NP-MRD: Showing NP-Card for (1s,2s,3s,5s,8r,9r,10s,11s,13r,16s)-5,8,9,16-tetrakis(acetyloxy)-2-(benzoyloxy)-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.0³,⁷.0¹³,¹⁶]hexadec-6-en-11-yl benzoate (NP0294374)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-10 02:52:57 UTC

Updated at

2022-09-10 02:52:57 UTC

NP-MRD ID

NP0294374

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,3s,5s,8r,9r,10s,11s,13r,16s)-5,8,9,16-tetrakis(acetyloxy)-2-(benzoyloxy)-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.0³,⁷.0¹³,¹⁶]hexadec-6-en-11-yl benzoate

Description

(1S,2S,3S,5S,8R,9R,10S,11S,13R,16S)-5,8,9,16-tetrakis(acetyloxy)-2-(benzoyloxy)-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.0³,⁷.0¹³,¹⁶]Hexadec-6-en-11-yl benzoate belongs to the class of organic compounds known as taxanes and derivatives. These are diterpenoids with a structure based either on the taxane skeleton, or a derivative thereof. In term of phytochemistry, several derivatives of the taxane skeleton exist: 2(3->20)-Abeotaxane, 3,11-cyclotaxane, 11(15->1),11(10->9)-abeotaxane, 3,8-seco-taxane, and 11(15->1)-abeotaxane, among others. More complex skeletons have been found recently, which include the taxane-derived [3.3.3] Propellane ring system. (1s,2s,3s,5s,8r,9r,10s,11s,13r,16s)-5,8,9,16-tetrakis(acetyloxy)-2-(benzoyloxy)-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.0³,⁷.0¹³,¹⁶]hexadec-6-en-11-yl benzoate is found in Taxus brevifolia. Based on a literature review very few articles have been published on (1S,2S,3S,5S,8R,9R,10S,11S,13R,16S)-5,8,9,16-tetrakis(acetyloxy)-2-(benzoyloxy)-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.0³,⁷.0¹³,¹⁶]Hexadec-6-en-11-yl benzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102204522D          

 56 61  0  0  1  0            999 V2000
    9.7206    1.4140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0348    0.8959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6899    0.3178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1407    0.9957    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2368    0.8280    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4735    1.1411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9399    0.5120    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1145    1.4935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0533    2.4325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3239    1.2878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0342    1.7261    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3733   -0.1900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1748    0.0053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9289   -0.4357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0947   -0.9665    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.8382   -1.4417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6609   -1.8092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1545   -1.1418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3010   -2.3993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3139   -1.2329    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6616   -2.1032    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0835   -2.9415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9368   -3.7948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8617   -3.3361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6188   -0.7885    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6393   -1.6351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9512   -1.2732    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2643   -1.8585    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6144   -2.4801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7855   -2.2655    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8423   -3.3344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6182   -3.6148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7633   -4.4269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1326   -4.9586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3567   -4.6783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2115   -3.8661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1976   -0.9374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1117   -0.1168    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6270    0.5508    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2946    1.0355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7793    0.3678    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6230    1.3844    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6976    2.0003    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8293    2.2778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0693    2.7519    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5329    0.0320    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1208    0.6108    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6324    1.4494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7651    1.9075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8188    1.4348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9369    2.7935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2558    3.2590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3183    4.0816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0620    4.4388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7431    3.9733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6806    3.1507    0.0000 C   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
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  8 11  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  2  0  0  0  0
  5 13  1  0  0  0  0
 13 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 20 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  0  0  0  0
 27 28  1  1  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 31 36  1  0  0  0  0
 27 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  1  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 38 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
 46 41  1  6  0  0  0
 25 46  1  0  0  0  0
 46 47  1  0  0  0  0
  7 47  1  0  0  0  0
 47 48  1  6  0  0  0
 48 49  1  0  0  0  0
 49 50  2  0  0  0  0
 49 51  1  0  0  0  0
 51 52  2  0  0  0  0
 52 53  1  0  0  0  0
 53 54  2  0  0  0  0
 54 55  1  0  0  0  0
 55 56  2  0  0  0  0
 51 56  1  0  0  0  0
M  END

     RDKit          3D

104109  0  0  0  0  0  0  0  0999 V2000
   -6.1964    0.4247    3.3269 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5514   -0.0112    2.0686 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2483   -0.6629    1.2181 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2419    0.2401    1.7519 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6869   -0.2322    0.4811 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0056    0.9158   -0.2006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8514    0.1962   -0.9733 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5714   -0.2424   -2.1777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9265   -0.9384   -3.3222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4762    0.8025   -2.8174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5259   -1.2383   -1.7315 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4827   -0.7551    0.0650 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5060   -1.0193    0.8993 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5264   -1.9448    2.0924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1822   -1.4714    0.3561 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4125   -2.8916    0.4569 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0662   -3.6092    1.5424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1944   -5.0771    1.6107 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7167   -3.0571    2.4755 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6717   -1.3358   -0.8503 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7138   -2.3489   -0.6294 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7331   -3.5541   -1.2784 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7704   -4.5978   -1.0867 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7851   -3.7845   -2.1052 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3249   -0.0935   -1.2246 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3318   -0.5218   -2.3217 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2073    0.3695   -0.0925 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1180   -0.7013    0.2247 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3374   -1.2089    1.4633 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6615   -0.6562    2.3840 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2565   -2.2942    1.7844 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4243   -2.7673    3.0650 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3042   -3.7963    3.3638 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0362   -4.3663    2.3499 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8832   -3.9071    1.0587 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9981   -2.8785    0.7868 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9996    1.6226   -0.4012 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0806    2.6792   -0.8780 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7534    3.4898   -1.8282 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3881    2.4591   -2.7562 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1696    2.2993   -1.9768 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3201    3.3981   -2.3200 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4434    3.4929   -3.4395 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2842    4.6765   -3.6805 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4256    2.5552   -4.2725 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4562    0.9867   -1.8011 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8267    1.3062   -1.1457 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7585    2.1530   -0.0446 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2216    3.3342    0.3090 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9447    3.9325   -0.5058 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8908    3.9136    1.6174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0763    3.2041    2.4797 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2141    3.7657    3.6976 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2672    4.9843    4.0816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0914    5.6944    3.2004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3950    5.1477    1.9719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2348    0.0888    3.3610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2024    1.5261    3.4463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6975    0.0213    4.2375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4973   -0.7275    0.0131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6079    1.5179    0.6369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5965    1.5560   -0.8198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8469   -1.1879   -4.0013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5538   -1.9533   -3.1456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3496   -0.3146   -4.0193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5141    0.7759   -2.4280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6454    0.5435   -3.9084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0476    1.8081   -2.8665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9375   -1.6536   -2.5204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6688   -3.0016    1.8005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4814   -1.7062    2.6606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6680   -1.7450    2.7514 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2921   -1.1847    1.2836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2201   -5.2791    1.9485 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4959   -5.5530    2.3309 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0143   -5.5544    0.6195 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1272   -1.8052   -1.6720 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6912   -4.2228   -1.6246 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4755   -5.5115   -1.6320 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9813   -4.7915   -0.0152 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3690   -0.3482   -2.0592 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9769   -0.0803   -3.2820 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2957   -1.6152   -2.5424 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7077    0.5773    0.8521 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8686   -2.3467    3.8884 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4427   -4.1761    4.3689 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7209   -5.1702    2.5984 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4813   -4.3889    0.2994 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8909   -2.5314   -0.2290 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3910    1.9784    0.6043 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8848    1.4504   -1.0039 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6868    3.3823   -0.0967 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2129    1.7987   -2.8329 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3071    3.0252   -3.7353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2031    5.4100   -2.8524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0308    5.1632   -4.6458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3581    4.3580   -3.7650 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3096    0.6761   -2.8426 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4026    1.9548   -1.8113 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3262    2.2265    2.2017 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8592    3.1927    4.3711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0324    5.4282    5.0552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4963    6.6612    3.4572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0264    5.6484    1.2432 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7 47  1  0
 47 48  1  0
 48 49  1  0
 49 50  2  0
 49 51  1  0
 51 52  2  0
 52 53  1  0
 53 54  2  0
 54 55  1  0
 55 56  2  0
 47 46  1  0
 46 41  1  0
 41 40  1  0
 40 39  1  0
 39 38  1  0
 38 37  1  0
 37 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  2  0
 29 31  1  0
 31 32  2  0
 32 33  1  0
 33 34  2  0
 34 35  1  0
 35 36  2  0
 27 25  1  0
 25 26  1  6
 25 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  2  0
 20 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 15 12  1  0
 12 13  2  0
 13 14  1  0
 41 42  1  6
 42 43  1  0
 43 44  1  0
 43 45  2  0
  7  8  1  6
  8  9  1  0
  8 10  1  0
  8 11  1  0
 13  5  1  0
 12  7  1  0
 56 51  1  0
 25 46  1  0
 38 41  1  0
 36 31  1  0
  1 57  1  0
  1 58  1  0
  1 59  1  0
  5 60  1  6
  6 61  1  0
  6 62  1  0
 47 99  1  6
 52100  1  0
 53101  1  0
 54102  1  0
 55103  1  0
 56104  1  0
 46 98  1  6
 40 93  1  0
 40 94  1  0
 38 92  1  1
 37 90  1  0
 37 91  1  0
 27 84  1  1
 32 85  1  0
 33 86  1  0
 34 87  1  0
 35 88  1  0
 36 89  1  0
 26 81  1  0
 26 82  1  0
 26 83  1  0
 20 77  1  6
 23 78  1  0
 23 79  1  0
 23 80  1  0
 15 73  1  1
 18 74  1  0
 18 75  1  0
 18 76  1  0
 14 70  1  0
 14 71  1  0
 14 72  1  0
 44 95  1  0
 44 96  1  0
 44 97  1  0
  9 63  1  0
  9 64  1  0
  9 65  1  0
 10 66  1  0
 10 67  1  0
 10 68  1  0
 11 69  1  0
M  END


  Mrv1652309102204522D          

 56 61  0  0  1  0            999 V2000
    9.7206    1.4140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0348    0.8959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6899    0.3178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1407    0.9957    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2368    0.8280    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4735    1.1411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9399    0.5120    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1145    1.4935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0533    2.4325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3239    1.2878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0342    1.7261    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3733   -0.1900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1748    0.0053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9289   -0.4357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0947   -0.9665    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.8382   -1.4417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6609   -1.8092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1545   -1.1418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3010   -2.3993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3139   -1.2329    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6616   -2.1032    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0835   -2.9415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9368   -3.7948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8617   -3.3361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6188   -0.7885    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6393   -1.6351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9512   -1.2732    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2643   -1.8585    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6144   -2.4801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7855   -2.2655    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8423   -3.3344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6182   -3.6148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7633   -4.4269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1326   -4.9586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3567   -4.6783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2115   -3.8661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1976   -0.9374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1117   -0.1168    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6270    0.5508    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2946    1.0355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7793    0.3678    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6230    1.3844    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6976    2.0003    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8293    2.2778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0693    2.7519    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5329    0.0320    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1208    0.6108    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6324    1.4494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7651    1.9075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8188    1.4348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9369    2.7935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2558    3.2590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3183    4.0816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0620    4.4388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7431    3.9733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6806    3.1507    0.0000 C   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
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  8 11  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  2  0  0  0  0
  5 13  1  0  0  0  0
 13 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 20 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  0  0  0  0
 27 28  1  1  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 31 36  1  0  0  0  0
 27 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  1  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 38 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
 46 41  1  6  0  0  0
 25 46  1  0  0  0  0
 46 47  1  0  0  0  0
  7 47  1  0  0  0  0
 47 48  1  6  0  0  0
 48 49  1  0  0  0  0
 49 50  2  0  0  0  0
 49 51  1  0  0  0  0
 51 52  2  0  0  0  0
 52 53  1  0  0  0  0
 53 54  2  0  0  0  0
 54 55  1  0  0  0  0
 55 56  2  0  0  0  0
 51 56  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0294374

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@H]1C[C@]2([C@@H](OC(=O)C3=CC=CC=C3)[C@H]3[C@@]4(CO[C@@H]4C[C@H](OC(=O)C4=CC=CC=C4)[C@@]3(C)[C@@H](OC(C)=O)[C@H](OC(C)=O)C2=C1C)OC(C)=O)C(C)(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C42H48O14/c1-22-29(51-23(2)43)20-41(39(6,7)49)32(22)33(52-24(3)44)35(53-25(4)45)40(8)30(54-37(47)27-15-11-9-12-16-27)19-31-42(21-50-31,56-26(5)46)34(40)36(41)55-38(48)28-17-13-10-14-18-28/h9-18,29-31,33-36,49H,19-21H2,1-8H3/t29-,30-,31+,33+,34+,35-,36-,40+,41-,42-/m0/s1

> <INCHI_KEY>
RKJDSDDVYHZEED-OXXKWLEUSA-N

> <FORMULA>
C42H48O14

> <MOLECULAR_WEIGHT>
776.832

> <EXACT_MASS>
776.304406226

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
104

> <JCHEM_AVERAGE_POLARIZABILITY>
78.6528566575183

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,3S,5S,8R,9R,10S,11S,13R,16S)-5,8,9,16-tetrakis(acetyloxy)-2-(benzoyloxy)-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.0^{3,7}.0^{13,16}]hexadec-6-en-11-yl benzoate

> <JCHEM_LOGP>
3.4138933113333323

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.648750520553122

> <JCHEM_PKA_STRONGEST_BASIC>
-2.952436522310064

> <JCHEM_POLAR_SURFACE_AREA>
187.26

> <JCHEM_REFRACTIVITY>
194.51679999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,3S,5S,8R,9R,10S,11S,13R,16S)-5,8,9,16-tetrakis(acetyloxy)-2-(benzoyloxy)-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.0^{3,7}.0^{13,16}]hexadec-6-en-11-yl benzoate

> <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      18.145   2.639   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      16.865   1.672   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      18.088   0.593   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      15.196   1.859   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      13.509   1.546   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      12.084   2.130   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.088   0.956   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.414   2.788   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      11.300   4.541   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.938   2.404   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      13.131   3.222   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      11.897  -0.355   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.393   0.010   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.801  -0.813   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.377  -1.804   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      12.765  -2.691   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      14.300  -3.377   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      15.222  -2.131   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      15.495  -4.479   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       9.919  -2.301   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      10.568  -3.926   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      11.356  -5.491   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.082  -7.084   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      12.808  -6.227   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       8.622  -1.472   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.660  -3.052   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.376  -2.377   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       6.093  -3.469   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       4.880  -4.630   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       3.333  -4.229   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       5.306  -6.224   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.754  -6.748   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       7.025  -8.264   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.847  -9.256   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.399  -8.733   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       4.128  -7.217   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       5.969  -1.750   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       5.809  -0.218   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       4.904   1.028   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       6.150   1.933   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       7.055   0.687   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       6.763   2.584   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       5.036   3.734   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       3.415   4.252   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       5.729   5.137   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       8.461   0.060   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       9.559   1.140   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0       8.647   2.706   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0       7.028   3.561   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0       5.262   2.678   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0       7.349   5.215   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       6.077   6.083   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0       6.194   7.619   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0       7.582   8.286   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0       8.854   7.417   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0       8.737   5.881   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   13                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   12   47                                             
CONECT    8    7    9   10   11                                             
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    8                                                            
CONECT   12    7   13   15                                                  
CONECT   13   12    5   14                                                  
CONECT   14   13                                                            
CONECT   15   12   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   15   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   20   26   27   46                                             
CONECT   26   25                                                            
CONECT   27   25   28   37                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   36                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   31                                                       
CONECT   37   27   38                                                       
CONECT   38   37   39   41                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   38   42   46                                             
CONECT   42   41   43                                                       
CONECT   43   42   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43                                                            
CONECT   46   41   25   47                                                  
CONECT   47   46    7   48                                                  
CONECT   48   47   49                                                       
CONECT   49   48   50   51                                                  
CONECT   50   49                                                            
CONECT   51   49   52   56                                                  
CONECT   52   51   53                                                       
CONECT   53   52   54                                                       
CONECT   54   53   55                                                       
CONECT   55   54   56                                                       
CONECT   56   55   51                                                       
MASTER        0    0    0    0    0    0    0    0   56    0  122    0
END

View in JSmol

Synonyms

Value	Source
(1S,2S,3S,5S,8R,9R,10S,11S,13R,16S)-5,8,9,16-Tetrakis(acetyloxy)-2-(benzoyloxy)-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.0,.0,]hexadec-6-en-11-yl benzoic acid	Generator

Chemical Formula

C₄₂H₄₈O₁₄

Average Mass

776.8320 Da

Monoisotopic Mass

776.30441 Da

IUPAC Name

(1S,2S,3S,5S,8R,9R,10S,11S,13R,16S)-5,8,9,16-tetrakis(acetyloxy)-2-(benzoyloxy)-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.0^{3,7}.0^{13,16}]hexadec-6-en-11-yl benzoate

Traditional Name

(1S,2S,3S,5S,8R,9R,10S,11S,13R,16S)-5,8,9,16-tetrakis(acetyloxy)-2-(benzoyloxy)-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.0^{3,7}.0^{13,16}]hexadec-6-en-11-yl benzoate

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@H]1C[C@]2([C@@H](OC(=O)C3=CC=CC=C3)[C@H]3[C@@]4(CO[C@@H]4C[C@H](OC(=O)C4=CC=CC=C4)[C@@]3(C)[C@@H](OC(C)=O)[C@H](OC(C)=O)C2=C1C)OC(C)=O)C(C)(C)O

InChI Identifier

InChI=1S/C42H48O14/c1-22-29(51-23(2)43)20-41(39(6,7)49)32(22)33(52-24(3)44)35(53-25(4)45)40(8)30(54-37(47)27-15-11-9-12-16-27)19-31-42(21-50-31,56-26(5)46)34(40)36(41)55-38(48)28-17-13-10-14-18-28/h9-18,29-31,33-36,49H,19-21H2,1-8H3/t29-,30-,31+,33+,34+,35-,36-,40+,41-,42-/m0/s1

InChI Key

RKJDSDDVYHZEED-OXXKWLEUSA-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
Taxus brevifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as taxanes and derivatives. These are diterpenoids with a structure based either on the taxane skeleton, or a derivative thereof. In term of phytochemistry, several derivatives of the taxane skeleton exist: 2(3->20)-Abeotaxane, 3,11-cyclotaxane, 11(15->1),11(10->9)-abeotaxane, 3,8-seco-taxane, and 11(15->1)-abeotaxane, among others. More complex skeletons have been found recently, which include the taxane-derived [3.3.3] Propellane ring system.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Taxanes and derivatives

Alternative Parents

Substituents

Hexacarboxylic acid or derivatives
11(15->1)-abeotaxane diterpenoid
Benzoate ester
Benzoic acid or derivatives
Benzoyl
Benzenoid
Monocyclic benzene moiety
Tertiary alcohol
Oxetane
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Carboxylic acid derivative
Organooxygen compound
Carbonyl group
Alcohol
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	3.41	ChemAxon
pKa (Strongest Acidic)	14.65	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	187.26 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	194.52 m³·mol⁻¹	ChemAxon
Polarizability	78.65 Å³	ChemAxon
Number of Rings	6	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

162870998

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2s,3s,5s,8r,9r,10s,11s,13r,16s)-5,8,9,16-tetrakis(acetyloxy)-2-(benzoyloxy)-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.0³,⁷.0¹³,¹⁶]hexadec-6-en-11-yl benzoate (NP0294374)

MOL for NP0294374 ((1s,2s,3s,5s,8r,9r,10s,11s,13r,16s)-5,8,9,16-tetrakis(acetyloxy)-2-(benzoyloxy)-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.0³,⁷.0¹³,¹⁶]hexadec-6-en-11-yl benzoate)

3D MOL for NP0294374 ((1s,2s,3s,5s,8r,9r,10s,11s,13r,16s)-5,8,9,16-tetrakis(acetyloxy)-2-(benzoyloxy)-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.0³,⁷.0¹³,¹⁶]hexadec-6-en-11-yl benzoate)

3D SDF for NP0294374 ((1s,2s,3s,5s,8r,9r,10s,11s,13r,16s)-5,8,9,16-tetrakis(acetyloxy)-2-(benzoyloxy)-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.0³,⁷.0¹³,¹⁶]hexadec-6-en-11-yl benzoate)

3D-SDF for NP0294374 ((1s,2s,3s,5s,8r,9r,10s,11s,13r,16s)-5,8,9,16-tetrakis(acetyloxy)-2-(benzoyloxy)-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.0³,⁷.0¹³,¹⁶]hexadec-6-en-11-yl benzoate)

PDB for NP0294374 ((1s,2s,3s,5s,8r,9r,10s,11s,13r,16s)-5,8,9,16-tetrakis(acetyloxy)-2-(benzoyloxy)-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.0³,⁷.0¹³,¹⁶]hexadec-6-en-11-yl benzoate)

3D PDB for NP0294374 ((1s,2s,3s,5s,8r,9r,10s,11s,13r,16s)-5,8,9,16-tetrakis(acetyloxy)-2-(benzoyloxy)-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.0³,⁷.0¹³,¹⁶]hexadec-6-en-11-yl benzoate)

SMILES for NP0294374 ((1s,2s,3s,5s,8r,9r,10s,11s,13r,16s)-5,8,9,16-tetrakis(acetyloxy)-2-(benzoyloxy)-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.0³,⁷.0¹³,¹⁶]hexadec-6-en-11-yl benzoate)

INCHI for NP0294374 ((1s,2s,3s,5s,8r,9r,10s,11s,13r,16s)-5,8,9,16-tetrakis(acetyloxy)-2-(benzoyloxy)-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.0³,⁷.0¹³,¹⁶]hexadec-6-en-11-yl benzoate)

Structure for NP0294374 ((1s,2s,3s,5s,8r,9r,10s,11s,13r,16s)-5,8,9,16-tetrakis(acetyloxy)-2-(benzoyloxy)-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.0³,⁷.0¹³,¹⁶]hexadec-6-en-11-yl benzoate)

3D Structure for NP0294374 ((1s,2s,3s,5s,8r,9r,10s,11s,13r,16s)-5,8,9,16-tetrakis(acetyloxy)-2-(benzoyloxy)-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.0³,⁷.0¹³,¹⁶]hexadec-6-en-11-yl benzoate)