NP-MRD: Showing NP-Card for 14,17-dihydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-13-yl acetate (NP0198560)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 17:02:01 UTC

Updated at

2022-09-04 17:02:01 UTC

NP-MRD ID

NP0198560

Secondary Accession Numbers

None

Natural Product Identification

Common Name

14,17-dihydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-13-yl acetate

Description

14,17-Dihydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]Octadecan-13-yl acetate belongs to the class of organic compounds known as 3-hydroxysteroids. These are steroids carrying a hydroxyl group at the 3-position of the steroid backbone. 14,17-dihydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-13-yl acetate is found in Actaea vaginata. 14,17-Dihydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]Octadecan-13-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191514002D          

 48 54  0  0  0  0            999 V2000
    2.1239    3.1521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1507    2.3275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4500    1.8920    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8782    1.9385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9050    1.1139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5879    0.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3638    0.9312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3586   -0.1416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8649   -0.7929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1642   -1.2284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4598   -0.2212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1873   -0.6103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0420   -1.4224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2248   -1.5353    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6137   -2.0172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1854   -2.6121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2085   -1.4456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0189   -2.5889    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5340   -0.1684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8939   -0.9107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0022   -0.7991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2825   -1.5750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1901   -0.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9098    0.1221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3779   -0.5086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0976    0.2673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4342   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2463   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5266    0.5577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3387    0.7029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6190    1.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4311    1.6241    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7114    2.4000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1796    3.0307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4599    3.8066    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3675    2.8855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8357    3.5162    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0872    2.1096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2751    1.9643    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9948    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7082    1.6026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7107    1.9630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1827    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3492    1.6739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1613    1.5287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4416    0.7528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2537    0.6076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0560    1.4085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  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
  9 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
  9 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 15 18  1  0  0  0  0
  8 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  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
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 31 38  1  0  0  0  0
 38 39  1  0  0  0  0
 29 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 40 43  1  0  0  0  0
 26 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 24 46  1  0  0  0  0
 46 47  1  0  0  0  0
  5 47  1  0  0  0  0
 19 47  1  0  0  0  0
 47 48  1  0  0  0  0
M  END

     RDKit          3D

108114  0  0  0  0  0  0  0  0999 V2000
   -0.7279    0.7844    4.1953 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8314   -0.3851    3.2747 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3263   -1.4903    3.6578 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4301   -0.3344    2.0610 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5075   -1.4732    1.2094 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0387   -1.7468    1.4463 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2915   -1.6531    2.8373 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5367   -0.5053    0.7956 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9938   -0.3147    0.7722 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.4257   -0.2478    2.2646 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8351   -1.3969    0.1929 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5623   -0.7567   -0.9672 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3770    0.7045   -0.6955 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.7188    1.3301   -0.4378 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6205    1.0012   -1.6092 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6306    2.8464   -0.3990 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3355    0.8393    0.7074 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4277    0.8721    0.2520 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7098   -0.2702   -0.4165 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3275   -0.6458   -1.7285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2205    1.1533   -0.5390 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4460    1.6404   -1.8578 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8906    1.5189   -0.0014 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1902    0.5235    0.0106 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2729    1.3779    0.5114 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5384    0.1114    0.0950 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1785   -0.7867    1.1536 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6318   -0.4287    1.3653 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4619   -0.5597    0.1135 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3868    0.4781    0.0475 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7009    0.0685    0.2574 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1779    0.5725    1.4745 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1568    1.5289    1.3360 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4175    0.9739    0.7016 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.2087    0.3433    1.6575 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0476    0.0336   -0.4344 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.9228    0.1919   -1.5071 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6289    0.3421   -0.8756 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5510    1.6296   -1.3622 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6343   -0.7172   -1.1156 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5323   -0.1796   -2.2577 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5574   -2.1927   -1.4244 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3822    0.0432   -1.1963 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5306   -0.4953   -2.3025 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5643   -1.4367   -1.6003 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3424   -0.4778   -0.8445 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4981   -1.2179   -0.2360 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7630   -2.5327   -0.9332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3938    0.6519    5.0816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1140    1.6734    3.6559 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3143    0.9958    4.4858 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9815   -2.3516    1.5948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3552   -2.7008    1.1424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1519   -2.5221    3.2720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1499    0.3194    1.5065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5762   -1.2317    2.6942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6017    0.2495    2.8576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2989    0.3776    2.4190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6585   -1.7484    0.8863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3576   -2.2970   -0.1553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1758   -1.0736   -1.9569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6507   -1.0380   -0.9951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0153    1.1761   -1.6593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0000    0.7043   -2.4584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2733    0.1356   -1.3294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2491    1.8696   -1.9004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6053    3.2134   -0.0222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5106    3.2059   -1.4334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8536    3.2120    0.2948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3728    1.5050    1.4364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8033   -1.6100   -1.7976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4836   -0.6739   -2.4860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9413    0.2011   -2.1625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0380    1.7245    0.0179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2335    2.6114   -1.8327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5656    2.3595   -0.7129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0680    2.1103    0.9405 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2048    1.6385    1.6149 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6252    2.3092   -0.0226 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7198   -0.4801    2.1457 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9461   -1.8327    1.0934 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6511    0.6402    1.6637 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0070   -1.0132    2.2000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0793   -1.4914    0.2861 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6720   -1.0443    0.4161 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8216    2.4501    0.8092 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4407    1.8524    2.3579 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9810    1.8309    0.2888 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7318   -0.4714    1.9842 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1332   -1.0129   -0.0885 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4903   -0.6071   -1.6304 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4145   -0.3734   -1.6934 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9711    1.6994   -2.2491 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2722   -0.9112   -2.5683 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0131    0.7650   -1.9862 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8555    0.0419   -3.1293 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2762   -2.8389   -0.5983 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0054   -2.4659   -2.3171 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6283   -2.5035   -1.6475 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6579    1.0878   -1.5436 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8805    0.3297   -2.7233 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0450   -0.9102   -3.1551 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0578   -1.9216   -2.4658 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0005   -2.2275   -1.0267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7785    0.0373   -1.7784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7406   -2.9267   -0.6704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9952   -3.2450   -0.5624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7620   -2.4863   -2.0361 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  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  1
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 18  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 14 17  1  0
  8 19  1  0
 19 20  1  6
 19 21  1  0
 21 22  1  0
 21 23  1  0
 24 23  1  6
 24 25  1  0
 26 25  1  1
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  1  0
 36 38  1  0
 38 39  1  0
 29 40  1  0
 40 41  1  0
 40 42  1  0
 40 43  1  0
 43 44  1  0
 44 45  1  0
 45 46  1  0
 46 47  1  0
 47 48  1  6
 47  5  1  0
 18  9  1  0
 47 19  1  0
 26 24  1  0
 43 26  1  0
 46 24  1  0
 38 31  1  0
  1 49  1  0
  1 50  1  0
  1 51  1  0
  5 52  1  6
  6 53  1  6
  7 54  1  0
  8 55  1  1
 10 56  1  0
 10 57  1  0
 10 58  1  0
 11 59  1  0
 11 60  1  0
 12 61  1  0
 12 62  1  0
 13 63  1  6
 15 64  1  0
 15 65  1  0
 15 66  1  0
 16 67  1  0
 16 68  1  0
 16 69  1  0
 17 70  1  0
 20 71  1  0
 20 72  1  0
 20 73  1  0
 21 74  1  1
 22 75  1  0
 23 76  1  0
 23 77  1  0
 25 78  1  0
 25 79  1  0
 27 80  1  0
 27 81  1  0
 28 82  1  0
 28 83  1  0
 29 84  1  1
 31 85  1  1
 33 86  1  0
 33 87  1  0
 34 88  1  6
 35 89  1  0
 36 90  1  1
 37 91  1  0
 38 92  1  6
 39 93  1  0
 41 94  1  0
 41 95  1  0
 41 96  1  0
 42 97  1  0
 42 98  1  0
 42 99  1  0
 43100  1  6
 44101  1  0
 44102  1  0
 45103  1  0
 45104  1  0
 46105  1  6
 48106  1  0
 48107  1  0
 48108  1  0
M  END


  Mrv1533004191514002D          

 48 54  0  0  0  0            999 V2000
    2.1239    3.1521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1507    2.3275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4500    1.8920    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8782    1.9385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9050    1.1139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5879    0.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3638    0.9312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3586   -0.1416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8649   -0.7929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1642   -1.2284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4598   -0.2212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1873   -0.6103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0420   -1.4224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2248   -1.5353    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6137   -2.0172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1854   -2.6121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2085   -1.4456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0189   -2.5889    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5340   -0.1684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8939   -0.9107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0022   -0.7991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2825   -1.5750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1901   -0.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9098    0.1221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3779   -0.5086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0976    0.2673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4342   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2463   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5266    0.5577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3387    0.7029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6190    1.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4311    1.6241    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7114    2.4000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1796    3.0307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4599    3.8066    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3675    2.8855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8357    3.5162    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0872    2.1096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2751    1.9643    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9948    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7082    1.6026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7107    1.9630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1827    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3492    1.6739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1613    1.5287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4416    0.7528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2537    0.6076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0560    1.4085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  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
  9 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
  9 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 15 18  1  0  0  0  0
  8 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  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
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 31 38  1  0  0  0  0
 38 39  1  0  0  0  0
 29 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 40 43  1  0  0  0  0
 26 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 24 46  1  0  0  0  0
 46 47  1  0  0  0  0
  5 47  1  0  0  0  0
 19 47  1  0  0  0  0
 47 48  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0198560

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1C(O)C(C2(C)CCC(O2)C(C)(C)O)C2(C)C(O)CC34CC33CCC(OC5OCC(O)C(O)C5O)C(C)(C)C3CCC4C12C

> <INCHI_IDENTIFIER>
InChI=1S/C37H60O11/c1-18(38)46-29-27(43)28(33(6)13-11-24(48-33)32(4,5)44)35(8)22(40)15-37-17-36(37)14-12-23(47-30-26(42)25(41)19(39)16-45-30)31(2,3)20(36)9-10-21(37)34(29,35)7/h19-30,39-44H,9-17H2,1-8H3

> <INCHI_KEY>
FRLGNHGNKSPOGU-UHFFFAOYSA-N

> <FORMULA>
C37H60O11

> <MOLECULAR_WEIGHT>
680.876

> <EXACT_MASS>
680.413562752

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
108

> <JCHEM_AVERAGE_POLARIZABILITY>
76.20776334590687

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
14,17-dihydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-13-yl acetate

> <ALOGPS_LOGP>
2.05

> <JCHEM_LOGP>
1.0593756086666672

> <ALOGPS_LOGS>
-4.17

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.220973673481119

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.2291414958951

> <JCHEM_PKA_STRONGEST_BASIC>
-2.950688216682245

> <JCHEM_POLAR_SURFACE_AREA>
175.37

> <JCHEM_REFRACTIVITY>
172.44880000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.61e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
14,17-dihydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-13-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0       3.965   5.884   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.015   4.345   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       2.707   3.532   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       5.373   3.618   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       5.423   2.079   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.697   1.215   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       8.146   1.738   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.269  -0.264   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.215  -1.480   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.907  -2.293   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.325  -0.413   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.683  -1.139   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.412  -2.655   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       7.886  -2.866   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      10.479  -3.766   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.546  -4.876   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.589  -2.698   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       9.369  -4.833   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.730  -0.314   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.402  -1.700   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.737  -1.492   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       4.261  -2.940   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       2.221  -1.221   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.698   0.228   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.706  -0.949   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.182   0.499   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.810  -0.678   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -2.326  -0.407   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -2.850   1.041   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -4.366   1.312   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -4.889   2.761   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -6.405   3.032   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -6.928   4.480   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -5.935   5.657   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -6.458   7.106   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -4.419   5.386   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -3.427   6.564   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -3.896   3.938   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -2.380   3.667   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      -1.857   2.218   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -3.189   2.992   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -1.327   3.664   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -0.341   1.947   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       0.652   3.125   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       2.168   2.854   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       2.691   1.405   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       4.207   1.134   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       3.838   2.629   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   47                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   19                                                  
CONECT    9    8   10   11   14                                             
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13    9                                                       
CONECT   15   13   16   17   18                                             
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   15                                                            
CONECT   19    8   20   21   47                                             
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25   26   46                                             
CONECT   25   24   26                                                       
CONECT   26   25   24   27   43                                             
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   40                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   38                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   31   39                                                  
CONECT   39   38                                                            
CONECT   40   29   41   42   43                                             
CONECT   41   40                                                            
CONECT   42   40                                                            
CONECT   43   40   26   44                                                  
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   24   47                                                  
CONECT   47   46    5   19   48                                             
CONECT   48   47                                                            
MASTER        0    0    0    0    0    0    0    0   48    0  108    0
END

View in JSmol

Synonyms

Value	Source
14,17-Dihydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0,.0,.0,]octadecan-13-yl acetic acid	Generator
14,17-Dihydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-13-yl acetic acid	Generator

Chemical Formula

C₃₇H₆₀O₁₁

Average Mass

680.8760 Da

Monoisotopic Mass

680.41356 Da

IUPAC Name

14,17-dihydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-13-yl acetate

Traditional Name

14,17-dihydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-13-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC1C(O)C(C2(C)CCC(O2)C(C)(C)O)C2(C)C(O)CC34CC33CCC(OC5OCC(O)C(O)C5O)C(C)(C)C3CCC4C12C

InChI Identifier

InChI=1S/C37H60O11/c1-18(38)46-29-27(43)28(33(6)13-11-24(48-33)32(4,5)44)35(8)22(40)15-37-17-36(37)14-12-23(47-30-26(42)25(41)19(39)16-45-30)31(2,3)20(36)9-10-21(37)34(29,35)7/h19-30,39-44H,9-17H2,1-8H3

InChI Key

FRLGNHGNKSPOGU-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
Actaea vaginata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 3-hydroxysteroids. These are steroids carrying a hydroxyl group at the 3-position of the steroid backbone.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Hydroxysteroids

Direct Parent

3-hydroxysteroids

Alternative Parents

Substituents

3-hydroxysteroid
Cyclic alcohol
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	2.05	ALOGPS
logP	1.06	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	12.23	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	175.37 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	172.45 m³·mol⁻¹	ChemAxon
Polarizability	76.21 Å³	ChemAxon
Number of Rings	7	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

73818232

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 14,17-dihydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-13-yl acetate (NP0198560)

MOL for NP0198560 (14,17-dihydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-13-yl acetate)

3D MOL for NP0198560 (14,17-dihydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-13-yl acetate)

3D SDF for NP0198560 (14,17-dihydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-13-yl acetate)

3D-SDF for NP0198560 (14,17-dihydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-13-yl acetate)

PDB for NP0198560 (14,17-dihydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-13-yl acetate)

3D PDB for NP0198560 (14,17-dihydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-13-yl acetate)

SMILES for NP0198560 (14,17-dihydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-13-yl acetate)

INCHI for NP0198560 (14,17-dihydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-13-yl acetate)

Structure for NP0198560 (14,17-dihydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-13-yl acetate)

3D Structure for NP0198560 (14,17-dihydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-13-yl acetate)