NP-MRD: Showing NP-Card for 4-hydroxy-2-{[4-hydroxy-2-methyl-5-(octanoyloxy)-6-{[7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.0³,⁸]hexacosan-6-yl]oxy}oxan-3-yl]oxy}-6-methyl-5-(octanoyloxy)oxan-3-yl octanoate (NP0220311)

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Record Information

Version

2.0

Created at

2022-09-05 21:35:03 UTC

Updated at

2022-09-05 21:35:03 UTC

NP-MRD ID

NP0220311

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-hydroxy-2-{[4-hydroxy-2-methyl-5-(octanoyloxy)-6-{[7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.0³,⁸]hexacosan-6-yl]oxy}oxan-3-yl]oxy}-6-methyl-5-(octanoyloxy)oxan-3-yl octanoate

Description

4-Hydroxy-2-{[4-hydroxy-2-methyl-5-(octanoyloxy)-6-{[7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.0³,⁸]Hexacosan-6-yl]oxy}oxan-3-yl]oxy}-6-methyl-5-(octanoyloxy)oxan-3-yl octanoate 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. 4-hydroxy-2-{[4-hydroxy-2-methyl-5-(octanoyloxy)-6-{[7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.0³,⁸]hexacosan-6-yl]oxy}oxan-3-yl]oxy}-6-methyl-5-(octanoyloxy)oxan-3-yl octanoate is found in Ipomoea purpurea. 4-Hydroxy-2-{[4-hydroxy-2-methyl-5-(octanoyloxy)-6-{[7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.0³,⁸]Hexacosan-6-yl]oxy}oxan-3-yl]oxy}-6-methyl-5-(octanoyloxy)oxan-3-yl octanoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004241505122D          

 86 90  0  0  0  0            999 V2000
  -10.0026    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
   -9.2881   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5737   -1.6500    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
   -7.8592   -2.8875    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
   -7.1447   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  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  2  0  0  0  0
  8 10  1  0  0  0  0
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 12 14  1  0  0  0  0
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 17 18  1  0  0  0  0
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 32 33  1  0  0  0  0
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M  END


  Mrv1533004241505122D          

 86 90  0  0  0  0            999 V2000
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   -8.5737   -2.4750    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
   -7.8592   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.5724  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868  -12.3750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579  -12.3750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868  -11.5500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013  -10.3125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5737  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -5.3625    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
   -0.7145   -5.3625    0.0000 C   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
    0.7145   -5.3625    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
   -5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -4.1250    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  2  0  0  0  0
  8 10  1  0  0  0  0
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 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 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
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  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
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 34 37  1  0  0  0  0
 37 38  1  0  0  0  0
 29 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 40 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  1  0  0  0  0
 50 51  1  0  0  0  0
 51 52  1  0  0  0  0
 52 53  1  0  0  0  0
 53 54  1  0  0  0  0
 54 55  1  0  0  0  0
 55 56  2  0  0  0  0
 55 57  1  0  0  0  0
 57 58  1  0  0  0  0
 27 58  1  0  0  0  0
 58 59  1  0  0  0  0
 23 59  1  0  0  0  0
 59 60  1  0  0  0  0
 21 61  1  0  0  0  0
 61 62  1  0  0  0  0
 62 63  1  0  0  0  0
 63 64  2  0  0  0  0
 63 65  1  0  0  0  0
 65 66  1  0  0  0  0
 66 67  1  0  0  0  0
 67 68  1  0  0  0  0
 68 69  1  0  0  0  0
 69 70  1  0  0  0  0
 70 71  1  0  0  0  0
 61 72  1  0  0  0  0
 17 72  1  0  0  0  0
 72 73  1  0  0  0  0
 15 74  1  0  0  0  0
 74 75  1  0  0  0  0
 75 76  1  0  0  0  0
 76 77  2  0  0  0  0
 76 78  1  0  0  0  0
 78 79  1  0  0  0  0
 79 80  1  0  0  0  0
 80 81  1  0  0  0  0
 81 82  1  0  0  0  0
 82 83  1  0  0  0  0
 83 84  1  0  0  0  0
 74 85  1  0  0  0  0
 11 85  1  0  0  0  0
 85 86  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0220311

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCC(=O)OC1C(C)OC(OC2C(C)OC(OC3C(C)OC4OC5C(O)C(O)C(CO)OC5OC(CCCCC)CCCCCCCCCC(=O)OC4C3O)C(OC(=O)CCCCCCC)C2O)C(OC(=O)CCCCCCC)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C64H112O22/c1-8-12-16-22-29-35-45(66)80-54-40(5)75-61(58(51(54)72)81-46(67)36-30-23-17-13-9-2)84-55-41(6)76-62(59(52(55)73)82-47(68)37-31-24-18-14-10-3)85-56-42(7)77-63-60(53(56)74)83-48(69)38-32-26-21-19-20-25-28-34-43(33-27-15-11-4)78-64-57(86-63)50(71)49(70)44(39-65)79-64/h40-44,49-65,70-74H,8-39H2,1-7H3

> <INCHI_KEY>
LRKQAUUKLJJTOD-UHFFFAOYSA-N

> <FORMULA>
C64H112O22

> <MOLECULAR_WEIGHT>
1233.578

> <EXACT_MASS>
1232.764525246

> <JCHEM_ACCEPTOR_COUNT>
18

> <JCHEM_ATOM_COUNT>
198

> <JCHEM_AVERAGE_POLARIZABILITY>
137.4778216330683

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-hydroxy-2-{[4-hydroxy-2-methyl-5-(octanoyloxy)-6-{[7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.0³,⁸]hexacosan-6-yl]oxy}oxan-3-yl]oxy}-6-methyl-5-(octanoyloxy)oxan-3-yl octanoate

> <ALOGPS_LOGP>
5.41

> <JCHEM_LOGP>
11.685236439666665

> <ALOGPS_LOGS>
-4.76

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.693538751238727

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.265094490007318

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810837668751677

> <JCHEM_POLAR_SURFACE_AREA>
300.41999999999996

> <JCHEM_REFRACTIVITY>
310.6332

> <JCHEM_ROTATABLE_BOND_COUNT>
33

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.14e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-hydroxy-2-{[4-hydroxy-2-methyl-5-(octanoyloxy)-6-{[7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.0³,⁸]hexacosan-6-yl]oxy}oxan-3-yl]oxy}-6-methyl-5-(octanoyloxy)oxan-3-yl octanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0     -18.672   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -17.338  -0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -17.338  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -16.004  -3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -16.004  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -14.670  -5.390   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -14.670  -6.930   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -13.337  -7.700   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0     -12.003  -6.930   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0     -13.337  -9.240   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0     -12.003 -10.010   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -12.003 -11.550   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -13.337 -12.320   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0     -10.669 -12.320   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -9.336 -11.550   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -8.002 -12.320   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -8.002 -13.860   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -6.668 -14.630   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -5.335 -13.860   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -6.668 -16.170   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -8.002 -16.940   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -8.002 -18.480   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -6.668 -19.250   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -5.335 -18.480   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -5.335 -16.940   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -4.001 -19.250   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -4.001 -20.790   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -2.667 -21.560   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -1.334 -20.790   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -1.334 -19.250   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -2.667 -18.480   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -0.000 -18.480   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -0.000 -16.940   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       1.334 -19.250   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       2.667 -18.480   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       4.001 -19.250   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       1.334 -20.790   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -0.000 -21.560   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -0.000 -23.100   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      -1.334 -23.870   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -0.000 -24.640   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -0.000 -26.180   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       1.334 -26.950   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       1.334 -28.490   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       2.667 -29.260   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -1.334 -25.410   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      -2.667 -26.180   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      -2.667 -27.720   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      -4.001 -28.490   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      -5.335 -27.720   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      -6.668 -28.490   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      -8.002 -27.720   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      -8.002 -26.180   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      -6.668 -25.410   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      -6.668 -23.870   0.000  0.00  0.00           C+0
HETATM   56  O   UNK     0      -8.002 -23.100   0.000  0.00  0.00           O+0
HETATM   57  O   UNK     0      -5.335 -23.100   0.000  0.00  0.00           O+0
HETATM   58  C   UNK     0      -5.335 -21.560   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0      -6.668 -20.790   0.000  0.00  0.00           C+0
HETATM   60  O   UNK     0      -8.002 -21.560   0.000  0.00  0.00           O+0
HETATM   61  C   UNK     0      -9.336 -16.170   0.000  0.00  0.00           C+0
HETATM   62  O   UNK     0     -10.669 -16.940   0.000  0.00  0.00           O+0
HETATM   63  C   UNK     0     -10.669 -18.480   0.000  0.00  0.00           C+0
HETATM   64  O   UNK     0      -9.336 -19.250   0.000  0.00  0.00           O+0
HETATM   65  C   UNK     0     -12.003 -19.250   0.000  0.00  0.00           C+0
HETATM   66  C   UNK     0     -12.003 -20.790   0.000  0.00  0.00           C+0
HETATM   67  C   UNK     0     -13.337 -21.560   0.000  0.00  0.00           C+0
HETATM   68  C   UNK     0     -13.337 -23.100   0.000  0.00  0.00           C+0
HETATM   69  C   UNK     0     -14.670 -23.870   0.000  0.00  0.00           C+0
HETATM   70  C   UNK     0     -14.670 -25.410   0.000  0.00  0.00           C+0
HETATM   71  C   UNK     0     -16.004 -26.180   0.000  0.00  0.00           C+0
HETATM   72  C   UNK     0      -9.336 -14.630   0.000  0.00  0.00           C+0
HETATM   73  O   UNK     0     -10.669 -13.860   0.000  0.00  0.00           O+0
HETATM   74  C   UNK     0      -9.336 -10.010   0.000  0.00  0.00           C+0
HETATM   75  O   UNK     0      -8.002  -9.240   0.000  0.00  0.00           O+0
HETATM   76  C   UNK     0      -6.668 -10.010   0.000  0.00  0.00           C+0
HETATM   77  O   UNK     0      -6.668 -11.550   0.000  0.00  0.00           O+0
HETATM   78  C   UNK     0      -5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   79  C   UNK     0      -4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   80  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   81  C   UNK     0      -1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   82  C   UNK     0      -0.000  -9.240   0.000  0.00  0.00           C+0
HETATM   83  C   UNK     0       1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   84  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   85  C   UNK     0     -10.669  -9.240   0.000  0.00  0.00           C+0
HETATM   86  O   UNK     0     -10.669  -7.700   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   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   85                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   74                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   72                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   61                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   59                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28   58                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   38                                                  
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   37                                                  
CONECT   35   34   36                                                       
CONECT   36   35                                                            
CONECT   37   34   38                                                       
CONECT   38   37   29   39                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41   46                                                  
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44                                                            
CONECT   46   40   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   51                                                       
CONECT   51   50   52                                                       
CONECT   52   51   53                                                       
CONECT   53   52   54                                                       
CONECT   54   53   55                                                       
CONECT   55   54   56   57                                                  
CONECT   56   55                                                            
CONECT   57   55   58                                                       
CONECT   58   57   27   59                                                  
CONECT   59   58   23   60                                                  
CONECT   60   59                                                            
CONECT   61   21   62   72                                                  
CONECT   62   61   63                                                       
CONECT   63   62   64   65                                                  
CONECT   64   63                                                            
CONECT   65   63   66                                                       
CONECT   66   65   67                                                       
CONECT   67   66   68                                                       
CONECT   68   67   69                                                       
CONECT   69   68   70                                                       
CONECT   70   69   71                                                       
CONECT   71   70                                                            
CONECT   72   61   17   73                                                  
CONECT   73   72                                                            
CONECT   74   15   75   85                                                  
CONECT   75   74   76                                                       
CONECT   76   75   77   78                                                  
CONECT   77   76                                                            
CONECT   78   76   79                                                       
CONECT   79   78   80                                                       
CONECT   80   79   81                                                       
CONECT   81   80   82                                                       
CONECT   82   81   83                                                       
CONECT   83   82   84                                                       
CONECT   84   83                                                            
CONECT   85   74   11   86                                                  
CONECT   86   85                                                            
MASTER        0    0    0    0    0    0    0    0   86    0  180    0
END

View in JSmol

Synonyms

Value	Source
4-Hydroxy-2-{[4-hydroxy-2-methyl-5-(octanoyloxy)-6-{[7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.0,]hexacosan-6-yl]oxy}oxan-3-yl]oxy}-6-methyl-5-(octanoyloxy)oxan-3-yl octanoic acid	Generator
4-Hydroxy-2-{[4-hydroxy-2-methyl-5-(octanoyloxy)-6-{[7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.0³,⁸]hexacosan-6-yl]oxy}oxan-3-yl]oxy}-6-methyl-5-(octanoyloxy)oxan-3-yl octanoic acid	Generator

Chemical Formula

C₆₄H₁₁₂O₂₂

Average Mass

1233.5780 Da

Monoisotopic Mass

1232.76453 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

CCCCCCCC(=O)OC1C(C)OC(OC2C(C)OC(OC3C(C)OC4OC5C(O)C(O)C(CO)OC5OC(CCCCC)CCCCCCCCCC(=O)OC4C3O)C(OC(=O)CCCCCCC)C2O)C(OC(=O)CCCCCCC)C1O

InChI Identifier

InChI=1S/C64H112O22/c1-8-12-16-22-29-35-45(66)80-54-40(5)75-61(58(51(54)72)81-46(67)36-30-23-17-13-9-2)84-55-41(6)76-62(59(52(55)73)82-47(68)37-31-24-18-14-10-3)85-56-42(7)77-63-60(53(56)74)83-48(69)38-32-26-21-19-20-25-28-34-43(33-27-15-11-4)78-64-57(86-63)50(71)49(70)44(39-65)79-64/h40-44,49-65,70-74H,8-39H2,1-7H3

InChI Key

LRKQAUUKLJJTOD-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Ipomoea purpurea	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
Tetracarboxylic acid or derivatives
Alkyl glycoside
Glycosyl compound
O-glycosyl compound
Fatty acid ester
Oxane
Fatty acyl
Secondary alcohol
Lactone
Carboxylic acid ester
Organoheterocyclic compound
Polyol
Oxacycle
Acetal
Carboxylic acid derivative
Primary alcohol
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	5.41	ALOGPS
logP	11.69	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	12.27	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	18	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	300.42 Å²	ChemAxon
Rotatable Bond Count	33	ChemAxon
Refractivity	310.63 m³·mol⁻¹	ChemAxon
Polarizability	137.48 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

85156816

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-hydroxy-2-{[4-hydroxy-2-methyl-5-(octanoyloxy)-6-{[7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.0³,⁸]hexacosan-6-yl]oxy}oxan-3-yl]oxy}-6-methyl-5-(octanoyloxy)oxan-3-yl octanoate (NP0220311)

MOL for NP0220311 (4-hydroxy-2-{[4-hydroxy-2-methyl-5-(octanoyloxy)-6-{[7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.0³,⁸]hexacosan-6-yl]oxy}oxan-3-yl]oxy}-6-methyl-5-(octanoyloxy)oxan-3-yl octanoate)

3D MOL for NP0220311 (4-hydroxy-2-{[4-hydroxy-2-methyl-5-(octanoyloxy)-6-{[7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.0³,⁸]hexacosan-6-yl]oxy}oxan-3-yl]oxy}-6-methyl-5-(octanoyloxy)oxan-3-yl octanoate)

3D SDF for NP0220311 (4-hydroxy-2-{[4-hydroxy-2-methyl-5-(octanoyloxy)-6-{[7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.0³,⁸]hexacosan-6-yl]oxy}oxan-3-yl]oxy}-6-methyl-5-(octanoyloxy)oxan-3-yl octanoate)

3D-SDF for NP0220311 (4-hydroxy-2-{[4-hydroxy-2-methyl-5-(octanoyloxy)-6-{[7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.0³,⁸]hexacosan-6-yl]oxy}oxan-3-yl]oxy}-6-methyl-5-(octanoyloxy)oxan-3-yl octanoate)

PDB for NP0220311 (4-hydroxy-2-{[4-hydroxy-2-methyl-5-(octanoyloxy)-6-{[7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.0³,⁸]hexacosan-6-yl]oxy}oxan-3-yl]oxy}-6-methyl-5-(octanoyloxy)oxan-3-yl octanoate)

3D PDB for NP0220311 (4-hydroxy-2-{[4-hydroxy-2-methyl-5-(octanoyloxy)-6-{[7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.0³,⁸]hexacosan-6-yl]oxy}oxan-3-yl]oxy}-6-methyl-5-(octanoyloxy)oxan-3-yl octanoate)

SMILES for NP0220311 (4-hydroxy-2-{[4-hydroxy-2-methyl-5-(octanoyloxy)-6-{[7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.0³,⁸]hexacosan-6-yl]oxy}oxan-3-yl]oxy}-6-methyl-5-(octanoyloxy)oxan-3-yl octanoate)

INCHI for NP0220311 (4-hydroxy-2-{[4-hydroxy-2-methyl-5-(octanoyloxy)-6-{[7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.0³,⁸]hexacosan-6-yl]oxy}oxan-3-yl]oxy}-6-methyl-5-(octanoyloxy)oxan-3-yl octanoate)

Structure for NP0220311 (4-hydroxy-2-{[4-hydroxy-2-methyl-5-(octanoyloxy)-6-{[7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.0³,⁸]hexacosan-6-yl]oxy}oxan-3-yl]oxy}-6-methyl-5-(octanoyloxy)oxan-3-yl octanoate)

3D Structure for NP0220311 (4-hydroxy-2-{[4-hydroxy-2-methyl-5-(octanoyloxy)-6-{[7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.0³,⁸]hexacosan-6-yl]oxy}oxan-3-yl]oxy}-6-methyl-5-(octanoyloxy)oxan-3-yl octanoate)