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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 00:12:06 UTC

Update Date

2022-03-07 02:55:57 UTC

HMDB ID

HMDB0038854

Secondary Accession Numbers

HMDB38854

Metabolite Identification

Common Name

3-O-beta-D-Galactopyranosyl-L-arabinose

Description

3-O-beta-D-Galactopyranosyl-L-arabinose, also known as 3-O-galactosylarabinose or arabinosylgalactose, belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. Based on a literature review very few articles have been published on 3-O-beta-D-Galactopyranosyl-L-arabinose.

Structure

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

HMDB0038854
     RDKit          3D
3-O-beta-D-Galactopyranosyl-L-arabinose
 41 42  0  0  0  0  0  0  0  0999 V2000
    1.6912    0.0840   -2.6236 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3261   -0.4307   -1.4855 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7094    0.6514   -0.5243 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6249    1.3565   -0.0811 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6943    0.6215    0.6299 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0969   -0.0328   -0.2750 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3907    0.3299   -0.3572 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9148    0.5894   -1.7390 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1963   -0.6355   -2.3873 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2764    1.2654   -1.5580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8056    0.9231   -0.3067 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6766   -0.4314   -0.0368 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4367   -0.7316    1.0829 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2323   -0.8536    0.1458 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9229   -1.1282    1.4581 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3823   -0.1995    1.6381 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7667   -0.2178    2.8912 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7524    0.3901    1.8868 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3328   -0.2346    2.9845 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5714    0.1881    0.6225 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9235   -1.1408    0.5543 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1178   -0.1998   -3.4571 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7018   -1.2310   -1.0932 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2772   -0.8984   -1.8506 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3249    1.3932   -1.1163 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0917    1.4062    1.1925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6709    1.1579    0.3562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2504    1.1390   -2.3917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9199   -0.4365   -3.0443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9730    0.9374   -2.3584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1437    2.3582   -1.5992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1237   -0.9631   -0.9270 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6801   -1.6734    1.1524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9593   -1.6981   -0.5497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5098   -1.8419    1.7755 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5377   -1.2481    1.2796 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8906    0.6014    3.3940 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6303    1.4782    2.0280 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1345    0.2213    3.8369 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5086    0.8012    0.6682 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1894   -1.6665    0.1843 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
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
  5 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20  3  1  0
 14  7  1  0
  1 22  1  0
  2 23  1  0
  2 24  1  0
  3 25  1  6
  5 26  1  1
  7 27  1  1
  8 28  1  6
  9 29  1  0
 10 30  1  0
 10 31  1  0
 12 32  1  0
 13 33  1  0
 14 34  1  6
 15 35  1  0
 16 36  1  6
 17 37  1  0
 18 38  1  1
 19 39  1  0
 20 40  1  1
 21 41  1  0
M  END


  Mrv0541 02011301562D          

 21 22  0  0  0  0            999 V2000
   -7.2548    4.7851    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9693    4.3725    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.9693    3.5475    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.2548    3.1350    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.5403    3.5475    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.5403    4.3725    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.8258    3.1350    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2548    2.3100    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6837    3.1350    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6837    4.7850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3982    4.3725    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5883    6.9285    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4133    6.9285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8258    6.2140    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.4133    5.4995    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5883    5.4995    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1758    6.2140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3508    6.2140    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1758    4.7850    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8258    4.7850    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6508    6.2140    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6 20  1  1  0  0  0
  5  7  1  6  0  0  0
  4  8  1  1  0  0  0
  3  9  1  1  0  0  0
  2 10  1  1  0  0  0
 10 11  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  0  0  0  0
 16 19  1  6  0  0  0
 15 20  1  1  0  0  0
 14 21  1  1  0  0  0
M  END
> <DATABASE_ID>
HMDB0038854

> <DATABASE_NAME>
hmdb

> <SMILES>
OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C11H20O10/c12-1-4-5(14)6(15)7(16)11(20-4)21-9-3(13)2-19-10(18)8(9)17/h3-18H,1-2H2/t3-,4+,5-,6-,7+,8+,9-,10?,11-/m0/s1

> <INCHI_KEY>
XSXQXHMPBBNYRD-ANYLNHRWSA-N

> <FORMULA>
C11H20O10

> <MOLECULAR_WEIGHT>
312.2705

> <EXACT_MASS>
312.10564686

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_AVERAGE_POLARIZABILITY>
28.099966875029196

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-{[(3R,4S,5S)-2,3,5-trihydroxyoxan-4-yl]oxy}oxane-3,4,5-triol

> <ALOGPS_LOGP>
-2.96

> <JCHEM_LOGP>
-4.073039921666666

> <ALOGPS_LOGS>
0.29

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.193359532781551

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.26510860852641

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810835653347967

> <JCHEM_POLAR_SURFACE_AREA>
169.29999999999998

> <JCHEM_REFRACTIVITY>
62.3742

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.12e+02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-{[(3R,4S,5S)-2,3,5-trihydroxyoxan-4-yl]oxy}oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0038854
     RDKit          3D
3-O-beta-D-Galactopyranosyl-L-arabinose
 41 42  0  0  0  0  0  0  0  0999 V2000
    1.6912    0.0840   -2.6236 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3261   -0.4307   -1.4855 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7094    0.6514   -0.5243 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6249    1.3565   -0.0811 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6943    0.6215    0.6299 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0969   -0.0328   -0.2750 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3907    0.3299   -0.3572 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9148    0.5894   -1.7390 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1963   -0.6355   -2.3873 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2764    1.2654   -1.5580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8056    0.9231   -0.3067 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6766   -0.4314   -0.0368 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4367   -0.7316    1.0829 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2323   -0.8536    0.1458 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9229   -1.1282    1.4581 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3823   -0.1995    1.6381 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7667   -0.2178    2.8912 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7524    0.3901    1.8868 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3328   -0.2346    2.9845 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5714    0.1881    0.6225 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9235   -1.1408    0.5543 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1178   -0.1998   -3.4571 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7018   -1.2310   -1.0932 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2772   -0.8984   -1.8506 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3249    1.3932   -1.1163 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0917    1.4062    1.1925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6709    1.1579    0.3562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2504    1.1390   -2.3917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9199   -0.4365   -3.0443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9730    0.9374   -2.3584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1437    2.3582   -1.5992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1237   -0.9631   -0.9270 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6801   -1.6734    1.1524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9593   -1.6981   -0.5497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5098   -1.8419    1.7755 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5377   -1.2481    1.2796 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8906    0.6014    3.3940 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6303    1.4782    2.0280 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1345    0.2213    3.8369 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5086    0.8012    0.6682 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1894   -1.6665    0.1843 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
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
  5 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20  3  1  0
 14  7  1  0
  1 22  1  0
  2 23  1  0
  2 24  1  0
  3 25  1  6
  5 26  1  1
  7 27  1  1
  8 28  1  6
  9 29  1  0
 10 30  1  0
 10 31  1  0
 12 32  1  0
 13 33  1  0
 14 34  1  6
 15 35  1  0
 16 36  1  6
 17 37  1  0
 18 38  1  1
 19 39  1  0
 20 40  1  1
 21 41  1  0
M  END

HEADER    PROTEIN                                 01-FEB-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   01-FEB-13         0                                  
HETATM    1  O   UNK     0     -13.542   8.932   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0     -14.876   8.162   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -14.876   6.622   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -13.542   5.852   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -12.209   6.622   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -12.209   8.162   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0     -10.875   5.852   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0     -13.542   4.312   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0     -16.210   5.852   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0     -16.210   8.932   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0     -17.543   8.162   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0      -8.565  12.933   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0     -10.105  12.933   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -10.875  11.599   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -10.105  10.266   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -8.565  10.266   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -7.795  11.599   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -6.255  11.599   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -7.795   8.932   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0     -10.875   8.932   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0     -12.415  11.599   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   10                                                  
CONECT    3    2    4    9                                                  
CONECT    4    3    5    8                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1   20                                                  
CONECT    7    5                                                            
CONECT    8    4                                                            
CONECT    9    3                                                            
CONECT   10    2   11                                                       
CONECT   11   10                                                            
CONECT   12   13   17                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   21                                                  
CONECT   15   14   16   20                                                  
CONECT   16   15   17   19                                                  
CONECT   17   16   12   18                                                  
CONECT   18   17                                                            
CONECT   19   16                                                            
CONECT   20    6   15                                                       
CONECT   21   14                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   44    0
END

COMPND    HMDB0038854
HETATM    1  O1  UNL     1       1.691   0.084  -2.624  1.00  0.00           O  
HETATM    2  C1  UNL     1       2.326  -0.431  -1.485  1.00  0.00           C  
HETATM    3  C2  UNL     1       2.709   0.651  -0.524  1.00  0.00           C  
HETATM    4  O2  UNL     1       1.625   1.357  -0.081  1.00  0.00           O  
HETATM    5  C3  UNL     1       0.694   0.621   0.630  1.00  0.00           C  
HETATM    6  O3  UNL     1      -0.097  -0.033  -0.275  1.00  0.00           O  
HETATM    7  C4  UNL     1      -1.391   0.330  -0.357  1.00  0.00           C  
HETATM    8  C5  UNL     1      -1.915   0.589  -1.739  1.00  0.00           C  
HETATM    9  O4  UNL     1      -2.196  -0.636  -2.387  1.00  0.00           O  
HETATM   10  C6  UNL     1      -3.276   1.265  -1.558  1.00  0.00           C  
HETATM   11  O5  UNL     1      -3.806   0.923  -0.307  1.00  0.00           O  
HETATM   12  C7  UNL     1      -3.677  -0.431  -0.037  1.00  0.00           C  
HETATM   13  O6  UNL     1      -4.437  -0.732   1.083  1.00  0.00           O  
HETATM   14  C8  UNL     1      -2.232  -0.854   0.146  1.00  0.00           C  
HETATM   15  O7  UNL     1      -1.923  -1.128   1.458  1.00  0.00           O  
HETATM   16  C9  UNL     1       1.382  -0.199   1.638  1.00  0.00           C  
HETATM   17  O8  UNL     1       0.767  -0.218   2.891  1.00  0.00           O  
HETATM   18  C10 UNL     1       2.752   0.390   1.887  1.00  0.00           C  
HETATM   19  O9  UNL     1       3.333  -0.235   2.985  1.00  0.00           O  
HETATM   20  C11 UNL     1       3.571   0.188   0.622  1.00  0.00           C  
HETATM   21  O10 UNL     1       3.924  -1.141   0.554  1.00  0.00           O  
HETATM   22  H1  UNL     1       2.118  -0.200  -3.457  1.00  0.00           H  
HETATM   23  H2  UNL     1       1.702  -1.231  -1.093  1.00  0.00           H  
HETATM   24  H3  UNL     1       3.277  -0.898  -1.851  1.00  0.00           H  
HETATM   25  H4  UNL     1       3.325   1.393  -1.116  1.00  0.00           H  
HETATM   26  H5  UNL     1       0.092   1.406   1.193  1.00  0.00           H  
HETATM   27  H6  UNL     1      -1.671   1.158   0.356  1.00  0.00           H  
HETATM   28  H7  UNL     1      -1.250   1.139  -2.392  1.00  0.00           H  
HETATM   29  H8  UNL     1      -2.920  -0.437  -3.044  1.00  0.00           H  
HETATM   30  H9  UNL     1      -3.973   0.937  -2.358  1.00  0.00           H  
HETATM   31  H10 UNL     1      -3.144   2.358  -1.599  1.00  0.00           H  
HETATM   32  H11 UNL     1      -4.124  -0.963  -0.927  1.00  0.00           H  
HETATM   33  H12 UNL     1      -4.680  -1.673   1.152  1.00  0.00           H  
HETATM   34  H13 UNL     1      -1.959  -1.698  -0.550  1.00  0.00           H  
HETATM   35  H14 UNL     1      -2.510  -1.842   1.776  1.00  0.00           H  
HETATM   36  H15 UNL     1       1.538  -1.248   1.280  1.00  0.00           H  
HETATM   37  H16 UNL     1       0.891   0.601   3.394  1.00  0.00           H  
HETATM   38  H17 UNL     1       2.630   1.478   2.028  1.00  0.00           H  
HETATM   39  H18 UNL     1       3.135   0.221   3.837  1.00  0.00           H  
HETATM   40  H19 UNL     1       4.509   0.801   0.668  1.00  0.00           H  
HETATM   41  H20 UNL     1       3.189  -1.667   0.184  1.00  0.00           H  
CONECT    1    2   22
CONECT    2    3   23   24
CONECT    3    4   20   25
CONECT    4    5
CONECT    5    6   16   26
CONECT    6    7
CONECT    7    8   14   27
CONECT    8    9   10   28
CONECT    9   29
CONECT   10   11   30   31
CONECT   11   12
CONECT   12   13   14   32
CONECT   13   33
CONECT   14   15   34
CONECT   15   35
CONECT   16   17   18   36
CONECT   17   37
CONECT   18   19   20   38
CONECT   19   39
CONECT   20   21   40
CONECT   21   41
END

HMDB0038854
     RDKit          3D
3-O-beta-D-Galactopyranosyl-L-arabinose
 41 42  0  0  0  0  0  0  0  0999 V2000
    1.6912    0.0840   -2.6236 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3261   -0.4307   -1.4855 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7094    0.6514   -0.5243 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6249    1.3565   -0.0811 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6943    0.6215    0.6299 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0969   -0.0328   -0.2750 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3907    0.3299   -0.3572 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9148    0.5894   -1.7390 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1963   -0.6355   -2.3873 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2764    1.2654   -1.5580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8056    0.9231   -0.3067 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6766   -0.4314   -0.0368 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4367   -0.7316    1.0829 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2323   -0.8536    0.1458 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9229   -1.1282    1.4581 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3823   -0.1995    1.6381 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7667   -0.2178    2.8912 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7524    0.3901    1.8868 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3328   -0.2346    2.9845 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5714    0.1881    0.6225 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9235   -1.1408    0.5543 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1178   -0.1998   -3.4571 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7018   -1.2310   -1.0932 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2772   -0.8984   -1.8506 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3249    1.3932   -1.1163 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0917    1.4062    1.1925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6709    1.1579    0.3562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2504    1.1390   -2.3917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9199   -0.4365   -3.0443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9730    0.9374   -2.3584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1437    2.3582   -1.5992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1237   -0.9631   -0.9270 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6801   -1.6734    1.1524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9593   -1.6981   -0.5497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5098   -1.8419    1.7755 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5377   -1.2481    1.2796 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8906    0.6014    3.3940 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6303    1.4782    2.0280 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1345    0.2213    3.8369 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5086    0.8012    0.6682 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1894   -1.6665    0.1843 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
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
  5 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20  3  1  0
 14  7  1  0
  1 22  1  0
  2 23  1  0
  2 24  1  0
  3 25  1  6
  5 26  1  1
  7 27  1  1
  8 28  1  6
  9 29  1  0
 10 30  1  0
 10 31  1  0
 12 32  1  0
 13 33  1  0
 14 34  1  6
 15 35  1  0
 16 36  1  6
 17 37  1  0
 18 38  1  1
 19 39  1  0
 20 40  1  1
 21 41  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
3-O-Galactosylarabinose	ChEBI
O(3)-beta-D-Galactopyranosyl-D-arabinose	ChEBI
O(3)-b-D-Galactopyranosyl-D-arabinose	Generator
O(3)-Β-D-galactopyranosyl-D-arabinose	Generator
3-O-b-D-Galactopyranosyl-L-arabinose	Generator
3-O-Β-D-galactopyranosyl-L-arabinose	Generator
3-O-Galactosylarabinose, (L-ara)-isomer	MeSH
Arabinosylgalactose	MeSH
Galactosylarabinose	MeSH
2-Methyl-3-(2-methylphenyl)-4(3H)-quinazolinone	HMDB
2-Methyl-3-(2-methylphenyl)-4-quinazolinone	HMDB
2-Methyl-3-(2-methylphenyl)quinazolin-4(3H)-one	HMDB
2-Methyl-3-(2-methylphenyl)quinazolin-4-one	HMDB
2-Methyl-3-(2-tolyl)quinazol-4-one	HMDB
2-Methyl-3-(O-tolyl)-3,4-dihydro-4-quinazolinone	HMDB
2-Methyl-3-(O-tolyl)-4(3H)-quinazolinone hydrochloride	HMDB
2-Methyl-3-(O-tolyl)-4-quinazolone hydrochloride	HMDB
2-Methyl-3-O--tolyl-4(3H)-quinazolinone	HMDB
2-Methyl-3-O-tolyl-3H-quinazolin-4-one	HMDB
2-Methyl-3-O-tolyl-4 (3H)-chinazolinon	HMDB
2-Methyl-3-O-tolyl-4(3H)-chinazolinon	HMDB
2-Methyl-3-O-tolyl-4(3H)-chinazolone	HMDB
2-Methyl-3-O-tolyl-4(3H)-quinazolinone	HMDB
2-Methyl-3-O-tolyl-4-quinazolone	HMDB
2-Methyl-3-tolyl-4-oxybensdiazine	HMDB
2-Methyl-3-tolylchinazolon-4 hydrochloride	HMDB
3,4-dihydro-2-Methyl-4-oxo-3-O-tolylquinazoline	HMDB
Aqual	HMDB
Cateudyl	HMDB
Citexal	HMDB
Diamthazole dihydrochloride	HMDB
Dormigoa	HMDB
Dormigoa-schlafmittel	HMDB
Dormogen	HMDB
Dormutil	HMDB
Dorsedin	HMDB
Fadormir	HMDB
Holodorm	HMDB
Hyminal	HMDB
Hypocol	HMDB
Hyptor	HMDB
Hyptor base	HMDB
Ipnofil	HMDB
MAOA	HMDB
Melsed	HMDB
Melsedin base	HMDB
Melsomin	HMDB
Mequin	HMDB
Metachalon	HMDB
Metacualona	HMDB
Metakvalon	HMDB
Metaqualon	HMDB
Metaqualone	HMDB
Methachalonum	HMDB
Methaqualon	HMDB
Methaqualone	HMDB
Methaqualone hydrochloride	HMDB
Methaqualoneinone	HMDB
Methaqualonum	HMDB
Methased	HMDB
Methyl-O-tolylquinazolone	HMDB
Methylquinazolone hydrochloride	HMDB
Metolquizolone	HMDB
Mollinox	HMDB
Motolon	HMDB
Mozambin	HMDB
MTQ	HMDB
MTQ Hydrochloride	HMDB
Nethaqualone	HMDB
Nobedorm	HMDB
Noctilene	HMDB
Normi-nox	HMDB
Omnyl	HMDB
Optinoxan	HMDB
Orthonal	HMDB
Ortonal	HMDB
Parminal	HMDB
pro-Dorm	HMDB
Qu.lovin.a.lovin.alude	HMDB
Quaalude	HMDB
Revonal	HMDB
Rorer 148	HMDB
Rorer 714	HMDB
Roulone	HMDB
Rouqualone	HMDB
Sindesvel	HMDB
Somberol	HMDB
Somnafac	HMDB
Somnomed	HMDB
Sonal	HMDB
Sopor	HMDB
Soverin	HMDB
Torinal	HMDB
Tuazole	HMDB
Tuazolone	HMDB

Chemical Formula

C₁₁H₂₀O₁₀

Average Molecular Weight

312.2705

Monoisotopic Molecular Weight

312.10564686

IUPAC Name

(2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-{[(3R,4S,5S)-2,3,5-trihydroxyoxan-4-yl]oxy}oxane-3,4,5-triol

Traditional Name

(2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-{[(3R,4S,5S)-2,3,5-trihydroxyoxan-4-yl]oxy}oxane-3,4,5-triol

CAS Registry Number

6055-00-1

SMILES

OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O

InChI Identifier

InChI=1S/C11H20O10/c12-1-4-5(14)6(15)7(16)11(20-4)21-9-3(13)2-19-10(18)8(9)17/h3-18H,1-2H2/t3-,4+,5-,6-,7+,8+,9-,10?,11-/m0/s1

InChI Key

XSXQXHMPBBNYRD-ANYLNHRWSA-N

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

O-glycosyl compounds

Alternative Parents

Substituents

Disaccharide
O-glycosyl compound
Oxane
Alpha-hydroxyaldehyde
Secondary alcohol
Acetal
Oxacycle
Polyol
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
Alcohol
Aldehyde
Primary alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

disaccharide (CHEBI:73916 )

Ontology

Not Available

Ingestion (HMDB: HMDB0038854)

Source

Exogenous

Food

Food (HMDB: HMDB0038854)

Fruit

Fruits (FooDB: FOOD00871)

Endogenous

Plant

Plant (HMDB: HMDB0038854)

Process

Not Available

Role

Industrial application

Drug (HMDB: HMDB0038854)

Biological role

Nutrient

Nutrient (HMDB: HMDB0038854)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	202 - 204 °C	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	612 g/L	ALOGPS
logP	-3	ALOGPS
logP	-4.1	ChemAxon
logS	0.29	ALOGPS
pKa (Strongest Acidic)	11.27	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	169.3 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	62.37 m³·mol⁻¹	ChemAxon
Polarizability	28.1 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	167.984	31661259
DarkChem	[M-H]-	165.399	31661259
DeepCCS	[M+H]+	169.336	30932474
DeepCCS	[M-H]-	167.118	30932474
DeepCCS	[M-2H]-	201.077	30932474
DeepCCS	[M+Na]+	175.255	30932474
AllCCS	[M+H]+	171.8	32859911
AllCCS	[M+H-H2O]+	168.5	32859911
AllCCS	[M+NH4]+	174.8	32859911
AllCCS	[M+Na]+	175.6	32859911
AllCCS	[M-H]-	167.3	32859911
AllCCS	[M+Na-2H]-	166.9	32859911
AllCCS	[M+HCOO]-	166.6	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
3-O-beta-D-Galactopyranosyl-L-arabinose	OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O	3206.8	Standard polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose	OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O	2839.3	Standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose	OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O	2673.4	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
3-O-beta-D-Galactopyranosyl-L-arabinose,1TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O	2580.8	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,1TMS,isomer #2	C[Si](C)(C)O[C@H]1COC(O)[C@H](O)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	2575.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,1TMS,isomer #3	C[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@H]1O	2584.6	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,1TMS,isomer #4	C[Si](C)(C)O[C@H]1C(O)OC[C@H](O)[C@@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	2584.0	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,1TMS,isomer #5	C[Si](C)(C)O[C@H]1[C@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)O[C@H](CO)[C@H](O)[C@@H]1O	2566.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,1TMS,isomer #6	C[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@@H]1O	2568.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,1TMS,isomer #7	C[Si](C)(C)O[C@H]1[C@@H](CO)O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@H](O)[C@H]1O	2564.0	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O	2581.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TMS,isomer #10	C[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O)[C@@H]2O)[C@@H]1O	2562.9	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TMS,isomer #11	C[Si](C)(C)O[C@H]1COC(O)[C@H](O)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	2568.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TMS,isomer #12	C[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H]1O	2578.8	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TMS,isomer #13	C[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H]1O	2569.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TMS,isomer #14	C[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H]1O	2578.1	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TMS,isomer #15	C[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@H]1O[Si](C)(C)C	2596.9	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TMS,isomer #16	C[Si](C)(C)O[C@H]1C(O)OC[C@H](O)[C@@H]1O[C@@H]1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2572.0	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TMS,isomer #17	C[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O[Si](C)(C)C)[C@@H]1O	2564.0	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TMS,isomer #18	C[Si](C)(C)O[C@H]1C(O)OC[C@H](O)[C@@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	2570.6	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TMS,isomer #19	C[Si](C)(C)O[C@H]1[C@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)O[C@H](CO)[C@H](O[Si](C)(C)C)[C@@H]1O	2538.1	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O	2578.1	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TMS,isomer #20	C[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@@H]1O[Si](C)(C)C	2549.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TMS,isomer #21	C[Si](C)(C)O[C@H]1[C@@H](CO)O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C	2540.7	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O	2574.9	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O	2549.0	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O	2537.8	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C	2566.0	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TMS,isomer #7	C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@H]1O	2578.7	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TMS,isomer #8	C[Si](C)(C)O[C@H]1COC(O)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	2577.5	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TMS,isomer #9	C[Si](C)(C)O[C@H]1COC(O)[C@H](O)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2566.7	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O	2502.5	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #10	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O	2495.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #11	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O	2494.7	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #12	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C	2501.9	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #13	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	2447.8	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #14	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	2476.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #15	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2455.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #16	C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H]1O	2501.1	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #17	C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H]1O	2506.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #18	C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H]1O	2499.9	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #19	C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@H]1O[Si](C)(C)C	2540.5	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O	2506.7	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #20	C[Si](C)(C)O[C@H]1COC(O)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2510.8	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #21	C[Si](C)(C)O[C@H]1COC(O)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2515.5	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #22	C[Si](C)(C)O[C@H]1COC(O)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	2506.9	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #23	C[Si](C)(C)O[C@H]1COC(O)[C@H](O)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2482.9	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #24	C[Si](C)(C)O[C@H]1COC(O)[C@H](O)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2483.5	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #25	C[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O)[C@@H]2O)[C@@H]1O[Si](C)(C)C	2479.0	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #26	C[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H]1O	2502.8	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #27	C[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H]1O	2502.5	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #28	C[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H]1O[Si](C)(C)C	2531.7	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #29	C[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H]1O	2508.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O	2468.5	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #30	C[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H]1O[Si](C)(C)C	2532.5	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #31	C[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2533.8	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #32	C[Si](C)(C)O[C@H]1[C@@H](CO)O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2513.9	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #33	C[Si](C)(C)O[C@H]1C(O)OC[C@H](O)[C@@H]1O[C@@H]1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2504.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #34	C[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2519.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #35	C[Si](C)(C)O[C@@H]1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)O[C@@H]1CO	2472.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O	2476.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C	2479.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O	2532.0	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O	2486.7	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #8	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O	2490.0	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TMS,isomer #9	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C	2497.6	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O	2455.1	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #10	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2447.0	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #11	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O	2476.1	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #12	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O	2503.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #13	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C	2490.7	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #14	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	2462.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #15	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	2479.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #16	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2477.1	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #17	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	2476.5	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #18	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	2490.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #19	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2494.1	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O	2439.6	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #20	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2447.8	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #21	C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H]1O	2489.9	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #22	C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H]1O	2474.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #23	C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H]1O[Si](C)(C)C	2481.6	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #24	C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H]1O	2475.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #25	C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H]1O[Si](C)(C)C	2496.5	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #26	C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2469.7	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #27	C[Si](C)(C)O[C@H]1COC(O)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2500.9	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #28	C[Si](C)(C)O[C@H]1COC(O)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2479.6	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #29	C[Si](C)(C)O[C@H]1COC(O)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2483.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O	2463.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #30	C[Si](C)(C)O[C@@H]1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O)[C@@H]2O)O[C@@H]1CO	2457.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #31	C[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H]1O	2501.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #32	C[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H]1O[Si](C)(C)C	2525.5	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #33	C[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2516.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #34	C[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2515.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #35	C[Si](C)(C)O[C@@H]1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O[Si](C)(C)C)O[C@@H]1CO	2508.8	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C	2451.5	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O	2445.7	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O	2472.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C	2462.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #8	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	2426.8	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TMS,isomer #9	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	2454.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O	2441.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TMS,isomer #10	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2433.1	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TMS,isomer #11	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	2485.8	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TMS,isomer #12	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	2504.5	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TMS,isomer #13	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2505.0	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TMS,isomer #14	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2484.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TMS,isomer #15	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2474.0	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TMS,isomer #16	C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H]1O	2499.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TMS,isomer #17	C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H]1O[Si](C)(C)C	2489.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TMS,isomer #18	C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2465.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TMS,isomer #19	C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2472.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O	2470.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TMS,isomer #20	C[Si](C)(C)O[C@H]1COC(O)[C@H](O[Si](C)(C)C)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2481.9	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TMS,isomer #21	C[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2500.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C	2464.9	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	2465.6	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	2473.9	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2485.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	2448.1	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TMS,isomer #8	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	2464.9	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TMS,isomer #9	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2473.8	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,6TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	2475.5	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,6TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	2481.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,6TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2497.7	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,6TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2493.9	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,6TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2474.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,6TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2489.7	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,6TMS,isomer #7	C[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2493.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,7TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C)COC(O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2531.7	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O	2816.0	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@H]1COC(O)[C@H](O)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	2831.1	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@H]1O	2821.0	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@H]1C(O)OC[C@H](O)[C@@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	2829.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)O[C@H](CO)[C@H](O)[C@@H]1O	2824.6	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@@H]1O	2820.6	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](CO)O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@H](O)[C@H]1O	2812.1	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O	3008.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O)[C@@H]2O)[C@@H]1O	3044.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)O[C@H]1COC(O)[C@H](O)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3051.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@H]1O	3034.1	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@H]1O	3040.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H]1O	3050.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@H]1O[Si](C)(C)C(C)(C)C	3047.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)O[C@H]1C(O)OC[C@H](O)[C@@H]1O[C@@H]1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3036.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3037.1	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)O[C@H]1C(O)OC[C@H](O)[C@@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3048.5	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3003.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O	3020.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TBDMS,isomer #20	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3017.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](CO)O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3000.7	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]1O	3016.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O	3014.0	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3005.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3003.9	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@H]1O	3045.8	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@H]1COC(O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	3050.6	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@H]1COC(O)[C@H](O)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3038.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O	3208.1	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O	3227.7	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3220.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3213.7	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3169.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3175.1	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3172.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@H]1O	3218.5	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@H]1O	3226.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H]1O	3234.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@H]1O[Si](C)(C)C(C)(C)C	3224.7	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]1O	3203.8	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)O[C@H]1COC(O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3229.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #21	CC(C)(C)[Si](C)(C)O[C@H]1COC(O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3234.0	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #22	CC(C)(C)[Si](C)(C)O[C@H]1COC(O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3242.1	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #23	CC(C)(C)[Si](C)(C)O[C@H]1COC(O)[C@H](O)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3194.5	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #24	CC(C)(C)[Si](C)(C)O[C@H]1COC(O)[C@H](O)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3203.0	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #25	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O)[C@@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3203.8	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@H]1O	3202.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H]1O	3204.9	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@H]1O[Si](C)(C)C(C)(C)C	3228.7	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H]1O	3218.9	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O	3209.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@H]1O[Si](C)(C)C(C)(C)C	3232.8	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3239.5	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #32	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](CO)O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3213.0	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #33	CC(C)(C)[Si](C)(C)O[C@H]1C(O)OC[C@H](O)[C@@H]1O[C@@H]1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3218.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #34	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3227.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #35	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)O[C@@H]1CO	3174.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3195.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3195.9	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]1O	3198.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O	3214.0	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3207.9	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3205.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]1O	3366.9	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3364.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O	3400.1	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3394.8	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3387.1	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3382.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3387.1	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3381.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3402.7	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3409.1	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3405.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O	3383.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3362.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@H]1O	3380.8	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H]1O	3383.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@H]1O[Si](C)(C)C(C)(C)C	3392.0	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H]1O	3391.5	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@H]1O[Si](C)(C)C(C)(C)C	3394.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3405.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #27	CC(C)(C)[Si](C)(C)O[C@H]1COC(O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3391.1	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #28	CC(C)(C)[Si](C)(C)O[C@H]1COC(O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3389.0	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #29	CC(C)(C)[Si](C)(C)O[C@H]1COC(O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3400.9	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3375.7	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #30	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O)[C@@H]2O)O[C@@H]1CO	3367.0	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H]1O	3386.0	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@H]1O[Si](C)(C)C(C)(C)C	3397.5	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3400.6	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3408.5	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #35	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O[Si](C)(C)C(C)(C)C)O[C@@H]1CO	3396.1	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3369.9	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O	3394.6	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3392.8	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3387.8	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3361.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3371.7	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O	3542.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3527.0	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3564.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3565.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3564.1	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3561.1	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O)COC(O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3563.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H]1O	3543.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@H]1O[Si](C)(C)C(C)(C)C	3536.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3536.9	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3545.5	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3541.9	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TBDMS,isomer #20	CC(C)(C)[Si](C)(C)O[C@H]1COC(O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3537.2	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC1OC[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3554.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3536.8	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3551.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3555.3	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3551.6	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3547.4	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3550.9	Semi standard non polar	33892256
3-O-beta-D-Galactopyranosyl-L-arabinose,5TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2[C@@H](O[Si](C)(C)C(C)(C)C)COC(O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3550.8	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-beta-D-Galactopyranosyl-L-arabinose GC-MS (Non-derivatized) - 70eV, Positive	splash10-0ued-3490000000-6da41c40d63b32d0f2d7	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose GC-MS (5 TMS) - 70eV, Positive	splash10-0a4i-1412039000-2e4bee84b845529e3991	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose GC-MS (TBDMS_3_2) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose GC-MS (TBDMS_3_10) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose GC-MS (TBDMS_4_1) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose GC-MS (TBDMS_4_5) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose GC-MS (TBDMS_4_6) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose GC-MS (TBDMS_4_7) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose GC-MS (TBDMS_4_11) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose GC-MS (TBDMS_4_17) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose GC-MS (TBDMS_4_18) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose GC-MS (TBDMS_5_1) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose GC-MS (TBDMS_5_2) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose GC-MS (TBDMS_5_3) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose GC-MS (TBDMS_5_7) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose GC-MS (TBDMS_5_8) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose GC-MS (TBDMS_5_9) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose GC-MS (TBDMS_5_11) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose GC-MS (TBDMS_5_12) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose GC-MS (TBDMS_5_15) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose GC-MS ("3-O-beta-D-Galactopyranosyl-L-arabinose,3TBDMS,#2" TMS) - 70eV, Positive	Not Available	2021-10-14	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose 10V, Positive-QTOF	splash10-0gx1-0942000000-4cdfc3c9ce51dc8ad85a	2016-08-02	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose 20V, Positive-QTOF	splash10-0f89-0900000000-75b5c8254a3a9abdd855	2016-08-02	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose 40V, Positive-QTOF	splash10-001l-5900000000-c2c9bba8b1c896b1d8cc	2016-08-02	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose 10V, Negative-QTOF	splash10-03dj-3976000000-5d48d27cbb76392ac75a	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose 20V, Negative-QTOF	splash10-001j-1920000000-639ac4bea3e69b7cdbac	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose 40V, Negative-QTOF	splash10-000x-9700000000-7149fb1ae3f05b31012f	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose 10V, Negative-QTOF	splash10-03di-1319000000-5c4854eafd4d09e0ae90	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose 20V, Negative-QTOF	splash10-03fu-9553000000-531cb3b4ac907be2cf85	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose 40V, Negative-QTOF	splash10-0a4i-9100000000-62f418e8eeab9556f67f	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose 10V, Positive-QTOF	splash10-03dj-0927000000-935d1be331bb37e43817	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose 20V, Positive-QTOF	splash10-01qa-4900000000-927387d35509066c1725	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-O-beta-D-Galactopyranosyl-L-arabinose 40V, Positive-QTOF	splash10-002k-9300000000-ac8aede71de217875c89	2021-09-23	Wishart Lab	View Spectrum

NMR Spectra

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

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

167842

KEGG Compound ID

Not Available

BioCyc ID

CPD-3785

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

193417

PDB ID

Not Available

ChEBI ID

73916

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

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

Enzymes

Enzyme Details

1. Cytochrome P450 3A4

General function:: Involved in monooxygenase activity
Specific function:: Cytochromes P450 are a group of heme-thiolate monooxygenases. In liver microsomes, this enzyme is involved in an NADPH-dependent electron transport pathway. It performs a variety of oxidation reactions (e.g. caffeine 8-oxidation, omeprazole sulphoxidation, midazolam 1'-hydroxylation and midazolam 4-hydroxylation) of structurally unrelated compounds, including steroids, fatty acids, and xenobiotics. Acts as a 1,8-cineole 2-exo-monooxygenase. The enzyme also hydroxylates etoposide.
Gene Name:: CYP3A4
Uniprot ID:: P08684
Molecular weight:: 57255.585

References

Preissner S, Kroll K, Dunkel M, Senger C, Goldsobel G, Kuzman D, Guenther S, Winnenburg R, Schroeder M, Preissner R: SuperCYP: a comprehensive database on Cytochrome P450 enzymes including a tool for analysis of CYP-drug interactions. Nucleic Acids Res. 2010 Jan;38(Database issue):D237-43. doi: 10.1093/nar/gkp970. Epub 2009 Nov 24. [PubMed:19934256 ]

Showing metabocard for 3-O-beta-D-Galactopyranosyl-L-arabinose (HMDB0038854)

MOL for HMDB0038854 (3-O-beta-D-Galactopyranosyl-L-arabinose)

3D MOL for HMDB0038854 (3-O-beta-D-Galactopyranosyl-L-arabinose)

3D SDF for HMDB0038854 (3-O-beta-D-Galactopyranosyl-L-arabinose)

3D-SDF for HMDB0038854 (3-O-beta-D-Galactopyranosyl-L-arabinose)

PDB for HMDB0038854 (3-O-beta-D-Galactopyranosyl-L-arabinose)

3D PDB for HMDB0038854 (3-O-beta-D-Galactopyranosyl-L-arabinose)

SMILES for HMDB0038854 (3-O-beta-D-Galactopyranosyl-L-arabinose)

INCHI for HMDB0038854 (3-O-beta-D-Galactopyranosyl-L-arabinose)

Structure for HMDB0038854 (3-O-beta-D-Galactopyranosyl-L-arabinose)

3D Structure for HMDB0038854 (3-O-beta-D-Galactopyranosyl-L-arabinose)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

Enzymes

References