NP-MRD: Showing NP-Card for 2-[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosan-22-yl]propan-2-yl acetate (NP0216967)

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Record Information

Version

2.0

Created at

2022-09-05 17:08:32 UTC

Updated at

2022-09-05 17:08:32 UTC

NP-MRD ID

NP0216967

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosan-22-yl]propan-2-yl acetate

Description

(23R,24S)-3beta-(beta-D-Galactopyranosyloxy)-9beta,19-cyclo-16beta,23:16,24-Diepoxy-5alpha-lanostane-15alpha,25-diol 25-acetate belongs to the class of organic compounds known as cucurbitacin glycosides. These are polycyclic compounds containing a carbohydrate derivative glycosidically linked to a curcubitane nucleus. 2-[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosan-22-yl]propan-2-yl acetate is found in Actaea cimicifuga and Actaea simplex. Based on a literature review very few articles have been published on (23R,24S)-3beta-(beta-D-Galactopyranosyloxy)-9beta,19-cyclo-16beta,23:16,24-Diepoxy-5alpha-lanostane-15alpha,25-diol 25-acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052219082D          

 49 56  0  0  1  0            999 V2000
    7.8818    1.6800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1877    1.2341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2267    0.4101    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4545    1.6124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7604    1.1665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3145    1.8607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2062    0.4724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0662    0.7207    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2518    1.0383    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6551    0.3776    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3266    0.0746    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0165   -0.1487    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7079   -0.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8619   -1.1274    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5715   -1.8997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3290   -0.4393    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4861   -0.3913    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7861   -1.1598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9120   -0.9838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1119   -0.7828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8858    0.0106    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3117   -0.5819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0857    0.2116    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4884   -0.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2886   -0.1800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5146    0.6134    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3148    0.8144    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5408    1.6078    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3410    1.8088    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5670    2.6022    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3672    2.8031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9413    2.2106    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9929    3.1947    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2190    3.9881    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1928    2.9937    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6187    3.5862    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9667    2.2003    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1666    1.9994    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9405    1.2059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6237    1.6684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6037    1.9590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1404    1.0050    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4337    1.5975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2339    1.3965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4599    0.6031    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2587    0.4069    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1209    1.2204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9555    0.8600    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9666    1.6849    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
  5  7  1  0  0  0  0
  8  5  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 12 11  1  6  0  0  0
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 16 10  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  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  6  0  0  0
 23 22  1  6  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  6  0  0  0
 28 27  1  6  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  6  0  0  0
 31 32  1  0  0  0  0
 30 33  1  0  0  0  0
 33 34  1  6  0  0  0
 33 35  1  0  0  0  0
 35 36  1  6  0  0  0
 35 37  1  0  0  0  0
 28 37  1  0  0  0  0
 37 38  1  1  0  0  0
 26 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
 39 42  1  0  0  0  0
 23 42  1  0  0  0  0
 42 43  1  6  0  0  0
 43 44  1  0  0  0  0
 45 44  1  1  0  0  0
 21 45  1  0  0  0  0
 45 46  1  0  0  0  0
 17 46  1  0  0  0  0
 46 47  1  1  0  0  0
 46 48  1  0  0  0  0
 10 48  1  0  0  0  0
 48 49  1  1  0  0  0
M  END

     RDKit          3D

109116  0  0  0  0  0  0  0  0999 V2000
  -10.8041   -0.2403    0.0579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3963   -0.6288   -0.3118 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8991   -1.7070    0.1091 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6287    0.1731   -1.1073 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3025   -0.0786   -1.5198 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2515   -1.3252   -2.3870 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9121    1.0821   -2.4223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3846   -0.1894   -0.3324 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0719   -0.4388   -0.6935 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2921    0.5510   -0.1369 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1174    1.6730   -0.2183 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2997    1.1563    0.3523 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.1596    0.9473    1.8247 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7205    1.0440    2.2822 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.6247    0.3677    3.6398 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8785    0.2470    1.2909 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4414    0.6047    1.2997 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2683    2.1013    1.3221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5890    0.0017    2.3502 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2029    0.4897    2.1964 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3459    0.6222    0.8268 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4298    1.7402    0.6637 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7664    0.3120    0.6697 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5961   -0.1412    1.8549 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0261    0.2580    1.4567 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5261   -0.6683    0.3677 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7752   -0.2324    0.0078 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7809   -1.1621    0.0833 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.6558   -0.8135    1.0612 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6980    0.0043    0.7560 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.1749    1.3708    0.3762 C   0  0  0  0  0  0  0  0  0  0  0  0
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    9.5802   -0.5403   -0.3391 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.6620    0.4195   -1.3435 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.8333   -1.7924   -1.6818 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1711   -0.4770   -0.5087 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -0.5557    0.5143   -0.3107 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9611    0.0775   -0.0316 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1590   -1.4032   -0.2051 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9939    0.7529   -0.9318 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0624    0.1443   -2.1706 O   0  0  0  0  0  0  0  0  0  0  0  0
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  -11.3970   -0.0603   -0.8540 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.3823   -2.2508   -1.8296 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.6201   -1.0934    2.4193 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4593   -0.1805    2.8213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1189    1.4937    2.7087 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.7232   -0.5885   -2.5938 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6026   -0.2657   -2.3486 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0340   -1.4567   -1.0767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6505    1.5214   -0.8205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9795   -1.5998   -1.3044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2080   -1.6856   -0.0474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4259   -2.0122    0.3371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8159    1.8310   -0.9742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3242    0.8437   -2.8212 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11 10  1  0
 10  9  1  6
  9  8  1  0
  8  5  1  0
  5  6  1  0
  5  7  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
 10 48  1  0
 48 49  1  0
 48 46  1  0
 46 47  1  1
 46 45  1  0
 45 44  1  0
 44 43  1  0
 43 42  1  0
 42 23  1  0
 23 22  1  6
 21 22  1  1
 21 20  1  0
 20 19  1  0
 19 17  1  0
 17 18  1  6
 17 16  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 30 33  1  0
 33 34  1  0
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 35 36  1  0
 35 37  1  0
 37 38  1  0
 26 39  1  0
 39 40  1  0
 39 41  1  0
 16 14  1  0
 37 28  1  0
  8 12  1  0
 17 46  1  0
 16 10  1  0
 21 45  1  0
 39 42  1  0
 21 23  1  0
 15 64  1  0
 15 65  1  0
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 14 63  1  1
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 13 62  1  0
 12 60  1  1
  8 59  1  1
  6 53  1  0
  6 54  1  0
  6 55  1  0
  7 56  1  0
  7 57  1  0
  7 58  1  0
  1 50  1  0
  1 51  1  0
  1 52  1  0
 48108  1  6
 49109  1  0
 47105  1  0
 47106  1  0
 47107  1  0
 45104  1  6
 44102  1  0
 44103  1  0
 43100  1  0
 43101  1  0
 42 99  1  1
 22 75  1  0
 22 76  1  0
 20 73  1  0
 20 74  1  0
 19 71  1  0
 19 72  1  0
 18 68  1  0
 18 69  1  0
 18 70  1  0
 16 67  1  1
 24 77  1  0
 24 78  1  0
 25 79  1  0
 25 80  1  0
 26 81  1  1
 28 82  1  1
 30 83  1  1
 31 84  1  0
 31 85  1  0
 32 86  1  0
 33 87  1  1
 34 88  1  0
 35 89  1  1
 36 90  1  0
 37 91  1  6
 38 92  1  0
 40 93  1  0
 40 94  1  0
 40 95  1  0
 41 96  1  0
 41 97  1  0
 41 98  1  0
M  END


  Mrv1652309052219082D          

 49 56  0  0  1  0            999 V2000
    7.8818    1.6800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1877    1.2341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2267    0.4101    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4545    1.6124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7604    1.1665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3145    1.8607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2062    0.4724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0662    0.7207    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2518    1.0383    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6551    0.3776    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3266    0.0746    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0165   -0.1487    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7079   -0.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8619   -1.1274    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5715   -1.8997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3290   -0.4393    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4861   -0.3913    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7861   -1.1598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9120   -0.9838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1119   -0.7828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8858    0.0106    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3117   -0.5819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0857    0.2116    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4884   -0.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2886   -0.1800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5146    0.6134    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3148    0.8144    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5408    1.6078    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3410    1.8088    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5670    2.6022    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3672    2.8031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9413    2.2106    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9929    3.1947    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2190    3.9881    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1928    2.9937    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6187    3.5862    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9667    2.2003    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1666    1.9994    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9405    1.2059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6237    1.6684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6037    1.9590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1404    1.0050    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4337    1.5975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2339    1.3965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4599    0.6031    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2587    0.4069    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1209    1.2204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9555    0.8600    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9666    1.6849    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
  5  7  1  0  0  0  0
  8  5  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 12 11  1  6  0  0  0
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 16 10  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  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  6  0  0  0
 23 22  1  6  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  6  0  0  0
 28 27  1  6  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  6  0  0  0
 31 32  1  0  0  0  0
 30 33  1  0  0  0  0
 33 34  1  6  0  0  0
 33 35  1  0  0  0  0
 35 36  1  6  0  0  0
 35 37  1  0  0  0  0
 28 37  1  0  0  0  0
 37 38  1  1  0  0  0
 26 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
 39 42  1  0  0  0  0
 23 42  1  0  0  0  0
 42 43  1  6  0  0  0
 43 44  1  0  0  0  0
 45 44  1  1  0  0  0
 21 45  1  0  0  0  0
 45 46  1  0  0  0  0
 17 46  1  0  0  0  0
 46 47  1  1  0  0  0
 46 48  1  0  0  0  0
 10 48  1  0  0  0  0
 48 49  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0216967

