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Record Information

Version

5.0

Status

Detected and Quantified

Creation Date

2005-11-16 15:48:42 UTC

Update Date

2021-11-15 21:04:28 UTC

HMDB ID

HMDB0000163

Secondary Accession Numbers

HMDB00163

Metabolite Identification

Common Name

D-Maltose

Description

D-Maltose, also known as maltose, maltobiose or malt sugar, is a disaccharide formed from two units of glucose joined with an alpha (1‚Üí4) bond. Its name comes from malt, combined with the suffix '-ose' which is used in names of sugars. Maltose is a key structural motif of starch. When alpha-amylase breaks down starch, it removes two glucose units at a time, producing maltose. Maltose can be further broken down to glucose by the maltase enzyme, which catalyses the hydrolysis of the glycosidic bond. D-maltose exists in all living species, ranging from bacteria to plants to humans. Within humans, D-maltose participates in a number of enzymatic reactions. In particular, maltose can be converted into glucose; which is mediated by the enzyme maltase-glucoamylase. In addition, maltose can be converted into glucose through its interaction with the enzyme glycogen debranching enzyme. Maltose is found in high concentrations in oriental wheats and in a lower concentrations in sweet potato, grape wines, yellow pond-lilies, sunflowers, and spinach. Maltose is a component of malt, a substance which is obtained in the process of allowing grain to soften in water and germinate. It is also present in highly variable quantities in partially hydrolysed starch products like maltodextrin, corn syrup and acid-thinned starch. Maltose has a sweet taste but is only about 30-60% as sweet as sucrose, depending on the concentration.

Structure

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

HMDB0000163
     RDKit          3D
D-Maltose
 45 46  0  0  0  0  0  0  0  0999 V2000
   -3.8477    1.8134    1.7693 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9644    2.0500    0.7427 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3963    0.8045    0.1277 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6949    0.0215    1.0420 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8945   -0.8383    0.2422 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0735   -0.0179   -0.5134 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2573   -0.0656   -0.1929 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7937    1.2653    0.2999 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7239    1.4077    1.7867 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5640    0.5719    2.4788 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0650    1.5378   -0.1311 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9623    0.5100   -0.0489 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1113    0.9080   -0.7731 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4967   -0.7764   -0.6919 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1903   -1.7504    0.2688 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1491   -0.4487   -1.3535 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6927   -1.4705   -2.1290 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7386   -1.7869   -0.5350 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9704   -2.7013   -1.1960 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7013   -1.0152   -1.4241 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5418   -1.8527   -2.1149 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4637   -0.0897   -0.4653 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4505    0.6211   -1.1232 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8795    2.6381    2.3323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1114    2.6382    1.1390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4038    2.6520   -0.0776 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6707    1.1142   -0.6516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2997   -1.4083    0.9850 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3713   -0.8102    0.6380 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1162    2.0440   -0.1354 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7024    1.2742    2.1956 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0137    2.4530    2.0310 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2350   -0.3437    2.6084 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3396    0.3095    0.9833 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8730    0.3852   -0.4499 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2116   -1.1785   -1.4287 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0023   -2.1322    0.6816 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3454    0.4945   -1.9250 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1876   -1.1928   -2.9288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3665   -2.3423    0.2078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5632   -3.4503   -1.4995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1065   -0.3446   -2.0746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1016   -1.2911   -2.7084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8704   -0.7408    0.3331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2936    0.5341   -0.5880 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  8 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
  5 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 22  3  1  0
 16  7  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  6
  5 28  1  1
  7 29  1  1
  8 30  1  6
  9 31  1  0
  9 32  1  0
 10 33  1  0
 12 34  1  1
 13 35  1  0
 14 36  1  6
 15 37  1  0
 16 38  1  6
 17 39  1  0
 18 40  1  1
 19 41  1  0
 20 42  1  6
 21 43  1  0
 22 44  1  1
 23 45  1  0
M  END

  Mrv1652304202019412D          

 23 24  0  0  1  0            999 V2000
    8.7262  -12.2877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1551  -13.1127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7262  -13.1127    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.8696  -13.5252    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.0117  -13.5252    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.0117  -14.3502    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.5840  -14.7627    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.2985  -14.3502    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.7262  -14.7627    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.8696  -14.3502    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.2985  -13.5252    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.4406  -14.3502    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.0117  -11.8752    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1551  -12.2877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2972  -13.1127    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2972  -14.7627    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.5840  -15.5877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.0130  -14.7627    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7262  -15.5877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.0130  -13.1127    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.5840  -13.1127    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4406  -13.5252    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1551  -14.7627    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1 13  1  0  0  0  0
  3  1  1  1  0  0  0
  4  2  1  1  0  0  0
  2 14  1  0  0  0  0
  3  5  1  0  0  0  0
  3 22  1  0  0  0  0
  4 10  1  0  0  0  0
  4 21  1  0  0  0  0
  5 15  1  6  0  0  0
  5  6  1  0  0  0  0
  6 16  1  1  0  0  0
  6  9  1  0  0  0  0
  7  8  1  0  0  0  0
  7 10  1  0  0  0  0
  7 17  1  1  0  0  0
  8 11  1  0  0  0  0
  8 18  1  1  0  0  0
  9 19  1  6  0  0  0
  9 12  1  0  0  0  0
 10 23  1  6  0  0  0
 11 21  1  0  0  0  0
 11 20  1  6  0  0  0
 12 22  1  0  0  0  0
 12 23  1  6  0  0  0
M  END
> <DATABASE_ID>
HMDB0000163

> <DATABASE_NAME>
hmdb

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

> <INCHI_IDENTIFIER>
InChI=1S/C12H22O11/c13-1-3-5(15)6(16)9(19)12(22-3)23-10-4(2-14)21-11(20)8(18)7(10)17/h3-20H,1-2H2/t3-,4-,5-,6+,7-,8+,9-,10-,11+,12-/m1/s1

> <INCHI_KEY>
GUBGYTABKSRVRQ-DKBJLJRDSA-N

> <FORMULA>
C12H22O11

> <MOLECULAR_WEIGHT>
342.2965

> <EXACT_MASS>
342.116211546

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
31.42931831870777

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <ALOGPS_LOGP>
-3.01

> <JCHEM_LOGP>
-4.703374863666666

> <ALOGPS_LOGS>
0.23

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.17368931723461

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.254374125721942

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810835652988272

> <JCHEM_POLAR_SURFACE_AREA>
189.52999999999997

> <JCHEM_REFRACTIVITY>
68.3367

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.86e+02 g/l

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

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0000163
     RDKit          3D
D-Maltose
 45 46  0  0  0  0  0  0  0  0999 V2000
   -3.8477    1.8134    1.7693 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9644    2.0500    0.7427 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3963    0.8045    0.1277 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6949    0.0215    1.0420 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8945   -0.8383    0.2422 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0735   -0.0179   -0.5134 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2573   -0.0656   -0.1929 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7937    1.2653    0.2999 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7239    1.4077    1.7867 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5640    0.5719    2.4788 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0650    1.5378   -0.1311 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9623    0.5100   -0.0489 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1113    0.9080   -0.7731 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4967   -0.7764   -0.6919 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1903   -1.7504    0.2688 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1491   -0.4487   -1.3535 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6927   -1.4705   -2.1290 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7386   -1.7869   -0.5350 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9704   -2.7013   -1.1960 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7013   -1.0152   -1.4241 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5418   -1.8527   -2.1149 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4637   -0.0897   -0.4653 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4505    0.6211   -1.1232 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8795    2.6381    2.3323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1114    2.6382    1.1390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4038    2.6520   -0.0776 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6707    1.1142   -0.6516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2997   -1.4083    0.9850 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3713   -0.8102    0.6380 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1162    2.0440   -0.1354 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7024    1.2742    2.1956 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0137    2.4530    2.0310 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2350   -0.3437    2.6084 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3396    0.3095    0.9833 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8730    0.3852   -0.4499 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2116   -1.1785   -1.4287 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0023   -2.1322    0.6816 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3454    0.4945   -1.9250 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1876   -1.1928   -2.9288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3665   -2.3423    0.2078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5632   -3.4503   -1.4995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1065   -0.3446   -2.0746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1016   -1.2911   -2.7084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8704   -0.7408    0.3331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2936    0.5341   -0.5880 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  8 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
  5 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 22  3  1  0
 16  7  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  6
  5 28  1  1
  7 29  1  1
  8 30  1  6
  9 31  1  0
  9 32  1  0
 10 33  1  0
 12 34  1  1
 13 35  1  0
 14 36  1  6
 15 37  1  0
 16 38  1  6
 17 39  1  0
 18 40  1  1
 19 41  1  0
 20 42  1  6
 21 43  1  0
 22 44  1  1
 23 45  1  0
M  END

HEADER    PROTEIN                                 20-APR-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-APR-20         0                                  
HETATM    1  C   UNK     0      16.289 -22.937   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      18.956 -24.477   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      16.289 -24.477   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      20.290 -25.247   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      14.955 -25.247   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      14.955 -26.787   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      21.623 -27.557   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      22.957 -26.787   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      16.289 -27.557   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      20.290 -26.787   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      22.957 -25.247   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      17.622 -26.787   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      14.955 -22.167   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      18.956 -22.937   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0      13.621 -24.477   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      13.621 -27.557   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      21.623 -29.097   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      24.291 -27.557   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      16.289 -29.097   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      24.291 -24.477   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      21.623 -24.477   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      17.622 -25.247   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      18.956 -27.557   0.000  0.00  0.00           O+0
CONECT    1   13    3                                                       
CONECT    2    4   14                                                       
CONECT    3    1    5   22                                                  
CONECT    4    2   10   21                                                  
CONECT    5    3   15    6                                                  
CONECT    6    5   16    9                                                  
CONECT    7    8   10   17                                                  
CONECT    8    7   11   18                                                  
CONECT    9    6   19   12                                                  
CONECT   10    4    7   23                                                  
CONECT   11    8   21   20                                                  
CONECT   12    9   22   23                                                  
CONECT   13    1                                                            
CONECT   14    2                                                            
CONECT   15    5                                                            
CONECT   16    6                                                            
CONECT   17    7                                                            
CONECT   18    8                                                            
CONECT   19    9                                                            
CONECT   20   11                                                            
CONECT   21    4   11                                                       
CONECT   22    3   12                                                       
CONECT   23   10   12                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

COMPND    HMDB0000163
HETATM    1  O1  UNL     1      -3.848   1.813   1.769  1.00  0.00           O  
HETATM    2  C1  UNL     1      -2.964   2.050   0.743  1.00  0.00           C  
HETATM    3  C2  UNL     1      -2.396   0.805   0.128  1.00  0.00           C  
HETATM    4  O2  UNL     1      -1.695   0.022   1.042  1.00  0.00           O  
HETATM    5  C3  UNL     1      -0.895  -0.838   0.242  1.00  0.00           C  
HETATM    6  O3  UNL     1      -0.073  -0.018  -0.513  1.00  0.00           O  
HETATM    7  C4  UNL     1       1.257  -0.066  -0.193  1.00  0.00           C  
HETATM    8  C5  UNL     1       1.794   1.265   0.300  1.00  0.00           C  
HETATM    9  C6  UNL     1       1.724   1.408   1.787  1.00  0.00           C  
HETATM   10  O4  UNL     1       2.564   0.572   2.479  1.00  0.00           O  
HETATM   11  O5  UNL     1       3.065   1.538  -0.131  1.00  0.00           O  
HETATM   12  C7  UNL     1       3.962   0.510  -0.049  1.00  0.00           C  
HETATM   13  O6  UNL     1       5.111   0.908  -0.773  1.00  0.00           O  
HETATM   14  C8  UNL     1       3.497  -0.776  -0.692  1.00  0.00           C  
HETATM   15  O7  UNL     1       3.190  -1.750   0.269  1.00  0.00           O  
HETATM   16  C9  UNL     1       2.149  -0.449  -1.353  1.00  0.00           C  
HETATM   17  O8  UNL     1       1.693  -1.470  -2.129  1.00  0.00           O  
HETATM   18  C10 UNL     1      -1.739  -1.787  -0.535  1.00  0.00           C  
HETATM   19  O9  UNL     1      -0.970  -2.701  -1.196  1.00  0.00           O  
HETATM   20  C11 UNL     1      -2.701  -1.015  -1.424  1.00  0.00           C  
HETATM   21  O10 UNL     1      -3.542  -1.853  -2.115  1.00  0.00           O  
HETATM   22  C12 UNL     1      -3.464  -0.090  -0.465  1.00  0.00           C  
HETATM   23  O11 UNL     1      -4.451   0.621  -1.123  1.00  0.00           O  
HETATM   24  H1  UNL     1      -3.879   2.638   2.332  1.00  0.00           H  
HETATM   25  H2  UNL     1      -2.111   2.638   1.139  1.00  0.00           H  
HETATM   26  H3  UNL     1      -3.404   2.652  -0.078  1.00  0.00           H  
HETATM   27  H4  UNL     1      -1.671   1.114  -0.652  1.00  0.00           H  
HETATM   28  H5  UNL     1      -0.300  -1.408   0.985  1.00  0.00           H  
HETATM   29  H6  UNL     1       1.371  -0.810   0.638  1.00  0.00           H  
HETATM   30  H7  UNL     1       1.116   2.044  -0.135  1.00  0.00           H  
HETATM   31  H8  UNL     1       0.702   1.274   2.196  1.00  0.00           H  
HETATM   32  H9  UNL     1       2.014   2.453   2.031  1.00  0.00           H  
HETATM   33  H10 UNL     1       2.235  -0.344   2.608  1.00  0.00           H  
HETATM   34  H11 UNL     1       4.340   0.310   0.983  1.00  0.00           H  
HETATM   35  H12 UNL     1       5.873   0.385  -0.450  1.00  0.00           H  
HETATM   36  H13 UNL     1       4.212  -1.178  -1.429  1.00  0.00           H  
HETATM   37  H14 UNL     1       4.002  -2.132   0.682  1.00  0.00           H  
HETATM   38  H15 UNL     1       2.345   0.494  -1.925  1.00  0.00           H  
HETATM   39  H16 UNL     1       1.188  -1.193  -2.929  1.00  0.00           H  
HETATM   40  H17 UNL     1      -2.366  -2.342   0.208  1.00  0.00           H  
HETATM   41  H18 UNL     1      -1.563  -3.450  -1.499  1.00  0.00           H  
HETATM   42  H19 UNL     1      -2.106  -0.345  -2.075  1.00  0.00           H  
HETATM   43  H20 UNL     1      -4.102  -1.291  -2.708  1.00  0.00           H  
HETATM   44  H21 UNL     1      -3.870  -0.741   0.333  1.00  0.00           H  
HETATM   45  H22 UNL     1      -5.294   0.534  -0.588  1.00  0.00           H  
CONECT    1    2   24
CONECT    2    3   25   26
CONECT    3    4   22   27
CONECT    4    5
CONECT    5    6   18   28
CONECT    6    7
CONECT    7    8   16   29
CONECT    8    9   11   30
CONECT    9   10   31   32
CONECT   10   33
CONECT   11   12
CONECT   12   13   14   34
CONECT   13   35
CONECT   14   15   16   36
CONECT   15   37
CONECT   16   17   38
CONECT   17   39
CONECT   18   19   20   40
CONECT   19   41
CONECT   20   21   22   42
CONECT   21   43
CONECT   22   23   44
CONECT   23   45
END

HMDB0000163
     RDKit          3D
D-Maltose
 45 46  0  0  0  0  0  0  0  0999 V2000
   -3.8477    1.8134    1.7693 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9644    2.0500    0.7427 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3963    0.8045    0.1277 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6949    0.0215    1.0420 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8945   -0.8383    0.2422 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0735   -0.0179   -0.5134 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2573   -0.0656   -0.1929 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7937    1.2653    0.2999 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7239    1.4077    1.7867 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5640    0.5719    2.4788 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0650    1.5378   -0.1311 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9623    0.5100   -0.0489 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1113    0.9080   -0.7731 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4967   -0.7764   -0.6919 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1903   -1.7504    0.2688 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1491   -0.4487   -1.3535 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6927   -1.4705   -2.1290 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7386   -1.7869   -0.5350 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9704   -2.7013   -1.1960 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7013   -1.0152   -1.4241 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5418   -1.8527   -2.1149 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4637   -0.0897   -0.4653 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4505    0.6211   -1.1232 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8795    2.6381    2.3323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1114    2.6382    1.1390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4038    2.6520   -0.0776 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6707    1.1142   -0.6516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2997   -1.4083    0.9850 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3713   -0.8102    0.6380 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1162    2.0440   -0.1354 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7024    1.2742    2.1956 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0137    2.4530    2.0310 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2350   -0.3437    2.6084 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3396    0.3095    0.9833 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8730    0.3852   -0.4499 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2116   -1.1785   -1.4287 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0023   -2.1322    0.6816 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3454    0.4945   -1.9250 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1876   -1.1928   -2.9288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3665   -2.3423    0.2078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5632   -3.4503   -1.4995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1065   -0.3446   -2.0746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1016   -1.2911   -2.7084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8704   -0.7408    0.3331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2936    0.5341   -0.5880 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  8 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
  5 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 22  3  1  0
 16  7  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  6
  5 28  1  1
  7 29  1  1
  8 30  1  6
  9 31  1  0
  9 32  1  0
 10 33  1  0
 12 34  1  1
 13 35  1  0
 14 36  1  6
 15 37  1  0
 16 38  1  6
 17 39  1  0
 18 40  1  1
 19 41  1  0
 20 42  1  6
 21 43  1  0
 22 44  1  1
 23 45  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
4-O-alpha-D-Glucopyranosyl-alpha-D-mannopyranose	ChEBI
4-O-a-D-Glucopyranosyl-a-D-mannopyranose	Generator
4-O-Α-D-glucopyranosyl-α-D-mannopyranose	Generator
1-alpha-D-Glucopyranosyl-4-alpha-D-glucopyranose	HMDB
1-alpha-delta-Glucopyranosyl-4-alpha-delta-glucopyranose	HMDB
4-(alpha-D-Glucopyranosido)-alpha-glucopyranose	HMDB
4-(alpha-D-Glucosido)-D-glucose	HMDB
4-(alpha-delta-Glucopyranosido)-alpha-glucopyranose	HMDB
4-(alpha-delta-Glucosido)-delta-glucose	HMDB
4-O-a-D-Glucopyranosyl-D-glucose	HMDB
4-O-alpha-D-Glucopyranosyl-D-glucopyranose	HMDB
4-O-alpha-D-Glucopyranosyl-D-glucose	HMDB
4-O-alpha-delta-Glucopyranosyl-delta-glucopyranose	HMDB
4-O-alpha-delta-Glucopyranosyl-delta-glucose	HMDB
Advantose 100	HMDB
alpha-D-GLCP-(1->4)-D-GLCP	HMDB
alpha-D-Glucopyranosyl-(1->4)-D-glucopyranose	HMDB
alpha-D-Glucopyranosyl-(1->4)-D-glucose	HMDB
alpha-delta-GLCP-(1->4)-delta-GLCP	HMDB
alpha-delta-Glucopyranosyl-(1->4)-delta-glucopyranose	HMDB
alpha-delta-Glucopyranosyl-(1->4)-delta-glucose	HMDB
alpha-Malt sugar	HMDB
Cextromaltose	HMDB
D-(+)-Maltose	HMDB
delta-(+)-Maltose	HMDB
delta-Maltose	HMDB
Finetose	HMDB
Finetose F	HMDB
Madoros	HMDB
Malt sugar	HMDB
Maltobiose	HMDB
Maltodiose	HMDB
Maltos	HMDB
Maltose	HMDB
Maltose HH	HMDB
Maltose HHH	HMDB
Maltose solution	HMDB
Malzzucker	HMDB
Martos-10	HMDB
Sunmalt	HMDB
Sunmalt S	HMDB

Chemical Formula

C₁₂H₂₂O₁₁

Average Molecular Weight

342.2965

Monoisotopic Molecular Weight

342.116211546

IUPAC Name

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

Traditional Name

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

CAS Registry Number

69-79-4

SMILES

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

InChI Identifier

InChI=1S/C12H22O11/c13-1-3-5(15)6(16)9(19)12(22-3)23-10-4(2-14)21-11(20)8(18)7(10)17/h3-20H,1-2H2/t3-,4-,5-,6+,7-,8+,9-,10-,11+,12-/m1/s1

