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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-01 03:00:02 UTC

Update Date

2021-09-26 22:48:59 UTC

HMDB ID

HMDB0242526

Secondary Accession Numbers

None

Metabolite Identification

Common Name

(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

Description

2-{3-hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol belongs to the class of organic compounds known as stilbene glycosides. Stilbene glycosides are compounds structurally characterized by the presence of a carbohydrate moiety glycosidically linked to the stilbene skeleton. Based on a literature review very few articles have been published on 2-{3-hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol. This compound has been identified in human blood as reported by (PMID: 31557052 ). (2s,3r,4s,5s,6r)-2-[3-hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically (2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

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


  Mrv1533004171515222D          

 30 32  0  0  0  0            999 V2000
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 O   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
    0.7145   -3.7125    0.0000 O   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
    2.1434   -2.8875    0.0000 O   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
    3.5724   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  7  6  1  4  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 16 25  1  0  0  0  0
 25 26  1  0  0  0  0
 14 27  2  0  0  0  0
  9 27  1  0  0  0  0
  6 28  1  0  0  0  0
 28 29  2  0  0  0  0
  3 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END

HMDB0257194
     RDKit          3D
Rhapontin
 54 56  0  0  0  0  0  0  0  0999 V2000
    9.9364    0.3868   -0.6402 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8049    1.1265   -1.0140 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5161    0.6906   -0.6709 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3316   -0.4729    0.0406 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0435   -0.8788    0.3656 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9240   -0.1593    0.0032 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6034   -0.6408    0.3758 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4870   -0.0196    0.0723 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1846   -0.5391    0.4666 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0029   -1.6960    1.1739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2837   -2.1378    1.5205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4037   -3.3283    2.2441 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4162   -1.4395    1.1716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2464   -0.2725    0.4590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2986    0.4893    0.0670 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6447    0.3460    0.2377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2705    0.2138   -1.0163 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5653   -0.2705   -0.8855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1991   -0.2221   -2.2623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5105   -0.6916   -2.2365 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4163    0.5237    0.0462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4944   -0.3063    0.4324 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7314    0.9565    1.3011 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6012   -0.1827    2.1246 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3425    1.4758    0.9459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5316    2.5827    0.1239 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0168    0.1588    0.1203 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1288    1.0008   -0.7074 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4189    1.4264   -1.0445 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6292    2.5966   -1.7616 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.8708    0.0668    0.4056 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.8298    1.0616   -0.7378 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1452   -0.4624   -1.3472 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1782   -1.0710    0.3471 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9658   -1.8160    0.9343 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6002   -1.5796    0.9407 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5726    0.9081   -0.4911 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8673   -2.2903    1.4770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3991   -3.2983    3.2501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3930   -1.8158    1.4593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8652   -0.5782    0.8074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5223   -1.3296   -0.5440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1403    0.8382   -2.5998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5684   -0.8101   -2.9468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4957   -1.6839   -2.2903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8462    1.4414   -0.4447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0730    0.1475    1.0991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3433    1.7334    1.7927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7164   -1.0202    1.6039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8676    1.7889    1.8729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2791    3.1434    0.4247 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1775    1.0819   -0.4451 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3362    1.6280   -1.0349 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8943    3.1992   -2.0779 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  3
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 11 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 18 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 14 27  2  0
  6 28  1  0
 28 29  2  0
 29 30  1  0
 29  3  1  0
 27  9  1  0
 25 16  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  4 34  1  0
  5 35  1  0
  7 36  1  0
  8 37  1  0
 10 38  1  0
 12 39  1  0
 13 40  1  0
 16 41  1  0
 18 42  1  0
 19 43  1  0
 19 44  1  0
 20 45  1  0
 21 46  1  0
 22 47  1  0
 23 48  1  0
 24 49  1  0
 25 50  1  0
 26 51  1  0
 27 52  1  0
 28 53  1  0
 30 54  1  0
M  END


  Mrv1533004171515222D          

 30 32  0  0  0  0            999 V2000
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 O   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
    0.7145   -3.7125    0.0000 O   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
    2.1434   -2.8875    0.0000 O   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
    3.5724   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  7  6  1  4  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 16 25  1  0  0  0  0
 25 26  1  0  0  0  0
 14 27  2  0  0  0  0
  9 27  1  0  0  0  0
  6 28  1  0  0  0  0
 28 29  2  0  0  0  0
  3 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0242526

> <DATABASE_NAME>
hmdb

> <SMILES>
COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O)C3O)=C2)C=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C21H24O9/c1-28-16-5-4-11(8-15(16)24)2-3-12-6-13(23)9-14(7-12)29-21-20(27)19(26)18(25)17(10-22)30-21/h2-9,17-27H,10H2,1H3

> <INCHI_KEY>
GKAJCVFOJGXVIA-UHFFFAOYSA-N

> <FORMULA>
C21H24O9

> <MOLECULAR_WEIGHT>
420.414

> <EXACT_MASS>
420.142032353

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
42.61132213676318

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-{3-hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <ALOGPS_LOGP>
0.70

> <JCHEM_LOGP>
0.9766515273333334

> <ALOGPS_LOGS>
-2.86

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.95643046969659

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.21091603590187

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981092343730565

> <JCHEM_POLAR_SURFACE_AREA>
149.07

> <JCHEM_REFRACTIVITY>
106.06310000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.85e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
rhaponticin

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0257194
     RDKit          3D
Rhapontin
 54 56  0  0  0  0  0  0  0  0999 V2000
    9.9364    0.3868   -0.6402 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8049    1.1265   -1.0140 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5161    0.6906   -0.6709 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3316   -0.4729    0.0406 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0435   -0.8788    0.3656 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9240   -0.1593    0.0032 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6034   -0.6408    0.3758 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4870   -0.0196    0.0723 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1846   -0.5391    0.4666 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0029   -1.6960    1.1739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2837   -2.1378    1.5205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4037   -3.3283    2.2441 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4162   -1.4395    1.1716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2464   -0.2725    0.4590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2986    0.4893    0.0670 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6447    0.3460    0.2377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2705    0.2138   -1.0163 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5653   -0.2705   -0.8855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1991   -0.2221   -2.2623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5105   -0.6916   -2.2365 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4163    0.5237    0.0462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4944   -0.3063    0.4324 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7314    0.9565    1.3011 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6012   -0.1827    2.1246 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3425    1.4758    0.9459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5316    2.5827    0.1239 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0168    0.1588    0.1203 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1288    1.0008   -0.7074 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4189    1.4264   -1.0445 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6292    2.5966   -1.7616 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.8708    0.0668    0.4056 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.8298    1.0616   -0.7378 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1452   -0.4624   -1.3472 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1782   -1.0710    0.3471 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9658   -1.8160    0.9343 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6002   -1.5796    0.9407 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5726    0.9081   -0.4911 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8673   -2.2903    1.4770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3991   -3.2983    3.2501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3930   -1.8158    1.4593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8652   -0.5782    0.8074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5223   -1.3296   -0.5440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1403    0.8382   -2.5998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5684   -0.8101   -2.9468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4957   -1.6839   -2.2903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8462    1.4414   -0.4447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0730    0.1475    1.0991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3433    1.7334    1.7927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7164   -1.0202    1.6039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8676    1.7889    1.8729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2791    3.1434    0.4247 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1775    1.0819   -0.4451 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3362    1.6280   -1.0349 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8943    3.1992   -2.0779 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  3
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 11 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 18 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 14 27  2  0
  6 28  1  0
 28 29  2  0
 29 30  1  0
 29  3  1  0
 27  9  1  0
 25 16  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  4 34  1  0
  5 35  1  0
  7 36  1  0
  8 37  1  0
 10 38  1  0
 12 39  1  0
 13 40  1  0
 16 41  1  0
 18 42  1  0
 19 43  1  0
 19 44  1  0
 20 45  1  0
 21 46  1  0
 22 47  1  0
 23 48  1  0
 24 49  1  0
 25 50  1  0
 26 51  1  0
 27 52  1  0
 28 53  1  0
 30 54  1  0
M  END

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      10.669   1.540   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      10.669   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.003  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.003  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.669  -7.700   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.669  -9.240   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      12.003 -10.010   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       9.336 -10.010   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       6.668 -10.010   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       4.001 -10.010   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.334 -11.550   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.334  -6.930   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       6.668  -6.930   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       8.002   0.000   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   29                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   28                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   27                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   27                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   25                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   16   26                                                  
CONECT   26   25                                                            
CONECT   27   14    9                                                       
CONECT   28    6   29                                                       
CONECT   29   28    3   30                                                  
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

COMPND    HMDB0257194
HETATM    1  C1  UNL     1       9.936   0.387  -0.640  1.00  0.00           C  
HETATM    2  O1  UNL     1       8.805   1.126  -1.014  1.00  0.00           O  
HETATM    3  C2  UNL     1       7.516   0.691  -0.671  1.00  0.00           C  
HETATM    4  C3  UNL     1       7.332  -0.473   0.041  1.00  0.00           C  
HETATM    5  C4  UNL     1       6.044  -0.879   0.366  1.00  0.00           C  
HETATM    6  C5  UNL     1       4.924  -0.159   0.003  1.00  0.00           C  
HETATM    7  C6  UNL     1       3.603  -0.641   0.376  1.00  0.00           C  
HETATM    8  C7  UNL     1       2.487  -0.020   0.072  1.00  0.00           C  
HETATM    9  C8  UNL     1       1.185  -0.539   0.467  1.00  0.00           C  
HETATM   10  C9  UNL     1       1.003  -1.696   1.174  1.00  0.00           C  
HETATM   11  C10 UNL     1      -0.284  -2.138   1.520  1.00  0.00           C  
HETATM   12  O2  UNL     1      -0.404  -3.328   2.244  1.00  0.00           O  
HETATM   13  C11 UNL     1      -1.416  -1.439   1.172  1.00  0.00           C  
HETATM   14  C12 UNL     1      -1.246  -0.273   0.459  1.00  0.00           C  
HETATM   15  O3  UNL     1      -2.299   0.489   0.067  1.00  0.00           O  
HETATM   16  C13 UNL     1      -3.645   0.346   0.238  1.00  0.00           C  
HETATM   17  O4  UNL     1      -4.271   0.214  -1.016  1.00  0.00           O  
HETATM   18  C14 UNL     1      -5.565  -0.271  -0.886  1.00  0.00           C  
HETATM   19  C15 UNL     1      -6.199  -0.222  -2.262  1.00  0.00           C  
HETATM   20  O5  UNL     1      -7.510  -0.692  -2.236  1.00  0.00           O  
HETATM   21  C16 UNL     1      -6.416   0.524   0.046  1.00  0.00           C  
HETATM   22  O6  UNL     1      -7.494  -0.306   0.432  1.00  0.00           O  
HETATM   23  C17 UNL     1      -5.731   0.956   1.301  1.00  0.00           C  
HETATM   24  O7  UNL     1      -5.601  -0.183   2.125  1.00  0.00           O  
HETATM   25  C18 UNL     1      -4.342   1.476   0.946  1.00  0.00           C  
HETATM   26  O8  UNL     1      -4.532   2.583   0.124  1.00  0.00           O  
HETATM   27  C19 UNL     1       0.017   0.159   0.120  1.00  0.00           C  
HETATM   28  C20 UNL     1       5.129   1.001  -0.707  1.00  0.00           C  
HETATM   29  C21 UNL     1       6.419   1.426  -1.045  1.00  0.00           C  
HETATM   30  O9  UNL     1       6.629   2.597  -1.762  1.00  0.00           O  
HETATM   31  H1  UNL     1       9.871   0.067   0.406  1.00  0.00           H  
HETATM   32  H2  UNL     1      10.830   1.062  -0.738  1.00  0.00           H  
HETATM   33  H3  UNL     1      10.145  -0.462  -1.347  1.00  0.00           H  
HETATM   34  H4  UNL     1       8.178  -1.071   0.347  1.00  0.00           H  
HETATM   35  H5  UNL     1       5.966  -1.816   0.934  1.00  0.00           H  
HETATM   36  H6  UNL     1       3.600  -1.580   0.941  1.00  0.00           H  
HETATM   37  H7  UNL     1       2.573   0.908  -0.491  1.00  0.00           H  
HETATM   38  H8  UNL     1       1.867  -2.290   1.477  1.00  0.00           H  
HETATM   39  H9  UNL     1      -0.399  -3.298   3.250  1.00  0.00           H  
HETATM   40  H10 UNL     1      -2.393  -1.816   1.459  1.00  0.00           H  
HETATM   41  H11 UNL     1      -3.865  -0.578   0.807  1.00  0.00           H  
HETATM   42  H12 UNL     1      -5.522  -1.330  -0.544  1.00  0.00           H  
HETATM   43  H13 UNL     1      -6.140   0.838  -2.600  1.00  0.00           H  
HETATM   44  H14 UNL     1      -5.568  -0.810  -2.947  1.00  0.00           H  
HETATM   45  H15 UNL     1      -7.496  -1.684  -2.290  1.00  0.00           H  
HETATM   46  H16 UNL     1      -6.846   1.441  -0.445  1.00  0.00           H  
HETATM   47  H17 UNL     1      -8.073   0.147   1.099  1.00  0.00           H  
HETATM   48  H18 UNL     1      -6.343   1.733   1.793  1.00  0.00           H  
HETATM   49  H19 UNL     1      -5.716  -1.020   1.604  1.00  0.00           H  
HETATM   50  H20 UNL     1      -3.868   1.789   1.873  1.00  0.00           H  
HETATM   51  H21 UNL     1      -5.279   3.143   0.425  1.00  0.00           H  
HETATM   52  H22 UNL     1       0.177   1.082  -0.445  1.00  0.00           H  
HETATM   53  H23 UNL     1       4.336   1.628  -1.035  1.00  0.00           H  
HETATM   54  H24 UNL     1       5.894   3.199  -2.078  1.00  0.00           H  
CONECT    1    2   31   32   33
CONECT    2    3
CONECT    3    4    4   29
CONECT    4    5   34
CONECT    5    6    6   35
CONECT    6    7   28
CONECT    7    8    8   36
CONECT    8    9   37
CONECT    9   10   10   27
CONECT   10   11   38
CONECT   11   12   13   13
CONECT   12   39
CONECT   13   14   40
CONECT   14   15   27   27
CONECT   15   16
CONECT   16   17   25   41
CONECT   17   18
CONECT   18   19   21   42
CONECT   19   20   43   44
CONECT   20   45
CONECT   21   22   23   46
CONECT   22   47
CONECT   23   24   25   48
CONECT   24   49
CONECT   25   26   50
CONECT   26   51
CONECT   27   52
CONECT   28   29   29   53
CONECT   29   30
CONECT   30   54
END

HMDB0257194
     RDKit          3D
Rhapontin
 54 56  0  0  0  0  0  0  0  0999 V2000
    9.9364    0.3868   -0.6402 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8049    1.1265   -1.0140 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5161    0.6906   -0.6709 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3316   -0.4729    0.0406 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0435   -0.8788    0.3656 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9240   -0.1593    0.0032 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6034   -0.6408    0.3758 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4870   -0.0196    0.0723 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1846   -0.5391    0.4666 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0029   -1.6960    1.1739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2837   -2.1378    1.5205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4037   -3.3283    2.2441 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4162   -1.4395    1.1716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2464   -0.2725    0.4590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2986    0.4893    0.0670 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6447    0.3460    0.2377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2705    0.2138   -1.0163 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5653   -0.2705   -0.8855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1991   -0.2221   -2.2623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5105   -0.6916   -2.2365 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4163    0.5237    0.0462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4944   -0.3063    0.4324 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7314    0.9565    1.3011 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6012   -0.1827    2.1246 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3425    1.4758    0.9459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5316    2.5827    0.1239 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0168    0.1588    0.1203 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1288    1.0008   -0.7074 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4189    1.4264   -1.0445 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6292    2.5966   -1.7616 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.8708    0.0668    0.4056 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.8298    1.0616   -0.7378 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1452   -0.4624   -1.3472 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1782   -1.0710    0.3471 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9658   -1.8160    0.9343 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6002   -1.5796    0.9407 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5726    0.9081   -0.4911 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8673   -2.2903    1.4770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3991   -3.2983    3.2501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3930   -1.8158    1.4593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8652   -0.5782    0.8074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5223   -1.3296   -0.5440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1403    0.8382   -2.5998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5684   -0.8101   -2.9468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4957   -1.6839   -2.2903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8462    1.4414   -0.4447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0730    0.1475    1.0991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3433    1.7334    1.7927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7164   -1.0202    1.6039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8676    1.7889    1.8729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2791    3.1434    0.4247 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1775    1.0819   -0.4451 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3362    1.6280   -1.0349 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8943    3.1992   -2.0779 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  3
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 11 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 18 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 14 27  2  0
  6 28  1  0
 28 29  2  0
 29 30  1  0
 29  3  1  0
 27  9  1  0
 25 16  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  4 34  1  0
  5 35  1  0
  7 36  1  0
  8 37  1  0
 10 38  1  0
 12 39  1  0
 13 40  1  0
 16 41  1  0
 18 42  1  0
 19 43  1  0
 19 44  1  0
 20 45  1  0
 21 46  1  0
 22 47  1  0
 23 48  1  0
 24 49  1  0
 25 50  1  0
 26 51  1  0
 27 52  1  0
 28 53  1  0
 30 54  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₁H₂₄O₉

Average Molecular Weight

420.414

Monoisotopic Molecular Weight

420.142032353

IUPAC Name

2-{3-hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol

Traditional Name

rhaponticin

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O)C3O)=C2)C=C1O

InChI Identifier

InChI=1S/C21H24O9/c1-28-16-5-4-11(8-15(16)24)2-3-12-6-13(23)9-14(7-12)29-21-20(27)19(26)18(25)17(10-22)30-21/h2-9,17-27H,10H2,1H3

InChI Key

GKAJCVFOJGXVIA-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as stilbene glycosides. Stilbene glycosides are compounds structurally characterized by the presence of a carbohydrate moiety glycosidically linked to the stilbene skeleton.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Stilbenes

Sub Class

Stilbene glycosides

Direct Parent

Stilbene glycosides

Alternative Parents

Substituents

Stilbene glycoside
Phenolic glycoside
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Methoxyphenol
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
Styrene
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Oxane
Monosaccharide
Monocyclic benzene moiety
Benzenoid
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Acetal
Ether
Polyol
Alcohol
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Primary alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	0.7	ALOGPS
logP	0.98	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	9.21	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	149.07 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	106.06 m³·mol⁻¹	ChemAxon
Polarizability	42.61 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	193.453	30932474
DeepCCS	[M-H]-	191.095	30932474
DeepCCS	[M-2H]-	225.143	30932474
DeepCCS	[M+Na]+	200.724	30932474
AllCCS	[M+H]+	200.2	32859911
AllCCS	[M+H-H2O]+	197.8	32859911
AllCCS	[M+NH4]+	202.3	32859911
AllCCS	[M+Na]+	202.9	32859911
AllCCS	[M-H]-	193.6	32859911
AllCCS	[M+Na-2H]-	194.0	32859911
AllCCS	[M+HCOO]-	194.7	32859911

Predicted Kovats Retention Indices

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O	4029.9	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O	3677.3	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O	5961.4	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TMS,isomer #2	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O)=C2)C=C1O	4014.2	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TMS,isomer #2	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O)=C2)C=C1O	3698.4	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TMS,isomer #2	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O)=C2)C=C1O	6104.1	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TMS,isomer #3	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2)C=C1O	3969.0	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TMS,isomer #3	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2)C=C1O	3594.9	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TMS,isomer #3	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2)C=C1O	5957.0	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TMS,isomer #4	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2)C=C1O	3958.4	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TMS,isomer #4	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2)C=C1O	3610.0	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TMS,isomer #4	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2)C=C1O	5964.9	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TMS,isomer #5	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2)C=C1O	3981.1	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TMS,isomer #5	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2)C=C1O	3624.0	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TMS,isomer #5	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2)C=C1O	5975.6	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TMS,isomer #6	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O)C3O)=C2)C=C1O[Si](C)(C)C	4021.0	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TMS,isomer #6	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O)C3O)=C2)C=C1O[Si](C)(C)C	3665.0	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TMS,isomer #6	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O)C3O)=C2)C=C1O[Si](C)(C)C	5958.1	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O	3928.7	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O	3794.1	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O	5365.6	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #10	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2)C=C1O	3868.0	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #10	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2)C=C1O	3628.8	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #10	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2)C=C1O	5223.6	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #11	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2)C=C1O	3877.5	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #11	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2)C=C1O	3650.3	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #11	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2)C=C1O	5260.4	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #12	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2)C=C1O[Si](C)(C)C	3903.7	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #12	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2)C=C1O[Si](C)(C)C	3685.8	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #12	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2)C=C1O[Si](C)(C)C	5264.0	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #13	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1O	3891.8	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #13	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1O	3653.4	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #13	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1O	5267.2	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #14	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2)C=C1O[Si](C)(C)C	3883.4	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #14	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2)C=C1O[Si](C)(C)C	3704.8	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #14	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2)C=C1O[Si](C)(C)C	5288.9	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #15	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3917.3	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #15	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3712.4	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #15	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	5283.8	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #2	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O	3895.5	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #2	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O	3698.1	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #2	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O	5259.5	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #3	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O	3911.1	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #3	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O	3715.5	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #3	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O	5285.1	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #4	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O	3899.4	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #4	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O	3721.4	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #4	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O	5280.4	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #5	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3930.4	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #5	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3770.4	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #5	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	5286.8	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #6	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O)=C2)C=C1O	3909.6	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #6	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O)=C2)C=C1O	3712.0	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #6	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O)=C2)C=C1O	5355.1	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #7	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O)=C2)C=C1O	3903.3	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #7	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O)=C2)C=C1O	3731.8	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #7	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O)=C2)C=C1O	5375.7	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #8	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O[Si](C)(C)C)=C2)C=C1O	3921.2	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #8	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O[Si](C)(C)C)=C2)C=C1O	3734.0	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #8	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O[Si](C)(C)C)=C2)C=C1O	5371.0	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #9	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O)=C2)C=C1O[Si](C)(C)C	3932.0	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #9	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O)=C2)C=C1O[Si](C)(C)C	3777.9	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TMS,isomer #9	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O)=C2)C=C1O[Si](C)(C)C	5370.7	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O	3842.0	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O	3784.4	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O	4870.0	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #10	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3845.2	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #10	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3783.5	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #10	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	4867.5	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #11	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2)C=C1O	3830.0	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #11	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2)C=C1O	3704.7	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #11	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2)C=C1O	4811.1	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #12	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2)C=C1O	3862.2	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #12	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2)C=C1O	3738.5	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #12	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2)C=C1O	4855.1	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #13	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O)=C2)C=C1O[Si](C)(C)C	3843.4	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #13	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O)=C2)C=C1O[Si](C)(C)C	3773.7	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #13	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O)=C2)C=C1O[Si](C)(C)C	4884.5	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #14	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1O	3837.7	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #14	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1O	3717.2	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #14	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1O	4846.6	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #15	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O)=C2)C=C1O[Si](C)(C)C	3822.3	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #15	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O)=C2)C=C1O[Si](C)(C)C	3793.0	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #15	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O)=C2)C=C1O[Si](C)(C)C	4917.6	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #16	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3858.2	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #16	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3797.6	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #16	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	4901.8	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #17	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1O	3837.4	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #17	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1O	3627.4	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #17	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1O	4726.7	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #18	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2)C=C1O[Si](C)(C)C	3821.5	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #18	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2)C=C1O[Si](C)(C)C	3677.6	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #18	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2)C=C1O[Si](C)(C)C	4806.0	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #19	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3832.1	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #19	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3713.6	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #19	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	4839.9	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #2	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O	3856.7	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #2	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O	3800.8	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #2	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O	4906.2	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #20	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3835.5	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #20	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3699.1	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #20	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	4837.1	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #3	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O	3850.1	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #3	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O	3804.3	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #3	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O	4888.2	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #4	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3849.1	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #4	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3870.6	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #4	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	4916.6	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #5	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O	3827.5	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #5	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O	3681.8	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #5	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O	4791.8	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #6	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O	3839.2	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #6	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O	3716.1	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #6	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O	4827.8	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #7	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3843.3	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #7	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3758.9	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #7	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	4849.0	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #8	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O	3837.8	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #8	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O	3702.3	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #8	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O	4824.0	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #9	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3859.6	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #9	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3770.6	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #9	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	4882.7	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O	3800.6	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O	3723.0	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O	4498.0	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #10	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3809.0	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #10	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3724.6	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #10	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	4543.8	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #11	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1O	3815.8	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #11	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1O	3673.8	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #11	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1O	4405.6	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #12	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2)C=C1O[Si](C)(C)C	3803.5	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #12	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2)C=C1O[Si](C)(C)C	3723.2	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #12	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2)C=C1O[Si](C)(C)C	4517.9	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #13	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3826.0	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #13	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3780.0	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #13	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	4554.9	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #14	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3800.0	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #14	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3738.9	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #14	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	4545.0	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #15	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3801.6	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #15	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3648.8	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #15	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	4449.6	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #2	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O	3813.4	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #2	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O	3778.6	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #2	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O	4536.1	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #3	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3813.3	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #3	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3812.9	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #3	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	4571.2	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #4	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O	3793.3	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #4	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O	3737.1	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #4	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O	4525.8	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #5	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3818.9	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #5	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3824.9	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #5	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	4611.7	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #6	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3827.8	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #6	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3832.8	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #6	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	4586.8	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #7	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O	3770.6	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #7	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O	3647.4	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #7	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O	4429.5	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #8	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3800.7	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #8	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3705.3	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #8	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	4518.4	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #9	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3821.0	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #9	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3755.5	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #9	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	4551.6	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O	3784.6	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O	3677.1	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O	4157.9	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #2	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3805.8	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #2	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3742.8	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #2	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	4277.6	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #3	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3817.3	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #3	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3793.0	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #3	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	4311.8	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #4	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3792.4	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #4	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3754.2	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #4	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	4302.5	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #5	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3769.4	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #5	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3668.8	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #5	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	4214.8	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #6	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3808.2	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #6	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3684.9	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #6	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	4179.8	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,6TMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3813.0	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,6TMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3706.7	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,6TMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C=C1O[Si](C)(C)C	3999.3	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4303.3	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	3913.9	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	5850.9	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #2	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O)=C2)C=C1O	4274.2	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #2	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O)=C2)C=C1O	3943.8	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #2	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O)=C2)C=C1O	5974.0	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #3	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C2)C=C1O	4252.0	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #3	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C2)C=C1O	3839.2	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #3	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C2)C=C1O	5848.0	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #4	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1O	4243.4	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #4	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1O	3852.7	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #4	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1O	5857.6	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #5	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4267.8	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #5	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O	3869.8	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #5	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O	5865.6	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #6	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O)C3O)=C2)C=C1O[Si](C)(C)C(C)(C)C	4288.7	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #6	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O)C3O)=C2)C=C1O[Si](C)(C)C(C)(C)C	3910.5	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #6	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O)C3O)=C2)C=C1O[Si](C)(C)C(C)(C)C	5838.5	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4433.8	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4262.3	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	5297.9	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #10	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1O	4389.1	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #10	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1O	4110.5	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #10	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1O	5185.2	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #11	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4399.7	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #11	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4129.8	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #11	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O	5218.7	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #12	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C2)C=C1O[Si](C)(C)C(C)(C)C	4405.3	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #12	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C2)C=C1O[Si](C)(C)C(C)(C)C	4170.9	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #12	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C2)C=C1O[Si](C)(C)C(C)(C)C	5228.8	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #13	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4400.1	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #13	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4131.1	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #13	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O	5217.6	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #14	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1O[Si](C)(C)C(C)(C)C	4389.4	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #14	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1O[Si](C)(C)C(C)(C)C	4182.2	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #14	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1O[Si](C)(C)C(C)(C)C	5250.3	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #15	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4415.2	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #15	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4199.1	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #15	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	5245.8	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #2	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4443.0	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #2	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4175.2	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #2	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	5220.2	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #3	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4447.9	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #3	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4185.1	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #3	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	5242.9	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #4	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4444.1	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #4	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4200.2	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #4	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	5238.3	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #5	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4454.6	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #5	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4248.3	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #5	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	5250.1	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #6	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C2)C=C1O	4386.9	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #6	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C2)C=C1O	4178.2	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #6	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C2)C=C1O	5279.4	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #7	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1O	4397.0	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #7	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1O	4193.1	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #7	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1O	5298.8	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #8	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4406.1	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #8	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4204.4	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #8	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O	5295.0	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #9	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O)=C2)C=C1O[Si](C)(C)C(C)(C)C	4414.1	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #9	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O)=C2)C=C1O[Si](C)(C)C(C)(C)C	4257.8	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #9	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O)=C2)C=C1O[Si](C)(C)C(C)(C)C	5304.9	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4583.6	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4440.9	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4929.3	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #10	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4595.7	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #10	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4465.2	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #10	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4931.7	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #11	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1O	4526.2	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #11	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1O	4364.9	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #11	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1O	4878.6	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #12	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4553.9	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #12	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4406.4	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #12	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4909.4	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #13	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C2)C=C1O[Si](C)(C)C(C)(C)C	4531.8	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #13	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C2)C=C1O[Si](C)(C)C(C)(C)C	4438.1	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #13	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C2)C=C1O[Si](C)(C)C(C)(C)C	4940.8	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #14	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4531.6	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #14	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4376.1	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #14	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4900.3	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #15	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1O[Si](C)(C)C(C)(C)C	4533.0	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #15	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1O[Si](C)(C)C(C)(C)C	4445.3	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #15	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1O[Si](C)(C)C(C)(C)C	4965.5	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #16	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4545.3	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #16	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4466.9	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #16	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4953.7	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #17	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4528.8	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #17	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4304.6	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #17	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4811.8	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #18	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1O[Si](C)(C)C(C)(C)C	4526.4	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #18	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1O[Si](C)(C)C(C)(C)C	4350.5	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #18	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1O[Si](C)(C)C(C)(C)C	4876.2	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #19	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4528.7	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #19	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4392.9	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #19	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4904.6	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #2	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4600.1	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #2	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4448.1	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #2	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4955.2	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #20	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4542.4	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #20	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4370.4	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #20	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4898.0	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #3	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4584.6	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #3	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4464.6	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #3	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4942.7	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #4	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4596.6	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #4	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4527.4	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #4	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4972.8	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #5	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4589.5	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #5	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4352.7	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #5	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4865.3	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #6	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4592.5	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #6	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4391.7	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #6	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4895.2	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #7	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4608.3	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #7	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4432.7	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #7	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4916.0	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #8	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4603.2	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #8	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4369.8	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #8	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4888.2	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #9	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4606.3	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #9	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4432.6	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #9	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4941.4	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4739.8	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4541.6	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #1	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4651.8	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #10	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4749.1	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #10	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4536.3	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #10	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4679.7	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #11	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4711.4	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #11	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4498.0	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #11	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4575.3	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #12	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1O[Si](C)(C)C(C)(C)C	4672.7	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #12	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1O[Si](C)(C)C(C)(C)C	4538.8	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #12	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=C2)C=C1O[Si](C)(C)C(C)(C)C	4661.6	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #13	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4700.4	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #13	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4591.8	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #13	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4690.7	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #14	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4675.3	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #14	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4547.8	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #14	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4682.6	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #15	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4657.5	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #15	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4460.9	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #15	COC1=CC=C(C=CC2=CC(O)=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4604.7	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #2	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4771.3	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #2	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4590.0	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #2	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4681.7	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #3	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4744.0	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #3	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4613.1	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #3	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4714.8	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #4	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4742.3	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #4	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4548.1	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #4	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4673.3	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #5	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4753.5	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #5	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4621.5	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #5	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4734.4	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #6	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4733.0	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #6	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4641.0	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #6	COC1=CC=C(C=CC2=CC(OC3OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4724.7	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #7	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4728.9	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #7	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4461.0	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #7	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O	4594.9	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #8	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4735.1	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #8	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4514.1	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #8	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4657.7	Standard polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #9	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4739.9	Semi standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #9	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4570.5	Standard non polar	33892256
(2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #9	COC1=CC=C(C=CC2=CC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2)C=C1O[Si](C)(C)C(C)(C)C	4688.9	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - (2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (Non-derivatized) - 70eV, Positive	splash10-0pi9-9214200000-4048d74b86ce9fa3f759	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 10V, Positive-QTOF	splash10-0a4i-0090200000-373cefeb757eab8d0b12	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 20V, Positive-QTOF	splash10-0a4u-0592100000-9e3552bdf2e3e417cc4f	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 40V, Positive-QTOF	splash10-0aba-5393100000-f5f0eef87fae86135cf0	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 10V, Negative-QTOF	splash10-0a4i-0090100000-855b88ecb0376cc6f423	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 20V, Negative-QTOF	splash10-0a4l-0090100000-2bb69bc3074f78638faa	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 40V, Negative-QTOF	splash10-054o-0090000000-e66d3e031a18962d6874	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

4886

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5062

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for (2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol (HMDB0242526)

MOL for HMDB0242526 ((2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

3D MOL for HMDB0242526 ((2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

3D SDF for HMDB0242526 ((2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

3D-SDF for HMDB0242526 ((2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

PDB for HMDB0242526 ((2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

3D PDB for HMDB0242526 ((2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

SMILES for HMDB0242526 ((2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

INCHI for HMDB0242526 ((2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

Structure for HMDB0242526 ((2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

3D Structure for HMDB0242526 ((2S,3R,4S,5S,6R)-2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Derivatized

GC-MS Spectra

MS/MS Spectra