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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 01:16:53 UTC

Update Date

2022-03-07 02:56:19 UTC

HMDB ID

HMDB0039742

Secondary Accession Numbers

HMDB39742

Metabolite Identification

Common Name

4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose

Description

4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds. 4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose has been detected, but not quantified in, breakfast cereal and cereals and cereal products. This could make 4-O-methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on 4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose.

Structure

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


  Mrv0541 05061311222D          

 32 34  0  0  0  0            999 V2000
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  4  2  1  0  0  0  0
  5  3  1  0  0  0  0
  6  4  1  0  0  0  0
  7  5  1  0  0  0  0
  9  7  1  0  0  0  0
 10  8  1  0  0  0  0
 11  8  1  0  0  0  0
 12  6  1  0  0  0  0
 13 11  1  0  0  0  0
 14 13  1  0  0  0  0
 15  9  1  0  0  0  0
 16 10  1  0  0  0  0
 17 12  1  0  0  0  0
 18  4  1  0  0  0  0
 19  6  1  0  0  0  0
 20  7  1  0  0  0  0
 21  8  1  0  0  0  0
 22  9  1  0  0  0  0
 23 10  1  0  0  0  0
 24 14  2  0  0  0  0
 25 14  1  0  0  0  0
 26 15  1  0  0  0  0
 27  1  1  0  0  0  0
 27 11  1  0  0  0  0
 28  3  1  0  0  0  0
 28 15  1  0  0  0  0
 29  2  1  0  0  0  0
 29 17  1  0  0  0  0
 30  5  1  0  0  0  0
 30 17  1  0  0  0  0
 31 12  1  0  0  0  0
 31 16  1  0  0  0  0
 32 13  1  0  0  0  0
 32 16  1  0  0  0  0
M  END

HMDB0039742
     RDKit          3D
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose
 60 62  0  0  0  0  0  0  0  0999 V2000
   -5.7097    2.6578   -0.8439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6762    2.1618   -0.0540 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7625    1.4408   -0.8299 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8204    0.0129   -0.3735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0024   -0.1079    1.0845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2514   -0.8835    1.7223 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9637    0.5932    1.7919 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8104   -0.7569   -0.8741 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5303   -0.3418   -0.6541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8420   -1.1149    0.2806 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2268   -1.8027   -0.2515 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4665   -1.3957    0.5402 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0095   -0.2139    0.1168 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2992   -0.3741   -0.3833 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4213    0.0470   -1.8121 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3195    1.4155   -1.9744 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4098    2.0009   -1.3301 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5853    3.3250   -1.6568 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1438    1.8489    0.1681 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8425    2.2241    0.4186 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2960    0.3827    0.4831 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9962    0.1167    1.8267 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1314   -1.4020    1.8699 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8349   -2.6660    2.3339 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2836   -3.3131    1.5543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4934   -4.6053    2.0062 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0515   -3.2713    0.0786 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8850   -3.8959   -0.7028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3362    1.0882   -0.2961 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1541    1.2969    1.0900 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3927    2.0139   -0.7739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0228    2.5413   -2.0127 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4139    3.2166   -0.2282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2576    1.8220   -1.3624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2972    3.3113   -1.6524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1239    1.4636   -1.8927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7748   -0.4101   -0.8220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5128    0.0333    2.4597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9798   -0.5177   -1.6288 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3671   -1.6319   -1.3348 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2344   -2.2046    0.3639 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5796   -1.4586   -0.3133 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4286   -0.2709   -2.1699 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6320   -0.4649   -2.3953 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3264    1.4153   -1.5706 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5317    3.6031   -1.5685 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8844    2.4581    0.7470 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7599    2.9309    1.0941 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3167    0.0461    0.2817 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1782    0.9292    2.3813 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6887   -3.3563    2.3194 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4918   -2.5733    3.3852 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1836   -2.6894    1.6982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1507   -4.5480    2.7466 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0370   -3.7748   -0.0875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5976   -4.7593   -1.0719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3594    1.4504   -0.7386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2666    0.9645    1.3759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4303    2.9013   -0.0798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2059    3.0914   -1.8501 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  2  0
  5  7  1  0
  4  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 12 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
  9 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31  3  1  0
 27 11  1  0
 21 14  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  3 36  1  0
  4 37  1  0
  7 38  1  0
  9 39  1  0
 11 40  1  0
 12 41  1  0
 14 42  1  0
 15 43  1  0
 15 44  1  0
 17 45  1  0
 18 46  1  0
 19 47  1  0
 20 48  1  0
 21 49  1  0
 22 50  1  0
 24 51  1  0
 24 52  1  0
 25 53  1  0
 26 54  1  0
 27 55  1  0
 28 56  1  0
 29 57  1  0
 30 58  1  0
 31 59  1  0
 32 60  1  0
M  END


  Mrv0541 05061311222D          

 32 34  0  0  0  0            999 V2000
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  4  2  1  0  0  0  0
  5  3  1  0  0  0  0
  6  4  1  0  0  0  0
  7  5  1  0  0  0  0
  9  7  1  0  0  0  0
 10  8  1  0  0  0  0
 11  8  1  0  0  0  0
 12  6  1  0  0  0  0
 13 11  1  0  0  0  0
 14 13  1  0  0  0  0
 15  9  1  0  0  0  0
 16 10  1  0  0  0  0
 17 12  1  0  0  0  0
 18  4  1  0  0  0  0
 19  6  1  0  0  0  0
 20  7  1  0  0  0  0
 21  8  1  0  0  0  0
 22  9  1  0  0  0  0
 23 10  1  0  0  0  0
 24 14  2  0  0  0  0
 25 14  1  0  0  0  0
 26 15  1  0  0  0  0
 27  1  1  0  0  0  0
 27 11  1  0  0  0  0
 28  3  1  0  0  0  0
 28 15  1  0  0  0  0
 29  2  1  0  0  0  0
 29 17  1  0  0  0  0
 30  5  1  0  0  0  0
 30 17  1  0  0  0  0
 31 12  1  0  0  0  0
 31 16  1  0  0  0  0
 32 13  1  0  0  0  0
 32 16  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0039742

> <DATABASE_NAME>
hmdb

> <SMILES>
COC1C(O)C(O)C(OC2C(O)C(O)COC2OC2COC(O)C(O)C2O)OC1C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C17H28O15/c1-27-11-8(21)10(23)16(32-13(11)14(24)25)31-12-6(19)4(18)2-29-17(12)30-5-3-28-15(26)9(22)7(5)20/h4-13,15-23,26H,2-3H2,1H3,(H,24,25)

> <INCHI_KEY>
XZGRJCXNJVJWKJ-UHFFFAOYSA-N

> <FORMULA>
C17H28O15

> <MOLECULAR_WEIGHT>
472.3952

> <EXACT_MASS>
472.142820226

> <JCHEM_ACCEPTOR_COUNT>
15

> <JCHEM_AVERAGE_POLARIZABILITY>
43.45892588280626

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-({4,5-dihydroxy-2-[(4,5,6-trihydroxyoxan-3-yl)oxy]oxan-3-yl}oxy)-4,5-dihydroxy-3-methoxyoxane-2-carboxylic acid

> <ALOGPS_LOGP>
-2.53

> <JCHEM_LOGP>
-4.250139583666667

> <ALOGPS_LOGS>
-0.26

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
11.26150547283007

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.2608676675218167

> <JCHEM_PKA_STRONGEST_BASIC>
-3.679382853304687

> <JCHEM_POLAR_SURFACE_AREA>
234.28999999999994

> <JCHEM_REFRACTIVITY>
93.44360000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.61e+02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-({4,5-dihydroxy-2-[(4,5,6-trihydroxyoxan-3-yl)oxy]oxan-3-yl}oxy)-4,5-dihydroxy-3-methoxyoxane-2-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0039742
     RDKit          3D
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose
 60 62  0  0  0  0  0  0  0  0999 V2000
   -5.7097    2.6578   -0.8439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6762    2.1618   -0.0540 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7625    1.4408   -0.8299 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8204    0.0129   -0.3735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0024   -0.1079    1.0845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2514   -0.8835    1.7223 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9637    0.5932    1.7919 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8104   -0.7569   -0.8741 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5303   -0.3418   -0.6541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8420   -1.1149    0.2806 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2268   -1.8027   -0.2515 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4665   -1.3957    0.5402 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0095   -0.2139    0.1168 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2992   -0.3741   -0.3833 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4213    0.0470   -1.8121 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3195    1.4155   -1.9744 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4098    2.0009   -1.3301 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5853    3.3250   -1.6568 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1438    1.8489    0.1681 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8425    2.2241    0.4186 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2960    0.3827    0.4831 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9962    0.1167    1.8267 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1314   -1.4020    1.8699 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8349   -2.6660    2.3339 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2836   -3.3131    1.5543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4934   -4.6053    2.0062 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0515   -3.2713    0.0786 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8850   -3.8959   -0.7028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3362    1.0882   -0.2961 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1541    1.2969    1.0900 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3927    2.0139   -0.7739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0228    2.5413   -2.0127 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4139    3.2166   -0.2282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2576    1.8220   -1.3624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2972    3.3113   -1.6524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1239    1.4636   -1.8927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7748   -0.4101   -0.8220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5128    0.0333    2.4597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9798   -0.5177   -1.6288 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3671   -1.6319   -1.3348 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2344   -2.2046    0.3639 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5796   -1.4586   -0.3133 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4286   -0.2709   -2.1699 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6320   -0.4649   -2.3953 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3264    1.4153   -1.5706 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5317    3.6031   -1.5685 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8844    2.4581    0.7470 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7599    2.9309    1.0941 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3167    0.0461    0.2817 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1782    0.9292    2.3813 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6887   -3.3563    2.3194 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4918   -2.5733    3.3852 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1836   -2.6894    1.6982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1507   -4.5480    2.7466 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0370   -3.7748   -0.0875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5976   -4.7593   -1.0719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3594    1.4504   -0.7386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2666    0.9645    1.3759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4303    2.9013   -0.0798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2059    3.0914   -1.8501 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  2  0
  5  7  1  0
  4  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 12 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
  9 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31  3  1  0
 27 11  1  0
 21 14  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  3 36  1  0
  4 37  1  0
  7 38  1  0
  9 39  1  0
 11 40  1  0
 12 41  1  0
 14 42  1  0
 15 43  1  0
 15 44  1  0
 17 45  1  0
 18 46  1  0
 19 47  1  0
 20 48  1  0
 21 49  1  0
 22 50  1  0
 24 51  1  0
 24 52  1  0
 25 53  1  0
 26 54  1  0
 27 55  1  0
 28 56  1  0
 29 57  1  0
 30 58  1  0
 31 59  1  0
 32 60  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       6.668  -5.390   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       9.336  -6.930   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       2.667   4.620   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       0.000   4.620   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      12.003  -5.390   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      10.669  -3.080   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       8.002   0.000   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       6.668  -2.310   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
CONECT    1   27                                                            
CONECT    2    4   29                                                       
CONECT    3    5   28                                                       
CONECT    4    2    6   18                                                  
CONECT    5    3    7   30                                                  
CONECT    6    4   12   19                                                  
CONECT    7    5    9   20                                                  
CONECT    8   10   11   21                                                  
CONECT    9    7   15   22                                                  
CONECT   10    8   16   23                                                  
CONECT   11    8   13   27                                                  
CONECT   12    6   17   31                                                  
CONECT   13   11   14   32                                                  
CONECT   14   13   24   25                                                  
CONECT   15    9   26   28                                                  
CONECT   16   10   31   32                                                  
CONECT   17   12   29   30                                                  
CONECT   18    4                                                            
CONECT   19    6                                                            
CONECT   20    7                                                            
CONECT   21    8                                                            
CONECT   22    9                                                            
CONECT   23   10                                                            
CONECT   24   14                                                            
CONECT   25   14                                                            
CONECT   26   15                                                            
CONECT   27    1   11                                                       
CONECT   28    3   15                                                       
CONECT   29    2   17                                                       
CONECT   30    5   17                                                       
CONECT   31   12   16                                                       
CONECT   32   13   16                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

