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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2007-05-30 13:37:56 UTC

Update Date

2021-09-14 15:18:17 UTC

HMDB ID

HMDB0006701

Secondary Accession Numbers

HMDB06701

Metabolite Identification

Common Name

3-O-a-L-Fucopyranosyl-D-glucose

Description

3-O-a-L-Fucopyranosyl-D-glucose belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol. Based on a literature review very few articles have been published on 3-O-a-L-Fucopyranosyl-D-glucose.

Structure

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

HMDB0006701
     RDKit          3D
3-O-a-L-Fucopyranosyl-D-glucose
 44 44  0  0  0  0  0  0  0  0999 V2000
   -3.6315    0.7043    1.3982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5186    1.1932    0.4841 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4044    0.4494    0.7358 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8602   -0.1686   -0.3887 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2452   -0.8596    0.0363 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4388   -0.5085   -0.4858 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8951   -1.6931   -1.3568 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1120   -1.4488   -1.9470 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0301   -2.9271   -0.5254 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0260   -3.2888    0.0757 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5370   -0.2073    0.4761 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8674   -1.2652    1.3104 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2801    1.0085    1.3377 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2600    0.8321    2.2434 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5396    1.3667    2.1244 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6291    1.5628    1.2661 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9417   -1.0309   -0.9809 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6314   -1.7458   -0.0143 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9581   -0.0790   -1.6202 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5795    0.1441   -2.9635 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9324    1.2636   -0.9430 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2034    1.8689   -0.9871 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2517   -0.0412    2.1292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1040    1.5359    1.9626 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3970    0.2213    0.7536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2969    2.2494    0.8176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6205    0.6057   -1.1164 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3933    0.3428   -1.2248 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1517   -1.9178   -2.1364 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5651   -2.3053   -2.1035 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9559   -3.4800   -0.4492 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5065    0.0343   -0.0569 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6134   -1.0569    2.2538 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0426    1.9058    0.7019 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7091    1.6306    2.3725 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8029    0.5622    2.8366 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3992    2.3126    2.6797 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2802    2.1552    1.7542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6043   -1.6957   -1.7747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7933   -2.6952   -0.2830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9658   -0.5077   -1.6240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8329    0.8115   -2.9114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2526    1.9905   -1.4588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4999    2.1713   -0.0988 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
  7  8  1  0
  7  9  1  0
  9 10  2  0
  6 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
  4 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21  2  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  4 27  1  6
  6 28  1  0
  7 29  1  6
  8 30  1  0
  9 31  1  0
 11 32  1  6
 12 33  1  0
 13 34  1  0
 14 35  1  0
 15 36  1  0
 15 37  1  0
 16 38  1  0
 17 39  1  6
 18 40  1  0
 19 41  1  0
 20 42  1  0
 21 43  1  0
 22 44  1  0
M  END


  Mrv0541 02231220482D          

 22 22  0  0  1  0            999 V2000
   14.7241  -10.2457    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.7241  -11.0707    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.0096  -11.4832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2951  -11.0707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2951  -10.2457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0096   -9.8332    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.4385  -11.4832    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.0096  -12.3082    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.5806  -11.4832    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.5806   -9.8332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4385   -9.8332    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.4385   -9.0082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7241   -8.5957    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.7241   -7.7707    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.0096   -9.0082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1021   -8.1558    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.1530   -8.5957    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   16.8675   -9.0082    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.1530   -7.7707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4385   -7.3582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.8675   -7.3582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8675   -6.5332    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  3  2  1  0  0  0  0
  4  3  1  0  0  0  0
  5  4  1  0  0  0  0
  6  5  1  0  0  0  0
  6  1  1  0  0  0  0
  2  7  1  1  0  0  0
  8  3  1  6  0  0  0
  9  4  1  6  0  0  0
 10  5  1  6  0  0  0
  1 11  1  1  0  0  0
 12 11  1  0  0  0  0
 13 12  1  6  0  0  0
 14 13  1  6  0  0  0
 15 13  1  0  0  0  0
 16 15  2  0  0  0  0
 17 12  1  0  0  0  0
 17 18  1  1  0  0  0
 19 17  1  0  0  0  0
 20 19  1  6  0  0  0
 21 19  1  0  0  0  0
 22 21  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0006701

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO)[C@@H](O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C12H22O10/c1-4-7(17)9(19)10(20)12(21-4)22-11(6(16)3-14)8(18)5(15)2-13/h3-13,15-20H,2H2,1H3/t4?,5?,6-,7?,8+,9?,10-,11?,12-/m0/s1

> <INCHI_KEY>
WFLGVJKIXANXQV-CJVZSHCUSA-N

> <FORMULA>
C12H22O10

> <MOLECULAR_WEIGHT>
326.2971

> <EXACT_MASS>
326.121296924

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_AVERAGE_POLARIZABILITY>
30.383739720215694

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,4R)-2,4,5,6-tetrahydroxy-3-{[(2S,3S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}hexanal

> <ALOGPS_LOGP>
-2.22

> <JCHEM_LOGP>
-4.292286241999999

> <ALOGPS_LOGS>
-0.18

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.944210353623241

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.631870125206154

> <JCHEM_PKA_STRONGEST_BASIC>
-2.974227102423715

> <JCHEM_POLAR_SURFACE_AREA>
177.14

> <JCHEM_REFRACTIVITY>
68.2152

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.16e+02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,4R)-2,4,5,6-tetrahydroxy-3-{[(2S,3S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}hexanal

