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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 00:12:40 UTC

Update Date

2022-03-07 02:55:57 UTC

HMDB ID

HMDB0038863

Secondary Accession Numbers

HMDB38863

Metabolite Identification

Common Name

2-O-b-D-Galactopyranosyl-D-xylose

Description

2-O-b-D-Galactopyranosyl-D-xylose 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 2-O-b-D-Galactopyranosyl-D-xylose.

Structure

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

HMDB0038863
     RDKit          3D
2-O-b-D-Galactopyranosyl-D-xylose
 41 42  0  0  0  0  0  0  0  0999 V2000
   -3.1432    2.4935   -0.9115 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0433    1.6418   -0.9892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4444    0.2256   -1.3130 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3317   -0.5379   -1.3770 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6128   -0.7832   -0.2334 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3319    0.1778   -0.1329 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6351   -0.1262   -0.2929 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2682    0.8531   -1.2588 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5814    0.9870   -2.4363 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6169    0.5944   -1.4543 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1572   -0.2203   -0.4689 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7963    0.2181    0.9248 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3247    1.4832    1.1801 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3061    0.1633    1.0642 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8787   -0.7404    2.0218 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4847   -1.0607    0.9028 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0962   -2.1235    1.7185 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8453   -1.4683    0.3739 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6468   -1.9971    1.3587 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4302   -0.2151   -0.2505 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5514    0.7315    0.7476 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1787    2.9950   -1.7693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3221    2.0069   -1.7756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4745    1.6221   -0.0403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9748    0.2782   -2.3090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0450   -1.7505   -0.4560 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8845   -1.1717   -0.5044 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2229    1.8557   -0.7402 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0401    0.4168   -3.1276 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2760   -0.1381   -0.5478 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9226   -1.2812   -0.5960 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2647   -0.4884    1.6265 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6380    2.1393    1.4273 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9392    1.1675    1.3571 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9692   -0.3328    2.9199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6841   -0.1461    1.5394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8188   -2.2393    2.3882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6554   -2.2033   -0.4387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6453   -2.9861    1.2389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3725   -0.4922   -0.7390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2528    0.4513    1.3731 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  6
  7 27  1  6
  8 28  1  0
  9 29  1  0
 11 30  1  0
 11 31  1  0
 12 32  1  1
 13 33  1  0
 14 34  1  1
 15 35  1  0
 16 36  1  1
 17 37  1  0
 18 38  1  6
 19 39  1  0
 20 40  1  6
 21 41  1  0
M  END

  Mrv0541 02011302092D          

 21 22  0  0  0  0            999 V2000
   -4.5964    4.1643    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3109    3.7518    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3109    2.9268    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5964    2.5143    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8820    2.9268    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8820    3.7518    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1675    2.5143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5964    1.6893    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0254    2.5143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0254    4.1643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7398    3.7518    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5175    5.5932    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9300    6.3077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7550    6.3077    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1675    5.5932    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7550    4.8788    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9300    4.8788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5175    4.1643    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1675    4.1643    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9925    5.5932    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1675    7.0222    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 19  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  6  0  0  0
M  END
> <DATABASE_ID>
HMDB0038863

> <DATABASE_NAME>
hmdb

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

> <INCHI_IDENTIFIER>
InChI=1S/C11H20O10/c12-1-4-6(15)7(16)8(17)11(20-4)21-9-5(14)3(13)2-19-10(9)18/h3-18H,1-2H2/t3-,4-,5+,6+,7+,8-,9-,10?,11+/m1/s1

> <INCHI_KEY>
NTQWZXRSBBGWFC-NCRZSTDJSA-N

> <FORMULA>
C11H20O10

> <MOLECULAR_WEIGHT>
312.2705

> <EXACT_MASS>
312.10564686

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_AVERAGE_POLARIZABILITY>
28.076754792039907

> <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,5R)-2,4,5-trihydroxyoxan-3-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>
12.181504932565241

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.279323991455367

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981083576684803

> <JCHEM_POLAR_SURFACE_AREA>
169.29999999999998

> <JCHEM_REFRACTIVITY>
62.3742

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.15e+02 g/l

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

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0038863
     RDKit          3D
2-O-b-D-Galactopyranosyl-D-xylose
 41 42  0  0  0  0  0  0  0  0999 V2000
   -3.1432    2.4935   -0.9115 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0433    1.6418   -0.9892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4444    0.2256   -1.3130 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3317   -0.5379   -1.3770 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6128   -0.7832   -0.2334 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3319    0.1778   -0.1329 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6351   -0.1262   -0.2929 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2682    0.8531   -1.2588 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5814    0.9870   -2.4363 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6169    0.5944   -1.4543 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1572   -0.2203   -0.4689 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7963    0.2181    0.9248 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3247    1.4832    1.1801 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3061    0.1633    1.0642 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8787   -0.7404    2.0218 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4847   -1.0607    0.9028 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0962   -2.1235    1.7185 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8453   -1.4683    0.3739 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6468   -1.9971    1.3587 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4302   -0.2151   -0.2505 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5514    0.7315    0.7476 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1787    2.9950   -1.7693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3221    2.0069   -1.7756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4745    1.6221   -0.0403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9748    0.2782   -2.3090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0450   -1.7505   -0.4560 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8845   -1.1717   -0.5044 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2229    1.8557   -0.7402 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0401    0.4168   -3.1276 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2760   -0.1381   -0.5478 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9226   -1.2812   -0.5960 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2647   -0.4884    1.6265 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6380    2.1393    1.4273 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9392    1.1675    1.3571 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9692   -0.3328    2.9199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6841   -0.1461    1.5394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8188   -2.2393    2.3882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6554   -2.2033   -0.4387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6453   -2.9861    1.2389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3725   -0.4922   -0.7390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2528    0.4513    1.3731 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  6
  7 27  1  6
  8 28  1  0
  9 29  1  0
 11 30  1  0
 11 31  1  0
 12 32  1  1
 13 33  1  0
 14 34  1  1
 15 35  1  0
 16 36  1  1
 17 37  1  0
 18 38  1  6
 19 39  1  0
 20 40  1  6
 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      -8.580   7.773   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -9.914   7.003   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -9.914   5.463   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -8.580   4.693   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -7.246   5.463   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -7.246   7.003   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -5.913   4.693   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0      -8.580   3.153   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0     -11.247   4.693   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0     -11.247   7.773   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0     -12.581   7.003   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0      -2.833  10.441   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -3.603  11.774   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -5.143  11.774   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -5.913  10.441   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -5.143   9.107   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.603   9.107   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -2.833   7.773   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -5.913   7.773   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -7.453  10.441   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -5.913  13.108   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   19                                                  
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    6   16                                                       
CONECT   20   15                                                            
CONECT   21   14                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   44    0
END

COMPND    HMDB0038863
HETATM    1  O1  UNL     1      -3.143   2.494  -0.912  1.00  0.00           O  
HETATM    2  C1  UNL     1      -2.043   1.642  -0.989  1.00  0.00           C  
HETATM    3  C2  UNL     1      -2.444   0.226  -1.313  1.00  0.00           C  
HETATM    4  O2  UNL     1      -1.332  -0.538  -1.377  1.00  0.00           O  
HETATM    5  C3  UNL     1      -0.613  -0.783  -0.233  1.00  0.00           C  
HETATM    6  O3  UNL     1       0.332   0.178  -0.133  1.00  0.00           O  
HETATM    7  C4  UNL     1       1.635  -0.126  -0.293  1.00  0.00           C  
HETATM    8  C5  UNL     1       2.268   0.853  -1.259  1.00  0.00           C  
HETATM    9  O4  UNL     1       1.581   0.987  -2.436  1.00  0.00           O  
HETATM   10  O5  UNL     1       3.617   0.594  -1.454  1.00  0.00           O  
HETATM   11  C6  UNL     1       4.157  -0.220  -0.469  1.00  0.00           C  
HETATM   12  C7  UNL     1       3.796   0.218   0.925  1.00  0.00           C  
HETATM   13  O6  UNL     1       4.325   1.483   1.180  1.00  0.00           O  
HETATM   14  C8  UNL     1       2.306   0.163   1.064  1.00  0.00           C  
HETATM   15  O7  UNL     1       1.879  -0.740   2.022  1.00  0.00           O  
HETATM   16  C9  UNL     1      -1.485  -1.061   0.903  1.00  0.00           C  
HETATM   17  O8  UNL     1      -1.096  -2.124   1.718  1.00  0.00           O  
HETATM   18  C10 UNL     1      -2.845  -1.468   0.374  1.00  0.00           C  
HETATM   19  O9  UNL     1      -3.647  -1.997   1.359  1.00  0.00           O  
HETATM   20  C11 UNL     1      -3.430  -0.215  -0.251  1.00  0.00           C  
HETATM   21  O10 UNL     1      -3.551   0.732   0.748  1.00  0.00           O  
HETATM   22  H1  UNL     1      -3.179   2.995  -1.769  1.00  0.00           H  
HETATM   23  H2  UNL     1      -1.322   2.007  -1.776  1.00  0.00           H  
HETATM   24  H3  UNL     1      -1.474   1.622  -0.040  1.00  0.00           H  
HETATM   25  H4  UNL     1      -2.975   0.278  -2.309  1.00  0.00           H  
HETATM   26  H5  UNL     1      -0.045  -1.751  -0.456  1.00  0.00           H  
HETATM   27  H6  UNL     1       1.885  -1.172  -0.504  1.00  0.00           H  
HETATM   28  H7  UNL     1       2.223   1.856  -0.740  1.00  0.00           H  
HETATM   29  H8  UNL     1       2.040   0.417  -3.128  1.00  0.00           H  
HETATM   30  H9  UNL     1       5.276  -0.138  -0.548  1.00  0.00           H  
HETATM   31  H10 UNL     1       3.923  -1.281  -0.596  1.00  0.00           H  
HETATM   32  H11 UNL     1       4.265  -0.488   1.627  1.00  0.00           H  
HETATM   33  H12 UNL     1       3.638   2.139   1.427  1.00  0.00           H  
HETATM   34  H13 UNL     1       1.939   1.168   1.357  1.00  0.00           H  
HETATM   35  H14 UNL     1       1.969  -0.333   2.920  1.00  0.00           H  
HETATM   36  H15 UNL     1      -1.684  -0.146   1.539  1.00  0.00           H  
HETATM   37  H16 UNL     1      -1.819  -2.239   2.388  1.00  0.00           H  
HETATM   38  H17 UNL     1      -2.655  -2.203  -0.439  1.00  0.00           H  
HETATM   39  H18 UNL     1      -3.645  -2.986   1.239  1.00  0.00           H  
HETATM   40  H19 UNL     1      -4.372  -0.492  -0.739  1.00  0.00           H  
HETATM   41  H20 UNL     1      -4.253   0.451   1.373  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
CONECT   11   12   30   31
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

HMDB0038863
     RDKit          3D
2-O-b-D-Galactopyranosyl-D-xylose
 41 42  0  0  0  0  0  0  0  0999 V2000
   -3.1432    2.4935   -0.9115 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0433    1.6418   -0.9892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4444    0.2256   -1.3130 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3317   -0.5379   -1.3770 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6128   -0.7832   -0.2334 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3319    0.1778   -0.1329 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6351   -0.1262   -0.2929 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2682    0.8531   -1.2588 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5814    0.9870   -2.4363 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6169    0.5944   -1.4543 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1572   -0.2203   -0.4689 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7963    0.2181    0.9248 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3247    1.4832    1.1801 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3061    0.1633    1.0642 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8787   -0.7404    2.0218 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4847   -1.0607    0.9028 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0962   -2.1235    1.7185 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8453   -1.4683    0.3739 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6468   -1.9971    1.3587 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4302   -0.2151   -0.2505 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5514    0.7315    0.7476 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1787    2.9950   -1.7693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3221    2.0069   -1.7756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4745    1.6221   -0.0403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9748    0.2782   -2.3090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0450   -1.7505   -0.4560 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8845   -1.1717   -0.5044 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2229    1.8557   -0.7402 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0401    0.4168   -3.1276 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2760   -0.1381   -0.5478 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9226   -1.2812   -0.5960 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2647   -0.4884    1.6265 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6380    2.1393    1.4273 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9392    1.1675    1.3571 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9692   -0.3328    2.9199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6841   -0.1461    1.5394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8188   -2.2393    2.3882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6554   -2.2033   -0.4387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6453   -2.9861    1.2389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3725   -0.4922   -0.7390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2528    0.4513    1.3731 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  6
  7 27  1  6
  8 28  1  0
  9 29  1  0
 11 30  1  0
 11 31  1  0
 12 32  1  1
 13 33  1  0
 14 34  1  1
 15 35  1  0
 16 36  1  1
 17 37  1  0
 18 38  1  6
 19 39  1  0
 20 40  1  6
 21 41  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Not Available

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,5R)-2,4,5-trihydroxyoxan-3-yl]oxy}oxane-3,4,5-triol

Traditional Name

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

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C11H20O10/c12-1-4-6(15)7(16)8(17)11(20-4)21-9-5(14)3(13)2-19-10(9)18/h3-18H,1-2H2/t3-,4-,5+,6+,7+,8-,9-,10?,11+/m1/s1

InChI Key

NTQWZXRSBBGWFC-NCRZSTDJSA-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

O-glycosyl compound
Disaccharide
Oxane
Secondary alcohol
Hemiacetal
Oxacycle
Organoheterocyclic compound
Polyol
Acetal
Hydrocarbon derivative
Primary alcohol
Alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Exogenous (HMDB: HMDB0038863)

Food

Food (HMDB: HMDB0038863)

Process

Not Available

Role

Biological role

Nutrient (HMDB: HMDB0038863)

Physical Properties

State

Not Available

Experimental Molecular Properties

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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	615 g/L	ALOGPS
logP	-3	ALOGPS
logP	-4.1	ChemAxon
logS	0.29	ALOGPS
pKa (Strongest Acidic)	11.28	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	28.08 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]+	168.263	31661259
DarkChem	[M-H]-	164.546	31661259
DeepCCS	[M+H]+	165.867	30932474
DeepCCS	[M-H]-	163.589	30932474
DeepCCS	[M-2H]-	197.411	30932474
DeepCCS	[M+Na]+	171.78	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
2-O-b-D-Galactopyranosyl-D-xylose	OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O	3227.6	Standard polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose	OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O	2914.6	Standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose	OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O	2666.5	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
2-O-b-D-Galactopyranosyl-D-xylose,1TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O	2597.2	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,1TMS,isomer #2	C[Si](C)(C)OC1OC[C@@H](O)[C@H](O)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	2595.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,1TMS,isomer #3	C[Si](C)(C)O[C@@H]1COC(O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@H]1O	2593.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,1TMS,isomer #4	C[Si](C)(C)O[C@H]1[C@H](O)COC(O)[C@@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	2579.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,1TMS,isomer #5	C[Si](C)(C)O[C@H]1[C@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O)O[C@H](CO)[C@H](O)[C@@H]1O	2581.2	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,1TMS,isomer #6	C[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O)[C@@H]1O	2582.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,1TMS,isomer #7	C[Si](C)(C)O[C@H]1[C@@H](CO)O[C@@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O)[C@H](O)[C@H]1O	2578.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O	2598.6	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TMS,isomer #10	C[Si](C)(C)OC1OC[C@@H](O)[C@H](O)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2574.7	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TMS,isomer #11	C[Si](C)(C)OC1OC[C@@H](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	2588.7	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TMS,isomer #12	C[Si](C)(C)O[C@@H]1COC(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	2578.6	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TMS,isomer #13	C[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]2C(O)OC[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@@H]1O	2569.2	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TMS,isomer #14	C[Si](C)(C)O[C@H]1[C@H](O[C@H]2C(O)OC[C@@H](O[Si](C)(C)C)[C@@H]2O)O[C@H](CO)[C@H](O)[C@@H]1O	2577.9	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TMS,isomer #15	C[Si](C)(C)O[C@@H]1COC(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	2573.1	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TMS,isomer #16	C[Si](C)(C)O[C@H]1[C@H](O)COC(O)[C@@H]1O[C@@H]1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2549.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TMS,isomer #17	C[Si](C)(C)O[C@H]1[C@H](O)COC(O)[C@@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2542.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TMS,isomer #18	C[Si](C)(C)O[C@H]1[C@H](O)COC(O)[C@@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	2538.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TMS,isomer #19	C[Si](C)(C)O[C@H]1[C@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O)O[C@H](CO)[C@H](O[Si](C)(C)C)[C@@H]1O	2550.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O	2588.1	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TMS,isomer #20	C[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O)[C@@H]1O[Si](C)(C)C	2564.2	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TMS,isomer #21	C[Si](C)(C)O[C@H]1[C@@H](CO)O[C@@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C	2558.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O	2543.2	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O	2559.9	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O	2552.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C	2584.2	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TMS,isomer #7	C[Si](C)(C)OC1OC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	2585.7	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TMS,isomer #8	C[Si](C)(C)OC1OC[C@@H](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	2573.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TMS,isomer #9	C[Si](C)(C)OC1OC[C@@H](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	2588.6	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O	2505.0	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #10	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O	2472.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #11	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O	2471.1	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #12	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C	2478.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #13	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	2472.6	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #14	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	2496.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #15	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2472.6	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #16	C[Si](C)(C)OC1OC[C@@H](O[Si](C)(C)C)[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	2504.6	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #17	C[Si](C)(C)OC1OC[C@@H](O[Si](C)(C)C)[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	2496.6	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #18	C[Si](C)(C)OC1OC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2495.2	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #19	C[Si](C)(C)OC1OC[C@@H](O[Si](C)(C)C)[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	2502.0	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O	2490.6	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #20	C[Si](C)(C)OC1OC[C@@H](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	2493.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #21	C[Si](C)(C)OC1OC[C@@H](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	2500.