NP-MRD: Showing NP-Card for 2-({4,5-dihydroxy-2-[4-(14-hydroxy-6-methoxy-7,9,13-trimethyl-16-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icos-18-en-6-yl)-2-methylbutoxy]-6-(hydroxymethyl)oxan-3-yl}oxy)-6-methyloxane-3,4,5-triol (NP0229194)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-06 09:09:09 UTC

Updated at

2022-09-06 09:09:09 UTC

NP-MRD ID

NP0229194

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-({4,5-dihydroxy-2-[4-(14-hydroxy-6-methoxy-7,9,13-trimethyl-16-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icos-18-en-6-yl)-2-methylbutoxy]-6-(hydroxymethyl)oxan-3-yl}oxy)-6-methyloxane-3,4,5-triol

Description

2-({4,5-Dihydroxy-2-[4-(14-hydroxy-6-methoxy-7,9,13-trimethyl-16-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]Icos-18-en-6-yl)-2-methylbutoxy]-6-(hydroxymethyl)oxan-3-yl}oxy)-6-methyloxane-3,4,5-triol 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. 2-({4,5-dihydroxy-2-[4-(14-hydroxy-6-methoxy-7,9,13-trimethyl-16-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icos-18-en-6-yl)-2-methylbutoxy]-6-(hydroxymethyl)oxan-3-yl}oxy)-6-methyloxane-3,4,5-triol is found in Allium triquetrum. 2-({4,5-Dihydroxy-2-[4-(14-hydroxy-6-methoxy-7,9,13-trimethyl-16-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]Icos-18-en-6-yl)-2-methylbutoxy]-6-(hydroxymethyl)oxan-3-yl}oxy)-6-methyloxane-3,4,5-triol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171504192D          

 65 72  0  0  0  0            999 V2000
    3.1293   -1.3136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1339   -2.1386    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8507   -2.5471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3696   -3.2172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5486   -3.1356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0675   -3.8058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4073   -4.5576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2465   -3.7242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7654   -4.3943    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0556   -4.3127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5367   -4.9829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3577   -4.9013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8389   -5.5714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6598   -5.4898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6975   -4.1495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5185   -4.0679    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2163   -3.4793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5562   -2.7276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3954   -3.5610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0858   -2.8908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2540   -2.1390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0750   -2.0574    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4148   -1.3056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2358   -1.2240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9336   -0.6355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2734    0.1163    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1127   -0.7171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3685   -0.0469    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2271   -1.4689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0481   -1.5505    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1820   -1.7915    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0030   -1.8731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7151   -1.4566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3313   -2.0052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1513   -1.9143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4826   -1.1588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3026   -1.0679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7913   -1.7326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6112   -1.6417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0999   -2.3064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7686   -3.0620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9486   -3.1529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6173   -3.9084    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4600   -2.4882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1286   -3.2437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6400   -2.5790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3087   -3.3346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4887   -3.4254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0000   -2.7607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5915   -3.4775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1791   -2.6791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4669   -3.0956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3853   -3.9166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9199   -2.2156    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4086   -2.8803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2286   -2.7894    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.7172   -3.4541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5372   -3.3633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0259   -4.0279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.3859   -4.2097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8746   -4.8744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.5659   -4.3005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2346   -5.0561    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.0773   -3.6358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2573   -3.7267    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
  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
 12 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 10 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
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 21 29  1  0  0  0  0
 29 30  1  0  0  0  0
  3 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 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  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 38 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 35 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 34 49  1  0  0  0  0
 49 50  1  0  0  0  0
 49 51  1  0  0  0  0
 32 51  1  0  0  0  0
 51 52  1  0  0  0  0
  3 52  1  0  0  0  0
 52 53  1  0  0  0  0
 40 54  1  0  0  0  0
 54 55  1  0  0  0  0
 55 56  1  0  0  0  0
 56 57  1  0  0  0  0
 57 58  1  0  0  0  0
 58 59  1  0  0  0  0
 57 60  1  0  0  0  0
 60 61  1  0  0  0  0
 60 62  1  0  0  0  0
 62 63  1  0  0  0  0
 62 64  1  0  0  0  0
 55 64  1  0  0  0  0
 64 65  1  0  0  0  0
M  END

     RDKit          3D

141148  0  0  0  0  0  0  0  0999 V2000
    0.7989    3.1710    3.6277 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8082    2.5970    2.8941 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4222    1.7251    1.9133 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6431    1.3583    1.1308 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7580    0.7365    1.8861 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9640    0.4453    0.9736 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5249    1.6667    0.3393 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9222   -0.3633    1.7827 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0867   -0.7258    1.1416 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9438   -1.4751    0.0068 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5981   -2.6933    0.2132 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2653   -3.6285   -0.7572 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.4456   -4.5717   -1.0180 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7641   -5.2355    0.1855 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7277   -3.0418   -2.0099 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0947   -3.9142   -3.0632 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2334   -1.6929   -2.3860 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1508   -0.9997   -2.9791 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6628   -0.8577   -1.1992 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.0177   -1.0064   -0.9181 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7124    0.1984   -0.8542 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.6974    0.2366   -1.8009 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.5528    1.3022   -1.7578 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.9611    2.4065   -2.6460 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7609    1.9089   -0.4109 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.9712    3.0541   -0.2153 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.5543    0.9265    0.7137 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.6837    1.6213    1.9333 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1817    0.3407    0.5669 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.1788   -0.8778    1.2455 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5717    2.4626    0.9812 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0264    1.4833    0.1786 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3290    1.8577   -0.3879 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1013    0.5794   -0.2205 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5710    0.7082   -0.3774 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8353    1.0211   -1.8446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2554    0.7105   -2.1865 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0397   -0.0662   -1.4905 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4583   -0.2980   -1.9453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3337   -0.3717   -0.7389 C   0  0  2  0  0  0  0  0  0  0  0  0
   -9.6299   -0.0015   -0.9871 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5726   -0.9421   -0.5830 C   0  0  1  0  0  0  0  0  0  0  0  0
  -11.3342   -0.4748    0.4824 O   0  0  0  0  0  0  0  0  0  0  0  0
  -12.3070    0.4164    0.1580 C   0  0  1  0  0  0  0  0  0  0  0  0
  -12.0459    1.7537    0.8304 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.0371    2.6748    0.5054 O   0  0  0  0  0  0  0  0  0  0  0  0
  -12.5660    0.6146   -1.2911 C   0  0  1  0  0  0  0  0  0  0  0  0
  -11.6996    1.5128   -1.9059 O   0  0  0  0  0  0  0  0  0  0  0  0
  -12.6318   -0.7082   -1.9929 C   0  0  2  0  0  0  0  0  0  0  0  0
  -13.7749   -1.3726   -1.4906 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3911   -1.5148   -1.6918 C   0  0  1  0  0  0  0  0  0  0  0  0
  -10.6442   -1.6184   -2.8482 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6977    0.5253    0.3220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4748   -0.1771    0.8693 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.8888   -1.2262    1.6766 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6335   -0.7547   -0.2500 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.9396   -2.2291   -0.4343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1794   -0.6279   -0.0171 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7623   -1.0267    1.3812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2588   -1.1469    1.4564 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6945    0.2278    1.2203 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1675    1.2475    2.1933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2135    0.2659    1.0830 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5223    0.6634    2.3579 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1003   -0.5900    2.9258 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0594    3.7309    2.9913 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3610    2.4468    4.3111 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2789    3.9882    4.2493 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3876    0.7467    0.2183 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0262    2.3271    0.6906 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5357   -0.2375    2.3453 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1154    1.4457    2.6890 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5356   -0.2477    0.1895 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4516    1.5644   -0.7833 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6092    1.7381    0.5887 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0293    2.5921    0.6232 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4504   -1.3051    2.1644 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2489    0.2288    2.6889 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8963   -1.6840   -0.2698 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4756   -4.2777   -0.3106 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3122   -4.0523   -1.4358 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1508   -5.3721   -1.7259 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9356   -5.4841    0.6642 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5985   -3.0878   -2.0101 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9611   -3.6300   -3.4657 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0138   -1.7176   -3.1769 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8316   -0.2544   -2.4108 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3700    0.1999   -1.3265 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9746    0.9932   -1.0592 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.5412    1.0722   -2.2222 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6861    3.2465   -2.5980 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7511    2.0591   -3.6569 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0580    2.7618   -2.0899 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.8092    2.2632   -0.3406 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7013    3.0402    0.7409 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.3650    0.1695    0.7186 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0154    1.1764    2.5464 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4638    0.9874    1.1052 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0807   -1.1832    1.5129 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6509    1.2090   -0.6982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8255    2.6426    0.2032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2516    2.1584   -1.4622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7509   -0.2469   -0.8492 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0358    1.5432    0.1803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6759    2.0949   -2.0717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1897    0.4423   -2.5280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6474    1.1748   -3.0844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8094    0.5795   -2.5500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5518   -1.1956   -2.5532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3559   -1.3881   -0.2565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9733   -1.7956   -0.1472 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.2695    0.0435    0.6183 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0367    2.1315    0.6211 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.1681    1.5637    1.9372 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.1743    3.3561    1.2089 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.5910    1.0751   -1.3853 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5078    1.1600   -2.8273 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.8150   -0.5716   -3.0639 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.6797   -2.3505   -1.5644 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.7192   -2.5507   -1.3911 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2440   -2.5314   -2.9464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4091    1.5054   -0.1480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4468    0.6608    1.1256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9247    0.5576    1.4727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1017   -0.9511    2.5996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4962   -2.4504   -1.3662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4440   -2.6479    0.4685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9950   -2.8421   -0.5283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6687   -1.3727   -0.6943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0943   -0.2567    2.0770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2723   -1.9685    1.6726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8405   -1.8236    0.6861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0133   -1.4462    2.4927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5672    2.1659    2.1639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2178    1.5738    2.0308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1998    0.7645    3.2142 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1762   -0.6562    0.6473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2026    1.0503    3.1123 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7361   -0.3939    3.8015 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4840   -1.3020    2.1882 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1986   -1.1453    3.3706 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  3  2  1  1
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 12 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
  3 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 35 36  1  0
 36 37  1  0
 37 38  2  0
 38 39  1  0
 39 40  1  0
 40 53  1  0
 53 54  1  0
 54 55  1  0
 54 56  1  0
 56 57  1  6
 56 58  1  0
 58 59  1  0
 59 60  1  0
 60 61  1  0
 61 62  1  1
 61 63  1  0
 63 64  1  0
 64 65  1  0
 40 41  1  0
 41 42  1  0
 42 43  1  0
 43 44  1  0
 44 45  1  0
 45 46  1  0
 44 47  1  0
 47 48  1  0
 47 49  1  0
 49 50  1  0
 49 51  1  0
 51 52  1  0
 64  3  1  0
 51 42  1  0
 19 10  1  0
 29 21  1  0
 63 32  1  0
 61 34  1  0
 58 35  1  0
 56 38  1  0
  1 66  1  0
  1 67  1  0
  1 68  1  0
  4 69  1  0
  4 70  1  0
  5 71  1  0
  5 72  1  0
  6 73  1  6
  7 74  1  0
  7 75  1  0
  7 76  1  0
  8 77  1  0
  8 78  1  0
 10 79  1  6
 12 80  1  1
 13 81  1  0
 13 82  1  0
 14 83  1  0
 15 84  1  1
 16 85  1  0
 17 86  1  6
 18 87  1  0
 19 88  1  6
 21 89  1  6
 23 90  1  6
 24 91  1  0
 24 92  1  0
 24 93  1  0
 25 94  1  6
 26 95  1  0
 27 96  1  1
 28 97  1  0
 29 98  1  1
 30 99  1  0
 32100  1  6
 33101  1  0
 33102  1  0
 34103  1  6
 35104  1  1
 36105  1  0
 36106  1  0
 37107  1  0
 39108  1  0
 39109  1  0
 40110  1  1
 53122  1  0
 53123  1  0
 54124  1  1
 55125  1  0
 57126  1  0
 57127  1  0
 57128  1  0
 58129  1  6
 59130  1  0
 59131  1  0
 60132  1  0
 60133  1  0
 62134  1  0
 62135  1  0
 62136  1  0
 63137  1  6
 64138  1  1
 65139  1  0
 65140  1  0
 65141  1  0
 42111  1  1
 44112  1  1
 45113  1  0
 45114  1  0
 46115  1  0
 47116  1  1
 48117  1  0
 49118  1  6
 50119  1  0
 51120  1  1
 52121  1  0
M  END


  Mrv1533004171504192D          

 65 72  0  0  0  0            999 V2000
    3.1293   -1.3136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1339   -2.1386    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8507   -2.5471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3696   -3.2172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5486   -3.1356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0675   -3.8058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4073   -4.5576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2465   -3.7242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7654   -4.3943    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0556   -4.3127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5367   -4.9829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3577   -4.9013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8389   -5.5714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6598   -5.4898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6975   -4.1495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5185   -4.0679    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2163   -3.4793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5562   -2.7276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3954   -3.5610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0858   -2.8908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2540   -2.1390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0750   -2.0574    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4148   -1.3056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2358   -1.2240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9336   -0.6355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2734    0.1163    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1127   -0.7171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3685   -0.0469    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2271   -1.4689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0481   -1.5505    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1820   -1.7915    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0030   -1.8731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7151   -1.4566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3313   -2.0052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1513   -1.9143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4826   -1.1588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3026   -1.0679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7913   -1.7326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6112   -1.6417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0999   -2.3064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7686   -3.0620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9486   -3.1529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6173   -3.9084    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4600   -2.4882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1286   -3.2437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6400   -2.5790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3087   -3.3346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4887   -3.4254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0000   -2.7607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5915   -3.4775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1791   -2.6791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4669   -3.0956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3853   -3.9166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9199   -2.2156    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4086   -2.8803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2286   -2.7894    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.7172   -3.4541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5372   -3.3633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0259   -4.0279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.3859   -4.2097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8746   -4.8744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.5659   -4.3005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2346   -5.0561    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.0773   -3.6358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2573   -3.7267    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
  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
 12 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 10 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
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 21 29  1  0  0  0  0
 29 30  1  0  0  0  0
  3 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 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  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 38 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 35 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 34 49  1  0  0  0  0
 49 50  1  0  0  0  0
 49 51  1  0  0  0  0
 32 51  1  0  0  0  0
 51 52  1  0  0  0  0
  3 52  1  0  0  0  0
 52 53  1  0  0  0  0
 40 54  1  0  0  0  0
 54 55  1  0  0  0  0
 55 56  1  0  0  0  0
 56 57  1  0  0  0  0
 57 58  1  0  0  0  0
 58 59  1  0  0  0  0
 57 60  1  0  0  0  0
 60 61  1  0  0  0  0
 60 62  1  0  0  0  0
 62 63  1  0  0  0  0
 62 64  1  0  0  0  0
 55 64  1  0  0  0  0
 64 65  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0229194

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1(CCC(C)COC2OC(CO)C(O)C(O)C2OC2OC(C)C(O)C(O)C2O)OC2CC3C4CC=C5CC(CC(O)C5(C)C4CCC3(C)C2C1C)OC1OC(CO)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C46H76O19/c1-19(18-59-43-40(37(55)34(52)29(17-48)63-43)64-41-38(56)35(53)32(50)21(3)60-41)9-12-46(58-6)20(2)31-27(65-46)15-26-24-8-7-22-13-23(61-42-39(57)36(54)33(51)28(16-47)62-42)14-30(49)45(22,5)25(24)10-11-44(26,31)4/h7,19-21,23-43,47-57H,8-18H2,1-6H3

> <INCHI_KEY>
XGHOUJIJRQMORR-UHFFFAOYSA-N

> <FORMULA>
C46H76O19

> <MOLECULAR_WEIGHT>
933.095

> <EXACT_MASS>
932.498080227

> <JCHEM_ACCEPTOR_COUNT>
19

> <JCHEM_ATOM_COUNT>
141

> <JCHEM_AVERAGE_POLARIZABILITY>
101.22033269184472

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
11

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-({4,5-dihydroxy-2-[4-(14-hydroxy-6-methoxy-7,9,13-trimethyl-16-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icos-18-en-6-yl)-2-methylbutoxy]-6-(hydroxymethyl)oxan-3-yl}oxy)-6-methyloxane-3,4,5-triol

> <ALOGPS_LOGP>
-0.06

> <JCHEM_LOGP>
-1.1604736580000001

> <ALOGPS_LOGS>
-3.29

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.320343136640162

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.852502941255844

> <JCHEM_PKA_STRONGEST_BASIC>
-3.612182629439543

> <JCHEM_POLAR_SURFACE_AREA>
296.36999999999995

> <JCHEM_REFRACTIVITY>
225.69530000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.75e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-({4,5-dihydroxy-2-[4-(14-hydroxy-6-methoxy-7,9,13-trimethyl-16-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icos-18-en-6-yl)-2-methylbutoxy]-6-(hydroxymethyl)oxan-3-yl}oxy)-6-methyloxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       5.841  -2.452   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.850  -3.992   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       7.188  -4.755   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.290  -6.006   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.757  -5.853   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.859  -7.104   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.494  -8.507   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.327  -6.952   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       1.429  -8.203   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -0.104  -8.050   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -1.002  -9.301   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -2.534  -9.149   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.433 -10.400   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -4.965 -10.248   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -3.169  -7.746   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -4.701  -7.593   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -2.271  -6.495   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -2.905  -5.091   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -0.738  -6.647   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.160  -5.396   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -0.474  -3.993   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -2.007  -3.841   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -2.641  -2.437   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -4.173  -2.285   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.743  -1.186   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -2.377   0.217   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -0.210  -1.339   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       0.688  -0.088   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       0.424  -2.742   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       1.956  -2.894   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       7.806  -3.344   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       9.339  -3.497   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      10.668  -2.719   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      11.818  -3.743   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      13.349  -3.573   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      13.968  -2.163   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      15.498  -1.993   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      16.410  -3.234   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      17.941  -3.065   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      18.853  -4.305   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      18.235  -5.716   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      16.704  -5.885   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      16.086  -7.296   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      15.792  -4.645   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      15.173  -6.055   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      14.261  -4.814   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      13.643  -6.225   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      12.112  -6.394   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      11.200  -5.153   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      10.438  -6.491   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       9.668  -5.001   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       8.338  -5.779   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0       8.186  -7.311   0.000  0.00  0.00           C+0
HETATM   54  O   UNK     0      20.384  -4.136   0.000  0.00  0.00           O+0
HETATM   55  C   UNK     0      21.296  -5.377   0.000  0.00  0.00           C+0
HETATM   56  O   UNK     0      22.827  -5.207   0.000  0.00  0.00           O+0
HETATM   57  C   UNK     0      23.739  -6.448   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0      25.269  -6.278   0.000  0.00  0.00           C+0
HETATM   59  O   UNK     0      26.182  -7.519   0.000  0.00  0.00           O+0
HETATM   60  C   UNK     0      23.120  -7.858   0.000  0.00  0.00           C+0
HETATM   61  O   UNK     0      24.033  -9.099   0.000  0.00  0.00           O+0
HETATM   62  C   UNK     0      21.590  -8.028   0.000  0.00  0.00           C+0
HETATM   63  O   UNK     0      20.971  -9.438   0.000  0.00  0.00           O+0
HETATM   64  C   UNK     0      20.678  -6.787   0.000  0.00  0.00           C+0
HETATM   65  O   UNK     0      19.147  -6.956   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   31   52                                             
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   19                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15   12   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   10   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   29                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   21   30                                                  
CONECT   30   29                                                            
CONECT   31    3   32                                                       
CONECT   32   31   33   51                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   49                                                  
CONECT   35   34   36   46                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39   44                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41   54                                                  
CONECT   41   40   42                                                       
CONECT   42   41   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   38   45   46                                             
CONECT   45   44                                                            
CONECT   46   44   35   47                                                  
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   34   50   51                                             
CONECT   50   49                                                            
CONECT   51   49   32   52                                                  
CONECT   52   51    3   53                                                  
CONECT   53   52                                                            
CONECT   54   40   55                                                       
CONECT   55   54   56   64                                                  
CONECT   56   55   57                                                       
CONECT   57   56   58   60                                                  
CONECT   58   57   59                                                       
CONECT   59   58                                                            
CONECT   60   57   61   62                                                  
CONECT   61   60                                                            
CONECT   62   60   63   64                                                  
CONECT   63   62                                                            
CONECT   64   62   55   65                                                  
CONECT   65   64                                                            
MASTER        0    0    0    0    0    0    0    0   65    0  144    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₆H₇₆O₁₉

Average Mass

933.0950 Da

Monoisotopic Mass

932.49808 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1(CCC(C)COC2OC(CO)C(O)C(O)C2OC2OC(C)C(O)C(O)C2O)OC2CC3C4CC=C5CC(CC(O)C5(C)C4CCC3(C)C2C1C)OC1OC(CO)C(O)C(O)C1O

InChI Identifier

InChI=1S/C46H76O19/c1-19(18-59-43-40(37(55)34(52)29(17-48)63-43)64-41-38(56)35(53)32(50)21(3)60-41)9-12-46(58-6)20(2)31-27(65-46)15-26-24-8-7-22-13-23(61-42-39(57)36(54)33(51)28(16-47)62-42)14-30(49)45(22,5)25(24)10-11-44(26,31)4/h7,19-21,23-43,47-57H,8-18H2,1-6H3

InChI Key

XGHOUJIJRQMORR-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
Allium triquetrum	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
Furostane-skeleton
Diterpene glycoside
Diterpenoid
Hydroxysteroid
1-hydroxysteroid
Delta-5-steroid
Terpene glycoside
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
O-glycosyl compound
Glycosyl compound
Disaccharide
Ketal
Oxane
Fatty acyl
Cyclic alcohol
Tetrahydrofuran
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Acetal
Polyol
Primary alcohol
Alcohol
Hydrocarbon derivative
Organic oxygen compound
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	-0.06	ALOGPS
logP	-1.2	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	11.85	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	19	ChemAxon
Hydrogen Donor Count	11	ChemAxon
Polar Surface Area	296.37 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	225.7 m³·mol⁻¹	ChemAxon
Polarizability	101.22 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

72973703

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-({4,5-dihydroxy-2-[4-(14-hydroxy-6-methoxy-7,9,13-trimethyl-16-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icos-18-en-6-yl)-2-methylbutoxy]-6-(hydroxymethyl)oxan-3-yl}oxy)-6-methyloxane-3,4,5-triol (NP0229194)

MOL for NP0229194 (2-({4,5-dihydroxy-2-[4-(14-hydroxy-6-methoxy-7,9,13-trimethyl-16-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icos-18-en-6-yl)-2-methylbutoxy]-6-(hydroxymethyl)oxan-3-yl}oxy)-6-methyloxane-3,4,5-triol)

3D MOL for NP0229194 (2-({4,5-dihydroxy-2-[4-(14-hydroxy-6-methoxy-7,9,13-trimethyl-16-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icos-18-en-6-yl)-2-methylbutoxy]-6-(hydroxymethyl)oxan-3-yl}oxy)-6-methyloxane-3,4,5-triol)

3D SDF for NP0229194 (2-({4,5-dihydroxy-2-[4-(14-hydroxy-6-methoxy-7,9,13-trimethyl-16-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icos-18-en-6-yl)-2-methylbutoxy]-6-(hydroxymethyl)oxan-3-yl}oxy)-6-methyloxane-3,4,5-triol)

3D-SDF for NP0229194 (2-({4,5-dihydroxy-2-[4-(14-hydroxy-6-methoxy-7,9,13-trimethyl-16-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icos-18-en-6-yl)-2-methylbutoxy]-6-(hydroxymethyl)oxan-3-yl}oxy)-6-methyloxane-3,4,5-triol)

PDB for NP0229194 (2-({4,5-dihydroxy-2-[4-(14-hydroxy-6-methoxy-7,9,13-trimethyl-16-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icos-18-en-6-yl)-2-methylbutoxy]-6-(hydroxymethyl)oxan-3-yl}oxy)-6-methyloxane-3,4,5-triol)

3D PDB for NP0229194 (2-({4,5-dihydroxy-2-[4-(14-hydroxy-6-methoxy-7,9,13-trimethyl-16-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icos-18-en-6-yl)-2-methylbutoxy]-6-(hydroxymethyl)oxan-3-yl}oxy)-6-methyloxane-3,4,5-triol)

SMILES for NP0229194 (2-({4,5-dihydroxy-2-[4-(14-hydroxy-6-methoxy-7,9,13-trimethyl-16-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icos-18-en-6-yl)-2-methylbutoxy]-6-(hydroxymethyl)oxan-3-yl}oxy)-6-methyloxane-3,4,5-triol)

INCHI for NP0229194 (2-({4,5-dihydroxy-2-[4-(14-hydroxy-6-methoxy-7,9,13-trimethyl-16-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icos-18-en-6-yl)-2-methylbutoxy]-6-(hydroxymethyl)oxan-3-yl}oxy)-6-methyloxane-3,4,5-triol)

Structure for NP0229194 (2-({4,5-dihydroxy-2-[4-(14-hydroxy-6-methoxy-7,9,13-trimethyl-16-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icos-18-en-6-yl)-2-methylbutoxy]-6-(hydroxymethyl)oxan-3-yl}oxy)-6-methyloxane-3,4,5-triol)

3D Structure for NP0229194 (2-({4,5-dihydroxy-2-[4-(14-hydroxy-6-methoxy-7,9,13-trimethyl-16-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icos-18-en-6-yl)-2-methylbutoxy]-6-(hydroxymethyl)oxan-3-yl}oxy)-6-methyloxane-3,4,5-triol)