COMPND    HMDB0039742
HETATM    1  C1  UNL     1      -5.710   2.658  -0.844  1.00  0.00           C  
HETATM    2  O1  UNL     1      -4.676   2.162  -0.054  1.00  0.00           O  
HETATM    3  C2  UNL     1      -3.762   1.441  -0.830  1.00  0.00           C  
HETATM    4  C3  UNL     1      -3.820   0.013  -0.374  1.00  0.00           C  
HETATM    5  C4  UNL     1      -4.002  -0.108   1.085  1.00  0.00           C  
HETATM    6  O2  UNL     1      -3.251  -0.884   1.722  1.00  0.00           O  
HETATM    7  O3  UNL     1      -4.964   0.593   1.792  1.00  0.00           O  
HETATM    8  O4  UNL     1      -2.810  -0.757  -0.874  1.00  0.00           O  
HETATM    9  C5  UNL     1      -1.530  -0.342  -0.654  1.00  0.00           C  
HETATM   10  O5  UNL     1      -0.842  -1.115   0.281  1.00  0.00           O  
HETATM   11  C6  UNL     1       0.227  -1.803  -0.252  1.00  0.00           C  
HETATM   12  C7  UNL     1       1.466  -1.396   0.540  1.00  0.00           C  
HETATM   13  O6  UNL     1       2.010  -0.214   0.117  1.00  0.00           O  
HETATM   14  C8  UNL     1       3.299  -0.374  -0.383  1.00  0.00           C  
HETATM   15  C9  UNL     1       3.421   0.047  -1.812  1.00  0.00           C  
HETATM   16  O7  UNL     1       3.319   1.416  -1.974  1.00  0.00           O  
HETATM   17  C10 UNL     1       4.410   2.001  -1.330  1.00  0.00           C  
HETATM   18  O8  UNL     1       4.585   3.325  -1.657  1.00  0.00           O  
HETATM   19  C11 UNL     1       4.144   1.849   0.168  1.00  0.00           C  
HETATM   20  O9  UNL     1       2.842   2.224   0.419  1.00  0.00           O  
HETATM   21  C12 UNL     1       4.296   0.383   0.483  1.00  0.00           C  
HETATM   22  O10 UNL     1       3.996   0.117   1.827  1.00  0.00           O  
HETATM   23  O11 UNL     1       1.131  -1.402   1.870  1.00  0.00           O  
HETATM   24  C13 UNL     1       0.835  -2.666   2.334  1.00  0.00           C  
HETATM   25  C14 UNL     1      -0.284  -3.313   1.554  1.00  0.00           C  
HETATM   26  O12 UNL     1      -0.493  -4.605   2.006  1.00  0.00           O  
HETATM   27  C15 UNL     1       0.051  -3.271   0.079  1.00  0.00           C  
HETATM   28  O13 UNL     1      -0.885  -3.896  -0.703  1.00  0.00           O  
HETATM   29  C16 UNL     1      -1.336   1.088  -0.296  1.00  0.00           C  
HETATM   30  O14 UNL     1      -1.154   1.297   1.090  1.00  0.00           O  
HETATM   31  C17 UNL     1      -2.393   2.014  -0.774  1.00  0.00           C  
HETATM   32  O15 UNL     1      -2.023   2.541  -2.013  1.00  0.00           O  
HETATM   33  H1  UNL     1      -6.414   3.217  -0.228  1.00  0.00           H  
HETATM   34  H2  UNL     1      -6.258   1.822  -1.362  1.00  0.00           H  
HETATM   35  H3  UNL     1      -5.297   3.311  -1.652  1.00  0.00           H  
HETATM   36  H4  UNL     1      -4.124   1.464  -1.893  1.00  0.00           H  
HETATM   37  H5  UNL     1      -4.775  -0.410  -0.822  1.00  0.00           H  
HETATM   38  H6  UNL     1      -5.513   0.033   2.460  1.00  0.00           H  
HETATM   39  H7  UNL     1      -0.980  -0.518  -1.629  1.00  0.00           H  
HETATM   40  H8  UNL     1       0.367  -1.632  -1.335  1.00  0.00           H  
HETATM   41  H9  UNL     1       2.234  -2.205   0.364  1.00  0.00           H  
HETATM   42  H10 UNL     1       3.580  -1.459  -0.313  1.00  0.00           H  
HETATM   43  H11 UNL     1       4.429  -0.271  -2.170  1.00  0.00           H  
HETATM   44  H12 UNL     1       2.632  -0.465  -2.395  1.00  0.00           H  
HETATM   45  H13 UNL     1       5.326   1.415  -1.571  1.00  0.00           H  
HETATM   46  H14 UNL     1       5.532   3.603  -1.569  1.00  0.00           H  
HETATM   47  H15 UNL     1       4.884   2.458   0.747  1.00  0.00           H  
HETATM   48  H16 UNL     1       2.760   2.931   1.094  1.00  0.00           H  
HETATM   49  H17 UNL     1       5.317   0.046   0.282  1.00  0.00           H  
HETATM   50  H18 UNL     1       4.178   0.929   2.381  1.00  0.00           H  
HETATM   51  H19 UNL     1       1.689  -3.356   2.319  1.00  0.00           H  
HETATM   52  H20 UNL     1       0.492  -2.573   3.385  1.00  0.00           H  
HETATM   53  H21 UNL     1      -1.184  -2.689   1.698  1.00  0.00           H  
HETATM   54  H22 UNL     1      -1.151  -4.548   2.747  1.00  0.00           H  
HETATM   55  H23 UNL     1       1.037  -3.775  -0.087  1.00  0.00           H  
HETATM   56  H24 UNL     1      -0.598  -4.759  -1.072  1.00  0.00           H  
HETATM   57  H25 UNL     1      -0.359   1.450  -0.739  1.00  0.00           H  
HETATM   58  H26 UNL     1      -0.267   0.964   1.376  1.00  0.00           H  
HETATM   59  H27 UNL     1      -2.430   2.901  -0.080  1.00  0.00           H  
HETATM   60  H28 UNL     1      -1.206   3.091  -1.850  1.00  0.00           H  
CONECT    1    2   33   34   35
CONECT    2    3
CONECT    3    4   31   36
CONECT    4    5    8   37
CONECT    5    6    6    7
CONECT    7   38
CONECT    8    9
CONECT    9   10   29   39
CONECT   10   11
CONECT   11   12   27   40
CONECT   12   13   23   41
CONECT   13   14
CONECT   14   15   21   42
CONECT   15   16   43   44
CONECT   16   17
CONECT   17   18   19   45
CONECT   18   46
CONECT   19   20   21   47
CONECT   20   48
CONECT   21   22   49
CONECT   22   50
CONECT   23   24
CONECT   24   25   51   52
CONECT   25   26   27   53
CONECT   26   54
CONECT   27   28   55
CONECT   28   56
CONECT   29   30   31   57
CONECT   30   58
CONECT   31   32   59
CONECT   32   60
END

HMDB0039742
     RDKit          3D
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose
 60 62  0  0  0  0  0  0  0  0999 V2000
   -5.7097    2.6578   -0.8439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6762    2.1618   -0.0540 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7625    1.4408   -0.8299 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8204    0.0129   -0.3735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0024   -0.1079    1.0845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2514   -0.8835    1.7223 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9637    0.5932    1.7919 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8104   -0.7569   -0.8741 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5303   -0.3418   -0.6541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8420   -1.1149    0.2806 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2268   -1.8027   -0.2515 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4665   -1.3957    0.5402 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0095   -0.2139    0.1168 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2992   -0.3741   -0.3833 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4213    0.0470   -1.8121 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3195    1.4155   -1.9744 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4098    2.0009   -1.3301 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5853    3.3250   -1.6568 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1438    1.8489    0.1681 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8425    2.2241    0.4186 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2960    0.3827    0.4831 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9962    0.1167    1.8267 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1314   -1.4020    1.8699 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8349   -2.6660    2.3339 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2836   -3.3131    1.5543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4934   -4.6053    2.0062 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0515   -3.2713    0.0786 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8850   -3.8959   -0.7028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3362    1.0882   -0.2961 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1541    1.2969    1.0900 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3927    2.0139   -0.7739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0228    2.5413   -2.0127 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4139    3.2166   -0.2282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2576    1.8220   -1.3624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2972    3.3113   -1.6524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1239    1.4636   -1.8927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7748   -0.4101   -0.8220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5128    0.0333    2.4597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9798   -0.5177   -1.6288 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3671   -1.6319   -1.3348 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2344   -2.2046    0.3639 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5796   -1.4586   -0.3133 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4286   -0.2709   -2.1699 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6320   -0.4649   -2.3953 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3264    1.4153   -1.5706 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5317    3.6031   -1.5685 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8844    2.4581    0.7470 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7599    2.9309    1.0941 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3167    0.0461    0.2817 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1782    0.9292    2.3813 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6887   -3.3563    2.3194 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4918   -2.5733    3.3852 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1836   -2.6894    1.6982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1507   -4.5480    2.7466 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0370   -3.7748   -0.0875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5976   -4.7593   -1.0719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3594    1.4504   -0.7386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2666    0.9645    1.3759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4303    2.9013   -0.0798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2059    3.0914   -1.8501 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  2  0
  5  7  1  0
  4  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 12 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
  9 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31  3  1  0
 27 11  1  0
 21 14  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  3 36  1  0
  4 37  1  0
  7 38  1  0
  9 39  1  0
 11 40  1  0
 12 41  1  0
 14 42  1  0
 15 43  1  0
 15 44  1  0
 17 45  1  0
 18 46  1  0
 19 47  1  0
 20 48  1  0
 21 49  1  0
 22 50  1  0
 24 51  1  0
 24 52  1  0
 25 53  1  0
 26 54  1  0
 27 55  1  0
 28 56  1  0
 29 57  1  0
 30 58  1  0
 31 59  1  0
 32 60  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
4-O-Methyl-a-D-glucopyranosyl-(1->2)-b-D-xylopyranosyl-(1->4)-D-xylose	HMDB
6-({4,5-dihydroxy-2-[(4,5,6-trihydroxyoxan-3-yl)oxy]oxan-3-yl}oxy)-4,5-dihydroxy-3-methoxyoxane-2-carboxylate	Generator

Chemical Formula

C₁₇H₂₈O₁₅

Average Molecular Weight

472.3952

Monoisotopic Molecular Weight

472.142820226

IUPAC Name

6-({4,5-dihydroxy-2-[(4,5,6-trihydroxyoxan-3-yl)oxy]oxan-3-yl}oxy)-4,5-dihydroxy-3-methoxyoxane-2-carboxylic acid

Traditional Name

6-({4,5-dihydroxy-2-[(4,5,6-trihydroxyoxan-3-yl)oxy]oxan-3-yl}oxy)-4,5-dihydroxy-3-methoxyoxane-2-carboxylic acid

CAS Registry Number

10365-86-3

SMILES

COC1C(O)C(O)C(OC2C(O)C(O)COC2OC2COC(O)C(O)C2O)OC1C(O)=O

InChI Identifier

InChI=1S/C17H28O15/c1-27-11-8(21)10(23)16(32-13(11)14(24)25)31-12-6(19)4(18)2-29-17(12)30-5-3-28-15(26)9(22)7(5)20/h4-13,15-23,26H,2-3H2,1H3,(H,24,25)

InChI Key

XZGRJCXNJVJWKJ-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Oligosaccharides

Alternative Parents

Substituents

Oligosaccharide
1-o-glucuronide
O-glucuronide
Glucuronic acid or derivatives
Glycosyl compound
O-glycosyl compound
Pyran
Oxane
Secondary alcohol
Hemiacetal
Acetal
Organoheterocyclic compound
Oxacycle
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid
Carboxylic acid derivative
Polyol
Hydrocarbon derivative
Organic oxide
Carbonyl group
Alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Extracellular (HMDB: HMDB0039742)
Cytoplasm (HMDB: HMDB0039742)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0039742)

Source

Exogenous

Food

Food (HMDB: HMDB0039742)

Cereal and cereal product

Cereal product

Breakfast cereal (FooDB: FOOD00270)

Cereals and cereal products (FooDB: FOOD00858)

Endogenous

Plant

Poaceae (HMDB: HMDB0039742)

Not Available

Nutrient (HMDB: HMDB0039742)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	180 - 187 °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	261 g/L	ALOGPS
logP	-2.5	ALOGPS
logP	-4.3	ChemAxon
logS	-0.26	ALOGPS
pKa (Strongest Acidic)	3.26	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	15	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	234.29 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	93.44 m³·mol⁻¹	ChemAxon
Polarizability	43.46 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	202.979	31661259
DarkChem	[M-H]-	196.82	31661259
DeepCCS	[M+H]+	195.247	30932474
DeepCCS	[M-H]-	192.889	30932474
DeepCCS	[M-2H]-	227.167	30932474
DeepCCS	[M+Na]+	202.575	30932474
AllCCS	[M+H]+	204.9	32859911
AllCCS	[M+H-H2O]+	202.9	32859911
AllCCS	[M+NH4]+	206.6	32859911
AllCCS	[M+Na]+	207.2	32859911
AllCCS	[M-H]-	202.3	32859911
AllCCS	[M+Na-2H]-	202.5	32859911
AllCCS	[M+HCOO]-	202.9	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose	COC1C(O)C(O)C(OC2C(O)C(O)COC2OC2COC(O)C(O)C2O)OC1C(O)=O	3881.8	Standard polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose	COC1C(O)C(O)C(OC2C(O)C(O)COC2OC2COC(O)C(O)C2O)OC1C(O)=O	3810.5	Standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose	COC1C(O)C(O)C(OC2C(O)C(O)COC2OC2COC(O)C(O)C2O)OC1C(O)=O	3754.1	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,1TMS,isomer #1	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O)C(O)C1O[Si](C)(C)C	3794.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,1TMS,isomer #2	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O)C(O[Si](C)(C)C)C1O	3791.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,1TMS,isomer #3	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O[Si](C)(C)C)C(O)C1O	3785.5	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,1TMS,isomer #4	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C)C2O)C(O)C1O	3805.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,1TMS,isomer #5	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O)C2O)C(O)C1O	3803.6	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,1TMS,isomer #6	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O)C2O)C(O)C1O	3794.6	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,1TMS,isomer #7	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O)C2O)C(O)C1O	3795.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,1TMS,isomer #8	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O)C(O)C1O	3788.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #1	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O)C(O)C1O[Si](C)(C)C	3751.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #10	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O)C2O)C(O[Si](C)(C)C)C1O	3766.6	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #11	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O)C2O)C(O[Si](C)(C)C)C1O	3760.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #12	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	3774.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #13	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3752.6	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #14	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O[Si](C)(C)C)C(O)C1O	3733.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #15	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O)C2O[Si](C)(C)C)C(O)C1O	3758.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #16	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O)C2O[Si](C)(C)C)C(O)C1O	3748.6	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #17	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O)C2O[Si](C)(C)C)C(O)C1O	3742.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #18	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	3784.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #19	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C)C2O)C(O)C1O	3753.6	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #2	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O)C2O)C(O)C1O[Si](C)(C)C	3774.6	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #20	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O[Si](C)(C)C)C2O)C(O)C1O	3782.5	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #21	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O[Si](C)(C)C)C2O)C(O)C1O	3766.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #22	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O)C(O)C1O	3761.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #23	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O)C2O)C(O)C1O	3762.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #24	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)OCC(O)C2O)C(O)C1O	3773.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #25	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)OCC(O)C2O)C(O)C1O	3751.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #26	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O)C2O)C(O)C1O	3743.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #27	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O)C2O)C(O)C1O	3773.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #28	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O)C2O)C(O)C1O	3745.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #3	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O)C2O)C(O)C1O[Si](C)(C)C	3762.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #4	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O)C2O)C(O)C1O[Si](C)(C)C	3760.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #5	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	3770.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #6	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3751.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #7	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3787.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #8	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O)C(O[Si](C)(C)C)C1O	3760.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TMS,isomer #9	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O)C2O)C(O[Si](C)(C)C)C1O	3776.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #1	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O)C2O)C(O)C1O[Si](C)(C)C	3725.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #10	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3724.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #11	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3768.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #12	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O)C2O)C(O)C1O[Si](C)(C)C	3750.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #13	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	3743.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #14	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3714.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #15	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3764.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #16	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	3739.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #17	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3713.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #18	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3757.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #19	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3750.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #2	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O)C2O)C(O)C1O[Si](C)(C)C	3694.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #20	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3759.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #21	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3731.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #22	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O)C2O)C(O[Si](C)(C)C)C1O	3743.5	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #23	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O)C2O)C(O[Si](C)(C)C)C1O	3719.5	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #24	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O)C2O)C(O[Si](C)(C)C)C1O	3727.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #25	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	3723.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #26	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3673.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #27	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)OCC(O)C2O)C(O[Si](C)(C)C)C1O	3759.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #28	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)OCC(O)C2O)C(O[Si](C)(C)C)C1O	3740.6	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #29	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	3758.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #3	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O)C2O)C(O)C1O[Si](C)(C)C	3708.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #30	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3736.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #31	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O)C2O)C(O[Si](C)(C)C)C1O	3760.5	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #32	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	3753.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #33	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3730.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #34	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	3747.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #35	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3724.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #36	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3754.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #37	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O)C2O[Si](C)(C)C)C(O)C1O	3679.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #38	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O)C2O[Si](C)(C)C)C(O)C1O	3644.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #39	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O)C2O[Si](C)(C)C)C(O)C1O	3658.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #4	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	3703.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #40	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	3715.6	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #41	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)OCC(O)C2O[Si](C)(C)C)C(O)C1O	3730.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #42	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)OCC(O)C2O[Si](C)(C)C)C(O)C1O	3697.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #43	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	3757.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #44	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O)C2O[Si](C)(C)C)C(O)C1O	3702.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #45	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	3752.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #46	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	3740.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #47	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O[Si](C)(C)C)C2O)C(O)C1O	3725.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #48	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O[Si](C)(C)C)C2O)C(O)C1O	3697.6	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #49	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O)C(O)C1O	3703.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #5	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3651.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #50	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)OCC(O[Si](C)(C)C)C2O)C(O)C1O	3753.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #51	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O)C(O)C1O	3734.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #52	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O)C(O)C1O	3745.5	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #53	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)OCC(O)C2O)C(O)C1O	3727.6	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #54	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)OCC(O)C2O)C(O)C1O	3695.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #55	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O)C2O)C(O)C1O	3747.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #56	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O)C2O)C(O)C1O	3689.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #6	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3718.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #7	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)OCC(O)C2O)C(O)C1O[Si](C)(C)C	3753.6	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #8	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)OCC(O)C2O)C(O)C1O[Si](C)(C)C	3731.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TMS,isomer #9	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	3751.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #1	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)OCC(O)C2O)C(O)C1O[Si](C)(C)C	3526.6	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #10	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	3496.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #11	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3447.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #12	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3515.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #13	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3512.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #14	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3530.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #15	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3487.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #16	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O)C2O)C(O)C1O[Si](C)(C)C	3589.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #17	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)OCC(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	3577.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #18	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)OCC(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3515.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #19	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)OCC(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3593.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #2	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)OCC(O)C2O)C(O)C1O[Si](C)(C)C	3488.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #20	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	3546.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #21	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)OCC(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3499.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #22	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)OCC(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3552.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #23	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3588.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #24	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3598.5	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #25	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3535.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #26	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	3551.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #27	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3510.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #28	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3565.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #29	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3560.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #3	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	3520.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #30	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3574.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #31	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3536.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #32	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3574.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #33	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3590.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #34	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3531.6	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #35	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3594.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #36	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)OCC(O)C2O)C(O[Si](C)(C)C)C1O	3535.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #37	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)OCC(O)C2O)C(O[Si](C)(C)C)C1O	3501.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #38	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	3533.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #39	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3478.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #4	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3466.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #40	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O)C2O)C(O[Si](C)(C)C)C1O	3508.5	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #41	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	3512.5	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #42	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3465.6	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #43	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	3508.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #44	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3454.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #45	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3525.6	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #46	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O)C2O)C(O[Si](C)(C)C)C1O	3591.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #47	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)OCC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	3577.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #48	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)OCC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3519.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #49	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	3538.5	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #5	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3536.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #50	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)OCC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3494.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #51	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3591.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #52	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	3545.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #53	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3512.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #54	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3561.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #55	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3577.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #56	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)OCC(O)C2O[Si](C)(C)C)C(O)C1O	3474.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #57	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)OCC(O)C2O[Si](C)(C)C)C(O)C1O	3451.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #58	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	3523.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #59	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O)C2O[Si](C)(C)C)C(O)C1O	3469.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #6	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O)C2O)C(O)C1O[Si](C)(C)C	3502.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #60	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	3503.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #61	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	3499.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #62	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O)C2O[Si](C)(C)C)C(O)C1O	3517.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #63	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	3579.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #64	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	3535.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #65	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	3549.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #66	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)OCC(O[Si](C)(C)C)C2O)C(O)C1O	3527.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #67	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O)C(O)C1O	3499.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #68	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O)C(O)C1O	3502.6	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #69	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O)C(O)C1O	3580.6	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #7	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	3502.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #70	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O)C2O)C(O)C1O	3529.5	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #8	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3457.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,4TMS,isomer #9	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3519.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #1	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O)C2O)C(O)C1O[Si](C)(C)C	3353.6	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #10	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3300.6	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #11	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	3311.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #12	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3273.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #13	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3370.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #14	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3302.5	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #15	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3341.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #16	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3297.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #17	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3294.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #18	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3331.5	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #19	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3289.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #2	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)OCC(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	3315.5	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #20	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3380.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #21	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	3382.5	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #22	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3351.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #23	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3425.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #24	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3368.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #25	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)OCC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3399.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #26	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)OCC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3360.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #27	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3336.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #28	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3371.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #29	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)OCC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3329.6	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #3	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)OCC(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3274.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #30	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3387.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #31	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3365.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #32	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3399.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #33	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3362.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #34	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3400.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #35	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3378.6	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #36	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O)C2O)C(O[Si](C)(C)C)C1O	3374.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #37	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)OCC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	3336.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #38	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)OCC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3296.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #39	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	3309.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #4	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)OCC(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3365.5	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #40	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)OCC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3266.5	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #41	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3329.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #42	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	3339.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #43	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3299.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #44	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3322.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #45	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3313.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #46	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	3386.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #47	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3350.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #48	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3364.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #49	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3333.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #5	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	3285.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #50	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3365.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #51	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O)C2O[Si](C)(C)C)C(O)C1O	3323.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #52	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	3337.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #53	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	3303.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #54	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	3342.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #55	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	3388.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #56	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)OCC(O[Si](C)(C)C)C2O)C(O)C1O	3360.6	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #6	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)OCC(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3242.6	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #7	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)OCC(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3322.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #8	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3313.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,5TMS,isomer #9	COC1C(C(=O)O[Si](C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C)C(O)C3O)OCC(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3345.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,1TBDMS,isomer #1	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	4022.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,1TBDMS,isomer #2	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	4020.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,1TBDMS,isomer #3	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	4021.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,1TBDMS,isomer #4	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	4032.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,1TBDMS,isomer #5	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O)C3O)OCC(O)C2O)C(O)C1O	4045.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,1TBDMS,isomer #6	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C(C)(C)C)C3O)OCC(O)C2O)C(O)C1O	4023.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,1TBDMS,isomer #7	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C(C)(C)C)OCC(O)C2O)C(O)C1O	4021.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,1TBDMS,isomer #8	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O)C(O)C1O	4015.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #1	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	4143.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #10	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C(C)(C)C)C3O)OCC(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	4144.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #11	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C(C)(C)C)OCC(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	4145.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #12	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C(C)(C)C)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	4172.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #13	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	4144.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #14	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	4140.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #15	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O)C3O)OCC(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	4162.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #16	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C(C)(C)C)C3O)OCC(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	4134.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #17	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C(C)(C)C)OCC(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	4133.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #18	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	4187.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #19	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	4162.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #2	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O)C3O)OCC(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	4168.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #20	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O)C3O)OCC(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	4188.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #21	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C(C)(C)C)C3O)OCC(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	4155.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #22	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C(C)(C)C)OCC(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	4157.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #23	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O)C3O)OCC(O)C2O)C(O)C1O	4165.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #24	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)OCC(O)C2O)C(O)C1O	4169.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #25	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)OCC(O)C2O)C(O)C1O	4153.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #26	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C(C)(C)C)C3O)OCC(O)C2O)C(O)C1O	4135.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #27	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)OCC(O)C2O)C(O)C1O	4148.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #28	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C(C)(C)C)OCC(O)C2O)C(O)C1O	4143.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #3	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C(C)(C)C)C3O)OCC(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	4137.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #4	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C(C)(C)C)OCC(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	4142.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #5	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	4165.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #6	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	4137.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #7	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4159.5	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #8	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	4155.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,2TBDMS,isomer #9	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O)C3O)OCC(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	4173.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #1	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O)C3O)OCC(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	4264.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #10	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O)C3O)OCC(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	4272.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #11	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O)C3O)OCC(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4290.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #12	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)OCC(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	4269.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #13	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C(C)(C)C)C3O)OCC(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	4265.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #14	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C(C)(C)C)C3O)OCC(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	4249.5	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #15	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C(C)(C)C)C3O)OCC(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4262.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #16	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C(C)(C)C)OCC(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	4271.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #17	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C(C)(C)C)OCC(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	4247.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #18	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C(C)(C)C)OCC(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4269.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #19	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	4283.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #2	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C(C)(C)C)C3O)OCC(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	4242.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #20	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C(C)(C)C)C2O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4294.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #21	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4262.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #22	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O)C3O)OCC(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	4278.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #23	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C(C)(C)C)C3O)OCC(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	4256.5	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #24	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C(C)(C)C)OCC(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	4263.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #25	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C(C)(C)C)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	4287.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #26	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	4252.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #27	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)OCC(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	4276.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #28	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)OCC(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	4273.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #29	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O)C3O)OCC(O[Si](C)(C)C(C)(C)C)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	4299.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #3	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C(C)(C)C)OCC(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	4246.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #30	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O)C3O)OCC(O)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	4268.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #31	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)OCC(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	4273.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #32	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C(C)(C)C)C3O)OCC(O[Si](C)(C)C(C)(C)C)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	4265.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #33	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C(C)(C)C)C3O)OCC(O)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	4242.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #34	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C(C)(C)C)OCC(O[Si](C)(C)C(C)(C)C)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	4272.8	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #35	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C(C)(C)C)OCC(O)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	4244.5	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #36	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	4289.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #37	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O)C3O)OCC(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	4251.2	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #38	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C(C)(C)C)C3O)OCC(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	4235.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #39	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C(C)(C)C)OCC(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	4237.5	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #4	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	4269.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #40	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	4275.5	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #41	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)OCC(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	4263.5	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #42	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)OCC(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	4256.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #43	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O)C3O)OCC(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	4298.0	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #44	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)OCC(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	4259.5	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #45	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C(C)(C)C)C3O)OCC(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	4276.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #46	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C(C)(C)C)OCC(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	4273.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #47	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O)C3O)OCC(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	4278.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #48	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C(C)(C)C)C3O)OCC(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	4253.6	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #49	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O[Si](C)(C)C(C)(C)C)OCC(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	4258.4	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #5	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	4240.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #50	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)OCC(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	4286.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #51	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)OCC(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	4288.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #52	COC1C(C(=O)O)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)OCC(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	4278.9	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #53	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)OCC(O)C2O)C(O)C1O	4250.5	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #54	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)OCC(O)C2O)C(O)C1O	4256.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #55	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)OCC(O)C2O)C(O)C1O	4278.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #56	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)OCC(O)C2O)C(O)C1O	4260.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #6	COC1C(C(=O)O[Si](C)(C)C(C)(C)C)OC(OC2C(OC3COC(O)C(O)C3O)OCC(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4277.3	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #7	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)OCC(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	4272.1	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #8	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)OCC(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	4273.7	Semi standard non polar	33892256
4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,isomer #9	COC1C(C(=O)O)OC(OC2C(OC3COC(O[Si](C)(C)C(C)(C)C)C(O)C3O)OCC(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	4297.7	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 - 4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose GC-MS (Non-derivatized) - 70eV, Positive	splash10-05fu-7514900000-15092d24635160d900da	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose GC-MS (3 TMS) - 70eV, Positive	splash10-00di-4901167000-120cd9f7bb254b2e059b	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose GC-MS (TBDMS_3_31) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose GC-MS ("4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose,3TBDMS,#31" 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 - 4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose 10V, Positive-QTOF	splash10-0fsi-0960400000-06b90c11e2c6be5391a3	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose 20V, Positive-QTOF	splash10-0f89-0940000000-528b12f3d590a35e5994	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose 40V, Positive-QTOF	splash10-001i-2920000000-84e657cdc5a0407325b2	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose 10V, Negative-QTOF	splash10-001i-2962500000-fcb397ff970921af8571	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose 20V, Negative-QTOF	splash10-001j-2941000000-926eacd895de9f8e2e3b	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose 40V, Negative-QTOF	splash10-0btd-4930000000-406a579b283adfd9305f	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose 10V, Negative-QTOF	splash10-00di-0101900000-cda482ec9950ad6f1cd2	2021-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose 20V, Negative-QTOF	splash10-0ac1-8726900000-4b5959b76fc926f3d73a	2021-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose 40V, Negative-QTOF	splash10-0a4j-9702000000-b2a0276f3a8c22d047d8	2021-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose 10V, Positive-QTOF	splash10-05fr-0100900000-38c862b9e36d0c422dbe	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose 20V, Positive-QTOF	splash10-0awc-4924400000-2c50c2cc3e7dfdd97092	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose 40V, Positive-QTOF	splash10-015d-9503000000-b07275fb49b0e14f50b7	2021-09-25	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

Cytoplasm
Extracellular

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

FDB019388

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

78382737

PDB ID

Not Available

ChEBI ID

168540

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 4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose (HMDB0039742)

MOL for HMDB0039742 (4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose)

3D MOL for HMDB0039742 (4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose)

3D SDF for HMDB0039742 (4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose)

3D-SDF for HMDB0039742 (4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose)

PDB for HMDB0039742 (4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose)

3D PDB for HMDB0039742 (4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose)

SMILES for HMDB0039742 (4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose)

INCHI for HMDB0039742 (4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose)

Structure for HMDB0039742 (4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose)

3D Structure for HMDB0039742 (4-O-Methyl-a-D-glucosyl-(1->2)-b-D-xylosyl-(1->4)-D-xylose)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra