NP-MRD: Showing NP-Card for (2r,3r,4s,5s,6r)-2-{[(1r,3ar,5ar,6r,7s,9ar,11ar)-1-[(2r)-6-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol (NP0234737)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-06 16:57:41 UTC

Updated at

2022-09-06 16:57:41 UTC

NP-MRD ID

NP0234737

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3r,4s,5s,6r)-2-{[(1r,3ar,5ar,6r,7s,9ar,11ar)-1-[(2r)-6-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

Description

(2R,3R,4S,5S,6R)-2-{[(2R,5S,6R,7R,11R,14R,15R)-14-[(2R)-6-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6-(hydroxymethyl)-2,6,11,15-tetramethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-1(10)-en-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. (2r,3r,4s,5s,6r)-2-{[(1r,3ar,5ar,6r,7s,9ar,11ar)-1-[(2r)-6-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol is found in Silybum marianum. Based on a literature review very few articles have been published on (2R,3R,4S,5S,6R)-2-{[(2R,5S,6R,7R,11R,14R,15R)-14-[(2R)-6-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6-(hydroxymethyl)-2,6,11,15-tetramethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-1(10)-en-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062218572D          

 45 49  0  0  1  0            999 V2000
    4.3612   -3.0854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1784   -2.9726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4893   -2.2084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9830   -1.5571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2939   -0.7929    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1111   -0.6800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875   -0.1416    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0168    0.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340    1.1139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826    0.6076    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4850    1.4085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8705    0.7528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387    0.1221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190   -0.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311   -0.7991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629   -0.1684    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3228   -0.9107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266    0.2673    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8069   -0.5086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976    0.5577    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9098    0.7029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1901    1.4789    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0022    1.6241    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2825    2.4000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0946    2.5452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3749    3.3211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7507    3.0307    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0310    3.8066    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9385    2.8855    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4067    3.5162    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6582    2.1096    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1539    1.9643    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342    1.1884    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2793    1.6026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7182    1.9630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1894    2.5962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463    1.0432    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7781    1.6739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5902    1.5287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6848   -3.6239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1911   -4.2752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0335   -4.1303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3361   -3.1176    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  6  0  0  0
  7  5  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  7 16  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  1  6  0  0  0
 13 18  1  0  0  0  0
 18 19  1  1  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
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  6  0  0  0
 27 28  1  0  0  0  0
 26 29  1  0  0  0  0
 29 30  1  1  0  0  0
 29 31  1  0  0  0  0
 31 32  1  6  0  0  0
 31 33  1  0  0  0  0
 24 33  1  0  0  0  0
 33 34  1  1  0  0  0
 22 35  1  0  0  0  0
 35 36  1  6  0  0  0
 35 37  1  1  0  0  0
 37 38  1  0  0  0  0
 35 39  1  0  0  0  0
 18 39  1  0  0  0  0
 39 40  1  6  0  0  0
 40 41  1  0  0  0  0
 12 41  1  0  0  0  0
  2 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 42 45  1  0  0  0  0
M  END

     RDKit          3D

107111  0  0  0  0  0  0  0  0999 V2000
   -8.5056   -2.2777    0.5593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3494   -0.9818    0.5412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1107   -0.3998   -0.0347 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1410   -1.4394   -0.5001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8955   -0.8553   -1.1007 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2842   -0.0215   -2.2886 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9926   -0.1775   -0.1506 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6599   -1.0549    1.0603 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2147   -0.7831    1.4261 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9860    0.4991    0.7069 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8490    1.5429    1.3795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6273    0.9300    0.4551 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0525    0.8843   -0.7357 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8679    1.0197   -2.0060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3449    1.1790   -1.5704 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6195    0.0861   -0.6444 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0393   -1.2133   -1.1379 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4225    0.6945   -0.8386 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8371    0.7257   -2.2956 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8145   -0.6863   -0.3513 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2431   -0.8989   -0.1161 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1809    0.2621   -0.1610 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2078   -0.0356    0.7678 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4455   -0.2108    0.1812 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.7413   -1.5840    0.3892 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8237   -2.0187   -0.3300 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.4099   -3.2284    0.4081 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5193   -3.7369   -0.2542 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9319   -1.0159   -0.4727 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.8056   -0.2524   -1.6328 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9100   -0.0960    0.7066 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.2929   -0.7181    1.8972 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5669    0.5392    0.8238 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.6676    1.8674    0.3702 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5919    1.5843    0.1179 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0158    1.9670    1.5593 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1799    2.7297   -0.7083 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0556    2.5991   -2.0536 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1051    1.6723    0.0486 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6008    1.4231    1.4650 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1293    1.4595    1.6231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4152   -0.1143    1.0993 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5709   -0.9489    1.6044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8650    0.6739    2.2614 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9333    0.7235    0.1054 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3936   -2.7208    0.9713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7509   -2.9298    0.1597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6271    0.1605    0.8202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3095    0.3788   -0.7955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6354   -2.0348   -1.2935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8993   -2.1841    0.3114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3383   -1.7392   -1.5316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6915   -0.2351   -3.2003 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2430    1.0642   -2.0770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3913   -0.1832   -2.5313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4585    0.7766    0.1604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3556   -0.8078    1.9106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7732   -2.1165    0.8886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0687   -0.6705    2.5241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5505   -1.6107    1.1075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6472    1.0890    2.0006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2401    2.3047    0.7109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1836    2.0720    2.1125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8740    0.1130   -2.6069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5736    1.8990   -2.5874 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4057    2.2002   -1.1511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9444    1.1296   -2.4764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5381   -2.0929   -0.6850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2946   -1.2930   -2.2359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9702   -1.3510   -0.9520 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6424    1.6658   -2.8068 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8103    0.2427   -2.4944 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1258   -0.0082   -2.8093 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1738   -0.9022    0.5301 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4178   -1.3899   -1.1456 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3451   -1.4426    0.8711 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6324   -1.6522   -0.8572 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7227    0.2901   -1.1297 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3523   -0.0687   -0.9060 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5474   -2.3892   -1.3463 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7270   -2.9283    1.4264 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6281   -4.0156    0.4450 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2765   -3.9363    0.3620 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9411   -1.4972   -0.5224 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6719   -0.8559   -2.4146 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6824    0.7030    0.5257 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6391   -0.0095    2.4933 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3180    0.5797    1.9245 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9875    2.4453    1.1336 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7848    1.1989    2.2851 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7883    3.0023    1.7977 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1491    1.9459    1.4761 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2670    2.8648   -0.4835 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7281    3.7074   -0.3658 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8658    2.7386   -2.5939 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8197    2.7412   -0.1781 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9787    0.4252    1.8402 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0179    2.1727    2.1679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1303    0.8925    2.5548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1739    2.5250    1.8457 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2543   -1.6077    2.4364 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3794   -0.2761    2.0137 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0403   -1.5520    0.7996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7214    1.2014    2.7401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1730    1.4500    1.8853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3666   -0.0422    2.9427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8187    0.2502   -0.7787 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
  2 42  1  0
 42 43  1  0
 42 44  1  0
 42 45  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  1
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  6
 13 18  1  0
 18 19  1  6
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 26 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31 33  1  0
 33 34  1  0
 22 35  1  0
 35 36  1  1
 35 37  1  0
 37 38  1  0
 35 39  1  0
 39 40  1  0
 40 41  1  0
 16  7  1  0
 39 18  1  0
 16 10  1  0
 33 24  1  0
 41 12  1  0
  6 53  1  0
  6 54  1  0
  6 55  1  0
  5 52  1  6
  4 50  1  0
  4 51  1  0
  3 48  1  0
  3 49  1  0
  1 46  1  0
  1 47  1  0
 43101  1  0
 43102  1  0
 43103  1  0
 44104  1  0
 44105  1  0
 44106  1  0
 45107  1  0
  7 56  1  1
  8 57  1  0
  8 58  1  0
  9 59  1  0
  9 60  1  0
 11 61  1  0
 11 62  1  0
 11 63  1  0
 14 64  1  0
 14 65  1  0
 15 66  1  0
 15 67  1  0
 17 68  1  0
 17 69  1  0
 17 70  1  0
 19 71  1  0
 19 72  1  0
 19 73  1  0
 20 74  1  0
 20 75  1  0
 21 76  1  0
 21 77  1  0
 22 78  1  6
 24 79  1  6
 26 80  1  6
 27 81  1  0
 27 82  1  0
 28 83  1  0
 29 84  1  6
 30 85  1  0
 31 86  1  6
 32 87  1  0
 33 88  1  1
 34 89  1  0
 36 90  1  0
 36 91  1  0
 36 92  1  0
 37 93  1  0
 37 94  1  0
 38 95  1  0
 39 96  1  6
 40 97  1  0
 40 98  1  0
 41 99  1  0
 41100  1  0
M  END


  Mrv1652309062218572D          

 45 49  0  0  1  0            999 V2000
    4.3612   -3.0854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1784   -2.9726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4893   -2.2084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9830   -1.5571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2939   -0.7929    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1111   -0.6800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875   -0.1416    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0168    0.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340    1.1139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826    0.6076    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4850    1.4085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8705    0.7528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387    0.1221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190   -0.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311   -0.7991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629   -0.1684    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3228   -0.9107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266    0.2673    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8069   -0.5086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976    0.5577    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9098    0.7029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1901    1.4789    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0022    1.6241    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2825    2.4000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0946    2.5452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3749    3.3211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7507    3.0307    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0310    3.8066    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9385    2.8855    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4067    3.5162    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6582    2.1096    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1539    1.9643    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342    1.1884    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2793    1.6026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7182    1.9630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1894    2.5962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463    1.0432    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7781    1.6739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5902    1.5287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6848   -3.6239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1911   -4.2752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0335   -4.1303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3361   -3.1176    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  6  0  0  0
  7  5  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  7 16  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  1  6  0  0  0
 13 18  1  0  0  0  0
 18 19  1  1  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
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  6  0  0  0
 27 28  1  0  0  0  0
 26 29  1  0  0  0  0
 29 30  1  1  0  0  0
 29 31  1  0  0  0  0
 31 32  1  6  0  0  0
 31 33  1  0  0  0  0
 24 33  1  0  0  0  0
 33 34  1  1  0  0  0
 22 35  1  0  0  0  0
 35 36  1  6  0  0  0
 35 37  1  1  0  0  0
 37 38  1  0  0  0  0
 35 39  1  0  0  0  0
 18 39  1  0  0  0  0
 39 40  1  6  0  0  0
 40 41  1  0  0  0  0
 12 41  1  0  0  0  0
  2 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 42 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0234737

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](CCC(=C)C(C)(C)O)[C@H]1CC[C@@]2(C)C3=C(CC[C@]12C)[C@]1(C)CC[C@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@](C)(CO)[C@@H]1CC3

> <INCHI_IDENTIFIER>
InChI=1S/C37H62O8/c1-21(9-10-22(2)33(3,4)43)23-13-17-37(8)25-11-12-27-34(5,24(25)14-18-36(23,37)7)16-15-28(35(27,6)20-39)45-32-31(42)30(41)29(40)26(19-38)44-32/h21,23,26-32,38-43H,2,9-20H2,1,3-8H3/t21-,23-,26-,27-,28+,29-,30+,31-,32+,34+,35+,36-,37+/m1/s1

> <INCHI_KEY>
BQSKVEDRDUPKAI-ZZYPIIGCSA-N

> <FORMULA>
C37H62O8

> <MOLECULAR_WEIGHT>
634.895

> <EXACT_MASS>
634.444468956

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
107

> <JCHEM_AVERAGE_POLARIZABILITY>
73.86777749044847

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3R,4S,5S,6R)-2-{[(2R,5S,6R,7R,11R,14R,15R)-14-[(2R)-6-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6-(hydroxymethyl)-2,6,11,15-tetramethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-1(10)-en-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_LOGP>
3.684811260333332

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.194355758583875

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.209888357530982

> <JCHEM_PKA_STRONGEST_BASIC>
-1.3398960924439418

> <JCHEM_POLAR_SURFACE_AREA>
139.84

> <JCHEM_REFRACTIVITY>
173.89090000000007

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R,4S,5S,6R)-2-{[(2R,5S,6R,7R,11R,14R,15R)-14-[(2R)-6-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6-(hydroxymethyl)-2,6,11,15-tetramethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-1(10)-en-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       8.141  -5.759   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.666  -5.549   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.247  -4.122   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.302  -2.907   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.882  -1.480   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.407  -1.269   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.937  -0.264   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.365   1.215   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.090   2.079   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.874   1.134   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.505   2.629   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.358   1.405   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.366   0.228   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.889  -1.221   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.405  -1.492   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.398  -0.314   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.069  -1.700   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.850   0.499   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.373  -0.949   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.857  -0.678   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.341  -0.407   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.182   1.041   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -1.698   1.312   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -2.221   2.761   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -3.737   3.032   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -4.261   4.480   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -5.777   4.751   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -6.300   6.199   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -3.268   5.657   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -3.791   7.106   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -1.752   5.386   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -0.759   6.564   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -1.229   3.938   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       0.287   3.667   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       0.810   2.218   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -0.521   2.992   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       1.341   3.664   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       0.354   4.846   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       2.326   1.947   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       3.319   3.125   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       4.835   2.854   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      10.612  -6.765   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      11.557  -7.980   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       9.396  -7.710   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      11.827  -5.819   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   42                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   16                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12   16                                             
CONECT   11   10                                                            
CONECT   12   10   13   41                                                  
CONECT   13   12   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15    7   10   17                                             
CONECT   17   16                                                            
CONECT   18   13   19   20   39                                             
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   35                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   33                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   29                                                  
CONECT   27   26   28                                                       
CONECT   28   27                                                            
CONECT   29   26   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   24   34                                                  
CONECT   34   33                                                            
CONECT   35   22   36   37   39                                             
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37                                                            
CONECT   39   35   18   40                                                  
CONECT   40   39   41                                                       
CONECT   41   40   12                                                       
CONECT   42    2   43   44   45                                             
CONECT   43   42                                                            
CONECT   44   42                                                            
CONECT   45   42                                                            
MASTER        0    0    0    0    0    0    0    0   45    0   98    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₇H₆₂O₈

Average Mass

634.8950 Da

Monoisotopic Mass

634.44447 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@H](CCC(=C)C(C)(C)O)[C@H]1CC[C@@]2(C)C3=C(CC[C@]12C)[C@]1(C)CC[C@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@](C)(CO)[C@@H]1CC3

InChI Identifier

InChI=1S/C37H62O8/c1-21(9-10-22(2)33(3,4)43)23-13-17-37(8)25-11-12-27-34(5,24(25)14-18-36(23,37)7)16-15-28(35(27,6)20-39)45-32-31(42)30(41)29(40)26(19-38)44-32/h21,23,26-32,38-43H,2,9-20H2,1,3-8H3/t21-,23-,26-,27-,28+,29-,30+,31-,32+,34+,35+,36-,37+/m1/s1

InChI Key

BQSKVEDRDUPKAI-ZZYPIIGCSA-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
Silybum marianum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Steroidal glycoside
25-hydroxysteroid
14-alpha-methylsteroid
Steroid
O-glycosyl compound
Glycosyl compound
Oxane
Monosaccharide
Tertiary alcohol
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Polyol
Acetal
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source

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

162822179

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3r,4s,5s,6r)-2-{[(1r,3ar,5ar,6r,7s,9ar,11ar)-1-[(2r)-6-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol (NP0234737)

MOL for NP0234737 ((2r,3r,4s,5s,6r)-2-{[(1r,3ar,5ar,6r,7s,9ar,11ar)-1-[(2r)-6-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D MOL for NP0234737 ((2r,3r,4s,5s,6r)-2-{[(1r,3ar,5ar,6r,7s,9ar,11ar)-1-[(2r)-6-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D SDF for NP0234737 ((2r,3r,4s,5s,6r)-2-{[(1r,3ar,5ar,6r,7s,9ar,11ar)-1-[(2r)-6-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D-SDF for NP0234737 ((2r,3r,4s,5s,6r)-2-{[(1r,3ar,5ar,6r,7s,9ar,11ar)-1-[(2r)-6-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

PDB for NP0234737 ((2r,3r,4s,5s,6r)-2-{[(1r,3ar,5ar,6r,7s,9ar,11ar)-1-[(2r)-6-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D PDB for NP0234737 ((2r,3r,4s,5s,6r)-2-{[(1r,3ar,5ar,6r,7s,9ar,11ar)-1-[(2r)-6-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

SMILES for NP0234737 ((2r,3r,4s,5s,6r)-2-{[(1r,3ar,5ar,6r,7s,9ar,11ar)-1-[(2r)-6-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

INCHI for NP0234737 ((2r,3r,4s,5s,6r)-2-{[(1r,3ar,5ar,6r,7s,9ar,11ar)-1-[(2r)-6-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

Structure for NP0234737 ((2r,3r,4s,5s,6r)-2-{[(1r,3ar,5ar,6r,7s,9ar,11ar)-1-[(2r)-6-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D Structure for NP0234737 ((2r,3r,4s,5s,6r)-2-{[(1r,3ar,5ar,6r,7s,9ar,11ar)-1-[(2r)-6-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)