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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 19:53:23 UTC

Update Date

2022-03-07 02:54:17 UTC

HMDB ID

HMDB0034955

Secondary Accession Numbers

HMDB34955

Metabolite Identification

Common Name

Zizybeoside II

Description

Zizybeoside II belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds. Zizybeoside II has been detected, but not quantified in, fruits. This could make zizybeoside II a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on Zizybeoside II.

Structure

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

  Mrv0541 05061308092D          

 41 44  0  0  0  0            999 V2000
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   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    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.0013    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    4.5375    0.0000 O   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
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    2.1434    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  3  1  1  0  0  0  0
  4  2  1  0  0  0  0
  5  3  2  0  0  0  0
 10  4  2  0  0  0  0
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 11  6  1  0  0  0  0
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 40 21  1  0  0  0  0
 40 23  1  0  0  0  0
 41 22  1  0  0  0  0
 41 24  1  0  0  0  0
M  END

HMDB0034955
     RDKit          3D
Zizybeoside II
 79 82  0  0  0  0  0  0  0  0999 V2000
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 38 76  1  0
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 41 79  1  0
M  END

  Mrv0541 05061308092D          

 41 44  0  0  0  0            999 V2000
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    5.0013    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    4.5375    0.0000 O   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
   -0.7145    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  3  1  1  0  0  0  0
  4  2  1  0  0  0  0
  5  3  2  0  0  0  0
 10  4  2  0  0  0  0
 10  5  1  0  0  0  0
 10  9  1  0  0  0  0
 11  6  1  0  0  0  0
 12  7  1  0  0  0  0
 13  8  1  0  0  0  0
 14 11  1  0  0  0  0
 15 12  1  0  0  0  0
 16 13  1  0  0  0  0
 17 14  1  0  0  0  0
 18 15  1  0  0  0  0
 19 17  1  0  0  0  0
 20 18  1  0  0  0  0
 21 16  1  0  0  0  0
 22 21  1  0  0  0  0
 23 19  1  0  0  0  0
 24 20  1  0  0  0  0
 25 22  1  0  0  0  0
 26  6  1  0  0  0  0
 27  7  1  0  0  0  0
 28  8  1  0  0  0  0
 29 14  1  0  0  0  0
 30 15  1  0  0  0  0
 31 16  1  0  0  0  0
 32 17  1  0  0  0  0
 33 18  1  0  0  0  0
 34 19  1  0  0  0  0
 35 20  1  0  0  0  0
 36  9  1  0  0  0  0
 36 25  1  0  0  0  0
 37 11  1  0  0  0  0
 37 23  1  0  0  0  0
 38 12  1  0  0  0  0
 38 24  1  0  0  0  0
 39 13  1  0  0  0  0
 39 25  1  0  0  0  0
 40 21  1  0  0  0  0
 40 23  1  0  0  0  0
 41 22  1  0  0  0  0
 41 24  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0034955

> <DATABASE_NAME>
hmdb

> <SMILES>
OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C25H38O16/c26-6-11-14(29)17(32)19(34)23(37-11)40-21-16(31)13(8-28)39-25(36-9-10-4-2-1-3-5-10)22(21)41-24-20(35)18(33)15(30)12(7-27)38-24/h1-5,11-35H,6-9H2

> <INCHI_KEY>
BEDWWZCYHCGAKV-UHFFFAOYSA-N

> <FORMULA>
C25H38O16

> <MOLECULAR_WEIGHT>
594.5596

> <EXACT_MASS>
594.215985168

> <JCHEM_ACCEPTOR_COUNT>
16

> <JCHEM_AVERAGE_POLARIZABILITY>
58.11351357639356

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
10

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <ALOGPS_LOGP>
-1.83

> <JCHEM_LOGP>
-4.106610888333333

> <ALOGPS_LOGS>
-0.88

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.367885763809404

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.87916306496445

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810910032065756

> <JCHEM_POLAR_SURFACE_AREA>
257.67999999999995

> <JCHEM_REFRACTIVITY>
130.11379999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.79e+01 g/l

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

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0034955
     RDKit          3D
Zizybeoside II
 79 82  0  0  0  0  0  0  0  0999 V2000
   -5.4239   -0.9920   -1.4950 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4101   -0.0528   -1.5546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0744   -0.7819   -1.4541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0396    0.1168   -1.5099 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9172   -0.4741   -0.9214 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1291    0.4340   -0.8770 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4225    0.7238    0.4243 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1256    2.1944    0.7635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2125    2.3930    1.0043 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7351    3.3139    0.1030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1782    3.5537    0.3293 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8707    2.9156    1.3420 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2198    3.1468    1.5454 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8870    4.0314    0.7211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1839    4.6694   -0.2953 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8298    4.4359   -0.4974 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8444    2.5904    1.8873 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0042    1.5669    2.8053 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6217    2.1186    4.0599 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7664    1.0495    4.9624 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8356    0.4253    2.3296 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1760   -0.7569    2.6911 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8731    0.5045    0.8070 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4299   -0.6250    0.2506 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4812   -0.4520   -0.5727 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6553   -0.9582   -0.0303 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7148   -2.3407   -0.0746 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7719   -3.0437    0.8428 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0525   -2.6650    2.1624 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6224   -2.8852   -1.5020 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6151   -2.2999   -2.2915 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2922   -2.4056   -2.0508 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0737   -2.8635   -3.3443 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3467   -0.8906   -1.9802 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4758   -0.5062   -2.7168 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5552   -1.7704   -1.6018 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6089   -2.8474   -0.7204 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4646   -2.0824   -2.7634 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3267   -3.4397   -3.0638 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9028   -1.7925   -2.5368 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6623   -2.9315   -2.2765 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4968   -1.3023   -0.5644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4856    0.5905   -0.6563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4242    0.5363   -2.4924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1107   -1.3100   -0.4632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2141   -0.7083    0.1167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2374    0.1630    1.1508 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4425    2.8143   -0.0822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5897    3.0056   -0.9520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2393    4.3140    0.2296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3084    2.2287    1.9668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7657    2.6514    2.3349 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9374    4.1991    0.8952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7424    5.3614   -0.9270 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3535    4.9629   -1.3013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0379    1.2471    3.0901 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9889    2.8642    4.5658 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6484    2.4977    3.8665 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8578    1.4132    5.8882 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8407    0.3717    2.7722 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0770   -0.7812    3.6676 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3944    1.4417    0.4809 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6634    0.6692   -0.6134 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7615   -2.5917    0.2878 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7111   -2.8980    0.6217 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9852   -4.1350    0.7646 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2312   -2.5858    2.6983 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7340   -3.9649   -1.5363 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3469   -2.0516   -1.6755 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5030   -2.8025   -1.4001 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2303   -2.2048   -4.0423 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4776   -0.5122   -2.5239 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6430    0.4440   -2.4851 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4650   -1.6965   -1.9890 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0562   -2.7654    0.0127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0434   -1.5401   -3.6533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9965   -4.0053   -2.6278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3196   -1.3691   -3.4929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5830   -2.8780   -2.6231 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
  8 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
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 27 30  1  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
 32 34  1  0
 34 35  1  0
  5 36  1  0
 36 37  1  0
 36 38  1  0
 38 39  1  0
 38 40  1  0
 40 41  1  0
 40  3  1  0
 23  7  1  0
 34 25  1  0
 16 11  1  0
  1 42  1  0
  2 43  1  0
  2 44  1  0
  3 45  1  0
  5 46  1  0
  7 47  1  0
  8 48  1  0
 10 49  1  0
 10 50  1  0
 12 51  1  0
 13 52  1  0
 14 53  1  0
 15 54  1  0
 16 55  1  0
 18 56  1  0
 19 57  1  0
 19 58  1  0
 20 59  1  0
 21 60  1  0
 22 61  1  0
 23 62  1  0
 25 63  1  0
 27 64  1  0
 28 65  1  0
 28 66  1  0
 29 67  1  0
 30 68  1  0
 31 69  1  0
 32 70  1  0
 33 71  1  0
 34 72  1  0
 35 73  1  0
 36 74  1  0
 37 75  1  0
 38 76  1  0
 39 77  1  0
 40 78  1  0
 41 79  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.001   3.850   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.001   8.470   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.667   6.160   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.667   9.240   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.667  10.780   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.002   6.160   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.334  11.550   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.668   6.930   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.000  10.780   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.667   6.160   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.334   6.930   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.335   6.160   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.000   9.240   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       8.002   1.540   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      -4.001   6.930   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       9.336   3.850   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -4.001  11.550   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       9.336   6.930   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0      -1.334  13.090   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0       6.668   8.470   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0       1.334  11.550   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      -1.334   6.930   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       5.335   4.620   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      -1.334   8.470   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0       0.000   4.620   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       4.001   6.930   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0       1.334   8.470   0.000  0.00  0.00           O+0
CONECT    1    2    3                                                       
CONECT    2    1    4                                                       
CONECT    3    1    5                                                       
CONECT    4    2   10                                                       
CONECT    5    3   10                                                       
CONECT    6   11   26                                                       
CONECT    7   12   27                                                       
CONECT    8   13   28                                                       
CONECT    9   10   36                                                       
CONECT   10    4    5    9                                                  
CONECT   11    6   14   37                                                  
CONECT   12    7   15   38                                                  
CONECT   13    8   16   39                                                  
CONECT   14   11   17   29                                                  
CONECT   15   12   18   30                                                  
CONECT   16   13   21   31                                                  
CONECT   17   14   19   32                                                  
CONECT   18   15   20   33                                                  
CONECT   19   17   23   34                                                  
CONECT   20   18   24   35                                                  
CONECT   21   16   22   40                                                  
CONECT   22   21   25   41                                                  
CONECT   23   19   37   40                                                  
CONECT   24   20   38   41                                                  
CONECT   25   22   36   39                                                  
CONECT   26    6                                                            
CONECT   27    7                                                            
CONECT   28    8                                                            
CONECT   29   14                                                            
CONECT   30   15                                                            
CONECT   31   16                                                            
CONECT   32   17                                                            
CONECT   33   18                                                            
CONECT   34   19                                                            
CONECT   35   20                                                            
CONECT   36    9   25                                                       
CONECT   37   11   23                                                       
CONECT   38   12   24                                                       
CONECT   39   13   25                                                       
CONECT   40   21   23                                                       
CONECT   41   22   24                                                       
MASTER        0    0    0    0    0    0    0    0   41    0   88    0
END

COMPND    HMDB0034955
HETATM    1  O1  UNL     1      -5.424  -0.992  -1.495  1.00  0.00           O  
HETATM    2  C1  UNL     1      -4.410  -0.053  -1.555  1.00  0.00           C  
HETATM    3  C2  UNL     1      -3.074  -0.782  -1.454  1.00  0.00           C  
HETATM    4  O2  UNL     1      -2.040   0.117  -1.510  1.00  0.00           O  
HETATM    5  C3  UNL     1      -0.917  -0.474  -0.921  1.00  0.00           C  
HETATM    6  O3  UNL     1       0.129   0.434  -0.877  1.00  0.00           O  
HETATM    7  C4  UNL     1       0.423   0.724   0.424  1.00  0.00           C  
HETATM    8  C5  UNL     1       0.126   2.194   0.763  1.00  0.00           C  
HETATM    9  O4  UNL     1      -1.213   2.393   1.004  1.00  0.00           O  
HETATM   10  C6  UNL     1      -1.735   3.314   0.103  1.00  0.00           C  
HETATM   11  C7  UNL     1      -3.178   3.554   0.329  1.00  0.00           C  
HETATM   12  C8  UNL     1      -3.871   2.916   1.342  1.00  0.00           C  
HETATM   13  C9  UNL     1      -5.220   3.147   1.545  1.00  0.00           C  
HETATM   14  C10 UNL     1      -5.887   4.031   0.721  1.00  0.00           C  
HETATM   15  C11 UNL     1      -5.184   4.669  -0.295  1.00  0.00           C  
HETATM   16  C12 UNL     1      -3.830   4.436  -0.497  1.00  0.00           C  
HETATM   17  O5  UNL     1       0.844   2.590   1.887  1.00  0.00           O  
HETATM   18  C13 UNL     1       1.004   1.567   2.805  1.00  0.00           C  
HETATM   19  C14 UNL     1       1.622   2.119   4.060  1.00  0.00           C  
HETATM   20  O6  UNL     1       1.766   1.050   4.962  1.00  0.00           O  
HETATM   21  C15 UNL     1       1.836   0.425   2.330  1.00  0.00           C  
HETATM   22  O7  UNL     1       1.176  -0.757   2.691  1.00  0.00           O  
HETATM   23  C16 UNL     1       1.873   0.505   0.807  1.00  0.00           C  
HETATM   24  O8  UNL     1       2.430  -0.625   0.251  1.00  0.00           O  
HETATM   25  C17 UNL     1       3.481  -0.452  -0.573  1.00  0.00           C  
HETATM   26  O9  UNL     1       4.655  -0.958  -0.030  1.00  0.00           O  
HETATM   27  C18 UNL     1       4.715  -2.341  -0.075  1.00  0.00           C  
HETATM   28  C19 UNL     1       3.772  -3.044   0.843  1.00  0.00           C  
HETATM   29  O10 UNL     1       4.053  -2.665   2.162  1.00  0.00           O  
HETATM   30  C20 UNL     1       4.622  -2.885  -1.502  1.00  0.00           C  
HETATM   31  O11 UNL     1       5.615  -2.300  -2.292  1.00  0.00           O  
HETATM   32  C21 UNL     1       3.292  -2.406  -2.051  1.00  0.00           C  
HETATM   33  O12 UNL     1       3.074  -2.863  -3.344  1.00  0.00           O  
HETATM   34  C22 UNL     1       3.347  -0.891  -1.980  1.00  0.00           C  
HETATM   35  O13 UNL     1       4.476  -0.506  -2.717  1.00  0.00           O  
HETATM   36  C23 UNL     1      -0.555  -1.770  -1.602  1.00  0.00           C  
HETATM   37  O14 UNL     1      -0.609  -2.847  -0.720  1.00  0.00           O  
HETATM   38  C24 UNL     1      -1.465  -2.082  -2.763  1.00  0.00           C  
HETATM   39  O15 UNL     1      -1.327  -3.440  -3.064  1.00  0.00           O  
HETATM   40  C25 UNL     1      -2.903  -1.793  -2.537  1.00  0.00           C  
HETATM   41  O16 UNL     1      -3.662  -2.932  -2.277  1.00  0.00           O  
HETATM   42  H1  UNL     1      -5.497  -1.302  -0.564  1.00  0.00           H  
HETATM   43  H2  UNL     1      -4.486   0.590  -0.656  1.00  0.00           H  
HETATM   44  H3  UNL     1      -4.424   0.536  -2.492  1.00  0.00           H  
HETATM   45  H4  UNL     1      -3.111  -1.310  -0.463  1.00  0.00           H  
HETATM   46  H5  UNL     1      -1.214  -0.708   0.117  1.00  0.00           H  
HETATM   47  H6  UNL     1      -0.237   0.163   1.151  1.00  0.00           H  
HETATM   48  H7  UNL     1       0.442   2.814  -0.082  1.00  0.00           H  
HETATM   49  H8  UNL     1      -1.590   3.006  -0.952  1.00  0.00           H  
HETATM   50  H9  UNL     1      -1.239   4.314   0.230  1.00  0.00           H  
HETATM   51  H10 UNL     1      -3.308   2.229   1.967  1.00  0.00           H  
HETATM   52  H11 UNL     1      -5.766   2.651   2.335  1.00  0.00           H  
HETATM   53  H12 UNL     1      -6.937   4.199   0.895  1.00  0.00           H  
HETATM   54  H13 UNL     1      -5.742   5.361  -0.927  1.00  0.00           H  
HETATM   55  H14 UNL     1      -3.354   4.963  -1.301  1.00  0.00           H  
HETATM   56  H15 UNL     1      -0.038   1.247   3.090  1.00  0.00           H  
HETATM   57  H16 UNL     1       0.989   2.864   4.566  1.00  0.00           H  
HETATM   58  H17 UNL     1       2.648   2.498   3.867  1.00  0.00           H  
HETATM   59  H18 UNL     1       1.858   1.413   5.888  1.00  0.00           H  
HETATM   60  H19 UNL     1       2.841   0.372   2.772  1.00  0.00           H  
HETATM   61  H20 UNL     1       1.077  -0.781   3.668  1.00  0.00           H  
HETATM   62  H21 UNL     1       2.394   1.442   0.481  1.00  0.00           H  
HETATM   63  H22 UNL     1       3.663   0.669  -0.613  1.00  0.00           H  
HETATM   64  H23 UNL     1       5.761  -2.592   0.288  1.00  0.00           H  
HETATM   65  H24 UNL     1       2.711  -2.898   0.622  1.00  0.00           H  
HETATM   66  H25 UNL     1       3.985  -4.135   0.765  1.00  0.00           H  
HETATM   67  H26 UNL     1       3.231  -2.586   2.698  1.00  0.00           H  
HETATM   68  H27 UNL     1       4.734  -3.965  -1.536  1.00  0.00           H  
HETATM   69  H28 UNL     1       6.347  -2.052  -1.675  1.00  0.00           H  
HETATM   70  H29 UNL     1       2.503  -2.803  -1.400  1.00  0.00           H  
HETATM   71  H30 UNL     1       3.230  -2.205  -4.042  1.00  0.00           H  
HETATM   72  H31 UNL     1       2.478  -0.512  -2.524  1.00  0.00           H  
HETATM   73  H32 UNL     1       4.643   0.444  -2.485  1.00  0.00           H  
HETATM   74  H33 UNL     1       0.465  -1.696  -1.989  1.00  0.00           H  
HETATM   75  H34 UNL     1       0.056  -2.765   0.013  1.00  0.00           H  
HETATM   76  H35 UNL     1      -1.043  -1.540  -3.653  1.00  0.00           H  
HETATM   77  H36 UNL     1      -1.997  -4.005  -2.628  1.00  0.00           H  
HETATM   78  H37 UNL     1      -3.320  -1.369  -3.493  1.00  0.00           H  
HETATM   79  H38 UNL     1      -4.583  -2.878  -2.623  1.00  0.00           H  
CONECT    1    2   42
CONECT    2    3   43   44
CONECT    3    4   40   45
CONECT    4    5
CONECT    5    6   36   46
CONECT    6    7
CONECT    7    8   23   47
CONECT    8    9   17   48
CONECT    9   10
CONECT   10   11   49   50
CONECT   11   12   12   16
CONECT   12   13   51
CONECT   13   14   14   52
CONECT   14   15   53
CONECT   15   16   16   54
CONECT   16   55
CONECT   17   18
CONECT   18   19   21   56
CONECT   19   20   57   58
CONECT   20   59
CONECT   21   22   23   60
CONECT   22   61
CONECT   23   24   62
CONECT   24   25
CONECT   25   26   34   63
CONECT   26   27
CONECT   27   28   30   64
CONECT   28   29   65   66
CONECT   29   67
CONECT   30   31   32   68
CONECT   31   69
CONECT   32   33   34   70
CONECT   33   71
CONECT   34   35   72
CONECT   35   73
CONECT   36   37   38   74
CONECT   37   75
CONECT   38   39   40   76
CONECT   39   77
CONECT   40   41   78
CONECT   41   79
END

HMDB0034955
     RDKit          3D
Zizybeoside II
 79 82  0  0  0  0  0  0  0  0999 V2000
   -5.4239   -0.9920   -1.4950 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4101   -0.0528   -1.5546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0744   -0.7819   -1.4541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0396    0.1168   -1.5099 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9172   -0.4741   -0.9214 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1291    0.4340   -0.8770 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4225    0.7238    0.4243 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1256    2.1944    0.7635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2125    2.3930    1.0043 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7351    3.3139    0.1030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1782    3.5537    0.3293 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8707    2.9156    1.3420 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2198    3.1468    1.5454 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8870    4.0314    0.7211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1839    4.6694   -0.2953 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8298    4.4359   -0.4974 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8444    2.5904    1.8873 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0042    1.5669    2.8053 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6217    2.1186    4.0599 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7664    1.0495    4.9624 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8356    0.4253    2.3296 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1760   -0.7569    2.6911 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8731    0.5045    0.8070 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4299   -0.6250    0.2506 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4812   -0.4520   -0.5727 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6553   -0.9582   -0.0303 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7148   -2.3407   -0.0746 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7719   -3.0437    0.8428 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0525   -2.6650    2.1624 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6224   -2.8852   -1.5020 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6151   -2.2999   -2.2915 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2922   -2.4056   -2.0508 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0737   -2.8635   -3.3443 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3467   -0.8906   -1.9802 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4758   -0.5062   -2.7168 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5552   -1.7704   -1.6018 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6089   -2.8474   -0.7204 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4646   -2.0824   -2.7634 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3267   -3.4397   -3.0638 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9028   -1.7925   -2.5368 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6623   -2.9315   -2.2765 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4968   -1.3023   -0.5644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4856    0.5905   -0.6563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4242    0.5363   -2.4924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1107   -1.3100   -0.4632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2141   -0.7083    0.1167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2374    0.1630    1.1508 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4425    2.8143   -0.0822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5897    3.0056   -0.9520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2393    4.3140    0.2296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3084    2.2287    1.9668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7657    2.6514    2.3349 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9374    4.1991    0.8952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7424    5.3614   -0.9270 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3535    4.9629   -1.3013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0379    1.2471    3.0901 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9889    2.8642    4.5658 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6484    2.4977    3.8665 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8578    1.4132    5.8882 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8407    0.3717    2.7722 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0770   -0.7812    3.6676 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3944    1.4417    0.4809 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6634    0.6692   -0.6134 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7615   -2.5917    0.2878 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7111   -2.8980    0.6217 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9852   -4.1350    0.7646 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2312   -2.5858    2.6983 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7340   -3.9649   -1.5363 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3469   -2.0516   -1.6755 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5030   -2.8025   -1.4001 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2303   -2.2048   -4.0423 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4776   -0.5122   -2.5239 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6430    0.4440   -2.4851 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4650   -1.6965   -1.9890 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0562   -2.7654    0.0127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0434   -1.5401   -3.6533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9965   -4.0053   -2.6278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3196   -1.3691   -3.4929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5830   -2.8780   -2.6231 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
  8 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
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 27 30  1  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
 32 34  1  0
 34 35  1  0
  5 36  1  0
 36 37  1  0
 36 38  1  0
 38 39  1  0
 38 40  1  0
 40 41  1  0
 40  3  1  0
 23  7  1  0
 34 25  1  0
 16 11  1  0
  1 42  1  0
  2 43  1  0
  2 44  1  0
  3 45  1  0
  5 46  1  0
  7 47  1  0
  8 48  1  0
 10 49  1  0
 10 50  1  0
 12 51  1  0
 13 52  1  0
 14 53  1  0
 15 54  1  0
 16 55  1  0
 18 56  1  0
 19 57  1  0
 19 58  1  0
 20 59  1  0
 21 60  1  0
 22 61  1  0
 23 62  1  0
 25 63  1  0
 27 64  1  0
 28 65  1  0
 28 66  1  0
 29 67  1  0
 30 68  1  0
 31 69  1  0
 32 70  1  0
 33 71  1  0
 34 72  1  0
 35 73  1  0
 36 74  1  0
 37 75  1  0
 38 76  1  0
 39 77  1  0
 40 78  1  0
 41 79  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₅H₃₈O₁₆

Average Molecular Weight

594.5596

Monoisotopic Molecular Weight

594.215985168

IUPAC Name

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

Traditional Name

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

CAS Registry Number

81417-79-0

SMILES

OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O

InChI Identifier

InChI=1S/C25H38O16/c26-6-11-14(29)17(32)19(34)23(37-11)40-21-16(31)13(8-28)39-25(36-9-10-4-2-1-3-5-10)22(21)41-24-20(35)18(33)15(30)12(7-27)38-24/h1-5,11-35H,6-9H2

InChI Key

BEDWWZCYHCGAKV-UHFFFAOYSA-N

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Oligosaccharides

Alternative Parents

Substituents

Oligosaccharide
O-glycosyl compound
Glycosyl compound
Benzenoid
Oxane
Monocyclic benzene moiety
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Polyol
Acetal
Hydrocarbon derivative
Primary alcohol
Alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Extracellular (HMDB: HMDB0034955)
Cytoplasm (HMDB: HMDB0034955)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0034955)

Source

Exogenous

Exogenous (HMDB: HMDB0034955)

Food

Food (HMDB: HMDB0034955)

Fruit

Fruits (FooDB: FOOD00871)

Endogenous

Plant

Plant (HMDB: HMDB0034955)

Process

Not Available

Role

Biological role

Nutrient (HMDB: HMDB0034955)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	237 - 238 °C	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	77.9 g/L	ALOGPS
logP	-1.8	ALOGPS
logP	-4.1	ChemAxon
logS	-0.88	ALOGPS
pKa (Strongest Acidic)	11.88	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	16	ChemAxon
Hydrogen Donor Count	10	ChemAxon
Polar Surface Area	257.68 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	130.11 m³·mol⁻¹	ChemAxon
Polarizability	58.11 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	232.967	31661259
DarkChem	[M-H]-	223.132	31661259
DeepCCS	[M+H]+	223.173	30932474
DeepCCS	[M-H]-	220.777	30932474
DeepCCS	[M-2H]-	253.661	30932474
DeepCCS	[M+Na]+	229.204	30932474
AllCCS	[M+H]+	229.5	32859911
AllCCS	[M+H-H2O]+	228.4	32859911
AllCCS	[M+NH4]+	230.4	32859911
AllCCS	[M+Na]+	230.7	32859911
AllCCS	[M-H]-	224.1	32859911
AllCCS	[M+Na-2H]-	225.7	32859911
AllCCS	[M+HCOO]-	227.6	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Zizybeoside II	OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O	4298.0	Standard polar	33892256
Zizybeoside II	OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O	4917.3	Standard non polar	33892256
Zizybeoside II	OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O	5060.1	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Zizybeoside II,1TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O	4794.7	Semi standard non polar	33892256
Zizybeoside II,1TMS,isomer #10	C[Si](C)(C)OC1C(CO)OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C1O	4798.1	Semi standard non polar	33892256
Zizybeoside II,1TMS,isomer #2	C[Si](C)(C)OC1C(CO)OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C1OC1OC(CO)C(O)C(O)C1O	4809.2	Semi standard non polar	33892256
Zizybeoside II,1TMS,isomer #3	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C(OC2OC(CO)C(O)C(O)C2O)C1O	4810.7	Semi standard non polar	33892256
Zizybeoside II,1TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O	4794.8	Semi standard non polar	33892256
Zizybeoside II,1TMS,isomer #5	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O)C(O)C1O	4798.3	Semi standard non polar	33892256
Zizybeoside II,1TMS,isomer #6	C[Si](C)(C)OC1C(O)C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O)C1O	4770.2	Semi standard non polar	33892256
Zizybeoside II,1TMS,isomer #7	C[Si](C)(C)OC1C(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O)OC(CO)C(O)C1O	4796.8	Semi standard non polar	33892256
Zizybeoside II,1TMS,isomer #8	C[Si](C)(C)OC1C(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)OC(CO)C(O)C1O	4798.6	Semi standard non polar	33892256
Zizybeoside II,1TMS,isomer #9	C[Si](C)(C)OC1C(O)C(CO)OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C1O	4768.8	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O	4718.0	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #10	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C(OC2OC(CO)C(O)C(O)C2O)C1O[Si](C)(C)C	4729.4	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #11	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O	4718.5	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #12	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O)C2O)C(O)C1O	4748.3	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #13	C[Si](C)(C)OC1C(O)C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O)C2O)C1O	4709.4	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #14	C[Si](C)(C)OC1C(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O)C2O)OC(CO)C(O)C1O	4734.6	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #15	C[Si](C)(C)OC1C(CO)OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C1O	4748.2	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #16	C[Si](C)(C)OC1C(O)C(CO)OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C1O	4708.6	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #17	C[Si](C)(C)OC1C(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)OC(CO)C(O)C1O	4734.3	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #18	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O	4708.7	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #19	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(OC2OC(CO)C(O)C(O)C2O)C1O	4736.1	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2C(O)C(CO[Si](C)(C)C)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O	4708.9	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #20	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(OC2OC(CO)C(O)C(O)C2O)C1O	4692.8	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #21	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(OC2OC(CO)C(O)C(O)C2O)C1O	4721.3	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #22	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C1O	4736.0	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #23	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C1O	4692.0	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #24	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C1O	4724.8	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #25	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O	4720.4	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #26	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	4680.2	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #27	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	4711.1	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #28	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	4716.0	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #29	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	4688.4	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C(O)C1O	4689.8	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #30	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C	4717.8	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #31	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	4742.8	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #32	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	4708.0	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #33	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	4738.0	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #34	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	4714.0	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #35	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	4732.0	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #36	C[Si](C)(C)OC1C(CO)OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	4708.3	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #37	C[Si](C)(C)OC1C(O)C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C1O	4674.5	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #38	C[Si](C)(C)OC1C(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)OC(CO)C(O)C1O	4704.0	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #39	C[Si](C)(C)OC1C(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O)OC(CO)C(O)C1O[Si](C)(C)C	4731.7	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O	4720.4	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #40	C[Si](C)(C)OC1C(CO)OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	4736.1	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #41	C[Si](C)(C)OC1C(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)OC(CO)C(O)C1O	4700.8	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #42	C[Si](C)(C)OC1C(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)OC(CO)C(O)C1O	4730.7	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #43	C[Si](C)(C)OC1C(CO)OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	4715.8	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #44	C[Si](C)(C)OC1C(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)OC(CO)C(O)C1O[Si](C)(C)C	4734.5	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #45	C[Si](C)(C)OC1C(CO)OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	4731.7	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	4681.2	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	4707.8	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	4718.5	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #8	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	4688.5	Semi standard non polar	33892256
Zizybeoside II,2TMS,isomer #9	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C	4717.5	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO[Si](C)(C)C)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O	4584.4	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #10	C[Si](C)(C)OCC1OC(OC2C(O)C(CO[Si](C)(C)C)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O	4610.1	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #100	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4595.7	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #101	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O	4638.5	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #102	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O	4630.5	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #103	C[Si](C)(C)OC1C(CO)OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O	4629.3	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #104	C[Si](C)(C)OC1C(CO)OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O	4638.8	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #105	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	4633.8	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #106	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	4593.9	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #107	C[Si](C)(C)OC1C(O)C(CO)OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C1O	4605.4	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #108	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4613.3	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #109	C[Si](C)(C)OC1C(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)OC(CO)C(O)C1O	4624.5	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #11	C[Si](C)(C)OCC1OC(OC2C(O)C(CO[Si](C)(C)C)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	4564.8	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #110	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4639.4	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #111	C[Si](C)(C)OC1C(CO)OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	4631.2	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #112	C[Si](C)(C)OC1C(CO)OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	4593.7	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #113	C[Si](C)(C)OC1C(O)C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C1O	4605.2	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #114	C[Si](C)(C)OC1C(O)C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C1O	4595.1	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #115	C[Si](C)(C)OC1C(O)C(CO)OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C1O	4593.2	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #116	C[Si](C)(C)OC1C(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)OC(CO)C(O)C1O	4617.9	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #117	C[Si](C)(C)OC1C(CO)OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4613.4	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #118	C[Si](C)(C)OC1C(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)OC(CO)C(O)C1O	4622.3	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #119	C[Si](C)(C)OC1C(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)OC(CO)C(O)C1O	4618.8	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #12	C[Si](C)(C)OCC1OC(OC2C(O)C(CO[Si](C)(C)C)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	4586.8	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #120	C[Si](C)(C)OC1C(CO)OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4640.6	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #13	C[Si](C)(C)OCC1OC(OC2C(O)C(CO[Si](C)(C)C)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	4603.0	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #14	C[Si](C)(C)OCC1OC(OC2C(O)C(CO[Si](C)(C)C)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	4577.8	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #15	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C1O	4605.2	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #16	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O	4572.6	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #17	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	4545.3	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #18	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	4565.7	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #19	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	4564.7	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C(O)C1O	4565.9	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #20	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	4545.9	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #21	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O	4573.1	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #22	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	4602.6	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #23	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	4591.1	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #24	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	4618.7	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #25	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	4594.6	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #26	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C	4620.3	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #27	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O	4591.0	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #28	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O	4573.0	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #29	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O	4558.9	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O	4622.9	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #30	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C	4582.1	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #31	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O	4603.0	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #32	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O	4573.8	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #33	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C	4600.3	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #34	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4596.4	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #35	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4588.9	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #36	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4595.5	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #37	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O	4584.9	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #38	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(OC2OC(CO)C(O)C(O)C2O)C1O[Si](C)(C)C	4634.7	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #39	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(OC2OC(CO)C(O)C(O)C2O)C1O[Si](C)(C)C	4588.1	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	4582.0	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #40	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(OC2OC(CO)C(O)C(O)C2O)C1O[Si](C)(C)C	4613.7	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #41	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C1O[Si](C)(C)C	4635.0	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #42	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C1O[Si](C)(C)C	4587.2	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #43	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C1O[Si](C)(C)C	4615.5	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #44	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O	4623.4	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #45	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	4580.9	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #46	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	4605.3	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #47	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	4612.7	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #48	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	4592.9	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #49	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C	4616.0	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	4603.6	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #50	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	4661.8	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #51	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	4622.7	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #52	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	4646.0	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #53	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	4629.9	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #54	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	4640.3	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #55	C[Si](C)(C)OC1C(CO)OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	4623.1	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #56	C[Si](C)(C)OC1C(O)C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C1O	4588.0	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #57	C[Si](C)(C)OC1C(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)OC(CO)C(O)C1O	4604.4	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #58	C[Si](C)(C)OC1C(CO)OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C1OC1OC(CO)C(O)C(O)C1O	4635.5	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #59	C[Si](C)(C)OC1C(CO)OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	4644.3	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	4614.0	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #60	C[Si](C)(C)OC1C(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)OC(CO)C(O)C1O	4602.5	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #61	C[Si](C)(C)OC1C(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)OC(CO)C(O)C1O	4630.8	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #62	C[Si](C)(C)OC1C(CO)OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	4630.6	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #63	C[Si](C)(C)OC1C(CO)OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	4639.3	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #64	C[Si](C)(C)OC1C(CO)OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C1OC1OC(CO)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4635.4	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #65	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O	4609.8	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #66	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	4564.2	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #67	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	4590.0	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #68	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	4600.6	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #69	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	4579.0	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	4591.8	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #70	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(OC2OC(CO)C(O)C(O)C2O)C1O	4605.6	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #71	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(OC2OC(CO)C(O)C(O)C2O)C1O	4623.2	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #72	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(OC2OC(CO)C(O)C(O)C2O)C1O	4615.6	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #73	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C1O	4646.4	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #74	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C1O	4604.6	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #75	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C1O	4633.6	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #76	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(OC2OC(CO)C(O)C(O)C2O)C1O	4613.2	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #77	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C1O	4604.0	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #78	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C1O	4567.9	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #79	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C1O	4587.2	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #8	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C	4616.0	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #80	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C1O	4631.1	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #81	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C1O	4585.1	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #82	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C1O	4620.9	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #83	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C1O	4622.6	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #84	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C1O	4618.0	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #85	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C1O	4617.3	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #86	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	4601.2	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #87	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	4591.6	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #88	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	4617.5	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #89	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	4594.0	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #9	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O)C2OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C(O)C1O	4561.8	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #90	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C	4620.2	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #91	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O	4592.6	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #92	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O	4571.4	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #93	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O	4558.2	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #94	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C	4581.2	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #95	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O	4603.6	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #96	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O	4574.8	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #97	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C	4601.4	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #98	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4594.5	Semi standard non polar	33892256
Zizybeoside II,3TMS,isomer #99	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4587.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C2OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C(O)C1O	4400.6	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #10	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	4408.8	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #100	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C1O[Si](C)(C)C	4476.3	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #101	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C1O[Si](C)(C)C	4437.1	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #102	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C1O[Si](C)(C)C	4451.8	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #103	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C1O[Si](C)(C)C	4476.7	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #104	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C1O[Si](C)(C)C	4469.4	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #105	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C1O[Si](C)(C)C	4466.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #106	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	4460.2	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #107	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	4451.5	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #108	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	4471.7	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #109	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	4469.5	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #11	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	4407.6	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #110	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C	4490.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #111	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O	4448.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #112	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O	4430.6	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #113	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O	4424.8	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #114	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C	4451.3	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #115	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O	4442.5	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #116	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O	4432.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #117	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C	4457.3	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #118	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4453.4	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #119	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4445.8	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #12	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	4409.4	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #120	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4460.1	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #121	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O	4526.8	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #122	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O	4511.6	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #123	C[Si](C)(C)OC1C(CO)OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O	4509.6	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #124	C[Si](C)(C)OC1C(CO)OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O	4528.1	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #125	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	4518.0	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #126	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	4468.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #127	C[Si](C)(C)OC1C(O)C(CO)OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C1O	4476.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #128	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4481.2	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #129	C[Si](C)(C)OC1C(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)OC(CO)C(O)C1O	4493.3	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #13	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O	4425.8	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #130	C[Si](C)(C)OC1C(CO)OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C1OC1OC(CO)C(O)C(O)C1O	4506.3	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #131	C[Si](C)(C)OC1C(CO)OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	4518.1	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #132	C[Si](C)(C)OC1C(CO)OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	4470.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #133	C[Si](C)(C)OC1C(O)C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C1O	4476.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #134	C[Si](C)(C)OC1C(O)C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C1O	4470.2	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #135	C[Si](C)(C)OC1C(O)C(CO)OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C1O	4469.6	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #136	C[Si](C)(C)OC1C(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)OC(CO)C(O)C1O	4483.6	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #137	C[Si](C)(C)OC1C(CO)OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4481.2	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #138	C[Si](C)(C)OC1C(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)OC(CO)C(O)C1O	4490.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #139	C[Si](C)(C)OC1C(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)OC(CO)C(O)C1O	4482.7	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #14	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	4460.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #140	C[Si](C)(C)OC1C(CO)OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C1OC1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4507.8	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #141	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	4458.8	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #142	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	4451.8	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #143	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	4471.5	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #144	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	4471.5	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #145	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C1O	4490.2	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #146	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O	4447.1	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #147	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O	4434.2	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #148	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O	4428.6	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #149	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C1O	4455.8	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #15	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	4450.7	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #150	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O	4439.2	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #151	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O	4436.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #152	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C1O	4455.8	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #153	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(OC2OC(CO)C(O)C(O)C2O)C1O	4458.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #154	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(OC2OC(CO)C(O)C(O)C2O)C1O	4458.8	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #155	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(OC2OC(CO)C(O)C(O)C2O)C1O	4466.2	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #156	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(OC2OC(CO)C(O)C(O)C2O)C1O	4496.3	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #157	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C1O	4517.4	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #158	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C1O	4469.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #159	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C1O	4482.2	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #16	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	4472.4	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #160	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C1O	4505.5	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #161	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C1O	4467.2	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #162	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C1O	4473.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #163	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C1O	4515.6	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #164	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C1O	4504.3	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #165	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C1O	4505.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #166	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C1O	4506.1	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #167	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C1O	4459.2	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #168	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C1O	4471.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #169	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C1O	4469.2	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #17	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	4468.2	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #170	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C1O	4467.2	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #171	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C1O	4461.7	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #172	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C1O	4480.3	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #173	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C1O	4474.2	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #174	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C1O	4471.0	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #175	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C1O	4493.6	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #176	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O	4458.8	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #177	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O	4461.4	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #178	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O	4451.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #179	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C	4480.7	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #18	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C	4490.8	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #180	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O	4451.8	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #181	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O	4447.3	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #182	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C	4469.7	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #183	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4476.5	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #184	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4470.7	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #185	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4483.6	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #186	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O	4447.3	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #187	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O	4441.8	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #188	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C	4466.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #189	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4433.0	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #19	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O	4448.4	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #190	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4435.3	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #191	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4438.8	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #192	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4441.3	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #193	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4436.3	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #194	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4449.5	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #195	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4454.0	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #196	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	4526.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #197	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	4497.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #198	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	4501.6	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #199	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4485.3	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO[Si](C)(C)C)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O	4446.2	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #20	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O	4432.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #200	C[Si](C)(C)OC1C(CO)OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	4499.0	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #201	C[Si](C)(C)OC1C(CO)OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	4528.7	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #202	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4486.2	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #203	C[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4493.3	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #204	C[Si](C)(C)OC1C(O)C(CO)OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C1O	4485.4	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #205	C[Si](C)(C)OC1C(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)OC(CO)C(O)C1O	4493.1	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #206	C[Si](C)(C)OC1C(CO)OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4487.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #207	C[Si](C)(C)OC1C(CO)OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4491.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #208	C[Si](C)(C)OC1C(O)C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C1O	4485.2	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #209	C[Si](C)(C)OC1C(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)OC(CO)C(O)C1O[Si](C)(C)C	4481.3	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #21	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O	4425.5	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #210	C[Si](C)(C)OC1C(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)OC(CO)C(O)C1O	4492.0	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #22	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C	4452.5	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #23	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O	4442.2	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #24	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O	4430.3	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #25	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C	4455.8	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #26	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4453.6	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #27	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4447.6	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #28	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4459.5	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #29	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O)C2OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O	4437.5	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO[Si](C)(C)C)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	4415.5	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #30	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O)C2OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	4420.4	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #31	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O)C2OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	4416.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #32	C[Si](C)(C)OCC1OC(OC2C(O)C(CO[Si](C)(C)C)OC(OCC3=CC=CC=C3)C2OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	4419.2	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #33	C[Si](C)(C)OCC1OC(OC2C(O)C(CO[Si](C)(C)C)OC(OCC3=CC=CC=C3)C2OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	4420.4	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #34	C[Si](C)(C)OCC1OC(OC2C(O)C(CO[Si](C)(C)C)OC(OCC3=CC=CC=C3)C2OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O	4437.7	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #35	C[Si](C)(C)OCC1OC(OC2C(O)C(CO[Si](C)(C)C)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	4459.5	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #36	C[Si](C)(C)OCC1OC(OC2C(O)C(CO[Si](C)(C)C)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	4453.5	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #37	C[Si](C)(C)OCC1OC(OC2C(O)C(CO[Si](C)(C)C)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	4470.7	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #38	C[Si](C)(C)OCC1OC(OC2C(O)C(CO[Si](C)(C)C)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	4470.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #39	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C1O	4489.6	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO[Si](C)(C)C)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	4418.3	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #40	C[Si](C)(C)OCC1OC(OC2C(O)C(CO[Si](C)(C)C)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O	4448.0	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #41	C[Si](C)(C)OCC1OC(OC2C(O)C(CO[Si](C)(C)C)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O	4435.2	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #42	C[Si](C)(C)OCC1OC(OC2C(O)C(CO[Si](C)(C)C)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O	4428.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #43	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C1O	4455.8	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #44	C[Si](C)(C)OCC1OC(OC2C(O)C(CO[Si](C)(C)C)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O	4438.3	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #45	C[Si](C)(C)OCC1OC(OC2C(O)C(CO[Si](C)(C)C)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O	4436.0	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #46	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C1O	4455.2	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #47	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C1O	4457.7	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #48	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C1O	4458.1	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #49	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C1O	4465.5	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO[Si](C)(C)C)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	4434.7	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #50	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	4424.6	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #51	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	4414.4	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #52	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	4430.6	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #53	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	4433.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #54	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C	4451.8	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #55	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O	4415.4	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #56	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O	4411.6	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #57	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O	4408.5	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #58	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	4434.5	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #59	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O	4412.5	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO[Si](C)(C)C)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	4433.6	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #60	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O	4412.1	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #61	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	4430.5	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #62	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	4416.5	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #63	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O	4417.6	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #64	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	4425.2	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #65	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O	4462.5	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #66	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O	4463.0	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #67	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O	4452.7	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #68	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C	4481.3	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #69	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O	4450.7	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C)C(CO[Si](C)(C)C)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C	4449.3	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #70	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O	4447.0	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #71	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C	4470.0	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #72	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4474.9	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #73	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4469.4	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #74	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4482.3	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #75	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O	4447.8	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #76	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O	4441.0	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #77	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C	4465.7	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #78	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4432.8	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #79	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4435.4	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #8	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O	4426.0	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #80	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4438.3	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #81	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4439.8	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #82	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4436.6	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #83	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4448.7	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #84	C[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4450.0	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #85	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C2OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O	4446.4	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #86	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	4415.0	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #87	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	4419.1	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #88	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	4434.0	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #89	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	4433.1	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #9	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C)C2OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	4409.6	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #90	C[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C	4449.2	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #91	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(OC2OC(CO)C(O)C(O)C2O)C1O[Si](C)(C)C	4477.2	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #92	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(OC2OC(CO)C(O)C(O)C2O)C1O[Si](C)(C)C	4467.6	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #93	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C1O[Si](C)(C)C	4509.7	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #94	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C1O[Si](C)(C)C	4470.7	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #95	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C1O[Si](C)(C)C	4478.1	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #96	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(OC2OC(CO)C(O)C(O)C2O)C1O[Si](C)(C)C	4466.5	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #97	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C1O[Si](C)(C)C	4470.8	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #98	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C1O[Si](C)(C)C	4426.8	Semi standard non polar	33892256
Zizybeoside II,4TMS,isomer #99	C[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C1O[Si](C)(C)C	4439.0	Semi standard non polar	33892256
Zizybeoside II,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O	4981.6	Semi standard non polar	33892256
Zizybeoside II,1TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5037.6	Semi standard non polar	33892256
Zizybeoside II,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C1OC1OC(CO)C(O)C(O)C1O	5048.5	Semi standard non polar	33892256
Zizybeoside II,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C(OC2OC(CO)C(O)C(O)C2O)C1O	4999.2	Semi standard non polar	33892256
Zizybeoside II,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O	4981.7	Semi standard non polar	33892256
Zizybeoside II,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5038.0	Semi standard non polar	33892256
Zizybeoside II,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O)C1O	5005.6	Semi standard non polar	33892256
Zizybeoside II,1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1C(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O)OC(CO)C(O)C1O	5016.6	Semi standard non polar	33892256
Zizybeoside II,1TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1C(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)OC(CO)C(O)C1O	5018.0	Semi standard non polar	33892256
Zizybeoside II,1TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C1O	5005.1	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(O[Si](C)(C)C(C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O	5056.6	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C(OC2OC(CO)C(O)C(O)C2O)C1O[Si](C)(C)C(C)(C)C	5076.6	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C(C)(C)C)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O	5057.7	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C(C)(C)C)C2OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5135.3	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C(C)(C)C)C2OC2OC(CO)C(O)C(O)C2O)C1O	5095.4	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC1C(OC2C(OCC3=CC=CC=C3)OC(CO)C(O[Si](C)(C)C(C)(C)C)C2OC2OC(CO)C(O)C(O)C2O)OC(CO)C(O)C1O	5113.4	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2C(O[Si](C)(C)C(C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5135.2	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(OC2C(O[Si](C)(C)C(C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C1O	5094.9	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC1C(OC2C(O[Si](C)(C)C(C)(C)C)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)OC(CO)C(O)C1O	5113.7	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO[Si](C)(C)C(C)(C)C)C(O)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O	4999.1	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(OC2OC(CO)C(O)C(O)C2O)C1O	5084.7	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(O)C(CO[Si](C)(C)C(C)(C)C)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O	4998.7	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(OC2OC(CO)C(O)C(O)C2O)C1O	5035.7	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(OC2OC(CO)C(O)C(O)C2O)C1O	5045.4	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C1O	5085.4	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C1O	5035.1	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OCC1OC(OCC2=CC=CC=C2)C(OC2OC(CO)C(O)C(O)C2O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C1O	5049.8	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)C(O)C1O	5049.4	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C(O)C1O	5001.1	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O	5018.1	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	5033.0	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	5027.0	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C2O)C(O)C(O)C1O	4952.5	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	5046.1	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)C1O	5123.6	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	5090.6	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	5106.2	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	5091.3	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	5110.1	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #36	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	5090.8	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #37	CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C1O	5064.7	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #38	CC(C)(C)[Si](C)(C)OC1C(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)OC(CO)C(O)C1O	5073.7	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #39	CC(C)(C)[Si](C)(C)OC1C(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	5101.4	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)C(O)C1O	5049.2	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #40	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	5104.7	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #41	CC(C)(C)[Si](C)(C)OC1C(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)OC(CO)C(O)C1O	5071.7	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #42	CC(C)(C)[Si](C)(C)OC1C(OC2C(OCC3=CC=CC=C3)OC(CO)C(O)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)OC(CO)C(O)C1O	5091.2	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #43	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	5093.5	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #44	CC(C)(C)[Si](C)(C)OC1C(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	5103.7	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #45	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	5109.4	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C(O)C1O	5001.6	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O	5013.8	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	5036.5	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	5026.4	Semi standard non polar	33892256
Zizybeoside II,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(O)C(CO)OC(OCC3=CC=CC=C3)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	5046.3	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Zizybeoside II GC-MS (Non-derivatized) - 70eV, Positive	splash10-0hk9-3200390000-caf78280d99a1ba2954e	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Zizybeoside II GC-MS (1 TMS) - 70eV, Positive	splash10-0k9e-6410139000-e645af8c46730ffb0f40	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Zizybeoside II GC-MS ("Zizybeoside II,1TMS,#1" TMS) - 70eV, Positive	Not Available	2021-10-14	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Zizybeoside II GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Zizybeoside II GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Zizybeoside II GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Zizybeoside II GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Zizybeoside II GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Zizybeoside II GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Zizybeoside II GC-MS (TMS_1_8) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Zizybeoside II GC-MS (TMS_1_9) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Zizybeoside II GC-MS (TMS_1_10) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Zizybeoside II GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Zizybeoside II GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Zizybeoside II GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Zizybeoside II GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Zizybeoside II GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Zizybeoside II GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Zizybeoside II GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Zizybeoside II GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Zizybeoside II GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Zizybeoside II GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Zizybeoside II GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Zizybeoside II GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Zizybeoside II GC-MS (TMS_2_13) - 70eV, Positive	Not Available	2021-10-15	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 - Zizybeoside II 10V, Positive-QTOF	splash10-015c-4130940000-8a27fddf094b2fe6ede9	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Zizybeoside II 20V, Positive-QTOF	splash10-014i-5681900000-9f4de848f1a469be1890	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Zizybeoside II 40V, Positive-QTOF	splash10-014i-3291410000-eade8419c607a1bc0fc3	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Zizybeoside II 10V, Negative-QTOF	splash10-01rx-1402970000-8b8b1fd4d9527bac38b5	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Zizybeoside II 20V, Negative-QTOF	splash10-01u0-1835940000-cbceecab392a0819f8c5	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Zizybeoside II 40V, Negative-QTOF	splash10-004i-3933100000-26b5f36ae3d1c67336f7	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Zizybeoside II 10V, Negative-QTOF	splash10-0006-0000190000-d96ff1320a442b525e7d	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Zizybeoside II 20V, Negative-QTOF	splash10-0016-4100790000-fb8797e539b41f6cff8c	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Zizybeoside II 40V, Negative-QTOF	splash10-014r-5195200000-9919544b148b0579044d	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Zizybeoside II 10V, Positive-QTOF	splash10-00yi-2060930000-ee814ba06c7e6961d146	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Zizybeoside II 20V, Positive-QTOF	splash10-01b9-4460940000-ba6c2727518dc351335d	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Zizybeoside II 40V, Positive-QTOF	splash10-05g3-9321420000-6b9d417da0c4f718df7c	2021-09-22	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm
Extracellular

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB013549

KNApSAcK ID

C00058208

Chemspider ID

Not Available

KEGG Compound ID

C17565

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

73156985

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

(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .

Showing metabocard for Zizybeoside II (HMDB0034955)

MOL for HMDB0034955 (Zizybeoside II)

3D MOL for HMDB0034955 (Zizybeoside II)

3D SDF for HMDB0034955 (Zizybeoside II)

3D-SDF for HMDB0034955 (Zizybeoside II)

PDB for HMDB0034955 (Zizybeoside II)

3D PDB for HMDB0034955 (Zizybeoside II)

SMILES for HMDB0034955 (Zizybeoside II)

INCHI for HMDB0034955 (Zizybeoside II)

Structure for HMDB0034955 (Zizybeoside II)

3D Structure for HMDB0034955 (Zizybeoside II)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra