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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-06 15:16:52 UTC

Update Date

2022-03-07 02:52:02 UTC

HMDB ID

HMDB0015598

Secondary Accession Numbers

HMDB15598

Metabolite Identification

Common Name

Voglibose

Description

Voglibose is only found in individuals that have used or taken this drug. Voglibose (INN and USAN) is an alpha-glucosidase inhibitor used for lowering post-prandial blood glucose levels in people with diabetes mellitus. It is made in India by Ranbaxy Labs and sold under the trade name Volix. [Wikipedia ]Alpha-glucosidase inhibitors are saccharides that act as competitive inhibitors of enzymes needed to digest carbohydrates: specifically alpha-glucosidase enzymes in the brush border of the small intestines. The membrane-bound intestinal alpha-glucosidases hydrolyze oligosaccharides, trisaccharides, and disaccharides to glucose and other monosaccharides in the small intestine. Acarbose also blocks pancreatic alpha-amylase in addition to inhibiting membrane-bound alpha-glucosidases. Pancreatic alpha-amylase hydrolyzes complex starches to oligosaccharides in the lumen of the small intestine. Inhibition of these enzyme systems reduces the rate of digestion of complex carbohydrates. Less glucose is absorbed because the carbohydrates are not broken down into glucose molecules. In diabetic patients, the short-term effect of these drugs therapies is to decrease current blood glucose levels: the long term effect is a small reduction in hemoglobin-A1c level. (From Drug Therapy in Nursing, 2nd ed)

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

HMDB0015598
     RDKit          3D
Voglibose
 39 39  0  0  0  0  0  0  0  0999 V2000
   -4.6904    0.3517    1.2084 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4753   -0.2972    1.3249 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6291   -0.0502    0.0457 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6956    1.4117   -0.1901 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1357    1.9100   -1.3336 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4455   -0.7192    0.1986 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2062   -0.4515   -0.4129 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4523    0.7821    0.0191 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9360    0.7702    0.2227 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2838    1.3186    1.4529 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6345    1.6312   -0.8304 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2559    2.9511   -0.7647 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6016   -0.5696    0.1588 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8067   -0.6248    0.8147 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6192   -1.5653    0.7606 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2367   -2.7509    1.1167 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5896   -1.7380   -0.3240 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2225   -2.8356   -0.1161 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2823   -0.2303    0.6514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5516   -1.4045    1.4183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8530    0.0812    2.1441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2993   -0.5683   -0.7615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2262    1.9219    0.6925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7916    1.7184   -0.2321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5856    1.7106   -2.1640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3497   -1.2772    1.1008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4374   -0.3864   -1.5421 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2795    1.5800   -0.7338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0139    1.1716    0.9681 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2823    1.2491    1.5224 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2522    1.2512   -1.8271 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7259    1.5514   -0.8139 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6744    3.4234    0.0205 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7717   -0.8885   -0.8874 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1336   -1.5604    0.7575 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1356   -1.0523    1.6045 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9584   -2.9882    2.0190 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1326   -1.9198   -1.2896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8720   -2.9071   -0.8471 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  3  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  1
  9 11  1  0
 11 12  1  0
  9 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17  7  1  0
  1 19  1  0
  2 20  1  0
  2 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  5 25  1  0
  6 26  1  0
  7 27  1  6
  8 28  1  0
  8 29  1  0
 10 30  1  0
 11 31  1  0
 11 32  1  0
 12 33  1  0
 13 34  1  6
 14 35  1  0
 15 36  1  1
 16 37  1  0
 17 38  1  6
 18 39  1  0
M  END

  Mrv0541 02231217592D          

 18 18  0  0  1  0            999 V2000
    3.1095    1.5011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0930    0.7867    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5220   -1.6884    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0930   -0.8634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7595    1.5011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0944   -0.4509    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3799    0.7867    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9509   -0.8634    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5220    0.7867    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2365   -0.4509    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2365    0.3741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8075    0.3741    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5220   -0.8634    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8075   -0.4509    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9345    1.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6655   -0.4509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3799   -0.8634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6655    0.3741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  9  1  1  6  0  0  0
 12  2  1  6  0  0  0
 13  3  1  6  0  0  0
 14  4  1  1  0  0  0
  5 15  1  0  0  0  0
  6 17  1  0  0  0  0
  7 18  1  0  0  0  0
 10  8  1  6  0  0  0
  8 16  1  0  0  0  0
  9 11  1  0  0  0  0
  9 12  1  0  0  0  0
  9 15  1  0  0  0  0
 10 11  1  0  0  0  0
 10 13  1  0  0  0  0
 12 14  1  0  0  0  0
 13 14  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0015598

> <DATABASE_NAME>
hmdb

> <SMILES>
OCC(CO)N[C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C10H21NO7/c12-2-5(3-13)11-6-1-10(18,4-14)9(17)8(16)7(6)15/h5-9,11-18H,1-4H2/t6-,7-,8+,9-,10-/m0/s1

> <INCHI_KEY>
FZNCGRZWXLXZSZ-CIQUZCHMSA-N

> <FORMULA>
C10H21NO7

> <MOLECULAR_WEIGHT>
267.2762

> <EXACT_MASS>
267.131802031

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_AVERAGE_POLARIZABILITY>
26.020633135118675

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,3R,4S,5S)-5-[(1,3-dihydroxypropan-2-yl)amino]-1-(hydroxymethyl)cyclohexane-1,2,3,4-tetrol

> <ALOGPS_LOGP>
-2.34

> <JCHEM_LOGP>
-4.852786626333334

> <ALOGPS_LOGS>
-0.15

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
13.265209747663402

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.45583891661365

> <JCHEM_PKA_STRONGEST_BASIC>
7.658290741647424

> <JCHEM_POLAR_SURFACE_AREA>
153.64000000000001

> <JCHEM_REFRACTIVITY>
59.546700000000016

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.90e+02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
voglibose

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0015598
     RDKit          3D
Voglibose
 39 39  0  0  0  0  0  0  0  0999 V2000
   -4.6904    0.3517    1.2084 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4753   -0.2972    1.3249 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6291   -0.0502    0.0457 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6956    1.4117   -0.1901 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1357    1.9100   -1.3336 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4455   -0.7192    0.1986 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2062   -0.4515   -0.4129 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4523    0.7821    0.0191 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9360    0.7702    0.2227 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2838    1.3186    1.4529 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6345    1.6312   -0.8304 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2559    2.9511   -0.7647 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6016   -0.5696    0.1588 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8067   -0.6248    0.8147 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6192   -1.5653    0.7606 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2367   -2.7509    1.1167 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5896   -1.7380   -0.3240 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2225   -2.8356   -0.1161 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2823   -0.2303    0.6514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5516   -1.4045    1.4183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8530    0.0812    2.1441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2993   -0.5683   -0.7615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2262    1.9219    0.6925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7916    1.7184   -0.2321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5856    1.7106   -2.1640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3497   -1.2772    1.1008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4374   -0.3864   -1.5421 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2795    1.5800   -0.7338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0139    1.1716    0.9681 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2823    1.2491    1.5224 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2522    1.2512   -1.8271 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7259    1.5514   -0.8139 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6744    3.4234    0.0205 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7717   -0.8885   -0.8874 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1336   -1.5604    0.7575 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1356   -1.0523    1.6045 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9584   -2.9882    2.0190 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1326   -1.9198   -1.2896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8720   -2.9071   -0.8471 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  3  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  1
  9 11  1  0
 11 12  1  0
  9 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17  7  1  0
  1 19  1  0
  2 20  1  0
  2 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  5 25  1  0
  6 26  1  0
  7 27  1  6
  8 28  1  0
  8 29  1  0
 10 30  1  0
 11 31  1  0
 11 32  1  0
 12 33  1  0
 13 34  1  6
 14 35  1  0
 15 36  1  1
 16 37  1  0
 17 38  1  6
 18 39  1  0
M  END

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  O   UNK     0       5.804   2.802   0.000  0.00  0.00           O+0
HETATM    2  O   UNK     0       3.907   1.469   0.000  0.00  0.00           O+0
HETATM    3  O   UNK     0       6.574  -3.152   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       3.907  -1.612   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0       8.884   2.802   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      13.243  -0.842   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      11.909   1.469   0.000  0.00  0.00           O+0
HETATM    8  N   UNK     0       9.242  -1.612   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       6.574   1.469   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.908  -0.842   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.908   0.698   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.241   0.698   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.574  -1.612   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.241  -0.842   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.344   2.802   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.576  -0.842   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.909  -1.612   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.576   0.698   0.000  0.00  0.00           C+0
CONECT    1    9                                                            
CONECT    2   12                                                            
CONECT    3   13                                                            
CONECT    4   14                                                            
CONECT    5   15                                                            
CONECT    6   17                                                            
CONECT    7   18                                                            
CONECT    8   10   16                                                       
CONECT    9    1   11   12   15                                             
CONECT   10    8   11   13                                                  
CONECT   11    9   10                                                       
CONECT   12    2    9   14                                                  
CONECT   13    3   10   14                                                  
CONECT   14    4   12   13                                                  
CONECT   15    5    9                                                       
CONECT   16    8   17   18                                                  
CONECT   17    6   16                                                       
CONECT   18    7   16                                                       
MASTER        0    0    0    0    0    0    0    0   18    0   36    0
END

COMPND    HMDB0015598
HETATM    1  O1  UNL     1      -4.690   0.352   1.208  1.00  0.00           O  
HETATM    2  C1  UNL     1      -3.475  -0.297   1.325  1.00  0.00           C  
HETATM    3  C2  UNL     1      -2.629  -0.050   0.046  1.00  0.00           C  
HETATM    4  C3  UNL     1      -2.696   1.412  -0.190  1.00  0.00           C  
HETATM    5  O2  UNL     1      -2.136   1.910  -1.334  1.00  0.00           O  
HETATM    6  N1  UNL     1      -1.445  -0.719   0.199  1.00  0.00           N  
HETATM    7  C4  UNL     1      -0.206  -0.451  -0.413  1.00  0.00           C  
HETATM    8  C5  UNL     1       0.452   0.782   0.019  1.00  0.00           C  
HETATM    9  C6  UNL     1       1.936   0.770   0.223  1.00  0.00           C  
HETATM   10  O3  UNL     1       2.284   1.319   1.453  1.00  0.00           O  
HETATM   11  C7  UNL     1       2.635   1.631  -0.830  1.00  0.00           C  
HETATM   12  O4  UNL     1       2.256   2.951  -0.765  1.00  0.00           O  
HETATM   13  C8  UNL     1       2.602  -0.570   0.159  1.00  0.00           C  
HETATM   14  O5  UNL     1       3.807  -0.625   0.815  1.00  0.00           O  
HETATM   15  C9  UNL     1       1.619  -1.565   0.761  1.00  0.00           C  
HETATM   16  O6  UNL     1       2.237  -2.751   1.117  1.00  0.00           O  
HETATM   17  C10 UNL     1       0.590  -1.738  -0.324  1.00  0.00           C  
HETATM   18  O7  UNL     1      -0.223  -2.836  -0.116  1.00  0.00           O  
HETATM   19  H1  UNL     1      -5.282  -0.230   0.651  1.00  0.00           H  
HETATM   20  H2  UNL     1      -3.552  -1.404   1.418  1.00  0.00           H  
HETATM   21  H3  UNL     1      -2.853   0.081   2.144  1.00  0.00           H  
HETATM   22  H4  UNL     1      -3.299  -0.568  -0.761  1.00  0.00           H  
HETATM   23  H5  UNL     1      -2.226   1.922   0.693  1.00  0.00           H  
HETATM   24  H6  UNL     1      -3.792   1.718  -0.232  1.00  0.00           H  
HETATM   25  H7  UNL     1      -2.586   1.711  -2.164  1.00  0.00           H  
HETATM   26  H8  UNL     1      -1.350  -1.277   1.101  1.00  0.00           H  
HETATM   27  H9  UNL     1      -0.437  -0.386  -1.542  1.00  0.00           H  
HETATM   28  H10 UNL     1       0.280   1.580  -0.734  1.00  0.00           H  
HETATM   29  H11 UNL     1      -0.014   1.172   0.968  1.00  0.00           H  
HETATM   30  H12 UNL     1       3.282   1.249   1.522  1.00  0.00           H  
HETATM   31  H13 UNL     1       2.252   1.251  -1.827  1.00  0.00           H  
HETATM   32  H14 UNL     1       3.726   1.551  -0.814  1.00  0.00           H  
HETATM   33  H15 UNL     1       2.674   3.423   0.020  1.00  0.00           H  
HETATM   34  H16 UNL     1       2.772  -0.888  -0.887  1.00  0.00           H  
HETATM   35  H17 UNL     1       4.134  -1.560   0.758  1.00  0.00           H  
HETATM   36  H18 UNL     1       1.136  -1.052   1.604  1.00  0.00           H  
HETATM   37  H19 UNL     1       1.958  -2.988   2.019  1.00  0.00           H  
HETATM   38  H20 UNL     1       1.133  -1.920  -1.290  1.00  0.00           H  
HETATM   39  H21 UNL     1      -0.872  -2.907  -0.847  1.00  0.00           H  
CONECT    1    2   19
CONECT    2    3   20   21
CONECT    3    4    6   22
CONECT    4    5   23   24
CONECT    5   25
CONECT    6    7   26
CONECT    7    8   17   27
CONECT    8    9   28   29
CONECT    9   10   11   13
CONECT   10   30
CONECT   11   12   31   32
CONECT   12   33
CONECT   13   14   15   34
CONECT   14   35
CONECT   15   16   17   36
CONECT   16   37
CONECT   17   18   38
CONECT   18   39
END

HMDB0015598
     RDKit          3D
Voglibose
 39 39  0  0  0  0  0  0  0  0999 V2000
   -4.6904    0.3517    1.2084 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4753   -0.2972    1.3249 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6291   -0.0502    0.0457 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6956    1.4117   -0.1901 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1357    1.9100   -1.3336 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4455   -0.7192    0.1986 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2062   -0.4515   -0.4129 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4523    0.7821    0.0191 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9360    0.7702    0.2227 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2838    1.3186    1.4529 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6345    1.6312   -0.8304 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2559    2.9511   -0.7647 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6016   -0.5696    0.1588 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8067   -0.6248    0.8147 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6192   -1.5653    0.7606 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2367   -2.7509    1.1167 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5896   -1.7380   -0.3240 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2225   -2.8356   -0.1161 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2823   -0.2303    0.6514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5516   -1.4045    1.4183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8530    0.0812    2.1441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2993   -0.5683   -0.7615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2262    1.9219    0.6925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7916    1.7184   -0.2321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5856    1.7106   -2.1640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3497   -1.2772    1.1008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4374   -0.3864   -1.5421 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2795    1.5800   -0.7338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0139    1.1716    0.9681 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2823    1.2491    1.5224 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2522    1.2512   -1.8271 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7259    1.5514   -0.8139 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6744    3.4234    0.0205 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7717   -0.8885   -0.8874 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1336   -1.5604    0.7575 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1356   -1.0523    1.6045 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9584   -2.9882    2.0190 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1326   -1.9198   -1.2896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8720   -2.9071   -0.8471 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  3  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  1
  9 11  1  0
 11 12  1  0
  9 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17  7  1  0
  1 19  1  0
  2 20  1  0
  2 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  5 25  1  0
  6 26  1  0
  7 27  1  6
  8 28  1  0
  8 29  1  0
 10 30  1  0
 11 31  1  0
 11 32  1  0
 12 33  1  0
 13 34  1  6
 14 35  1  0
 15 36  1  1
 16 37  1  0
 17 38  1  6
 18 39  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
Basen	Kegg
N-(1,3-Dihydroxy-2-propyl)valiolamine	HMDB
3,4-Dideoxy-4-((2-hydroxy-1-(hydroxymethyl)ethyl)amino)-2-C-(hydroxymethyl)-D-epi-inositol	HMDB

Chemical Formula

C₁₀H₂₁NO₇

Average Molecular Weight

267.2762

Monoisotopic Molecular Weight

267.131802031

IUPAC Name

(1S,2S,3R,4S,5S)-5-[(1,3-dihydroxypropan-2-yl)amino]-1-(hydroxymethyl)cyclohexane-1,2,3,4-tetrol

Traditional Name

voglibose

CAS Registry Number

83480-29-9

SMILES

OCC(CO)N[C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C10H21NO7/c12-2-5(3-13)11-6-1-10(18,4-14)9(17)8(16)7(6)15/h5-9,11-18H,1-4H2/t6-,7-,8+,9-,10-/m0/s1

InChI Key

FZNCGRZWXLXZSZ-CIQUZCHMSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aminocyclitols. These are cyclitols with at least one hydroxyl group replace by an amino group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Alcohols and polyols

Direct Parent

Aminocyclitols

Alternative Parents

Substituents

Aminocyclitol
Cyclohexanol
Cyclohexylamine
Tertiary alcohol
1,2-aminoalcohol
Secondary alcohol
Secondary amine
Secondary aliphatic amine
Polyol
Organic nitrogen compound
Organonitrogen compound
Primary alcohol
Hydrocarbon derivative
Organopnictogen compound
Amine
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 21059682)

Excreta

Biofluid or Excreta

Urine (PMID: 21059682)

Cellular substructure

Membrane (HMDB: HMDB0015598)

Source

Exogenous

Exogenous (HMDB: HMDB0015598)

Process

Not Available

Role

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	190 g/L	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	190 g/L	ALOGPS
logP	-2.3	ALOGPS
logP	-4.9	ChemAxon
logS	-0.15	ALOGPS
pKa (Strongest Acidic)	12.46	ChemAxon
pKa (Strongest Basic)	7.66	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	153.64 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	59.55 m³·mol⁻¹	ChemAxon
Polarizability	26.02 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	163.146	31661259
DarkChem	[M-H]-	160.791	31661259
DeepCCS	[M+H]+	169.398	30932474
DeepCCS	[M-H]-	167.04	30932474
DeepCCS	[M-2H]-	201.302	30932474
DeepCCS	[M+Na]+	177.468	30932474
AllCCS	[M+H]+	159.5	32859911
AllCCS	[M+H-H2O]+	156.2	32859911
AllCCS	[M+NH4]+	162.5	32859911
AllCCS	[M+Na]+	163.4	32859911
AllCCS	[M-H]-	158.2	32859911
AllCCS	[M+Na-2H]-	158.2	32859911
AllCCS	[M+HCOO]-	158.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Voglibose	OCC(CO)N[C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O)[C@H]1O	4234.1	Standard polar	33892256
Voglibose	OCC(CO)N[C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O)[C@H]1O	2670.1	Standard non polar	33892256
Voglibose	OCC(CO)N[C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O)[C@H]1O	2646.2	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Voglibose,1TMS,isomer #1	C[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O)[C@H]1O	2537.7	Semi standard non polar	33892256
Voglibose,1TMS,isomer #2	C[Si](C)(C)O[C@]1(CO)C[C@H](NC(CO)CO)[C@H](O)[C@@H](O)[C@@H]1O	2500.3	Semi standard non polar	33892256
Voglibose,1TMS,isomer #3	C[Si](C)(C)OC[C@@]1(O)C[C@H](NC(CO)CO)[C@H](O)[C@@H](O)[C@@H]1O	2506.1	Semi standard non polar	33892256
Voglibose,1TMS,isomer #4	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O)[C@@H](NC(CO)CO)C[C@]1(O)CO	2492.4	Semi standard non polar	33892256
Voglibose,1TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](NC(CO)CO)C[C@](O)(CO)[C@H]1O	2474.1	Semi standard non polar	33892256
Voglibose,1TMS,isomer #6	C[Si](C)(C)O[C@H]1[C@@H](NC(CO)CO)C[C@](O)(CO)[C@@H](O)[C@@H]1O	2459.6	Semi standard non polar	33892256
Voglibose,1TMS,isomer #7	C[Si](C)(C)N(C(CO)CO)[C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O)[C@H]1O	2468.8	Semi standard non polar	33892256
Voglibose,2TMS,isomer #1	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O)[C@H]1O	2528.0	Semi standard non polar	33892256
Voglibose,2TMS,isomer #10	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](NC(CO)CO)C[C@@](CO)(O[Si](C)(C)C)[C@H]1O	2447.4	Semi standard non polar	33892256
Voglibose,2TMS,isomer #11	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O)[C@@H](NC(CO)CO)C[C@@]1(CO)O[Si](C)(C)C	2457.7	Semi standard non polar	33892256
Voglibose,2TMS,isomer #12	C[Si](C)(C)O[C@]1(CO)C[C@H](N(C(CO)CO)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	2437.0	Semi standard non polar	33892256
Voglibose,2TMS,isomer #13	C[Si](C)(C)OC[C@@]1(O)C[C@H](NC(CO)CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2418.2	Semi standard non polar	33892256
Voglibose,2TMS,isomer #14	C[Si](C)(C)OC[C@@]1(O)C[C@H](NC(CO)CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2426.6	Semi standard non polar	33892256
Voglibose,2TMS,isomer #15	C[Si](C)(C)OC[C@@]1(O)C[C@H](NC(CO)CO)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2453.7	Semi standard non polar	33892256
Voglibose,2TMS,isomer #16	C[Si](C)(C)OC[C@@]1(O)C[C@H](N(C(CO)CO)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	2443.4	Semi standard non polar	33892256
Voglibose,2TMS,isomer #17	C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](NC(CO)CO)C[C@]1(O)CO	2431.4	Semi standard non polar	33892256
Voglibose,2TMS,isomer #18	C[Si](C)(C)O[C@H]1[C@@H](NC(CO)CO)C[C@](O)(CO)[C@@H](O[Si](C)(C)C)[C@@H]1O	2399.8	Semi standard non polar	33892256
Voglibose,2TMS,isomer #19	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O)[C@@H](N(C(CO)CO)[Si](C)(C)C)C[C@]1(O)CO	2405.3	Semi standard non polar	33892256
Voglibose,2TMS,isomer #2	C[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O	2466.3	Semi standard non polar	33892256
Voglibose,2TMS,isomer #20	C[Si](C)(C)O[C@H]1[C@@H](NC(CO)CO)C[C@](O)(CO)[C@@H](O)[C@@H]1O[Si](C)(C)C	2388.8	Semi standard non polar	33892256
Voglibose,2TMS,isomer #21	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](N(C(CO)CO)[Si](C)(C)C)C[C@](O)(CO)[C@H]1O	2405.1	Semi standard non polar	33892256
Voglibose,2TMS,isomer #22	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@](O)(CO)C[C@@H]1N(C(CO)CO)[Si](C)(C)C	2415.6	Semi standard non polar	33892256
Voglibose,2TMS,isomer #3	C[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O	2480.6	Semi standard non polar	33892256
Voglibose,2TMS,isomer #4	C[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2454.8	Semi standard non polar	33892256
Voglibose,2TMS,isomer #5	C[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2437.3	Semi standard non polar	33892256
Voglibose,2TMS,isomer #6	C[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	2426.0	Semi standard non polar	33892256
Voglibose,2TMS,isomer #7	C[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	2465.9	Semi standard non polar	33892256
Voglibose,2TMS,isomer #8	C[Si](C)(C)OC[C@@]1(O[Si](C)(C)C)C[C@H](NC(CO)CO)[C@H](O)[C@@H](O)[C@@H]1O	2464.1	Semi standard non polar	33892256
Voglibose,2TMS,isomer #9	C[Si](C)(C)O[C@H]1[C@@H](NC(CO)CO)C[C@@](CO)(O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2429.3	Semi standard non polar	33892256
Voglibose,3TMS,isomer #1	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O	2398.9	Semi standard non polar	33892256
Voglibose,3TMS,isomer #10	C[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	2380.5	Semi standard non polar	33892256
Voglibose,3TMS,isomer #11	C[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	2441.9	Semi standard non polar	33892256
Voglibose,3TMS,isomer #12	C[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2385.7	Semi standard non polar	33892256
Voglibose,3TMS,isomer #13	C[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2364.6	Semi standard non polar	33892256
Voglibose,3TMS,isomer #14	C[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	2352.8	Semi standard non polar	33892256
Voglibose,3TMS,isomer #15	C[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	2433.8	Semi standard non polar	33892256
Voglibose,3TMS,isomer #16	C[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2368.8	Semi standard non polar	33892256
Voglibose,3TMS,isomer #17	C[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2352.2	Semi standard non polar	33892256
Voglibose,3TMS,isomer #18	C[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C	2412.6	Semi standard non polar	33892256
Voglibose,3TMS,isomer #19	C[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2339.6	Semi standard non polar	33892256
Voglibose,3TMS,isomer #2	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O	2386.3	Semi standard non polar	33892256
Voglibose,3TMS,isomer #20	C[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	2412.0	Semi standard non polar	33892256
Voglibose,3TMS,isomer #21	C[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2417.3	Semi standard non polar	33892256
Voglibose,3TMS,isomer #22	C[Si](C)(C)OC[C@@]1(O[Si](C)(C)C)C[C@H](NC(CO)CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2382.6	Semi standard non polar	33892256
Voglibose,3TMS,isomer #23	C[Si](C)(C)OC[C@@]1(O[Si](C)(C)C)C[C@H](NC(CO)CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2417.3	Semi standard non polar	33892256
Voglibose,3TMS,isomer #24	C[Si](C)(C)OC[C@@]1(O[Si](C)(C)C)C[C@H](NC(CO)CO)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2426.5	Semi standard non polar	33892256
Voglibose,3TMS,isomer #25	C[Si](C)(C)OC[C@@]1(O[Si](C)(C)C)C[C@H](N(C(CO)CO)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	2423.7	Semi standard non polar	33892256
Voglibose,3TMS,isomer #26	C[Si](C)(C)O[C@H]1[C@@H](NC(CO)CO)C[C@@](CO)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2392.2	Semi standard non polar	33892256
Voglibose,3TMS,isomer #27	C[Si](C)(C)O[C@H]1[C@@H](NC(CO)CO)C[C@@](CO)(O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2401.5	Semi standard non polar	33892256
Voglibose,3TMS,isomer #28	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@](CO)(O[Si](C)(C)C)C[C@@H]1N(C(CO)CO)[Si](C)(C)C	2413.1	Semi standard non polar	33892256
Voglibose,3TMS,isomer #29	C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](NC(CO)CO)C[C@@]1(CO)O[Si](C)(C)C	2418.1	Semi standard non polar	33892256
Voglibose,3TMS,isomer #3	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2367.8	Semi standard non polar	33892256
Voglibose,3TMS,isomer #30	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](N(C(CO)CO)[Si](C)(C)C)C[C@@](CO)(O[Si](C)(C)C)[C@H]1O	2432.8	Semi standard non polar	33892256
Voglibose,3TMS,isomer #31	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O)[C@@H](N(C(CO)CO)[Si](C)(C)C)C[C@@]1(CO)O[Si](C)(C)C	2407.2	Semi standard non polar	33892256
Voglibose,3TMS,isomer #32	C[Si](C)(C)OC[C@@]1(O)C[C@H](NC(CO)CO)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2351.4	Semi standard non polar	33892256
Voglibose,3TMS,isomer #33	C[Si](C)(C)OC[C@@]1(O)C[C@H](NC(CO)CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2389.6	Semi standard non polar	33892256
Voglibose,3TMS,isomer #34	C[Si](C)(C)OC[C@@]1(O)C[C@H](N(C(CO)CO)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2393.7	Semi standard non polar	33892256
Voglibose,3TMS,isomer #35	C[Si](C)(C)OC[C@@]1(O)C[C@H](NC(CO)CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2412.1	Semi standard non polar	33892256
Voglibose,3TMS,isomer #36	C[Si](C)(C)OC[C@@]1(O)C[C@H](N(C(CO)CO)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2394.3	Semi standard non polar	33892256
Voglibose,3TMS,isomer #37	C[Si](C)(C)OC[C@@]1(O)C[C@H](N(C(CO)CO)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2398.8	Semi standard non polar	33892256
Voglibose,3TMS,isomer #38	C[Si](C)(C)O[C@H]1[C@@H](NC(CO)CO)C[C@](O)(CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2369.0	Semi standard non polar	33892256
Voglibose,3TMS,isomer #39	C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](N(C(CO)CO)[Si](C)(C)C)C[C@]1(O)CO	2388.0	Semi standard non polar	33892256
Voglibose,3TMS,isomer #4	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2365.8	Semi standard non polar	33892256
Voglibose,3TMS,isomer #40	C[Si](C)(C)O[C@H]1[C@@H](N(C(CO)CO)[Si](C)(C)C)C[C@](O)(CO)[C@@H](O[Si](C)(C)C)[C@@H]1O	2386.8	Semi standard non polar	33892256
Voglibose,3TMS,isomer #41	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](O)[C@@](O)(CO)C[C@@H]1N(C(CO)CO)[Si](C)(C)C	2387.3	Semi standard non polar	33892256
Voglibose,3TMS,isomer #5	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	2328.7	Semi standard non polar	33892256
Voglibose,3TMS,isomer #6	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	2476.4	Semi standard non polar	33892256
Voglibose,3TMS,isomer #7	C[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O	2393.7	Semi standard non polar	33892256
Voglibose,3TMS,isomer #8	C[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2394.4	Semi standard non polar	33892256
Voglibose,3TMS,isomer #9	C[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2403.7	Semi standard non polar	33892256
Voglibose,4TMS,isomer #1	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O	2324.6	Semi standard non polar	33892256
Voglibose,4TMS,isomer #10	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2324.1	Semi standard non polar	33892256
Voglibose,4TMS,isomer #11	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2304.7	Semi standard non polar	33892256
Voglibose,4TMS,isomer #12	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C	2414.6	Semi standard non polar	33892256
Voglibose,4TMS,isomer #13	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2278.3	Semi standard non polar	33892256
Voglibose,4TMS,isomer #14	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	2424.2	Semi standard non polar	33892256
Voglibose,4TMS,isomer #15	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2418.5	Semi standard non polar	33892256
Voglibose,4TMS,isomer #16	C[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2329.7	Semi standard non polar	33892256
Voglibose,4TMS,isomer #17	C[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2360.0	Semi standard non polar	33892256
Voglibose,4TMS,isomer #18	C[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	2332.9	Semi standard non polar	33892256
Voglibose,4TMS,isomer #19	C[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	2420.4	Semi standard non polar	33892256
Voglibose,4TMS,isomer #2	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2329.3	Semi standard non polar	33892256
Voglibose,4TMS,isomer #20	C[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2368.7	Semi standard non polar	33892256
Voglibose,4TMS,isomer #21	C[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2352.2	Semi standard non polar	33892256
Voglibose,4TMS,isomer #22	C[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C	2408.9	Semi standard non polar	33892256
Voglibose,4TMS,isomer #23	C[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2348.9	Semi standard non polar	33892256
Voglibose,4TMS,isomer #24	C[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	2437.9	Semi standard non polar	33892256
Voglibose,4TMS,isomer #25	C[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2422.3	Semi standard non polar	33892256
Voglibose,4TMS,isomer #26	C[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2351.8	Semi standard non polar	33892256
Voglibose,4TMS,isomer #27	C[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2346.4	Semi standard non polar	33892256
Voglibose,4TMS,isomer #28	C[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C	2408.2	Semi standard non polar	33892256
Voglibose,4TMS,isomer #29	C[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2303.5	Semi standard non polar	33892256
Voglibose,4TMS,isomer #3	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2371.8	Semi standard non polar	33892256
Voglibose,4TMS,isomer #30	C[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	2407.7	Semi standard non polar	33892256
Voglibose,4TMS,isomer #31	C[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2397.5	Semi standard non polar	33892256
Voglibose,4TMS,isomer #32	C[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2302.0	Semi standard non polar	33892256
Voglibose,4TMS,isomer #33	C[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	2392.5	Semi standard non polar	33892256
Voglibose,4TMS,isomer #34	C[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2391.6	Semi standard non polar	33892256
Voglibose,4TMS,isomer #35	C[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2396.1	Semi standard non polar	33892256
Voglibose,4TMS,isomer #36	C[Si](C)(C)OC[C@@]1(O[Si](C)(C)C)C[C@H](NC(CO)CO)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2356.3	Semi standard non polar	33892256
Voglibose,4TMS,isomer #37	C[Si](C)(C)OC[C@@]1(O[Si](C)(C)C)C[C@H](NC(CO)CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2382.0	Semi standard non polar	33892256
Voglibose,4TMS,isomer #38	C[Si](C)(C)OC[C@@]1(O[Si](C)(C)C)C[C@H](N(C(CO)CO)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2399.2	Semi standard non polar	33892256
Voglibose,4TMS,isomer #39	C[Si](C)(C)OC[C@@]1(O[Si](C)(C)C)C[C@H](NC(CO)CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2386.4	Semi standard non polar	33892256
Voglibose,4TMS,isomer #4	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	2334.4	Semi standard non polar	33892256
Voglibose,4TMS,isomer #40	C[Si](C)(C)OC[C@@]1(O[Si](C)(C)C)C[C@H](N(C(CO)CO)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2416.4	Semi standard non polar	33892256
Voglibose,4TMS,isomer #41	C[Si](C)(C)OC[C@@]1(O[Si](C)(C)C)C[C@H](N(C(CO)CO)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2409.6	Semi standard non polar	33892256
Voglibose,4TMS,isomer #42	C[Si](C)(C)O[C@H]1[C@@H](NC(CO)CO)C[C@@](CO)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2371.2	Semi standard non polar	33892256
Voglibose,4TMS,isomer #43	C[Si](C)(C)O[C@H]1[C@@H](N(C(CO)CO)[Si](C)(C)C)C[C@@](CO)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2398.4	Semi standard non polar	33892256
Voglibose,4TMS,isomer #44	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](O)[C@](CO)(O[Si](C)(C)C)C[C@@H]1N(C(CO)CO)[Si](C)(C)C	2406.6	Semi standard non polar	33892256
Voglibose,4TMS,isomer #45	C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](N(C(CO)CO)[Si](C)(C)C)C[C@@]1(CO)O[Si](C)(C)C	2428.9	Semi standard non polar	33892256
Voglibose,4TMS,isomer #46	C[Si](C)(C)OC[C@@]1(O)C[C@H](NC(CO)CO)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2361.8	Semi standard non polar	33892256
Voglibose,4TMS,isomer #47	C[Si](C)(C)OC[C@@]1(O)C[C@H](N(C(CO)CO)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2379.6	Semi standard non polar	33892256
Voglibose,4TMS,isomer #48	C[Si](C)(C)OC[C@@]1(O)C[C@H](N(C(CO)CO)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2402.9	Semi standard non polar	33892256
Voglibose,4TMS,isomer #49	C[Si](C)(C)OC[C@@]1(O)C[C@H](N(C(CO)CO)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2410.0	Semi standard non polar	33892256
Voglibose,4TMS,isomer #5	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	2450.1	Semi standard non polar	33892256
Voglibose,4TMS,isomer #50	C[Si](C)(C)O[C@H]1[C@@H](N(C(CO)CO)[Si](C)(C)C)C[C@](O)(CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2382.3	Semi standard non polar	33892256
Voglibose,4TMS,isomer #6	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2328.1	Semi standard non polar	33892256
Voglibose,4TMS,isomer #7	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2324.2	Semi standard non polar	33892256
Voglibose,4TMS,isomer #8	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	2305.4	Semi standard non polar	33892256
Voglibose,4TMS,isomer #9	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	2432.3	Semi standard non polar	33892256
Voglibose,5TMS,isomer #1	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2319.4	Semi standard non polar	33892256
Voglibose,5TMS,isomer #10	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2452.8	Semi standard non polar	33892256
Voglibose,5TMS,isomer #11	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2344.1	Semi standard non polar	33892256
Voglibose,5TMS,isomer #12	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2346.5	Semi standard non polar	33892256
Voglibose,5TMS,isomer #13	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C	2428.4	Semi standard non polar	33892256
Voglibose,5TMS,isomer #14	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2279.7	Semi standard non polar	33892256
Voglibose,5TMS,isomer #15	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	2427.7	Semi standard non polar	33892256
Voglibose,5TMS,isomer #16	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2429.1	Semi standard non polar	33892256
Voglibose,5TMS,isomer #17	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2307.5	Semi standard non polar	33892256
Voglibose,5TMS,isomer #18	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	2426.9	Semi standard non polar	33892256
Voglibose,5TMS,isomer #19	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2425.4	Semi standard non polar	33892256
Voglibose,5TMS,isomer #2	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2346.1	Semi standard non polar	33892256
Voglibose,5TMS,isomer #20	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2429.9	Semi standard non polar	33892256
Voglibose,5TMS,isomer #21	C[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2347.4	Semi standard non polar	33892256
Voglibose,5TMS,isomer #22	C[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2347.9	Semi standard non polar	33892256
Voglibose,5TMS,isomer #23	C[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C	2426.7	Semi standard non polar	33892256
Voglibose,5TMS,isomer #24	C[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2332.0	Semi standard non polar	33892256
Voglibose,5TMS,isomer #25	C[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	2435.0	Semi standard non polar	33892256
Voglibose,5TMS,isomer #26	C[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2425.3	Semi standard non polar	33892256
Voglibose,5TMS,isomer #27	C[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2348.4	Semi standard non polar	33892256
Voglibose,5TMS,isomer #28	C[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	2440.3	Semi standard non polar	33892256
Voglibose,5TMS,isomer #29	C[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2428.3	Semi standard non polar	33892256
Voglibose,5TMS,isomer #3	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	2309.3	Semi standard non polar	33892256
Voglibose,5TMS,isomer #30	C[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2435.1	Semi standard non polar	33892256
Voglibose,5TMS,isomer #31	C[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2328.4	Semi standard non polar	33892256
Voglibose,5TMS,isomer #32	C[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	2422.4	Semi standard non polar	33892256
Voglibose,5TMS,isomer #33	C[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2431.0	Semi standard non polar	33892256
Voglibose,5TMS,isomer #34	C[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2394.7	Semi standard non polar	33892256
Voglibose,5TMS,isomer #35	C[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2405.9	Semi standard non polar	33892256
Voglibose,5TMS,isomer #36	C[Si](C)(C)OC[C@@]1(O[Si](C)(C)C)C[C@H](NC(CO)CO)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2376.0	Semi standard non polar	33892256
Voglibose,5TMS,isomer #37	C[Si](C)(C)OC[C@@]1(O[Si](C)(C)C)C[C@H](N(C(CO)CO)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2421.8	Semi standard non polar	33892256
Voglibose,5TMS,isomer #38	C[Si](C)(C)OC[C@@]1(O[Si](C)(C)C)C[C@H](N(C(CO)CO)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2429.2	Semi standard non polar	33892256
Voglibose,5TMS,isomer #39	C[Si](C)(C)OC[C@@]1(O[Si](C)(C)C)C[C@H](N(C(CO)CO)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2448.2	Semi standard non polar	33892256
Voglibose,5TMS,isomer #4	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C	2436.1	Semi standard non polar	33892256
Voglibose,5TMS,isomer #40	C[Si](C)(C)O[C@H]1[C@@H](N(C(CO)CO)[Si](C)(C)C)C[C@@](CO)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2434.9	Semi standard non polar	33892256
Voglibose,5TMS,isomer #41	C[Si](C)(C)OC[C@@]1(O)C[C@H](N(C(CO)CO)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2421.3	Semi standard non polar	33892256
Voglibose,5TMS,isomer #5	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2353.2	Semi standard non polar	33892256
Voglibose,5TMS,isomer #6	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2341.9	Semi standard non polar	33892256
Voglibose,5TMS,isomer #7	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C	2432.9	Semi standard non polar	33892256
Voglibose,5TMS,isomer #8	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2343.3	Semi standard non polar	33892256
Voglibose,5TMS,isomer #9	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	2462.0	Semi standard non polar	33892256
Voglibose,6TMS,isomer #1	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2362.1	Semi standard non polar	33892256
Voglibose,6TMS,isomer #10	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2492.2	Semi standard non polar	33892256
Voglibose,6TMS,isomer #11	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2340.4	Semi standard non polar	33892256
Voglibose,6TMS,isomer #12	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	2461.7	Semi standard non polar	33892256
Voglibose,6TMS,isomer #13	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2483.7	Semi standard non polar	33892256
Voglibose,6TMS,isomer #14	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2450.3	Semi standard non polar	33892256
Voglibose,6TMS,isomer #15	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2463.0	Semi standard non polar	33892256
Voglibose,6TMS,isomer #16	C[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2376.5	Semi standard non polar	33892256
Voglibose,6TMS,isomer #17	C[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	2468.8	Semi standard non polar	33892256
Voglibose,6TMS,isomer #18	C[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2468.1	Semi standard non polar	33892256
Voglibose,6TMS,isomer #19	C[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2459.7	Semi standard non polar	33892256
Voglibose,6TMS,isomer #2	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2346.3	Semi standard non polar	33892256
Voglibose,6TMS,isomer #20	C[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2480.6	Semi standard non polar	33892256
Voglibose,6TMS,isomer #21	C[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2458.7	Semi standard non polar	33892256
Voglibose,6TMS,isomer #22	C[Si](C)(C)OC[C@@]1(O[Si](C)(C)C)C[C@H](N(C(CO)CO)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2485.7	Semi standard non polar	33892256
Voglibose,6TMS,isomer #3	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C	2473.7	Semi standard non polar	33892256
Voglibose,6TMS,isomer #4	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2326.4	Semi standard non polar	33892256
Voglibose,6TMS,isomer #5	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	2470.0	Semi standard non polar	33892256
Voglibose,6TMS,isomer #6	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2482.3	Semi standard non polar	33892256
Voglibose,6TMS,isomer #7	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2364.3	Semi standard non polar	33892256
Voglibose,6TMS,isomer #8	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	2486.3	Semi standard non polar	33892256
Voglibose,6TMS,isomer #9	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2486.6	Semi standard non polar	33892256
Voglibose,7TMS,isomer #1	C[Si](C)(C)OCC(CO[Si](C)(C)C)N[C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2410.6	Semi standard non polar	33892256
Voglibose,7TMS,isomer #2	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	2522.8	Semi standard non polar	33892256
Voglibose,7TMS,isomer #3	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2537.5	Semi standard non polar	33892256
Voglibose,7TMS,isomer #4	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2527.6	Semi standard non polar	33892256
Voglibose,7TMS,isomer #5	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@@](CO)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2553.3	Semi standard non polar	33892256
Voglibose,7TMS,isomer #6	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@](O)(CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2528.3	Semi standard non polar	33892256
Voglibose,7TMS,isomer #7	C[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2533.9	Semi standard non polar	33892256
Voglibose,8TMS,isomer #1	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2614.7	Semi standard non polar	33892256
Voglibose,8TMS,isomer #1	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2690.5	Standard non polar	33892256
Voglibose,8TMS,isomer #1	C[Si](C)(C)OCC(CO[Si](C)(C)C)N([C@H]1C[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2576.4	Standard polar	33892256
Voglibose,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O)[C@H]1O	2745.9	Semi standard non polar	33892256
Voglibose,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@]1(CO)C[C@H](NC(CO)CO)[C@H](O)[C@@H](O)[C@@H]1O	2722.9	Semi standard non polar	33892256
Voglibose,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@@]1(O)C[C@H](NC(CO)CO)[C@H](O)[C@@H](O)[C@@H]1O	2730.4	Semi standard non polar	33892256
Voglibose,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O)[C@@H](NC(CO)CO)C[C@]1(O)CO	2700.7	Semi standard non polar	33892256
Voglibose,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](NC(CO)CO)C[C@](O)(CO)[C@H]1O	2701.4	Semi standard non polar	33892256
Voglibose,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](NC(CO)CO)C[C@](O)(CO)[C@@H](O)[C@@H]1O	2686.0	Semi standard non polar	33892256
Voglibose,1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N(C(CO)CO)[C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O)[C@H]1O	2716.5	Semi standard non polar	33892256
Voglibose,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N[C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O)[C@H]1O	2988.8	Semi standard non polar	33892256
Voglibose,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](NC(CO)CO)C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@H]1O	2874.6	Semi standard non polar	33892256
Voglibose,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O)[C@@H](NC(CO)CO)C[C@@]1(CO)O[Si](C)(C)C(C)(C)C	2862.4	Semi standard non polar	33892256
Voglibose,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)O[C@]1(CO)C[C@H](N(C(CO)CO)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	2919.6	Semi standard non polar	33892256
Voglibose,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC[C@@]1(O)C[C@H](NC(CO)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	2867.5	Semi standard non polar	33892256
Voglibose,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC[C@@]1(O)C[C@H](NC(CO)CO)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	2872.3	Semi standard non polar	33892256
Voglibose,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC[C@@]1(O)C[C@H](NC(CO)CO)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	2885.2	Semi standard non polar	33892256
Voglibose,2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC[C@@]1(O)C[C@H](N(C(CO)CO)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	2921.4	Semi standard non polar	33892256
Voglibose,2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](NC(CO)CO)C[C@]1(O)CO	2863.5	Semi standard non polar	33892256
Voglibose,2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](NC(CO)CO)C[C@](O)(CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	2849.3	Semi standard non polar	33892256
Voglibose,2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O)[C@@H](N(C(CO)CO)[Si](C)(C)C(C)(C)C)C[C@]1(O)CO	2898.4	Semi standard non polar	33892256
Voglibose,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O	2880.3	Semi standard non polar	33892256
Voglibose,2TBDMS,isomer #20	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](NC(CO)CO)C[C@](O)(CO)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	2832.3	Semi standard non polar	33892256
Voglibose,2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](N(C(CO)CO)[Si](C)(C)C(C)(C)C)C[C@](O)(CO)[C@H]1O	2891.4	Semi standard non polar	33892256
Voglibose,2TBDMS,isomer #22	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@](O)(CO)C[C@@H]1N(C(CO)CO)[Si](C)(C)C(C)(C)C	2880.7	Semi standard non polar	33892256
Voglibose,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O	2920.5	Semi standard non polar	33892256
Voglibose,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	2883.4	Semi standard non polar	33892256
Voglibose,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	2870.6	Semi standard non polar	33892256
Voglibose,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	2871.3	Semi standard non polar	33892256
Voglibose,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	2945.9	Semi standard non polar	33892256
Voglibose,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC[C@@]1(O[Si](C)(C)C(C)(C)C)C[C@H](NC(CO)CO)[C@H](O)[C@@H](O)[C@@H]1O	2878.4	Semi standard non polar	33892256
Voglibose,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](NC(CO)CO)C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	2858.3	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N[C@H]1C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O	3088.1	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3058.4	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	3144.4	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3067.1	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3058.0	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3047.6	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	3143.4	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3044.1	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3049.4	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	3149.5	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3018.5	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N[C@H]1C[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O	3141.4	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)[Si](C)(C)C(C)(C)C	3127.3	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3110.3	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC[C@@]1(O[Si](C)(C)C(C)(C)C)C[C@H](NC(CO)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3044.7	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC[C@@]1(O[Si](C)(C)C(C)(C)C)C[C@H](NC(CO)CO)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3062.2	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC[C@@]1(O[Si](C)(C)C(C)(C)C)C[C@H](NC(CO)CO)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3075.9	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC[C@@]1(O[Si](C)(C)C(C)(C)C)C[C@H](N(C(CO)CO)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3125.4	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #26	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](NC(CO)CO)C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3057.1	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #27	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](NC(CO)CO)C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3052.0	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #28	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@](CO)(O[Si](C)(C)C(C)(C)C)C[C@@H]1N(C(CO)CO)[Si](C)(C)C(C)(C)C	3119.3	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #29	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](NC(CO)CO)C[C@@]1(CO)O[Si](C)(C)C(C)(C)C	3073.5	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N[C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3091.2	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #30	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](N(C(CO)CO)[Si](C)(C)C(C)(C)C)C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@H]1O	3133.5	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #31	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O)[C@@H](N(C(CO)CO)[Si](C)(C)C(C)(C)C)C[C@@]1(CO)O[Si](C)(C)C(C)(C)C	3118.9	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC[C@@]1(O)C[C@H](NC(CO)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3018.2	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC[C@@]1(O)C[C@H](NC(CO)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3057.8	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC[C@@]1(O)C[C@H](N(C(CO)CO)[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3102.6	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OC[C@@]1(O)C[C@H](NC(CO)CO)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3061.5	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #36	CC(C)(C)[Si](C)(C)OC[C@@]1(O)C[C@H](N(C(CO)CO)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3121.5	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #37	CC(C)(C)[Si](C)(C)OC[C@@]1(O)C[C@H](N(C(CO)CO)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3128.3	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #38	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](NC(CO)CO)C[C@](O)(CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3041.3	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #39	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](N(C(CO)CO)[Si](C)(C)C(C)(C)C)C[C@]1(O)CO	3108.0	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N[C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3058.5	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #40	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](N(C(CO)CO)[Si](C)(C)C(C)(C)C)C[C@](O)(CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3107.9	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #41	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@](O)(CO)C[C@@H]1N(C(CO)CO)[Si](C)(C)C(C)(C)C	3084.7	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N[C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3056.9	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N([C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	3179.3	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O	3054.0	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3062.2	Semi standard non polar	33892256
Voglibose,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3076.2	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N[C@H]1C[C@@](CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O	3264.9	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N[C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3218.7	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N[C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3223.6	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N([C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	3378.8	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N[C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3179.3	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N([C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)[Si](C)(C)C(C)(C)C	3354.6	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N([C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3328.5	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3222.5	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3236.6	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3213.9	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	3341.2	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N[C@H]1C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3238.9	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3231.3	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3216.9	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	3346.1	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3220.8	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)[Si](C)(C)C(C)(C)C	3357.0	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3338.4	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3219.7	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3228.8	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	3353.5	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3185.4	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N[C@H]1C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3269.5	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)[Si](C)(C)C(C)(C)C	3341.0	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3320.1	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3187.8	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)[Si](C)(C)C(C)(C)C	3328.5	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3322.1	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3297.4	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #36	CC(C)(C)[Si](C)(C)OC[C@@]1(O[Si](C)(C)C(C)(C)C)C[C@H](NC(CO)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3209.0	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #37	CC(C)(C)[Si](C)(C)OC[C@@]1(O[Si](C)(C)C(C)(C)C)C[C@H](NC(CO)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3223.5	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #38	CC(C)(C)[Si](C)(C)OC[C@@]1(O[Si](C)(C)C(C)(C)C)C[C@H](N(C(CO)CO)[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3321.7	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #39	CC(C)(C)[Si](C)(C)OC[C@@]1(O[Si](C)(C)C(C)(C)C)C[C@H](NC(CO)CO)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3237.7	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N[C@H]1C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3232.8	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #40	CC(C)(C)[Si](C)(C)OC[C@@]1(O[Si](C)(C)C(C)(C)C)C[C@H](N(C(CO)CO)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3338.5	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #41	CC(C)(C)[Si](C)(C)OC[C@@]1(O[Si](C)(C)C(C)(C)C)C[C@H](N(C(CO)CO)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3341.4	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #42	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](NC(CO)CO)C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3225.5	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #43	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](N(C(CO)CO)[Si](C)(C)C(C)(C)C)C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3318.5	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #44	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@](CO)(O[Si](C)(C)C(C)(C)C)C[C@@H]1N(C(CO)CO)[Si](C)(C)C(C)(C)C	3315.8	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #45	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](N(C(CO)CO)[Si](C)(C)C(C)(C)C)C[C@@]1(CO)O[Si](C)(C)C(C)(C)C	3336.7	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #46	CC(C)(C)[Si](C)(C)OC[C@@]1(O)C[C@H](NC(CO)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3207.4	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #47	CC(C)(C)[Si](C)(C)OC[C@@]1(O)C[C@H](N(C(CO)CO)[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3297.9	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #48	CC(C)(C)[Si](C)(C)OC[C@@]1(O)C[C@H](N(C(CO)CO)[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3316.5	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #49	CC(C)(C)[Si](C)(C)OC[C@@]1(O)C[C@H](N(C(CO)CO)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3320.6	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N([C@H]1C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	3373.3	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #50	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](N(C(CO)CO)[Si](C)(C)C(C)(C)C)C[C@](O)(CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3291.9	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N[C@H]1C[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3249.7	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N[C@H]1C[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3245.7	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N[C@H]1C[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3230.3	Semi standard non polar	33892256
Voglibose,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N([C@H]1C[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	3372.7	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N[C@H]1C[C@@](CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3392.2	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N([C@H]1C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3541.9	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N[C@H]1C[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3389.3	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N[C@H]1C[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3396.0	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N([C@H]1C[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	3534.4	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N[C@H]1C[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3369.0	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N([C@H]1C[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)[Si](C)(C)C(C)(C)C	3532.4	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N([C@H]1C[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3525.7	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N[C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3353.1	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N([C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)[Si](C)(C)C(C)(C)C	3536.7	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N([C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3528.8	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N[C@H]1C[C@@](CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3423.1	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N([C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3504.6	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3395.3	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3397.9	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	3536.0	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3389.1	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)[Si](C)(C)C(C)(C)C	3538.8	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3523.4	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3390.7	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)[Si](C)(C)C(C)(C)C	3538.5	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3529.9	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N[C@H]1C[C@@](CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3395.2	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OCC(CO)N([C@H]1C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3527.8	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OCC(CO)N[C@H]1C[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3369.2	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)[Si](C)(C)C(C)(C)C	3527.3	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3512.7	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3503.5	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OCC(CO)N([C@H]1C[C@](O)(CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3503.7	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #36	CC(C)(C)[Si](C)(C)OC[C@@]1(O[Si](C)(C)C(C)(C)C)C[C@H](NC(CO)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3396.1	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #37	CC(C)(C)[Si](C)(C)OC[C@@]1(O[Si](C)(C)C(C)(C)C)C[C@H](N(C(CO)CO)[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3510.2	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #38	CC(C)(C)[Si](C)(C)OC[C@@]1(O[Si](C)(C)C(C)(C)C)C[C@H](N(C(CO)CO)[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3517.3	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #39	CC(C)(C)[Si](C)(C)OC[C@@]1(O[Si](C)(C)C(C)(C)C)C[C@H](N(C(CO)CO)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3532.6	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N([C@H]1C[C@@](CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	3555.6	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #40	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](N(C(CO)CO)[Si](C)(C)C(C)(C)C)C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3512.2	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #41	CC(C)(C)[Si](C)(C)OC[C@@]1(O)C[C@H](N(C(CO)CO)[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3499.5	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N[C@H]1C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3400.7	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N[C@H]1C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3385.1	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N([C@H]1C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	3543.0	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N[C@H]1C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3390.3	Semi standard non polar	33892256
Voglibose,5TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)N([C@H]1C[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)[Si](C)(C)C(C)(C)C	3553.3	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Voglibose GC-MS (Non-derivatized) - 70eV, Positive	splash10-002s-1980000000-33cb901e6f81818552e5	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Voglibose GC-MS (5 TMS) - 70eV, Positive	splash10-03di-1100289000-80acf509a06c3f901374	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Voglibose GC-MS (TBDMS_4_25) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Voglibose GC-MS (TBDMS_5_10) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Voglibose GC-MS (TBDMS_5_24) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Voglibose GC-MS (TBDMS_5_26) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Voglibose GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Voglibose GC-MS ("Voglibose,4TBDMS,#25" TMS) - 70eV, Positive	Not Available	2021-10-14	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Voglibose 10V, Positive-QTOF	splash10-0gb9-0090000000-59803c398938b40db072	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Voglibose 20V, Positive-QTOF	splash10-0f89-0290000000-955c2e1243d80e33f3a8	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Voglibose 40V, Positive-QTOF	splash10-004i-3920000000-bb6db0ffc0532e3e2d96	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Voglibose 10V, Negative-QTOF	splash10-014i-0290000000-b1e8f1611dd963f0fbfe	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Voglibose 20V, Negative-QTOF	splash10-014j-0490000000-be40686c577d84c8e289	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Voglibose 40V, Negative-QTOF	splash10-05tf-8930000000-686045d50b36df2726db	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Voglibose 10V, Positive-QTOF	splash10-014i-0090000000-96ef009448daa89a94dd	2021-10-11	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Voglibose 20V, Positive-QTOF	splash10-00di-9180000000-393eff67c3726ac2c61a	2021-10-11	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Voglibose 40V, Positive-QTOF	splash10-00di-9200000000-8a27d4ca4bdc7c0b47c0	2021-10-11	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Voglibose 10V, Negative-QTOF	splash10-014i-0090000000-247c6c97f730cbfb281d	2021-10-11	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Voglibose 20V, Negative-QTOF	splash10-014i-0290000000-f52101a9f96855a2f770	2021-10-11	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Voglibose 40V, Negative-QTOF	splash10-0rk9-7960000000-059ee9ff297f0b3d55bf	2021-10-11	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Membrane

Biospecimen Locations

Blood
Urine

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Expected but not Quantified	Not Quantified	Not Available	Not Available	Taking drug identified by DrugBank entry DB04878	21059682	details
Urine	Expected but not Quantified	Not Quantified	Not Available	Not Available	Taking drug identified by DrugBank entry DB04878	21059682	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

DB04878

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

392046

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Voglibose

METLIN ID

Not Available

PubChem Compound

444020

PDB ID

Not Available

ChEBI ID

590151

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Satoh N, Shimatsu A, Yamada K, Aizawa-Abe M, Suganami T, Kuzuya H, Ogawa Y: An alpha-glucosidase inhibitor, voglibose, reduces oxidative stress markers and soluble intercellular adhesion molecule 1 in obese type 2 diabetic patients. Metabolism. 2006 Jun;55(6):786-93. [PubMed:16713439 ]
Kurebayashi S, Watada H, Tanaka Y, Kawasumi M, Kawamori R, Hirose T: Efficacy and adverse effects of nateglinide in early type 2 diabetes. Comparison with voglibose in a cross-over study. Endocr J. 2006 Apr;53(2):213-7. [PubMed:16618980 ]
Aso Y, Yamamoto R, Suetsugu M, Matsumoto S, Wakabayashi S, Matsutomo R, Takebayashi K, Inukai T: Comparison of the effects of pioglitazone and voglibose on circulating total and high-molecular-weight adiponectin, and on two fibrinolysis inhibitors, in patients with Type 2 diabetes. Diabet Med. 2007 Sep;24(9):962-8. Epub 2007 May 17. [PubMed:17509067 ]

Enzymes

Enzyme Details

1. Maltase-glucoamylase, intestinal

General function:: Involved in catalytic activity
Specific function:: May serve as an alternate pathway for starch digestion when luminal alpha-amylase activity is reduced because of immaturity or malnutrition. May play a unique role in the digestion of malted dietary oligosaccharides used in food manufacturing.
Gene Name:: MGAM
Uniprot ID:: O43451
Molecular weight:: Not Available

References

Satoh N, Shimatsu A, Yamada K, Aizawa-Abe M, Suganami T, Kuzuya H, Ogawa Y: An alpha-glucosidase inhibitor, voglibose, reduces oxidative stress markers and soluble intercellular adhesion molecule 1 in obese type 2 diabetic patients. Metabolism. 2006 Jun;55(6):786-93. [PubMed:16713439 ]
Chen X, Ji ZL, Chen YZ: TTD: Therapeutic Target Database. Nucleic Acids Res. 2002 Jan 1;30(1):412-5. [PubMed:11752352 ]
Matsumura M, Monden T, Miyashita Y, Kawagoe Y, Shimizu H, Nakatani Y, Domeki N, Yanagi K, Ikeda S, Kasai K: Effects of changeover from voglibose to acarbose on postprandial triglycerides in type 2 diabetes mellitus patients. Adv Ther. 2009 Jun;26(6):660-6. doi: 10.1007/s12325-009-0040-7. Epub 2009 Jun 30. [PubMed:19568704 ]
Abe M, Okada K, Maruyama T, Maruyama N, Matsumoto K: Combination therapy with mitiglinide and voglibose improves glycemic control in type 2 diabetic patients on hemodialysis. Expert Opin Pharmacother. 2010 Feb;11(2):169-76. doi: 10.1517/14656560903530683. [PubMed:20025554 ]
Iwasa M, Kobayashi H, Yasuda S, Kawamura I, Sumi S, Yamada Y, Shiraki T, Yamaki T, Ushikoshi H, Aoyama T, Nishigaki K, Takemura G, Fujiwara T, Fujiwara H, Minatoguchi S: Antidiabetic drug voglibose is protective against ischemia-reperfusion injury through glucagon-like peptide 1 receptors and the phosphoinositide 3-kinase-Akt-endothelial nitric oxide synthase pathway in rabbits. J Cardiovasc Pharmacol. 2010 Jun;55(6):625-34. doi: 10.1097/FJC.0b013e3181dcd240. [PubMed:20351564 ]
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Showing metabocard for Voglibose (HMDB0015598)

MOL for HMDB0015598 (Voglibose)

3D MOL for HMDB0015598 (Voglibose)

3D SDF for HMDB0015598 (Voglibose)

3D-SDF for HMDB0015598 (Voglibose)

PDB for HMDB0015598 (Voglibose)

3D PDB for HMDB0015598 (Voglibose)

SMILES for HMDB0015598 (Voglibose)

INCHI for HMDB0015598 (Voglibose)

Structure for HMDB0015598 (Voglibose)

3D Structure for HMDB0015598 (Voglibose)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

Enzymes

References