NP-MRD: Showing NP-Card for (3,4-dihydroxy-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-oloxy}-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl)methyl acetate (NP0142651)

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Record Information

Version

2.0

Created at

2022-09-01 21:14:27 UTC

Updated at

2022-09-01 21:14:27 UTC

NP-MRD ID

NP0142651

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3,4-dihydroxy-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-oloxy}-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl)methyl acetate

Description

(3,4-Dihydroxy-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]Icosan]-18'-en-16'-oloxy}-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl)methyl acetate belongs to the class of organic compounds known as steroidal saponins. These are saponins in which the aglycone moiety is a steroid. (3,4-dihydroxy-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-oloxy}-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl)methyl acetate is found in Ruscus aculeatus. The steroidal aglycone is usually a spirostane, furostane, spirosolane, solanidane, or curcubitacin derivative (3,4-dihydroxy-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]Icosan]-18'-en-16'-oloxy}-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl)methyl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004201503192D          

 55 62  0  0  0  0            999 V2000
    4.3030   -3.2858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1170   -3.1521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4082   -2.3802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2223   -2.2464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7452   -2.8845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4540   -3.6564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6399   -3.7902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1155   -2.1473    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9311   -2.2716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6640   -1.8929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2507   -2.4728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0743   -2.4249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4446   -1.6877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2682   -1.6397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7215   -2.3290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5451   -2.2811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9984   -2.9704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8221   -2.9224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.6282   -3.7076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8046   -3.7555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4343   -4.4928    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.8876   -5.1821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7112   -5.1341    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.1645   -5.8234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9881   -5.7755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3584   -5.0382    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.9051   -4.3489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0815   -4.3969    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2754   -3.6117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7942   -6.5606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2476   -7.2499    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.9706   -6.6086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6003   -7.3458    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.5173   -5.9193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6937   -5.9672    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.3234   -6.7045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7767   -7.3938    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.4065   -8.1310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8598   -8.8203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5829   -8.1789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2126   -8.9162    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1295   -7.4896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3059   -7.5376    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4998   -6.7524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0465   -6.0631    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.3512   -3.0662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9810   -3.8035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5276   -3.1142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1573   -3.8514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3337   -3.8994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8804   -3.2101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4351   -3.9046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0648   -3.0857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3319   -3.4645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2076   -4.2801    0.0000 C   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
  2  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 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  2  0  0  0  0
 27 29  1  0  0  0  0
 24 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 22 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 36 44  1  0  0  0  0
 44 45  1  0  0  0  0
 20 46  1  0  0  0  0
 15 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
 12 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 11 51  1  0  0  0  0
 51 52  1  0  0  0  0
 51 53  1  0  0  0  0
  9 53  1  0  0  0  0
 53 54  1  0  0  0  0
  5 54  1  0  0  0  0
 54 55  1  0  0  0  0
M  END

     RDKit          3D

119126  0  0  0  0  0  0  0  0999 V2000
   -5.9938   -5.4571    4.4648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8210   -4.7614    3.8674 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6874   -5.2785    3.9123 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0787   -3.5320    3.2755 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0009   -2.7983    2.6766 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5309   -1.5010    2.1007 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5577   -0.7408    1.5092 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2113   -1.2334    0.2550 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9904   -0.7528   -0.2012 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0996   -1.7522   -0.4695 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7548   -1.9255   -1.9356 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2942   -3.3572   -2.1141 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3878   -4.1067   -2.4725 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3426   -3.9174   -0.8464 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0586   -2.8053   -0.1707 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3375   -2.7004    0.0069 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0738   -1.5956    0.6789 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0979   -0.5906    1.2449 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9798   -0.4903    0.2362 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3363    0.8350    0.3299 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4207    1.8040   -0.1813 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4522    1.9070    0.9027 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9128    3.0545    1.7947 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7872    2.4129    0.4399 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7260    1.9171    1.5044 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1579    0.6086    1.9265 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6643    0.6883    1.7065 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9387    1.7065    0.8758 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7400    1.4627   -0.4526 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.7475    2.3305   -1.2191 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0441    2.1916   -0.4139 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4037    0.7483   -0.2119 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.2446    0.6726    1.0694 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2366   -0.1544   -0.0188 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1102    0.1482   -0.7389 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3288    1.7967   -0.8053 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3866    2.8402   -1.9358 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1420   -1.7014    0.3434 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2446   -2.0170    1.7858 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3736   -0.8081   -0.6580 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5859    0.5137   -0.3753 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5093    1.4001   -1.4059 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5541    2.4188   -1.1728 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3033    3.0214   -2.3757 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2705    4.1461   -2.2042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4871    3.6204   -3.0490 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5819    4.9938   -2.7552 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7889    2.9510   -2.7801 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.1501    2.0904   -3.8235 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8345    2.1655   -1.5077 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.8625    1.2593   -1.4567 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.1662   -3.0069   -0.5984 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.5827   -3.4728    1.9163 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.8787   -0.9159    3.0120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2318   -2.3304    0.2901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6262   -2.7219   -0.2016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6881   -1.7194   -2.5026 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0340   -1.2447   -2.2712 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4649   -3.4212   -2.9162 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0162   -4.2839   -1.7270 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0368   -4.7200   -1.1759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4078   -4.4110   -0.1993 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9704   -3.5172   -0.3785 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6871   -2.0753    1.4694 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7237   -1.1637   -0.1350 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6457   -1.1341    2.1329 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4778   -0.5298   -0.7815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5136    1.0098   -0.3447 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1277    1.1496    1.3801 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8815    2.7661   -0.3634 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7604    1.3935   -1.1289 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6620    3.9020    1.1005 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7001    3.4404    2.4538 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9991    2.7259    2.3300 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7956    3.5353    0.3740 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8317    2.6434    2.3422 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4042    0.4055    2.9978 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6417   -0.2048    1.3660 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2462    0.9012    2.7432 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9876    1.8835   -2.2122 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4632    3.3779   -1.2429 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8549    2.6382    0.5825 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8730    2.7054   -0.9349 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0729    0.4028   -1.0313 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1533004201503192D          

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M  END
> <DATABASE_ID>
NP0142651

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C2C(CC3C4CC=C5CC(O)CC(OC6OC(COC(C)=O)C(O)C(O)C6OC6OC(C)C(O)C(O)C6O)C5(C)C4CCC23C)OC11CCC(C)CO1

> <INCHI_IDENTIFIER>
InChI=1S/C41H64O14/c1-18-9-12-41(50-16-18)19(2)30-27(55-41)15-26-24-8-7-22-13-23(43)14-29(40(22,6)25(24)10-11-39(26,30)5)53-38-36(34(47)32(45)28(52-38)17-49-21(4)42)54-37-35(48)33(46)31(44)20(3)51-37/h7,18-20,23-38,43-48H,8-17H2,1-6H3

> <INCHI_KEY>
SZGNYKUYAYFOKL-UHFFFAOYSA-N

> <FORMULA>
C41H64O14

> <MOLECULAR_WEIGHT>
780.949

> <EXACT_MASS>
780.429606741

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
119

> <JCHEM_AVERAGE_POLARIZABILITY>
84.83951886872916

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3,4-dihydroxy-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-oloxy}-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl)methyl acetate

> <ALOGPS_LOGP>
1.74

> <JCHEM_LOGP>
1.5700644666666659

> <ALOGPS_LOGS>
-3.76

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.722771508289156

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.101084439173789

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7504752725714825

> <JCHEM_POLAR_SURFACE_AREA>
203.05999999999997

> <JCHEM_REFRACTIVITY>
194.1722000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.35e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3,4-dihydroxy-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-oloxy}-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl)methyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 20-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-APR-15         0                                  
HETATM    1  C   UNK     0       8.032  -6.134   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.552  -5.884   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.095  -4.443   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.615  -4.193   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.591  -5.384   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      12.048  -6.825   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      10.528  -7.075   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      13.282  -4.008   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      14.805  -4.240   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      16.173  -3.533   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      17.268  -4.616   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      18.805  -4.526   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      19.497  -3.150   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      21.034  -3.061   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      21.880  -4.347   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      23.418  -4.258   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      24.264  -5.545   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      25.801  -5.455   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      23.573  -6.921   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      22.035  -7.010   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      21.344  -8.386   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      22.190  -9.673   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      23.728  -9.584   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      24.574 -10.870   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      26.111 -10.781   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      26.802  -9.405   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      25.956  -8.118   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      24.419  -8.208   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      26.647  -6.742   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      23.883 -12.247   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      24.729 -13.533   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      22.345 -12.336   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      21.654 -13.712   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      21.499 -11.049   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      19.962 -11.139   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      19.270 -12.515   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      20.117 -13.802   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      19.425 -15.178   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      20.272 -16.465   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      17.888 -15.267   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      17.197 -16.644   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      17.042 -13.981   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      15.504 -14.070   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      17.733 -12.605   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      16.887 -11.318   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      21.189  -5.724   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      20.498  -7.100   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      19.652  -5.813   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      18.960  -7.189   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      17.423  -7.279   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      16.577  -5.992   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      15.746  -7.289   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      15.054  -5.760   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      13.686  -6.467   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      13.454  -7.989   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    8   54                                             
CONECT    6    5    7                                                       
CONECT    7    6    2                                                       
CONECT    8    5    9                                                       
CONECT    9    8   10   53                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   51                                                  
CONECT   12   11   13   48                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   46                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   46                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   34                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   30                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   24   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   22   35                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37   44                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   36   45                                                  
CONECT   45   44                                                            
CONECT   46   20   15   47   48                                             
CONECT   47   46                                                            
CONECT   48   46   12   49                                                  
CONECT   49   48   50                                                       
CONECT   50   49   51                                                       
CONECT   51   50   11   52   53                                             
CONECT   52   51                                                            
CONECT   53   51    9   54                                                  
CONECT   54   53    5   55                                                  
CONECT   55   54                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  124    0
END

View in JSmol

Synonyms

Value	Source
(3,4-Dihydroxy-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0,.0,.0,]icosan]-18'-en-16'-oloxy}-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl)methyl acetic acid	Generator
(3,4-Dihydroxy-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-oloxy}-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl)methyl acetic acid	Generator

Chemical Formula

C₄₁H₆₄O₁₄

Average Mass

780.9490 Da

Monoisotopic Mass

780.42961 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

CC1C2C(CC3C4CC=C5CC(O)CC(OC6OC(COC(C)=O)C(O)C(O)C6OC6OC(C)C(O)C(O)C6O)C5(C)C4CCC23C)OC11CCC(C)CO1

InChI Identifier

InChI=1S/C41H64O14/c1-18-9-12-41(50-16-18)19(2)30-27(55-41)15-26-24-8-7-22-13-23(43)14-29(40(22,6)25(24)10-11-39(26,30)5)53-38-36(34(47)32(45)28(52-38)17-49-21(4)42)54-37-35(48)33(46)31(44)20(3)51-37/h7,18-20,23-38,43-48H,8-17H2,1-6H3

InChI Key

SZGNYKUYAYFOKL-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Ruscus aculeatus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as steroidal saponins. These are saponins in which the aglycone moiety is a steroid. The steroidal aglycone is usually a spirostane, furostane, spirosolane, solanidane, or curcubitacin derivative.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroidal glycosides

Direct Parent

Steroidal saponins

Alternative Parents

Substituents

Steroidal saponin
Triterpenoid
Spirostane skeleton
3-hydroxy-delta-5-steroid
3-hydroxysteroid
Hydroxysteroid
Delta-5-steroid
Disaccharide
Glycosyl compound
O-glycosyl compound
Ketal
Oxane
Cyclic alcohol
Tetrahydrofuran
Secondary alcohol
Carboxylic acid ester
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Acetal
Polyol
Organic oxide
Hydrocarbon derivative
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	1.74	ALOGPS
logP	1.57	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	12.1	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	203.06 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	194.17 m³·mol⁻¹	ChemAxon
Polarizability	84.84 Å³	ChemAxon
Number of Rings	8	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3,4-dihydroxy-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-oloxy}-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl)methyl acetate (NP0142651)

MOL for NP0142651 ((3,4-dihydroxy-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-oloxy}-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl)methyl acetate)

3D MOL for NP0142651 ((3,4-dihydroxy-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-oloxy}-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl)methyl acetate)

3D SDF for NP0142651 ((3,4-dihydroxy-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-oloxy}-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl)methyl acetate)

3D-SDF for NP0142651 ((3,4-dihydroxy-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-oloxy}-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl)methyl acetate)

PDB for NP0142651 ((3,4-dihydroxy-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-oloxy}-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl)methyl acetate)

3D PDB for NP0142651 ((3,4-dihydroxy-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-oloxy}-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl)methyl acetate)

SMILES for NP0142651 ((3,4-dihydroxy-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-oloxy}-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl)methyl acetate)

INCHI for NP0142651 ((3,4-dihydroxy-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-oloxy}-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl)methyl acetate)

Structure for NP0142651 ((3,4-dihydroxy-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-oloxy}-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl)methyl acetate)

3D Structure for NP0142651 ((3,4-dihydroxy-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-18'-en-16'-oloxy}-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl)methyl acetate)