InChI Key

GUBGYTABKSRVRQ-DKBJLJRDSA-N

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

O-glycosyl compounds

Alternative Parents

Substituents

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

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

alpha-D-glucosyl-(1->4)-D-mannopyranose (CHEBI:47937 )

Ontology

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	102 - 103 °C	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	780 mg/mL	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Experimental Collision Cross Sections

Adduct Type	Data Source	CCS Value (Å²)	Reference
[M-H]-	Baker	205.9	30932474

Predicted Molecular Properties

Property	Value	Source
Water Solubility	586 g/L	ALOGPS
logP	-3	ALOGPS
logP	-4.7	ChemAxon
logS	0.23	ALOGPS
pKa (Strongest Acidic)	11.25	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	189.53 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	68.34 m³·mol⁻¹	ChemAxon
Polarizability	31.43 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	174.901	31661259
DarkChem	[M-H]-	171.04	31661259
AllCCS	[M+H]+	176.311	32859911
AllCCS	[M-H]-	174.376	32859911
DeepCCS	[M+H]+	174.444	30932474
DeepCCS	[M-H]-	172.297	30932474
DeepCCS	[M-2H]-	205.685	30932474
DeepCCS	[M+Na]+	180.24	30932474
AllCCS	[M+H]+	176.3	32859911
AllCCS	[M+H-H2O]+	173.5	32859911
AllCCS	[M+NH4]+	178.9	32859911
AllCCS	[M+Na]+	179.7	32859911
AllCCS	[M-H]-	174.4	32859911
AllCCS	[M+Na-2H]-	173.9	32859911
AllCCS	[M+HCOO]-	173.6	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
D-Maltose	OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O)[C@@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O	3876.3	Standard polar	33892256
D-Maltose	OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O)[C@@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O	3234.2	Standard non polar	33892256
D-Maltose	OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O)[C@@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O	2939.5	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
D-Maltose,1TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	2784.2	Semi standard non polar	33892256
D-Maltose,1TMS,isomer #2	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](O)O[C@H](CO)[C@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	2790.8	Semi standard non polar	33892256
D-Maltose,1TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	2785.3	Semi standard non polar	33892256
D-Maltose,1TMS,isomer #4	C[Si](C)(C)O[C@H]1O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@@H]1O	2809.6	Semi standard non polar	33892256
D-Maltose,1TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	2802.6	Semi standard non polar	33892256
D-Maltose,1TMS,isomer #6	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]1O	2787.1	Semi standard non polar	33892256
D-Maltose,1TMS,isomer #7	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)[C@@H]1O	2784.3	Semi standard non polar	33892256
D-Maltose,1TMS,isomer #8	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)[C@H](O)[C@H]1O	2776.5	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O)[C@@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	2814.6	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #10	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	2789.3	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #11	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O	2781.6	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #12	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	2776.0	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #13	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C	2774.6	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #14	C[Si](C)(C)O[C@H]1[C@@H](O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](CO)O[C@@H]1O[Si](C)(C)C	2793.5	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #15	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	2790.7	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #16	C[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	2777.7	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #17	C[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	2771.1	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #18	C[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	2775.0	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #19	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	2808.5	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	2805.0	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #20	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)[C@H](O)[C@H]1O	2798.1	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #21	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)[C@@H]1O	2790.1	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #22	C[Si](C)(C)O[C@H]1O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H]1O	2801.4	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #23	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2800.5	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #24	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2788.6	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #25	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	2796.4	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #26	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	2782.6	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #27	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)O[C@@H]1CO	2774.3	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #28	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C	2784.1	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O	2775.6	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	2776.8	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2780.2	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2778.5	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2796.3	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #8	C[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	2785.8	Semi standard non polar	33892256
D-Maltose,2TMS,isomer #9	C[Si](C)(C)O[C@H]1O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H]1O	2796.3	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	2681.4	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #10	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2679.0	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #11	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2697.5	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #12	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O	2676.5	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #13	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2682.6	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #14	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2674.6	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #15	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2693.0	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #16	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2660.3	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #17	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2664.1	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #18	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2681.5	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #19	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2663.4	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)O[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	2685.2	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #20	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2696.8	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #21	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2670.8	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #22	C[Si](C)(C)O[C@H]1[C@@H](O[Si](C)(C)C)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](CO)O[C@@H]1O[Si](C)(C)C	2710.7	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #23	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	2689.3	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #24	C[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	2719.7	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #25	C[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C	2706.3	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #26	C[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2699.7	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #27	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	2687.0	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #28	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O	2720.1	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #29	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	2697.4	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	2670.8	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #30	C[Si](C)(C)O[C@H]1O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O	2702.9	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #31	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2682.3	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #32	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2678.8	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #33	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	2670.0	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #34	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H]1CO	2700.2	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #35	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](O)O[C@H](CO)[C@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2706.5	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #36	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2685.6	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #37	C[Si](C)(C)O[C@H]1[C@@H](O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H](CO)O[C@@H]1O[Si](C)(C)C	2727.2	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #38	C[Si](C)(C)O[C@H]1[C@@H](O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H](CO)O[C@@H]1O[Si](C)(C)C	2706.1	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #39	C[Si](C)(C)O[C@H]1[C@@H](O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H](CO)O[C@@H]1O[Si](C)(C)C	2717.2	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O)[C@@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2679.3	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #40	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	2681.5	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #41	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2696.3	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #42	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2688.1	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #43	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	2693.3	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #44	C[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	2711.0	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #45	C[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	2707.2	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #46	C[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O	2700.3	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #47	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2694.2	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #48	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2687.0	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #49	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	2695.2	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2678.2	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #50	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)O[C@@H]1CO	2723.8	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #51	C[Si](C)(C)O[C@H]1O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H](O)[C@@H]1O	2719.4	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #52	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	2709.6	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #53	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2680.7	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #54	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2691.2	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #55	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2678.2	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #56	C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	2689.9	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2692.3	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O	2679.2	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #8	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	2685.6	Semi standard non polar	33892256
D-Maltose,3TMS,isomer #9	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2693.0	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	2619.9	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #10	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2585.5	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #11	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2612.7	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #12	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2609.9	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #13	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2604.8	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #14	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O)[C@@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2626.9	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #15	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2623.0	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #16	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O	2634.1	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #17	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2619.1	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #18	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2635.9	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #19	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2630.7	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	2613.3	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #20	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2604.3	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #21	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2628.5	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #22	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2620.9	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #23	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2610.9	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #24	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2631.9	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #25	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2631.9	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #26	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2614.3	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #27	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2643.8	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #28	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2628.6	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #29	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2638.8	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2606.2	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #30	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2654.8	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #31	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2652.3	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #32	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2604.7	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #33	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2620.9	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #34	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2625.9	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #35	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2626.1	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #36	C[Si](C)(C)O[C@H]1[C@@H](O[Si](C)(C)C)[C@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H](CO)O[C@@H]1O[Si](C)(C)C	2654.4	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #37	C[Si](C)(C)O[C@H]1[C@@H](O[Si](C)(C)C)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H](CO)O[C@@H]1O[Si](C)(C)C	2670.3	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #38	C[Si](C)(C)O[C@H]1[C@@H](O[Si](C)(C)C)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H](CO)O[C@@H]1O[Si](C)(C)C	2643.5	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #39	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	2632.5	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2614.8	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #40	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2623.0	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #41	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2643.3	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #42	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	2615.1	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #43	C[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C	2683.9	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #44	C[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2660.8	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #45	C[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2665.3	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #46	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2616.5	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #47	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2633.3	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #48	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	2605.6	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #49	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)O[C@@H]1CO	2644.7	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2618.8	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #50	C[Si](C)(C)O[C@H]1O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H]1O	2668.4	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #51	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2646.5	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #52	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2623.6	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #53	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2606.1	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #54	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2601.1	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #55	C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2630.1	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #56	C[Si](C)(C)O[C@H]1[C@@H](O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H](CO)O[C@@H]1O[Si](C)(C)C	2677.6	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #57	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]2CO)O[C@@H]1CO	2659.2	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #58	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2620.7	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #59	C[Si](C)(C)O[C@H]1[C@@H](O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H](CO)O[C@@H]1O[Si](C)(C)C	2656.9	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)O[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	2620.7	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #60	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2635.3	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #61	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	2617.3	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #62	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2656.7	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #63	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2645.1	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #64	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2640.4	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #65	C[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O	2669.7	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #66	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2624.4	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #67	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2614.2	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #68	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2607.7	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #69	C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	2637.2	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)O[C@@H]2CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2625.1	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #70	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2623.8	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #8	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2640.5	Semi standard non polar	33892256
D-Maltose,4TMS,isomer #9	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2632.0	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	2629.2	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #10	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2609.3	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #11	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)O[C@@H]2CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2597.7	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #12	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)O[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2622.2	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #13	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)O[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2612.4	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #14	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2634.0	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #15	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2646.1	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #16	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2646.3	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #17	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2595.9	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #18	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2609.2	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #19	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2614.9	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]2CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2602.0	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #20	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2625.8	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #21	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2630.1	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #22	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2646.8	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #23	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2650.2	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #24	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2630.5	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #25	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2639.9	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #26	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2643.7	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #27	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2615.2	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #28	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2624.7	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #29	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2637.4	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2620.1	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #30	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2630.1	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #31	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2637.8	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #32	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2646.8	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #33	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2652.5	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #34	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2665.6	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #35	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2635.7	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #36	C[Si](C)(C)O[C@H]1[C@@H](O[Si](C)(C)C)[C@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H](CO)O[C@@H]1O[Si](C)(C)C	2675.3	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #37	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]2CO)O[C@@H]1CO	2649.5	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #38	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2647.2	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #39	C[Si](C)(C)O[C@H]1[C@@H](O[Si](C)(C)C)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H](CO)O[C@@H]1O[Si](C)(C)C	2656.2	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	2611.3	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #40	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	2656.0	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #41	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	2631.2	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #42	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2652.8	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #43	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2621.1	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #44	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2631.3	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #45	C[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2661.7	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #46	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2638.1	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #47	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2607.8	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #48	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2613.6	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #49	C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2650.0	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2582.4	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #50	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2633.2	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #51	C[Si](C)(C)O[C@H]1[C@@H](O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H](CO)O[C@@H]1O[Si](C)(C)C	2663.7	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #52	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2644.0	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #53	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2620.7	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #54	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2626.6	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #55	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2659.7	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #56	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2634.1	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2613.9	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2599.8	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #8	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2594.9	Semi standard non polar	33892256
D-Maltose,5TMS,isomer #9	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2601.6	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]2CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2618.4	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #10	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2618.8	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #11	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)O[C@@H]2CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2614.4	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #12	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)O[C@@H]2CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2620.8	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #13	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2634.3	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #14	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2635.5	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #15	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2618.7	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #16	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2632.2	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #17	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2636.6	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #18	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2658.1	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #19	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2644.7	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2637.0	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #20	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2621.8	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #21	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2635.3	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #22	C[Si](C)(C)O[C@H]1[C@@H](O[Si](C)(C)C)[C@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H](CO)O[C@@H]1O[Si](C)(C)C	2662.9	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #23	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2662.0	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #24	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2636.5	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #25	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2634.8	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #26	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2637.7	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #27	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2629.4	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #28	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2650.2	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2642.1	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2623.5	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2623.0	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2638.0	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2600.9	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #8	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2607.3	Semi standard non polar	33892256
D-Maltose,6TMS,isomer #9	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2626.6	Semi standard non polar	33892256
D-Maltose,7TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]2CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2646.1	Semi standard non polar	33892256
D-Maltose,7TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]2CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2657.6	Semi standard non polar	33892256
D-Maltose,7TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2671.2	Semi standard non polar	33892256
D-Maltose,7TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2661.4	Semi standard non polar	33892256
D-Maltose,7TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2647.5	Semi standard non polar	33892256
D-Maltose,7TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2652.5	Semi standard non polar	33892256
D-Maltose,7TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)O[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2656.5	Semi standard non polar	33892256
D-Maltose,7TMS,isomer #8	C[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2652.5	Semi standard non polar	33892256
D-Maltose,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	3021.0	Semi standard non polar	33892256
D-Maltose,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](O)O[C@H](CO)[C@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	3038.0	Semi standard non polar	33892256
D-Maltose,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	3022.2	Semi standard non polar	33892256
D-Maltose,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@H]1O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@@H]1O	3040.0	Semi standard non polar	33892256
D-Maltose,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	3039.3	Semi standard non polar	33892256
D-Maltose,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]1O	3043.4	Semi standard non polar	33892256
D-Maltose,1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)[C@@H]1O	3036.1	Semi standard non polar	33892256
D-Maltose,1TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)[C@H](O)[C@H]1O	3029.3	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@H](O)[C@@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	3246.7	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	3251.6	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3257.2	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3247.3	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3263.1	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](CO)O[C@@H]1O[Si](C)(C)C(C)(C)C	3248.0	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	3248.4	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	3245.9	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O	3242.8	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3255.7	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	3260.0	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	3253.9	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #20	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)[C@H](O)[C@H]1O	3265.0	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)[C@@H]1O	3257.0	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #22	CC(C)(C)[Si](C)(C)O[C@H]1O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O	3278.7	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3267.6	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3257.1	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3269.7	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #26	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3254.7	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #27	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)O[C@@H]1CO	3244.3	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #28	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3248.2	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O	3229.8	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3235.7	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3251.9	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3243.6	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3251.1	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3255.9	Semi standard non polar	33892256
D-Maltose,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@H]1O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3248.3	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	3392.8	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3399.9	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3406.1	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O	3394.6	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3412.3	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3400.4	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3404.3	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3409.2	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3390.8	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3396.0	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3393.4	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)O[C@@H]2CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3395.1	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3396.2	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3395.1	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #22	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](CO)O[C@@H]1O[Si](C)(C)C(C)(C)C	3426.3	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	3414.7	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #24	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3422.5	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #25	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3422.4	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #26	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3432.4	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	3401.6	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #28	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3412.8	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #29	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3410.8	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3383.6	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #30	CC(C)(C)[Si](C)(C)O[C@H]1O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3427.3	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3402.7	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3402.6	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3416.6	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #34	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@@H]1CO	3405.4	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #35	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](O)O[C@H](CO)[C@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3397.6	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #36	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3410.9	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #37	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H](CO)O[C@@H]1O[Si](C)(C)C(C)(C)C	3412.1	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #38	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H](CO)O[C@@H]1O[Si](C)(C)C(C)(C)C	3409.0	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #39	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@@H]1O[Si](C)(C)C(C)(C)C	3427.7	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@H](O)[C@@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3407.5	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #40	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	3398.6	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #41	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3417.8	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #42	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3420.7	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #43	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3430.7	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #44	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O	3407.5	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #45	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3411.3	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #46	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3419.6	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #47	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3410.0	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #48	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3409.1	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #49	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3429.8	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3395.3	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #50	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)O[C@@H]1CO	3417.7	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #51	CC(C)(C)[Si](C)(C)O[C@H]1O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@H](O)[C@@H]1O	3411.0	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #52	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3423.9	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #53	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3401.3	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #54	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3403.1	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #55	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3410.6	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #56	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3405.9	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3403.4	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O	3387.6	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3386.0	Semi standard non polar	33892256
D-Maltose,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3421.6	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)O[C@@H]2CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3520.0	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3543.5	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3535.5	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3533.0	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3544.9	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@H](O)[C@@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3546.1	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3546.2	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O	3541.0	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)O[C@@H]2CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3548.7	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)O[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3546.1	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3544.5	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3526.1	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3552.7	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3548.0	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3544.4	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3553.1	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3555.5	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3554.7	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3554.3	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3555.1	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3550.8	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3559.1	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3546.9	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3561.2	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3561.6	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3547.3	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3551.2	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3548.3	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3552.5	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #36	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H](CO)O[C@@H]1O[Si](C)(C)C(C)(C)C	3568.2	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #37	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H](CO)O[C@@H]1O[Si](C)(C)C(C)(C)C	3573.9	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #38	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@@H]1O[Si](C)(C)C(C)(C)C	3572.5	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #39	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	3555.3	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3540.0	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #40	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3558.5	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #41	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3566.9	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #42	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3567.1	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #43	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3565.5	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #44	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3568.4	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #45	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3574.9	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #46	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3547.3	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #47	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3553.5	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #48	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3559.1	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #49	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@@H]1CO	3558.4	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3536.7	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #50	CC(C)(C)[Si](C)(C)O[C@H]1O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3557.1	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #51	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3565.7	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #52	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3539.4	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #53	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3541.3	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #54	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3545.5	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #55	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3547.2	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #56	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H](CO)O[C@@H]1O[Si](C)(C)C(C)(C)C	3555.7	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #57	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)O[C@@H]2CO)O[C@@H]1CO	3557.4	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #58	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3539.9	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #59	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@@H]1O[Si](C)(C)C(C)(C)C	3564.0	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)O[C@@H]2CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3538.2	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #60	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3546.7	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #61	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3547.7	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #62	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3563.4	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #63	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3562.9	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #64	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3569.0	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #65	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	3570.2	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #66	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3543.3	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #67	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3543.8	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #68	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3550.1	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #69	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3558.0	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)O[C@@H]2CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3559.5	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #70	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3545.2	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3555.7	Semi standard non polar	33892256
D-Maltose,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3549.7	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 - D-Maltose GC-MS (Non-derivatized) - 70eV, Positive	splash10-03e9-4897000000-332d470623cd7f1e1ced	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - D-Maltose GC-MS (4 TMS) - 70eV, Positive	splash10-014i-3421129000-03a98898fd3278f95502	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - D-Maltose GC-MS (TBDMS_3_3) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - D-Maltose GC-MS (TBDMS_3_16) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - D-Maltose GC-MS (TBDMS_4_2) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - D-Maltose GC-MS (TBDMS_4_10) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - D-Maltose GC-MS (TBDMS_4_11) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - D-Maltose GC-MS (TBDMS_4_12) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - D-Maltose GC-MS (TBDMS_4_20) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - D-Maltose GC-MS (TBDMS_4_32) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - D-Maltose GC-MS (TBDMS_4_33) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - D-Maltose GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - D-Maltose GC-MS ("D-Maltose,3TBDMS,#3" TMS) - 70eV, Positive	Not Available	2021-10-14	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - D-Maltose GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - D-Maltose GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - D-Maltose GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - D-Maltose GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - D-Maltose GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - D-Maltose GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - D-Maltose GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - D-Maltose GC-MS (TMS_1_8) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - D-Maltose GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - D-Maltose GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - D-Maltose GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - D-Maltose GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Experimental LC-MS/MS	LC-MS/MS Spectrum - D-Maltose Quattro_QQQ 10V, Positive-QTOF (Annotated)	splash10-01ox-0149000000-74748828832d87932342	2012-07-24	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - D-Maltose Quattro_QQQ 25V, Positive-QTOF (Annotated)	splash10-008c-2950000000-4ebee22b86c2cc9ee3ab	2012-07-24	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - D-Maltose Quattro_QQQ 40V, Positive-QTOF (Annotated)	splash10-00kg-9710000000-041dbc580f99b8881518	2012-07-24	HMDB team, MONA	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - D-Maltose 10V, Positive-QTOF	splash10-03gl-0907000000-a1de7813fbe8b5258c10	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - D-Maltose 20V, Positive-QTOF	splash10-03e9-0900000000-79cc5059a3f338e8c1dd	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - D-Maltose 40V, Positive-QTOF	splash10-03di-3900000000-851d0bc84d91b6e09579	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - D-Maltose 10V, Negative-QTOF	splash10-002f-0749000000-af1d18f2bc3ab8e02883	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - D-Maltose 20V, Negative-QTOF	splash10-0200-2902000000-67218697344afb9e70fa	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - D-Maltose 40V, Negative-QTOF	splash10-01td-4900000000-40aa2d8125769803cfbb	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - D-Maltose 10V, Positive-QTOF	splash10-0006-0109000000-9d0f9a68a67bafd734ab	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - D-Maltose 20V, Positive-QTOF	splash10-01rw-3898000000-7f495a1bcfdbed6466c4	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - D-Maltose 40V, Positive-QTOF	splash10-01ti-9210000000-b8a83657f0266d372bee	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - D-Maltose 10V, Negative-QTOF	splash10-000x-1069000000-9cd867711bca0eecf935	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - D-Maltose 20V, Negative-QTOF	splash10-0006-9365000000-65403961bfb5e35eaa0d	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - D-Maltose 40V, Negative-QTOF	splash10-000l-9200000000-0de9785c1c5df1430dd2	2021-09-22	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Experimental 1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, experimental)	2012-12-04	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Experimental 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, experimental)	2021-10-10	Wishart Lab	View Spectrum
Experimental 2D NMR	[¹H, ¹³C]-HSQC NMR Spectrum (2D, 600 MHz, H₂O, experimental)	2012-12-05	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm
Extracellular
Lysosome

Biospecimen Locations

Blood
Feces
Sweat
Urine

Tissue Locations

Kidney
Liver
Placenta
Platelet

Pathways

Name	SMPDB/PathBank	KEGG
Starch and Sucrose Metabolism
Glycogen synthetase deficiency		Not Available
Glycogenosis, Type III. Cori disease, Debrancher glycogenosis		Not Available
Glycogenosis, Type IV. Amylopectinosis, Anderson disease		Not Available
Glycogenosis, Type VI. Hers disease		Not Available

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Feces	Detected but not Quantified	Not Quantified	Infant (0-1 year old)	Both	Normal	22411374	details
Feces	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Normal	27543620	details
Feces	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Normal	25037050	details
Feces	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Normal	29808030	details
Feces	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	20669995	details
Sweat	Detected but not Quantified	Not Quantified	Adult	Both	Normal	26755145	details
Urine	Detected and Quantified	16.424 +/- 6.538 umol/mmol creatinine	Children (1 - 13 years old)	Not Specified	Normal	Analysis of 30 no...	details
Urine	Detected and Quantified	6.0 (1.3-21.4) umol/mmol creatinine	Adult (>18 years old)	Both	Normal	24023812	details
Urine	Detected and Quantified	6.14 +/- 5.12 umol/mmol creatinine	Infant (0-1 year old)	Both	Normal	2026685	details

Abnormal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected and Quantified	1169.0 +/- 526.0 uM	Adult (>18 years old)	Both	Peritoneal dialysis	15796147	details
Feces	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Colorectal Cancer	27275383	details
Feces	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Colorectal cancer	25037050	details
Urine	Detected and Quantified	8.332 +/- 5.36 umol/mmol creatinine	Children (1 - 13 years old)	Not Specified	Eosinophilic esophagitis	Analysis of 30 no...	details
Urine	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Bladder cancer	28157703	details

Associated Disorders and Diseases

Disease References

Peritoneal dialysis
Garcia-Lopez E, Anderstam B, Heimburger O, Amici G, Werynski A, Lindholm B: Determination of high and low molecular weight molecules of icodextrin in plasma and dialysate, using gel filtration chromatography, in peritoneal dialysis patients. Perit Dial Int. 2005 Mar-Apr;25(2):181-91. [PubMed:15796147 ]
Colorectal cancer
Brown DG, Rao S, Weir TL, O'Malia J, Bazan M, Brown RJ, Ryan EP: Metabolomics and metabolic pathway networks from human colorectal cancers, adjacent mucosa, and stool. Cancer Metab. 2016 Jun 6;4:11. doi: 10.1186/s40170-016-0151-y. eCollection 2016. [PubMed:27275383 ] Goedert JJ, Sampson JN, Moore SC, Xiao Q, Xiong X, Hayes RB, Ahn J, Shi J, Sinha R: Fecal metabolomics: assay performance and association with colorectal cancer. Carcinogenesis. 2014 Sep;35(9):2089-96. doi: 10.1093/carcin/bgu131. Epub 2014 Jul 18. [PubMed:25037050 ]
Eosinophilic esophagitis
Slae, M., Huynh, H., Wishart, D.S. (2014). Analysis of 30 normal pediatric urine samples via NMR spectroscopy (unpublished work). NA.

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

Not Available

BiGG ID

Wikipedia Link

METLIN ID

PubChem Compound

PDB ID

Not Available

ChEBI ID

47937

Food Biomarker Ontology

Not Available

VMH ID

MALT

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Pedersen, Sven; Vang Hendriksen, Hanne. Method for production of maltose and/or enzymatically modified starch. PCT Int. Appl. (2001), 99 pp.

Material Safety Data Sheet (MSDS)

Not Available

General References

Lu J, Willis AC, Reid KB: Purification, characterization and cDNA cloning of human lung surfactant protein D. Biochem J. 1992 Jun 15;284 ( Pt 3):795-802. [PubMed:1339284 ]
Rubaltelli FF, Biadaioli R, Pecile P, Nicoletti P: Intestinal flora in breast- and bottle-fed infants. J Perinat Med. 1998;26(3):186-91. [PubMed:9773376 ]
Andrews RK, Suzuki-Inoue K, Shen Y, Tulasne D, Watson SP, Berndt MC: Interaction of calmodulin with the cytoplasmic domain of platelet glycoprotein VI. Blood. 2002 Jun 1;99(11):4219-21. [PubMed:12010829 ]
Hirooka EY, Muller EE, Freitas JC, Vicente E, Yoshimoto Y, Bergdoll MS: Enterotoxigenicity of Staphylococcus intermedius of canine origin. Int J Food Microbiol. 1988 Dec;7(3):185-91. [PubMed:3275321 ]
Daly JJ, Sherman JK, Green L, Hostetler TL: Survival of Trichomonas vaginalis in human semen. Genitourin Med. 1989 Apr;65(2):106-8. [PubMed:2787774 ]
Sherman JK, Hostetler TL, McHenry K, Daly JJ: Cryosurvival of Trichomonas vaginalis during cryopreservation of human semen. Cryobiology. 1991 Jun;28(3):246-50. [PubMed:1864083 ]
van Leeuwen L: New saccharogenic determination of alpha-amylase in serum and urine. Clin Chem. 1979 Feb;25(2):215-7. [PubMed:215341 ]
Miller LJ, Malagelada JR, Taylor WF, Go VL: Intestinal control of human postprandial gastric function: the role of components of jejunoileal chyme in regulating gastric secretion and gastric emptying. Gastroenterology. 1981 Apr;80(4):763-9. [PubMed:7202948 ]
Roy E, Stavropoulos E, Brennan J, Coade S, Grigorieva E, Walker B, Dagg B, Tascon RE, Lowrie DB, Colston MJ, Jolles S: Therapeutic efficacy of high-dose intravenous immunoglobulin in Mycobacterium tuberculosis infection in mice. Infect Immun. 2005 Sep;73(9):6101-9. [PubMed:16113331 ]
Wyss C, Choi BK, Schupbach P, Guggenheim B, Gobel UB: Treponema maltophilum sp. nov., a small oral spirochete isolated from human periodontal lesions. Int J Syst Bacteriol. 1996 Jul;46(3):745-52. [PubMed:8782684 ]
Morse DR, Schacterle GR, Furst L, Zaydenberg M, Pollack RL: Oral digestion of a complex-carbohydrate cereal: effects of stress and relaxation on physiological and salivary measures. Am J Clin Nutr. 1989 Jan;49(1):97-105. [PubMed:2463752 ]
Yamamoto T, Kajiura S, Hirai Y, Watanabe T: Capnocytophaga haemolytica sp. nov. and Capnocytophaga granulosa sp. nov., from human dental plaque. Int J Syst Bacteriol. 1994 Apr;44(2):324-9. [PubMed:8186098 ]
Zhu J, Marchant RE: Dendritic saccharide surfactant polymers as antifouling interface materials to reduce platelet adhesion. Biomacromolecules. 2006 Apr;7(4):1036-41. [PubMed:16602718 ]
Lingstrom P, Birkhed D, Granfeldt Y, Bjorck I: pH measurements of human dental plaque after consumption of starchy foods using the microtouch and the sampling method. Caries Res. 1993;27(5):394-401. [PubMed:8242677 ]
Leth-Larsen R, Holmskov U, Hojrup P: Structural characterization of human and bovine lung surfactant protein D. Biochem J. 1999 Nov 1;343 Pt 3:645-52. [PubMed:10527944 ]
Janoshazi A, Solomon AK: Initial steps of alpha- and beta-D-glucose binding to intact red cell membrane. J Membr Biol. 1993 Mar;132(2):167-78. [PubMed:8496948 ]
Tiwari F, Singh DK: Behavioural responses of the snail Lymnaea acuminata to carbohydrates in snail-attractant pellets. Naturwissenschaften. 2004 Aug;91(8):378-80. Epub 2004 Jun 2. [PubMed:15309310 ]
Chiba S, Hiromi K, Minamiura N, Ohnishi M, Shimomura T, Suga K, Suganuma T, Tanaka A, Tomioka S, Yamamoto T: Quantitative study on anomeric forms of glucose produced by alpha-glucosidases. J Biochem. 1979 May;85(5):1135-41. [PubMed:376499 ]
McCue JP, Hein RH, Tenold R: Three generations of immunoglobulin G preparations for clinical use. Rev Infect Dis. 1986 Jul-Aug;8 Suppl 4:S374-81. [PubMed:3092303 ]
Dorner KM: Quantitative determination of lactose, maltose, and sucrose in urine. Eur J Pediatr. 1977 Aug 23;126(1-2):45-52. [PubMed:902663 ]
Sigman-Grant M, Morita J: Defining and interpreting intakes of sugars. Am J Clin Nutr. 2003 Oct;78(4):815S-826S. [PubMed:14522745 ]
Elshenawy S, Pinney SE, Stuart T, Doulias PT, Zura G, Parry S, Elovitz MA, Bennett MJ, Bansal A, Strauss JF 3rd, Ischiropoulos H, Simmons RA: The Metabolomic Signature of the Placenta in Spontaneous Preterm Birth. Int J Mol Sci. 2020 Feb 4;21(3). pii: ijms21031043. doi: 10.3390/ijms21031043. [PubMed:32033212 ]

Enzymes

Enzyme Details

1. Glycogen debranching enzyme

General function:: Involved in catalytic activity
Specific function:: Multifunctional enzyme acting as 1,4-alpha-D-glucan:1,4-alpha-D-glucan 4-alpha-D-glycosyltransferase and amylo-1,6-glucosidase in glycogen degradation.
Gene Name:: AGL
Uniprot ID:: P35573
Molecular weight:: Not Available

Enzyme Details

2. Lysosomal alpha-glucosidase

General function:: Involved in catalytic activity
Specific function:: Essential for the degradation of glygogen to glucose in lysosomes.
Gene Name:: GAA
Uniprot ID:: P10253
Molecular weight:: Not Available

Reactions

D-Maltose + Water → alpha-D-Glucose	details

Enzyme Details

3. Alpha-amylase 1

General function:: Involved in catalytic activity
Specific function:: Not Available
Gene Name:: AMY1A
Uniprot ID:: P04745
Molecular weight:: Not Available

Enzyme Details

4. Alpha-amylase 2B

General function:: Involved in catalytic activity
Specific function:: Not Available
Gene Name:: AMY2B
Uniprot ID:: P19961
Molecular weight:: Not Available

References

Overington JP, Al-Lazikani B, Hopkins AL: How many drug targets are there? Nat Rev Drug Discov. 2006 Dec;5(12):993-6. [PubMed:17139284 ]
Imming P, Sinning C, Meyer A: Drugs, their targets and the nature and number of drug targets. Nat Rev Drug Discov. 2006 Oct;5(10):821-34. [PubMed:17016423 ]
Berman HM, Westbrook J, Feng Z, Gilliland G, Bhat TN, Weissig H, Shindyalov IN, Bourne PE: The Protein Data Bank. Nucleic Acids Res. 2000 Jan 1;28(1):235-42. [PubMed:10592235 ]

Enzyme Details

5. Maltase-glucoamylase, intestinal

General function:: Involved in catalytic activity
Specific function:: May serve as an alternate pathway for starch digestion when luminal alpha-amylase activity is reduced because of immaturity or malnutrition. May play a unique role in the digestion of malted dietary oligosaccharides used in food manufacturing.
Gene Name:: MGAM
Uniprot ID:: O43451
Molecular weight:: Not Available

Reactions

D-Maltose + Water → alpha-D-Glucose	details

Enzyme Details

6. Neutral alpha-glucosidase C

General function:: Involved in catalytic activity
Specific function:: Has alpha-glucosidase activity.
Gene Name:: GANC
Uniprot ID:: Q8TET4
Molecular weight:: Not Available

Reactions

D-Maltose + Water → alpha-D-Glucose	details

Showing metabocard for D-Maltose (HMDB0000163)

MOL for HMDB0000163 (D-Maltose)

3D MOL for HMDB0000163 (D-Maltose)

3D SDF for HMDB0000163 (D-Maltose)

3D-SDF for HMDB0000163 (D-Maltose)

PDB for HMDB0000163 (D-Maltose)

3D PDB for HMDB0000163 (D-Maltose)

SMILES for HMDB0000163 (D-Maltose)

INCHI for HMDB0000163 (D-Maltose)

Structure for HMDB0000163 (D-Maltose)

3D Structure for HMDB0000163 (D-Maltose)

Experimental Collision Cross Sections

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

Enzymes

Reactions

References

Reactions

Reactions