NP-MRD: Showing NP-Card for 3-({3,4-dihydroxy-6-methyl-5-[(2-methylbutanoyl)oxy]oxan-2-yl}oxy)-5-hydroxy-2-methyl-6-({4,5,26-trihydroxy-6,24-dimethyl-20-oxo-10-pentyl-2,7,9,21,25-pentaoxatricyclo[20.3.1.0³,⁸]hexacosan-23-yl}oxy)oxan-4-yl decanoate (NP0172784)

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Record Information

Version

2.0

Created at

2022-09-03 09:47:20 UTC

Updated at

2022-09-03 09:47:20 UTC

NP-MRD ID

NP0172784

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-({3,4-dihydroxy-6-methyl-5-[(2-methylbutanoyl)oxy]oxan-2-yl}oxy)-5-hydroxy-2-methyl-6-({4,5,26-trihydroxy-6,24-dimethyl-20-oxo-10-pentyl-2,7,9,21,25-pentaoxatricyclo[20.3.1.0³,⁸]hexacosan-23-yl}oxy)oxan-4-yl decanoate

Description

3-({3,4-Dihydroxy-6-methyl-5-[(2-methylbutanoyl)oxy]oxan-2-yl}oxy)-5-hydroxy-2-methyl-6-({4,5,26-trihydroxy-6,24-dimethyl-20-oxo-10-pentyl-2,7,9,21,25-pentaoxatricyclo[20.3.1.0³,⁸]Hexacosan-23-yl}oxy)oxan-4-yl decanoate belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds. 3-({3,4-dihydroxy-6-methyl-5-[(2-methylbutanoyl)oxy]oxan-2-yl}oxy)-5-hydroxy-2-methyl-6-({4,5,26-trihydroxy-6,24-dimethyl-20-oxo-10-pentyl-2,7,9,21,25-pentaoxatricyclo[20.3.1.0³,⁸]hexacosan-23-yl}oxy)oxan-4-yl decanoate is found in Ipomoea imperati. 3-({3,4-Dihydroxy-6-methyl-5-[(2-methylbutanoyl)oxy]oxan-2-yl}oxy)-5-hydroxy-2-methyl-6-({4,5,26-trihydroxy-6,24-dimethyl-20-oxo-10-pentyl-2,7,9,21,25-pentaoxatricyclo[20.3.1.0³,⁸]Hexacosan-23-yl}oxy)oxan-4-yl decanoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004171515082D          

 75 79  0  0  0  0            999 V2000
    6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.3845   -6.6724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1915   -6.5009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4464   -5.7163    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.7435   -7.1140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5505   -6.9424    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.4886   -7.8986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0406   -8.5117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6816   -8.0701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.1296   -7.4570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3046   -7.4570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0496   -6.6724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3974   -7.1776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6338   -6.8652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9815   -7.3704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2179   -7.0581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5656   -7.5632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   -0.4125    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  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 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
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 24 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 34 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  2  0  0  0  0
 49 51  1  0  0  0  0
 51 52  1  0  0  0  0
 18 52  1  0  0  0  0
 52 53  1  0  0  0  0
 22 53  1  0  0  0  0
 53 54  1  0  0  0  0
 16 55  1  0  0  0  0
 55 56  1  0  0  0  0
 56 57  1  0  0  0  0
 56 58  1  0  0  0  0
 13 58  1  0  0  0  0
 58 59  1  0  0  0  0
 59 60  1  0  0  0  0
 60 61  1  0  0  0  0
 61 62  1  0  0  0  0
 62 63  1  0  0  0  0
 62 64  1  0  0  0  0
 64 65  1  0  0  0  0
 65 66  1  0  0  0  0
 66 67  2  0  0  0  0
 66 68  1  0  0  0  0
 68 69  1  0  0  0  0
 68 70  1  0  0  0  0
 70 71  1  0  0  0  0
 64 72  1  0  0  0  0
 72 73  1  0  0  0  0
 72 74  1  0  0  0  0
 60 74  1  0  0  0  0
 74 75  1  0  0  0  0
M  END


  Mrv1533004171515082D          

 75 79  0  0  0  0            999 V2000
    6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.3845   -6.6724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1915   -6.5009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4464   -5.7163    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.7435   -7.1140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5505   -6.9424    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.4886   -7.8986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0406   -8.5117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6816   -8.0701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.1296   -7.4570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3046   -7.4570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0496   -6.6724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3974   -7.1776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6338   -6.8652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9815   -7.3704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2179   -7.0581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5656   -7.5632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   -0.4125    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  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 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
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 24 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 34 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  2  0  0  0  0
 49 51  1  0  0  0  0
 51 52  1  0  0  0  0
 18 52  1  0  0  0  0
 52 53  1  0  0  0  0
 22 53  1  0  0  0  0
 53 54  1  0  0  0  0
 16 55  1  0  0  0  0
 55 56  1  0  0  0  0
 56 57  1  0  0  0  0
 56 58  1  0  0  0  0
 13 58  1  0  0  0  0
 58 59  1  0  0  0  0
 59 60  1  0  0  0  0
 60 61  1  0  0  0  0
 61 62  1  0  0  0  0
 62 63  1  0  0  0  0
 62 64  1  0  0  0  0
 64 65  1  0  0  0  0
 65 66  1  0  0  0  0
 66 67  2  0  0  0  0
 66 68  1  0  0  0  0
 68 69  1  0  0  0  0
 68 70  1  0  0  0  0
 70 71  1  0  0  0  0
 64 72  1  0  0  0  0
 72 73  1  0  0  0  0
 72 74  1  0  0  0  0
 60 74  1  0  0  0  0
 74 75  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0172784

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCC(=O)OC1C(O)C(OC2C(C)OC3OC4C(O)C(O)C(C)OC4OC(CCCCC)CCCCCCCCCC(=O)OC2C3O)OC(C)C1OC1OC(C)C(OC(=O)C(C)CC)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C55H96O20/c1-9-12-14-15-17-21-25-29-37(56)70-48-43(62)53(67-34(7)46(48)73-52-42(61)41(60)45(33(6)66-52)72-51(64)31(4)11-3)74-47-35(8)68-54-44(63)49(47)71-38(57)30-26-22-19-16-18-20-24-28-36(27-23-13-10-2)69-55-50(75-54)40(59)39(58)32(5)65-55/h31-36,39-50,52-55,58-63H,9-30H2,1-8H3

> <INCHI_KEY>
FXXHXZAOBHOCMZ-UHFFFAOYSA-N

> <FORMULA>
C55H96O20

> <MOLECULAR_WEIGHT>
1077.353

> <EXACT_MASS>
1076.649495491

> <JCHEM_ACCEPTOR_COUNT>
17

> <JCHEM_ATOM_COUNT>
171

> <JCHEM_AVERAGE_POLARIZABILITY>
119.0570732995412

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-({3,4-dihydroxy-6-methyl-5-[(2-methylbutanoyl)oxy]oxan-2-yl}oxy)-5-hydroxy-2-methyl-6-({4,5,26-trihydroxy-6,24-dimethyl-20-oxo-10-pentyl-2,7,9,21,25-pentaoxatricyclo[20.3.1.0³,⁸]hexacosan-23-yl}oxy)oxan-4-yl decanoate

> <ALOGPS_LOGP>
4.64

> <JCHEM_LOGP>
9.021490772333333

> <ALOGPS_LOGS>
-4.29

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.227081949449108

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.788312996379535

> <JCHEM_PKA_STRONGEST_BASIC>
-3.612479403269223

> <JCHEM_POLAR_SURFACE_AREA>
274.11999999999995

> <JCHEM_REFRACTIVITY>
267.6786000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
22

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.51e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-({3,4-dihydroxy-6-methyl-5-[(2-methylbutanoyl)oxy]oxan-2-yl}oxy)-5-hydroxy-2-methyl-6-({4,5,26-trihydroxy-6,24-dimethyl-20-oxo-10-pentyl-2,7,9,21,25-pentaoxatricyclo[20.3.1.0³,⁸]hexacosan-23-yl}oxy)oxan-4-yl decanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      12.003  -0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.337  -0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      14.670  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      16.004  -0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      17.338  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      18.672  -0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      20.005  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      21.339  -0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      22.673  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      24.006  -0.000   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      24.006   1.540   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0      25.340  -0.770   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      25.340  -2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      24.006  -3.080   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      22.673  -2.310   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      24.006  -4.620   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      22.673  -5.390   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      22.673  -6.930   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      24.006  -7.700   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      25.340  -6.930   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      24.006  -9.240   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      22.673 -10.010   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      22.673 -11.550   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      21.251 -12.455   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      22.757 -12.135   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      23.233 -10.670   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      23.788 -13.279   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      25.294 -12.959   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      23.312 -14.744   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      24.342 -15.888   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      21.806 -15.064   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      20.775 -13.920   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      19.235 -13.920   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      18.759 -12.455   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      17.542 -13.398   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      16.116 -12.815   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      14.899 -13.758   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      13.473 -13.175   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      12.256 -14.118   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      17.338 -11.550   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      17.338 -10.010   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      16.004  -9.240   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      16.004  -7.700   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      14.670  -6.930   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      14.670  -5.390   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      16.004  -4.620   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      17.338  -5.390   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      18.672  -4.620   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      20.005  -5.390   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0      21.339  -4.620   0.000  0.00  0.00           O+0
HETATM   51  O   UNK     0      20.005  -6.930   0.000  0.00  0.00           O+0
HETATM   52  C   UNK     0      21.339  -7.700   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      21.339  -9.240   0.000  0.00  0.00           C+0
HETATM   54  O   UNK     0      20.005 -10.010   0.000  0.00  0.00           O+0
HETATM   55  O   UNK     0      25.340  -5.390   0.000  0.00  0.00           O+0
HETATM   56  C   UNK     0      26.674  -4.620   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0      28.007  -5.390   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0      26.674  -3.080   0.000  0.00  0.00           C+0
HETATM   59  O   UNK     0      28.007  -2.310   0.000  0.00  0.00           O+0
HETATM   60  C   UNK     0      28.007  -0.770   0.000  0.00  0.00           C+0
HETATM   61  O   UNK     0      26.674  -0.000   0.000  0.00  0.00           O+0
HETATM   62  C   UNK     0      26.674   1.540   0.000  0.00  0.00           C+0
HETATM   63  C   UNK     0      25.340   2.310   0.000  0.00  0.00           C+0
HETATM   64  C   UNK     0      28.007   2.310   0.000  0.00  0.00           C+0
HETATM   65  O   UNK     0      28.007   3.850   0.000  0.00  0.00           O+0
HETATM   66  C   UNK     0      26.674   4.620   0.000  0.00  0.00           C+0
HETATM   67  O   UNK     0      25.340   3.850   0.000  0.00  0.00           O+0
HETATM   68  C   UNK     0      26.674   6.160   0.000  0.00  0.00           C+0
HETATM   69  C   UNK     0      28.007   6.930   0.000  0.00  0.00           C+0
HETATM   70  C   UNK     0      25.340   6.930   0.000  0.00  0.00           C+0
HETATM   71  C   UNK     0      25.340   8.470   0.000  0.00  0.00           C+0
HETATM   72  C   UNK     0      29.341   1.540   0.000  0.00  0.00           C+0
HETATM   73  O   UNK     0      30.675   2.310   0.000  0.00  0.00           O+0
HETATM   74  C   UNK     0      29.341  -0.000   0.000  0.00  0.00           C+0
HETATM   75  O   UNK     0      30.675  -0.770   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   58                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   55                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   52                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23   53                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   32                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   24   33                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   40                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38                                                            
CONECT   40   34   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   50   51                                                  
CONECT   50   49                                                            
CONECT   51   49   52                                                       
CONECT   52   51   18   53                                                  
CONECT   53   52   22   54                                                  
CONECT   54   53                                                            
CONECT   55   16   56                                                       
CONECT   56   55   57   58                                                  
CONECT   57   56                                                            
CONECT   58   56   13   59                                                  
CONECT   59   58   60                                                       
CONECT   60   59   61   74                                                  
CONECT   61   60   62                                                       
CONECT   62   61   63   64                                                  
CONECT   63   62                                                            
CONECT   64   62   65   72                                                  
CONECT   65   64   66                                                       
CONECT   66   65   67   68                                                  
CONECT   67   66                                                            
CONECT   68   66   69   70                                                  
CONECT   69   68                                                            
CONECT   70   68   71                                                       
CONECT   71   70                                                            
CONECT   72   64   73   74                                                  
CONECT   73   72                                                            
CONECT   74   72   60   75                                                  
CONECT   75   74                                                            
MASTER        0    0    0    0    0    0    0    0   75    0  158    0
END

View in JSmol

Synonyms

Value	Source
3-({3,4-dihydroxy-6-methyl-5-[(2-methylbutanoyl)oxy]oxan-2-yl}oxy)-5-hydroxy-2-methyl-6-({4,5,26-trihydroxy-6,24-dimethyl-20-oxo-10-pentyl-2,7,9,21,25-pentaoxatricyclo[20.3.1.0,]hexacosan-23-yl}oxy)oxan-4-yl decanoic acid	Generator
3-({3,4-dihydroxy-6-methyl-5-[(2-methylbutanoyl)oxy]oxan-2-yl}oxy)-5-hydroxy-2-methyl-6-({4,5,26-trihydroxy-6,24-dimethyl-20-oxo-10-pentyl-2,7,9,21,25-pentaoxatricyclo[20.3.1.0³,⁸]hexacosan-23-yl}oxy)oxan-4-yl decanoic acid	Generator

Chemical Formula

C₅₅H₉₆O₂₀

Average Mass

1077.3530 Da

Monoisotopic Mass

1076.64950 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

CCCCCCCCCC(=O)OC1C(O)C(OC2C(C)OC3OC4C(O)C(O)C(C)OC4OC(CCCCC)CCCCCCCCCC(=O)OC2C3O)OC(C)C1OC1OC(C)C(OC(=O)C(C)CC)C(O)C1O

InChI Identifier

InChI=1S/C55H96O20/c1-9-12-14-15-17-21-25-29-37(56)70-48-43(62)53(67-34(7)46(48)73-52-42(61)41(60)45(33(6)66-52)72-51(64)31(4)11-3)74-47-35(8)68-54-44(63)49(47)71-38(57)30-26-22-19-16-18-20-24-28-36(27-23-13-10-2)69-55-50(75-54)40(59)39(58)32(5)65-55/h31-36,39-50,52-55,58-63H,9-30H2,1-8H3

InChI Key

FXXHXZAOBHOCMZ-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Ipomoea imperati	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Oligosaccharides

Alternative Parents

Substituents

Oligosaccharide
Fatty acyl glycoside
Macrolide
Alkyl glycoside
Glycosyl compound
O-glycosyl compound
Tricarboxylic acid or derivatives
Fatty acid ester
Fatty acyl
Oxane
Carboxylic acid ester
Lactone
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Acetal
Carboxylic acid derivative
Polyol
Hydrocarbon derivative
Carbonyl group
Organic oxide
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	4.64	ALOGPS
logP	9.02	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	11.79	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	17	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	274.12 Å²	ChemAxon
Rotatable Bond Count	22	ChemAxon
Refractivity	267.68 m³·mol⁻¹	ChemAxon
Polarizability	119.06 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-({3,4-dihydroxy-6-methyl-5-[(2-methylbutanoyl)oxy]oxan-2-yl}oxy)-5-hydroxy-2-methyl-6-({4,5,26-trihydroxy-6,24-dimethyl-20-oxo-10-pentyl-2,7,9,21,25-pentaoxatricyclo[20.3.1.0³,⁸]hexacosan-23-yl}oxy)oxan-4-yl decanoate (NP0172784)

MOL for NP0172784 (3-({3,4-dihydroxy-6-methyl-5-[(2-methylbutanoyl)oxy]oxan-2-yl}oxy)-5-hydroxy-2-methyl-6-({4,5,26-trihydroxy-6,24-dimethyl-20-oxo-10-pentyl-2,7,9,21,25-pentaoxatricyclo[20.3.1.0³,⁸]hexacosan-23-yl}oxy)oxan-4-yl decanoate)

3D MOL for NP0172784 (3-({3,4-dihydroxy-6-methyl-5-[(2-methylbutanoyl)oxy]oxan-2-yl}oxy)-5-hydroxy-2-methyl-6-({4,5,26-trihydroxy-6,24-dimethyl-20-oxo-10-pentyl-2,7,9,21,25-pentaoxatricyclo[20.3.1.0³,⁸]hexacosan-23-yl}oxy)oxan-4-yl decanoate)

3D SDF for NP0172784 (3-({3,4-dihydroxy-6-methyl-5-[(2-methylbutanoyl)oxy]oxan-2-yl}oxy)-5-hydroxy-2-methyl-6-({4,5,26-trihydroxy-6,24-dimethyl-20-oxo-10-pentyl-2,7,9,21,25-pentaoxatricyclo[20.3.1.0³,⁸]hexacosan-23-yl}oxy)oxan-4-yl decanoate)

3D-SDF for NP0172784 (3-({3,4-dihydroxy-6-methyl-5-[(2-methylbutanoyl)oxy]oxan-2-yl}oxy)-5-hydroxy-2-methyl-6-({4,5,26-trihydroxy-6,24-dimethyl-20-oxo-10-pentyl-2,7,9,21,25-pentaoxatricyclo[20.3.1.0³,⁸]hexacosan-23-yl}oxy)oxan-4-yl decanoate)

PDB for NP0172784 (3-({3,4-dihydroxy-6-methyl-5-[(2-methylbutanoyl)oxy]oxan-2-yl}oxy)-5-hydroxy-2-methyl-6-({4,5,26-trihydroxy-6,24-dimethyl-20-oxo-10-pentyl-2,7,9,21,25-pentaoxatricyclo[20.3.1.0³,⁸]hexacosan-23-yl}oxy)oxan-4-yl decanoate)

3D PDB for NP0172784 (3-({3,4-dihydroxy-6-methyl-5-[(2-methylbutanoyl)oxy]oxan-2-yl}oxy)-5-hydroxy-2-methyl-6-({4,5,26-trihydroxy-6,24-dimethyl-20-oxo-10-pentyl-2,7,9,21,25-pentaoxatricyclo[20.3.1.0³,⁸]hexacosan-23-yl}oxy)oxan-4-yl decanoate)

SMILES for NP0172784 (3-({3,4-dihydroxy-6-methyl-5-[(2-methylbutanoyl)oxy]oxan-2-yl}oxy)-5-hydroxy-2-methyl-6-({4,5,26-trihydroxy-6,24-dimethyl-20-oxo-10-pentyl-2,7,9,21,25-pentaoxatricyclo[20.3.1.0³,⁸]hexacosan-23-yl}oxy)oxan-4-yl decanoate)

INCHI for NP0172784 (3-({3,4-dihydroxy-6-methyl-5-[(2-methylbutanoyl)oxy]oxan-2-yl}oxy)-5-hydroxy-2-methyl-6-({4,5,26-trihydroxy-6,24-dimethyl-20-oxo-10-pentyl-2,7,9,21,25-pentaoxatricyclo[20.3.1.0³,⁸]hexacosan-23-yl}oxy)oxan-4-yl decanoate)

Structure for NP0172784 (3-({3,4-dihydroxy-6-methyl-5-[(2-methylbutanoyl)oxy]oxan-2-yl}oxy)-5-hydroxy-2-methyl-6-({4,5,26-trihydroxy-6,24-dimethyl-20-oxo-10-pentyl-2,7,9,21,25-pentaoxatricyclo[20.3.1.0³,⁸]hexacosan-23-yl}oxy)oxan-4-yl decanoate)

3D Structure for NP0172784 (3-({3,4-dihydroxy-6-methyl-5-[(2-methylbutanoyl)oxy]oxan-2-yl}oxy)-5-hydroxy-2-methyl-6-({4,5,26-trihydroxy-6,24-dimethyl-20-oxo-10-pentyl-2,7,9,21,25-pentaoxatricyclo[20.3.1.0³,⁸]hexacosan-23-yl}oxy)oxan-4-yl decanoate)