NP-MRD: Showing NP-Card for 2-({1-[4-hydroxy-3-(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethylidene)butyl]-1,2,5-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-4a-yl}methoxy)-6-(hydroxymethyl)oxane-3,4,5-triol (NP0154632)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-02 11:34:45 UTC

Updated at

2022-09-02 11:34:45 UTC

NP-MRD ID

NP0154632

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-({1-[4-hydroxy-3-(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethylidene)butyl]-1,2,5-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-4a-yl}methoxy)-6-(hydroxymethyl)oxane-3,4,5-triol

Description

2-[(4-Hydroxy-3-{2-[1,2,5-trimethyl-4a-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl]ethyl}but-2-en-1-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol belongs to the class of organic compounds known as diterpene glycosides. These are diterpenoids in which an isoprene unit is glycosylated. 2-[(4-Hydroxy-3-{2-[1,2,5-trimethyl-4a-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl]ethyl}but-2-en-1-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251505152D          

 45 48  0  0  0  0            999 V2000
   -1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3873    0.7284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3873    0.7284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0499    1.4281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3374    2.1565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0997    2.8561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2876    3.5846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1121    3.6134    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4994    4.3418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3239    4.3706    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7112    5.0990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5357    5.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9729    4.4282    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2740    5.7987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6613    6.5271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4495    5.7699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0123    6.4695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0622    5.0414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2377    5.0126    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1619    2.1853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5493    2.9137    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
  7  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
 10 13  1  0  0  0  0
 13 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
  8 17  1  0  0  0  0
 17 18  1  0  0  0  0
  5 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  2  0  0  0  0
  5 23  1  0  0  0  0
 23 24  1  0  0  0  0
 19 25  1  0  0  0  0
  2 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
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  4  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
 35 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 33 42  1  0  0  0  0
 42 43  1  0  0  0  0
 29 44  1  0  0  0  0
 44 45  1  0  0  0  0
M  END

     RDKit          3D

 99102  0  0  0  0  0  0  0  0999 V2000
   -4.0298    2.9797    0.6649 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8227    2.0878    0.8138 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9075    2.4007    1.7153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6768    1.6446    1.9747 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2261    0.8616    0.7715 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1439    0.8405   -0.3879 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5965    0.8642   -0.0139 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5697    0.9687   -1.1387 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8819    0.9939   -0.9179 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7043    0.1138   -0.4169 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.5192    0.7612    0.5455 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2671   -0.1377    1.2751 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.4262    0.6591    1.8898 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2486   -0.1390    2.6474 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7742   -1.2909    0.4760 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.0361   -2.4464    0.7400 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8805   -1.0034   -0.9927 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.9218   -2.2267   -1.6695 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7481   -0.2036   -1.5437 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.2339    1.0310   -1.9697 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7812   -0.4156    0.7529 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6147   -1.5893   -0.1674 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2653   -1.6320   -0.8571 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4088   -2.5487   -0.0593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7284   -0.3280   -1.2815 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1010    0.0506   -2.7094 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8109   -0.2890   -1.3040 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4243   -1.2649   -2.2117 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9400   -1.1373   -2.1683 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5006   -0.2533   -1.4309 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9162    0.0779   -1.2091 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2801   -0.0776    0.1433 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6178    0.2394    0.3306 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.7378    1.2766    1.2369 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0466    1.7525    1.2799 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.1909    2.6349    2.5059 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9063    1.8487    3.6260 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0629    0.6422    1.3887 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.0353    0.9400    2.3637 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3555   -0.6010    1.8542 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.2457   -1.6412    2.1221 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3182   -0.9967    0.8527 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.8984   -1.6789   -0.2027 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6772   -2.1141   -3.0089 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0253   -1.9784   -2.9155 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3274    3.1490   -0.3768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8419    2.7155    1.3667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7546    4.0298    1.0140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0928    3.3058    2.3191 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1039    2.3993    2.2937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8205    1.0366    2.8911 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7679    1.3150    0.5030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0128   -0.1471    1.1677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9518    1.7706   -0.9966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4280    0.1356   -1.8949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3304    1.9595   -1.6499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4157   -0.8744   -0.0798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6753   -0.5050    2.1465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0495    1.5255    2.4556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0150    1.0954    1.0335 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0931    0.3586    2.7958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8150   -1.5153    0.8527 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0964   -2.5782    1.7317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8780   -0.5174   -1.1706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0254   -2.4482   -2.0429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2129   -0.6644   -2.3760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2214    1.0863   -1.9443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9401   -0.5356    1.5100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6791   -0.5184    1.3339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7555   -2.4909    0.4677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4409   -1.6331   -0.9020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4793   -2.1905   -1.8248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2546   -3.5419   -0.5873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9310   -2.9068    0.8886 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5794   -2.2298    0.2256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5048    1.0991   -2.7738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6953   -0.7013   -3.2324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1918    0.1424   -3.3816 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2153   -0.4048   -0.2844 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0463    0.7267   -1.6583 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2423   -1.0797   -3.3139 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2141   -2.3389   -2.0279 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7949    0.4077   -0.8431 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9740    1.2243   -1.3297 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6560   -0.2832   -1.8905 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0436    0.5344   -0.6546 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2945    2.3861    0.3994 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4622    3.4831    2.4780 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2008    3.0442    2.6137 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9090    1.8953    3.7386 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5809    0.4869    0.4121 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.8553    0.4301    2.2286 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8736   -0.3518    2.8287 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5411   -2.0030    1.2651 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5881   -1.6612    1.3730 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2316   -2.2587   -0.6742 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4119   -1.8698   -4.0902 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3221   -3.1589   -2.8101 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5457   -2.8147   -2.9174 H   0  0  0  0  0  0  0  0  0  0  0  0
 24 23  1  0
 23 22  1  0
 22 21  1  0
 21  7  1  0
  7  8  1  6
  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
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  6 25  1  0
 25 26  1  6
 25 27  1  0
 27 28  1  0
 28 29  1  0
 29 44  1  0
 44 45  1  0
 29 30  2  0
 30 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
 35 38  1  0
 38 39  1  0
 38 40  1  0
 40 41  1  0
 40 42  1  0
 42 43  1  0
 25 23  1  0
 42 33  1  0
  2  7  1  0
 19 10  1  0
 24 73  1  0
 24 74  1  0
 24 75  1  0
 23 72  1  6
 22 70  1  0
 22 71  1  0
 21 68  1  0
 21 69  1  0
  8 55  1  0
  8 56  1  0
 10 57  1  1
 12 58  1  1
 13 59  1  0
 13 60  1  0
 14 61  1  0
 15 62  1  1
 16 63  1  0
 17 64  1  1
 18 65  1  0
 19 66  1  6
 20 67  1  0
  6 54  1  6
  5 52  1  0
  5 53  1  0
  4 50  1  0
  4 51  1  0
  3 49  1  0
  1 46  1  0
  1 47  1  0
  1 48  1  0
 26 76  1  0
 26 77  1  0
 26 78  1  0
 27 79  1  0
 27 80  1  0
 28 81  1  0
 28 82  1  0
 44 97  1  0
 44 98  1  0
 45 99  1  0
 30 83  1  0
 31 84  1  0
 31 85  1  0
 33 86  1  6
 35 87  1  6
 36 88  1  0
 36 89  1  0
 37 90  1  0
 38 91  1  6
 39 92  1  0
 40 93  1  1
 41 94  1  0
 42 95  1  1
 43 96  1  0
M  END


  Mrv1533004251505152D          

 45 48  0  0  0  0            999 V2000
   -1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3873    0.7284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3873    0.7284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0499    1.4281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3374    2.1565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0997    2.8561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2876    3.5846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1121    3.6134    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4994    4.3418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3239    4.3706    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7112    5.0990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5357    5.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9729    4.4282    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2740    5.7987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6613    6.5271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4495    5.7699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0123    6.4695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0622    5.0414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2377    5.0126    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1619    2.1853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5493    2.9137    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
  7  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
 10 13  1  0  0  0  0
 13 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
  8 17  1  0  0  0  0
 17 18  1  0  0  0  0
  5 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  2  0  0  0  0
  5 23  1  0  0  0  0
 23 24  1  0  0  0  0
 19 25  1  0  0  0  0
  2 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
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  4  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
 35 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 33 42  1  0  0  0  0
 42 43  1  0  0  0  0
 29 44  1  0  0  0  0
 44 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0154632

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CCC2(COC3OC(CO)C(O)C(O)C3O)C(CCC=C2C)C1(C)CCC(CO)=CCOC1OC(CO)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C32H54O13/c1-17-7-11-32(16-43-30-28(41)26(39)24(37)21(15-35)45-30)18(2)5-4-6-22(32)31(17,3)10-8-19(13-33)9-12-42-29-27(40)25(38)23(36)20(14-34)44-29/h5,9,17,20-30,33-41H,4,6-8,10-16H2,1-3H3

> <INCHI_KEY>
MKMAHELGRJTPPQ-UHFFFAOYSA-N

> <FORMULA>
C32H54O13

> <MOLECULAR_WEIGHT>
646.771

> <EXACT_MASS>
646.356441799

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
99

> <JCHEM_AVERAGE_POLARIZABILITY>
68.66923193922895

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-({1-[4-hydroxy-3-(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethylidene)butyl]-1,2,5-trimethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-4a-yl}methoxy)-6-(hydroxymethyl)oxane-3,4,5-triol

> <ALOGPS_LOGP>
-0.15

> <JCHEM_LOGP>
-1.0018368286666652

> <ALOGPS_LOGS>
-3.07

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.4308022544136

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.909704152818223

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810834144146003

> <JCHEM_POLAR_SURFACE_AREA>
218.98999999999998

> <JCHEM_REFRACTIVITY>
161.50230000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.57e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-({1-[4-hydroxy-3-(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethylidene)butyl]-1,2,5-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-4a-yl}methoxy)-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0      -2.667   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -3.850   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.000  -6.160   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -1.334  -6.930   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -1.334  -8.470   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -2.667 -10.780   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.000  -9.240   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       0.000 -10.780   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       1.334  -8.470   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.667  -9.240   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.667  -6.160   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.723   1.360   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.723   1.360   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.093   2.666   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -0.630   4.025   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.186   5.331   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -0.537   6.691   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -2.076   6.745   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -2.799   8.105   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -4.338   8.158   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -5.061   9.518   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -6.600   9.572   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -7.416   8.266   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -4.245  10.824   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -4.968  12.184   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      -2.706  10.770   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      -1.890  12.076   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      -1.983   9.411   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      -0.444   9.357   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      -2.169   4.079   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      -2.892   5.439   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   25                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   19   23                                             
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   17                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15    8   18                                                  
CONECT   18   17                                                            
CONECT   19    5   20   25                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22    5   24                                                  
CONECT   24   23                                                            
CONECT   25   19    2   26   27                                             
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   44                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   42                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   38                                                  
CONECT   36   35   37                                                       
CONECT   37   36                                                            
CONECT   38   35   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   33   43                                                  
CONECT   43   42                                                            
CONECT   44   29   45                                                       
CONECT   45   44                                                            
MASTER        0    0    0    0    0    0    0    0   45    0   96    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₂H₅₄O₁₃

Average Mass

646.7710 Da

Monoisotopic Mass

646.35644 Da

IUPAC Name

2-({1-[4-hydroxy-3-(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethylidene)butyl]-1,2,5-trimethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-4a-yl}methoxy)-6-(hydroxymethyl)oxane-3,4,5-triol

Traditional Name

2-({1-[4-hydroxy-3-(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethylidene)butyl]-1,2,5-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-4a-yl}methoxy)-6-(hydroxymethyl)oxane-3,4,5-triol

CAS Registry Number

Not Available

SMILES

CC1CCC2(COC3OC(CO)C(O)C(O)C3O)C(CCC=C2C)C1(C)CCC(CO)=CCOC1OC(CO)C(O)C(O)C1O

InChI Identifier

InChI=1S/C32H54O13/c1-17-7-11-32(16-43-30-28(41)26(39)24(37)21(15-35)45-30)18(2)5-4-6-22(32)31(17,3)10-8-19(13-33)9-12-42-29-27(40)25(38)23(36)20(14-34)44-29/h5,9,17,20-30,33-41H,4,6-8,10-16H2,1-3H3

InChI Key

MKMAHELGRJTPPQ-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene glycosides. These are diterpenoids in which an isoprene unit is glycosylated.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Diterpene glycosides

Alternative Parents

Substituents

Diterpene glycoside
Diterpenoid
Clerodane diterpenoid
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
Glycosyl compound
O-glycosyl compound
Fatty alcohol
Oxane
Monosaccharide
Fatty acyl
Secondary alcohol
Polyol
Acetal
Organoheterocyclic compound
Oxacycle
Organooxygen compound
Alcohol
Hydrocarbon derivative
Organic oxygen compound
Primary 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
logP	-0.15	ALOGPS
logP	-1	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	11.91	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	218.99 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	161.5 m³·mol⁻¹	ChemAxon
Polarizability	68.67 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-({1-[4-hydroxy-3-(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethylidene)butyl]-1,2,5-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-4a-yl}methoxy)-6-(hydroxymethyl)oxane-3,4,5-triol (NP0154632)

MOL for NP0154632 (2-({1-[4-hydroxy-3-(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethylidene)butyl]-1,2,5-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-4a-yl}methoxy)-6-(hydroxymethyl)oxane-3,4,5-triol)

3D MOL for NP0154632 (2-({1-[4-hydroxy-3-(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethylidene)butyl]-1,2,5-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-4a-yl}methoxy)-6-(hydroxymethyl)oxane-3,4,5-triol)

3D SDF for NP0154632 (2-({1-[4-hydroxy-3-(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethylidene)butyl]-1,2,5-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-4a-yl}methoxy)-6-(hydroxymethyl)oxane-3,4,5-triol)

3D-SDF for NP0154632 (2-({1-[4-hydroxy-3-(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethylidene)butyl]-1,2,5-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-4a-yl}methoxy)-6-(hydroxymethyl)oxane-3,4,5-triol)

PDB for NP0154632 (2-({1-[4-hydroxy-3-(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethylidene)butyl]-1,2,5-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-4a-yl}methoxy)-6-(hydroxymethyl)oxane-3,4,5-triol)

3D PDB for NP0154632 (2-({1-[4-hydroxy-3-(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethylidene)butyl]-1,2,5-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-4a-yl}methoxy)-6-(hydroxymethyl)oxane-3,4,5-triol)

SMILES for NP0154632 (2-({1-[4-hydroxy-3-(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethylidene)butyl]-1,2,5-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-4a-yl}methoxy)-6-(hydroxymethyl)oxane-3,4,5-triol)

INCHI for NP0154632 (2-({1-[4-hydroxy-3-(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethylidene)butyl]-1,2,5-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-4a-yl}methoxy)-6-(hydroxymethyl)oxane-3,4,5-triol)

Structure for NP0154632 (2-({1-[4-hydroxy-3-(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethylidene)butyl]-1,2,5-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-4a-yl}methoxy)-6-(hydroxymethyl)oxane-3,4,5-triol)

3D Structure for NP0154632 (2-({1-[4-hydroxy-3-(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}ethylidene)butyl]-1,2,5-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-4a-yl}methoxy)-6-(hydroxymethyl)oxane-3,4,5-triol)