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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 17:45:03 UTC

Update Date

2022-03-07 02:53:05 UTC

HMDB ID

HMDB0031726

Secondary Accession Numbers

HMDB31726

Metabolite Identification

Common Name

cis-Mulberroside A

Description

cis-Mulberroside A, also known as diazepine, belongs to the class of organic compounds known as stilbene glycosides. Stilbene glycosides are compounds structurally characterized by the presence of a carbohydrate moiety glycosidically linked to the stilbene skeleton. Based on a literature review a significant number of articles have been published on cis-Mulberroside A.

Structure

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


  Mrv0541 05061306052D          

 40 43  0  0  0  0            999 V2000
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    4.5375    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
   -1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    7.0125    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
    0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    8.2500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.8579    5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  4  3  2  0  0  0  0
 11  1  1  0  0  0  0
 11  5  2  0  0  0  0
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 12  3  1  0  0  0  0
 13  5  1  0  0  0  0
 13  7  2  0  0  0  0
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 15  6  2  0  0  0  0
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 16  8  1  0  0  0  0
 16 12  2  0  0  0  0
 17  9  1  0  0  0  0
 18 10  1  0  0  0  0
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 27  9  1  0  0  0  0
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 38 15  1  0  0  0  0
 38 26  1  0  0  0  0
 39 17  1  0  0  0  0
 39 25  1  0  0  0  0
 40 18  1  0  0  0  0
 40 26  1  0  0  0  0
M  END

HMDB0031726
     RDKit          3D
cis-Mulberroside A
 72 75  0  0  0  0  0  0  0  0999 V2000
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    5.8626    0.4416   -0.0208 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7913    1.0762   -0.6293 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.8632   -0.1074   -1.1675 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2348    1.1130   -1.6405 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.7838    2.3937   -2.0086 C   0  0  0  0  0  0  0  0  0  0  0  0
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 40 72  1  0
M  END


  Mrv0541 05061306052D          

 40 43  0  0  0  0            999 V2000
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 13  5  1  0  0  0  0
 13  7  2  0  0  0  0
 14  4  1  0  0  0  0
 14  8  2  0  0  0  0
 15  6  2  0  0  0  0
 15  7  1  0  0  0  0
 16  8  1  0  0  0  0
 16 12  2  0  0  0  0
 17  9  1  0  0  0  0
 18 10  1  0  0  0  0
 19 17  1  0  0  0  0
 20 18  1  0  0  0  0
 21 19  1  0  0  0  0
 22 20  1  0  0  0  0
 23 21  1  0  0  0  0
 24 22  1  0  0  0  0
 25 23  1  0  0  0  0
 26 24  1  0  0  0  0
 27  9  1  0  0  0  0
 28 10  1  0  0  0  0
 29 13  1  0  0  0  0
 30 16  1  0  0  0  0
 31 19  1  0  0  0  0
 32 20  1  0  0  0  0
 33 21  1  0  0  0  0
 34 22  1  0  0  0  0
 35 23  1  0  0  0  0
 36 24  1  0  0  0  0
 37 14  1  0  0  0  0
 37 25  1  0  0  0  0
 38 15  1  0  0  0  0
 38 26  1  0  0  0  0
 39 17  1  0  0  0  0
 39 25  1  0  0  0  0
 40 18  1  0  0  0  0
 40 26  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0031726

> <DATABASE_NAME>
hmdb

> <SMILES>
OCC1OC(OC2=CC(O)=C(\C=C/C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C=C2)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C26H32O14/c27-9-17-19(31)21(33)23(35)25(39-17)37-14-4-3-12(16(30)8-14)2-1-11-5-13(29)7-15(6-11)38-26-24(36)22(34)20(32)18(10-28)40-26/h1-8,17-36H,9-10H2/b2-1-

> <INCHI_KEY>
HPSWAEGGWLOOKT-UPHRSURJSA-N

> <FORMULA>
C26H32O14

> <MOLECULAR_WEIGHT>
568.5239

> <EXACT_MASS>
568.179205732

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_AVERAGE_POLARIZABILITY>
55.775681082593564

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
10

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <ALOGPS_LOGP>
-0.70

> <JCHEM_LOGP>
-1.4373106219999991

> <ALOGPS_LOGS>
-2.64

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.560689786696871

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.94685640416481

> <JCHEM_PKA_STRONGEST_BASIC>
-3.648395345694367

> <JCHEM_POLAR_SURFACE_AREA>
239.21999999999994

> <JCHEM_REFRACTIVITY>
133.72519999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.30e+00 g/l