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0006701
     RDKit          3D
3-O-a-L-Fucopyranosyl-D-glucose
 44 44  0  0  0  0  0  0  0  0999 V2000
   -3.6315    0.7043    1.3982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5186    1.1932    0.4841 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4044    0.4494    0.7358 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8602   -0.1686   -0.3887 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2452   -0.8596    0.0363 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4388   -0.5085   -0.4858 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8951   -1.6931   -1.3568 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1120   -1.4488   -1.9470 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0301   -2.9271   -0.5254 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0260   -3.2888    0.0757 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5370   -0.2073    0.4761 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8674   -1.2652    1.3104 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2801    1.0085    1.3377 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2600    0.8321    2.2434 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5396    1.3667    2.1244 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6291    1.5628    1.2661 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9417   -1.0309   -0.9809 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6314   -1.7458   -0.0143 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9581   -0.0790   -1.6202 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5795    0.1441   -2.9635 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9324    1.2636   -0.9430 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2034    1.8689   -0.9871 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2517   -0.0412    2.1292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1040    1.5359    1.9626 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3970    0.2213    0.7536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2969    2.2494    0.8176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6205    0.6057   -1.1164 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3933    0.3428   -1.2248 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1517   -1.9178   -2.1364 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5651   -2.3053   -2.1035 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9559   -3.4800   -0.4492 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5065    0.0343   -0.0569 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6134   -1.0569    2.2538 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0426    1.9058    0.7019 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7091    1.6306    2.3725 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8029    0.5622    2.8366 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3992    2.3126    2.6797 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2802    2.1552    1.7542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6043   -1.6957   -1.7747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7933   -2.6952   -0.2830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9658   -0.5077   -1.6240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8329    0.8115   -2.9114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2526    1.9905   -1.4588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4999    2.1713   -0.0988 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
  7  8  1  0
  7  9  1  0
  9 10  2  0
  6 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
  4 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21  2  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  4 27  1  6
  6 28  1  0
  7 29  1  6
  8 30  1  0
  9 31  1  0
 11 32  1  6
 12 33  1  0
 13 34  1  0
 14 35  1  0
 15 36  1  0
 15 37  1  0
 16 38  1  0
 17 39  1  6
 18 40  1  0
 19 41  1  0
 20 42  1  0
 21 43  1  0
 22 44  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  C   UNK     0      27.485 -19.125   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      27.485 -20.665   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      26.151 -21.435   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      24.818 -20.665   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      24.818 -19.125   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      26.151 -18.355   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      28.819 -21.435   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0      26.151 -22.975   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0      23.484 -21.435   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      23.484 -18.355   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      28.819 -18.355   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      28.819 -16.815   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      27.485 -16.045   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      27.485 -14.505   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      26.151 -16.815   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      24.457 -15.224   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      30.152 -16.045   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      31.486 -16.815   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      30.152 -14.505   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      28.819 -13.735   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      31.486 -13.735   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      31.486 -12.195   0.000  0.00  0.00           O+0
CONECT    1    2    6   11                                                  
CONECT    2    1    3    7                                                  
CONECT    3    2    4    8                                                  
CONECT    4    3    5    9                                                  
CONECT    5    4    6   10                                                  
CONECT    6    5    1                                                       
CONECT    7    2                                                            
CONECT    8    3                                                            
CONECT    9    4                                                            
CONECT   10    5                                                            
CONECT   11    1   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15                                                            
CONECT   17   12   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   44    0
END

COMPND    HMDB0006701
HETATM    1  C1  UNL     1      -3.632   0.704   1.398  1.00  0.00           C  
HETATM    2  C2  UNL     1      -2.519   1.193   0.484  1.00  0.00           C  
HETATM    3  O1  UNL     1      -1.404   0.449   0.736  1.00  0.00           O  
HETATM    4  C3  UNL     1      -0.860  -0.169  -0.389  1.00  0.00           C  
HETATM    5  O2  UNL     1       0.245  -0.860   0.036  1.00  0.00           O  
HETATM    6  C4  UNL     1       1.439  -0.508  -0.486  1.00  0.00           C  
HETATM    7  C5  UNL     1       1.895  -1.693  -1.357  1.00  0.00           C  
HETATM    8  O3  UNL     1       3.112  -1.449  -1.947  1.00  0.00           O  
HETATM    9  C6  UNL     1       2.030  -2.927  -0.525  1.00  0.00           C  
HETATM   10  O4  UNL     1       1.026  -3.289   0.076  1.00  0.00           O  
HETATM   11  C7  UNL     1       2.537  -0.207   0.476  1.00  0.00           C  
HETATM   12  O5  UNL     1       2.867  -1.265   1.310  1.00  0.00           O  
HETATM   13  C8  UNL     1       2.280   1.008   1.338  1.00  0.00           C  
HETATM   14  O6  UNL     1       1.260   0.832   2.243  1.00  0.00           O  
HETATM   15  C9  UNL     1       3.540   1.367   2.124  1.00  0.00           C  
HETATM   16  O7  UNL     1       4.629   1.563   1.266  1.00  0.00           O  
HETATM   17  C10 UNL     1      -1.942  -1.031  -0.981  1.00  0.00           C  
HETATM   18  O8  UNL     1      -2.631  -1.746  -0.014  1.00  0.00           O  
HETATM   19  C11 UNL     1      -2.958  -0.079  -1.620  1.00  0.00           C  
HETATM   20  O9  UNL     1      -2.580   0.144  -2.963  1.00  0.00           O  
HETATM   21  C12 UNL     1      -2.932   1.264  -0.943  1.00  0.00           C  
HETATM   22  O10 UNL     1      -4.203   1.869  -0.987  1.00  0.00           O  
HETATM   23  H1  UNL     1      -3.252  -0.041   2.129  1.00  0.00           H  
HETATM   24  H2  UNL     1      -4.104   1.536   1.963  1.00  0.00           H  
HETATM   25  H3  UNL     1      -4.397   0.221   0.754  1.00  0.00           H  
HETATM   26  H4  UNL     1      -2.297   2.249   0.818  1.00  0.00           H  
HETATM   27  H5  UNL     1      -0.621   0.606  -1.116  1.00  0.00           H  
HETATM   28  H6  UNL     1       1.393   0.343  -1.225  1.00  0.00           H  
HETATM   29  H7  UNL     1       1.152  -1.918  -2.136  1.00  0.00           H  
HETATM   30  H8  UNL     1       3.565  -2.305  -2.104  1.00  0.00           H  
HETATM   31  H9  UNL     1       2.956  -3.480  -0.449  1.00  0.00           H  
HETATM   32  H10 UNL     1       3.507   0.034  -0.057  1.00  0.00           H  
HETATM   33  H11 UNL     1       2.613  -1.057   2.254  1.00  0.00           H  
HETATM   34  H12 UNL     1       2.043   1.906   0.702  1.00  0.00           H  
HETATM   35  H13 UNL     1       0.709   1.631   2.372  1.00  0.00           H  
HETATM   36  H14 UNL     1       3.803   0.562   2.837  1.00  0.00           H  
HETATM   37  H15 UNL     1       3.399   2.313   2.680  1.00  0.00           H  
HETATM   38  H16 UNL     1       5.280   2.155   1.754  1.00  0.00           H  
HETATM   39  H17 UNL     1      -1.604  -1.696  -1.775  1.00  0.00           H  
HETATM   40  H18 UNL     1      -2.793  -2.695  -0.283  1.00  0.00           H  
HETATM   41  H19 UNL     1      -3.966  -0.508  -1.624  1.00  0.00           H  
HETATM   42  H20 UNL     1      -1.833   0.811  -2.911  1.00  0.00           H  
HETATM   43  H21 UNL     1      -2.253   1.990  -1.459  1.00  0.00           H  
HETATM   44  H22 UNL     1      -4.500   2.171  -0.099  1.00  0.00           H  
CONECT    1    2   23   24   25
CONECT    2    3   21   26
CONECT    3    4
CONECT    4    5   17   27
CONECT    5    6
CONECT    6    7   11   28
CONECT    7    8    9   29
CONECT    8   30
CONECT    9   10   10   31
CONECT   11   12   13   32
CONECT   12   33
CONECT   13   14   15   34
CONECT   14   35
CONECT   15   16   36   37
CONECT   16   38
CONECT   17   18   19   39
CONECT   18   40
CONECT   19   20   21   41
CONECT   20   42
CONECT   21   22   43
CONECT   22   44
END

HMDB0006701
     RDKit          3D
3-O-a-L-Fucopyranosyl-D-glucose
 44 44  0  0  0  0  0  0  0  0999 V2000
   -3.6315    0.7043    1.3982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5186    1.1932    0.4841 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4044    0.4494    0.7358 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8602   -0.1686   -0.3887 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2452   -0.8596    0.0363 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4388   -0.5085   -0.4858 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8951   -1.6931   -1.3568 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1120   -1.4488   -1.9470 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0301   -2.9271   -0.5254 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0260   -3.2888    0.0757 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5370   -0.2073    0.4761 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8674   -1.2652    1.3104 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2801    1.0085    1.3377 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2600    0.8321    2.2434 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5396    1.3667    2.1244 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6291    1.5628    1.2661 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9417   -1.0309   -0.9809 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6314   -1.7458   -0.0143 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9581   -0.0790   -1.6202 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5795    0.1441   -2.9635 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9324    1.2636   -0.9430 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2034    1.8689   -0.9871 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2517   -0.0412    2.1292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1040    1.5359    1.9626 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3970    0.2213    0.7536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2969    2.2494    0.8176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6205    0.6057   -1.1164 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3933    0.3428   -1.2248 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1517   -1.9178   -2.1364 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5651   -2.3053   -2.1035 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9559   -3.4800   -0.4492 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5065    0.0343   -0.0569 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6134   -1.0569    2.2538 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0426    1.9058    0.7019 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7091    1.6306    2.3725 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8029    0.5622    2.8366 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3992    2.3126    2.6797 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2802    2.1552    1.7542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6043   -1.6957   -1.7747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7933   -2.6952   -0.2830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9658   -0.5077   -1.6240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8329    0.8115   -2.9114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2526    1.9905   -1.4588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4999    2.1713   -0.0988 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
  7  8  1  0
  7  9  1  0
  9 10  2  0
  6 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
  4 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21  2  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  4 27  1  6
  6 28  1  0
  7 29  1  6
  8 30  1  0
  9 31  1  0
 11 32  1  6
 12 33  1  0
 13 34  1  0
 14 35  1  0
 15 36  1  0
 15 37  1  0
 16 38  1  0
 17 39  1  6
 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
3-O-(6-Deoxy-alpha-L-galactopyranosyl)- D-glucose	HMDB
3-O-alpha-L-Fucopyranosyl-D-glucose	HMDB
3-O-alpha-L-Fucopyranosyl-delta-glucose	HMDB
3-O-a-L-Fucopyranosyl-D-glucose	Generator
3-O-Α-L-fucopyranosyl-D-glucose	Generator

Chemical Formula

C₁₂H₂₂O₁₀

Average Molecular Weight

326.2971

Monoisotopic Molecular Weight

326.121296924

IUPAC Name

(2R,4R)-2,4,5,6-tetrahydroxy-3-{[(2S,3S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}hexanal

Traditional Name

(2R,4R)-2,4,5,6-tetrahydroxy-3-{[(2S,3S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}hexanal

CAS Registry Number

56822-52-7

SMILES

CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO)[C@@H](O)C(O)C1O

InChI Identifier

InChI=1S/C12H22O10/c1-4-7(17)9(19)10(20)12(21-4)22-11(6(16)3-14)8(18)5(15)2-13/h3-13,15-20H,2H2,1H3/t4?,5?,6-,7?,8+,9?,10-,11?,12-/m0/s1

InChI Key

WFLGVJKIXANXQV-CJVZSHCUSA-N

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acyl glycosides

Direct Parent

Fatty acyl glycosides of mono- and disaccharides

Alternative Parents

Substituents

Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
Disaccharide
O-glycosyl compound
Glycosyl compound
Fatty alcohol
Oxane
Alpha-hydroxyaldehyde
Secondary alcohol
Acetal
Oxacycle
Organoheterocyclic compound
Polyol
Organic oxygen compound
Organooxygen compound
Primary alcohol
Hydrocarbon derivative
Carbonyl group
Organic oxide
Aldehyde
Alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Cytoplasm (HMDB: HMDB0006701)
Cell membrane (HMDB: HMDB0006701)

Excreta

Biofluid or Excreta

Urine (HMDB: HMDB0006701)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0006701)

Source

Endogenous

Endogenous (HMDB: HMDB0006701)

Animal

Animal (HMDB: HMDB0006701)

Exogenous

Food

Food (HMDB: HMDB0006701)

Animal origin

Poultry

Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)
Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Equine

Horse (FooDB: FOOD00378)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0006701)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0006701)

Lipid metabolism pathway (HMDB: HMDB0006701)

Biochemical process

Lipid transport (HMDB: HMDB0006701)

Role

Biological role

Energy source (HMDB: HMDB0006701)

Physical Properties

State

Solid

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	216 g/L	ALOGPS
logP	-2.2	ALOGPS
logP	-4.3	ChemAxon
logS	-0.18	ALOGPS
pKa (Strongest Acidic)	11.63	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	177.14 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	68.22 m³·mol⁻¹	ChemAxon
Polarizability	30.38 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]+	176.3	31661259
DarkChem	[M-H]-	169.632	31661259
DeepCCS	[M+H]+	173.73	30932474
DeepCCS	[M-H]-	171.334	30932474
DeepCCS	[M-2H]-	205.47	30932474
DeepCCS	[M+Na]+	180.143	30932474
AllCCS	[M+H]+	173.4	32859911
AllCCS	[M+H-H2O]+	170.6	32859911
AllCCS	[M+NH4]+	176.1	32859911
AllCCS	[M+Na]+	176.8	32859911
AllCCS	[M-H]-	172.0	32859911
AllCCS	[M+Na-2H]-	171.8	32859911
AllCCS	[M+HCOO]-	171.8	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.	1.63 minutes	32390414
Predicted by Siyang on May 30, 2022	11.044 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	8.18 minutes	32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid	354.2 seconds	40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	757.5 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	258.6 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	25.8 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	173.1 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	77.3 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	303.8 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	268.1 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	637.0 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	594.1 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	66.4 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	951.9 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	205.5 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	282.9 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	613.0 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	409.6 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	410.4 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
3-O-a-L-Fucopyranosyl-D-glucose	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO)[C@@H](O)C(O)C1O	4068.7	Standard polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO)[C@@H](O)C(O)C1O	2762.6	Standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO)[C@@H](O)C(O)C1O	2624.8	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
3-O-a-L-Fucopyranosyl-D-glucose,1TMS,isomer #1	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O)C(O)CO)[C@@H](O)C(O)C1O	2706.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,1TMS,isomer #2	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O)C(O)C1O	2702.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,1TMS,isomer #3	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O)C1O	2725.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,1TMS,isomer #4	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O)C(O)C1O	2712.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,1TMS,isomer #5	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C)C(O)C1O	2679.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,1TMS,isomer #6	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO)[C@@H](O)C(O[Si](C)(C)C)C1O	2671.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,1TMS,isomer #7	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO)[C@@H](O)C(O)C1O[Si](C)(C)C	2739.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,1TMS,isomer #8	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(O)CO)[C@@H](O)C(O)C1O	2784.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #1	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O)C(O)C1O	2730.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #10	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C)C(O)C1O	2720.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #11	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O)C(O[Si](C)(C)C)C1O	2697.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #12	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O)C(O)C1O[Si](C)(C)C	2762.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #13	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O)C(O)C1O	2781.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #14	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O)C1O	2722.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #15	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C)C(O)C1O	2741.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #16	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O[Si](C)(C)C)C1O	2724.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #17	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O)C1O[Si](C)(C)C	2783.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #18	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C)[C@@H](O)C(O)C1O	2791.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #19	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O	2722.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #2	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O)C(O)C1O	2753.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #20	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O	2698.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #21	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C	2762.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #22	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O)C(O)C1O	2787.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #23	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2715.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #24	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2716.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #25	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C)C(O)C1O	2782.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #26	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2723.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #27	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(O)CO)[C@@H](O)C(O[Si](C)(C)C)C1O	2761.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #28	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(O)CO)[C@@H](O)C(O)C1O[Si](C)(C)C	2808.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #3	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O)C(O)C1O	2757.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #4	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C)C(O)C1O	2739.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #5	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O)C(O)CO)[C@@H](O)C(O[Si](C)(C)C)C1O	2722.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #6	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O)C(O)CO)[C@@H](O)C(O)C1O[Si](C)(C)C	2783.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #7	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(O)CO)[C@@H](O)C(O)C1O	2808.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #8	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O)C1O	2726.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TMS,isomer #9	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O)C(O)C1O	2714.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #1	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O)C(O)C1O	2672.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #10	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C	2787.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #11	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C)[C@@H](O)C(O)C1O	2780.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #12	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O	2737.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #13	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O	2723.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #14	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C	2775.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #15	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O)C(O)C1O	2776.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #16	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2737.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #17	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2726.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #18	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C)C(O)C1O	2768.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #19	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O)C(O)CO)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2743.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #2	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O)C(O)C1O	2661.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #20	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(O)CO)[C@@H](O)C(O[Si](C)(C)C)C1O	2744.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #21	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(O)CO)[C@@H](O)C(O)C1O[Si](C)(C)C	2790.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #22	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O)C1O	2635.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #23	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C)C(O)C1O	2702.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #24	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O[Si](C)(C)C)C1O	2696.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #25	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O)C1O[Si](C)(C)C	2728.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #26	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@@H](O)C(O)C1O	2786.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #27	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O	2669.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #28	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O	2663.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #29	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C	2699.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #3	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C)C(O)C1O	2707.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #30	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O)C(O)C1O	2758.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #31	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2703.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #32	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2697.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #33	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C)C(O)C1O	2772.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #34	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2706.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #35	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O)C(O[Si](C)(C)C)C1O	2753.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #36	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O)C(O)C1O[Si](C)(C)C	2800.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #37	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C)C(O)C1O	2705.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #38	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O[Si](C)(C)C)C1O	2694.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #39	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O)C1O[Si](C)(C)C	2737.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #4	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O)C(O[Si](C)(C)C)C1O	2695.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #40	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C(O)C1O	2787.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #41	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2749.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #42	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2742.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #43	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O	2809.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #44	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2753.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #45	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O	2796.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #46	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C	2837.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #47	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2717.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #48	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2712.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #49	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O	2784.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #5	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O)C(O)C1O[Si](C)(C)C	2744.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #50	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2724.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #51	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O	2773.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #52	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C	2808.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #53	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2739.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #54	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2788.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #55	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2776.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #56	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(O)CO)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2780.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #6	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O)C(O)C1O	2757.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #7	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O)C(O)C1O	2706.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #8	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O	2750.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TMS,isomer #9	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O	2743.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #1	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O)C(O)C1O	2579.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #10	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2634.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #11	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2641.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #12	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C)C(O)C1O	2625.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #13	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2646.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #14	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O)C(O[Si](C)(C)C)C1O	2613.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #15	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O)C(O)C1O[Si](C)(C)C	2644.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #16	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O	2652.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #17	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O	2646.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #18	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C	2678.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #19	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C(O)C1O	2640.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #2	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O	2638.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #20	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2680.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #21	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2685.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #22	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O	2676.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #23	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2688.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #24	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O	2673.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #25	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C	2688.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #26	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2650.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #27	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2658.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #28	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O	2642.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #29	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2662.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #3	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O	2637.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #30	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O	2629.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #31	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C	2664.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #32	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2666.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #33	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2639.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #34	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2626.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #35	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(O)CO)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2628.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #36	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C)C(O)C1O	2607.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #37	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O[Si](C)(C)C)C1O	2604.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #38	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O)C1O[Si](C)(C)C	2623.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #39	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C(O)C1O	2667.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #4	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C	2655.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #40	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2656.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #41	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2654.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #42	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O	2706.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #43	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2655.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #44	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O	2703.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #45	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C	2714.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #46	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2629.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #47	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2626.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #48	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O	2698.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #49	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2623.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #5	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@@H](O)C(O)C1O	2636.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #50	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O	2692.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #51	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C	2701.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #52	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2659.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #53	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2697.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #54	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2679.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #55	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2678.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #56	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2648.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #57	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2652.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #58	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O	2701.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #59	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2653.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #6	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O	2630.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #60	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O	2695.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #61	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C	2718.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #62	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2704.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #63	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2753.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #64	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2727.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #65	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2734.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #66	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2675.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #67	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2719.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #68	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2700.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #69	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2699.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #7	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O	2629.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #70	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2729.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #8	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C	2649.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TMS,isomer #9	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O)C(O)C1O	2617.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #1	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O	2599.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #10	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C	2624.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #11	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2612.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #12	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2623.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #13	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O	2586.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #14	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2618.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #15	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O	2596.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #16	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C	2609.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #17	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2632.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #18	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2608.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #19	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2615.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #2	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O	2610.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #20	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2599.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #21	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2635.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #22	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2645.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #23	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O	2596.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #24	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2642.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #25	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O	2608.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #26	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C	2623.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #27	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2661.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #28	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2647.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #29	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2643.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #3	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C	2623.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #30	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2633.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #31	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2636.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #32	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2606.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #33	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2614.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #34	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2602.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #35	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2638.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #36	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2612.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #37	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2617.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #38	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O	2630.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #39	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2616.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #4	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C(O)C1O	2577.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #40	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O	2650.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #41	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C	2661.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #42	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2651.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #43	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2686.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #44	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2681.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #45	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2682.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #46	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2617.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #47	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2667.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #48	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2664.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #49	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2660.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #5	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2633.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #50	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2690.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #51	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2639.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #52	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2682.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #53	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2680.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #54	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2679.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #55	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2722.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #56	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2698.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #6	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2634.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #7	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O	2607.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #8	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2635.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TMS,isomer #9	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O	2614.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #1	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2633.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #10	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2641.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #11	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2612.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #12	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2628.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #13	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2636.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #14	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2614.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #15	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2641.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #16	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2626.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #17	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2636.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #18	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2640.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #19	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2629.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #2	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2629.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #20	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2656.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #21	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2626.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #22	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2613.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #23	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2649.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #24	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2650.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #25	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2635.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #26	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2672.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #27	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2649.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #28	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2657.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #3	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O	2613.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #4	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2621.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #5	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O	2627.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #6	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C	2636.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #7	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2631.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #8	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2655.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,6TMS,isomer #9	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2659.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,7TMS,isomer #1	CC1O[C@@H](OC([C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](C=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2648.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,7TMS,isomer #2	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2670.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,7TMS,isomer #3	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2666.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,7TMS,isomer #4	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2642.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,7TMS,isomer #5	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2671.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,7TMS,isomer #6	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O)CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2644.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,7TMS,isomer #7	CC1O[C@@H](OC(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2651.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,7TMS,isomer #8	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2660.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,1TBDMS,isomer #1	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO)[C@@H](O)C(O)C1O	2931.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,1TBDMS,isomer #2	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO)[C@@H](O)C(O)C1O	2934.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,1TBDMS,isomer #3	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O)C1O	2980.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,1TBDMS,isomer #4	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O	2954.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,1TBDMS,isomer #5	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	2925.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,1TBDMS,isomer #6	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	2932.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,1TBDMS,isomer #7	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	2998.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,1TBDMS,isomer #8	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO)[C@@H](O)C(O)C1O	3015.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #1	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO)[C@@H](O)C(O)C1O	3130.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #10	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	3100.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #11	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3109.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #12	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3161.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #13	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO)[C@@H](O)C(O)C1O	3166.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #14	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O)C1O	3156.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #15	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	3185.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #16	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3198.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #17	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3248.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #18	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O	3232.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #19	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	3135.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #2	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O	3184.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #20	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3150.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #21	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3192.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #22	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O	3199.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #23	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3123.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #24	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3129.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #25	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	3165.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #26	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3150.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #27	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3172.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #28	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3221.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #3	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O	3169.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #4	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	3130.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #5	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3139.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #6	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3201.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #7	CC1O[C@@H](OC(C(=CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO)[C@@H](O)C(O)C1O	3190.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #8	CC1O[C@@H](OC([C@H](O[Si](C)(C)C(C)(C)C)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O)C1O	3156.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,2TBDMS,isomer #9	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O	3128.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #1	CC1O[C@@H](OC([C@H](O[Si](C)(C)C(C)(C)C)C(CO)O[Si](C)(C)C(C)(C)C)[C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O	3352.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #10	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3431.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #11	CC1O[C@@H](OC(C(=CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O	3382.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #12	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	3334.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #13	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3365.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #14	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3396.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #15	CC1O[C@@H](OC(C(=CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O	3363.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #16	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3296.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #17	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3304.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #18	CC1O[C@@H](OC(C(=CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	3307.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #19	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3322.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #2	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O	3346.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #20	CC1O[C@@H](OC(C(=CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3313.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #21	CC1O[C@@H](OC(C(=CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3356.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #22	CC1O[C@@H](OC([C@H](O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O)C1O	3301.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #23	CC1O[C@@H](OC([C@H](O[Si](C)(C)C(C)(C)C)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	3337.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #24	CC1O[C@@H](OC([C@H](O[Si](C)(C)C(C)(C)C)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3355.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #25	CC1O[C@@H](OC([C@H](O[Si](C)(C)C(C)(C)C)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3380.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #26	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O	3383.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #27	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	3303.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #28	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3321.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #29	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3345.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #3	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	3301.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #30	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O	3352.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #31	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3288.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #32	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3281.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #33	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	3313.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #34	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3301.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #35	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3329.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #36	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3357.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #37	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	3323.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #38	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3337.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #39	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3372.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #4	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3321.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #40	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O	3371.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #41	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3365.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #42	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3368.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #43	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	3382.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #44	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3394.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #45	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3406.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #46	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3436.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #47	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3317.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #48	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3314.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #49	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	3343.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #5	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3355.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #50	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3341.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #51	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3366.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #52	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3392.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #53	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3302.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #54	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3330.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #55	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3332.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #56	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3347.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #6	CC1O[C@@H](OC(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(O)CO)[C@@H](O)C(O)C1O	3335.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #7	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O	3364.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #8	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	3376.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,3TBDMS,isomer #9	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3396.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #1	CC1O[C@@H](OC([C@H](O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O	3494.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #10	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3473.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #11	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3480.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #12	CC1O[C@@H](OC(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(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	3459.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #13	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3493.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #14	CC1O[C@@H](OC(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(O)CO)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3458.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #15	CC1O[C@@H](OC(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(O)CO)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3497.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #16	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	3508.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #17	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3538.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #18	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3564.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #19	CC1O[C@@H](OC(C(=CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O	3503.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #2	CC1O[C@@H](OC([C@H](O[Si](C)(C)C(C)(C)C)C(CO)O[Si](C)(C)C(C)(C)C)[C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	3501.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #20	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3537.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #21	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3552.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #22	CC1O[C@@H](OC(C(=CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	3509.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #23	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3571.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #24	CC1O[C@@H](OC(C(=CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3538.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #25	CC1O[C@@H](OC(C(=CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3564.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #26	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3501.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #27	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3512.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #28	CC1O[C@@H](OC(C(=CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	3485.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #29	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3533.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #3	CC1O[C@@H](OC([C@H](O[Si](C)(C)C(C)(C)C)C(CO)O[Si](C)(C)C(C)(C)C)[C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3526.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #30	CC1O[C@@H](OC(C(=CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3497.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #31	CC1O[C@@H](OC(C(=CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3538.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #32	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3481.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #33	CC1O[C@@H](OC(C(=CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3456.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #34	CC1O[C@@H](OC(C(=CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3464.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #35	CC1O[C@@H](OC(C(=CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3469.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #36	CC1O[C@@H](OC([C@H](O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	3461.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #37	CC1O[C@@H](OC([C@H](O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3471.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #38	CC1O[C@@H](OC([C@H](O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3489.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #39	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O	3505.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #4	CC1O[C@@H](OC([C@H](O[Si](C)(C)C(C)(C)C)C(CO)O[Si](C)(C)C(C)(C)C)[C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3548.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #40	CC1O[C@@H](OC([C@H](O[Si](C)(C)C(C)(C)C)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3492.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #41	CC1O[C@@H](OC([C@H](O[Si](C)(C)C(C)(C)C)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3504.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #42	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](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(O)C1O	3523.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #43	CC1O[C@@H](OC([C@H](O[Si](C)(C)C(C)(C)C)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3523.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #44	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3540.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #45	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3569.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #46	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3476.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #47	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3484.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #48	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	3498.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #49	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3502.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #5	CC1O[C@@H](OC(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(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O	3504.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #50	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3518.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #51	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3548.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #52	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3471.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #53	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3488.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #54	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3484.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #55	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3502.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #56	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3481.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #57	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3495.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #58	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)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(O)C1O	3512.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #59	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3516.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #6	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	3484.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #60	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3532.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #61	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3563.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #62	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3538.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #63	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3553.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #64	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3549.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #65	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3576.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #66	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3490.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #67	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3512.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #68	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3511.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #69	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3535.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #7	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3515.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #70	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3510.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #8	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3533.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,4TBDMS,isomer #9	CC1O[C@@H](OC(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(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O	3493.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #1	CC1O[C@@H](OC([C@H](O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	3655.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #10	CC1O[C@@H](OC(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(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3689.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #11	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3667.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #12	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3687.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #13	CC1O[C@@H](OC(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(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	3639.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #14	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3695.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #15	CC1O[C@@H](OC(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(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3652.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #16	CC1O[C@@H](OC(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(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3684.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #17	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3659.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #18	CC1O[C@@H](OC(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(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3621.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #19	CC1O[C@@H](OC(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(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3641.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #2	CC1O[C@@H](OC([C@H](O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3672.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #20	CC1O[C@@H](OC(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(O)CO)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3642.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #21	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3679.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #22	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3705.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #23	CC1O[C@@H](OC(C(=CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)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(O)C1O	3640.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #24	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3712.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #25	CC1O[C@@H](OC(C(=CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3655.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #26	CC1O[C@@H](OC(C(=CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3694.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #27	CC1O[C@@H](OC([C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3711.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #28	CC1O[C@@H](OC(C(=CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3664.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #29	CC1O[C@@H](OC(C(=CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3685.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #3	CC1O[C@@H](OC([C@H](O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3695.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #30	CC1O[C@@H](OC(C(=CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3692.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #31	CC1O[C@@H](OC([C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3677.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #32	CC1O[C@@H](OC(C(=CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3636.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #33	CC1O[C@@H](OC(C(=CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3661.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #34	CC1O[C@@H](OC(C(=CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3668.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #35	CC1O[C@@H](OC(C(=CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3634.9	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #36	CC1O[C@@H](OC([C@H](O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3650.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #37	CC1O[C@@H](OC([C@H](O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3671.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #38	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)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(O)C1O	3653.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #39	CC1O[C@@H](OC([C@H](O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3672.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #4	CC1O[C@@H](OC(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(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O	3647.7	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #40	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3661.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #41	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)C1O[Si](C)(C)C(C)(C)C	3692.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #42	CC1O[C@@H](OC([C@H](O[Si](C)(C)C(C)(C)C)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3690.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #43	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](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(O[Si](C)(C)C(C)(C)C)C1O	3674.0	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #44	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](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(O)C1O[Si](C)(C)C(C)(C)C	3694.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #45	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3699.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #46	CC1O[C@@H](OC([C@@H](O)C=O)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3672.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #47	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3666.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #48	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3683.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #49	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3689.8	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #5	CC1O[C@@H](OC([C@H](O[Si](C)(C)C(C)(C)C)C(CO)O[Si](C)(C)C(C)(C)C)[C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3678.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #50	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C(O)CO)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3666.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #51	CC1O[C@@H](OC([C@H](O)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)C=O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3677.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #52	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)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(O[Si](C)(C)C(C)(C)C)C1O	3665.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #53	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)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(O)C1O[Si](C)(C)C(C)(C)C	3683.4	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #54	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3689.6	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #55	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3710.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #56	CC1O[C@@H](OC(C(O)=CO[Si](C)(C)C(C)(C)C)[C@H](O)C(O)CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3672.5	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #6	CC1O[C@@H](OC([C@H](O[Si](C)(C)C(C)(C)C)C(CO)O[Si](C)(C)C(C)(C)C)[C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3692.3	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #7	CC1O[C@@H](OC(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(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)C1O	3651.2	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #8	CC1O[C@@H](OC([C@H](O[Si](C)(C)C(C)(C)C)C(CO)O[Si](C)(C)C(C)(C)C)[C@H](C=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3699.1	Semi standard non polar	33892256
3-O-a-L-Fucopyranosyl-D-glucose,5TBDMS,isomer #9	CC1O[C@@H](OC(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(CO)O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)C1O	3659.7	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 - 3-O-a-L-Fucopyranosyl-D-glucose GC-MS (Non-derivatized) - 70eV, Positive	splash10-0aos-9273000000-ec95f81eaa9248e3d40d	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-O-a-L-Fucopyranosyl-D-glucose GC-MS (5 TMS) - 70eV, Positive	splash10-00di-4101029000-db63e7852c62da20a8ab	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-O-a-L-Fucopyranosyl-D-glucose GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-O-a-L-Fucopyranosyl-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 - 3-O-a-L-Fucopyranosyl-D-glucose 10V, Positive-QTOF	splash10-0bw9-1916000000-39416eeae50a13a70f0f	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-O-a-L-Fucopyranosyl-D-glucose 20V, Positive-QTOF	splash10-08gi-5900000000-4aed1c81e58e01f174dc	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-O-a-L-Fucopyranosyl-D-glucose 40V, Positive-QTOF	splash10-08fr-9600000000-530d0e079e50a204c5bb	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-O-a-L-Fucopyranosyl-D-glucose 10V, Negative-QTOF	splash10-0cg3-7793000000-5cf8354c214843d41cf4	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-O-a-L-Fucopyranosyl-D-glucose 20V, Negative-QTOF	splash10-08fr-5931000000-99f88726f4243f3661b8	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-O-a-L-Fucopyranosyl-D-glucose 40V, Negative-QTOF	splash10-0bt9-9700000000-34215cca6c597371175e	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-O-a-L-Fucopyranosyl-D-glucose 10V, Negative-QTOF	splash10-004m-4389000000-91932607a5c34ee76a2e	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-O-a-L-Fucopyranosyl-D-glucose 20V, Negative-QTOF	splash10-01vn-6921000000-0cf03aef522636b140a2	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-O-a-L-Fucopyranosyl-D-glucose 40V, Negative-QTOF	splash10-0a4l-9100000000-1ffeca759e99ece2b9a3	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-O-a-L-Fucopyranosyl-D-glucose 10V, Positive-QTOF	splash10-0bt9-0935000000-2046baf2d5abcb317f61	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-O-a-L-Fucopyranosyl-D-glucose 20V, Positive-QTOF	splash10-022c-8900000000-22a35255a2741c1c6fbf	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-O-a-L-Fucopyranosyl-D-glucose 40V, Positive-QTOF	splash10-0a6r-9400000000-8fbcd220a856ecada0a3	2021-09-24	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	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

FDB024033

KNApSAcK ID

Not Available

Chemspider ID

35016017

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

53477882

PDB ID

Not Available

ChEBI ID

168871

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Ajisaka, Katsumi; Shirakabe, Mayumi. Regioselective synthesis of a-L-fucosyl-containing disaccharides by use of a-L-fucosidases of various origins. Carbohydrate Research (1992), 224 291-9.

Material Safety Data Sheet (MSDS)

Not Available

General References

DiCioccio RA, Barlow JJ, Matta KL: Substrate specificity and other properties of alpha-L-fucosidase from human serum. J Biol Chem. 1982 Jan 25;257(2):714-8. [PubMed:7054178 ]
Bachner M, Alain T: [Future of psychiatry--a medical specialty or an interdisciplinary activity?]. Lakartidningen. 1992 May 6;89(19):1652-3; discussion 1653-4. [PubMed:1579031 ]

Showing metabocard for 3-O-a-L-Fucopyranosyl-D-glucose (HMDB0006701)

MOL for HMDB0006701 (3-O-a-L-Fucopyranosyl-D-glucose)

3D MOL for HMDB0006701 (3-O-a-L-Fucopyranosyl-D-glucose)

3D SDF for HMDB0006701 (3-O-a-L-Fucopyranosyl-D-glucose)

3D-SDF for HMDB0006701 (3-O-a-L-Fucopyranosyl-D-glucose)

PDB for HMDB0006701 (3-O-a-L-Fucopyranosyl-D-glucose)

3D PDB for HMDB0006701 (3-O-a-L-Fucopyranosyl-D-glucose)

SMILES for HMDB0006701 (3-O-a-L-Fucopyranosyl-D-glucose)

INCHI for HMDB0006701 (3-O-a-L-Fucopyranosyl-D-glucose)

Structure for HMDB0006701 (3-O-a-L-Fucopyranosyl-D-glucose)

3D Structure for HMDB0006701 (3-O-a-L-Fucopyranosyl-D-glucose)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra