁷.0¹⁰,¹⁴]hexadecan-4-yl benzoate)

INCHI for NP0267821 ((1r,2r,3r,4s,5s,7r,8r,9r,10s,11s,14r,16s)-2,8,11,16-tetrakis(acetyloxy)-1-{[2-(acetyloxy)acetyl]oxy}-7-hydroxy-5,9,12,12-tetramethyl-13-oxotetracyclo[7.6.1.0³,⁷.0¹⁰,¹⁴]hexadecan-4-yl benzoate)

Structure for NP0267821 ((1r,2r,3r,4s,5s,7r,8r,9r,10s,11s,14r,16s)-2,8,11,16-tetrakis(acetyloxy)-1-{[2-(acetyloxy)acetyl]oxy}-7-hydroxy-5,9,12,12-tetramethyl-13-oxotetracyclo[7.6.1.0³,⁷.0¹⁰,¹⁴]hexadecan-4-yl benzoate)

3D Structure for NP0267821 ((1r,2r,3r,4s,5s,7r,8r,9r,10s,11s,14r,16s)-2,8,11,16-tetrakis(acetyloxy)-1-{[2-(acetyloxy)acetyl]oxy}-7-hydroxy-5,9,12,12-tetramethyl-13-oxotetracyclo[7.6.1.0³,⁷.0¹⁰,¹⁴]hexadecan-4-yl benzoate)