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

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0031726
     RDKit          3D
cis-Mulberroside A
 72 75  0  0  0  0  0  0  0  0999 V2000
    8.4136   -1.8527   -2.3132 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9577   -1.0206   -1.3349 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9100   -0.5779   -0.3393 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8846    0.1209   -0.9144 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8626    0.4416   -0.0208 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7913    1.0762   -0.6293 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4899    0.6357   -0.7835 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0644   -0.5843   -0.3225 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7373   -0.9567   -0.5181 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2970   -2.1924   -0.0541 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8632   -0.1074   -1.1675 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2348    1.1130   -1.6405 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4381    2.1353   -2.2438 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7838    2.3937   -2.0086 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6753    1.7806   -1.0879 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3253    1.3033    0.1416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2323    0.6519    0.9312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5537    0.4652    0.4828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4442   -0.1953    1.3017 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7889   -0.4829    1.0607 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8902   -1.8937    1.0213 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1229   -2.3350    0.6075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4182   -2.0989   -0.8449 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5053   -2.7319   -1.6745 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2664   -1.8271    1.4533 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4285   -1.9707    0.7037 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1044   -0.3758    1.8200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3397    0.4290    0.6976 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6677   -0.0894    2.2584 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5122    1.2519    2.5249 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9325    0.9365   -0.7466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0112    1.5894   -1.5342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4551    2.0386   -2.7637 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5702    1.4502   -1.4277 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3870    1.2577    1.1461 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8459    2.5127    0.7423 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4827    0.5214    1.8484 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9873   -0.6548    2.4313 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5251    0.1308    0.8440 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1848    1.2673    0.3744 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9406   -1.8879   -3.1337 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4137   -0.1604   -1.8680 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7578   -1.6031   -0.8366 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4653   -1.5313    0.0762 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5372   -0.5218    0.4062 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7393   -1.2674    0.1912 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9522   -2.7968    0.4170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1499   -0.4573   -1.3542 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9914    2.7664   -3.0308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2078    3.2582   -2.6227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3251    1.4861    0.5272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9337    0.2863    1.8881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2118   -0.1284    0.1248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1139   -3.4484    0.7458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4232   -2.5677   -1.0517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5192   -1.0497   -1.1294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4107   -2.1917   -2.4976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4011   -2.4280    2.3717 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1655   -1.5797    1.1998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8278   -0.1576    2.6246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0653    1.0880    0.9021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4084   -0.7664    3.0723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9994    1.3444    3.3542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9632    0.7852   -1.0823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8351    2.5071   -3.3806 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9349    2.4004   -1.7770 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5723    1.4248    1.8790 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0986    2.4321   -0.2205 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9084    1.1225    2.6607 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7643   -0.4773    3.3985 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2727   -0.4987    1.3640 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1425    1.0626    0.1364 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  2  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 22 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 18 31  1  0
 31 32  2  0
 32 33  1  0
 12 34  2  0
  5 35  1  0
 35 36  1  0
 35 37  1  0
 37 38  1  0
 37 39  1  0
 39 40  1  0
 39  3  1  0
 34  7  1  0
 32 15  1  0
 29 20  1  0
  1 41  1  0
  2 42  1  0
  2 43  1  0
  3 44  1  0
  5 45  1  0
  8 46  1  0
 10 47  1  0
 11 48  1  0
 13 49  1  0
 14 50  1  0
 16 51  1  0
 17 52  1  0
 20 53  1  0
 22 54  1  0
 23 55  1  0
 23 56  1  0
 24 57  1  0
 25 58  1  0
 26 59  1  0
 27 60  1  0
 28 61  1  0
 29 62  1  0
 30 63  1  0
 31 64  1  0
 33 65  1  0
 34 66  1  0
 35 67  1  0
 36 68  1  0
 37 69  1  0
 38 70  1  0
 39 71  1  0
 40 72  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      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334   6.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334   8.470   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      -2.667   6.160   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -5.335   6.160   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334   8.470   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335  10.780   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -6.668  13.090   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -5.335   4.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.000   9.240   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.001   6.930   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334   6.930   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.001  11.550   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -6.668  11.550   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.001  13.090   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -8.002  10.780   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.667  13.860   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -8.002   9.240   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.334  13.090   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -6.668   8.470   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.334  11.550   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -5.335   9.240   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       6.668  11.550   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      -8.002  13.860   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      -6.668   3.850   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       2.667   6.160   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       5.335  13.860   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      -9.336  11.550   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       2.667  15.400   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      -9.336   8.470   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0       0.000  13.860   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      -6.668   6.930   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       0.000  10.780   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      -4.001   8.470   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0       2.667  10.780   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      -5.335  10.780   0.000  0.00  0.00           O+0
CONECT    1    2   11                                                       
CONECT    2    1   12                                                       
CONECT    3    4   12                                                       
CONECT    4    3   14                                                       
CONECT    5   11   13                                                       
CONECT    6   11   15                                                       
CONECT    7   13   15                                                       
CONECT    8   14   16                                                       
CONECT    9   17   27                                                       
CONECT   10   18   28                                                       
CONECT   11    1    5    6                                                  
CONECT   12    2    3   16                                                  
CONECT   13    5    7   29                                                  
CONECT   14    4    8   37                                                  
CONECT   15    6    7   38                                                  
CONECT   16    8   12   30                                                  
CONECT   17    9   19   39                                                  
CONECT   18   10   20   40                                                  
CONECT   19   17   21   31                                                  
CONECT   20   18   22   32                                                  
CONECT   21   19   23   33                                                  
CONECT   22   20   24   34                                                  
CONECT   23   21   25   35                                                  
CONECT   24   22   26   36                                                  
CONECT   25   23   37   39                                                  
CONECT   26   24   38   40                                                  
CONECT   27    9                                                            
CONECT   28   10                                                            
CONECT   29   13                                                            
CONECT   30   16                                                            
CONECT   31   19                                                            
CONECT   32   20                                                            
CONECT   33   21                                                            
CONECT   34   22                                                            
CONECT   35   23                                                            
CONECT   36   24                                                            
CONECT   37   14   25                                                       
CONECT   38   15   26                                                       
CONECT   39   17   25                                                       
CONECT   40   18   26                                                       
MASTER        0    0    0    0    0    0    0    0   40    0   86    0
END

COMPND    HMDB0031726
HETATM    1  O1  UNL     1       8.414  -1.853  -2.313  1.00  0.00           O  
HETATM    2  C1  UNL     1       8.958  -1.021  -1.335  1.00  0.00           C  
HETATM    3  C2  UNL     1       7.910  -0.578  -0.339  1.00  0.00           C  
HETATM    4  O2  UNL     1       6.885   0.121  -0.914  1.00  0.00           O  
HETATM    5  C3  UNL     1       5.863   0.442  -0.021  1.00  0.00           C  
HETATM    6  O3  UNL     1       4.791   1.076  -0.629  1.00  0.00           O  
HETATM    7  C4  UNL     1       3.490   0.636  -0.783  1.00  0.00           C  
HETATM    8  C5  UNL     1       3.064  -0.584  -0.322  1.00  0.00           C  
HETATM    9  C6  UNL     1       1.737  -0.957  -0.518  1.00  0.00           C  
HETATM   10  O4  UNL     1       1.297  -2.192  -0.054  1.00  0.00           O  
HETATM   11  C7  UNL     1       0.863  -0.107  -1.168  1.00  0.00           C  
HETATM   12  C8  UNL     1       1.235   1.113  -1.641  1.00  0.00           C  
HETATM   13  C9  UNL     1       0.438   2.135  -2.244  1.00  0.00           C  
HETATM   14  C10 UNL     1      -0.784   2.394  -2.009  1.00  0.00           C  
HETATM   15  C11 UNL     1      -1.675   1.781  -1.088  1.00  0.00           C  
HETATM   16  C12 UNL     1      -1.325   1.303   0.142  1.00  0.00           C  
HETATM   17  C13 UNL     1      -2.232   0.652   0.931  1.00  0.00           C  
HETATM   18  C14 UNL     1      -3.554   0.465   0.483  1.00  0.00           C  
HETATM   19  O5  UNL     1      -4.444  -0.195   1.302  1.00  0.00           O  
HETATM   20  C15 UNL     1      -5.789  -0.483   1.061  1.00  0.00           C  
HETATM   21  O6  UNL     1      -5.890  -1.894   1.021  1.00  0.00           O  
HETATM   22  C16 UNL     1      -7.123  -2.335   0.608  1.00  0.00           C  
HETATM   23  C17 UNL     1      -7.418  -2.099  -0.845  1.00  0.00           C  
HETATM   24  O7  UNL     1      -6.505  -2.732  -1.675  1.00  0.00           O  
HETATM   25  C18 UNL     1      -8.266  -1.827   1.453  1.00  0.00           C  
HETATM   26  O8  UNL     1      -9.429  -1.971   0.704  1.00  0.00           O  
HETATM   27  C19 UNL     1      -8.104  -0.376   1.820  1.00  0.00           C  
HETATM   28  O9  UNL     1      -8.340   0.429   0.698  1.00  0.00           O  
HETATM   29  C20 UNL     1      -6.668  -0.089   2.258  1.00  0.00           C  
HETATM   30  O10 UNL     1      -6.512   1.252   2.525  1.00  0.00           O  
HETATM   31  C21 UNL     1      -3.932   0.936  -0.747  1.00  0.00           C  
HETATM   32  C22 UNL     1      -3.011   1.589  -1.534  1.00  0.00           C  
HETATM   33  O11 UNL     1      -3.455   2.039  -2.764  1.00  0.00           O  
HETATM   34  C23 UNL     1       2.570   1.450  -1.428  1.00  0.00           C  
HETATM   35  C24 UNL     1       6.387   1.258   1.146  1.00  0.00           C  
HETATM   36  O12 UNL     1       6.846   2.513   0.742  1.00  0.00           O  
HETATM   37  C25 UNL     1       7.483   0.521   1.848  1.00  0.00           C  
HETATM   38  O13 UNL     1       6.987  -0.655   2.431  1.00  0.00           O  
HETATM   39  C26 UNL     1       8.525   0.131   0.844  1.00  0.00           C  
HETATM   40  O14 UNL     1       9.185   1.267   0.374  1.00  0.00           O  
HETATM   41  H1  UNL     1       8.941  -1.888  -3.134  1.00  0.00           H  
HETATM   42  H2  UNL     1       9.414  -0.160  -1.868  1.00  0.00           H  
HETATM   43  H3  UNL     1       9.758  -1.603  -0.837  1.00  0.00           H  
HETATM   44  H4  UNL     1       7.465  -1.531   0.076  1.00  0.00           H  
HETATM   45  H5  UNL     1       5.537  -0.522   0.406  1.00  0.00           H  
HETATM   46  H6  UNL     1       3.739  -1.267   0.191  1.00  0.00           H  
HETATM   47  H7  UNL     1       1.952  -2.797   0.417  1.00  0.00           H  
HETATM   48  H8  UNL     1      -0.150  -0.457  -1.354  1.00  0.00           H  
HETATM   49  H9  UNL     1       0.991   2.766  -3.031  1.00  0.00           H  
HETATM   50  H10 UNL     1      -1.208   3.258  -2.623  1.00  0.00           H  
HETATM   51  H11 UNL     1      -0.325   1.486   0.527  1.00  0.00           H  
HETATM   52  H12 UNL     1      -1.934   0.286   1.888  1.00  0.00           H  
HETATM   53  H13 UNL     1      -6.212  -0.128   0.125  1.00  0.00           H  
HETATM   54  H14 UNL     1      -7.114  -3.448   0.746  1.00  0.00           H  
HETATM   55  H15 UNL     1      -8.423  -2.568  -1.052  1.00  0.00           H  
HETATM   56  H16 UNL     1      -7.519  -1.050  -1.129  1.00  0.00           H  
HETATM   57  H17 UNL     1      -6.411  -2.192  -2.498  1.00  0.00           H  
HETATM   58  H18 UNL     1      -8.401  -2.428   2.372  1.00  0.00           H  
HETATM   59  H19 UNL     1     -10.166  -1.580   1.200  1.00  0.00           H  
HETATM   60  H20 UNL     1      -8.828  -0.158   2.625  1.00  0.00           H  
HETATM   61  H21 UNL     1      -9.065   1.088   0.902  1.00  0.00           H  
HETATM   62  H22 UNL     1      -6.408  -0.766   3.072  1.00  0.00           H  
HETATM   63  H23 UNL     1      -5.999   1.344   3.354  1.00  0.00           H  
HETATM   64  H24 UNL     1      -4.963   0.785  -1.082  1.00  0.00           H  
HETATM   65  H25 UNL     1      -2.835   2.507  -3.381  1.00  0.00           H  
HETATM   66  H26 UNL     1       2.935   2.400  -1.777  1.00  0.00           H  
HETATM   67  H27 UNL     1       5.572   1.425   1.879  1.00  0.00           H  
HETATM   68  H28 UNL     1       7.099   2.432  -0.220  1.00  0.00           H  
HETATM   69  H29 UNL     1       7.908   1.122   2.661  1.00  0.00           H  
HETATM   70  H30 UNL     1       6.764  -0.477   3.399  1.00  0.00           H  
HETATM   71  H31 UNL     1       9.273  -0.499   1.364  1.00  0.00           H  
HETATM   72  H32 UNL     1      10.142   1.063   0.136  1.00  0.00           H  
CONECT    1    2   41
CONECT    2    3   42   43
CONECT    3    4   39   44
CONECT    4    5
CONECT    5    6   35   45
CONECT    6    7
CONECT    7    8    8   34
CONECT    8    9   46
CONECT    9   10   11   11
CONECT   10   47
CONECT   11   12   48
CONECT   12   13   34   34
CONECT   13   14   14   49
CONECT   14   15   50
CONECT   15   16   16   32
CONECT   16   17   51
CONECT   17   18   18   52
CONECT   18   19   31
CONECT   19   20
CONECT   20   21   29   53
CONECT   21   22
CONECT   22   23   25   54
CONECT   23   24   55   56
CONECT   24   57
CONECT   25   26   27   58
CONECT   26   59
CONECT   27   28   29   60
CONECT   28   61
CONECT   29   30   62
CONECT   30   63
CONECT   31   32   32   64
CONECT   32   33
CONECT   33   65
CONECT   34   66
CONECT   35   36   37   67
CONECT   36   68
CONECT   37   38   39   69
CONECT   38   70
CONECT   39   40   71
CONECT   40   72
END

HMDB0031726
     RDKit          3D
cis-Mulberroside A
 72 75  0  0  0  0  0  0  0  0999 V2000
    8.4136   -1.8527   -2.3132 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9577   -1.0206   -1.3349 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9100   -0.5779   -0.3393 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8846    0.1209   -0.9144 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8626    0.4416   -0.0208 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7913    1.0762   -0.6293 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4899    0.6357   -0.7835 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0644   -0.5843   -0.3225 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7373   -0.9567   -0.5181 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2970   -2.1924   -0.0541 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8632   -0.1074   -1.1675 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2348    1.1130   -1.6405 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4381    2.1353   -2.2438 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7838    2.3937   -2.0086 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6753    1.7806   -1.0879 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3253    1.3033    0.1416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2323    0.6519    0.9312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5537    0.4652    0.4828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4442   -0.1953    1.3017 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7889   -0.4829    1.0607 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8902   -1.8937    1.0213 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1229   -2.3350    0.6075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4182   -2.0989   -0.8449 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5053   -2.7319   -1.6745 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2664   -1.8271    1.4533 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4285   -1.9707    0.7037 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1044   -0.3758    1.8200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3397    0.4290    0.6976 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6677   -0.0894    2.2584 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5122    1.2519    2.5249 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9325    0.9365   -0.7466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0112    1.5894   -1.5342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4551    2.0386   -2.7637 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5702    1.4502   -1.4277 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3870    1.2577    1.1461 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8459    2.5127    0.7423 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4827    0.5214    1.8484 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9873   -0.6548    2.4313 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5251    0.1308    0.8440 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1848    1.2673    0.3744 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9406   -1.8879   -3.1337 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4137   -0.1604   -1.8680 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7578   -1.6031   -0.8366 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4653   -1.5313    0.0762 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5372   -0.5218    0.4062 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7393   -1.2674    0.1912 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9522   -2.7968    0.4170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1499   -0.4573   -1.3542 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9914    2.7664   -3.0308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2078    3.2582   -2.6227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3251    1.4861    0.5272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9337    0.2863    1.8881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2118   -0.1284    0.1248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1139   -3.4484    0.7458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4232   -2.5677   -1.0517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5192   -1.0497   -1.1294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4107   -2.1917   -2.4976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4011   -2.4280    2.3717 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1655   -1.5797    1.1998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8278   -0.1576    2.6246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0653    1.0880    0.9021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4084   -0.7664    3.0723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9994    1.3444    3.3542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9632    0.7852   -1.0823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8351    2.5071   -3.3806 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9349    2.4004   -1.7770 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5723    1.4248    1.8790 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0986    2.4321   -0.2205 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9084    1.1225    2.6607 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7643   -0.4773    3.3985 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2727   -0.4987    1.3640 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1425    1.0626    0.1364 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  2  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 22 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 18 31  1  0
 31 32  2  0
 32 33  1  0
 12 34  2  0
  5 35  1  0
 35 36  1  0
 35 37  1  0
 37 38  1  0
 37 39  1  0
 39 40  1  0
 39  3  1  0
 34  7  1  0
 32 15  1  0
 29 20  1  0
  1 41  1  0
  2 42  1  0
  2 43  1  0
  3 44  1  0
  5 45  1  0
  8 46  1  0
 10 47  1  0
 11 48  1  0
 13 49  1  0
 14 50  1  0
 16 51  1  0
 17 52  1  0
 20 53  1  0
 22 54  1  0
 23 55  1  0
 23 56  1  0
 24 57  1  0
 25 58  1  0
 26 59  1  0
 27 60  1  0
 28 61  1  0
 29 62  1  0
 30 63  1  0
 31 64  1  0
 33 65  1  0
 34 66  1  0
 35 67  1  0
 36 68  1  0
 37 69  1  0
 38 70  1  0
 39 71  1  0
 40 72  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
Diazepine	HMDB

Chemical Formula

C₂₆H₃₂O₁₄

Average Molecular Weight

568.5239

Monoisotopic Molecular Weight

568.179205732

IUPAC Name

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

Traditional Name

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

CAS Registry Number

166734-06-1

SMILES

OCC1OC(OC2=CC(O)=C(\C=C/C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C=C2)C(O)C(O)C1O

InChI Identifier

InChI=1S/C26H32O14/c27-9-17-19(31)21(33)23(35)25(39-17)37-14-4-3-12(16(30)8-14)2-1-11-5-13(29)7-15(6-11)38-26-24(36)22(34)20(32)18(10-28)40-26/h1-8,17-36H,9-10H2/b2-1-

InChI Key

HPSWAEGGWLOOKT-UPHRSURJSA-N

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Stilbenes

Sub Class

Stilbene glycosides

Direct Parent

Stilbene glycosides

Alternative Parents

Substituents

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

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Extracellular (HMDB: HMDB0031726)
Cytoplasm (HMDB: HMDB0031726)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0031726)

Source

Endogenous

Endogenous (HMDB: HMDB0031726)

Plant

Plant (HMDB: HMDB0031726)

Exogenous

Food

Food (HMDB: HMDB0031726)

Fruit

Fruits (FooDB: FOOD00871)

Exogenous (HMDB: HMDB0031726)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	35340 mg/L @ 25 °C (est)	The Good Scents Company Information System
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	1.3 g/L	ALOGPS
logP	-0.7	ALOGPS
logP	-1.4	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	8.95	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	10	ChemAxon
Polar Surface Area	239.22 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	133.73 m³·mol⁻¹	ChemAxon
Polarizability	55.78 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
DeepCCS	[M+H]+	225.767	30932474
DeepCCS	[M-H]-	223.372	30932474
DeepCCS	[M-2H]-	256.257	30932474
DeepCCS	[M+Na]+	231.68	30932474
AllCCS	[M+H]+	227.1	32859911
AllCCS	[M+H-H2O]+	225.8	32859911
AllCCS	[M+NH4]+	228.4	32859911
AllCCS	[M+Na]+	228.7	32859911
AllCCS	[M-H]-	218.9	32859911
AllCCS	[M+Na-2H]-	221.0	32859911
AllCCS	[M+HCOO]-	223.5	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.	3.59 minutes	32390414
Predicted by Siyang on May 30, 2022	10.94 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	5.95 minutes	32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid	270.6 seconds	40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	1265.8 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	206.3 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	98.3 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	187.9 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	76.2 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	360.8 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	373.2 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	806.0 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	678.9 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	296.3 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	1064.1 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	222.2 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	263.9 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	530.4 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	397.5 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	203.6 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
cis-Mulberroside A	OCC1OC(OC2=CC(O)=C(\C=C/C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C=C2)C(O)C(O)C1O	6237.2	Standard polar	33892256
cis-Mulberroside A	OCC1OC(OC2=CC(O)=C(\C=C/C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C=C2)C(O)C(O)C1O	5409.2	Standard non polar	33892256
cis-Mulberroside A	OCC1OC(OC2=CC(O)=C(\C=C/C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C=C2)C(O)C(O)C1O	5358.2	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
cis-Mulberroside A,1TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O)=C2)C(O)C(O)C1O	5230.7	Semi standard non polar	33892256
cis-Mulberroside A,1TMS,isomer #10	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O)=C2)C(O)C1O	5257.5	Semi standard non polar	33892256
cis-Mulberroside A,1TMS,isomer #2	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5260.7	Semi standard non polar	33892256
cis-Mulberroside A,1TMS,isomer #3	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O)C=C2O)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5294.5	Semi standard non polar	33892256
cis-Mulberroside A,1TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=C2)C(O)C(O)C1O	5230.3	Semi standard non polar	33892256
cis-Mulberroside A,1TMS,isomer #5	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=C2)C(O)C1O	5257.5	Semi standard non polar	33892256
cis-Mulberroside A,1TMS,isomer #6	C[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=C2)C1O	5245.9	Semi standard non polar	33892256
cis-Mulberroside A,1TMS,isomer #7	C[Si](C)(C)OC1C(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=C2)OC(CO)C(O)C1O	5268.9	Semi standard non polar	33892256
cis-Mulberroside A,1TMS,isomer #8	C[Si](C)(C)OC1C(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O)=C2)OC(CO)C(O)C1O	5271.3	Semi standard non polar	33892256
cis-Mulberroside A,1TMS,isomer #9	C[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O)=C2)C1O	5246.7	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O)C(O)C4O)=CC(O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O)C1O	5152.9	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #10	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5133.8	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #11	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5113.8	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #12	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5157.4	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #13	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O)C=C2O[Si](C)(C)C)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5165.0	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #14	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O[Si](C)(C)C)=C2)C(O)C(O)C1O	5123.7	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #15	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=C1	5134.0	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #16	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=C1	5112.7	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #17	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=C1	5156.0	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #18	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C=C2O)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5161.5	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #19	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C=C2O)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5145.3	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O)C=C3O)=C2)C(O)C(O)C1O	5138.1	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #20	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C=C2O)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5184.1	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #21	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=CC(O[Si](C)(C)C)=C2)C(O)C(O)C1O	5153.0	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #22	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O)C=C2O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=C1	5161.5	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #23	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O)C=C2O)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=C1	5148.0	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #24	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O)C=C2O)=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=C1	5184.5	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #25	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O)=C2)C(O)C(O)C1O	5146.9	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #26	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O)=C2)C(O)C(O)C1O	5138.8	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #27	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O)=C2)C(O)C(O)C1O	5176.4	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #28	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=C2)C(O[Si](C)(C)C)C(O)C1O	5188.7	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #29	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=C2)C(O)C(O[Si](C)(C)C)C1O	5158.0	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)=C3)C(O)=C2)C(O)C(O)C1O	5146.7	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #30	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=C2)C(O)C(O)C1O[Si](C)(C)C	5166.0	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #31	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O)=C2)C(O)C1O	5152.8	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #32	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O)=C2)C(O)C1O	5136.6	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #33	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O)=C2)C(O)C1O	5184.8	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #34	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=C2)C(O[Si](C)(C)C)C1O	5188.3	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #35	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=C2)C(O)C1O[Si](C)(C)C	5169.3	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #36	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)=C3)C(O)=C2)C(O)C1O	5136.6	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #37	C[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O)=C2)C1O	5119.6	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #38	C[Si](C)(C)OC1C(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)=C3)C(O)=C2)OC(CO)C(O)C1O	5166.8	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #39	C[Si](C)(C)OC1C(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=C2)OC(CO)C(O)C1O[Si](C)(C)C	5197.6	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)=C3)C(O)=C2)C(O)C(O)C1O	5138.5	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #40	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)=C3)C(O)=C2)C(O)C1O	5184.0	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #41	C[Si](C)(C)OC1C(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O)=C2)OC(CO)C(O)C1O	5166.2	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #42	C[Si](C)(C)OC1C(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O)=C2)OC(CO)C(O)C1O	5208.8	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #43	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O)=C2)C(O[Si](C)(C)C)C1O	5189.2	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #44	C[Si](C)(C)OC1C(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O)=C2)OC(CO)C(O)C1O[Si](C)(C)C	5199.4	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #45	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O)=C2)C(O)C1O[Si](C)(C)C	5168.3	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O)C1O	5174.9	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O	5123.2	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O	5188.9	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #8	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O	5158.5	Semi standard non polar	33892256
cis-Mulberroside A,2TMS,isomer #9	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C	5165.6	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O)C=C3O)=CC(O[Si](C)(C)C)=C2)C(O)C(O)C1O	5046.3	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #10	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C4O)C=C3O)=C2)C(O)C(O)C1O	5054.0	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #100	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5077.6	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #101	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O)=C2)C(O)C1O	5067.7	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #102	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O)=C2)C(O)C1O	5095.8	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #103	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=C3)C(O)=C2)C(O)C1O	5094.5	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #104	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C3)C(O)=C2)C(O)C1O	5067.7	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #105	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O)=C2)C(O)C1O	5106.6	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #106	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O)=C2)C(O[Si](C)(C)C)C1O	5071.7	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #107	C[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C3)C(O)=C2)C1O	5043.7	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #108	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O)=C2)C(O[Si](C)(C)C)C1O	5114.4	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #109	C[Si](C)(C)OC1C(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C3)C(O)=C2)OC(CO)C(O)C1O	5087.1	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #11	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O[Si](C)(C)C)C=C3O)=C2)C(O)C(O)C1O	5099.1	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #110	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=C2)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5129.7	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #111	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C3)C(O)=C2)C(O)C1O	5104.1	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #112	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)=C3)C(O)=C2)C(O[Si](C)(C)C)C1O	5072.5	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #113	C[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O)=C2)C1O	5042.9	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #114	C[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O)=C2)C1O	5083.3	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #115	C[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C3)C(O)=C2)C1O	5081.4	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #116	C[Si](C)(C)OC1C(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C3)C(O)=C2)OC(CO)C(O)C1O	5125.5	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #117	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)=C3)C(O)=C2)C(O[Si](C)(C)C)C1O	5114.0	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #118	C[Si](C)(C)OC1C(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O)=C2)OC(CO)C(O)C1O	5085.2	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #119	C[Si](C)(C)OC1C(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O)=C2)OC(CO)C(O)C1O	5125.8	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #12	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O)C=C3O[Si](C)(C)C)=C2)C(O)C(O)C1O	4999.7	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #120	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O)=C2)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5130.6	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #13	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O)C1O	5099.4	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #14	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C4O)=C3)C(O)=C2)C(O)C(O)C1O	5055.2	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #15	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C4O)=C3)C(O)=C2)C(O)C(O)C1O	5071.4	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #16	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C3)C(O)=C2)C(O)C(O)C1O	5059.0	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #17	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O)C1O	5083.0	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #18	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)=C3)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O	5026.4	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #19	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)=C3)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O	5105.5	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)=CC(O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O)C1O	5071.4	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #20	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)=C3)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O	5062.5	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #21	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)=C3)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C	5079.6	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #22	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O)C1O	5095.0	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #23	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)=C3)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4997.6	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #24	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)=C3)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O	5082.6	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #25	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)=C3)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O	5039.8	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #26	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)=C3)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C	5057.9	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #27	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)=C3)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O	5039.1	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #28	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)=C3)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O	5126.2	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #29	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O	5083.7	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)=CC(O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O)C1O	5053.8	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #30	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C	5101.4	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #31	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O	5064.3	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #32	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O	5022.3	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #33	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C	5040.4	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #34	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5107.4	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #35	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5120.3	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #36	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5074.7	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #37	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5039.8	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #38	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5064.2	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #39	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C=C2O[Si](C)(C)C)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5058.0	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O)C1O	5093.5	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #40	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O[Si](C)(C)C)=C2)C(O)C(O)C1O	5026.4	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #41	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=C1	5048.3	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #42	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=C1	5013.8	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #43	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=C1	5060.0	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #44	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5075.8	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #45	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C=C2O[Si](C)(C)C)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5019.5	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #46	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O[Si](C)(C)C)=C2)C(O)C(O)C1O	4998.2	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #47	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=C1	5014.7	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #48	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=C1	4975.8	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #49	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=C1	5028.3	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O)C(O)C4O)=CC(O[Si](C)(C)C)=C3)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O	5031.0	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #50	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C=C2O[Si](C)(C)C)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5075.9	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #51	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O[Si](C)(C)C)=C2)C(O)C(O)C1O	5041.1	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #52	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=C1	5062.3	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #53	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=C1	5030.2	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #54	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=C1	5075.9	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #55	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C(O)C(O)C1O	5030.8	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #56	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O)C=C2O[Si](C)(C)C)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=C1	5057.9	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #57	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O)C=C2O[Si](C)(C)C)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=C1	5021.8	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #58	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O)C=C2O[Si](C)(C)C)=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=C1	5075.6	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #59	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O	5063.1	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O)C(O)C4O)=CC(O[Si](C)(C)C)=C3)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O	5110.5	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #60	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O	5022.4	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #61	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O[Si](C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C	5041.8	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #62	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=C1	5039.6	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #63	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=C1	5062.6	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #64	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=C1	5073.3	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #65	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C=C2O)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5082.1	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #66	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C=C2O)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5108.9	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #67	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O)=CC(O[Si](C)(C)C)=C2)C(O)C(O)C1O	5071.4	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #68	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C=C2O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=C1	5090.4	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #69	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C=C2O)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=C1	5067.7	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O)C(O)C4O)=CC(O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O	5070.9	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #70	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C=C2O)=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=C1	5107.7	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #71	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C=C2O)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5118.9	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #72	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O)=CC(O[Si](C)(C)C)=C2)C(O)C(O)C1O	5050.9	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #73	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C=C2O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=C1	5064.6	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #74	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C=C2O)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=C1	5037.3	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #75	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C=C2O)=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=C1	5085.1	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #76	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O)=CC(O[Si](C)(C)C)=C2)C(O)C(O)C1O	5092.5	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #77	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C=C2O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=C1	5107.8	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #78	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C=C2O)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=C1	5087.6	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #79	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C=C2O)=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=C1	5126.7	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #8	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O)C(O)C4O)=CC(O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C	5086.9	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #80	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=CC(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O	5112.0	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #81	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=CC(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O	5075.9	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #82	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=CC(O[Si](C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C	5087.8	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #83	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O)C=C2O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=C1	5086.1	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #84	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O)C=C2O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=C1	5110.5	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #85	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O)C=C2O)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=C1	5119.0	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #86	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O)=C2)C(O)C(O)C1O	5057.6	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #87	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O)=C2)C(O)C(O)C1O	5083.6	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #88	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O)=C2)C(O[Si](C)(C)C)C(O)C1O	5103.7	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #89	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O)=C2)C(O)C(O[Si](C)(C)C)C1O	5062.6	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #9	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C4O)C=C3O)=C2)C(O)C(O)C1O	5071.3	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #90	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O)=C2)C(O)C(O)C1O[Si](C)(C)C	5079.4	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #91	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O)=C2)C(O)C(O)C1O	5096.1	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #92	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O)=C2)C(O[Si](C)(C)C)C(O)C1O	5081.2	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #93	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O)=C2)C(O)C(O[Si](C)(C)C)C1O	5039.6	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #94	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O)=C2)C(O)C(O)C1O[Si](C)(C)C	5057.9	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #95	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O)=C2)C(O[Si](C)(C)C)C(O)C1O	5126.4	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #96	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O)=C2)C(O)C(O[Si](C)(C)C)C1O	5084.8	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #97	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O)=C2)C(O)C(O)C1O[Si](C)(C)C	5102.5	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #98	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5107.0	Semi standard non polar	33892256
cis-Mulberroside A,3TMS,isomer #99	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5119.1	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C4O)C=C3O)=CC(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4944.9	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #10	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)=CC(O[Si](C)(C)C)=C3)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4910.0	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #100	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O	4936.0	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #101	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O	4887.3	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #102	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O[Si](C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C	4918.2	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #103	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=C1	4911.4	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #104	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=C1	4927.4	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #105	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=C1	4932.1	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #106	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C=C2O[Si](C)(C)C)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	4939.9	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #107	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O[Si](C)(C)C)=C2)C(O)C(O)C1O	4911.3	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #108	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=C1	4934.3	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #109	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=C1	4889.4	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #11	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)=CC(O[Si](C)(C)C)=C3)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O	4983.2	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #110	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=C1	4945.6	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #111	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4865.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #112	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C=C2O[Si](C)(C)C)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=C1	4893.8	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #113	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C=C2O[Si](C)(C)C)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=C1	4848.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #114	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C=C2O[Si](C)(C)C)=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=C1	4896.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #115	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O	4896.0	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #116	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O	4846.0	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #117	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O[Si](C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C	4879.3	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #118	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=C1	4864.4	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #119	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=C1	4884.7	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #12	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)=CC(O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O	4940.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #120	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=C1	4887.6	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #121	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4917.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #122	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C=C2O[Si](C)(C)C)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=C1	4951.6	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #123	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C=C2O[Si](C)(C)C)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=C1	4898.3	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #124	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C=C2O[Si](C)(C)C)=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=C1	4962.4	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #125	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O	4949.2	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #126	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O	4900.9	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #127	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O[Si](C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C	4926.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #128	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=C1	4920.9	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #129	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=C1	4939.4	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #13	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)=CC(O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C	4961.0	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #130	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=C1	4944.7	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #131	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O	4943.7	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #132	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O	4888.8	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #133	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C	4921.8	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #134	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O)C=C2O[Si](C)(C)C)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=C1	4912.4	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #135	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O)C=C2O[Si](C)(C)C)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=C1	4931.0	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #136	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O)C=C2O[Si](C)(C)C)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=C1	4939.1	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #137	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4937.0	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #138	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4955.6	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #139	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4920.0	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #14	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O)C1O	4961.0	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #140	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=C1	4959.2	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #141	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C=C2O)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5001.9	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #142	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O)=CC(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4936.0	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #143	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C=C2O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=C1	4954.2	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #144	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C=C2O)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=C1	4920.6	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #145	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C=C2O)=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=C1	4969.7	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #146	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O)=CC(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4953.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #147	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C=C2O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=C1	4974.1	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #148	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C=C2O)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=C1	4943.7	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #149	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C=C2O)=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=C1	4992.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #15	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)=CC(O[Si](C)(C)C)=C3)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4865.3	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #150	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O)=CC(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O	4986.6	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #151	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O)=CC(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O	4945.2	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #152	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O)=CC(O[Si](C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C	4962.7	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #153	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C=C2O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=C1	4958.6	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #154	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C=C2O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=C1	4976.0	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #155	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C=C2O)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=C1	4979.7	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #156	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O)=CC(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4959.0	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #157	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C=C2O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=C1	4977.1	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #158	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C=C2O)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=C1	4946.1	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #159	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C=C2O)=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=C1	4996.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #16	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)=CC(O[Si](C)(C)C)=C3)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O	4957.2	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #160	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O)=CC(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O	4956.1	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #161	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O)=CC(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O	4904.1	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #162	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O)=CC(O[Si](C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C	4935.0	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #163	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C=C2O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=C1	4920.9	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #164	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C=C2O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=C1	4941.9	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #165	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C=C2O)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=C1	4944.3	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #166	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O)=CC(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O	5002.8	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #167	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O)=CC(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O	4961.0	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #168	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O)=CC(O[Si](C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C	4977.8	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #169	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C=C2O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=C1	4972.4	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #17	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)=CC(O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O	4903.4	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #170	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C=C2O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=C1	4992.7	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #171	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C=C2O)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=C1	4996.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #172	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=CC(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4992.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #173	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=CC(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5011.2	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #174	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=CC(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4973.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #175	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O)C=C2O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=C1	5004.1	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #176	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O)=C2)C(O)C(O)C1O	4984.1	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #177	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O)=C2)C(O[Si](C)(C)C)C(O)C1O	4978.8	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #178	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O)=C2)C(O)C(O[Si](C)(C)C)C1O	4928.9	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #179	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O)=C2)C(O)C(O)C1O[Si](C)(C)C	4952.1	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #18	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)=CC(O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C	4935.9	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #180	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O)=C2)C(O[Si](C)(C)C)C(O)C1O	5005.2	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #181	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O)=C2)C(O)C(O[Si](C)(C)C)C1O	4953.1	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #182	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O)=C2)C(O)C(O)C1O[Si](C)(C)C	4975.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #183	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4986.6	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #184	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5007.8	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #185	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4969.6	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #186	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O)=C2)C(O[Si](C)(C)C)C(O)C1O	5005.2	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #187	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O)=C2)C(O)C(O[Si](C)(C)C)C1O	4956.3	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #188	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O)=C2)C(O)C(O)C1O[Si](C)(C)C	4977.3	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #189	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4958.6	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #19	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4917.0	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #190	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4980.0	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #191	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4938.7	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #192	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5008.8	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #193	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5032.0	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #194	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4991.3	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #195	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5033.7	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #196	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O)=C2)C(O)C1O	4993.2	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #197	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O)=C2)C(O[Si](C)(C)C)C1O	4958.7	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #198	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O)=C2)C(O)C1O[Si](C)(C)C	4935.2	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #199	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O)=C2)C(O[Si](C)(C)C)C1O	4987.3	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C4O)C=C3O)=CC(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4921.6	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #20	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O	5002.4	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #200	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C3)C(O)=C2)C(O[Si](C)(C)C)C1O	4961.1	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #201	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C3)C(O)=C2)C(O)C1O	4992.3	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #202	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O)=C2)C(O[Si](C)(C)C)C1O	4988.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #203	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O)=C2)C(O)C1O[Si](C)(C)C	4963.0	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #204	C[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C3)C(O)=C2)C1O	4967.1	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #205	C[Si](C)(C)OC1C(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C3)C(O)=C2)OC(CO)C(O)C1O	5015.6	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #206	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C3)C(O)=C2)C(O[Si](C)(C)C)C1O	4987.3	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #207	C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C3)C(O)=C2)C(O)C1O[Si](C)(C)C	4960.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #208	C[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O)=C2)C1O	4968.3	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #209	C[Si](C)(C)OC1C(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O)=C2)OC(CO)C(O)C1O[Si](C)(C)C	4987.6	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #21	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O	4958.6	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #210	C[Si](C)(C)OC1C(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O)=C2)OC(CO)C(O)C1O	5016.9	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #22	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C	4978.9	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #23	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O)C(O)C4O)=CC(O[Si](C)(C)C)=C3)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O	4944.3	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #24	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O)C(O)C4O)=CC(O[Si](C)(C)C)=C3)C(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O	4887.2	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #25	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O)C(O)C4O)=CC(O[Si](C)(C)C)=C3)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C	4921.4	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #26	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O)C(O)C4O)=CC(O[Si](C)(C)C)=C3)C(O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4989.7	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #27	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O)C(O)C4O)=CC(O[Si](C)(C)C)=C3)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5006.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #28	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O)C(O)C4O)=CC(O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4967.6	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #29	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O)=C2)C(O)C(O)C1O	4954.3	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O[Si](C)(C)C)C=C3O)=CC(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4968.1	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #30	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O)=C2)C(O)C(O)C1O	4995.1	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #31	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C4O)C=C3O[Si](C)(C)C)=C2)C(O)C(O)C1O	4889.7	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #32	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C4O)C=C3O)=C2)C(O[Si](C)(C)C)C(O)C1O	4982.6	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #33	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C4O)C=C3O)=C2)C(O)C(O[Si](C)(C)C)C1O	4937.1	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #34	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C4O)C=C3O)=C2)C(O)C(O)C1O[Si](C)(C)C	4954.3	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #35	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O)=C2)C(O)C(O)C1O	4976.1	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #36	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C4O)C=C3O[Si](C)(C)C)=C2)C(O)C(O)C1O	4861.7	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #37	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C4O)C=C3O)=C2)C(O[Si](C)(C)C)C(O)C1O	4965.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #38	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C4O)C=C3O)=C2)C(O)C(O[Si](C)(C)C)C1O	4912.8	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #39	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C4O)=C3)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O	4937.1	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O)C=C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4882.2	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #40	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O[Si](C)(C)C)C=C3O[Si](C)(C)C)=C2)C(O)C(O)C1O	4911.2	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #41	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O[Si](C)(C)C)C=C3O)=C2)C(O[Si](C)(C)C)C(O)C1O	5010.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #42	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C4O)=C3)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O	4966.9	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #43	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C4O)=C3)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O	4983.4	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #44	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O[Si](C)(C)C)=C3)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4908.7	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #45	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C4O)=C3)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4861.7	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #46	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C4O)=C3)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4890.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #47	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O)C1O	4996.8	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #48	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O)C1O	4975.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #49	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C3)C(O)=C2)C(O)C(O)C1O	4956.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O)C1O	4968.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #50	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O)C1O	4983.7	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #51	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C3)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4889.8	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #52	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C3)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O	4979.6	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #53	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C3)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O	4928.1	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #54	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C3)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C	4951.9	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #55	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=C3)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4903.8	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #56	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=C3)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O	5004.4	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #57	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O	4950.7	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #58	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C	4973.4	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #59	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)=C3)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O	4935.9	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C4O)=CC(O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O)C1O	4925.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #60	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)=C3)C(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O	4887.6	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #61	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)=C3)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C	4916.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #62	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)=C3)C(O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4985.8	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #63	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)=C3)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5008.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #64	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)=C3)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4966.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #65	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C3)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4909.7	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #66	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C3)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O	5003.3	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #67	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O	4952.9	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #68	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C	4974.8	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #69	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)=C3)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O	4896.9	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C4O)=CC(O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O)C1O	4945.3	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #70	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)=C3)C(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O	4845.2	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #71	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)=C3)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C	4877.4	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #72	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)=C3)C(O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4959.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #73	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)=C3)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4980.7	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #74	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)=C3)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4936.8	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #75	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)=C3)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O	4949.6	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #76	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)=C3)C(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O	4898.9	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #77	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)=C3)C(O[Si](C)(C)C)=C2)C(O)C(O)C1O[Si](C)(C)C	4925.9	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #78	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)=C3)C(O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5008.2	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #79	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)=C3)C(O)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5031.3	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #8	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=CC(O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O)C1O	4939.9	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #80	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4988.0	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #81	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4938.8	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #82	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O[Si](C)(C)C)=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4954.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #83	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O[Si](C)(C)C)=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4918.4	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #84	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O)=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5036.3	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #85	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	4960.6	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #86	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C=C2O[Si](C)(C)C)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	4911.6	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #87	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O[Si](C)(C)C)=C2)C(O)C(O)C1O	4890.7	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #88	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=C1	4911.6	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #89	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=C1	4864.4	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #9	C[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3)C(O)=C2)C(O)C(O)C1O	4955.3	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #90	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=C1	4919.4	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #91	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C=C2O[Si](C)(C)C)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	4930.8	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #92	C[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O[Si](C)(C)C)=C2)C(O)C(O)C1O	4904.5	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #93	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=C1	4929.7	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #94	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=C1	4887.2	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #95	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=C1	4939.4	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #96	C[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2)C(O)C(O)C1O	4909.9	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #97	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C=C2O[Si](C)(C)C)=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=C1	4943.0	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #98	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C=C2O[Si](C)(C)C)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=C1	4895.1	Semi standard non polar	33892256
cis-Mulberroside A,4TMS,isomer #99	C[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C=C2O[Si](C)(C)C)=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=C1	4950.4	Semi standard non polar	33892256
cis-Mulberroside A,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O)=C2)C(O)C(O)C1O	5441.3	Semi standard non polar	33892256
cis-Mulberroside A,1TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O)=C2)C(O)C1O	5485.3	Semi standard non polar	33892256
cis-Mulberroside A,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5459.2	Semi standard non polar	33892256
cis-Mulberroside A,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O)C=C2O)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5497.4	Semi standard non polar	33892256
cis-Mulberroside A,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=C2)C(O)C(O)C1O	5441.4	Semi standard non polar	33892256
cis-Mulberroside A,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=C2)C(O)C1O	5485.4	Semi standard non polar	33892256
cis-Mulberroside A,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=C2)C1O	5480.1	Semi standard non polar	33892256
cis-Mulberroside A,1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1C(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=C2)OC(CO)C(O)C1O	5499.5	Semi standard non polar	33892256
cis-Mulberroside A,1TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1C(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O)=C2)OC(CO)C(O)C1O	5502.2	Semi standard non polar	33892256
cis-Mulberroside A,1TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O)=C2)C1O	5480.4	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(OC4OC(CO)C(O)C(O)C4O)=CC(O[Si](C)(C)C(C)(C)C)=C3)C(O)=C2)C(O)C(O)C1O	5556.1	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5535.3	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5521.0	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5547.8	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O)C=C2O[Si](C)(C)C(C)(C)C)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5579.7	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O[Si](C)(C)C(C)(C)C)=C2)C(O)C(O)C1O	5503.7	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)=C1	5535.7	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)=C1	5519.5	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC=C1/C=C\C1=CC(O)=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)=C1	5546.0	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)C=C2O)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5571.3	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)C=C2O)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5560.7	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C4O)C=C3O)=C2)C(O)C(O)C1O	5518.9	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)C=C2O)=CC(OC2OC(CO)C(O)C(O)C2O)=C1	5588.1	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=CC(O[Si](C)(C)C(C)(C)C)=C2)C(O)C(O)C1O	5556.5	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O)C=C2O)=CC(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)=C1	5571.0	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O)C=C2O)=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)=C1	5564.2	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC1=CC(/C=C\C2=CC=C(OC3OC(CO)C(O)C(O)C3O)C=C2O)=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)=C1	5589.1	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C=C3O)=C2)C(O)C(O)C1O	5533.9	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C=C3O)=C2)C(O)C(O)C1O	5521.9	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C=C3O)=C2)C(O)C(O)C1O	5554.0	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=C2)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	5575.1	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=C2)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	5561.6	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)=C3)C(O)=C2)C(O)C(O)C1O	5534.1	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=C2)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	5540.8	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C=C3O)=C2)C(O)C1O	5548.6	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C=C3O)=C2)C(O)C1O	5534.9	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C=C3O)=C2)C(O)C1O	5571.7	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=C2)C(O[Si](C)(C)C(C)(C)C)C1O	5579.1	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=C2)C(O)C1O[Si](C)(C)C(C)(C)C	5563.0	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #36	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)=C3)C(O)=C2)C(O)C1O	5535.1	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #37	CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C=C3O)=C2)C1O	5517.8	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #38	CC(C)(C)[Si](C)(C)OC1C(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)=C3)C(O)=C2)OC(CO)C(O)C1O	5554.1	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #39	CC(C)(C)[Si](C)(C)OC1C(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)=C2)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	5590.3	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)=C3)C(O)=C2)C(O)C(O)C1O	5522.4	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #40	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)=C3)C(O)=C2)C(O)C1O	5570.6	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #41	CC(C)(C)[Si](C)(C)OC1C(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C=C3O)=C2)OC(CO)C(O)C1O	5553.0	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #42	CC(C)(C)[Si](C)(C)OC1C(OC2=CC(O)=CC(/C=C\C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C=C3O)=C2)OC(CO)C(O)C1O	5590.4	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #43	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O)=C2)C(O[Si](C)(C)C(C)(C)C)C1O	5578.7	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #44	CC(C)(C)[Si](C)(C)OC1C(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O)=C2)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	5591.3	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #45	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O)=C2)C(O)C1O[Si](C)(C)C(C)(C)C	5560.5	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)=C3)C(O)=C2)C(O)C(O)C1O	5554.0	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O[Si](C)(C)C(C)(C)C)=C2)C(O)C(O)C1O	5503.7	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O)=C2)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	5574.0	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O)=C2)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	5560.8	Semi standard non polar	33892256
cis-Mulberroside A,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(/C=C\C3=CC(O)=CC(OC4OC(CO)C(O)C(O)C4O)=C3)C(O)=C2)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	5540.7	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Mulberroside A GC-MS (Non-derivatized) - 70eV, Positive	splash10-0zfr-2400690000-1634534f000d30e9c462	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Mulberroside A GC-MS (1 TMS) - 70eV, Positive	splash10-00di-6820139000-4f44692f9fd736c02a81	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Mulberroside A GC-MS ("cis-Mulberroside A,1TMS,#1" TMS) - 70eV, Positive	Not Available	2021-10-14	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Mulberroside A GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Mulberroside A GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Mulberroside A GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Mulberroside A GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Mulberroside A GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Mulberroside A GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Mulberroside A GC-MS (TMS_1_8) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Mulberroside A GC-MS (TMS_1_9) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Mulberroside A GC-MS (TMS_1_10) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Mulberroside A GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Mulberroside A GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Mulberroside A GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Mulberroside A GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Mulberroside A GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Mulberroside A GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Mulberroside A GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Mulberroside A GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Mulberroside A GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Mulberroside A GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Mulberroside A GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Mulberroside A GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-Mulberroside A 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 - cis-Mulberroside A 10V, Positive-QTOF	splash10-0k9i-0198870000-76c9024d9189c0607779	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Mulberroside A 20V, Positive-QTOF	splash10-000f-0193100000-db082d65a20b428b509d	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Mulberroside A 40V, Positive-QTOF	splash10-0006-1392100000-2106604dc8204fef39b8	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Mulberroside A 10V, Negative-QTOF	splash10-0670-1223790000-e2559cbae0ec71ad8b55	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Mulberroside A 20V, Negative-QTOF	splash10-0a4r-1259730000-e7f183fbb345a4cad6ec	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Mulberroside A 40V, Negative-QTOF	splash10-0006-2191100000-bc3c4453ad45a3052251	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Mulberroside A 10V, Positive-QTOF	splash10-05mt-0296780000-9cea616adea841b11731	2021-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Mulberroside A 20V, Positive-QTOF	splash10-0002-0243930000-17e02290662b03d676c8	2021-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Mulberroside A 40V, Positive-QTOF	splash10-0a4j-8751910000-ec54362219ad9df4d391	2021-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Mulberroside A 10V, Negative-QTOF	splash10-066u-0350490000-ee71818c08d13a41b7b8	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Mulberroside A 20V, Negative-QTOF	splash10-0a4u-3151940000-2b67bbb3162bda350641	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-Mulberroside A 40V, Negative-QTOF	splash10-0006-0090000000-502d911c7cb3bdced749	2021-09-25	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-30	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-30	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

FDB008389

KNApSAcK ID

C00057132

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131751187

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1827641

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 cis-Mulberroside A (HMDB0031726)

MOL for HMDB0031726 (cis-Mulberroside A)

3D MOL for HMDB0031726 (cis-Mulberroside A)

3D SDF for HMDB0031726 (cis-Mulberroside A)

3D-SDF for HMDB0031726 (cis-Mulberroside A)

PDB for HMDB0031726 (cis-Mulberroside A)

3D PDB for HMDB0031726 (cis-Mulberroside A)

SMILES for HMDB0031726 (cis-Mulberroside A)

INCHI for HMDB0031726 (cis-Mulberroside A)

Structure for HMDB0031726 (cis-Mulberroside A)

3D Structure for HMDB0031726 (cis-Mulberroside A)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra