Jump To Section:

Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References XML

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 01:41:54 UTC

Update Date

2022-03-07 02:56:29 UTC

HMDB ID

HMDB0040154

Secondary Accession Numbers

HMDB40154

Metabolite Identification

Common Name

6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose

Description

6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose belongs to the class of organic compounds known as c-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a C-glycosidic bond. 6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose has been detected, but not quantified in, brassicas and pulses. This could make 6-O-b-D-fructofuranosyl-2-deoxy-D-glucose a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on 6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose.

Structure

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

HMDB0040154
     RDKit          3D
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose
 44 45  0  0  0  0  0  0  0  0999 V2000
   -3.4429    2.5499   -1.6352 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2018    1.8724   -0.7138 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4973    0.6911   -0.1073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3371    1.1008    0.5475 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6123   -0.0947    0.7957 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0479   -0.5469    2.1595 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4488   -1.7127    2.5962 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3011    0.2357    0.6793 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6599   -0.6666    0.8556 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0124    0.0332    0.6524 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9852   -0.9430    0.8453 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2304   -0.3204    0.9478 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1920   -1.2779    0.6372 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3189    0.8647    0.0228 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4535    0.6466   -1.2114 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8694   -0.4224   -1.9706 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0095    0.5265   -0.7798 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3139   -0.3325   -1.6077 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9696   -1.0441   -0.2984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7501   -2.1151    0.1063 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8778   -0.1923   -1.1979 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8476   -0.9624   -1.8125 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9131    3.2908   -1.2474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3953    2.5898    0.1377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2106    1.6064   -1.0897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1638    0.1414    0.5504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9384    0.2903    2.8712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1385   -0.7608    2.1114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3183   -2.3906    1.9250 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7409   -1.1715    1.8249 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6330   -1.4588    0.0797 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1415    0.8302    1.3896 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3817    0.0637    1.9828 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8930   -1.2873    1.3495 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3616    1.0616   -0.2966 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9430    1.7618    0.5417 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5334    1.5829   -1.8209 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0969   -1.2155   -1.4269 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5148    1.5186   -0.8179 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7855   -0.4283   -2.4844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1471   -1.4285   -0.8955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6319   -1.8623    0.4362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2952    0.4358   -1.8692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5840   -1.0596   -2.7625 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
  5  6  1  0
  6  7  1  0
  5  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
  5 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21  3  1  0
 17 10  1  0
  1 23  1  0
  2 24  1  0
  2 25  1  0
  3 26  1  0
  6 27  1  0
  6 28  1  0
  7 29  1  0
  9 30  1  0
  9 31  1  0
 10 32  1  0
 12 33  1  0
 13 34  1  0
 14 35  1  0
 14 36  1  0
 15 37  1  0
 16 38  1  0
 17 39  1  0
 18 40  1  0
 19 41  1  0
 20 42  1  0
 21 43  1  0
 22 44  1  0
M  END

  Mrv0541 05061311402D          

 22 23  0  0  0  0            999 V2000
   -3.2917    4.5884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4847    4.7599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1975    0.0584    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5330    0.8121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0481    1.4796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3030    2.2642    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3536    3.6322    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5466    3.8038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9946    3.1907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1876    3.3622    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6356    2.7491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0836    3.3622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2766    3.1907    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7126    4.0738    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9056    4.2453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6507    5.0300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8437    5.2015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5888    5.9861    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1835    2.5191    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9682    2.2642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2231    1.4796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7382    0.8121    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  8  1  0  0  0  0
  1 17  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5 21  1  0  0  0  0
  6 11  1  0  0  0  0
  7  8  1  0  0  0  0
  7 15  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 20  1  0  0  0  0
 12 13  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0040154

> <DATABASE_NAME>
hmdb

> <SMILES>
OCC1OC(CO)(OCC2OC(O)CC(O)C2O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C12H22O10/c13-2-6-10(18)11(19)12(4-14,22-6)20-3-7-9(17)5(15)1-8(16)21-7/h5-11,13-19H,1-4H2

> <INCHI_KEY>
SMVQCONTAPZYQB-UHFFFAOYSA-N

> <FORMULA>
C12H22O10

> <MOLECULAR_WEIGHT>
326.2971

> <EXACT_MASS>
326.121296924

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_AVERAGE_POLARIZABILITY>
30.96549897000905

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-({[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}methyl)oxane-2,4,5-triol

> <ALOGPS_LOGP>
-2.84

> <JCHEM_LOGP>
-3.6281969006666666

> <ALOGPS_LOGS>
0.12

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.441672396120008

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.880123402223042

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9814326514136305

> <JCHEM_POLAR_SURFACE_AREA>
169.29999999999998

> <JCHEM_REFRACTIVITY>
67.26339999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.28e+02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-({[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}methyl)oxane-2,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0040154
     RDKit          3D
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose
 44 45  0  0  0  0  0  0  0  0999 V2000
   -3.4429    2.5499   -1.6352 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2018    1.8724   -0.7138 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4973    0.6911   -0.1073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3371    1.1008    0.5475 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6123   -0.0947    0.7957 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0479   -0.5469    2.1595 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4488   -1.7127    2.5962 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3011    0.2357    0.6793 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6599   -0.6666    0.8556 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0124    0.0332    0.6524 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9852   -0.9430    0.8453 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2304   -0.3204    0.9478 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1920   -1.2779    0.6372 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3189    0.8647    0.0228 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4535    0.6466   -1.2114 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8694   -0.4224   -1.9706 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0095    0.5265   -0.7798 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3139   -0.3325   -1.6077 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9696   -1.0441   -0.2984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7501   -2.1151    0.1063 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8778   -0.1923   -1.1979 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8476   -0.9624   -1.8125 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9131    3.2908   -1.2474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3953    2.5898    0.1377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2106    1.6064   -1.0897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1638    0.1414    0.5504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9384    0.2903    2.8712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1385   -0.7608    2.1114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3183   -2.3906    1.9250 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7409   -1.1715    1.8249 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6330   -1.4588    0.0797 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1415    0.8302    1.3896 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3817    0.0637    1.9828 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8930   -1.2873    1.3495 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3616    1.0616   -0.2966 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9430    1.7618    0.5417 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5334    1.5829   -1.8209 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0969   -1.2155   -1.4269 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5148    1.5186   -0.8179 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7855   -0.4283   -2.4844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1471   -1.4285   -0.8955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6319   -1.8623    0.4362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2952    0.4358   -1.8692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5840   -1.0596   -2.7625 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
  5  6  1  0
  6  7  1  0
  5  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
  5 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21  3  1  0
 17 10  1  0
  1 23  1  0
  2 24  1  0
  2 25  1  0
  3 26  1  0
  6 27  1  0
  6 28  1  0
  7 29  1  0
  9 30  1  0
  9 31  1  0
 10 32  1  0
 12 33  1  0
 13 34  1  0
 14 35  1  0
 14 36  1  0
 15 37  1  0
 16 38  1  0
 17 39  1  0
 18 40  1  0
 19 41  1  0
 20 42  1  0
 21 43  1  0
 22 44  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      -6.145   8.565   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -4.638   8.885   0.000  0.00  0.00           O+0
HETATM    3  O   UNK     0      -4.102   0.109   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -4.728   1.516   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.823   2.762   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -4.299   4.227   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      -8.127   6.780   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -6.620   7.100   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -5.590   5.956   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -4.084   6.276   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -3.053   5.132   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.023   6.276   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.516   5.956   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0     -10.664   7.604   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -9.157   7.925   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -8.681   9.389   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -7.175   9.709   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -6.699  11.174   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -0.343   4.702   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -1.807   4.227   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.283   2.762   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -1.378   1.516   0.000  0.00  0.00           O+0
CONECT    1    2    8   17                                                  
CONECT    2    1                                                            
CONECT    3    4                                                            
CONECT    4    3    5                                                       
CONECT    5    4    6   21                                                  
CONECT    6    5   11                                                       
CONECT    7    8   15                                                       
CONECT    8    1    7    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11    6   10   12   20                                             
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14   15                                                            
CONECT   15    7   14   16                                                  
CONECT   16   15   17                                                       
CONECT   17    1   16   18                                                  
CONECT   18   17                                                            
CONECT   19   20                                                            
CONECT   20   11   19   21                                                  
CONECT   21    5   20   22                                                  
CONECT   22   21                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

COMPND    HMDB0040154
HETATM    1  O1  UNL     1      -3.443   2.550  -1.635  1.00  0.00           O  
HETATM    2  C1  UNL     1      -4.202   1.872  -0.714  1.00  0.00           C  
HETATM    3  C2  UNL     1      -3.497   0.691  -0.107  1.00  0.00           C  
HETATM    4  O2  UNL     1      -2.337   1.101   0.547  1.00  0.00           O  
HETATM    5  C3  UNL     1      -1.612  -0.095   0.796  1.00  0.00           C  
HETATM    6  C4  UNL     1      -2.048  -0.547   2.159  1.00  0.00           C  
HETATM    7  O3  UNL     1      -1.449  -1.713   2.596  1.00  0.00           O  
HETATM    8  O4  UNL     1      -0.301   0.236   0.679  1.00  0.00           O  
HETATM    9  C5  UNL     1       0.660  -0.667   0.856  1.00  0.00           C  
HETATM   10  C6  UNL     1       2.012   0.033   0.652  1.00  0.00           C  
HETATM   11  O5  UNL     1       2.985  -0.943   0.845  1.00  0.00           O  
HETATM   12  C7  UNL     1       4.230  -0.320   0.948  1.00  0.00           C  
HETATM   13  O6  UNL     1       5.192  -1.278   0.637  1.00  0.00           O  
HETATM   14  C8  UNL     1       4.319   0.865   0.023  1.00  0.00           C  
HETATM   15  C9  UNL     1       3.453   0.647  -1.211  1.00  0.00           C  
HETATM   16  O7  UNL     1       3.869  -0.422  -1.971  1.00  0.00           O  
HETATM   17  C10 UNL     1       2.010   0.527  -0.780  1.00  0.00           C  
HETATM   18  O8  UNL     1       1.314  -0.333  -1.608  1.00  0.00           O  
HETATM   19  C11 UNL     1      -1.970  -1.044  -0.298  1.00  0.00           C  
HETATM   20  O9  UNL     1      -2.750  -2.115   0.106  1.00  0.00           O  
HETATM   21  C12 UNL     1      -2.878  -0.192  -1.198  1.00  0.00           C  
HETATM   22  O10 UNL     1      -3.848  -0.962  -1.813  1.00  0.00           O  
HETATM   23  H1  UNL     1      -2.913   3.291  -1.247  1.00  0.00           H  
HETATM   24  H2  UNL     1      -4.395   2.590   0.138  1.00  0.00           H  
HETATM   25  H3  UNL     1      -5.211   1.606  -1.090  1.00  0.00           H  
HETATM   26  H4  UNL     1      -4.164   0.141   0.550  1.00  0.00           H  
HETATM   27  H5  UNL     1      -1.938   0.290   2.871  1.00  0.00           H  
HETATM   28  H6  UNL     1      -3.139  -0.761   2.111  1.00  0.00           H  
HETATM   29  H7  UNL     1      -1.318  -2.391   1.925  1.00  0.00           H  
HETATM   30  H8  UNL     1       0.741  -1.171   1.825  1.00  0.00           H  
HETATM   31  H9  UNL     1       0.633  -1.459   0.080  1.00  0.00           H  
HETATM   32  H10 UNL     1       2.141   0.830   1.390  1.00  0.00           H  
HETATM   33  H11 UNL     1       4.382   0.064   1.983  1.00  0.00           H  
HETATM   34  H12 UNL     1       5.893  -1.287   1.349  1.00  0.00           H  
HETATM   35  H13 UNL     1       5.362   1.062  -0.297  1.00  0.00           H  
HETATM   36  H14 UNL     1       3.943   1.762   0.542  1.00  0.00           H  
HETATM   37  H15 UNL     1       3.533   1.583  -1.821  1.00  0.00           H  
HETATM   38  H16 UNL     1       4.097  -1.215  -1.427  1.00  0.00           H  
HETATM   39  H17 UNL     1       1.515   1.519  -0.818  1.00  0.00           H  
HETATM   40  H18 UNL     1       1.785  -0.428  -2.484  1.00  0.00           H  
HETATM   41  H19 UNL     1      -1.147  -1.429  -0.895  1.00  0.00           H  
HETATM   42  H20 UNL     1      -3.632  -1.862   0.436  1.00  0.00           H  
HETATM   43  H21 UNL     1      -2.295   0.436  -1.869  1.00  0.00           H  
HETATM   44  H22 UNL     1      -3.584  -1.060  -2.763  1.00  0.00           H  
CONECT    1    2   23
CONECT    2    3   24   25
CONECT    3    4   21   26
CONECT    4    5
CONECT    5    6    8   19
CONECT    6    7   27   28
CONECT    7   29
CONECT    8    9
CONECT    9   10   30   31
CONECT   10   11   17   32
CONECT   11   12
CONECT   12   13   14   33
CONECT   13   34
CONECT   14   15   35   36
CONECT   15   16   17   37
CONECT   16   38
CONECT   17   18   39
CONECT   18   40
CONECT   19   20   21   41
CONECT   20   42
CONECT   21   22   43
CONECT   22   44
END

HMDB0040154
     RDKit          3D
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose
 44 45  0  0  0  0  0  0  0  0999 V2000
   -3.4429    2.5499   -1.6352 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2018    1.8724   -0.7138 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4973    0.6911   -0.1073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3371    1.1008    0.5475 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6123   -0.0947    0.7957 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0479   -0.5469    2.1595 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4488   -1.7127    2.5962 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3011    0.2357    0.6793 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6599   -0.6666    0.8556 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0124    0.0332    0.6524 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9852   -0.9430    0.8453 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2304   -0.3204    0.9478 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1920   -1.2779    0.6372 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3189    0.8647    0.0228 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4535    0.6466   -1.2114 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8694   -0.4224   -1.9706 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0095    0.5265   -0.7798 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3139   -0.3325   -1.6077 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9696   -1.0441   -0.2984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7501   -2.1151    0.1063 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8778   -0.1923   -1.1979 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8476   -0.9624   -1.8125 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9131    3.2908   -1.2474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3953    2.5898    0.1377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2106    1.6064   -1.0897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1638    0.1414    0.5504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9384    0.2903    2.8712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1385   -0.7608    2.1114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3183   -2.3906    1.9250 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7409   -1.1715    1.8249 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6330   -1.4588    0.0797 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1415    0.8302    1.3896 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3817    0.0637    1.9828 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8930   -1.2873    1.3495 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3616    1.0616   -0.2966 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9430    1.7618    0.5417 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5334    1.5829   -1.8209 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0969   -1.2155   -1.4269 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5148    1.5186   -0.8179 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7855   -0.4283   -2.4844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1471   -1.4285   -0.8955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6319   -1.8623    0.4362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2952    0.4358   -1.8692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5840   -1.0596   -2.7625 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
  5  6  1  0
  6  7  1  0
  5  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
  5 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21  3  1  0
 17 10  1  0
  1 23  1  0
  2 24  1  0
  2 25  1  0
  3 26  1  0
  6 27  1  0
  6 28  1  0
  7 29  1  0
  9 30  1  0
  9 31  1  0
 10 32  1  0
 12 33  1  0
 13 34  1  0
 14 35  1  0
 14 36  1  0
 15 37  1  0
 16 38  1  0
 17 39  1  0
 18 40  1  0
 19 41  1  0
 20 42  1  0
 21 43  1  0
 22 44  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
6-O-b-D-Fructofuranosyl-2-deoxy-D-arabino-hexose, 9ci	HMDB

Chemical Formula

C₁₂H₂₂O₁₀

Average Molecular Weight

326.2971

Monoisotopic Molecular Weight

326.121296924

IUPAC Name

6-({[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}methyl)oxane-2,4,5-triol

Traditional Name

6-({[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}methyl)oxane-2,4,5-triol

CAS Registry Number

57440-92-3

SMILES

OCC1OC(CO)(OCC2OC(O)CC(O)C2O)C(O)C1O

InChI Identifier

InChI=1S/C12H22O10/c13-2-6-10(18)11(19)12(4-14,22-6)20-3-7-9(17)5(15)1-8(16)21-7/h5-11,13-19H,1-4H2

InChI Key

SMVQCONTAPZYQB-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as c-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a C-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

C-glycosyl compounds

Alternative Parents

Substituents

C-glycosyl compound
Ketal
Oxane
Monosaccharide
Tetrahydrofuran
Secondary alcohol
Hemiacetal
Oxacycle
Organoheterocyclic compound
Polyol
Acetal
Hydrocarbon derivative
Primary alcohol
Alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Ingestion (HMDB: HMDB0040154)

Source

Exogenous

Exogenous (HMDB: HMDB0040154)

Food

Food (HMDB: HMDB0040154)

Vegetable

Brassica

Brassicas (FooDB: FOOD00857)

Pulse

Pulses (FooDB: FOOD00867)

Endogenous

Plant

Plant (HMDB: HMDB0040154)
Fabaceae (HMDB: HMDB0040154)

Process

Not Available

Role

Biological role

Nutrient (HMDB: HMDB0040154)

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	428 g/L	ALOGPS
logP	-2.8	ALOGPS
logP	-3.6	ChemAxon
logS	0.12	ALOGPS
pKa (Strongest Acidic)	11.88	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	169.3 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	67.26 m³·mol⁻¹	ChemAxon
Polarizability	30.97 Å³	ChemAxon
Number of Rings	2	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]+	174.397	31661259
DarkChem	[M-H]-	167.825	31661259
DeepCCS	[M+H]+	174.241	30932474
DeepCCS	[M-H]-	171.883	30932474
DeepCCS	[M-2H]-	204.833	30932474
DeepCCS	[M+Na]+	180.409	30932474
AllCCS	[M+H]+	174.5	32859911
AllCCS	[M+H-H2O]+	171.5	32859911
AllCCS	[M+NH4]+	177.3	32859911
AllCCS	[M+Na]+	178.2	32859911
AllCCS	[M-H]-	172.4	32859911
AllCCS	[M+Na-2H]-	172.0	32859911
AllCCS	[M+HCOO]-	171.7	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose	OCC1OC(CO)(OCC2OC(O)CC(O)C2O)C(O)C1O	3007.4	Standard polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose	OCC1OC(CO)(OCC2OC(O)CC(O)C2O)C(O)C1O	3030.5	Standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose	OCC1OC(CO)(OCC2OC(O)CC(O)C2O)C(O)C1O	2728.7	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,1TMS,isomer #1	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O)C2O)C(O)C1O	2848.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,1TMS,isomer #2	C[Si](C)(C)OCC1(OCC2OC(O)CC(O)C2O)OC(CO)C(O)C1O	2858.0	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,1TMS,isomer #3	C[Si](C)(C)OC1CC(O)C(O)C(COC2(CO)OC(CO)C(O)C2O)O1	2829.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,1TMS,isomer #4	C[Si](C)(C)OC1CC(O)OC(COC2(CO)OC(CO)C(O)C2O)C1O	2827.1	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,1TMS,isomer #5	C[Si](C)(C)OC1C(O)CC(O)OC1COC1(CO)OC(CO)C(O)C1O	2822.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,1TMS,isomer #6	C[Si](C)(C)OC1C(O)C(CO)OC1(CO)OCC1OC(O)CC(O)C1O	2873.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,1TMS,isomer #7	C[Si](C)(C)OC1C(CO)OC(CO)(OCC2OC(O)CC(O)C2O)C1O	2846.6	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TMS,isomer #1	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O)CC(O)C2O)C(O)C1O	2839.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TMS,isomer #10	C[Si](C)(C)OCC1(OCC2OC(O)CC(O)C2O)OC(CO)C(O[Si](C)(C)C)C1O	2831.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TMS,isomer #11	C[Si](C)(C)OCC1(OCC2OC(O)CC(O)C2O)OC(CO)C(O)C1O[Si](C)(C)C	2846.2	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TMS,isomer #12	C[Si](C)(C)OC1CC(O[Si](C)(C)C)C(O)C(COC2(CO)OC(CO)C(O)C2O)O1	2784.0	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TMS,isomer #13	C[Si](C)(C)OC1CC(O)C(O[Si](C)(C)C)C(COC2(CO)OC(CO)C(O)C2O)O1	2786.5	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TMS,isomer #14	C[Si](C)(C)OC1CC(O)C(O)C(COC2(CO)OC(CO)C(O[Si](C)(C)C)C2O)O1	2801.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TMS,isomer #15	C[Si](C)(C)OC1CC(O)C(O)C(COC2(CO)OC(CO)C(O)C2O[Si](C)(C)C)O1	2827.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TMS,isomer #16	C[Si](C)(C)OC1CC(O)OC(COC2(CO)OC(CO)C(O[Si](C)(C)C)C2O)C1O	2798.5	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TMS,isomer #17	C[Si](C)(C)OC1CC(O)OC(COC2(CO)OC(CO)C(O)C2O[Si](C)(C)C)C1O	2821.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TMS,isomer #18	C[Si](C)(C)OC1CC(O)OC(COC2(CO)OC(CO)C(O)C2O)C1O[Si](C)(C)C	2802.8	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TMS,isomer #19	C[Si](C)(C)OC1C(O)CC(O)OC1COC1(CO)OC(CO)C(O[Si](C)(C)C)C1O	2795.5	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TMS,isomer #2	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C)CC(O)C2O)C(O)C1O	2813.2	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TMS,isomer #20	C[Si](C)(C)OC1C(O)CC(O)OC1COC1(CO)OC(CO)C(O)C1O[Si](C)(C)C	2823.2	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TMS,isomer #21	C[Si](C)(C)OC1C(CO)OC(CO)(OCC2OC(O)CC(O)C2O)C1O[Si](C)(C)C	2857.8	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TMS,isomer #3	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O[Si](C)(C)C)C2O)C(O)C1O	2805.5	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TMS,isomer #4	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O)C2O[Si](C)(C)C)C(O)C1O	2805.8	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TMS,isomer #5	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O)C2O)C(O[Si](C)(C)C)C1O	2855.1	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TMS,isomer #6	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O)C2O)C(O)C1O[Si](C)(C)C	2824.5	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TMS,isomer #7	C[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C)CC(O)C2O)OC(CO)C(O)C1O	2809.5	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TMS,isomer #8	C[Si](C)(C)OCC1(OCC2OC(O)CC(O[Si](C)(C)C)C2O)OC(CO)C(O)C1O	2807.1	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TMS,isomer #9	C[Si](C)(C)OCC1(OCC2OC(O)CC(O)C2O[Si](C)(C)C)OC(CO)C(O)C1O	2812.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #1	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O[Si](C)(C)C)CC(O)C2O)C(O)C1O	2771.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #10	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	2769.6	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #11	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	2775.2	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #12	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	2752.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #13	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2780.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #14	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2761.8	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #15	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2804.2	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #16	C[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C)CC(O[Si](C)(C)C)C2O)OC(CO)C(O)C1O	2750.8	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #17	C[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C)CC(O)C2O[Si](C)(C)C)OC(CO)C(O)C1O	2763.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #18	C[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C)CC(O)C2O)OC(CO)C(O[Si](C)(C)C)C1O	2761.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #19	C[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C)CC(O)C2O)OC(CO)C(O)C1O[Si](C)(C)C	2767.1	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #2	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O)CC(O[Si](C)(C)C)C2O)C(O)C1O	2768.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #20	C[Si](C)(C)OCC1(OCC2OC(O)CC(O[Si](C)(C)C)C2O[Si](C)(C)C)OC(CO)C(O)C1O	2775.6	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #21	C[Si](C)(C)OCC1(OCC2OC(O)CC(O[Si](C)(C)C)C2O)OC(CO)C(O[Si](C)(C)C)C1O	2759.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #22	C[Si](C)(C)OCC1(OCC2OC(O)CC(O[Si](C)(C)C)C2O)OC(CO)C(O)C1O[Si](C)(C)C	2760.1	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #23	C[Si](C)(C)OCC1(OCC2OC(O)CC(O)C2O[Si](C)(C)C)OC(CO)C(O[Si](C)(C)C)C1O	2768.5	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #24	C[Si](C)(C)OCC1(OCC2OC(O)CC(O)C2O[Si](C)(C)C)OC(CO)C(O)C1O[Si](C)(C)C	2772.8	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #25	C[Si](C)(C)OCC1(OCC2OC(O)CC(O)C2O)OC(CO)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2800.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #26	C[Si](C)(C)OC1CC(O[Si](C)(C)C)C(O[Si](C)(C)C)C(COC2(CO)OC(CO)C(O)C2O)O1	2754.0	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #27	C[Si](C)(C)OC1CC(O[Si](C)(C)C)C(O)C(COC2(CO)OC(CO)C(O[Si](C)(C)C)C2O)O1	2746.1	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #28	C[Si](C)(C)OC1CC(O[Si](C)(C)C)C(O)C(COC2(CO)OC(CO)C(O)C2O[Si](C)(C)C)O1	2761.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #29	C[Si](C)(C)OC1CC(O)C(O[Si](C)(C)C)C(COC2(CO)OC(CO)C(O[Si](C)(C)C)C2O)O1	2750.1	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #3	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O)CC(O)C2O[Si](C)(C)C)C(O)C1O	2776.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #30	C[Si](C)(C)OC1CC(O)C(O[Si](C)(C)C)C(COC2(CO)OC(CO)C(O)C2O[Si](C)(C)C)O1	2768.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #31	C[Si](C)(C)OC1CC(O)C(O)C(COC2(CO)OC(CO)C(O[Si](C)(C)C)C2O[Si](C)(C)C)O1	2770.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #32	C[Si](C)(C)OC1CC(O)OC(COC2(CO)OC(CO)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C1O	2760.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #33	C[Si](C)(C)OC1CC(O)OC(COC2(CO)OC(CO)C(O[Si](C)(C)C)C2O)C1O[Si](C)(C)C	2770.1	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #34	C[Si](C)(C)OC1CC(O)OC(COC2(CO)OC(CO)C(O)C2O[Si](C)(C)C)C1O[Si](C)(C)C	2780.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #35	C[Si](C)(C)OC1C(O)CC(O)OC1COC1(CO)OC(CO)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2777.6	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #4	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O)CC(O)C2O)C(O[Si](C)(C)C)C1O	2796.8	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #5	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O)CC(O)C2O)C(O)C1O[Si](C)(C)C	2779.0	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #6	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C)CC(O[Si](C)(C)C)C2O)C(O)C1O	2741.6	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #7	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C)CC(O)C2O[Si](C)(C)C)C(O)C1O	2756.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #8	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C)CC(O)C2O)C(O[Si](C)(C)C)C1O	2776.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TMS,isomer #9	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C)CC(O)C2O)C(O)C1O[Si](C)(C)C	2751.6	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #1	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O[Si](C)(C)C)CC(O[Si](C)(C)C)C2O)C(O)C1O	2704.2	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #10	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O)CC(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2683.6	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #11	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C)CC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	2706.5	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #12	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C)CC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	2703.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #13	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C)CC(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	2687.1	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #14	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C)CC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2722.8	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #15	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C)CC(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2702.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #16	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C)CC(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2717.1	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #17	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2737.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #18	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2720.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #19	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2719.1	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #2	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O[Si](C)(C)C)CC(O)C2O[Si](C)(C)C)C(O)C1O	2718.5	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #20	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2723.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #21	C[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C)CC(O[Si](C)(C)C)C2O[Si](C)(C)C)OC(CO)C(O)C1O	2717.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #22	C[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C)CC(O[Si](C)(C)C)C2O)OC(CO)C(O[Si](C)(C)C)C1O	2696.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #23	C[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C)CC(O[Si](C)(C)C)C2O)OC(CO)C(O)C1O[Si](C)(C)C	2700.6	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #24	C[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C)CC(O)C2O[Si](C)(C)C)OC(CO)C(O[Si](C)(C)C)C1O	2718.2	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #25	C[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C)CC(O)C2O[Si](C)(C)C)OC(CO)C(O)C1O[Si](C)(C)C	2720.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #26	C[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C)CC(O)C2O)OC(CO)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2700.6	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #27	C[Si](C)(C)OCC1(OCC2OC(O)CC(O[Si](C)(C)C)C2O[Si](C)(C)C)OC(CO)C(O[Si](C)(C)C)C1O	2730.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #28	C[Si](C)(C)OCC1(OCC2OC(O)CC(O[Si](C)(C)C)C2O[Si](C)(C)C)OC(CO)C(O)C1O[Si](C)(C)C	2731.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #29	C[Si](C)(C)OCC1(OCC2OC(O)CC(O[Si](C)(C)C)C2O)OC(CO)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2707.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #3	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O[Si](C)(C)C)CC(O)C2O)C(O[Si](C)(C)C)C1O	2674.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #30	C[Si](C)(C)OCC1(OCC2OC(O)CC(O)C2O[Si](C)(C)C)OC(CO)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2712.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #31	C[Si](C)(C)OC1CC(O[Si](C)(C)C)C(O[Si](C)(C)C)C(COC2(CO)OC(CO)C(O[Si](C)(C)C)C2O)O1	2705.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #32	C[Si](C)(C)OC1CC(O[Si](C)(C)C)C(O[Si](C)(C)C)C(COC2(CO)OC(CO)C(O)C2O[Si](C)(C)C)O1	2715.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #33	C[Si](C)(C)OC1CC(O[Si](C)(C)C)C(O)C(COC2(CO)OC(CO)C(O[Si](C)(C)C)C2O[Si](C)(C)C)O1	2691.5	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #34	C[Si](C)(C)OC1CC(O)C(O[Si](C)(C)C)C(COC2(CO)OC(CO)C(O[Si](C)(C)C)C2O[Si](C)(C)C)O1	2706.0	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #35	C[Si](C)(C)OC1CC(O)OC(COC2(CO)OC(CO)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C1O[Si](C)(C)C	2731.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #4	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O[Si](C)(C)C)CC(O)C2O)C(O)C1O[Si](C)(C)C	2662.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #5	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O)CC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	2727.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #6	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O)CC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	2701.2	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #7	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O)CC(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	2698.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #8	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O)CC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2691.8	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TMS,isomer #9	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O)CC(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2679.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TMS,isomer #1	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O[Si](C)(C)C)CC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	2647.8	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TMS,isomer #10	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O)CC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2594.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TMS,isomer #11	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C)CC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2643.2	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TMS,isomer #12	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C)CC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2627.0	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TMS,isomer #13	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C)CC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2621.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TMS,isomer #14	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C)CC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2615.8	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TMS,isomer #15	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2620.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TMS,isomer #16	C[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C)CC(O[Si](C)(C)C)C2O[Si](C)(C)C)OC(CO)C(O[Si](C)(C)C)C1O	2630.2	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TMS,isomer #17	C[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C)CC(O[Si](C)(C)C)C2O[Si](C)(C)C)OC(CO)C(O)C1O[Si](C)(C)C	2643.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TMS,isomer #18	C[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C)CC(O[Si](C)(C)C)C2O)OC(CO)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2604.6	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TMS,isomer #19	C[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C)CC(O)C2O[Si](C)(C)C)OC(CO)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2605.2	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TMS,isomer #2	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O[Si](C)(C)C)CC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	2600.2	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TMS,isomer #20	C[Si](C)(C)OCC1(OCC2OC(O)CC(O[Si](C)(C)C)C2O[Si](C)(C)C)OC(CO)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2605.5	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TMS,isomer #21	C[Si](C)(C)OC1CC(O[Si](C)(C)C)C(O[Si](C)(C)C)C(COC2(CO)OC(CO)C(O[Si](C)(C)C)C2O[Si](C)(C)C)O1	2625.2	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TMS,isomer #3	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O[Si](C)(C)C)CC(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	2598.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TMS,isomer #4	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O[Si](C)(C)C)CC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2597.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TMS,isomer #5	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O[Si](C)(C)C)CC(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2598.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TMS,isomer #6	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O[Si](C)(C)C)CC(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2584.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TMS,isomer #7	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O)CC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2598.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TMS,isomer #8	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O)CC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2599.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TMS,isomer #9	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O)CC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2613.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,6TMS,isomer #1	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O[Si](C)(C)C)CC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2536.1	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,6TMS,isomer #2	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O[Si](C)(C)C)CC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2535.2	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,6TMS,isomer #3	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O[Si](C)(C)C)CC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2533.2	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,6TMS,isomer #4	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O[Si](C)(C)C)CC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2547.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,6TMS,isomer #5	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O)CC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2545.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,6TMS,isomer #6	C[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C)CC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2540.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,6TMS,isomer #7	C[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C)CC(O[Si](C)(C)C)C2O[Si](C)(C)C)OC(CO)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2523.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,7TMS,isomer #1	C[Si](C)(C)OCC1OC(CO[Si](C)(C)C)(OCC2OC(O[Si](C)(C)C)CC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2533.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O)C2O)C(O)C1O	3077.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O)CC(O)C2O)OC(CO)C(O)C1O	3092.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1CC(O)C(O)C(COC2(CO)OC(CO)C(O)C2O)O1	3061.1	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1CC(O)OC(COC2(CO)OC(CO)C(O)C2O)C1O	3068.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1C(O)CC(O)OC1COC1(CO)OC(CO)C(O)C1O	3067.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC1(CO)OCC1OC(O)CC(O)C1O	3108.2	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1C(CO)OC(CO)(OCC2OC(O)CC(O)C2O)C1O	3088.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(CO[Si](C)(C)C(C)(C)C)(OCC2OC(O)CC(O)C2O)C(O)C1O	3256.1	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O)CC(O)C2O)OC(CO)C(O[Si](C)(C)C(C)(C)C)C1O	3265.8	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O)CC(O)C2O)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	3279.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1CC(O[Si](C)(C)C(C)(C)C)C(O)C(COC2(CO)OC(CO)C(O)C2O)O1	3241.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1CC(O)C(O[Si](C)(C)C(C)(C)C)C(COC2(CO)OC(CO)C(O)C2O)O1	3229.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC1CC(O)C(O)C(COC2(CO)OC(CO)C(O[Si](C)(C)C(C)(C)C)C2O)O1	3254.0	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1CC(O)C(O)C(COC2(CO)OC(CO)C(O)C2O[Si](C)(C)C(C)(C)C)O1	3266.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1CC(O)OC(COC2(CO)OC(CO)C(O[Si](C)(C)C(C)(C)C)C2O)C1O	3256.1	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC1CC(O)OC(COC2(CO)OC(CO)C(O)C2O[Si](C)(C)C(C)(C)C)C1O	3273.6	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC1CC(O)OC(COC2(CO)OC(CO)C(O)C2O)C1O[Si](C)(C)C(C)(C)C	3244.8	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC1C(O)CC(O)OC1COC1(CO)OC(CO)C(O[Si](C)(C)C(C)(C)C)C1O	3247.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O)C2O)C(O)C1O	3239.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC1C(O)CC(O)OC1COC1(CO)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	3266.1	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC1C(CO)OC(CO)(OCC2OC(O)CC(O)C2O)C1O[Si](C)(C)C(C)(C)C	3304.0	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	3243.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	3230.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	3282.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	3255.5	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O)C2O)OC(CO)C(O)C1O	3249.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O)CC(O[Si](C)(C)C(C)(C)C)C2O)OC(CO)C(O)C1O	3249.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O)CC(O)C2O[Si](C)(C)C(C)(C)C)OC(CO)C(O)C1O	3238.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(CO[Si](C)(C)C(C)(C)C)(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O)C2O)C(O)C1O	3410.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	3411.2	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O[Si](C)(C)C(C)(C)C)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	3433.1	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	3416.6	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3427.0	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3409.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3445.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O[Si](C)(C)C(C)(C)C)C2O)OC(CO)C(O)C1O	3412.1	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O)C2O[Si](C)(C)C(C)(C)C)OC(CO)C(O)C1O	3406.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O)C2O)OC(CO)C(O[Si](C)(C)C(C)(C)C)C1O	3406.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O)C2O)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	3419.0	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(CO[Si](C)(C)C(C)(C)C)(OCC2OC(O)CC(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	3421.2	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O)CC(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)OC(CO)C(O)C1O	3412.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O)CC(O[Si](C)(C)C(C)(C)C)C2O)OC(CO)C(O[Si](C)(C)C(C)(C)C)C1O	3414.6	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O)CC(O[Si](C)(C)C(C)(C)C)C2O)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	3428.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O)CC(O)C2O[Si](C)(C)C(C)(C)C)OC(CO)C(O[Si](C)(C)C(C)(C)C)C1O	3405.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O)CC(O)C2O[Si](C)(C)C(C)(C)C)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	3420.2	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O)CC(O)C2O)OC(CO)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3439.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC1CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(COC2(CO)OC(CO)C(O)C2O)O1	3405.6	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC1CC(O[Si](C)(C)C(C)(C)C)C(O)C(COC2(CO)OC(CO)C(O[Si](C)(C)C(C)(C)C)C2O)O1	3415.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC1CC(O[Si](C)(C)C(C)(C)C)C(O)C(COC2(CO)OC(CO)C(O)C2O[Si](C)(C)C(C)(C)C)O1	3423.8	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OC1CC(O)C(O[Si](C)(C)C(C)(C)C)C(COC2(CO)OC(CO)C(O[Si](C)(C)C(C)(C)C)C2O)O1	3403.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(CO[Si](C)(C)C(C)(C)C)(OCC2OC(O)CC(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	3407.8	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OC1CC(O)C(O[Si](C)(C)C(C)(C)C)C(COC2(CO)OC(CO)C(O)C2O[Si](C)(C)C(C)(C)C)O1	3414.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC1CC(O)C(O)C(COC2(CO)OC(CO)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)O1	3423.6	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC1CC(O)OC(COC2(CO)OC(CO)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C1O	3436.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC1CC(O)OC(COC2(CO)OC(CO)C(O[Si](C)(C)C(C)(C)C)C2O)C1O[Si](C)(C)C(C)(C)C	3422.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC1CC(O)OC(COC2(CO)OC(CO)C(O)C2O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3434.0	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OC1C(O)CC(O)OC1COC1(CO)OC(CO)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3426.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(CO[Si](C)(C)C(C)(C)C)(OCC2OC(O)CC(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	3435.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(CO[Si](C)(C)C(C)(C)C)(OCC2OC(O)CC(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	3415.5	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	3406.5	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	3396.8	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	3424.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	3407.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(CO[Si](C)(C)C(C)(C)C)(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	3559.1	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OCC1OC(CO[Si](C)(C)C(C)(C)C)(OCC2OC(O)CC(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3567.2	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	3544.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O[Si](C)(C)C(C)(C)C)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	3566.8	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	3560.6	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3556.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3545.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3566.0	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3569.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3561.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O[Si](C)(C)C(C)(C)C)C2O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3588.0	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(CO[Si](C)(C)C(C)(C)C)(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	3550.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3573.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)OC(CO)C(O)C1O	3546.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O[Si](C)(C)C(C)(C)C)C2O)OC(CO)C(O[Si](C)(C)C(C)(C)C)C1O	3553.5	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O[Si](C)(C)C(C)(C)C)C2O)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	3561.0	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O)C2O[Si](C)(C)C(C)(C)C)OC(CO)C(O[Si](C)(C)C(C)(C)C)C1O	3538.2	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O)C2O[Si](C)(C)C(C)(C)C)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	3548.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O)C2O)OC(CO)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3548.5	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O)CC(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)OC(CO)C(O[Si](C)(C)C(C)(C)C)C1O	3550.1	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O)CC(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	3561.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O)CC(O[Si](C)(C)C(C)(C)C)C2O)OC(CO)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3570.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(CO[Si](C)(C)C(C)(C)C)(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	3554.2	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O)CC(O)C2O[Si](C)(C)C(C)(C)C)OC(CO)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3559.1	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC1CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(COC2(CO)OC(CO)C(O[Si](C)(C)C(C)(C)C)C2O)O1	3539.5	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC1CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(COC2(CO)OC(CO)C(O)C2O[Si](C)(C)C(C)(C)C)O1	3553.1	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC1CC(O[Si](C)(C)C(C)(C)C)C(O)C(COC2(CO)OC(CO)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)O1	3559.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC1CC(O)C(O[Si](C)(C)C(C)(C)C)C(COC2(CO)OC(CO)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)O1	3541.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OC1CC(O)OC(COC2(CO)OC(CO)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3561.8	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(CO[Si](C)(C)C(C)(C)C)(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	3552.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(CO[Si](C)(C)C(C)(C)C)(OCC2OC(O)CC(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	3556.1	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OCC1OC(CO[Si](C)(C)C(C)(C)C)(OCC2OC(O)CC(O[Si](C)(C)C(C)(C)C)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	3586.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OCC1OC(CO[Si](C)(C)C(C)(C)C)(OCC2OC(O)CC(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	3582.0	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(CO[Si](C)(C)C(C)(C)C)(OCC2OC(O)CC(O)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3574.5	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OCC1OC(CO[Si](C)(C)C(C)(C)C)(OCC2OC(O)CC(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3565.9	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(CO[Si](C)(C)C(C)(C)C)(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	3678.0	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OCC1OC(CO[Si](C)(C)C(C)(C)C)(OCC2OC(O)CC(O)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3699.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3683.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3680.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O[Si](C)(C)C(C)(C)C)C2O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3690.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3678.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OCC1OC(CO)(OCC2OC(O)CC(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3696.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)OC(CO)C(O[Si](C)(C)C(C)(C)C)C1O	3674.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	3666.2	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O[Si](C)(C)C(C)(C)C)C2O)OC(CO)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3665.1	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O)C2O[Si](C)(C)C(C)(C)C)OC(CO)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3656.5	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(CO[Si](C)(C)C(C)(C)C)(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O[Si](C)(C)C(C)(C)C)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	3679.2	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OCC1(OCC2OC(O)CC(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)OC(CO)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3676.4	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC1CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(COC2(CO)OC(CO)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)O1	3675.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(CO[Si](C)(C)C(C)(C)C)(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	3692.0	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(CO[Si](C)(C)C(C)(C)C)(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3673.6	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(CO[Si](C)(C)C(C)(C)C)(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3682.1	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OCC1OC(CO[Si](C)(C)C(C)(C)C)(OCC2OC(O[Si](C)(C)C(C)(C)C)CC(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3671.3	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OCC1OC(CO[Si](C)(C)C(C)(C)C)(OCC2OC(O)CC(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3685.7	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(CO[Si](C)(C)C(C)(C)C)(OCC2OC(O)CC(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3693.6	Semi standard non polar	33892256
6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose,5TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OCC1OC(CO[Si](C)(C)C(C)(C)C)(OCC2OC(O)CC(O[Si](C)(C)C(C)(C)C)C2O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3705.2	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 - 6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose GC-MS (Non-derivatized) - 70eV, Positive	splash10-0pi0-8492000000-8ee0667834db137634cc	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose GC-MS (5 TMS) - 70eV, Positive	splash10-00di-2911037000-f57b9c5da3774aabfdac	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	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 - 6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose 10V, Positive-QTOF	splash10-056r-1519000000-d1f5fe0f337f679d7998	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose 20V, Positive-QTOF	splash10-00kb-1900000000-2a5c5a9b8fcb68323e17	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose 40V, Positive-QTOF	splash10-01vp-9500000000-7c43833009d979c8c485	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose 10V, Negative-QTOF	splash10-01t9-3913000000-4360c9233ab97402f5ab	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose 20V, Negative-QTOF	splash10-01ta-1900000000-6cea3c68b796675d88be	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose 40V, Negative-QTOF	splash10-0007-9500000000-3fd8da6823d653a0b724	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose 10V, Negative-QTOF	splash10-004i-0439000000-e9b4a2304d643cdc2c35	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose 20V, Negative-QTOF	splash10-08fr-9841000000-e63723bd16adca0672c4	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose 40V, Negative-QTOF	splash10-0006-9100000000-6715d46715e22d00d015	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose 10V, Positive-QTOF	splash10-004i-0129000000-2f8ec3a1159f07daddb3	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose 20V, Positive-QTOF	splash10-004s-4921000000-bcf81770791774119538	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose 40V, Positive-QTOF	splash10-05mt-9600000000-7c2a36b6953ae65cee38	2021-09-23	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB019858

KNApSAcK ID

Not Available

Chemspider ID

35014917

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131752784

PDB ID

Not Available

ChEBI ID

167938

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

(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .

Showing metabocard for 6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose (HMDB0040154)

MOL for HMDB0040154 (6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose)

3D MOL for HMDB0040154 (6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose)

3D SDF for HMDB0040154 (6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose)

3D-SDF for HMDB0040154 (6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose)

PDB for HMDB0040154 (6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose)

3D PDB for HMDB0040154 (6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose)

SMILES for HMDB0040154 (6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose)

INCHI for HMDB0040154 (6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose)

Structure for HMDB0040154 (6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose)

3D Structure for HMDB0040154 (6-O-b-D-Fructofuranosyl-2-deoxy-D-glucose)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra