NP-MRD: Showing NP-Card for (2s,3r,4s,5r)-2-{[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-22-(2-butoxypropan-2-yl)-2-hydroxy-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosan-9-yl]oxy}oxane-3,4,5-triol (NP0298004)

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Record Information

Version

2.0

Created at

2022-09-10 08:52:06 UTC

Updated at

2022-09-10 08:52:06 UTC

NP-MRD ID

NP0298004

Secondary Accession Numbers

None

Natural Product Identification

Common Name

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

Description

(2S,3R,4S,5R)-2-{[(1S,2R,3S,4R,7R,9S,12R,14S,17R,18R,19R,21R,22S)-22-(2-butoxypropan-2-yl)-2-hydroxy-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]Tetracosan-9-yl]oxy}oxane-3,4,5-triol 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. (2s,3r,4s,5r)-2-{[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-22-(2-butoxypropan-2-yl)-2-hydroxy-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosan-9-yl]oxy}oxane-3,4,5-triol is found in Actaea yunnanensis. Based on a literature review very few articles have been published on (2S,3R,4S,5R)-2-{[(1S,2R,3S,4R,7R,9S,12R,14S,17R,18R,19R,21R,22S)-22-(2-butoxypropan-2-yl)-2-hydroxy-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]Tetracosan-9-yl]oxy}oxane-3,4,5-triol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102210522D          

 48 55  0  0  1  0            999 V2000
    9.3092    1.7476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6150    1.3018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    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
    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
   -2.8889    0.2219    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6628   -0.5715    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2369   -1.1640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0371   -0.9631    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.6112   -1.5555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2631   -0.1696    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0633    0.0313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6890    0.4228    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9151    1.2163    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  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  9  6  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 13 12  1  6  0  0  0
  9 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 11  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 24 23  1  6  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
 27 28  1  6  0  0  0
 29 28  1  6  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  1  0  0  0
 32 34  1  0  0  0  0
 34 35  1  6  0  0  0
 34 36  1  0  0  0  0
 29 36  1  0  0  0  0
 36 37  1  1  0  0  0
 27 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 38 41  1  0  0  0  0
 24 41  1  0  0  0  0
 41 42  1  6  0  0  0
 42 43  1  0  0  0  0
 44 43  1  1  0  0  0
 22 44  1  0  0  0  0
 44 45  1  0  0  0  0
 18 45  1  0  0  0  0
 45 46  1  1  0  0  0
 45 47  1  0  0  0  0
 11 47  1  0  0  0  0
 47 48  1  1  0  0  0
M  END

     RDKit          3D

112119  0  0  0  0  0  0  0  0999 V2000
  -10.8749    3.1433    0.5689 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4857    2.9726    0.0496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1904    1.4774   -0.1129 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7400    1.3504   -0.6528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4721    0.0376   -0.7982 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3191   -0.4188   -1.3005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0445    0.0473   -2.7300 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4856   -1.9489   -1.4537 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0610   -0.2386   -0.5250 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0203   -0.8835   -1.2374 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9003   -0.2239   -0.7379 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2479    1.0965   -1.0012 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5303    1.1407   -0.4064 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2749    1.4151    1.0600 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3337    0.4122    1.6710 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0973   -0.3775    2.7276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6342   -0.4768    0.7119 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1270   -0.3564    0.7658 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7753    1.0846    0.6460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4985   -1.0003    1.9432 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9590   -1.1338    1.7869 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5572   -0.7128    0.5066 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5320    0.4475    0.4330 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9997   -0.9227    0.3832 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8136   -1.3924    1.5807 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0950   -2.0600    1.1747 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7559   -1.2195    0.1105 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7800    0.0973    0.5618 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0950    0.5338    0.7222 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.2565    0.8808    2.0604 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6128    1.0535    2.3409 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1573    2.2128    1.5185 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.1964    1.8135    0.6852 O   0  0  0  0  0  0  0  0  0  0  0  0
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    7.2113    3.5476    1.5333 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.4976   -1.6422   -0.8080 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6400   -1.5066   -2.0394 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2576   -2.0229   -1.6044 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7292   -0.8897   -0.7096 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7128   -1.1424   -0.4608 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9639   -2.5992   -0.3291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6427   -0.5781   -1.5044 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9772   -1.6152   -2.3791 O   0  0  0  0  0  0  0  0  0  0  0  0
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  -11.6279    2.9114   -0.2368 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0148    4.1912    0.9300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3617    3.4815   -0.9241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7797    3.3996    0.8009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2681    1.0290    0.8915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9077    1.0379   -0.8055 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.6982    1.9892   -1.5315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2770   -0.6506   -3.1295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6380    1.0559   -2.7759 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.5357   -2.4226   -1.7191 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.1171   -0.7739    0.4459 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.0641   -1.4642    2.4888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7158   -0.2408    3.7372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9769   -1.5298    0.9240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2366    1.3984    1.5771 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.6728    1.7643    0.5900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0145   -1.9918    2.1079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7460   -0.4183    2.8789 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.0836   -0.5300    2.2276 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2552   -2.0965    2.2215 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7685   -2.0305    2.0744 H   0  0  0  0  0  0  0  0  0  0  0  0
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    9.2046    0.1472    2.0799 H   0  0  0  0  0  0  0  0  0  0  0  0
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    9.5315    3.0117    2.1878 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1276    2.2472   -0.2055 H   0  0  0  0  0  0  0  0  0  0  0  0
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    6.3710    2.2037   -0.4986 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.0299   -3.4334   -1.5147 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.1468   -2.4450   -2.9895 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5874    0.7875   -1.5858 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0900    0.0317   -2.3352 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4755   -0.3393   -2.9600 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4920   -2.7465   -0.5584 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0653   -2.0998   -2.8472 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5497   -0.4095   -2.2924 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6628   -2.0826   -2.5113 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4092   -2.9498   -1.0505 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7896    0.0100   -1.3950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4382   -3.1004    0.4933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0307   -2.8903   -0.2531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6094   -3.0855   -1.2766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2254    0.2559   -2.0695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7650   -1.4330   -3.3092 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  6  9  1  0
  9 10  1  0
 11 10  1  6
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  6
 18 20  1  0
 20 21  1  0
 22 21  1  1
 22 23  1  0
 24 23  1  6
 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
 32 33  1  0
 32 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  1  0
 27 38  1  0
 38 39  1  0
 38 40  1  0
 38 41  1  0
 41 42  1  0
 42 43  1  0
 43 44  1  0
 44 45  1  0
 45 46  1  1
 45 47  1  0
 47 48  1  0
 13  9  1  0
 45 18  1  0
 17 11  1  0
 24 22  1  0
 41 24  1  0
 47 11  1  0
 44 22  1  0
 36 29  1  0
  1 49  1  0
  1 50  1  0
  1 51  1  0
  2 52  1  0
  2 53  1  0
  3 54  1  0
  3 55  1  0
  4 56  1  0
  4 57  1  0
  7 58  1  0
  7 59  1  0
  7 60  1  0
  8 61  1  0
  8 62  1  0
  8 63  1  0
  9 64  1  1
 13 65  1  6
 14 66  1  0
 14 67  1  0
 15 68  1  1
 16 69  1  0
 16 70  1  0
 16 71  1  0
 17 72  1  1
 19 73  1  0
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 19 75  1  0
 20 76  1  0
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 21 78  1  0
 21 79  1  0
 23 80  1  0
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 25 82  1  0
 25 83  1  0
 26 84  1  0
 26 85  1  0
 27 86  1  6
 29 87  1  6
 31 88  1  0
 31 89  1  0
 32 90  1  1
 33 91  1  0
 34 92  1  6
 35 93  1  0
 36 94  1  6
 37 95  1  0
 39 96  1  0
 39 97  1  0
 39 98  1  0
 40 99  1  0
 40100  1  0
 40101  1  0
 41102  1  1
 42103  1  0
 42104  1  0
 43105  1  0
 43106  1  0
 44107  1  6
 46108  1  0
 46109  1  0
 46110  1  0
 47111  1  6
 48112  1  0
M  END


  Mrv1652309102210522D          

 48 55  0  0  1  0            999 V2000
    9.3092    1.7476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6150    1.3018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    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
    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
   -2.8889    0.2219    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6628   -0.5715    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2369   -1.1640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0371   -0.9631    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.6112   -1.5555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2631   -0.1696    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0633    0.0313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6890    0.4228    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9151    1.2163    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  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  9  6  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 13 12  1  6  0  0  0
  9 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 11  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 24 23  1  6  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
 27 28  1  6  0  0  0
 29 28  1  6  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  1  0  0  0
 32 34  1  0  0  0  0
 34 35  1  6  0  0  0
 34 36  1  0  0  0  0
 29 36  1  0  0  0  0
 36 37  1  1  0  0  0
 27 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 38 41  1  0  0  0  0
 24 41  1  0  0  0  0
 41 42  1  6  0  0  0
 42 43  1  0  0  0  0
 44 43  1  1  0  0  0
 22 44  1  0  0  0  0
 44 45  1  0  0  0  0
 18 45  1  0  0  0  0
 45 46  1  1  0  0  0
 45 47  1  0  0  0  0
 11 47  1  0  0  0  0
 47 48  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0298004

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCOC(C)(C)[C@H]1O[C@@]23O[C@@H]1C[C@@H](C)[C@@H]2[C@@]1(C)CC[C@@]24C[C@@]22CC[C@H](O[C@@H]5OC[C@@H](O)[C@H](O)[C@H]5O)C(C)(C)[C@@H]2CC[C@H]4[C@]1(C)[C@H]3O

> <INCHI_IDENTIFIER>
InChI=1S/C39H64O9/c1-9-10-17-45-34(5,6)30-23-18-21(2)29-35(7)15-16-38-20-37(38)14-13-26(46-31-28(42)27(41)22(40)19-44-31)33(3,4)24(37)11-12-25(38)36(35,8)32(43)39(29,47-23)48-30/h21-32,40-43H,9-20H2,1-8H3/t21-,22-,23-,24+,25+,26+,27+,28-,29-,30+,31+,32-,35-,36-,37-,38+,39+/m1/s1

> <INCHI_KEY>
AYNPTULQRUYIBL-KDSRJQFPSA-N

> <FORMULA>
C39H64O9

> <MOLECULAR_WEIGHT>
676.932

> <EXACT_MASS>
676.455033641

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
112

> <JCHEM_AVERAGE_POLARIZABILITY>
79.39160330174921

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <JCHEM_LOGP>
4.950456202333336

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.842644589740505

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.150778871031658

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5265806236668267

> <JCHEM_POLAR_SURFACE_AREA>
127.07000000000002

> <JCHEM_REFRACTIVITY>
178.12020000000007

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

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

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      17.377   3.262   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      16.081   2.430   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      14.713   3.136   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      13.417   2.304   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      12.048   3.010   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      10.753   2.177   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.920   3.473   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.585   0.882   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.457   1.345   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       7.937   1.938   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       6.823   0.705   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       8.076   0.139   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       9.364  -0.278   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.788  -1.797   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.209  -2.105   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.667  -3.546   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.214  -0.820   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.641  -0.730   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.201  -2.165   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.569  -1.836   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.076  -1.461   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.654   0.020   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.582  -1.086   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.160   0.395   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.912  -0.711   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -2.405  -0.336   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -2.827   1.145   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -4.321   1.520   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -5.393   0.414   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -4.971  -1.067   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -6.042  -2.173   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -7.536  -1.798   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -8.608  -2.904   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -7.958  -0.317   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -9.451   0.058   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -6.886   0.789   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -7.308   2.270   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -1.756   2.251   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -3.031   3.114   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -1.127   3.657   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -0.262   1.876   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       0.810   2.982   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       2.303   2.607   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       2.725   1.126   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       4.216   0.760   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       3.959   2.278   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       5.517   1.605   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0       5.538   3.145   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8    9                                             
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    6   10   13                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   17   47                                             
CONECT   12   11   13                                                       
CONECT   13   12    9   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   11   18                                                  
CONECT   18   17   19   20   45                                             
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24   44                                             
CONECT   23   22   24                                                       
CONECT   24   23   22   25   41                                             
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   38                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   36                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   29   37                                                  
CONECT   37   36                                                            
CONECT   38   27   39   40   41                                             
CONECT   39   38                                                            
CONECT   40   38                                                            
CONECT   41   38   24   42                                                  
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   22   45                                                  
CONECT   45   44   18   46   47                                             
CONECT   46   45                                                            
CONECT   47   45   11   48                                                  
CONECT   48   47                                                            
MASTER        0    0    0    0    0    0    0    0   48    0  110    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₉H₆₄O₉

Average Mass

676.9320 Da

Monoisotopic Mass

676.45503 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CCCCOC(C)(C)[C@H]1O[C@@]23O[C@@H]1C[C@@H](C)[C@@H]2[C@@]1(C)CC[C@@]24C[C@@]22CC[C@H](O[C@@H]5OC[C@@H](O)[C@H](O)[C@H]5O)C(C)(C)[C@@H]2CC[C@H]4[C@]1(C)[C@H]3O

InChI Identifier

InChI=1S/C39H64O9/c1-9-10-17-45-34(5,6)30-23-18-21(2)29-35(7)15-16-38-20-37(38)14-13-26(46-31-28(42)27(41)22(40)19-44-31)33(3,4)24(37)11-12-25(38)36(35,8)32(43)39(29,47-23)48-30/h21-32,40-43H,9-20H2,1-8H3/t21-,22-,23-,24+,25+,26+,27+,28-,29-,30+,31+,32-,35-,36-,37-,38+,39+/m1/s1

InChI Key

AYNPTULQRUYIBL-KDSRJQFPSA-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 yunnanensis	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
Cycloartane-skeleton
Triterpenoid
15-hydroxysteroid
Hydroxysteroid
Glycosyl compound
O-glycosyl compound
Pentose monosaccharide
Ketal
Oxepane
Oxane
Monosaccharide
Meta-dioxolane
Cyclic alcohol
Secondary alcohol
Polyol
Ether
Dialkyl ether
Organoheterocyclic compound
Oxacycle
Acetal
Hydrocarbon derivative
Organic oxygen compound
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

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

62954730

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131844764

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,3r,4s,5r)-2-{[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-22-(2-butoxypropan-2-yl)-2-hydroxy-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosan-9-yl]oxy}oxane-3,4,5-triol (NP0298004)

MOL for NP0298004 ((2s,3r,4s,5r)-2-{[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-22-(2-butoxypropan-2-yl)-2-hydroxy-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosan-9-yl]oxy}oxane-3,4,5-triol)

3D MOL for NP0298004 ((2s,3r,4s,5r)-2-{[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-22-(2-butoxypropan-2-yl)-2-hydroxy-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosan-9-yl]oxy}oxane-3,4,5-triol)

3D SDF for NP0298004 ((2s,3r,4s,5r)-2-{[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-22-(2-butoxypropan-2-yl)-2-hydroxy-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosan-9-yl]oxy}oxane-3,4,5-triol)

3D-SDF for NP0298004 ((2s,3r,4s,5r)-2-{[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-22-(2-butoxypropan-2-yl)-2-hydroxy-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosan-9-yl]oxy}oxane-3,4,5-triol)

PDB for NP0298004 ((2s,3r,4s,5r)-2-{[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-22-(2-butoxypropan-2-yl)-2-hydroxy-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosan-9-yl]oxy}oxane-3,4,5-triol)

3D PDB for NP0298004 ((2s,3r,4s,5r)-2-{[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-22-(2-butoxypropan-2-yl)-2-hydroxy-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosan-9-yl]oxy}oxane-3,4,5-triol)

SMILES for NP0298004 ((2s,3r,4s,5r)-2-{[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-22-(2-butoxypropan-2-yl)-2-hydroxy-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosan-9-yl]oxy}oxane-3,4,5-triol)

INCHI for NP0298004 ((2s,3r,4s,5r)-2-{[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-22-(2-butoxypropan-2-yl)-2-hydroxy-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosan-9-yl]oxy}oxane-3,4,5-triol)

Structure for NP0298004 ((2s,3r,4s,5r)-2-{[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-22-(2-butoxypropan-2-yl)-2-hydroxy-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosan-9-yl]oxy}oxane-3,4,5-triol)

3D Structure for NP0298004 ((2s,3r,4s,5r)-2-{[(1s,2r,3s,4r,7r,9s,12r,14s,17r,18r,19r,21r,22s)-22-(2-butoxypropan-2-yl)-2-hydroxy-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.0¹,¹⁸.0³,¹⁷.0⁴,¹⁴.0⁷,¹².0¹²,¹⁴]tetracosan-9-yl]oxy}oxane-3,4,5-triol)