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C[C@H]2O[C@@]3(O[C@@H]2C(C)(C)OC(C)=O)[C@H](O)[C@@]2(C)[C@@H]4CC[C@@H]5[C@]6(C[C@@]46CC[C@]2(C)[C@@H]13)CC[C@H](O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)C5(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C38H60O11/c1-18-15-20-29(33(5,6)47-19(2)40)49-38(48-20)28(18)34(7)13-14-37-17-36(37)12-11-24(46-30-27(43)26(42)25(41)21(16-39)45-30)32(3,4)22(36)9-10-23(37)35(34,8)31(38)44/h18,20-31,39,41-44H,9-17H2,1-8H3/t18-,20-,21-,22+,23+,24+,25+,26+,27-,28-,29+,30+,31-,34-,35-,36-,37+,38+/m1/s1

> <INCHI_KEY>
NCPUFUMYGPQEOY-SVPNHDCUSA-N

> <FORMULA>
C38H60O11

> <MOLECULAR_WEIGHT>
692.887

> <EXACT_MASS>
692.413562752

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
109

> <JCHEM_AVERAGE_POLARIZABILITY>
77.02828457566542

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(1S,2R,3S,4R,7R,9S,12R,14S,17R,18R,19R,21R,22S)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-23,24-dioxaheptacyclo[19.2.1.0^{1,18}.0^{3,17}.0^{4,14}.0^{7,12}.0^{12,14}]tetracosan-22-yl]propan-2-yl acetate

> <JCHEM_LOGP>
2.794221152333332

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.782106840267058

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.121883230629429

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810835440417778

> <JCHEM_POLAR_SURFACE_AREA>
164.37

> <JCHEM_REFRACTIVITY>
174.60940000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2-[(1S,2R,3S,4R,7R,9S,12R,14S,17R,18R,19R,21R,22S)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-23,24-dioxaheptacyclo[19.2.1.0^{1,18}.0^{3,17}.0^{4,14}.0^{7,12}.0^{12,14}]tetracosan-22-yl]propan-2-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      14.713   3.136   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.417   2.304   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      13.490   0.765   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      12.048   3.010   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      10.753   2.177   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.920   3.473   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.585   0.882   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.457   1.345   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       7.937   1.938   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.823   0.705   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       8.076   0.139   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       9.364  -0.278   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.788  -1.797   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.209  -2.105   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.667  -3.546   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.214  -0.820   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.641  -0.730   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.201  -2.165   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.569  -1.836   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.076  -1.461   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.654   0.020   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.582  -1.086   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.160   0.395   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.912  -0.711   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.405  -0.336   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -2.827   1.145   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -4.321   1.520   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -4.743   3.001   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -6.237   3.376   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -6.658   4.857   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -8.152   5.232   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -9.224   4.127   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -5.587   5.963   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -6.009   7.444   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -4.093   5.588   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -3.022   6.694   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -3.671   4.107   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      -2.178   3.732   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      -1.756   2.251   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -3.031   3.114   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -1.127   3.657   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -0.262   1.876   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       0.810   2.982   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       2.303   2.607   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       2.725   1.126   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       4.216   0.760   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       3.959   2.278   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       5.517   1.605   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0       5.538   3.145   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    7    8                                             
CONECT    6    5                                                            
CONECT    7    5                                                            
CONECT    8    5    9   12                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   16   48                                             
CONECT   11   10   12                                                       
CONECT   12   11    8   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   10   17                                                  
CONECT   17   16   18   19   46                                             
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23   45                                             
CONECT   22   21   23                                                       
CONECT   23   22   21   24   42                                             
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   39                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   37                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   33                                                  
CONECT   31   30   32                                                       
CONECT   32   31                                                            
CONECT   33   30   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   28   38                                                  
CONECT   38   37                                                            
CONECT   39   26   40   41   42                                             
CONECT   40   39                                                            
CONECT   41   39                                                            
CONECT   42   39   23   43                                                  
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   21   46                                                  
CONECT   46   45   17   47   48                                             
CONECT   47   46                                                            
CONECT   48   46   10   49                                                  
CONECT   49   48                                                            
MASTER        0    0    0    0    0    0    0    0   49    0  112    0
END

View in JSmol

Synonyms

Value	Source
(23R,24S)-3b-(b-D-Galactopyranosyloxy)-9b,19-cyclo-16b,23:16,24-diepoxy-5a-lanostane-15a,25-diol 25-acetate	Generator
(23R,24S)-3b-(b-D-Galactopyranosyloxy)-9b,19-cyclo-16b,23:16,24-diepoxy-5a-lanostane-15a,25-diol 25-acetic acid	Generator
(23R,24S)-3beta-(beta-D-Galactopyranosyloxy)-9beta,19-cyclo-16beta,23:16,24-diepoxy-5alpha-lanostane-15alpha,25-diol 25-acetic acid	Generator
(23R,24S)-3Β-(β-D-galactopyranosyloxy)-9β,19-cyclo-16β,23:16,24-diepoxy-5α-lanostane-15α,25-diol 25-acetate	Generator
(23R,24S)-3Β-(β-D-galactopyranosyloxy)-9β,19-cyclo-16β,23:16,24-diepoxy-5α-lanostane-15α,25-diol 25-acetic acid	Generator

Chemical Formula

C₃₈H₆₀O₁₁

Average Mass

692.8870 Da

Monoisotopic Mass

692.41356 Da

IUPAC Name

2-[(1S,2R,3S,4R,7R,9S,12R,14S,17R,18R,19R,21R,22S)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-23,24-dioxaheptacyclo[19.2.1.0^{1,18}.0^{3,17}.0^{4,14}.0^{7,12}.0^{12,14}]tetracosan-22-yl]propan-2-yl acetate

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@@H]1C[C@H]2O[C@@]3(O[C@@H]2C(C)(C)OC(C)=O)[C@H](O)[C@@]2(C)[C@@H]4CC[C@@H]5[C@]6(C[C@@]46CC[C@]2(C)[C@@H]13)CC[C@H](O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)C5(C)C

InChI Identifier

InChI=1S/C38H60O11/c1-18-15-20-29(33(5,6)47-19(2)40)49-38(48-20)28(18)34(7)13-14-37-17-36(37)12-11-24(46-30-27(43)26(42)25(41)21(16-39)45-30)32(3,4)22(36)9-10-23(37)35(34,8)31(38)44/h18,20-31,39,41-44H,9-17H2,1-8H3/t18-,20-,21-,22+,23+,24+,25+,26+,27-,28-,29+,30+,31-,34-,35-,36-,37+,38+/m1/s1

InChI Key

NCPUFUMYGPQEOY-SVPNHDCUSA-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
Actaea cimicifuga	LOTUS Database	35616633
Actaea simplex	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cucurbitacin glycosides. These are polycyclic compounds containing a carbohydrate derivative glycosidically linked to a curcubitane nucleus.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroidal glycosides

Direct Parent

Cucurbitacin glycosides

Alternative Parents

Substituents

Cucurbitacin glycoside skeleton
Triterpene saponin
Triterpene glycoside
Cycloartanol-skeleton
9b,19-cyclo-lanostane-skeleton
Cycloartane-skeleton
Triterpenoid
15-hydroxysteroid
Hydroxysteroid
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Ketal
Oxepane
Monosaccharide
Oxane
Meta-dioxolane
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Monocarboxylic acid or derivatives
Polyol
Acetal
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Organooxygen compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
Alcohol
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	2.79	ChemAxon
pKa (Strongest Acidic)	12.12	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	164.37 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	174.61 m³·mol⁻¹	ChemAxon
Polarizability	77.03 Å³	ChemAxon
Number of Rings	8	ChemAxon
Bioavailability	Yes	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

102600400

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

MOL for NP0216967 (2-[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosan-22-yl]propan-2-yl acetate)

3D MOL for NP0216967 (2-[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosan-22-yl]propan-2-yl acetate)

3D SDF for NP0216967 (2-[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosan-22-yl]propan-2-yl acetate)

3D-SDF for NP0216967 (2-[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosan-22-yl]propan-2-yl acetate)

PDB for NP0216967 (2-[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosan-22-yl]propan-2-yl acetate)

3D PDB for NP0216967 (2-[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosan-22-yl]propan-2-yl acetate)

SMILES for NP0216967 (2-[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosan-22-yl]propan-2-yl acetate)

INCHI for NP0216967 (2-[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosan-22-yl]propan-2-yl acetate)

Structure for NP0216967 (2-[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosan-22-yl]propan-2-yl acetate)