NP-MRD: Showing NP-Card for 2-[(1-{[3,4-dimethoxy-6-(methoxymethyl)-5-{[3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,4,5,6-tetramethoxyhexan-3-yl)oxy]-3,4,5-trimethoxy-6-(methoxymethyl)oxane (NP0311950)

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Record Information

Version

2.0

Created at

2022-09-11 08:18:00 UTC

Updated at

2022-09-11 08:18:00 UTC

NP-MRD ID

NP0311950

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[(1-{[3,4-dimethoxy-6-(methoxymethyl)-5-{[3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,4,5,6-tetramethoxyhexan-3-yl)oxy]-3,4,5-trimethoxy-6-(methoxymethyl)oxane

Description

2-[(1-{[3,4-Dimethoxy-6-(methoxymethyl)-5-{[3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,4,5,6-tetramethoxyhexan-3-yl)oxy]-3,4,5-trimethoxy-6-(methoxymethyl)oxane belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol. 2-[(1-{[3,4-dimethoxy-6-(methoxymethyl)-5-{[3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,4,5,6-tetramethoxyhexan-3-yl)oxy]-3,4,5-trimethoxy-6-(methoxymethyl)oxane is found in Rhizobium phaseoli. 2-[(1-{[3,4-Dimethoxy-6-(methoxymethyl)-5-{[3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,4,5,6-tetramethoxyhexan-3-yl)oxy]-3,4,5-trimethoxy-6-(methoxymethyl)oxane is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251509492D          

 60 62  0  0  0  0            999 V2000
   -4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -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 O   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
   -5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.5724    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.4289   -1.6500    0.0000 O   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   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    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 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
   -0.0000    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.8250    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
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   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.7145    2.0625    0.0000 O   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
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    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1434   -0.4125    0.0000 O   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
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    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
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   -0.7145   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 O   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
  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
  4  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 14 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 21 24  1  0  0  0  0
 12 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 10 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 32 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
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 38 50  1  0  0  0  0
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 51 52  1  0  0  0  0
 36 53  1  0  0  0  0
 53 54  1  0  0  0  0
 54 55  1  0  0  0  0
 53 56  1  0  0  0  0
 30 56  1  0  0  0  0
 56 57  1  0  0  0  0
 57 58  1  0  0  0  0
 27 59  1  0  0  0  0
 59 60  1  0  0  0  0
M  END

     RDKit          3D

134136  0  0  0  0  0  0  0  0999 V2000
   -5.4590   -4.6051   -2.8454 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6780   -4.8331   -1.7300 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0807   -3.6968   -1.2979 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0085   -2.5890   -0.8577 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1601   -1.5415   -0.4727 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8392   -0.3434   -0.2236 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9969    0.4742    0.5192 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6445    1.6630   -0.1052 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2353    2.8040    0.7255 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6855    2.9042    1.9514 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3647    2.3975    3.0186 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4861    4.0573    0.0014 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.5227    4.8800    0.8067 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0617    5.2591    2.0432 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.0916    3.8309   -1.2512 O   0  0  0  0  0  0  0  0  0  0  0  0
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   10.2312   -1.1082   -1.2514 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.3171   -3.2931   -2.0350 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


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M  END
> <DATABASE_ID>
NP0311950

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COCC(OC)C(OC)C(OC1OC(COC)C(OC)C(OC)C1OC)C(COC1OC(COC)C(OC2OC(COC)C(OC)C(OC)C2OC)C(OC)C1OC)OC

> <INCHI_IDENTIFIER>
InChI=1S/C39H74O21/c1-40-16-21(44-5)26(46-7)29(59-38-35(53-14)31(49-10)27(47-8)23(57-38)17-41-2)22(45-6)20-55-37-34(52-13)33(51-12)30(25(56-37)19-43-4)60-39-36(54-15)32(50-11)28(48-9)24(58-39)18-42-3/h21-39H,16-20H2,1-15H3

> <INCHI_KEY>
WDCPBTBFNJOCCY-UHFFFAOYSA-N

> <FORMULA>
C39H74O21

> <MOLECULAR_WEIGHT>
879.0

> <EXACT_MASS>
878.472259403

> <JCHEM_ACCEPTOR_COUNT>
21

> <JCHEM_ATOM_COUNT>
134

> <JCHEM_AVERAGE_POLARIZABILITY>
92.16294278286821

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(1-{[3,4-dimethoxy-6-(methoxymethyl)-5-{[3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,4,5,6-tetramethoxyhexan-3-yl)oxy]-3,4,5-trimethoxy-6-(methoxymethyl)oxane

> <ALOGPS_LOGP>
0.77

> <JCHEM_LOGP>
0.6043717693333354

> <ALOGPS_LOGS>
-3.49

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2358105761405844

> <JCHEM_POLAR_SURFACE_AREA>
193.82999999999996

> <JCHEM_REFRACTIVITY>
206.9114999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
29

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.83e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[(1-{[3,4-dimethoxy-6-(methoxymethyl)-5-{[3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,4,5,6-tetramethoxyhexan-3-yl)oxy]-3,4,5-trimethoxy-6-(methoxymethyl)oxane

> <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      -8.002  -7.700   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -9.336  -6.930   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -9.336  -5.390   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -8.002  -4.620   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -6.668  -5.390   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -8.002  -3.080   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -9.336  -2.310   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0     -10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -6.668  -0.770   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -8.002   0.000   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -9.336  -0.770   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0     -10.669   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -12.003  -0.770   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0     -13.337  -0.000   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0     -14.670  -0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0     -10.669   1.540   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0     -12.003   2.310   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0     -12.003   3.850   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -9.336   2.310   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -9.336   3.850   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -8.002   4.620   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -8.002   1.540   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -6.668   2.310   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -5.335   1.540   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -2.667  -3.080   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -0.000   0.000   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      -0.000   1.540   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      -1.334   3.850   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   52  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   54  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
HETATM   55  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   57  O   UNK     0      -1.334  -6.930   0.000  0.00  0.00           O+0
HETATM   58  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   59  O   UNK     0      -4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   60  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    7                                                  
CONECT    5    4    6                                                       
CONECT    6    5                                                            
CONECT    7    4    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    7   11   27                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   24                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   18                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16                                                            
CONECT   18   14   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18   22   24                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   21   12   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   10   28   59                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   56                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33   36                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34                                                            
CONECT   36   32   37   53                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39   50                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41   44                                                  
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42                                                            
CONECT   44   40   45   47                                                  
CONECT   45   44   46                                                       
CONECT   46   45                                                            
CONECT   47   44   48   50                                                  
CONECT   48   47   49                                                       
CONECT   49   48                                                            
CONECT   50   47   38   51                                                  
CONECT   51   50   52                                                       
CONECT   52   51                                                            
CONECT   53   36   54   56                                                  
CONECT   54   53   55                                                       
CONECT   55   54                                                            
CONECT   56   53   30   57                                                  
CONECT   57   56   58                                                       
CONECT   58   57                                                            
CONECT   59   27   60                                                       
CONECT   60   59                                                            
MASTER        0    0    0    0    0    0    0    0   60    0  124    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₉H₇₄O₂₁

Average Mass

879.0000 Da

Monoisotopic Mass

878.47226 Da

IUPAC Name

2-[(1-{[3,4-dimethoxy-6-(methoxymethyl)-5-{[3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,4,5,6-tetramethoxyhexan-3-yl)oxy]-3,4,5-trimethoxy-6-(methoxymethyl)oxane

Traditional Name

2-[(1-{[3,4-dimethoxy-6-(methoxymethyl)-5-{[3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,4,5,6-tetramethoxyhexan-3-yl)oxy]-3,4,5-trimethoxy-6-(methoxymethyl)oxane

CAS Registry Number

Not Available

SMILES

COCC(OC)C(OC)C(OC1OC(COC)C(OC)C(OC)C1OC)C(COC1OC(COC)C(OC2OC(COC)C(OC)C(OC)C2OC)C(OC)C1OC)OC

InChI Identifier

InChI=1S/C39H74O21/c1-40-16-21(44-5)26(46-7)29(59-38-35(53-14)31(49-10)27(47-8)23(57-38)17-41-2)22(45-6)20-55-37-34(52-13)33(51-12)30(25(56-37)19-43-4)60-39-36(54-15)32(50-11)28(48-9)24(58-39)18-42-3/h21-39H,16-20H2,1-15H3

InChI Key

WDCPBTBFNJOCCY-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Rhizobium phaseoli	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acyl glycosides

Direct Parent

Fatty acyl glycosides of mono- and disaccharides

Alternative Parents

Substituents

Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
O-glycosyl compound
Glycosyl compound
Disaccharide
Oxane
Oxacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Acetal
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	0.77	ALOGPS
logP	0.6	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	21	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	193.83 Å²	ChemAxon
Rotatable Bond Count	29	ChemAxon
Refractivity	206.91 m³·mol⁻¹	ChemAxon
Polarizability	92.16 Å³	ChemAxon
Number of Rings	3	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-{[3,4-dimethoxy-6-(methoxymethyl)-5-{[3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,4,5,6-tetramethoxyhexan-3-yl)oxy]-3,4,5-trimethoxy-6-(methoxymethyl)oxane (NP0311950)

MOL for NP0311950 (2-[(1-{[3,4-dimethoxy-6-(methoxymethyl)-5-{[3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,4,5,6-tetramethoxyhexan-3-yl)oxy]-3,4,5-trimethoxy-6-(methoxymethyl)oxane)

3D MOL for NP0311950 (2-[(1-{[3,4-dimethoxy-6-(methoxymethyl)-5-{[3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,4,5,6-tetramethoxyhexan-3-yl)oxy]-3,4,5-trimethoxy-6-(methoxymethyl)oxane)

3D SDF for NP0311950 (2-[(1-{[3,4-dimethoxy-6-(methoxymethyl)-5-{[3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,4,5,6-tetramethoxyhexan-3-yl)oxy]-3,4,5-trimethoxy-6-(methoxymethyl)oxane)

3D-SDF for NP0311950 (2-[(1-{[3,4-dimethoxy-6-(methoxymethyl)-5-{[3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,4,5,6-tetramethoxyhexan-3-yl)oxy]-3,4,5-trimethoxy-6-(methoxymethyl)oxane)

PDB for NP0311950 (2-[(1-{[3,4-dimethoxy-6-(methoxymethyl)-5-{[3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,4,5,6-tetramethoxyhexan-3-yl)oxy]-3,4,5-trimethoxy-6-(methoxymethyl)oxane)

3D PDB for NP0311950 (2-[(1-{[3,4-dimethoxy-6-(methoxymethyl)-5-{[3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,4,5,6-tetramethoxyhexan-3-yl)oxy]-3,4,5-trimethoxy-6-(methoxymethyl)oxane)

SMILES for NP0311950 (2-[(1-{[3,4-dimethoxy-6-(methoxymethyl)-5-{[3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,4,5,6-tetramethoxyhexan-3-yl)oxy]-3,4,5-trimethoxy-6-(methoxymethyl)oxane)

INCHI for NP0311950 (2-[(1-{[3,4-dimethoxy-6-(methoxymethyl)-5-{[3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,4,5,6-tetramethoxyhexan-3-yl)oxy]-3,4,5-trimethoxy-6-(methoxymethyl)oxane)

Structure for NP0311950 (2-[(1-{[3,4-dimethoxy-6-(methoxymethyl)-5-{[3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,4,5,6-tetramethoxyhexan-3-yl)oxy]-3,4,5-trimethoxy-6-(methoxymethyl)oxane)

3D Structure for NP0311950 (2-[(1-{[3,4-dimethoxy-6-(methoxymethyl)-5-{[3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,4,5,6-tetramethoxyhexan-3-yl)oxy]-3,4,5-trimethoxy-6-(methoxymethyl)oxane)