Hmdb loader

Showing metabocard for Glucodistylin (HMDB0041597)

Jump To Section:
IdentificationTaxonomyOntologyPhysical propertiesSpectraBiological propertiesConcentrationsLinksReferencesXML
Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-12 03:17:28 UTC
Update Date2022-03-07 02:57:05 UTC
HMDB IDHMDB0041597
Secondary Accession Numbers
  • HMDB41597
Metabolite Identification
Common NameGlucodistylin
DescriptionGlucodistylin belongs to the class of organic compounds known as flavonoid-3-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C3-position. Based on a literature review very few articles have been published on Glucodistylin.
Structure
Data?1563863681
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0041597 (Glucodistylin)


  Mrv1652307201900082D          

 33 36  0  0  0  0            999 V2000
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  7  1  1  0  0  0  0
  7  3  2  0  0  0  0
  8  4  2  0  0  0  0
  8  5  1  0  0  0  0
  9  2  1  0  0  0  0
 10  3  1  0  0  0  0
 10  9  2  0  0  0  0
 11  4  1  0  0  0  0
 12  5  2  0  0  0  0
 13  6  1  0  0  0  0
 14 11  2  0  0  0  0
 14 12  1  0  0  0  0
 15 13  1  0  0  0  0
 16 14  1  0  0  0  0
 17 15  1  0  0  0  0
 18 17  1  0  0  0  0
 19  7  1  0  0  0  0
 20 16  1  0  0  0  0
 20 19  1  0  0  0  0
 21 18  1  0  0  0  0
 22  6  1  0  0  0  0
 23  8  1  0  0  0  0
 24  9  1  0  0  0  0
 25 10  1  0  0  0  0
 26 11  1  0  0  0  0
 27 15  1  0  0  0  0
 28 16  2  0  0  0  0
 29 17  1  0  0  0  0
 30 18  1  0  0  0  0
 31 12  1  0  0  0  0
 31 19  1  0  0  0  0
 32 13  1  0  0  0  0
 32 21  1  0  0  0  0
 33 20  1  0  0  0  0
 33 21  1  0  0  0  0
M  END
Download

3D MOL for HMDB0041597 (Glucodistylin)

HMDB0041597
     RDKit          3D
Glucodistylin
 55 58  0  0  0  0  0  0  0  0999 V2000
    0.3429   -1.0463    2.2493 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9370   -1.2719    1.1800 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2237   -1.9496    1.2607 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6722   -2.5819    2.4070 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8832   -2.5875    3.5460 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8970   -3.2246    2.4773 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6774   -3.2166    1.3434 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9064   -3.8489    1.3783 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2530   -2.5945    0.1918 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0226   -1.9485    0.1205 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5578   -1.3201   -0.9915 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3919   -0.5629   -1.1506 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8162    0.8554   -1.1681 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3429    1.7089   -2.1349 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7178    3.0437   -2.1848 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5880    3.5311   -1.2415 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9906    4.8820   -1.2616 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0690    2.6865   -0.2684 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9444    3.1459    0.6930 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6857    1.3399   -0.2247 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3505   -0.8654   -0.0946 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5502    0.1411   -0.0582 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8217   -0.1288   -0.4596 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6022   -0.0023    0.7287 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8760   -0.5086    0.5241 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8300    0.2810    1.3840 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5139    0.1804    2.7389 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3287   -0.3580   -0.9081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7107   -0.4772   -1.0259 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8318    0.9820   -1.3915 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3516    1.1643   -2.6730 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3115    0.8534   -1.4944 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7337    2.1134   -1.3163 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1810   -3.0347    4.3838 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2305   -3.7152    3.3877 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9330   -4.8356    1.1162 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8503   -2.5702   -0.7272 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9980   -0.8438   -2.1785 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6544    1.3762   -2.9027 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3418    3.6937   -2.9412 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6125    5.4668   -1.9941 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2381    4.1187    0.6836 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0868    0.7015    0.5587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2074   -1.7714   -0.4975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8677   -1.1899   -0.7857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9394   -1.5793    0.8192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8842   -0.1083    1.2705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8864    1.3413    1.0712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5297    0.2393    2.8031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8310   -1.1608   -1.5031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9705   -1.2522   -0.4343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1063    1.8181   -0.7235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2298    1.6054   -2.5758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1206    0.5053   -2.5293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3620    2.7799   -1.6673 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  4  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  2  0
 12 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 25 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
 21  2  1  0
 32 23  1  0
 10  3  1  0
 20 13  1  0
  5 34  1  0
  6 35  1  0
  8 36  1  0
  9 37  1  0
 12 38  1  0
 14 39  1  0
 15 40  1  0
 17 41  1  0
 19 42  1  0
 20 43  1  0
 21 44  1  0
 23 45  1  0
 25 46  1  0
 26 47  1  0
 26 48  1  0
 27 49  1  0
 28 50  1  0
 29 51  1  0
 30 52  1  0
 31 53  1  0
 32 54  1  0
 33 55  1  0
M  END
Download

3D SDF for HMDB0041597 (Glucodistylin)


  Mrv1652307201900082D          

 33 36  0  0  0  0            999 V2000
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  7  1  1  0  0  0  0
  7  3  2  0  0  0  0
  8  4  2  0  0  0  0
  8  5  1  0  0  0  0
  9  2  1  0  0  0  0
 10  3  1  0  0  0  0
 10  9  2  0  0  0  0
 11  4  1  0  0  0  0
 12  5  2  0  0  0  0
 13  6  1  0  0  0  0
 14 11  2  0  0  0  0
 14 12  1  0  0  0  0
 15 13  1  0  0  0  0
 16 14  1  0  0  0  0
 17 15  1  0  0  0  0
 18 17  1  0  0  0  0
 19  7  1  0  0  0  0
 20 16  1  0  0  0  0
 20 19  1  0  0  0  0
 21 18  1  0  0  0  0
 22  6  1  0  0  0  0
 23  8  1  0  0  0  0
 24  9  1  0  0  0  0
 25 10  1  0  0  0  0
 26 11  1  0  0  0  0
 27 15  1  0  0  0  0
 28 16  2  0  0  0  0
 29 17  1  0  0  0  0
 30 18  1  0  0  0  0
 31 12  1  0  0  0  0
 31 19  1  0  0  0  0
 32 13  1  0  0  0  0
 32 21  1  0  0  0  0
 33 20  1  0  0  0  0
 33 21  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0041597

> <DATABASE_NAME>
hmdb

> <SMILES>
OCC1OC(OC2C(OC3=CC(O)=CC(O)=C3C2=O)C2=CC(O)=C(O)C=C2)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C21H22O12/c22-6-13-15(27)17(29)18(30)21(32-13)33-20-16(28)14-11(26)4-8(23)5-12(14)31-19(20)7-1-2-9(24)10(25)3-7/h1-5,13,15,17-27,29-30H,6H2

> <INCHI_KEY>
FVQOMEDMFUMIMO-UHFFFAOYSA-N

> <FORMULA>
C21H22O12

> <MOLECULAR_WEIGHT>
466.395

> <EXACT_MASS>
466.111126148

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
43.467577167515174

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,4-dihydro-2H-1-benzopyran-4-one

> <ALOGPS_LOGP>
0.02

> <JCHEM_LOGP>
0.045548622333333136

> <ALOGPS_LOGS>
-1.98

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.000668940710382

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.7413381211260734

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981083713221519

> <JCHEM_POLAR_SURFACE_AREA>
206.59999999999997

> <JCHEM_REFRACTIVITY>
107.0222

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.91e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,3-dihydro-1-benzopyran-4-one

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0041597 (Glucodistylin)

HMDB0041597
     RDKit          3D
Glucodistylin
 55 58  0  0  0  0  0  0  0  0999 V2000
    0.3429   -1.0463    2.2493 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9370   -1.2719    1.1800 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2237   -1.9496    1.2607 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6722   -2.5819    2.4070 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8832   -2.5875    3.5460 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8970   -3.2246    2.4773 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6774   -3.2166    1.3434 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9064   -3.8489    1.3783 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2530   -2.5945    0.1918 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0226   -1.9485    0.1205 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5578   -1.3201   -0.9915 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3919   -0.5629   -1.1506 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8162    0.8554   -1.1681 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3429    1.7089   -2.1349 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7178    3.0437   -2.1848 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5880    3.5311   -1.2415 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9906    4.8820   -1.2616 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0690    2.6865   -0.2684 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9444    3.1459    0.6930 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6857    1.3399   -0.2247 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3505   -0.8654   -0.0946 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5502    0.1411   -0.0582 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8217   -0.1288   -0.4596 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6022   -0.0023    0.7287 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8760   -0.5086    0.5241 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8300    0.2810    1.3840 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5139    0.1804    2.7389 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3287   -0.3580   -0.9081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7107   -0.4772   -1.0259 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8318    0.9820   -1.3915 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3516    1.1643   -2.6730 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3115    0.8534   -1.4944 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7337    2.1134   -1.3163 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1810   -3.0347    4.3838 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2305   -3.7152    3.3877 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9330   -4.8356    1.1162 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8503   -2.5702   -0.7272 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9980   -0.8438   -2.1785 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6544    1.3762   -2.9027 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3418    3.6937   -2.9412 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6125    5.4668   -1.9941 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2381    4.1187    0.6836 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0868    0.7015    0.5587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2074   -1.7714   -0.4975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8677   -1.1899   -0.7857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9394   -1.5793    0.8192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8842   -0.1083    1.2705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8864    1.3413    1.0712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5297    0.2393    2.8031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8310   -1.1608   -1.5031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9705   -1.2522   -0.4343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1063    1.8181   -0.7235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2298    1.6054   -2.5758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1206    0.5053   -2.5293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3620    2.7799   -1.6673 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  4  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  2  0
 12 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 25 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
 21  2  1  0
 32 23  1  0
 10  3  1  0
 20 13  1  0
  5 34  1  0
  6 35  1  0
  8 36  1  0
  9 37  1  0
 12 38  1  0
 14 39  1  0
 15 40  1  0
 17 41  1  0
 19 42  1  0
 20 43  1  0
 21 44  1  0
 23 45  1  0
 25 46  1  0
 26 47  1  0
 26 48  1  0
 27 49  1  0
 28 50  1  0
 29 51  1  0
 30 52  1  0
 31 53  1  0
 32 54  1  0
 33 55  1  0
M  END
Download

PDB for HMDB0041597 (Glucodistylin)

HEADER    PROTEIN                                 20-JUL-19   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUL-19         0                                  
HETATM    1  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       2.667  -9.240   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       9.336   2.310   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       9.336  -0.770   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       5.335  -9.240   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       8.002  -7.700   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       8.002  -4.620   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       2.667   0.000   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
CONECT    1    2    7                                                       
CONECT    2    1    9                                                       
CONECT    3    7   10                                                       
CONECT    4    8   11                                                       
CONECT    5    8   12                                                       
CONECT    6   13   22                                                       
CONECT    7    1    3   19                                                  
CONECT    8    4    5   23                                                  
CONECT    9    2   10   24                                                  
CONECT   10    3    9   25                                                  
CONECT   11    4   14   26                                                  
CONECT   12    5   14   31                                                  
CONECT   13    6   15   32                                                  
CONECT   14   11   12   16                                                  
CONECT   15   13   17   27                                                  
CONECT   16   14   20   28                                                  
CONECT   17   15   18   29                                                  
CONECT   18   17   21   30                                                  
CONECT   19    7   20   31                                                  
CONECT   20   16   19   33                                                  
CONECT   21   18   32   33                                                  
CONECT   22    6                                                            
CONECT   23    8                                                            
CONECT   24    9                                                            
CONECT   25   10                                                            
CONECT   26   11                                                            
CONECT   27   15                                                            
CONECT   28   16                                                            
CONECT   29   17                                                            
CONECT   30   18                                                            
CONECT   31   12   19                                                       
CONECT   32   13   21                                                       
CONECT   33   20   21                                                       
MASTER        0    0    0    0    0    0    0    0   33    0   72    0
END
Download

3D PDB for HMDB0041597 (Glucodistylin)

COMPND    HMDB0041597
HETATM    1  O1  UNL     1       0.343  -1.046   2.249  1.00  0.00           O  
HETATM    2  C1  UNL     1       0.937  -1.272   1.180  1.00  0.00           C  
HETATM    3  C2  UNL     1       2.224  -1.950   1.261  1.00  0.00           C  
HETATM    4  C3  UNL     1       2.672  -2.582   2.407  1.00  0.00           C  
HETATM    5  O2  UNL     1       1.883  -2.587   3.546  1.00  0.00           O  
HETATM    6  C4  UNL     1       3.897  -3.225   2.477  1.00  0.00           C  
HETATM    7  C5  UNL     1       4.677  -3.217   1.343  1.00  0.00           C  
HETATM    8  O3  UNL     1       5.906  -3.849   1.378  1.00  0.00           O  
HETATM    9  C6  UNL     1       4.253  -2.594   0.192  1.00  0.00           C  
HETATM   10  C7  UNL     1       3.023  -1.949   0.121  1.00  0.00           C  
HETATM   11  O4  UNL     1       2.558  -1.320  -0.992  1.00  0.00           O  
HETATM   12  C8  UNL     1       1.392  -0.563  -1.151  1.00  0.00           C  
HETATM   13  C9  UNL     1       1.816   0.855  -1.168  1.00  0.00           C  
HETATM   14  C10 UNL     1       1.343   1.709  -2.135  1.00  0.00           C  
HETATM   15  C11 UNL     1       1.718   3.044  -2.185  1.00  0.00           C  
HETATM   16  C12 UNL     1       2.588   3.531  -1.242  1.00  0.00           C  
HETATM   17  O5  UNL     1       2.991   4.882  -1.262  1.00  0.00           O  
HETATM   18  C13 UNL     1       3.069   2.687  -0.268  1.00  0.00           C  
HETATM   19  O6  UNL     1       3.944   3.146   0.693  1.00  0.00           O  
HETATM   20  C14 UNL     1       2.686   1.340  -0.225  1.00  0.00           C  
HETATM   21  C15 UNL     1       0.351  -0.865  -0.095  1.00  0.00           C  
HETATM   22  O7  UNL     1      -0.550   0.141  -0.058  1.00  0.00           O  
HETATM   23  C16 UNL     1      -1.822  -0.129  -0.460  1.00  0.00           C  
HETATM   24  O8  UNL     1      -2.602  -0.002   0.729  1.00  0.00           O  
HETATM   25  C17 UNL     1      -3.876  -0.509   0.524  1.00  0.00           C  
HETATM   26  C18 UNL     1      -4.830   0.281   1.384  1.00  0.00           C  
HETATM   27  O9  UNL     1      -4.514   0.180   2.739  1.00  0.00           O  
HETATM   28  C19 UNL     1      -4.329  -0.358  -0.908  1.00  0.00           C  
HETATM   29  O10 UNL     1      -5.711  -0.477  -1.026  1.00  0.00           O  
HETATM   30  C20 UNL     1      -3.832   0.982  -1.391  1.00  0.00           C  
HETATM   31  O11 UNL     1      -4.352   1.164  -2.673  1.00  0.00           O  
HETATM   32  C21 UNL     1      -2.312   0.853  -1.494  1.00  0.00           C  
HETATM   33  O12 UNL     1      -1.734   2.113  -1.316  1.00  0.00           O  
HETATM   34  H1  UNL     1       2.181  -3.035   4.384  1.00  0.00           H  
HETATM   35  H2  UNL     1       4.230  -3.715   3.388  1.00  0.00           H  
HETATM   36  H3  UNL     1       5.933  -4.836   1.116  1.00  0.00           H  
HETATM   37  H4  UNL     1       4.850  -2.570  -0.727  1.00  0.00           H  
HETATM   38  H5  UNL     1       0.998  -0.844  -2.179  1.00  0.00           H  
HETATM   39  H6  UNL     1       0.654   1.376  -2.903  1.00  0.00           H  
HETATM   40  H7  UNL     1       1.342   3.694  -2.941  1.00  0.00           H  
HETATM   41  H8  UNL     1       2.613   5.467  -1.994  1.00  0.00           H  
HETATM   42  H9  UNL     1       4.238   4.119   0.684  1.00  0.00           H  
HETATM   43  H10 UNL     1       3.087   0.701   0.559  1.00  0.00           H  
HETATM   44  H11 UNL     1      -0.207  -1.771  -0.497  1.00  0.00           H  
HETATM   45  H12 UNL     1      -1.868  -1.190  -0.786  1.00  0.00           H  
HETATM   46  H13 UNL     1      -3.939  -1.579   0.819  1.00  0.00           H  
HETATM   47  H14 UNL     1      -5.884  -0.108   1.271  1.00  0.00           H  
HETATM   48  H15 UNL     1      -4.886   1.341   1.071  1.00  0.00           H  
HETATM   49  H16 UNL     1      -3.530   0.239   2.803  1.00  0.00           H  
HETATM   50  H17 UNL     1      -3.831  -1.161  -1.503  1.00  0.00           H  
HETATM   51  H18 UNL     1      -5.970  -1.252  -0.434  1.00  0.00           H  
HETATM   52  H19 UNL     1      -4.106   1.818  -0.724  1.00  0.00           H  
HETATM   53  H20 UNL     1      -5.230   1.605  -2.576  1.00  0.00           H  
HETATM   54  H21 UNL     1      -2.121   0.505  -2.529  1.00  0.00           H  
HETATM   55  H22 UNL     1      -2.362   2.780  -1.667  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   21
CONECT    3    4    4   10
CONECT    4    5    6
CONECT    5   34
CONECT    6    7    7   35
CONECT    7    8    9
CONECT    8   36
CONECT    9   10   10   37
CONECT   10   11
CONECT   11   12
CONECT   12   13   21   38
CONECT   13   14   14   20
CONECT   14   15   39
CONECT   15   16   16   40
CONECT   16   17   18
CONECT   17   41
CONECT   18   19   20   20
CONECT   19   42
CONECT   20   43
CONECT   21   22   44
CONECT   22   23
CONECT   23   24   32   45
CONECT   24   25
CONECT   25   26   28   46
CONECT   26   27   47   48
CONECT   27   49
CONECT   28   29   30   50
CONECT   29   51
CONECT   30   31   32   52
CONECT   31   53
CONECT   32   33   54
CONECT   33   55
END
Download

SMILES for HMDB0041597 (Glucodistylin)

OCC1OC(OC2C(OC3=CC(O)=CC(O)=C3C2=O)C2=CC(O)=C(O)C=C2)C(O)C(O)C1O
Download

INCHI for HMDB0041597 (Glucodistylin)

InChI=1S/C21H22O12/c22-6-13-15(27)17(29)18(30)21(32-13)33-20-16(28)14-11(26)4-8(23)5-12(14)31-19(20)7-1-2-9(24)10(25)3-7/h1-5,13,15,17-27,29-30H,6H2
Download
View in JSmolView NMR AssignmentsView Stereo Labels
SynonymsNot Available
Chemical FormulaC21H22O12
Average Molecular Weight466.395
Monoisotopic Molecular Weight466.111126148
IUPAC Name2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,4-dihydro-2H-1-benzopyran-4-one
Traditional Name2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,3-dihydro-1-benzopyran-4-one
CAS Registry Number27297-45-6
SMILES
OCC1OC(OC2C(OC3=CC(O)=CC(O)=C3C2=O)C2=CC(O)=C(O)C=C2)C(O)C(O)C1O
InChI Identifier
InChI=1S/C21H22O12/c22-6-13-15(27)17(29)18(30)21(32-13)33-20-16(28)14-11(26)4-8(23)5-12(14)31-19(20)7-1-2-9(24)10(25)3-7/h1-5,13,15,17-27,29-30H,6H2
InChI KeyFVQOMEDMFUMIMO-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as flavonoid-3-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C3-position.
KingdomOrganic compounds
Super ClassPhenylpropanoids and polyketides
ClassFlavonoids
Sub ClassFlavonoid glycosides
Direct ParentFlavonoid-3-O-glycosides
Alternative Parents
Substituents
  • Flavonoid-3-o-glycoside
  • Hydroxyflavonoid
  • Flavanonol
  • Flavanone
  • 7-hydroxyflavonoid
  • 5-hydroxyflavonoid
  • 4'-hydroxyflavonoid
  • 3'-hydroxyflavonoid
  • Flavan
  • Hexose monosaccharide
  • Chromone
  • Glycosyl compound
  • O-glycosyl compound
  • Benzopyran
  • 1-benzopyran
  • Chromane
  • Aryl alkyl ketone
  • Aryl ketone
  • Catechol
  • 1-hydroxy-4-unsubstituted benzenoid
  • Alkyl aryl ether
  • Phenol
  • 1-hydroxy-2-unsubstituted benzenoid
  • Monocyclic benzene moiety
  • Benzenoid
  • Oxane
  • Monosaccharide
  • Vinylogous acid
  • Secondary alcohol
  • Ketone
  • Polyol
  • Ether
  • Organoheterocyclic compound
  • Acetal
  • Oxacycle
  • Primary alcohol
  • Organic oxide
  • Organic oxygen compound
  • Alcohol
  • Hydrocarbon derivative
  • Organooxygen compound
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Biological locationSource
ProcessNot Available
Role
Biological role
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point169 - 171 °CNot Available
Boiling PointNot AvailableNot Available
Water Solubility7694 mg/L @ 25 °C (est)The Good Scents Company Information System
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility4.91 g/LALOGPS
logP0.02ALOGPS
logP0.046ChemAxon
logS-2ALOGPS
pKa (Strongest Acidic)7.74ChemAxon
pKa (Strongest Basic)-3ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count12ChemAxon
Hydrogen Donor Count8ChemAxon
Polar Surface Area206.6 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity107.02 m³·mol⁻¹ChemAxon
Polarizability43.47 ųChemAxon
Number of Rings4ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+207.94831661259
DarkChem[M-H]-201.38631661259
DeepCCS[M+H]+200.20530932474
DeepCCS[M-H]-197.80930932474
DeepCCS[M-2H]-230.69230932474
DeepCCS[M+Na]+206.1530932474
AllCCS[M+H]+206.432859911
AllCCS[M+H-H2O]+204.132859911
AllCCS[M+NH4]+208.532859911
AllCCS[M+Na]+209.132859911
AllCCS[M-H]-202.532859911
AllCCS[M+Na-2H]-203.032859911
AllCCS[M+HCOO]-203.732859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
GlucodistylinOCC1OC(OC2C(OC3=CC(O)=CC(O)=C3C2=O)C2=CC(O)=C(O)C=C2)C(O)C(O)C1O5107.8Standard polar33892256
GlucodistylinOCC1OC(OC2C(OC3=CC(O)=CC(O)=C3C2=O)C2=CC(O)=C(O)C=C2)C(O)C(O)C1O4178.7Standard non polar33892256
GlucodistylinOCC1OC(OC2C(OC3=CC(O)=CC(O)=C3C2=O)C2=CC(O)=C(O)C=C2)C(O)C(O)C1O4392.2Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Glucodistylin,1TMS,isomer #1C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O)C(O)C1O4386.8Semi standard non polar33892256
Glucodistylin,1TMS,isomer #2C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O)C3O)C(C3=CC=C(O)C(O)=C3)OC2=C14434.7Semi standard non polar33892256
Glucodistylin,1TMS,isomer #3C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(OC1OC(CO)C(O)C(O)C1O)C(C1=CC=C(O)C(O)=C1)O24432.9Semi standard non polar33892256
Glucodistylin,1TMS,isomer #4C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O)C(O)C2O)=CC=C1O4418.1Semi standard non polar33892256
Glucodistylin,1TMS,isomer #5C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O)C(O)C2O)C=C1O4436.0Semi standard non polar33892256
Glucodistylin,1TMS,isomer #6C[Si](C)(C)OC1C(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)OC(CO)C(O)C1O4404.7Semi standard non polar33892256
Glucodistylin,1TMS,isomer #7C[Si](C)(C)OC1C(O)C(CO)OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C1O4407.0Semi standard non polar33892256
Glucodistylin,1TMS,isomer #8C[Si](C)(C)OC1C(CO)OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O)C1O4399.5Semi standard non polar33892256
Glucodistylin,2TMS,isomer #1C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O)=C2)C(O)C(O)C1O4359.8Semi standard non polar33892256
Glucodistylin,2TMS,isomer #10C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O)C3O)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC2=C14274.4Semi standard non polar33892256
Glucodistylin,2TMS,isomer #11C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(C3=CC=C(O)C(O)=C3)OC2=C14275.0Semi standard non polar33892256
Glucodistylin,2TMS,isomer #12C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(C3=CC=C(O)C(O)=C3)OC2=C14274.8Semi standard non polar33892256
Glucodistylin,2TMS,isomer #13C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=C14293.6Semi standard non polar33892256
Glucodistylin,2TMS,isomer #14C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(OC1OC(CO)C(O[Si](C)(C)C)C(O)C1O)C(C1=CC=C(O)C(O)=C1)O24354.5Semi standard non polar33892256
Glucodistylin,2TMS,isomer #15C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(OC1OC(CO)C(O)C(O[Si](C)(C)C)C1O)C(C1=CC=C(O)C(O)=C1)O24360.0Semi standard non polar33892256
Glucodistylin,2TMS,isomer #16C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(OC1OC(CO)C(O)C(O)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O24365.1Semi standard non polar33892256
Glucodistylin,2TMS,isomer #17C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(=O)C2OC2OC(CO)C(O)C(O)C2O)C=C1O4376.2Semi standard non polar33892256
Glucodistylin,2TMS,isomer #18C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(=O)C2OC2OC(CO)C(O)C(O)C2O)=CC=C1O4358.1Semi standard non polar33892256
Glucodistylin,2TMS,isomer #19C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=CC=C1O4248.1Semi standard non polar33892256
Glucodistylin,2TMS,isomer #2C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O)C(O)=C2)C(O)C(O)C1O4300.8Semi standard non polar33892256
Glucodistylin,2TMS,isomer #20C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=CC=C1O4242.2Semi standard non polar33892256
Glucodistylin,2TMS,isomer #21C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=CC=C1O4269.5Semi standard non polar33892256
Glucodistylin,2TMS,isomer #22C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O)C(O)C2O)C=C1O[Si](C)(C)C4292.0Semi standard non polar33892256
Glucodistylin,2TMS,isomer #23C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C=C1O4267.9Semi standard non polar33892256
Glucodistylin,2TMS,isomer #24C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C=C1O4263.8Semi standard non polar33892256
Glucodistylin,2TMS,isomer #25C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C=C1O4287.7Semi standard non polar33892256
Glucodistylin,2TMS,isomer #26C[Si](C)(C)OC1C(CO)OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)C1O4283.8Semi standard non polar33892256
Glucodistylin,2TMS,isomer #27C[Si](C)(C)OC1C(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)OC(CO)C(O)C1O[Si](C)(C)C4302.5Semi standard non polar33892256
Glucodistylin,2TMS,isomer #28C[Si](C)(C)OC1C(CO)OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O)C1O[Si](C)(C)C4288.7Semi standard non polar33892256
Glucodistylin,2TMS,isomer #3C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O)C(O)C1O4305.9Semi standard non polar33892256
Glucodistylin,2TMS,isomer #4C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O4285.2Semi standard non polar33892256
Glucodistylin,2TMS,isomer #5C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O4292.5Semi standard non polar33892256
Glucodistylin,2TMS,isomer #6C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O4291.0Semi standard non polar33892256
Glucodistylin,2TMS,isomer #7C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C4287.3Semi standard non polar33892256
Glucodistylin,2TMS,isomer #8C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O)C(O)C3O)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C14353.0Semi standard non polar33892256
Glucodistylin,2TMS,isomer #9C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O)C3O)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC2=C14299.5Semi standard non polar33892256
Glucodistylin,3TMS,isomer #1C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O)=C2)C(O)C(O)C1O4188.0Semi standard non polar33892256
Glucodistylin,3TMS,isomer #10C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O4137.4Semi standard non polar33892256
Glucodistylin,3TMS,isomer #11C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C4137.3Semi standard non polar33892256
Glucodistylin,3TMS,isomer #12C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O4130.5Semi standard non polar33892256
Glucodistylin,3TMS,isomer #13C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O4122.1Semi standard non polar33892256
Glucodistylin,3TMS,isomer #14C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O4115.3Semi standard non polar33892256
Glucodistylin,3TMS,isomer #15C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C4115.2Semi standard non polar33892256
Glucodistylin,3TMS,isomer #16C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O4108.6Semi standard non polar33892256
Glucodistylin,3TMS,isomer #17C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O4096.2Semi standard non polar33892256
Glucodistylin,3TMS,isomer #18C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C4097.3Semi standard non polar33892256
Glucodistylin,3TMS,isomer #19C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4151.7Semi standard non polar33892256
Glucodistylin,3TMS,isomer #2C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O)C(O)C1O4195.2Semi standard non polar33892256
Glucodistylin,3TMS,isomer #20C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4172.0Semi standard non polar33892256
Glucodistylin,3TMS,isomer #21C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4163.5Semi standard non polar33892256
Glucodistylin,3TMS,isomer #22C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C14196.5Semi standard non polar33892256
Glucodistylin,3TMS,isomer #23C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C14184.4Semi standard non polar33892256
Glucodistylin,3TMS,isomer #24C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C14201.3Semi standard non polar33892256
Glucodistylin,3TMS,isomer #25C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O)C(O)C3O)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)O2)C(O[Si](C)(C)C)=C14188.0Semi standard non polar33892256
Glucodistylin,3TMS,isomer #26C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O)C(O)C3O)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)O2)C(O[Si](C)(C)C)=C14165.0Semi standard non polar33892256
Glucodistylin,3TMS,isomer #27C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O)C3O)C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C14150.4Semi standard non polar33892256
Glucodistylin,3TMS,isomer #28C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC2=C14111.2Semi standard non polar33892256
Glucodistylin,3TMS,isomer #29C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC2=C14090.8Semi standard non polar33892256
Glucodistylin,3TMS,isomer #3C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O4178.9Semi standard non polar33892256
Glucodistylin,3TMS,isomer #30C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC2=C14107.1Semi standard non polar33892256
Glucodistylin,3TMS,isomer #31C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC2=C14091.2Semi standard non polar33892256
Glucodistylin,3TMS,isomer #32C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC2=C14069.1Semi standard non polar33892256
Glucodistylin,3TMS,isomer #33C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC2=C14084.8Semi standard non polar33892256
Glucodistylin,3TMS,isomer #34C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(C3=CC=C(O)C(O)=C3)OC2=C14150.2Semi standard non polar33892256
Glucodistylin,3TMS,isomer #35C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=C14158.2Semi standard non polar33892256
Glucodistylin,3TMS,isomer #36C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=C14154.4Semi standard non polar33892256
Glucodistylin,3TMS,isomer #37C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(OC1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)C(C1=CC=C(O)C(O)=C1)O24225.9Semi standard non polar33892256
Glucodistylin,3TMS,isomer #38C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(OC1OC(CO)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O24228.0Semi standard non polar33892256
Glucodistylin,3TMS,isomer #39C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C=C1O4177.9Semi standard non polar33892256
Glucodistylin,3TMS,isomer #4C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O4210.8Semi standard non polar33892256
Glucodistylin,3TMS,isomer #40C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=CC=C1O4158.6Semi standard non polar33892256
Glucodistylin,3TMS,isomer #41C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(OC1OC(CO)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O24228.7Semi standard non polar33892256
Glucodistylin,3TMS,isomer #42C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(=O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C=C1O4161.0Semi standard non polar33892256
Glucodistylin,3TMS,isomer #43C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(=O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=CC=C1O4137.8Semi standard non polar33892256
Glucodistylin,3TMS,isomer #44C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(=O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C=C1O4196.0Semi standard non polar33892256
Glucodistylin,3TMS,isomer #45C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(=O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=CC=C1O4178.8Semi standard non polar33892256
Glucodistylin,3TMS,isomer #46C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(=O)C2OC2OC(CO)C(O)C(O)C2O)C=C1O[Si](C)(C)C4229.4Semi standard non polar33892256
Glucodistylin,3TMS,isomer #47C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC=C1O4096.0Semi standard non polar33892256
Glucodistylin,3TMS,isomer #48C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC=C1O4110.2Semi standard non polar33892256
Glucodistylin,3TMS,isomer #49C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C=C1O[Si](C)(C)C4125.0Semi standard non polar33892256
Glucodistylin,3TMS,isomer #5C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O4211.7Semi standard non polar33892256
Glucodistylin,3TMS,isomer #50C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1O4105.5Semi standard non polar33892256
Glucodistylin,3TMS,isomer #51C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C=C1O[Si](C)(C)C4111.0Semi standard non polar33892256
Glucodistylin,3TMS,isomer #52C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C4138.0Semi standard non polar33892256
Glucodistylin,3TMS,isomer #53C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=C1O4113.8Semi standard non polar33892256
Glucodistylin,3TMS,isomer #54C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=C1O4127.9Semi standard non polar33892256
Glucodistylin,3TMS,isomer #55C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1O4122.0Semi standard non polar33892256
Glucodistylin,3TMS,isomer #56C[Si](C)(C)OC1C(CO)OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)C1O[Si](C)(C)C4175.3Semi standard non polar33892256
Glucodistylin,3TMS,isomer #6C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C4206.6Semi standard non polar33892256
Glucodistylin,3TMS,isomer #7C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O)C(O)C1O4119.2Semi standard non polar33892256
Glucodistylin,3TMS,isomer #8C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O4100.5Semi standard non polar33892256
Glucodistylin,3TMS,isomer #9C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O4142.5Semi standard non polar33892256
Glucodistylin,4TMS,isomer #1C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C)C=C3O[Si](C)(C)C)OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O)C(O)C1O4025.1Semi standard non polar33892256
Glucodistylin,4TMS,isomer #10C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O4025.6Semi standard non polar33892256
Glucodistylin,4TMS,isomer #11C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O3994.6Semi standard non polar33892256
Glucodistylin,4TMS,isomer #12C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C4027.7Semi standard non polar33892256
Glucodistylin,4TMS,isomer #13C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4058.9Semi standard non polar33892256
Glucodistylin,4TMS,isomer #14C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4093.2Semi standard non polar33892256
Glucodistylin,4TMS,isomer #15C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4082.1Semi standard non polar33892256
Glucodistylin,4TMS,isomer #16C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O4013.2Semi standard non polar33892256
Glucodistylin,4TMS,isomer #17C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O3990.2Semi standard non polar33892256
Glucodistylin,4TMS,isomer #18C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O3982.0Semi standard non polar33892256
Glucodistylin,4TMS,isomer #19C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C3986.7Semi standard non polar33892256
Glucodistylin,4TMS,isomer #2C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O4008.3Semi standard non polar33892256
Glucodistylin,4TMS,isomer #20C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O3973.6Semi standard non polar33892256
Glucodistylin,4TMS,isomer #21C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O3959.2Semi standard non polar33892256
Glucodistylin,4TMS,isomer #22C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C3969.7Semi standard non polar33892256
Glucodistylin,4TMS,isomer #23C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4018.1Semi standard non polar33892256
Glucodistylin,4TMS,isomer #24C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4050.3Semi standard non polar33892256
Glucodistylin,4TMS,isomer #25C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4036.4Semi standard non polar33892256
Glucodistylin,4TMS,isomer #26C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O4014.5Semi standard non polar33892256
Glucodistylin,4TMS,isomer #27C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O3989.6Semi standard non polar33892256
Glucodistylin,4TMS,isomer #28C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C4020.4Semi standard non polar33892256
Glucodistylin,4TMS,isomer #29C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3983.3Semi standard non polar33892256
Glucodistylin,4TMS,isomer #3C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O4067.8Semi standard non polar33892256
Glucodistylin,4TMS,isomer #30C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4010.3Semi standard non polar33892256
Glucodistylin,4TMS,isomer #31C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4004.1Semi standard non polar33892256
Glucodistylin,4TMS,isomer #32C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3969.5Semi standard non polar33892256
Glucodistylin,4TMS,isomer #33C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3997.2Semi standard non polar33892256
Glucodistylin,4TMS,isomer #34C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3990.0Semi standard non polar33892256
Glucodistylin,4TMS,isomer #35C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4073.8Semi standard non polar33892256
Glucodistylin,4TMS,isomer #36C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C14073.9Semi standard non polar33892256
Glucodistylin,4TMS,isomer #37C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C14082.8Semi standard non polar33892256
Glucodistylin,4TMS,isomer #38C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)O2)C(O[Si](C)(C)C)=C14050.0Semi standard non polar33892256
Glucodistylin,4TMS,isomer #39C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)O2)C(O[Si](C)(C)C)=C14030.3Semi standard non polar33892256
Glucodistylin,4TMS,isomer #4C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O4037.7Semi standard non polar33892256
Glucodistylin,4TMS,isomer #40C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C14065.8Semi standard non polar33892256
Glucodistylin,4TMS,isomer #41C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)O2)C(O[Si](C)(C)C)=C14024.5Semi standard non polar33892256
Glucodistylin,4TMS,isomer #42C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)O2)C(O[Si](C)(C)C)=C14004.2Semi standard non polar33892256
Glucodistylin,4TMS,isomer #43C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)O2)C(O[Si](C)(C)C)=C14033.9Semi standard non polar33892256
Glucodistylin,4TMS,isomer #44C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)O2)C(O[Si](C)(C)C)=C14016.4Semi standard non polar33892256
Glucodistylin,4TMS,isomer #45C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O)C(O)C3O)C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)O2)C(O[Si](C)(C)C)=C14086.9Semi standard non polar33892256
Glucodistylin,4TMS,isomer #46C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C14042.2Semi standard non polar33892256
Glucodistylin,4TMS,isomer #47C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C14020.9Semi standard non polar33892256
Glucodistylin,4TMS,isomer #48C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C14033.9Semi standard non polar33892256
Glucodistylin,4TMS,isomer #49C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC2=C13988.0Semi standard non polar33892256
Glucodistylin,4TMS,isomer #5C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C4070.5Semi standard non polar33892256
Glucodistylin,4TMS,isomer #50C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC2=C13994.8Semi standard non polar33892256
Glucodistylin,4TMS,isomer #51C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC2=C13983.3Semi standard non polar33892256
Glucodistylin,4TMS,isomer #52C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC2=C13967.9Semi standard non polar33892256
Glucodistylin,4TMS,isomer #53C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC2=C13976.2Semi standard non polar33892256
Glucodistylin,4TMS,isomer #54C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC2=C13964.0Semi standard non polar33892256
Glucodistylin,4TMS,isomer #55C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=C14046.4Semi standard non polar33892256
Glucodistylin,4TMS,isomer #56C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(OC1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O24092.8Semi standard non polar33892256
Glucodistylin,4TMS,isomer #57C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=C1O4032.9Semi standard non polar33892256
Glucodistylin,4TMS,isomer #58C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC=C1O4019.7Semi standard non polar33892256
Glucodistylin,4TMS,isomer #59C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=C1O4044.9Semi standard non polar33892256
Glucodistylin,4TMS,isomer #6C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O4067.8Semi standard non polar33892256
Glucodistylin,4TMS,isomer #60C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC=C1O4030.4Semi standard non polar33892256
Glucodistylin,4TMS,isomer #61C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C=C1O[Si](C)(C)C4088.7Semi standard non polar33892256
Glucodistylin,4TMS,isomer #62C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(=O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1O4026.7Semi standard non polar33892256
Glucodistylin,4TMS,isomer #63C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(=O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1O4011.0Semi standard non polar33892256
Glucodistylin,4TMS,isomer #64C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(=O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C=C1O[Si](C)(C)C4046.1Semi standard non polar33892256
Glucodistylin,4TMS,isomer #65C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(=O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C4077.2Semi standard non polar33892256
Glucodistylin,4TMS,isomer #66C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1O3996.8Semi standard non polar33892256
Glucodistylin,4TMS,isomer #67C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=C1O[Si](C)(C)C4026.0Semi standard non polar33892256
Glucodistylin,4TMS,isomer #68C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C4040.5Semi standard non polar33892256
Glucodistylin,4TMS,isomer #69C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C4026.4Semi standard non polar33892256
Glucodistylin,4TMS,isomer #7C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O4036.8Semi standard non polar33892256
Glucodistylin,4TMS,isomer #70C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1O4009.4Semi standard non polar33892256
Glucodistylin,4TMS,isomer #8C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O4013.1Semi standard non polar33892256
Glucodistylin,4TMS,isomer #9C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C4040.7Semi standard non polar33892256
Glucodistylin,5TMS,isomer #1C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C)C=C3O[Si](C)(C)C)OC2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O3953.2Semi standard non polar33892256
Glucodistylin,5TMS,isomer #10C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3962.2Semi standard non polar33892256
Glucodistylin,5TMS,isomer #11C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O3949.9Semi standard non polar33892256
Glucodistylin,5TMS,isomer #12C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O3940.1Semi standard non polar33892256
Glucodistylin,5TMS,isomer #13C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C3959.6Semi standard non polar33892256
Glucodistylin,5TMS,isomer #14C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3915.6Semi standard non polar33892256
Glucodistylin,5TMS,isomer #15C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3940.9Semi standard non polar33892256
Glucodistylin,5TMS,isomer #16C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3942.0Semi standard non polar33892256
Glucodistylin,5TMS,isomer #17C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3896.5Semi standard non polar33892256
Glucodistylin,5TMS,isomer #18C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3925.4Semi standard non polar33892256
Glucodistylin,5TMS,isomer #19C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3924.7Semi standard non polar33892256
Glucodistylin,5TMS,isomer #2C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C)C=C3O[Si](C)(C)C)OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O3914.2Semi standard non polar33892256
Glucodistylin,5TMS,isomer #20C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4014.0Semi standard non polar33892256
Glucodistylin,5TMS,isomer #21C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O3923.3Semi standard non polar33892256
Glucodistylin,5TMS,isomer #22C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O3916.7Semi standard non polar33892256
Glucodistylin,5TMS,isomer #23C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C3930.6Semi standard non polar33892256
Glucodistylin,5TMS,isomer #24C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3884.6Semi standard non polar33892256
Glucodistylin,5TMS,isomer #25C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3910.5Semi standard non polar33892256
Glucodistylin,5TMS,isomer #26C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3904.0Semi standard non polar33892256
Glucodistylin,5TMS,isomer #27C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3866.7Semi standard non polar33892256
Glucodistylin,5TMS,isomer #28C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3894.3Semi standard non polar33892256
Glucodistylin,5TMS,isomer #29C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3885.7Semi standard non polar33892256
Glucodistylin,5TMS,isomer #3C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C)C=C3O[Si](C)(C)C)OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O3926.9Semi standard non polar33892256
Glucodistylin,5TMS,isomer #30C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3965.5Semi standard non polar33892256
Glucodistylin,5TMS,isomer #31C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3925.6Semi standard non polar33892256
Glucodistylin,5TMS,isomer #32C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3950.1Semi standard non polar33892256
Glucodistylin,5TMS,isomer #33C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3951.6Semi standard non polar33892256
Glucodistylin,5TMS,isomer #34C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3935.2Semi standard non polar33892256
Glucodistylin,5TMS,isomer #35C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3923.5Semi standard non polar33892256
Glucodistylin,5TMS,isomer #36C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C13974.3Semi standard non polar33892256
Glucodistylin,5TMS,isomer #37C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)O2)C(O[Si](C)(C)C)=C13936.4Semi standard non polar33892256
Glucodistylin,5TMS,isomer #38C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)O2)C(O[Si](C)(C)C)=C13922.2Semi standard non polar33892256
Glucodistylin,5TMS,isomer #39C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)O2)C(O[Si](C)(C)C)=C13946.6Semi standard non polar33892256
Glucodistylin,5TMS,isomer #4C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C)C=C3O[Si](C)(C)C)OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C3923.7Semi standard non polar33892256
Glucodistylin,5TMS,isomer #40C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)O2)C(O[Si](C)(C)C)=C13931.5Semi standard non polar33892256
Glucodistylin,5TMS,isomer #41C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)O2)C(O[Si](C)(C)C)=C13998.5Semi standard non polar33892256
Glucodistylin,5TMS,isomer #42C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)O2)C(O[Si](C)(C)C)=C13919.0Semi standard non polar33892256
Glucodistylin,5TMS,isomer #43C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)O2)C(O[Si](C)(C)C)=C13904.0Semi standard non polar33892256
Glucodistylin,5TMS,isomer #44C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)O2)C(O[Si](C)(C)C)=C13975.1Semi standard non polar33892256
Glucodistylin,5TMS,isomer #45C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)O2)C(O[Si](C)(C)C)=C13978.1Semi standard non polar33892256
Glucodistylin,5TMS,isomer #46C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13943.6Semi standard non polar33892256
Glucodistylin,5TMS,isomer #47C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13962.4Semi standard non polar33892256
Glucodistylin,5TMS,isomer #48C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13931.3Semi standard non polar33892256
Glucodistylin,5TMS,isomer #49C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC2=C13899.2Semi standard non polar33892256
Glucodistylin,5TMS,isomer #5C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O3900.5Semi standard non polar33892256
Glucodistylin,5TMS,isomer #50C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC2=C13883.3Semi standard non polar33892256
Glucodistylin,5TMS,isomer #51C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1O3934.9Semi standard non polar33892256
Glucodistylin,5TMS,isomer #52C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1O3919.9Semi standard non polar33892256
Glucodistylin,5TMS,isomer #53C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C=C1O[Si](C)(C)C3974.8Semi standard non polar33892256
Glucodistylin,5TMS,isomer #54C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3981.5Semi standard non polar33892256
Glucodistylin,5TMS,isomer #55C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(=O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3958.6Semi standard non polar33892256
Glucodistylin,5TMS,isomer #56C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3950.9Semi standard non polar33892256
Glucodistylin,5TMS,isomer #6C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O3910.4Semi standard non polar33892256
Glucodistylin,5TMS,isomer #7C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C3909.7Semi standard non polar33892256
Glucodistylin,5TMS,isomer #8C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3937.4Semi standard non polar33892256
Glucodistylin,5TMS,isomer #9C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3975.6Semi standard non polar33892256
Glucodistylin,6TMS,isomer #1C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C)C=C3O[Si](C)(C)C)OC2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O3881.7Semi standard non polar33892256
Glucodistylin,6TMS,isomer #10C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3900.2Semi standard non polar33892256
Glucodistylin,6TMS,isomer #11C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3873.8Semi standard non polar33892256
Glucodistylin,6TMS,isomer #12C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3896.0Semi standard non polar33892256
Glucodistylin,6TMS,isomer #13C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3890.3Semi standard non polar33892256
Glucodistylin,6TMS,isomer #14C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3864.4Semi standard non polar33892256
Glucodistylin,6TMS,isomer #15C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3846.4Semi standard non polar33892256
Glucodistylin,6TMS,isomer #16C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3835.5Semi standard non polar33892256
Glucodistylin,6TMS,isomer #17C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3851.7Semi standard non polar33892256
Glucodistylin,6TMS,isomer #18C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3853.2Semi standard non polar33892256
Glucodistylin,6TMS,isomer #19C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3830.4Semi standard non polar33892256
Glucodistylin,6TMS,isomer #2C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C)C=C3O[Si](C)(C)C)OC2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O3881.5Semi standard non polar33892256
Glucodistylin,6TMS,isomer #20C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3814.8Semi standard non polar33892256
Glucodistylin,6TMS,isomer #21C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3877.2Semi standard non polar33892256
Glucodistylin,6TMS,isomer #22C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)O2)C(O[Si](C)(C)C)=C13828.7Semi standard non polar33892256
Glucodistylin,6TMS,isomer #23C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)O2)C(O[Si](C)(C)C)=C13814.8Semi standard non polar33892256
Glucodistylin,6TMS,isomer #24C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)O2)C(O[Si](C)(C)C)=C13880.2Semi standard non polar33892256
Glucodistylin,6TMS,isomer #25C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)O2)C(O[Si](C)(C)C)=C13897.2Semi standard non polar33892256
Glucodistylin,6TMS,isomer #26C[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)O2)C(O[Si](C)(C)C)=C13864.9Semi standard non polar33892256
Glucodistylin,6TMS,isomer #27C[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13843.2Semi standard non polar33892256
Glucodistylin,6TMS,isomer #28C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3889.2Semi standard non polar33892256
Glucodistylin,6TMS,isomer #3C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C)C=C3O[Si](C)(C)C)OC2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C3888.2Semi standard non polar33892256
Glucodistylin,6TMS,isomer #4C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C)C=C3O[Si](C)(C)C)OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3830.5Semi standard non polar33892256
Glucodistylin,6TMS,isomer #5C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C)C=C3O[Si](C)(C)C)OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3843.6Semi standard non polar33892256
Glucodistylin,6TMS,isomer #6C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C)C=C3O[Si](C)(C)C)OC2C2=CC=C(O[Si](C)(C)C)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3853.4Semi standard non polar33892256
Glucodistylin,6TMS,isomer #7C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3816.2Semi standard non polar33892256
Glucodistylin,6TMS,isomer #8C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3830.3Semi standard non polar33892256
Glucodistylin,6TMS,isomer #9C[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C)C=C3O[Si](C)(C)C)OC2C2=CC=C(O)C(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3840.2Semi standard non polar33892256
Glucodistylin,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O)C(O)C1O4652.1Semi standard non polar33892256
Glucodistylin,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O)C3O)C(C3=CC=C(O)C(O)=C3)OC2=C14656.7Semi standard non polar33892256
Glucodistylin,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(OC1OC(CO)C(O)C(O)C1O)C(C1=CC=C(O)C(O)=C1)O24681.6Semi standard non polar33892256
Glucodistylin,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O)C(O)C2O)=CC=C1O4662.9Semi standard non polar33892256
Glucodistylin,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O)C(O)C2O)C=C1O4678.4Semi standard non polar33892256
Glucodistylin,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC1C(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)OC(CO)C(O)C1O4673.8Semi standard non polar33892256
Glucodistylin,1TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C1O4674.2Semi standard non polar33892256
Glucodistylin,1TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O)C1O4677.5Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C(C)(C)C)OC2C2=CC=C(O)C(O)=C2)C(O)C(O)C1O4798.9Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O)C3O)C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14740.3Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)C(C3=CC=C(O)C(O)=C3)OC2=C14745.2Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)C(C3=CC=C(O)C(O)=C3)OC2=C14735.3Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=C14733.1Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(OC1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C1O)C(C1=CC=C(O)C(O)=C1)O24800.0Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(OC1OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C1O)C(C1=CC=C(O)C(O)=C1)O24803.6Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #16CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(OC1OC(CO)C(O)C(O)C1O[Si](C)(C)C(C)(C)C)C(C1=CC=C(O)C(O)=C1)O24795.7Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C2OC2OC(CO)C(O)C(O)C2O)C=C1O4817.1Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C2OC2OC(CO)C(O)C(O)C2O)=CC=C1O4796.3Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)=CC=C1O4713.0Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C3OC2C2=CC=C(O)C(O)=C2)C(O)C(O)C1O4740.3Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #20CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)=CC=C1O4716.5Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #21CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)=CC=C1O4707.5Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #22CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O)C(O)C2O)C=C1O[Si](C)(C)C(C)(C)C4755.5Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C=C1O4730.4Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #24CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C=C1O4735.1Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C=C1O4726.9Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #26CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C(C)(C)C)C1O4743.8Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC1C(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C4742.2Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O)C1O[Si](C)(C)C(C)(C)C4741.5Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C2)C(O)C(O)C1O4744.8Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C2)C(O)C(O)C1O4728.5Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4737.5Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4749.2Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4732.8Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O)C(O)C3O)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C(C)(C)C)=C14797.3Semi standard non polar33892256
Glucodistylin,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O)C3O)C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC2=C14760.0Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O[Si](C)(C)C(C)(C)C)C=C3O[Si](C)(C)C(C)(C)C)OC2C2=CC=C(O)C(O)=C2)C(O)C(O)C1O4857.7Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C3OC2C2=CC=C(O)C(O)=C2)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4799.3Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C3OC2C2=CC=C(O)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4796.2Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C2)C(O)C(O)C1O4807.3Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C2)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4772.3Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C2)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4798.8Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #15CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4773.4Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #16CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C2)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4752.7Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C2)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4777.4Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #18CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4754.0Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #19CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O4767.5Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C(C)(C)C)OC2C2=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C2)C(O)C(O)C1O4866.3Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #20CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C4782.8Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #21CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4781.0Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #22CC(C)(C)[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C(C)(C)C)=C14869.0Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C(C)(C)C)=C14851.7Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #24CC(C)(C)[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C(C)(C)C)=C14858.0Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O)C(O)C3O)C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)O2)C(O[Si](C)(C)C(C)(C)C)=C14915.2Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #26CC(C)(C)[Si](C)(C)OC1=CC2=C(C(=O)C(OC3OC(CO)C(O)C(O)C3O)C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)O2)C(O[Si](C)(C)C(C)(C)C)=C14889.2Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O)C3O)C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14854.9Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC2=C14838.0Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #29CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC2=C14844.7Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C(C)(C)C)OC2C2=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C2)C(O)C(O)C1O4844.4Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #30CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC2=C14814.1Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #31CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14816.3Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #32CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14818.9Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #33CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14791.2Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #34CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)C(C3=CC=C(O)C(O)=C3)OC2=C14785.8Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #35CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=C14795.9Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #36CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=C14783.0Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #37CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(OC1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O)C(C1=CC=C(O)C(O)=C1)O24830.7Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #38CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(OC1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C)C(C1=CC=C(O)C(O)=C1)O24837.3Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #39CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C=C1O4858.9Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C(C)(C)C)OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4826.0Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #40CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)=CC=C1O4839.4Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #41CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(OC1OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C)C(C1=CC=C(O)C(O)=C1)O24826.2Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #42CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C=C1O4852.1Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #43CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)=CC=C1O4828.3Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #44CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C=C1O4849.4Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #45CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)=CC=C1O4832.2Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #46CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C2OC2OC(CO)C(O)C(O)C2O)C=C1O[Si](C)(C)C(C)(C)C4912.9Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #47CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)=CC=C1O4754.8Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #48CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)=CC=C1O4756.6Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #49CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C=C1O[Si](C)(C)C(C)(C)C4806.5Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C(C)(C)C)OC2C2=CC=C(O)C(O)=C2)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4843.3Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #50CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)=CC=C1O4754.8Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #51CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C=C1O[Si](C)(C)C(C)(C)C4794.5Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #52CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C4796.1Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #53CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C=C1O4776.0Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #54CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C=C1O4779.0Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #55CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC(O)=C3C(=O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=C1O4776.8Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #56CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2C(=O)C3=C(O)C=C(O)C=C3OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4758.9Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(C=C(O)C=C3O[Si](C)(C)C(C)(C)C)OC2C2=CC=C(O)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4832.0Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C3OC2C2=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C2)C(O)C(O)C1O4837.2Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C3OC2C2=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C2)C(O)C(O)C1O4812.9Semi standard non polar33892256
Glucodistylin,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)OCC1OC(OC2C(=O)C3=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C3OC2C2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4796.8Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Glucodistylin GC-MS (Non-derivatized) - 70eV, Positivesplash10-0f7k-8902800000-5dbc23e1e6dd86574f1a2017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Glucodistylin GC-MS (3 TMS) - 70eV, Positivesplash10-014i-3620009000-14d69eadcad468e95fc22017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Glucodistylin GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glucodistylin 10V, Positive-QTOFsplash10-000i-0900000000-8079a05e43e9bd02a1d92015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glucodistylin 20V, Positive-QTOFsplash10-000i-4900000000-05a61cd09db39cf83d9e2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glucodistylin 40V, Positive-QTOFsplash10-052f-9100000000-86f0930544216341fffc2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glucodistylin 10V, Negative-QTOFsplash10-001i-0900000000-070d391ddaf16d6063332015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glucodistylin 20V, Negative-QTOFsplash10-001i-0900000000-071c96e42609ae2546612015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glucodistylin 40V, Negative-QTOFsplash10-00lr-6900000000-3b868142f127b511f3bd2015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glucodistylin 10V, Positive-QTOFsplash10-014i-0000900000-2ed003ec55664a72da2b2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glucodistylin 20V, Positive-QTOFsplash10-0uxs-0900400000-9c461fad1387597afd0d2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glucodistylin 40V, Positive-QTOFsplash10-0udi-0902000000-08bbf3b7d252acc550a52021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glucodistylin 10V, Negative-QTOFsplash10-014i-0000900000-5a3dbce4f08b722998352021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glucodistylin 20V, Negative-QTOFsplash10-0gb9-0900800000-cf782a8004ba5046a8352021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Glucodistylin 40V, Negative-QTOFsplash10-03di-0409000000-5b23a28375314f1fb6ad2021-09-25Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Cytoplasm
  • Extracellular
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB021739
KNApSAcK IDC00008699
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound14187088
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1894201
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Neveu V, Perez-Jimenez J, Vos F, Crespy V, du Chaffaut L, Mennen L, Knox C, Eisner R, Cruz J, Wishart D, Scalbert A: Phenol-Explorer: an online comprehensive database on polyphenol contents in foods. Database (Oxford). 2010;2010:bap024. doi: 10.1093/database/bap024. Epub 2010 Jan 8. [PubMed:20428313 ]
  2. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .