NP-MRD: Showing NP-Card for 2-[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22r)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-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 (NP0185749)

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Record Information

Version

2.0

Created at

2022-09-04 01:17:08 UTC

Updated at

2022-09-04 01:17:08 UTC

NP-MRD ID

NP0185749

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22r)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-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

2-[(1S,2R,3S,4R,7R,9S,12R,14S,17R,18R,19R,21R,22R)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-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 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,22r)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-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 asiatica and Actaea cimicifuga. Based on a literature review very few articles have been published on 2-[(1S,2R,3S,4R,7R,9S,12R,14S,17R,18R,19R,21R,22R)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-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

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042203172D          

 47 54  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  2  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  0  0  0  0  0  0  0  0  0  0
   -2.9929    3.1947    0.0000 C   0  0  1  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  1  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  0  0  0  0
 31 32  1  1  0  0  0
 31 33  1  0  0  0  0
 33 34  1  6  0  0  0
 33 35  1  0  0  0  0
 28 35  1  0  0  0  0
 35 36  1  1  0  0  0
 26 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 37 40  1  0  0  0  0
 23 40  1  0  0  0  0
 40 41  1  6  0  0  0
 41 42  1  0  0  0  0
 43 42  1  1  0  0  0
 21 43  1  0  0  0  0
 43 44  1  0  0  0  0
 17 44  1  0  0  0  0
 44 45  1  1  0  0  0
 44 46  1  0  0  0  0
 10 46  1  0  0  0  0
 46 47  1  1  0  0  0
M  END

     RDKit          3D

105112  0  0  0  0  0  0  0  0999 V2000
  -10.1637    1.7519   -1.7005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7063    1.5816   -2.0156 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.2724   -1.4116    0.8266 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0832   -2.0189    2.1727 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5495   -2.2789   -0.1739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0955   -2.1581   -0.2336 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5877   -1.1345    0.5939 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8470   -1.6175    1.3880 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9522   -0.7846    0.1981 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5594   -1.4461   -1.0371 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0341   -1.4611   -0.7991 C   0  0  0  0  0  0  0  0  0  0  0  0
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    9.4538   -0.9489    0.4646 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.4783   -1.7851    0.0799 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.5631   -1.4457   -0.0599 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.7749   -1.1829   -0.6272 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.2117   -1.9661   -1.3070 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.0674   -2.7182    1.2730 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.2294   -1.9962    0.1547 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.4490   -1.2069    1.2728 H   0  0  0  0  0  0  0  0  0  0  0  0
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    9.4956   -0.0384   -1.4633 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.1198    2.5973    1.2835 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.4682    1.5119    0.9601 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.6786    1.1266   -0.6066 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2124    0.7366    2.3823 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1436    2.3132    1.4892 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.1434    1.7947    2.2345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3558   -0.4882    2.3734 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6569    1.5732   -0.6557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3863    0.1148   -1.3316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5468    0.3039   -1.1788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4699    0.6742    2.5844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3689    2.7377    2.0489 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 14 13  1  0
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 12 11  1  0
 11 10  1  0
 10  9  1  6
  9  8  1  0
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  5  7  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
 10 46  1  0
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 44 45  1  6
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 40 23  1  0
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 37 38  1  0
 37 39  1  0
 16 14  1  0
 35 28  1  0
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 17 44  1  0
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 37 40  1  0
 21 23  1  0
 15 62  1  0
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 13 60  1  0
 12 58  1  1
  8 57  1  1
  6 51  1  0
  6 52  1  0
  6 53  1  0
  7 54  1  0
  7 55  1  0
  7 56  1  0
  1 48  1  0
  1 49  1  0
  1 50  1  0
 46104  1  1
 47105  1  0
 45101  1  0
 45102  1  0
 45103  1  0
 43100  1  1
 42 98  1  0
 42 99  1  0
 41 96  1  0
 41 97  1  0
 40 95  1  6
 22 73  1  0
 22 74  1  0
 20 71  1  0
 20 72  1  0
 19 69  1  0
 19 70  1  0
 18 66  1  0
 18 67  1  0
 18 68  1  0
 16 65  1  6
 24 75  1  0
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 26 79  1  6
 28 80  1  6
 30 81  1  0
 30 82  1  0
 31 83  1  1
 32 84  1  0
 33 85  1  6
 34 86  1  0
 35 87  1  1
 36 88  1  0
 38 89  1  0
 38 90  1  0
 38 91  1  0
 39 92  1  0
 39 93  1  0
 39 94  1  0
M  END


  Mrv1652309042203172D          

 47 54  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  2  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  0  0  0  0  0  0  0  0  0  0
   -2.9929    3.1947    0.0000 C   0  0  1  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  1  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  0  0  0  0
 31 32  1  1  0  0  0
 31 33  1  0  0  0  0
 33 34  1  6  0  0  0
 33 35  1  0  0  0  0
 28 35  1  0  0  0  0
 35 36  1  1  0  0  0
 26 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 37 40  1  0  0  0  0
 23 40  1  0  0  0  0
 40 41  1  6  0  0  0
 41 42  1  0  0  0  0
 43 42  1  1  0  0  0
 21 43  1  0  0  0  0
 43 44  1  0  0  0  0
 17 44  1  0  0  0  0
 44 45  1  1  0  0  0
 44 46  1  0  0  0  0
 10 46  1  0  0  0  0
 46 47  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0185749

> <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]1OC[C@@H](O)[C@H](O)[C@H]1O)C5(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C37H58O10/c1-18-15-21-28(32(5,6)45-19(2)38)47-37(46-21)27(18)33(7)13-14-36-17-35(36)12-11-24(44-29-26(41)25(40)20(39)16-43-29)31(3,4)22(35)9-10-23(36)34(33,8)30(37)42/h18,20-30,39-42H,9-17H2,1-8H3/t18-,20-,21-,22+,23+,24+,25+,26-,27-,28-,29+,30-,33-,34-,35-,36+,37+/m1/s1

> <INCHI_KEY>
NNFJPOSVDKIWPO-XPODHQTRSA-N

> <FORMULA>
C37H58O10

> <MOLECULAR_WEIGHT>
662.861

> <EXACT_MASS>
662.402998068

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
105

> <JCHEM_AVERAGE_POLARIZABILITY>
74.98395108494802

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(1S,2R,3S,4R,7R,9S,12R,14S,17R,18R,19R,21R,22R)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-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>
3.4245560943333317

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.842644272196601

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.150778763317401

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5265806236668267

> <JCHEM_POLAR_SURFACE_AREA>
144.14000000000001

> <JCHEM_REFRACTIVITY>
168.64690000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2-[(1S,2R,3S,4R,7R,9S,12R,14S,17R,18R,19R,21R,22R)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-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                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-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      -5.587   5.963   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -6.009   7.444   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -4.093   5.588   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -3.022   6.694   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -3.671   4.107   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -2.178   3.732   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -1.756   2.251   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -3.031   3.114   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -1.127   3.657   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -0.262   1.876   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       0.810   2.982   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       2.303   2.607   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       2.725   1.126   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       4.216   0.760   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       3.959   2.278   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       5.517   1.605   0.000  0.00  0.00           C+0
HETATM   47  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   46                                             
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   44                                             
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23   43                                             
CONECT   22   21   23                                                       
CONECT   23   22   21   24   40                                             
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   37                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   35                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   28   36                                                  
CONECT   36   35                                                            
CONECT   37   26   38   39   40                                             
CONECT   38   37                                                            
CONECT   39   37                                                            
CONECT   40   37   23   41                                                  
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   21   44                                                  
CONECT   44   43   17   45   46                                             
CONECT   45   44                                                            
CONECT   46   44   10   47                                                  
CONECT   47   46                                                            
MASTER        0    0    0    0    0    0    0    0   47    0  108    0
END

View in JSmol

Synonyms

Value	Source
2-[(1S,2R,3S,4R,7R,9S,12R,14S,17R,18R,19R,21R,22R)-2-Hydroxy-3,8,8,17,19-pentamethyl-9-{[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}-23,24-dioxaheptacyclo[19.2.1.0,.0,.0,.0,.0,]tetracosan-22-yl]propan-2-yl acetic acid	Generator

Chemical Formula

C₃₇H₅₈O₁₀

Average Mass

662.8610 Da

Monoisotopic Mass

662.40300 Da

IUPAC Name

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]1OC[C@@H](O)[C@H](O)[C@H]1O)C5(C)C

InChI Identifier

InChI=1S/C37H58O10/c1-18-15-21-28(32(5,6)45-19(2)38)47-37(46-21)27(18)33(7)13-14-36-17-35(36)12-11-24(44-29-26(41)25(40)20(39)16-43-29)31(3,4)22(35)9-10-23(36)34(33,8)30(37)42/h18,20-30,39-42H,9-17H2,1-8H3/t18-,20-,21-,22+,23+,24+,25+,26-,27-,28-,29+,30-,33-,34-,35-,36+,37+/m1/s1

InChI Key

NNFJPOSVDKIWPO-XPODHQTRSA-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 asiatica	LOTUS Database	35616633
Actaea cimicifuga	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
Cycloartanol-skeleton
9b,19-cyclo-lanostane-skeleton
Triterpenoid
Cycloartane-skeleton
15-hydroxysteroid
Hydroxysteroid
Glycosyl compound
O-glycosyl compound
Ketal
Oxepane
Oxane
Monosaccharide
Meta-dioxolane
Cyclic alcohol
Carboxylic acid ester
Secondary alcohol
Polyol
Acetal
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Alcohol
Organooxygen compound
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	3.42	ChemAxon
pKa (Strongest Acidic)	12.15	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	144.14 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	168.65 m³·mol⁻¹	ChemAxon
Polarizability	74.98 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	No	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

101427153

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22r)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-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 (NP0185749)

MOL for NP0185749 (2-[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22r)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-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 NP0185749 (2-[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22r)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-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 NP0185749 (2-[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22r)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-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 NP0185749 (2-[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22r)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-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 NP0185749 (2-[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22r)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-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 NP0185749 (2-[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22r)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-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 NP0185749 (2-[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22r)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-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 NP0185749 (2-[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22r)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-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 NP0185749 (2-[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22r)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-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 Structure for NP0185749 (2-[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22r)-2-hydroxy-3,8,8,17,19-pentamethyl-9-{[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-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)