NP-MRD: Showing NP-Card for methyl 3-{[4-(acetyloxy)-3-ethyl-4-methylpent-2-enoyl]oxy}-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-5,18-dioxapentacyclo[12.5.0.0¹,⁶.0²,¹⁷.0⁸,¹³]nonadec-11-ene-17-carboxylate (NP0252102)

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Record Information

Version

2.0

Created at

2022-09-07 15:30:21 UTC

Updated at

2022-09-07 15:30:21 UTC

NP-MRD ID

NP0252102

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 3-{[4-(acetyloxy)-3-ethyl-4-methylpent-2-enoyl]oxy}-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-5,18-dioxapentacyclo[12.5.0.0¹,⁶.0²,¹⁷.0⁸,¹³]nonadec-11-ene-17-carboxylate

Description

Methyl 3-{[4-(acetyloxy)-3-ethyl-4-methylpent-2-enoyl]oxy}-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-5,18-dioxapentacyclo[12.5.0.0¹,⁶.0²,¹⁷.0⁸,¹³]Nonadec-11-ene-17-carboxylate belongs to the class of organic compounds known as quassinoids. These are a group of compounds chemically degraded from triterpenes. According to their basic skeleton, quassinoids are categorized into five distinct groups, C-18, C-19, C-20, C-22 and C-25 types. The C-20 quassinoids can be further classified into two types, tetracyclic and the pentacyclic. The tetracyclic variety does not have oxygenation at C-20, while the pentacyclic quassinoids possess additional oxygenation at C-20 that allows for the formation of an additional ring. methyl 3-{[4-(acetyloxy)-3-ethyl-4-methylpent-2-enoyl]oxy}-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-5,18-dioxapentacyclo[12.5.0.0¹,⁶.0²,¹⁷.0⁸,¹³]nonadec-11-ene-17-carboxylate is found in Brucea javanica. Based on a literature review very few articles have been published on methyl 3-{[4-(acetyloxy)-3-ethyl-4-methylpent-2-enoyl]oxy}-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-5,18-dioxapentacyclo[12.5.0.0¹,⁶.0²,¹⁷.0⁸,¹³]Nonadec-11-ene-17-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072217302D          

 55 60  0  0  0  0            999 V2000
   -1.9432    4.6084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4404    3.9544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7554    3.1919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2526    2.5378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4348    2.6462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1197    3.4087    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0681    1.9922    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8859    2.1006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2319    2.8408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7719    3.5257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0553    2.8813    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5044    2.1874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3237    2.3628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8680    1.7463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6821    1.8796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9738    2.6513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2046    1.2412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0188    1.3744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9130    0.4694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4355   -0.1690    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1438   -0.9407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3297   -1.0740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8072   -0.4356    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0380   -1.8458    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5605   -2.4842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2689   -3.2559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7914   -3.8944    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3747   -2.3509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8972   -2.9893    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6664   -1.5792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4805   -1.4459    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0988    0.3361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5763    0.9746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2756    0.2064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7552    0.8600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5884    0.0576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2027   -0.4931    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8133   -0.1941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5880   -0.9877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2706    0.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7748   -0.2140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0441   -0.1144    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0980   -0.9731    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6023   -1.6325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5543    0.7672    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9811    1.4970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0807    1.4337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4803    1.3961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5733    3.0834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6817    3.9013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4648    2.2656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3911    2.9750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8939    3.6291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7118    3.5206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5789    4.3916    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  4  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 25 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 21 30  1  0  0  0  0
 30 31  1  0  0  0  0
 19 32  2  0  0  0  0
 32 33  1  0  0  0  0
 14 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 41 43  1  0  0  0  0
 43 44  1  0  0  0  0
 40 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 12 47  1  0  0  0  0
 35 47  1  0  0  0  0
 47 48  1  0  0  0  0
  8 48  1  0  0  0  0
 40 48  1  0  0  0  0
  3 49  1  0  0  0  0
 49 50  1  0  0  0  0
 49 51  1  0  0  0  0
 49 52  1  0  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

105110  0  0  0  0  0  0  0  0999 V2000
   -7.7689   -2.4688   -0.9625 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4150   -1.0639   -0.6200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9319   -0.7669   -0.9039 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6452    0.1716   -1.7559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4289    0.7095   -2.2675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5419    1.7061   -3.1228 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1184    0.3828   -2.0472 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0689    1.0007   -2.6434 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5550    0.0432   -3.7168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2556   -0.3244   -4.6828 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2638   -0.3987   -3.5625 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2767   -0.4934   -2.2848 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6333   -1.0764   -2.1599 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0098   -1.1759   -0.7327 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6229   -2.5161   -0.4343 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8290   -2.6449   -1.3751 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1507   -2.5277    0.9426 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8301   -3.5064    1.3341 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8782   -1.4051    1.8306 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6627   -1.1897    2.9843 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7901   -0.3591    3.0121 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8720   -0.8154    2.0421 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4376   -0.7086    0.7360 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0794    0.0490    2.3123 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.7439   -0.4139    3.4640 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7841    1.5069    2.4360 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.9974    2.2394    1.1063 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0000    3.6173    1.2950 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5968    1.8407    3.0217 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5000    1.0847    2.6590 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1548    1.1685    1.3335 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9010   -0.5953    1.5533 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0088   -0.7715    0.3165 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0991   -1.7996    0.8060 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4454    0.5960   -0.0454 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4889    1.2062    0.9134 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2047    0.3458    1.7131 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3299    2.2389    0.1904 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6022    3.3652    0.9304 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7578    2.6653   -1.1291 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4595    3.8693   -1.5834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7126    3.8462   -1.6465 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7749    5.0136   -1.9386 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4536    6.1834   -2.3803 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6321    2.8597   -1.1217 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2416    1.8375   -1.9085 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2122    0.7431   -1.4986 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9005    1.5415   -2.0627 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.9773   -1.6164   -0.1615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6014   -2.8743   -0.8718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8866   -0.8137    0.4407 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7181   -2.1169    1.0124 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9863   -2.9547    1.8552 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5889   -3.5517    3.0978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7879   -3.2741    1.6515 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1356   -3.2429   -0.5276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8111   -2.7003   -0.5927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8255   -2.6433   -2.0676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0366   -0.3409   -1.1443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5088   -0.9225    0.4738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5655    0.6743   -2.1922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5298    1.8409   -3.2960 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3764   -1.2257   -1.7596 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3496   -0.5131   -2.7970 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6178   -2.1120   -2.5923 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8811   -0.4543   -0.6048 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9634   -3.3682   -0.6720 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5762   -3.2632   -0.8372 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2215   -1.6463   -1.6606 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5538   -3.1694   -2.2892 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2467   -0.4400    4.0179 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1498   -1.8619    2.2354 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1300   -0.4577    0.0938 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7749   -0.0860    1.4351 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6007    0.0655    3.5684 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5976    1.9294    3.1040 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1917    2.0115    0.3912 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9515    1.9336    0.6641 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1845    3.9635    1.7028 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6561    1.4060    3.3189 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5940    1.9489    1.1008 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6837    0.2445    2.1989 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7088   -2.7651    0.8133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8201   -2.0627    0.3397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1503   -1.7155    1.9140 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3987    1.2222    0.1813 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0350    1.8451    1.7038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4886    0.6957    2.5709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3013    1.7511   -0.0310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2046    3.2486    1.8288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3514    5.8079   -2.9305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8037    6.7531   -3.0751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7878    6.7650   -1.5113 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2010    2.0512   -2.9713 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2214    1.6623   -1.4825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4705    2.0723   -3.0320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5039   -2.9440   -1.0708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8479   -3.8107   -0.3398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1734   -2.9116   -1.8447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7946   -0.9633    1.5775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1301    0.2833    0.3984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9140   -1.0993    0.0634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6790   -3.4660    3.1100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2301   -4.5971    3.2344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2139   -3.0018    3.9950 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8 48  1  0
 48 47  1  0
 47 46  1  6
 46 45  1  0
 45 40  1  0
 40 38  1  0
 38 39  1  0
 38 36  1  0
 36 37  1  0
 36 35  1  0
 35 33  1  0
 33 34  1  1
 33 32  1  0
 32 19  2  0
 19 20  1  0
 20 21  1  0
 21 30  1  0
 30 31  1  0
 30 29  1  0
 29 26  1  0
 26 27  1  0
 27 28  1  0
 26 24  1  0
 24 25  1  0
 24 22  1  0
 22 23  1  0
 19 17  1  0
 17 18  2  0
 17 15  1  0
 15 16  1  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11  9  1  0
  9 10  2  0
 40 41  1  6
 41 42  2  0
 41 43  1  0
 43 44  1  0
  3 49  1  0
 49 50  1  0
 49 51  1  0
 49 52  1  0
 52 53  1  0
 53 54  1  0
 53 55  2  0
  9  8  1  0
 40 48  1  0
 14 33  1  0
 35 47  1  0
 22 21  1  0
 12 47  1  0
  1 56  1  0
  1 57  1  0
  1 58  1  0
  2 59  1  0
  2 60  1  0
  4 61  1  0
  8 62  1  6
 48 96  1  6
 46 94  1  0
 46 95  1  0
 38 89  1  6
 39 90  1  0
 36 87  1  1
 37 88  1  0
 35 86  1  6
 34 83  1  0
 34 84  1  0
 34 85  1  0
 32 82  1  0
 21 71  1  1
 30 80  1  1
 31 81  1  0
 26 76  1  1
 27 77  1  0
 27 78  1  0
 28 79  1  0
 24 74  1  6
 25 75  1  0
 22 72  1  1
 23 73  1  0
 15 67  1  1
 16 68  1  0
 16 69  1  0
 16 70  1  0
 14 66  1  6
 13 64  1  0
 13 65  1  0
 12 63  1  1
 44 91  1  0
 44 92  1  0
 44 93  1  0
 50 97  1  0
 50 98  1  0
 50 99  1  0
 51100  1  0
 51101  1  0
 51102  1  0
 54103  1  0
 54104  1  0
 54105  1  0
M  END


  Mrv1652309072217302D          

 55 60  0  0  0  0            999 V2000
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   -1.4404    3.9544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7554    3.1919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2526    2.5378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4348    2.6462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1197    3.4087    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0681    1.9922    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8859    2.1006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2319    2.8408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7719    3.5257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0553    2.8813    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5044    2.1874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3237    2.3628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8680    1.7463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6821    1.8796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9738    2.6513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2046    1.2412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0188    1.3744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9130    0.4694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4355   -0.1690    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1438   -0.9407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3297   -1.0740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8072   -0.4356    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0380   -1.8458    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5605   -2.4842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2689   -3.2559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7914   -3.8944    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3747   -2.3509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8972   -2.9893    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6664   -1.5792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4805   -1.4459    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0988    0.3361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5763    0.9746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2756    0.2064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7552    0.8600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5884    0.0576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2027   -0.4931    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8133   -0.1941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5880   -0.9877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2706    0.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7748   -0.2140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0441   -0.1144    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0980   -0.9731    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6023   -1.6325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5543    0.7672    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9811    1.4970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0807    1.4337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4803    1.3961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5733    3.0834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6817    3.9013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4648    2.2656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3911    2.9750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8939    3.6291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7118    3.5206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5789    4.3916    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  4  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 25 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 21 30  1  0  0  0  0
 30 31  1  0  0  0  0
 19 32  2  0  0  0  0
 32 33  1  0  0  0  0
 14 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 41 43  1  0  0  0  0
 43 44  1  0  0  0  0
 40 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 12 47  1  0  0  0  0
 35 47  1  0  0  0  0
 47 48  1  0  0  0  0
  8 48  1  0  0  0  0
 40 48  1  0  0  0  0
  3 49  1  0  0  0  0
 49 50  1  0  0  0  0
 49 51  1  0  0  0  0
 49 52  1  0  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>
NP0252102

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(=CC(=O)OC1C2C34COC2(C(O)C(O)C3C2(C)C=C(OC3C(O)OC(CO)C(O)C3O)C(=O)C(C)C2CC4OC1=O)C(=O)OC)C(C)(C)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C37H50O18/c1-8-16(34(4,5)55-15(3)39)9-21(40)54-27-29-36-13-50-37(29,33(48)49-7)30(45)25(44)28(36)35(6)11-18(22(41)14(2)17(35)10-20(36)53-32(27)47)51-26-24(43)23(42)19(12-38)52-31(26)46/h9,11,14,17,19-20,23-31,38,42-46H,8,10,12-13H2,1-7H3

> <INCHI_KEY>
KUWUPYZTOZNFMS-UHFFFAOYSA-N

> <FORMULA>
C37H50O18

> <MOLECULAR_WEIGHT>
782.789

> <EXACT_MASS>
782.29971477

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
105

> <JCHEM_AVERAGE_POLARIZABILITY>
77.85404212571848

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 3-{[4-(acetyloxy)-3-ethyl-4-methylpent-2-enoyl]oxy}-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-5,18-dioxapentacyclo[12.5.0.0^{1,6}.0^{2,17}.0^{8,13}]nonadec-11-ene-17-carboxylate

> <JCHEM_LOGP>
-1.4611367916666658

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.475424911549926

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.291912745468835

> <JCHEM_PKA_STRONGEST_BASIC>
-2.98107983367416

> <JCHEM_POLAR_SURFACE_AREA>
271.34

> <JCHEM_REFRACTIVITY>
182.20730000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl 3-{[4-(acetyloxy)-3-ethyl-4-methylpent-2-enoyl]oxy}-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-5,18-dioxapentacyclo[12.5.0.0^{1,6}.0^{2,17}.0^{8,13}]nonadec-11-ene-17-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -3.627   8.602   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.689   7.381   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.277   5.958   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.338   4.737   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.812   4.940   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -0.224   6.363   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       0.127   3.719   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.654   3.921   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.299   5.303   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       1.441   6.581   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       3.837   5.378   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       4.675   4.083   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.204   4.411   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.220   3.260   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.740   3.509   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.284   4.949   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.715   2.317   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      11.235   2.566   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       9.171   0.876   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      10.146  -0.315   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       9.602  -1.756   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.082  -2.005   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       7.107  -0.813   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       7.538  -3.445   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       8.513  -4.637   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.969  -6.078   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       8.944  -7.269   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      10.033  -4.388   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      11.008  -5.580   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      10.577  -2.948   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      12.097  -2.699   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       7.651   0.627   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.676   1.819   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.114   0.385   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.143   1.605   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       4.832   0.108   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       5.978  -0.920   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       3.385  -0.362   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       2.964  -1.844   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       2.372   0.831   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       1.446  -0.400   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      -0.082  -0.214   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0       2.050  -1.816   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0       1.124  -3.047   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       1.035   1.432   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       1.831   2.794   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       3.884   2.676   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       2.763   2.606   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      -4.803   5.756   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      -5.006   7.282   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      -4.601   4.229   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0      -6.330   5.553   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0      -7.269   6.774   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      -8.795   6.572   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0      -6.681   8.198   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   49                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   48                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   47                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   33                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   32                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   30                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   28                                                  
CONECT   26   25   27                                                       
CONECT   27   26                                                            
CONECT   28   25   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   21   31                                                  
CONECT   31   30                                                            
CONECT   32   19   33                                                       
CONECT   33   32   14   34   35                                             
CONECT   34   33                                                            
CONECT   35   33   36   47                                                  
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41   45   48                                             
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   44                                                       
CONECT   44   43                                                            
CONECT   45   40   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   12   35   48                                             
CONECT   48   47    8   40                                                  
CONECT   49    3   50   51   52                                             
CONECT   50   49                                                            
CONECT   51   49                                                            
CONECT   52   49   53                                                       
CONECT   53   52   54   55                                                  
CONECT   54   53                                                            
CONECT   55   53                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  120    0
END

View in JSmol

Synonyms

Value	Source
Methyl 3-{[4-(acetyloxy)-3-ethyl-4-methylpent-2-enoyl]oxy}-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-5,18-dioxapentacyclo[12.5.0.0,.0,.0,]nonadec-11-ene-17-carboxylic acid	Generator

Chemical Formula

C₃₇H₅₀O₁₈

Average Mass

782.7890 Da

Monoisotopic Mass

782.29971 Da

IUPAC Name

methyl 3-{[4-(acetyloxy)-3-ethyl-4-methylpent-2-enoyl]oxy}-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-5,18-dioxapentacyclo[12.5.0.0^{1,6}.0^{2,17}.0^{8,13}]nonadec-11-ene-17-carboxylate

Traditional Name

methyl 3-{[4-(acetyloxy)-3-ethyl-4-methylpent-2-enoyl]oxy}-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-5,18-dioxapentacyclo[12.5.0.0^{1,6}.0^{2,17}.0^{8,13}]nonadec-11-ene-17-carboxylate

CAS Registry Number

Not Available

SMILES

CCC(=CC(=O)OC1C2C34COC2(C(O)C(O)C3C2(C)C=C(OC3C(O)OC(CO)C(O)C3O)C(=O)C(C)C2CC4OC1=O)C(=O)OC)C(C)(C)OC(C)=O

InChI Identifier

InChI=1S/C37H50O18/c1-8-16(34(4,5)55-15(3)39)9-21(40)54-27-29-36-13-50-37(29,33(48)49-7)30(45)25(44)28(36)35(6)11-18(22(41)14(2)17(35)10-20(36)53-32(27)47)51-26-24(43)23(42)19(12-38)52-31(26)46/h9,11,14,17,19-20,23-31,38,42-46H,8,10,12-13H2,1-7H3

InChI Key

KUWUPYZTOZNFMS-UHFFFAOYSA-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
Brucea javanica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quassinoids. These are a group of compounds chemically degraded from triterpenes. According to their basic skeleton, quassinoids are categorized into five distinct groups, C-18, C-19, C-20, C-22 and C-25 types. The C-20 quassinoids can be further classified into two types, tetracyclic and the pentacyclic. The tetracyclic variety does not have oxygenation at C-20, while the pentacyclic quassinoids possess additional oxygenation at C-20 that allows for the formation of an additional ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Quassinoids

Alternative Parents

Substituents

C-20 quassinoid skeleton
Quassinoid
Naphthopyranone
Naphthopyran
Tetracarboxylic acid or derivatives
Hexose monosaccharide
Naphthalene
Furopyran
Delta_valerolactone
Oxepane
Fatty acid ester
Cyclohexenone
Delta valerolactone
Beta-hydroxy acid
Pyranone
Monosaccharide
Fatty acyl
Pyran
Oxane
Hydroxy acid
Cyclic alcohol
Furan
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Tetrahydrofuran
Cyclic ketone
Lactone
Ketone
Secondary alcohol
Hemiacetal
Carboxylic acid ester
Polyol
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Ether
Dialkyl ether
Carbonyl group
Organic oxide
Alcohol
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
Primary alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	-1.5	ChemAxon
pKa (Strongest Acidic)	11.29	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	271.34 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	182.21 m³·mol⁻¹	ChemAxon
Polarizability	77.85 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

162904165

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 3-{[4-(acetyloxy)-3-ethyl-4-methylpent-2-enoyl]oxy}-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-5,18-dioxapentacyclo[12.5.0.0¹,⁶.0²,¹⁷.0⁸,¹³]nonadec-11-ene-17-carboxylate (NP0252102)

MOL for NP0252102 (methyl 3-{[4-(acetyloxy)-3-ethyl-4-methylpent-2-enoyl]oxy}-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-5,18-dioxapentacyclo[12.5.0.0¹,⁶.0²,¹⁷.0⁸,¹³]nonadec-11-ene-17-carboxylate)

3D MOL for NP0252102 (methyl 3-{[4-(acetyloxy)-3-ethyl-4-methylpent-2-enoyl]oxy}-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-5,18-dioxapentacyclo[12.5.0.0¹,⁶.0²,¹⁷.0⁸,¹³]nonadec-11-ene-17-carboxylate)

3D SDF for NP0252102 (methyl 3-{[4-(acetyloxy)-3-ethyl-4-methylpent-2-enoyl]oxy}-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-5,18-dioxapentacyclo[12.5.0.0¹,⁶.0²,¹⁷.0⁸,¹³]nonadec-11-ene-17-carboxylate)

3D-SDF for NP0252102 (methyl 3-{[4-(acetyloxy)-3-ethyl-4-methylpent-2-enoyl]oxy}-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-5,18-dioxapentacyclo[12.5.0.0¹,⁶.0²,¹⁷.0⁸,¹³]nonadec-11-ene-17-carboxylate)

PDB for NP0252102 (methyl 3-{[4-(acetyloxy)-3-ethyl-4-methylpent-2-enoyl]oxy}-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-5,18-dioxapentacyclo[12.5.0.0¹,⁶.0²,¹⁷.0⁸,¹³]nonadec-11-ene-17-carboxylate)

3D PDB for NP0252102 (methyl 3-{[4-(acetyloxy)-3-ethyl-4-methylpent-2-enoyl]oxy}-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-5,18-dioxapentacyclo[12.5.0.0¹,⁶.0²,¹⁷.0⁸,¹³]nonadec-11-ene-17-carboxylate)

SMILES for NP0252102 (methyl 3-{[4-(acetyloxy)-3-ethyl-4-methylpent-2-enoyl]oxy}-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-5,18-dioxapentacyclo[12.5.0.0¹,⁶.0²,¹⁷.0⁸,¹³]nonadec-11-ene-17-carboxylate)

INCHI for NP0252102 (methyl 3-{[4-(acetyloxy)-3-ethyl-4-methylpent-2-enoyl]oxy}-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-5,18-dioxapentacyclo[12.5.0.0¹,⁶.0²,¹⁷.0⁸,¹³]nonadec-11-ene-17-carboxylate)

Structure for NP0252102 (methyl 3-{[4-(acetyloxy)-3-ethyl-4-methylpent-2-enoyl]oxy}-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-5,18-dioxapentacyclo[12.5.0.0¹,⁶.0²,¹⁷.0⁸,¹³]nonadec-11-ene-17-carboxylate)

3D Structure for NP0252102 (methyl 3-{[4-(acetyloxy)-3-ethyl-4-methylpent-2-enoyl]oxy}-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-5,18-dioxapentacyclo[12.5.0.0¹,⁶.0²,¹⁷.0⁸,¹³]nonadec-11-ene-17-carboxylate)