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #22	C[Si](C)(C)OC1OC[C@@H](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	2490.9	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #23	C[Si](C)(C)OC1OC[C@@H](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	2498.0	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #24	C[Si](C)(C)OC1OC[C@@H](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	2503.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #25	C[Si](C)(C)OC1OC[C@@H](O)[C@H](O)[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	2497.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #26	C[Si](C)(C)O[C@H]1[C@@H](CO)O[C@@H](O[C@H]2C(O)OC[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C	2496.0	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #27	C[Si](C)(C)O[C@H]1[C@H](O[C@H]2C(O)OC[C@@H](O[Si](C)(C)C)[C@@H]2O)O[C@H](CO)[C@H](O[Si](C)(C)C)[C@@H]1O	2493.7	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #28	C[Si](C)(C)O[C@@H]1COC(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	2506.6	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #29	C[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]2C(O)OC[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H]1O	2517.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O	2487.6	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #30	C[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]2C(O)OC[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@@H]1O[Si](C)(C)C	2499.7	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #31	C[Si](C)(C)O[C@H]1[C@H](O[C@H]2C(O)OC[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[C@H](CO)[C@H](O)[C@@H]1O	2510.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #32	C[Si](C)(C)O[C@H]1[C@H](O)COC(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	2494.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #33	C[Si](C)(C)O[C@H]1[C@H](O)COC(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	2491.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #34	C[Si](C)(C)O[C@H]1[C@H](O)COC(O)[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	2504.2	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,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]2C(O)OC[C@@H](O)[C@@H]2O)O[C@@H]1CO	2494.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O	2487.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C	2508.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O	2485.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O	2478.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #8	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O	2475.7	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TMS,isomer #9	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C	2487.7	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O	2441.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #10	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2465.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #11	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	2463.0	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #12	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	2483.6	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #13	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	2472.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #14	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	2455.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #15	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	2472.9	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #16	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	2466.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #17	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	2471.1	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #18	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	2479.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #19	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	2482.0	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O	2435.7	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #20	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	2470.6	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #21	C[Si](C)(C)OC1OC[C@@H](O[Si](C)(C)C)[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	2470.6	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #22	C[Si](C)(C)OC1OC[C@@H](O[Si](C)(C)C)[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	2489.1	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #23	C[Si](C)(C)OC1OC[C@@H](O[Si](C)(C)C)[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	2457.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #24	C[Si](C)(C)OC1OC[C@@H](O[Si](C)(C)C)[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	2479.0	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #25	C[Si](C)(C)OC1OC[C@@H](O[Si](C)(C)C)[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	2471.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #26	C[Si](C)(C)OC1OC[C@@H](O[Si](C)(C)C)[C@H](O)[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	2467.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #27	C[Si](C)(C)OC1OC[C@@H](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	2503.1	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #28	C[Si](C)(C)OC1OC[C@@H](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	2479.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #29	C[Si](C)(C)OC1OC[C@@H](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	2492.7	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O	2459.1	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #30	C[Si](C)(C)OC1OC[C@@H](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[Si](C)(C)C	2474.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #31	C[Si](C)(C)O[C@H]1[C@@H](CO)O[C@@H](O[C@H]2C(O)OC[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2515.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #32	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]2C(O)OC[C@@H](O[Si](C)(C)C)[C@@H]2O)O[C@@H]1CO	2490.9	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #33	C[Si](C)(C)O[C@H]1[C@H](O[C@H]2C(O)OC[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[C@H](CO)[C@H](O[Si](C)(C)C)[C@@H]1O	2504.1	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #34	C[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]2C(O)OC[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2504.1	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,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]2C(O)OC[C@@H](O)[C@@H]2O[Si](C)(C)C)O[C@@H]1CO	2507.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C	2447.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O	2435.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]1O	2474.6	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C	2453.7	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #8	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	2451.2	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TMS,isomer #9	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	2476.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](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	2445.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TMS,isomer #10	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](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	2433.2	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TMS,isomer #11	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	2473.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TMS,isomer #12	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	2484.2	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TMS,isomer #13	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	2490.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TMS,isomer #14	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	2473.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TMS,isomer #15	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	2480.2	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TMS,isomer #16	C[Si](C)(C)OC1OC[C@@H](O[Si](C)(C)C)[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	2493.6	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TMS,isomer #17	C[Si](C)(C)OC1OC[C@@H](O[Si](C)(C)C)[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	2470.6	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TMS,isomer #18	C[Si](C)(C)OC1OC[C@@H](O[Si](C)(C)C)[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	2481.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TMS,isomer #19	C[Si](C)(C)OC1OC[C@@H](O[Si](C)(C)C)[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[Si](C)(C)C	2482.1	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](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	2473.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TMS,isomer #20	C[Si](C)(C)OC1OC[C@@H](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	2487.1	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TMS,isomer #21	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]2C(O)OC[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[C@@H]1CO	2509.7	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](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	2469.6	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](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	2451.0	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](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	2472.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](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	2468.0	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](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	2470.9	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TMS,isomer #8	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](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	2483.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TMS,isomer #9	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](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	2485.9	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,6TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](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	2480.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,6TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](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	2481.7	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,6TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](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	2495.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,6TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](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	2481.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,6TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](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	2475.6	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,6TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	2494.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,6TMS,isomer #7	C[Si](C)(C)OC1OC[C@@H](O[Si](C)(C)C)[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	2499.0	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,7TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C)OC[C@@H](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	2528.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O	2833.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1OC[C@@H](O)[C@H](O)[C@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	2832.9	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1COC(O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@H]1O	2835.0	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)COC(O)[C@@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	2832.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O)O[C@H](CO)[C@H](O)[C@@H]1O	2842.1	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,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]2C(O)OC[C@@H](O)[C@@H]2O)[C@@H]1O	2835.7	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](CO)O[C@@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O)[C@H](O)[C@H]1O	2830.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C(C)(C)C)OC[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O	3015.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1OC[C@@H](O)[C@H](O)[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	3036.2	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC1OC[C@@H](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	3052.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)O[C@@H]1COC(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	3049.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]2C(O)OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@@H]1O	3045.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[C@H]2C(O)OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)O[C@H](CO)[C@H](O)[C@@H]1O	3060.9	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)O[C@@H]1COC(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	3057.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)COC(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	3040.0	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)COC(O)[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	3039.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)COC(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	3053.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O)O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3020.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O	3023.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,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]2C(O)OC[C@@H](O)[C@@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3028.6	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](CO)O[C@@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3014.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]1O	3019.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O	3022.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3011.9	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3018.9	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,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]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	3037.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1OC[C@@H](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	3042.1	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1OC[C@@H](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	3039.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C(C)(C)C)OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O	3194.1	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	3222.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	3208.7	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	3209.0	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	3165.7	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	3174.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	3168.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1OC[C@@H](O[Si](C)(C)C(C)(C)C)[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	3230.7	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,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]1O[C@@H]1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3203.6	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,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]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3202.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,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]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3220.0	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C(C)(C)C)OC[C@@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]1O	3199.2	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC1OC[C@@H](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	3219.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC1OC[C@@H](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	3220.2	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC1OC[C@@H](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	3231.9	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC1OC[C@@H](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	3189.6	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC1OC[C@@H](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	3200.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC1OC[C@@H](O)[C@H](O)[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	3199.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #26	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](CO)O[C@@H](O[C@H]2C(O)OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3188.6	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #27	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[C@H]2C(O)OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3198.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #28	CC(C)(C)[Si](C)(C)O[C@@H]1COC(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	3238.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #29	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]2C(O)OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3240.0	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C(C)(C)C)OC[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O	3200.0	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #30	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]2C(O)OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3200.2	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #31	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[C@H]2C(O)OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@H](O)[C@@H]1O	3250.9	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #32	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)COC(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	3204.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #33	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)COC(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	3213.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #34	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)COC(O)[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	3215.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,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]2C(O)OC[C@@H](O)[C@@H]2O)O[C@@H]1CO	3176.9	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C(C)(C)C)OC[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3184.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C(C)(C)C)OC[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3190.0	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	3212.0	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	3206.2	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	3194.2	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	3196.2	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C(C)(C)C)OC[C@@H](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	3364.2	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C(C)(C)C)OC[C@@H](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	3364.1	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	3395.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	3390.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	3389.0	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	3368.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	3376.0	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	3370.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	3389.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	3398.2	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	3391.0	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C(C)(C)C)OC[C@@H](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	3377.1	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	3352.7	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC1OC[C@@H](O[Si](C)(C)C(C)(C)C)[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	3389.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC1OC[C@@H](O[Si](C)(C)C(C)(C)C)[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	3391.7	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC1OC[C@@H](O[Si](C)(C)C(C)(C)C)[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	3402.2	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,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]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	3366.0	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,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]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	3372.9	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,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]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	3375.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC1OC[C@@H](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	3383.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC1OC[C@@H](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	3385.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OC1OC[C@@H](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	3390.6	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C(C)(C)C)OC[C@@H](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	3368.0	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OC1OC[C@@H](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[Si](C)(C)C(C)(C)C	3365.9	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #31	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](CO)O[C@@H](O[C@H]2C(O)OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3390.1	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #32	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]2C(O)OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)O[C@@H]1CO	3368.7	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #33	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[C@H]2C(O)OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3394.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #34	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]2C(O)OC[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	3400.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,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]2C(O)OC[C@@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)O[C@@H]1CO	3383.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C(C)(C)C)OC[C@@H](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	3365.1	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C(C)(C)C)OC[C@@H](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	3389.0	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C(C)(C)C)OC[C@@H](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	3381.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C(C)(C)C)OC[C@@H](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	3377.7	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C(C)(C)C)OC[C@@H](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	3360.9	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C(C)(C)C)OC[C@@H](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	3372.6	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C(C)(C)C)OC[C@@H](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	3537.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C(C)(C)C)OC[C@@H](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	3516.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	3550.6	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	3556.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	3552.7	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	3533.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O)OC[C@@H](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	3550.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1OC[C@@H](O[Si](C)(C)C(C)(C)C)[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	3538.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC1OC[C@@H](O[Si](C)(C)C(C)(C)C)[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	3538.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC1OC[C@@H](O[Si](C)(C)C(C)(C)C)[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	3544.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,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]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	3524.9	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C(C)(C)C)OC[C@@H](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	3541.0	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC1OC[C@@H](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	3542.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TBDMS,isomer #21	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]2C(O)OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)O[C@@H]1CO	3542.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C(C)(C)C)OC[C@@H](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	3536.9	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C(C)(C)C)OC[C@@H](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	3531.3	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C(C)(C)C)OC[C@@H](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	3539.5	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C(C)(C)C)OC[C@@H](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	3534.4	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C(C)(C)C)OC[C@@H](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	3549.2	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C(C)(C)C)OC[C@@H](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	3553.8	Semi standard non polar	33892256
2-O-b-D-Galactopyranosyl-D-xylose,5TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@H]2C(O[Si](C)(C)C(C)(C)C)OC[C@@H](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	3551.7	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose GC-MS (Non-derivatized) - 70eV, Positive	splash10-0ff4-4590000000-bc07f9e1437654b0ee9a	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose GC-MS (5 TMS) - 70eV, Positive	splash10-0a4i-1412039000-ece1e7d06147bf74fe55	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose GC-MS (TBDMS_3_2) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose GC-MS (TBDMS_3_10) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose GC-MS (TBDMS_4_1) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose GC-MS (TBDMS_4_5) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose GC-MS (TBDMS_4_6) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose GC-MS (TBDMS_4_7) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose GC-MS (TBDMS_4_11) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose GC-MS (TBDMS_4_17) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose GC-MS (TBDMS_4_18) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose GC-MS (TBDMS_5_1) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose GC-MS (TBDMS_5_2) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose GC-MS (TBDMS_5_3) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose GC-MS (TBDMS_5_7) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose GC-MS (TBDMS_5_8) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose GC-MS (TBDMS_5_9) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose GC-MS (TBDMS_5_11) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose GC-MS (TBDMS_5_12) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose GC-MS (TBDMS_5_15) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose GC-MS (TBDMS_5_18) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose GC-MS ("2-O-b-D-Galactopyranosyl-D-xylose,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 - 2-O-b-D-Galactopyranosyl-D-xylose 10V, Positive-QTOF	splash10-0gx1-0932000000-51fae81af7992cf38d73	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose 20V, Positive-QTOF	splash10-0f89-0900000000-7e9d7cbc5c0c3013be54	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose 40V, Positive-QTOF	splash10-001l-7900000000-c307d886700d33411e9b	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose 10V, Negative-QTOF	splash10-03ea-3943000000-f4fec9e5cdb9dbb650e6	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose 20V, Negative-QTOF	splash10-01sj-2910000000-4bbfa7e6dafa6b4e26ac	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose 40V, Negative-QTOF	splash10-0006-9700000000-1e117813ad4b89b5b1aa	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose 10V, Negative-QTOF	splash10-03k9-2295000000-b0c860fc5563839880ad	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose 20V, Negative-QTOF	splash10-03di-8975000000-1c8a878591cc8ec56e47	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose 40V, Negative-QTOF	splash10-052f-9100000000-6b69a88091a29d3581c4	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose 10V, Positive-QTOF	splash10-03di-0139000000-a093396c7dfab97edf3d	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose 20V, Positive-QTOF	splash10-03ds-3963000000-cd89cc698b9c187ae9a7	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-O-b-D-Galactopyranosyl-D-xylose 40V, Positive-QTOF	splash10-052s-9210000000-dc98bf0df8686ecf2ffb	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

FDB018303

KNApSAcK ID

Not Available

Chemspider ID

9176639

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11001447

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

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

Showing metabocard for 2-O-b-D-Galactopyranosyl-D-xylose (HMDB0038863)

MOL for HMDB0038863 (2-O-b-D-Galactopyranosyl-D-xylose)

3D MOL for HMDB0038863 (2-O-b-D-Galactopyranosyl-D-xylose)

3D SDF for HMDB0038863 (2-O-b-D-Galactopyranosyl-D-xylose)

3D-SDF for HMDB0038863 (2-O-b-D-Galactopyranosyl-D-xylose)

PDB for HMDB0038863 (2-O-b-D-Galactopyranosyl-D-xylose)

3D PDB for HMDB0038863 (2-O-b-D-Galactopyranosyl-D-xylose)

SMILES for HMDB0038863 (2-O-b-D-Galactopyranosyl-D-xylose)

INCHI for HMDB0038863 (2-O-b-D-Galactopyranosyl-D-xylose)

Structure for HMDB0038863 (2-O-b-D-Galactopyranosyl-D-xylose)

3D Structure for HMDB0038863 (2-O-b-D-Galactopyranosyl-D-xylose)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra