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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2013-01-09 12:11:22 UTC

Update Date

2022-03-07 03:17:35 UTC

HMDB ID

HMDB0059718

Secondary Accession Numbers

HMDB59718

Metabolite Identification

Common Name

Glucopyranosylmoranoline

Description

Glucopyranosylmoranoline 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. Glucopyranosylmoranoline, or Glucopyranosylmoranoline (CAS Number 80312-32-9), is a white to off-white solid, soluble in methanol and water, with melting point 189-192C. Glucopyranosylmoranoline is a very strong basic compound (based on its pKa).

Structure

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

HMDB0059718
     RDKit          3D
Glucopyranosylmoranoline
 45 46  0  0  0  0  0  0  0  0999 V2000
   -2.4391   -2.1156   -1.7766 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1273   -2.2829   -0.5766 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7837   -1.1312    0.3722 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4554   -1.0683    0.6564 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8390    0.1293    0.3858 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4239    0.1008    0.9801 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4523    0.1576    0.0819 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4171   -1.0068    0.1839 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7113   -2.3294    0.1869 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6833   -3.3214    0.3466 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3589   -0.9520   -0.8918 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0634    0.2779   -1.0123 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1602    1.4833   -1.0186 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8769    2.6463   -1.1048 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3249    1.4074    0.2625 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5735    2.5333    0.4695 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5461    1.3293    0.9493 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1081    1.6138    2.2296 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0419    1.2006    0.9546 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6980    2.3736    0.6600 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3921    0.1561   -0.1131 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.7615    0.0501   -0.1379 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0045   -2.4704   -2.4950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8670   -3.2260   -0.0663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2042   -2.2718   -0.7590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3223   -1.3864    1.3321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6747    0.1938   -0.7128 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0747    0.2163   -0.9615 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9936   -0.9301    1.1459 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0143   -2.4110    1.0392 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2191   -2.4698   -0.7825 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1673   -3.1995    1.2119 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0294   -1.3625   -1.7760 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6036    0.2761   -1.9874 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8653    0.3789   -0.2321 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4418    1.3550   -1.8488 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2984    3.3125   -1.5937 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0594    1.1976    1.0798 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5648    2.7113    1.4573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2889    2.1957    0.3041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7319    2.5189    2.3301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3658    0.7536    1.9205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5720    2.9877    1.4425 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0120    0.4654   -1.1035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1417   -0.0870   -1.0324 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
 13 14  1  0
 13 15  1  0
 15 16  1  0
  5 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21  3  1  0
 15  7  1  0
  1 23  1  0
  2 24  1  0
  2 25  1  0
  3 26  1  1
  5 27  1  6
  7 28  1  6
  8 29  1  1
  9 30  1  0
  9 31  1  0
 10 32  1  0
 11 33  1  0
 12 34  1  0
 12 35  1  0
 13 36  1  6
 14 37  1  0
 15 38  1  1
 16 39  1  0
 17 40  1  6
 18 41  1  0
 19 42  1  1
 20 43  1  0
 21 44  1  6
 22 45  1  0
M  END

4-O-a-D-Glucopyranosylmoranoline, CAS:80312-32-9 
  Mrv0541 01091312052D          

 22 23  0  0  0  0            999 V2000
    0.7040   -0.6258    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7040    0.1876    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0117   -1.0362    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4218   -1.0362    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4218    0.5956    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0303    0.5792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7179   -0.6258    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1375   -0.6258    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4218   -1.8776    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1375    0.1876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0233    1.3741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7109    0.1993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4451   -1.0292    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8554   -1.0594    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4102    0.6258    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1375   -0.5956    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4638   -1.8427    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1375    0.2296    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4032    1.4440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8554   -0.9988    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8367    0.6632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0954    1.8776    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  3  1  6  0  0  0
  1  4  1  0  0  0  0
  2  5  1  0  0  0  0
  2  6  1  1  0  0  0
  7  3  1  6  0  0  0
  4  8  1  0  0  0  0
  4  9  1  1  0  0  0
  5 10  1  0  0  0  0
  6 11  1  0  0  0  0
  7 12  1  0  0  0  0
  7 13  1  0  0  0  0
  8 14  1  6  0  0  0
  8 10  1  0  0  0  0
 12 15  1  0  0  0  0
 13 16  1  0  0  0  0
 13 17  1  6  0  0  0
 15 18  1  0  0  0  0
 15 19  1  1  0  0  0
 16 20  1  1  0  0  0
 16 18  1  0  0  0  0
 18 21  1  6  0  0  0
 19 22  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0059718

> <DATABASE_NAME>
hmdb

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

> <INCHI_IDENTIFIER>
InChI=1S/C12H23NO9/c14-2-4-11(7(17)5(16)1-13-4)22-12-10(20)9(19)8(18)6(3-15)21-12/h4-20H,1-3H2/t4-,5+,6-,7-,8-,9+,10-,11-,12-/m1/s1

> <INCHI_KEY>
GNVIYGFSOIHFHK-NIKVEEOSSA-N

> <FORMULA>
C12H23NO9

> <MOLECULAR_WEIGHT>
325.3123

> <EXACT_MASS>
325.137281339

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_AVERAGE_POLARIZABILITY>
31.057379406499606

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <ALOGPS_LOGP>
-2.69

> <JCHEM_LOGP>
-4.656578828666667

> <ALOGPS_LOGS>
-0.06

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
12.86788699021352

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.149711780285399

> <JCHEM_PKA_STRONGEST_BASIC>
7.993734364947867

> <JCHEM_POLAR_SURFACE_AREA>
172.1

> <JCHEM_REFRACTIVITY>
68.9877

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.82e+02 g/l

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

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0059718
     RDKit          3D
Glucopyranosylmoranoline
 45 46  0  0  0  0  0  0  0  0999 V2000
   -2.4391   -2.1156   -1.7766 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1273   -2.2829   -0.5766 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7837   -1.1312    0.3722 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4554   -1.0683    0.6564 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8390    0.1293    0.3858 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4239    0.1008    0.9801 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4523    0.1576    0.0819 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4171   -1.0068    0.1839 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7113   -2.3294    0.1869 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6833   -3.3214    0.3466 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3589   -0.9520   -0.8918 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0634    0.2779   -1.0123 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1602    1.4833   -1.0186 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8769    2.6463   -1.1048 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3249    1.4074    0.2625 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5735    2.5333    0.4695 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5461    1.3293    0.9493 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1081    1.6138    2.2296 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0419    1.2006    0.9546 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6980    2.3736    0.6600 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3921    0.1561   -0.1131 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.7615    0.0501   -0.1379 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0045   -2.4704   -2.4950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8670   -3.2260   -0.0663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2042   -2.2718   -0.7590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3223   -1.3864    1.3321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6747    0.1938   -0.7128 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0747    0.2163   -0.9615 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9936   -0.9301    1.1459 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0143   -2.4110    1.0392 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2191   -2.4698   -0.7825 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1673   -3.1995    1.2119 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0294   -1.3625   -1.7760 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6036    0.2761   -1.9874 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8653    0.3789   -0.2321 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4418    1.3550   -1.8488 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2984    3.3125   -1.5937 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0594    1.1976    1.0798 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5648    2.7113    1.4573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2889    2.1957    0.3041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7319    2.5189    2.3301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3658    0.7536    1.9205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5720    2.9877    1.4425 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0120    0.4654   -1.1035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1417   -0.0870   -1.0324 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
 13 14  1  0
 13 15  1  0
 15 16  1  0
  5 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21  3  1  0
 15  7  1  0
  1 23  1  0
  2 24  1  0
  2 25  1  0
  3 26  1  1
  5 27  1  6
  7 28  1  6
  8 29  1  1
  9 30  1  0
  9 31  1  0
 10 32  1  0
 11 33  1  0
 12 34  1  0
 12 35  1  0
 13 36  1  6
 14 37  1  0
 15 38  1  1
 16 39  1  0
 17 40  1  6
 18 41  1  0
 19 42  1  1
 20 43  1  0
 21 44  1  6
 22 45  1  0
M  END

HEADER    PROTEIN                                 09-JAN-13   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: 4-O-a-D-Glucopyranosylmoranoline, CAS:80312-32-9  
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-JAN-13         0                                  
HETATM    1  C   UNK     0       1.314  -1.168   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.314   0.350   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -0.022  -1.934   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       2.654  -1.934   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       2.654   1.112   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      -0.057   1.081   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.340  -1.168   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.990  -1.168   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.654  -3.505   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       3.990   0.350   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -0.043   2.565   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0      -1.327   0.372   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -2.698  -1.921   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       5.330  -1.977   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -2.632   1.168   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.990  -1.112   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -2.732  -3.440   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -3.990   0.429   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.619   2.695   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -5.330  -1.864   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -5.295   1.238   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -3.911   3.505   0.000  0.00  0.00           O+0
CONECT    1    2    3    4                                                  
CONECT    2    1    5    6                                                  
CONECT    3    1    7                                                       
CONECT    4    1    8    9                                                  
CONECT    5    2   10                                                       
CONECT    6    2   11                                                       
CONECT    7    3   12   13                                                  
CONECT    8    4   14   10                                                  
CONECT    9    4                                                            
CONECT   10    5    8                                                       
CONECT   11    6                                                            
CONECT   12    7   15                                                       
CONECT   13    7   16   17                                                  
CONECT   14    8                                                            
CONECT   15   12   18   19                                                  
CONECT   16   13   20   18                                                  
CONECT   17   13                                                            
CONECT   18   15   16   21                                                  
CONECT   19   15   22                                                       
CONECT   20   16                                                            
CONECT   21   18                                                            
CONECT   22   19                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

COMPND    HMDB0059718
HETATM    1  O1  UNL     1      -2.439  -2.116  -1.777  1.00  0.00           O  
HETATM    2  C1  UNL     1      -3.127  -2.283  -0.577  1.00  0.00           C  
HETATM    3  C2  UNL     1      -2.784  -1.131   0.372  1.00  0.00           C  
HETATM    4  O2  UNL     1      -1.455  -1.068   0.656  1.00  0.00           O  
HETATM    5  C3  UNL     1      -0.839   0.129   0.386  1.00  0.00           C  
HETATM    6  O3  UNL     1       0.424   0.101   0.980  1.00  0.00           O  
HETATM    7  C4  UNL     1       1.452   0.158   0.082  1.00  0.00           C  
HETATM    8  C5  UNL     1       2.417  -1.007   0.184  1.00  0.00           C  
HETATM    9  C6  UNL     1       1.711  -2.329   0.187  1.00  0.00           C  
HETATM   10  O4  UNL     1       2.683  -3.321   0.347  1.00  0.00           O  
HETATM   11  N1  UNL     1       3.359  -0.952  -0.892  1.00  0.00           N  
HETATM   12  C7  UNL     1       4.063   0.278  -1.012  1.00  0.00           C  
HETATM   13  C8  UNL     1       3.160   1.483  -1.019  1.00  0.00           C  
HETATM   14  O5  UNL     1       3.877   2.646  -1.105  1.00  0.00           O  
HETATM   15  C9  UNL     1       2.325   1.407   0.263  1.00  0.00           C  
HETATM   16  O6  UNL     1       1.574   2.533   0.469  1.00  0.00           O  
HETATM   17  C10 UNL     1      -1.546   1.329   0.949  1.00  0.00           C  
HETATM   18  O7  UNL     1      -1.108   1.614   2.230  1.00  0.00           O  
HETATM   19  C11 UNL     1      -3.042   1.201   0.955  1.00  0.00           C  
HETATM   20  O8  UNL     1      -3.698   2.374   0.660  1.00  0.00           O  
HETATM   21  C12 UNL     1      -3.392   0.156  -0.113  1.00  0.00           C  
HETATM   22  O9  UNL     1      -4.761   0.050  -0.138  1.00  0.00           O  
HETATM   23  H1  UNL     1      -3.005  -2.470  -2.495  1.00  0.00           H  
HETATM   24  H2  UNL     1      -2.867  -3.226  -0.066  1.00  0.00           H  
HETATM   25  H3  UNL     1      -4.204  -2.272  -0.759  1.00  0.00           H  
HETATM   26  H4  UNL     1      -3.322  -1.386   1.332  1.00  0.00           H  
HETATM   27  H5  UNL     1      -0.675   0.194  -0.713  1.00  0.00           H  
HETATM   28  H6  UNL     1       1.075   0.216  -0.962  1.00  0.00           H  
HETATM   29  H7  UNL     1       2.994  -0.930   1.146  1.00  0.00           H  
HETATM   30  H8  UNL     1       1.014  -2.411   1.039  1.00  0.00           H  
HETATM   31  H9  UNL     1       1.219  -2.470  -0.783  1.00  0.00           H  
HETATM   32  H10 UNL     1       3.167  -3.199   1.212  1.00  0.00           H  
HETATM   33  H11 UNL     1       3.029  -1.363  -1.776  1.00  0.00           H  
HETATM   34  H12 UNL     1       4.604   0.276  -1.987  1.00  0.00           H  
HETATM   35  H13 UNL     1       4.865   0.379  -0.232  1.00  0.00           H  
HETATM   36  H14 UNL     1       2.442   1.355  -1.849  1.00  0.00           H  
HETATM   37  H15 UNL     1       3.298   3.312  -1.594  1.00  0.00           H  
HETATM   38  H16 UNL     1       3.059   1.198   1.080  1.00  0.00           H  
HETATM   39  H17 UNL     1       1.565   2.711   1.457  1.00  0.00           H  
HETATM   40  H18 UNL     1      -1.289   2.196   0.304  1.00  0.00           H  
HETATM   41  H19 UNL     1      -0.732   2.519   2.330  1.00  0.00           H  
HETATM   42  H20 UNL     1      -3.366   0.754   1.920  1.00  0.00           H  
HETATM   43  H21 UNL     1      -3.572   2.988   1.443  1.00  0.00           H  
HETATM   44  H22 UNL     1      -3.012   0.465  -1.103  1.00  0.00           H  
HETATM   45  H23 UNL     1      -5.142  -0.087  -1.032  1.00  0.00           H  
CONECT    1    2   23
CONECT    2    3   24   25
CONECT    3    4   21   26
CONECT    4    5
CONECT    5    6   17   27
CONECT    6    7
CONECT    7    8   15   28
CONECT    8    9   11   29
CONECT    9   10   30   31
CONECT   10   32
CONECT   11   12   33
CONECT   12   13   34   35
CONECT   13   14   15   36
CONECT   14   37
CONECT   15   16   38
CONECT   16   39
CONECT   17   18   19   40
CONECT   18   41
CONECT   19   20   21   42
CONECT   20   43
CONECT   21   22   44
CONECT   22   45
END

HMDB0059718
     RDKit          3D
Glucopyranosylmoranoline
 45 46  0  0  0  0  0  0  0  0999 V2000
   -2.4391   -2.1156   -1.7766 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1273   -2.2829   -0.5766 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7837   -1.1312    0.3722 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4554   -1.0683    0.6564 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8390    0.1293    0.3858 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4239    0.1008    0.9801 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4523    0.1576    0.0819 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4171   -1.0068    0.1839 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7113   -2.3294    0.1869 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6833   -3.3214    0.3466 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3589   -0.9520   -0.8918 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0634    0.2779   -1.0123 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1602    1.4833   -1.0186 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8769    2.6463   -1.1048 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3249    1.4074    0.2625 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5735    2.5333    0.4695 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5461    1.3293    0.9493 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1081    1.6138    2.2296 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0419    1.2006    0.9546 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6980    2.3736    0.6600 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3921    0.1561   -0.1131 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.7615    0.0501   -0.1379 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0045   -2.4704   -2.4950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8670   -3.2260   -0.0663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2042   -2.2718   -0.7590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3223   -1.3864    1.3321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6747    0.1938   -0.7128 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0747    0.2163   -0.9615 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9936   -0.9301    1.1459 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0143   -2.4110    1.0392 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2191   -2.4698   -0.7825 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1673   -3.1995    1.2119 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0294   -1.3625   -1.7760 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6036    0.2761   -1.9874 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8653    0.3789   -0.2321 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4418    1.3550   -1.8488 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2984    3.3125   -1.5937 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0594    1.1976    1.0798 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5648    2.7113    1.4573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2889    2.1957    0.3041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7319    2.5189    2.3301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3658    0.7536    1.9205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5720    2.9877    1.4425 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0120    0.4654   -1.1035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1417   -0.0870   -1.0324 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
 13 14  1  0
 13 15  1  0
 15 16  1  0
  5 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21  3  1  0
 15  7  1  0
  1 23  1  0
  2 24  1  0
  2 25  1  0
  3 26  1  1
  5 27  1  6
  7 28  1  6
  8 29  1  1
  9 30  1  0
  9 31  1  0
 10 32  1  0
 11 33  1  0
 12 34  1  0
 12 35  1  0
 13 36  1  6
 14 37  1  0
 15 38  1  1
 16 39  1  0
 17 40  1  6
 18 41  1  0
 19 42  1  1
 20 43  1  0
 21 44  1  6
 22 45  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
alpha-D-Glucopyranosyl-(1->4)-1-deoxynojirimycin	ChEBI
a-D-Glucopyranosyl-(1->4)-1-deoxynojirimycin	Generator
Α-D-glucopyranosyl-(1->4)-1-deoxynojirimycin	Generator
4-O-a-D-Glucopyranosylmoranoline	HMDB
4-O-Α-D-glucopyranosylmoranoline	HMDB
1-Deoxynojirimycin 4-O-alpha-D-glucopyranose	MeSH
MOR-502	MeSH
1-Deoxy-nojirimycin 4-O-alpha-D-glucopyranose	MeSH
4-O-Glucopyranosylmoranoline	MeSH

Chemical Formula

C₁₂H₂₃NO₉

Average Molecular Weight

325.3123

Monoisotopic Molecular Weight

325.137281339

IUPAC Name

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

Traditional Name

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

CAS Registry Number

80312-32-9

SMILES

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

InChI Identifier

InChI=1S/C12H23NO9/c14-2-4-11(7(17)5(16)1-13-4)22-12-10(20)9(19)8(18)6(3-15)21-12/h4-20H,1-3H2/t4-,5+,6-,7-,8-,9+,10-,11-,12-/m1/s1

InChI Key

GNVIYGFSOIHFHK-NIKVEEOSSA-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

Hexose monosaccharide
O-glycosyl compound
Monosaccharide
Oxane
Piperidine
1,2-aminoalcohol
Secondary alcohol
Acetal
Secondary aliphatic amine
Oxacycle
Azacycle
Organoheterocyclic compound
Polyol
Secondary amine
Hydrocarbon derivative
Alcohol
Organonitrogen compound
Amine
Organic nitrogen compound
Primary alcohol
Organopnictogen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

alpha-D-glucoside (CHEBI:70736 )
monosaccharide derivative (CHEBI:70736 )

Ontology

Not Available

Exogenous (HMDB: HMDB0059718)

Process

Not Available

Role

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	282 g/L	ALOGPS
logP	-2.7	ALOGPS
logP	-4.7	ChemAxon
logS	-0.06	ALOGPS
pKa (Strongest Acidic)	12.15	ChemAxon
pKa (Strongest Basic)	7.99	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	172.1 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	68.99 m³·mol⁻¹	ChemAxon
Polarizability	31.06 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	173.746	31661259
DarkChem	[M-H]-	171.375	31661259
DeepCCS	[M+H]+	168.871	30932474
DeepCCS	[M-H]-	166.673	30932474
DeepCCS	[M-2H]-	200.411	30932474
DeepCCS	[M+Na]+	174.733	30932474
AllCCS	[M+H]+	175.3	32859911
AllCCS	[M+H-H2O]+	172.3	32859911
AllCCS	[M+NH4]+	178.2	32859911
AllCCS	[M+Na]+	179.0	32859911
AllCCS	[M-H]-	172.3	32859911
AllCCS	[M+Na-2H]-	172.0	32859911
AllCCS	[M+HCOO]-	171.6	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.	0.51 minutes	32390414
Predicted by Siyang on May 30, 2022	10.8239 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	8.74 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	487.9 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	283.5 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	17.3 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	185.8 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	97.2 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	352.2 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	260.7 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	1000.4 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	584.7 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	57.1 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	789.4 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	212.1 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	336.6 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	937.4 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	664.0 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	456.8 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Glucopyranosylmoranoline	OC[C@H]1NC[C@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	3610.7	Standard polar	33892256
Glucopyranosylmoranoline	OC[C@H]1NC[C@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	3082.1	Standard non polar	33892256
Glucopyranosylmoranoline	OC[C@H]1NC[C@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	3024.2	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Glucopyranosylmoranoline,1TMS,isomer #1	C[Si](C)(C)OC[C@H]1NC[C@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	2728.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,1TMS,isomer #2	C[Si](C)(C)O[C@H]1CN[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	2695.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,1TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](O)CN[C@H](CO)[C@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	2722.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,1TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	2724.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,1TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O)[C@H](O)[C@H]1O	2720.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,1TMS,isomer #6	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O)O[C@H](CO)[C@H]1O	2710.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,1TMS,isomer #7	C[Si](C)(C)O[C@H]1[C@@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	2718.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,1TMS,isomer #8	C[Si](C)(C)N1C[C@H](O)[C@@H](O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H]1CO	2679.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #1	C[Si](C)(C)OC[C@H]1NC[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	2684.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #10	C[Si](C)(C)O[C@H]1CN[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	2666.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #11	C[Si](C)(C)O[C@H]1CN[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	2681.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #12	C[Si](C)(C)O[C@H]1CN[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	2686.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #13	C[Si](C)(C)O[C@H]1CN([Si](C)(C)C)[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	2689.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #14	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	2721.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #15	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O	2715.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #16	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O[Si](C)(C)C)O[C@H](CO)[C@H]1O	2707.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #17	C[Si](C)(C)O[C@H]1[C@@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O	2715.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #18	C[Si](C)(C)O[C@@H]1[C@@H](O)CN([Si](C)(C)C)[C@H](CO)[C@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	2699.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #19	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2716.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #2	C[Si](C)(C)OC[C@H]1NC[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	2712.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #20	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2717.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #21	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2734.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #22	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O	2714.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #23	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)NC[C@H](O)[C@H]2O)O[C@@H]1CO	2704.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #24	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C	2708.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #25	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O)[C@H]1O	2692.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #26	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O)O[C@H](CO)[C@H]1O	2709.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #27	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO)O[C@H](CO)[C@H]1O	2694.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #28	C[Si](C)(C)O[C@H]1[C@@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO)O[C@H](CO)[C@@H](O)[C@@H]1O	2691.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)NC[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	2717.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #4	C[Si](C)(C)OC[C@H]1NC[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	2707.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #5	C[Si](C)(C)OC[C@H]1NC[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	2697.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #6	C[Si](C)(C)OC[C@H]1NC[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	2700.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #7	C[Si](C)(C)OC[C@@H]1[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)CN1[Si](C)(C)C	2732.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #8	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)CN[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O	2691.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TMS,isomer #9	C[Si](C)(C)O[C@H]1CN[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	2681.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #1	C[Si](C)(C)OC[C@H]1NC[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	2621.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #10	C[Si](C)(C)OC[C@H]1NC[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	2629.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #11	C[Si](C)(C)OC[C@@H]1[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](O)CN1[Si](C)(C)C	2729.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #12	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)NC[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2613.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #13	C[Si](C)(C)OC[C@H]1NC[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	2632.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #14	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)NC[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2636.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #15	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	2718.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #16	C[Si](C)(C)OC[C@H]1NC[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	2623.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #17	C[Si](C)(C)OC[C@H]1NC[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	2621.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #18	C[Si](C)(C)OC[C@@H]1[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)CN1[Si](C)(C)C	2702.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #19	C[Si](C)(C)OC[C@H]1NC[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	2615.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,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)CN[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	2609.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #20	C[Si](C)(C)OC[C@@H]1[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H](O)[C@@H](O)CN1[Si](C)(C)C	2711.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #21	C[Si](C)(C)OC[C@@H]1[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](O)CN1[Si](C)(C)C	2706.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,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)CN[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O	2629.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #23	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)CN[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2628.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,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)CN[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2642.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,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)CN[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2644.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,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)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O	2716.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #27	C[Si](C)(C)O[C@H]1CN[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	2645.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #28	C[Si](C)(C)O[C@H]1CN[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	2643.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #29	C[Si](C)(C)O[C@H]1CN[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	2636.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #3	C[Si](C)(C)OC[C@H]1NC[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	2614.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #30	C[Si](C)(C)O[C@H]1CN([Si](C)(C)C)[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	2697.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #31	C[Si](C)(C)O[C@H]1CN[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	2634.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #32	C[Si](C)(C)O[C@H]1CN[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	2646.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #33	C[Si](C)(C)O[C@H]1CN([Si](C)(C)C)[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	2701.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #34	C[Si](C)(C)O[C@H]1CN[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	2633.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #35	C[Si](C)(C)O[C@H]1CN([Si](C)(C)C)[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	2699.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #36	C[Si](C)(C)O[C@H]1CN([Si](C)(C)C)[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	2722.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #37	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2660.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #38	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2664.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #39	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2672.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #4	C[Si](C)(C)OC[C@H]1NC[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	2627.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #40	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O	2706.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #41	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)NC[C@H](O)[C@H]2O[Si](C)(C)C)O[C@@H]1CO	2667.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #42	C[Si](C)(C)O[C@@H]1[C@@H](O)CN[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	2670.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #43	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O)[C@H]1O	2704.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #44	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O[Si](C)(C)C)O[C@H](CO)[C@H]1O	2672.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #45	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO)O[C@H](CO)[C@H]1O	2711.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #46	C[Si](C)(C)O[C@H]1[C@@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO)O[C@H](CO)[C@@H](O)[C@@H]1O	2704.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #47	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2658.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #48	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2690.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #49	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2681.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #5	C[Si](C)(C)OC[C@H]1NC[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	2604.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #50	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2673.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #51	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2701.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #52	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2701.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #53	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O)O[C@H](CO)[C@H]1O[Si](C)(C)C	2645.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #54	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)CN([Si](C)(C)C)[C@@H]2CO)O[C@@H]1CO	2691.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #55	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O)[C@H]1O[Si](C)(C)C	2693.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #56	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO)O[C@H](CO)[C@H]1O	2692.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #6	C[Si](C)(C)OC[C@@H]1[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)CN1[Si](C)(C)C	2740.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)NC[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	2627.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #8	C[Si](C)(C)OC[C@H]1NC[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	2637.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TMS,isomer #9	C[Si](C)(C)OC[C@H]1NC[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	2652.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,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)CN[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	2582.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #10	C[Si](C)(C)OC[C@H]1NC[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	2620.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #11	C[Si](C)(C)OC[C@H]1NC[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	2608.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #12	C[Si](C)(C)OC[C@@H]1[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)CN1[Si](C)(C)C	2726.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #13	C[Si](C)(C)OC[C@H]1NC[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	2599.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #14	C[Si](C)(C)OC[C@@H]1[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)CN1[Si](C)(C)C	2734.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #15	C[Si](C)(C)OC[C@@H]1[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](O[Si](C)(C)C)CN1[Si](C)(C)C	2722.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #16	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)NC[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2578.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #17	C[Si](C)(C)OC[C@H]1NC[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)[C@H](O[Si](C)(C)C)[C@H]1O	2626.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #18	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)NC[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2598.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #19	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	2692.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #2	C[Si](C)(C)OC[C@H]1NC[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	2607.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #20	C[Si](C)(C)OC[C@H]1NC[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	2635.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #21	C[Si](C)(C)OC[C@H]1NC[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	2619.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #22	C[Si](C)(C)OC[C@@H]1[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)CN1[Si](C)(C)C	2709.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #23	C[Si](C)(C)OC[C@H]1NC[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	2618.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #24	C[Si](C)(C)OC[C@@H]1[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)CN1[Si](C)(C)C	2728.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #25	C[Si](C)(C)OC[C@@H]1[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](O)CN1[Si](C)(C)C	2700.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #26	C[Si](C)(C)OC[C@H]1NC[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	2577.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #27	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)NC[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2615.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #28	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2667.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #29	C[Si](C)(C)OC[C@H]1NC[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	2602.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #3	C[Si](C)(C)OC[C@H]1NC[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	2634.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #30	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2695.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #31	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2684.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #32	C[Si](C)(C)OC[C@H]1NC[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	2574.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #33	C[Si](C)(C)OC[C@@H]1[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](O)CN1[Si](C)(C)C	2697.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #34	C[Si](C)(C)OC[C@@H]1[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](O)[C@@H](O)CN1[Si](C)(C)C	2698.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #35	C[Si](C)(C)OC[C@@H]1[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](O)[C@@H](O)CN1[Si](C)(C)C	2684.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #36	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)CN[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2601.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #37	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)CN[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2632.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #38	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)CN[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2621.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #39	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)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O	2705.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #4	C[Si](C)(C)OC[C@H]1NC[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	2597.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #40	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)CN[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2615.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #41	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)CN[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2646.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #42	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2696.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #43	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)CN[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2633.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #44	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2710.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #45	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2708.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #46	C[Si](C)(C)O[C@H]1CN[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	2619.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #47	C[Si](C)(C)O[C@H]1CN[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	2636.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #48	C[Si](C)(C)O[C@H]1CN([Si](C)(C)C)[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	2717.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #49	C[Si](C)(C)O[C@H]1CN[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	2630.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #5	C[Si](C)(C)OC[C@@H]1[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](O[Si](C)(C)C)CN1[Si](C)(C)C	2742.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #50	C[Si](C)(C)O[C@H]1CN([Si](C)(C)C)[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	2714.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #51	C[Si](C)(C)O[C@H]1CN([Si](C)(C)C)[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	2720.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #52	C[Si](C)(C)O[C@H]1CN[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	2627.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #53	C[Si](C)(C)O[C@H]1CN([Si](C)(C)C)[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	2707.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #54	C[Si](C)(C)O[C@H]1CN([Si](C)(C)C)[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	2723.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #55	C[Si](C)(C)O[C@H]1CN([Si](C)(C)C)[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	2719.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #56	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[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	2624.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #57	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[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	2656.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #58	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2687.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #59	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[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	2646.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)CN[C@@H]2CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2570.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #60	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2718.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #61	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2705.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #62	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O[Si](C)(C)C)O[C@H](CO)[C@H]1O[Si](C)(C)C	2619.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #63	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)CN([Si](C)(C)C)[C@@H]2CO)O[C@@H]1CO	2716.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #64	C[Si](C)(C)O[C@@H]1[C@@H](O)CN([Si](C)(C)C)[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	2724.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #65	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO)O[C@H](CO)[C@H]1O	2712.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #66	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[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	2624.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #67	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2673.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #68	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2699.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #69	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2697.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #7	C[Si](C)(C)OC[C@H]1NC[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	2610.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #70	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO)O[C@H](CO)[C@H]1O[Si](C)(C)C	2690.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #8	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)CN[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2584.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TMS,isomer #9	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	2714.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,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)CN[C@@H]2CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2589.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #10	C[Si](C)(C)OC[C@@H]1[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](O[Si](C)(C)C)CN1[Si](C)(C)C	2729.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #11	C[Si](C)(C)OC[C@H]1NC[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	2594.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #12	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)CN[C@@H]2CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2615.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,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)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2728.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #14	C[Si](C)(C)OC[C@H]1NC[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	2611.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,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)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2741.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #16	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2734.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #17	C[Si](C)(C)OC[C@H]1NC[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	2609.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #18	C[Si](C)(C)OC[C@@H]1[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](O[Si](C)(C)C)CN1[Si](C)(C)C	2743.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #19	C[Si](C)(C)OC[C@@H]1[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](O)[C@@H](O[Si](C)(C)C)CN1[Si](C)(C)C	2746.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #2	C[Si](C)(C)OC[C@H]1NC[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)[C@H](O[Si](C)(C)C)[C@H]1O	2620.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #20	C[Si](C)(C)OC[C@@H]1[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](O)[C@@H](O[Si](C)(C)C)CN1[Si](C)(C)C	2727.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #21	C[Si](C)(C)OC[C@H]1NC[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)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2582.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #22	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)NC[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	2603.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,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)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2695.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #24	C[Si](C)(C)OC[C@H]1NC[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	2606.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #25	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2733.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,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)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2715.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #27	C[Si](C)(C)OC[C@H]1NC[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	2583.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #28	C[Si](C)(C)OC[C@@H]1[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](O)CN1[Si](C)(C)C	2730.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #29	C[Si](C)(C)OC[C@@H]1[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](O[Si](C)(C)C)[C@@H](O)CN1[Si](C)(C)C	2718.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,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)CN[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2614.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #30	C[Si](C)(C)OC[C@@H]1[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](O[Si](C)(C)C)[C@@H](O)CN1[Si](C)(C)C	2704.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #31	C[Si](C)(C)OC[C@H]1NC[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	2560.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #32	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2687.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #33	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2715.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #34	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2708.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #35	C[Si](C)(C)OC[C@@H]1[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](O)[C@@H](O)CN1[Si](C)(C)C	2689.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #36	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)CN[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2589.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #37	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)CN[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2613.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #38	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)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2711.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #39	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)CN[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2610.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #4	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)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	2722.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #40	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)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2718.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #41	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)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2733.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #42	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)CN[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2604.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #43	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2709.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #44	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2731.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #45	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2725.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #46	C[Si](C)(C)O[C@H]1CN[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	2606.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #47	C[Si](C)(C)O[C@H]1CN([Si](C)(C)C)[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	2718.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #48	C[Si](C)(C)O[C@H]1CN([Si](C)(C)C)[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	2732.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #49	C[Si](C)(C)O[C@H]1CN([Si](C)(C)C)[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	2726.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #5	C[Si](C)(C)OC[C@H]1NC[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	2628.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #50	C[Si](C)(C)O[C@H]1CN([Si](C)(C)C)[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	2718.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #51	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[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	2605.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #52	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2701.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #53	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2722.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #54	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2725.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #55	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO)O[C@H](CO)[C@H]1O[Si](C)(C)C	2710.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #56	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2686.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #6	C[Si](C)(C)OC[C@H]1NC[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	2609.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #7	C[Si](C)(C)OC[C@@H]1[C@@H](O[C@H]2O[C@H](CO)[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)CN1[Si](C)(C)C	2737.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #8	C[Si](C)(C)OC[C@H]1NC[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	2603.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TMS,isomer #9	C[Si](C)(C)OC[C@@H]1[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)CN1[Si](C)(C)C	2732.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,6TMS,isomer #1	C[Si](C)(C)OC[C@H]1NC[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)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2605.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,6TMS,isomer #10	C[Si](C)(C)OC[C@@H]1[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](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)CN1[Si](C)(C)C	2728.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,6TMS,isomer #11	C[Si](C)(C)OC[C@H]1NC[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	2615.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,6TMS,isomer #12	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2728.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,6TMS,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)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2744.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,6TMS,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)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2745.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,6TMS,isomer #15	C[Si](C)(C)OC[C@@H]1[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](O)[C@@H](O[Si](C)(C)C)CN1[Si](C)(C)C	2733.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,6TMS,isomer #16	C[Si](C)(C)OC[C@H]1NC[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[Si](C)(C)C	2587.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,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)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2693.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,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)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2712.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,6TMS,isomer #19	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2721.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,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)CN[C@@H]2CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2622.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,6TMS,isomer #20	C[Si](C)(C)OC[C@@H]1[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](O[Si](C)(C)C)[C@@H](O)CN1[Si](C)(C)C	2692.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,6TMS,isomer #21	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C)[C@@H]2CO[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	2697.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,6TMS,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)CN[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2615.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,6TMS,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)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2720.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,6TMS,isomer #24	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)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2731.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,6TMS,isomer #25	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)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2742.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,6TMS,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)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2719.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,6TMS,isomer #27	C[Si](C)(C)O[C@H]1CN([Si](C)(C)C)[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	2733.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,6TMS,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)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2704.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,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)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2732.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,6TMS,isomer #4	C[Si](C)(C)OC[C@H]1NC[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	2629.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,6TMS,isomer #5	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)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2739.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,6TMS,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)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2748.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,6TMS,isomer #7	C[Si](C)(C)OC[C@H]1NC[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	2612.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,6TMS,isomer #8	C[Si](C)(C)OC[C@@H]1[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](O[Si](C)(C)C)CN1[Si](C)(C)C	2750.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,6TMS,isomer #9	C[Si](C)(C)OC[C@@H]1[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](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)CN1[Si](C)(C)C	2735.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,7TMS,isomer #1	C[Si](C)(C)OC[C@H]1NC[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	2664.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,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)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2752.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,7TMS,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)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2760.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,7TMS,isomer #4	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)CN([Si](C)(C)C)[C@@H]2CO[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2774.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,7TMS,isomer #5	C[Si](C)(C)OC[C@@H]1[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](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)CN1[Si](C)(C)C	2755.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,7TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[Si](C)(C)C)CN([Si](C)(C)C)[C@@H]2CO[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	2752.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,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)CN([Si](C)(C)C)[C@@H]2CO[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	2716.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,7TMS,isomer #8	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)CN([Si](C)(C)C)[C@@H]2CO)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2761.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1NC[C@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	2972.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@H]1CN[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	2942.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)CN[C@H](CO)[C@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	2975.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	2971.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O)[C@H](O)[C@H]1O	2973.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O)O[C@H](CO)[C@H]1O	2967.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	2972.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,1TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N1C[C@H](O)[C@@H](O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H]1CO	2994.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3161.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@H]1CN[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	3163.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)O[C@H]1CN[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	3174.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)O[C@H]1CN[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	3171.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)O[C@H]1CN([Si](C)(C)C(C)(C)C)[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	3217.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3162.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3183.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@H]1O	3180.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O	3192.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)CN([Si](C)(C)C(C)(C)C)[C@H](CO)[C@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	3226.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3159.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3181.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3153.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3157.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O	3211.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #23	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)NC[C@H](O)[C@H]2O)O[C@@H]1CO	3158.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #24	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3163.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #25	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)[C@H](O)[C@H]1O	3222.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #26	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]2[C@@H](CO)NC[C@H](O)[C@H]2O)O[C@H](CO)[C@H]1O	3167.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #27	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)O[C@H](CO)[C@H]1O	3218.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #28	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)O[C@H](CO)[C@@H](O)[C@@H]1O	3228.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,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)NC[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	3145.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3158.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3157.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3168.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC[C@@H]1[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)CN1[Si](C)(C)C(C)(C)C	3231.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #8	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)CN[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O	3145.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@H]1CN[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	3159.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3352.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3369.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC[C@@H]1[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](O)CN1[Si](C)(C)C(C)(C)C	3453.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,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)NC[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3331.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3333.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,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)NC[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3326.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,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)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3430.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3323.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3327.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC[C@@H]1[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](O)[C@@H](O)CN1[Si](C)(C)C(C)(C)C	3440.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3335.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,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)CN[C@@H]2CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3338.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC[C@@H]1[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](O)[C@@H](O)CN1[Si](C)(C)C(C)(C)C	3436.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC[C@@H]1[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](O)CN1[Si](C)(C)C(C)(C)C	3446.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #22	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)CN[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O	3348.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #23	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)CN[C@@H]2CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3360.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #24	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)CN[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3362.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #25	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)CN[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3353.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #26	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)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O	3417.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #27	CC(C)(C)[Si](C)(C)O[C@H]1CN[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	3342.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #28	CC(C)(C)[Si](C)(C)O[C@H]1CN[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	3351.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #29	CC(C)(C)[Si](C)(C)O[C@H]1CN[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	3366.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3333.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #30	CC(C)(C)[Si](C)(C)O[C@H]1CN([Si](C)(C)C(C)(C)C)[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	3436.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #31	CC(C)(C)[Si](C)(C)O[C@H]1CN[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	3353.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #32	CC(C)(C)[Si](C)(C)O[C@H]1CN[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	3371.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #33	CC(C)(C)[Si](C)(C)O[C@H]1CN([Si](C)(C)C(C)(C)C)[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	3434.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #34	CC(C)(C)[Si](C)(C)O[C@H]1CN[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	3377.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #35	CC(C)(C)[Si](C)(C)O[C@H]1CN([Si](C)(C)C(C)(C)C)[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	3443.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #36	CC(C)(C)[Si](C)(C)O[C@H]1CN([Si](C)(C)C(C)(C)C)[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	3434.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #37	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[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	3362.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #38	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[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	3362.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #39	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[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	3356.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3346.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #40	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)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O	3420.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #41	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)NC[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@@H]1CO	3370.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #42	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)CN[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	3358.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #43	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@H]2[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)[C@H](O)[C@H]1O	3440.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #44	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]2[C@@H](CO)NC[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@H]1O	3368.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #45	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O[C@H]2[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)O[C@H](CO)[C@H]1O	3434.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #46	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O[C@H]2[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)O[C@H](CO)[C@@H](O)[C@@H]1O	3448.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #47	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[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	3342.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #48	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[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	3356.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #49	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3414.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3348.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #50	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[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	3342.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #51	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3410.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #52	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3412.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #53	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]2[C@@H](CO)NC[C@H](O)[C@H]2O)O[C@H](CO)[C@H]1O[Si](C)(C)C(C)(C)C	3336.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #54	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)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)O[C@@H]1CO	3403.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #55	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3404.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,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](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)O[C@H](CO)[C@H]1O	3412.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC[C@@H]1[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)CN1[Si](C)(C)C(C)(C)C	3453.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #7	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)NC[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3341.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3353.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3368.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)CN[C@@H]2CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3497.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3498.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3499.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC[C@@H]1[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](O)[C@@H](O[Si](C)(C)C(C)(C)C)CN1[Si](C)(C)C(C)(C)C	3644.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3502.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC[C@@H]1[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](O)[C@@H](O[Si](C)(C)C(C)(C)C)CN1[Si](C)(C)C(C)(C)C	3648.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC[C@@H]1[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](O[Si](C)(C)C(C)(C)C)CN1[Si](C)(C)C(C)(C)C	3655.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #16	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)NC[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	3502.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC[C@H]1NC[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[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	3505.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #18	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)NC[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	3491.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #19	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)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3624.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3504.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3493.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3498.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC[C@@H]1[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](O[Si](C)(C)C(C)(C)C)[C@@H](O)CN1[Si](C)(C)C(C)(C)C	3645.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3499.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC[C@@H]1[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](O[Si](C)(C)C(C)(C)C)[C@@H](O)CN1[Si](C)(C)C(C)(C)C	3643.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC[C@@H]1[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](O)CN1[Si](C)(C)C(C)(C)C	3654.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3488.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #27	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)NC[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	3502.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C(C)(C)C)[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	3619.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3494.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3512.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,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)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3619.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,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)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3617.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3473.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC[C@@H]1[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](O)CN1[Si](C)(C)C(C)(C)C	3620.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC[C@@H]1[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](O)[C@@H](O)CN1[Si](C)(C)C(C)(C)C	3619.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OC[C@@H]1[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](O)[C@@H](O)CN1[Si](C)(C)C(C)(C)C	3622.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #36	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)CN[C@@H]2CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3525.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #37	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)CN[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3528.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #38	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)CN[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3521.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #39	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)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O	3611.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3516.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #40	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)CN[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	3523.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #41	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)CN[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	3537.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #42	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)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3621.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #43	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)CN[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	3527.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #44	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)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3620.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #45	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)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3614.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #46	CC(C)(C)[Si](C)(C)O[C@H]1CN[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	3506.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #47	CC(C)(C)[Si](C)(C)O[C@H]1CN[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	3514.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #48	CC(C)(C)[Si](C)(C)O[C@H]1CN([Si](C)(C)C(C)(C)C)[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	3621.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #49	CC(C)(C)[Si](C)(C)O[C@H]1CN[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	3524.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@@H]1[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](O[Si](C)(C)C(C)(C)C)CN1[Si](C)(C)C(C)(C)C	3648.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #50	CC(C)(C)[Si](C)(C)O[C@H]1CN([Si](C)(C)C(C)(C)C)[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	3623.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #51	CC(C)(C)[Si](C)(C)O[C@H]1CN([Si](C)(C)C(C)(C)C)[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	3630.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #52	CC(C)(C)[Si](C)(C)O[C@H]1CN[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	3522.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #53	CC(C)(C)[Si](C)(C)O[C@H]1CN([Si](C)(C)C(C)(C)C)[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	3627.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #54	CC(C)(C)[Si](C)(C)O[C@H]1CN([Si](C)(C)C(C)(C)C)[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	3634.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #55	CC(C)(C)[Si](C)(C)O[C@H]1CN([Si](C)(C)C(C)(C)C)[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	3644.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #56	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[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	3512.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #57	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[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	3528.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #58	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)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3624.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #59	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[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	3517.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #6	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)CN[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	3517.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #60	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)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3623.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #61	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)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3621.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #62	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]2[C@@H](CO)NC[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@H]1O[Si](C)(C)C(C)(C)C	3505.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #63	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[Si](C)(C)C(C)(C)C)[C@@H](O)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)O[C@@H]1CO	3629.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #64	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)CN([Si](C)(C)C(C)(C)C)[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	3623.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #65	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]2[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)O[C@H](CO)[C@H]1O	3626.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #66	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[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	3521.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #67	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C(C)(C)C)[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	3595.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #68	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C(C)(C)C)[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	3603.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #69	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C(C)(C)C)[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	3605.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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	3513.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #70	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]2[C@H](O)[C@@H](O)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)O[C@H](CO)[C@H]1O[Si](C)(C)C(C)(C)C	3597.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #8	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)CN[C@@H]2CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3506.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,4TBDMS,isomer #9	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)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3625.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)CN[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	3670.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC[C@@H]1[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](O[Si](C)(C)C(C)(C)C)CN1[Si](C)(C)C(C)(C)C	3819.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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[Si](C)(C)C(C)(C)C	3669.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #12	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)CN[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[Si](C)(C)C(C)(C)C	3675.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,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)CN([Si](C)(C)C(C)(C)C)[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	3816.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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[Si](C)(C)C(C)(C)C)[C@H]1O	3671.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,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)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3818.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #16	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)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3810.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC[C@H]1NC[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3650.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC[C@@H]1[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](O[Si](C)(C)C(C)(C)C)CN1[Si](C)(C)C(C)(C)C	3819.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC[C@@H]1[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](O)[C@@H](O[Si](C)(C)C(C)(C)C)CN1[Si](C)(C)C(C)(C)C	3822.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3667.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC[C@@H]1[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](O)[C@@H](O[Si](C)(C)C(C)(C)C)CN1[Si](C)(C)C(C)(C)C	3817.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC[C@H]1NC[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[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	3658.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #22	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)NC[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	3667.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #23	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)CN([Si](C)(C)C(C)(C)C)[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	3807.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC[C@H]1NC[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[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	3659.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #25	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)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3811.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,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)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3803.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC[C@H]1NC[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3642.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC[C@@H]1[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](O)CN1[Si](C)(C)C(C)(C)C	3811.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OC[C@@H]1[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](O[Si](C)(C)C(C)(C)C)[C@@H](O)CN1[Si](C)(C)C(C)(C)C	3817.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)CN[C@@H]2CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3665.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OC[C@@H]1[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](O[Si](C)(C)C(C)(C)C)[C@@H](O)CN1[Si](C)(C)C(C)(C)C	3811.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC[C@H]1NC[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[Si](C)(C)C(C)(C)C	3649.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO[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	3784.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C(C)(C)C)[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[Si](C)(C)C(C)(C)C	3786.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO[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	3796.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OC[C@@H]1[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](O)[C@@H](O)CN1[Si](C)(C)C(C)(C)C	3778.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #36	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)CN[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	3672.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #37	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)CN[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	3677.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #38	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)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3787.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #39	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)CN[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	3677.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	3792.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #40	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)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3795.2	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #41	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)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3784.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #42	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)CN[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[Si](C)(C)C(C)(C)C	3681.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #43	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)CN([Si](C)(C)C(C)(C)C)[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	3795.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #44	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)CN([Si](C)(C)C(C)(C)C)[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	3795.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #45	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)CN([Si](C)(C)C(C)(C)C)[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	3803.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #46	CC(C)(C)[Si](C)(C)O[C@H]1CN[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[Si](C)(C)C(C)(C)C	3656.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #47	CC(C)(C)[Si](C)(C)O[C@H]1CN([Si](C)(C)C(C)(C)C)[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	3792.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #48	CC(C)(C)[Si](C)(C)O[C@H]1CN([Si](C)(C)C(C)(C)C)[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	3792.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #49	CC(C)(C)[Si](C)(C)O[C@H]1CN([Si](C)(C)C(C)(C)C)[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	3798.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@H]1NC[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3654.0	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #50	CC(C)(C)[Si](C)(C)O[C@H]1CN([Si](C)(C)C(C)(C)C)[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	3798.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #51	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)NC[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3676.5	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #52	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)CN([Si](C)(C)C(C)(C)C)[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	3791.3	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #53	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)CN([Si](C)(C)C(C)(C)C)[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	3791.4	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #54	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)CN([Si](C)(C)C(C)(C)C)[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	3800.9	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #55	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]2[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)CN([Si](C)(C)C(C)(C)C)[C@@H]2CO)O[C@H](CO)[C@H]1O[Si](C)(C)C(C)(C)C	3788.6	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #56	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)CN([Si](C)(C)C(C)(C)C)[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[Si](C)(C)C(C)(C)C	3763.8	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC[C@H]1NC[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3651.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC[C@@H]1[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](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)CN1[Si](C)(C)C(C)(C)C	3814.1	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC[C@H]1NC[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3660.7	Semi standard non polar	33892256
Glucopyranosylmoranoline,5TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC[C@@H]1[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](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)CN1[Si](C)(C)C(C)(C)C	3821.9	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 - Glucopyranosylmoranoline GC-MS (Non-derivatized) - 70eV, Positive	splash10-0abc-6794000000-41aa346c86772d819fb5	2017-09-20	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Glucopyranosylmoranoline GC-MS (5 TMS) - 70eV, Positive	splash10-00di-1411039000-27458429e9ebc6448f19	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Glucopyranosylmoranoline GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Glucopyranosylmoranoline GC-MS (TMS_5_2) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Glucopyranosylmoranoline GC-MS (TMS_6_1) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Glucopyranosylmoranoline GC-MS (TMS_6_4) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Glucopyranosylmoranoline GC-MS (TMS_7_1) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Glucopyranosylmoranoline GC-MS (TBDMS_3_7) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Glucopyranosylmoranoline GC-MS (TBDMS_3_37) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Glucopyranosylmoranoline GC-MS (TBDMS_4_16) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Glucopyranosylmoranoline GC-MS (TBDMS_4_17) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Glucopyranosylmoranoline GC-MS (TBDMS_4_18) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Glucopyranosylmoranoline GC-MS (TBDMS_4_19) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Glucopyranosylmoranoline GC-MS (TBDMS_4_56) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Glucopyranosylmoranoline GC-MS (TBDMS_4_57) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Glucopyranosylmoranoline GC-MS (TBDMS_5_4) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Glucopyranosylmoranoline GC-MS (TBDMS_5_21) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Glucopyranosylmoranoline GC-MS (TBDMS_5_22) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Glucopyranosylmoranoline GC-MS (TBDMS_5_23) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Glucopyranosylmoranoline GC-MS (TBDMS_5_24) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Glucopyranosylmoranoline GC-MS (TBDMS_5_25) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Glucopyranosylmoranoline GC-MS (TBDMS_5_26) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Glucopyranosylmoranoline GC-MS (TBDMS_5_51) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Glucopyranosylmoranoline GC-MS ("Glucopyranosylmoranoline,5TMS,#2" TMS) - 70eV, Positive	Not Available	2021-10-14	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glucopyranosylmoranoline 10V, Positive-QTOF	splash10-06tb-0917000000-3fc9b4e303af88d92c4d	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glucopyranosylmoranoline 20V, Positive-QTOF	splash10-0002-0900000000-38902d1a5ec05f037ea2	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glucopyranosylmoranoline 40V, Positive-QTOF	splash10-0002-2900000000-bd3f648f2084d876a222	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glucopyranosylmoranoline 10V, Negative-QTOF	splash10-00di-0948000000-6dfa2855360f88346004	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glucopyranosylmoranoline 20V, Negative-QTOF	splash10-01rx-1931000000-f71469bd551956973c6f	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glucopyranosylmoranoline 40V, Negative-QTOF	splash10-0233-8900000000-5605181f93f054275660	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glucopyranosylmoranoline 10V, Positive-QTOF	splash10-004j-0609000000-4c6cfa8f59ac3620e8af	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glucopyranosylmoranoline 20V, Positive-QTOF	splash10-0002-0901000000-fde11656da00c496bc78	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glucopyranosylmoranoline 40V, Positive-QTOF	splash10-0k92-9430000000-0fa76cd0b02cf04092ac	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glucopyranosylmoranoline 10V, Negative-QTOF	splash10-00di-0109000000-9eb27f799fe07bc607b9	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glucopyranosylmoranoline 20V, Negative-QTOF	splash10-0zmi-8984000000-0d5722b05dcab214fba7	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glucopyranosylmoranoline 40V, Negative-QTOF	splash10-0006-9400000000-da6c283aeb50bcc5869b	2021-09-23	Wishart Lab	View Spectrum

NMR Spectra

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

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11324809

PDB ID

Not Available

ChEBI ID

70736

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Fujioka S, Matsuzawa Y, Tokunaga K, Keno Y, Kobatake T, Tarui S: Treatment of visceral fat obesity. Int J Obes. 1991 Sep;15 Suppl 2:59-65. [PubMed:1794940 ]

Showing metabocard for Glucopyranosylmoranoline (HMDB0059718)

MOL for HMDB0059718 (Glucopyranosylmoranoline)

3D MOL for HMDB0059718 (Glucopyranosylmoranoline)

3D SDF for HMDB0059718 (Glucopyranosylmoranoline)

3D-SDF for HMDB0059718 (Glucopyranosylmoranoline)

PDB for HMDB0059718 (Glucopyranosylmoranoline)

3D PDB for HMDB0059718 (Glucopyranosylmoranoline)

SMILES for HMDB0059718 (Glucopyranosylmoranoline)

INCHI for HMDB0059718 (Glucopyranosylmoranoline)

Structure for HMDB0059718 (Glucopyranosylmoranoline)

3D Structure for HMDB0059718 (Glucopyranosylmoranoline)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra